500D Service Manual

GE Medical Systems
gemedical.com
Technical
Publication
Direction 2360588-100
Revision 10
Book 1
Pages 1 - 172
of 3
GE Medical Systems
Precision 500D ®, R&F System Manual
Table of Contents, Preface, Chapters 1, 2 & 3

Introduction, Theory and Tube Specifications
Copyright © 2002, 2003, 2004 and 2005

by General Electric Company. All Rights Reserved
GE MEDICAL SYSTEMS
DIRECTION 2360588-100, REVISION 10 PRECISION 500D ®, R&F SYSTEM MANUAL
This page left intentionally blank
Published by GE Medical Systems

Editor in Chief (CEM)
Rick Fauska
Engineering and Technical
Nathan Hoyle Rita Pochert
Tom Voelzs Jon Omernick
Ojas Buck Andy Argersinger
Gulnar Siddiqi Richard Lemminger
John David Gary Hammel
Dan Beetcher
Page 2
GE MEDICAL SYSTEMS
LEGAL NOTES
TRADEMARKS
Adobe, the Adobe logo, Acrobat, the Acrobat logo, Exchange, and PostScript are trademarks of
Adobe Systems Incorporated or its subsidiaries and may be registered in certain jurisdictions.
Microsoft is a registered trademark and Windows is a trademark of Microsoft Corporation.
All other products and their name brands are trademarks of their respective holders.
COPYRIGHTS
All Material, Copyright © 2002, 2003, 2004 and 2005 by General Electric Company. All rights
reserved.
Legal Notes Page 3

GE MEDICAL SYSTEMS
Page 4 Legal Notes

GE MEDICAL SYSTEMS
IMPORTANT PRECAUTIONS
LANGUAGE
• THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY.

• IF A CUSTOMER’S SERVICE PROVIDER REQUIRES A LANGUAGE OTHER THAN
ENGLISH, IT IS THE CUSTOMER’S RESPONSIBILITY TO PROVIDE TRANSLATION
SERVICES.
• DO NOT ATTEMPT TO SERVICE THE EQUIPMENT UNLESS THIS SERVICE MANUAL
HAS BEEN CONSULTED AND IS UNDERSTOOD.
• FAILURE TO HEED THIS WARNING MAY RESULT IN INJURY TO THE SERVICE
PROVIDER, OPERATOR OR PATIENT FROM ELECTRIC SHOCK, MECHANICAL OR
OTHER HAZARDS.
• CE MANUEL DE MAINTENANCE N’EST DISPONIBLE QU’EN ANGLAIS.

• SI LE TECHNICIEN DU CLIENT A BESOIN DE CE MANUEL DANS UNE AUTRE LANGUE
QUE L’ANGLAIS, C’EST AU CLIENT QU’IL INCOMBE DE LE FAIRE TRADUIRE.
• NE PAS TENTER D’INTERVENTION SUR LES ÉQUIPEMENTS TANT QUE LE MANUEL
SERVICE N’A PAS ÉTÉ CONSULTÉ ET COMPRIS.
• LE NON-RESPECT DE CET AVERTISSEMENT PEUT ENTRAÎNER CHEZ LE
TECHNICIEN, L’OPÉRATEUR OU LE PATIENT DES BLESSURES DUES À DES
DANGERS ÉLECTRIQUES, MÉCANIQUES OU AUTRES.
• DIESES KUNDENDIENST-HANDBUCH EXISTIERT NUR IN ENGLISCHER SPRACHE.

• FALLS EIN FREMDER KUNDENDIENST EINE ANDERE SPRACHE BENÖTIGT, IST ES
AUFGABE DES KUNDEN FÜR EINE ENTSPRECHENDE ÜBERSETZUNG ZU SORGEN.
• VERSUCHEN SIE NICHT, DAS GERÄT ZU REPARIEREN, BEVOR DIESES
KUNDENDIENST-HANDBUCH ZU RATE GEZOGEN UND VERSTANDEN WURDE.
• WIRD DIESE WARNUNG NICHT BEACHTET, SO KANN ES ZU VERLETZUNGEN DES
KUNDENDIENSTTECHNIKERS, DES BEDIENERS ODER DES PATIENTEN DURCH
ELEKTRISCHE SCHLÄGE, MECHANISCHE ODER SONSTIGE GEFAHREN KOMMEN.
• ESTE MANUAL DE SERVICIO SÓLO EXISTE EN INGLÉS.

• SI ALGÚN PROVEEDOR DE SERVICIOS AJENO A GEMS SOLICITA UN IDIOMA QUE
NO SEA EL INGLÉS, ES RESPONSABILIDAD DEL CLIENTE OFRECER UN SERVICIO
DE TRADUCCIÓN.
• NO SE DEBERÁ DAR SERVICIO TÉCNICO AL EQUIPO, SIN HABER CONSULTADO Y
COMPRENDIDO ESTE MANUAL DE SERVICIO.
• LA NO OBSERVANCIA DEL PRESENTE AVISO PUEDE DAR LUGAR A QUE EL
PROVEEDOR DE SERVICIOS, EL OPERADOR O EL PACIENTE SUFRAN LESIONES
PROVOCADAS POR CAUSAS ELÉCTRICAS, MECÁNICAS O DE OTRA NATURALEZA.
Important Precautions Page 5

GE MEDICAL SYSTEMS
• ESTE MANUAL DE ASSISTÊNCIA TÉCNICA SÓ SE ENCONTRA DISPONÍVEL EM

INGLÊS.
• SE QUALQUER OUTRO SERVIÇO DE ASSISTÊNCIA TÉCNICA, QUE NÃO A GEMS,
SOLICITAR ESTES MANUAIS NOUTRO IDIOMA, É DA RESPONSABILIDADE DO
CLIENTE FORNECER OS SERVIÇOS DE TRADUÇÃO.
• NÃO TENTE REPARAR O EQUIPAMENTO SEM TER CONSULTADO E
COMPREENDIDO ESTE MANUAL DE ASSISTÊNCIA TÉCNICA.
• O NÃO CUMPRIMENTO DESTE AVISO PODE POR EM PERIGO A SEGURANÇA DO
TÉCNICO, OPERADOR OU PACIENTE DEVIDO A‘ CHOQUES ELÉTRICOS,
MECÂNICOS OU OUTROS.
• IL PRESENTE MANUALE DI MANUTENZIONE È DISPONIBILE SOLTANTO IN INGLESE.

• SE UN ADDETTO ALLA MANUTENZIONE ESTERNO ALLA GEMS RICHIEDE IL
MANUALE IN UNA LINGUA DIVERSA, IL CLIENTE È TENUTO A PROVVEDERE
DIRETTAMENTE ALLA TRADUZIONE.
• SI PROCEDA ALLA MANUTENZIONE DELL’APPARECCHIATURA SOLO DOPO AVER
CONSULTATO IL PRESENTE MANUALE ED AVERNE COMPRESO IL CONTENUTO.
• NON TENERE CONTO DELLA PRESENTE AVVERTENZA POTREBBE FAR COMPIERE
OPERAZIONI DA CUI DERIVINO LESIONI ALL’ADDETTO ALLA MANUTENZIONE,
ALL’UTILIZZATORE ED AL PAZIENTE PER FOLGORAZIONE ELETTRICA, PER URTI
MECCANICI OD ALTRI RISCHI.
DAMAGE IN TRANSPORTATION
All packages should be closely examined at time of delivery. If damage is apparent write “Damage
In Shipment” on ALL copies of the freight or express bill BEFORE delivery is accepted or “signed
for” by a GE representative or hospital receiving agent. Whether noted or concealed, damage
MUST be reported to the carrier immediately upon discovery, or in any event, within 14 days after
Page 6 Important Precautions

GE MEDICAL SYSTEMS
receipt, and the contents and containers held for inspection by the carrier. A transportation
company will not pay a claim for damage if an inspection is not requested within this 14 day period.
Call Traffic and Transportation, Milwaukee, WI (414) 785 5052 or 8*323 5052 immediately after
damage is found. At this time be ready to supply name of carrier, delivery date, consignee name,
freight or express bill number, item damaged and extent of damage.
Complete instructions regarding claim procedure are found in Section S of the Policy And
Procedures Bulletins.
14 July 1993
CERTIFIED ELECTRICAL CONTRACTOR STATEMENT

All electrical Installations that are preliminary to positioning of the equipment at the site prepared
for the equipment shall be performed by licensed electrical contractors. In addition, electrical feeds
into the Power Distribution Unit shall be performed by licensed electrical contractors. Other
connections between pieces of electrical equipment, calibrations and testing shall be performed by
qualified GE Medical personnel. The products involved (and the accompanying electrical
installations) are highly sophisticated, and special engineering competence is required. In
performing all electrical work on these products, GE will use its own specially trained field
engineers. All of GE’s electrical work on these products will comply with the requirements of the
applicable electrical codes.
The purchaser of GE equipment shall only utilize qualified personnel (i.e., GE’s field engineers,
personnel of third-party service companies with equivalent training, or licensed electricians) to
perform electrical servicing on the equipment.
IMPORTANT...X-RAY PROTECTION
X-ray equipment if not properly used may cause injury. Accordingly, the instructions herein
contained should be thoroughly read and understood by everyone who will use the equipment
before you attempt to place this equipment in operation. The General Electric Company, Medical
Systems Group, will be glad to assist and cooperate in placing this equipment in use.
Although this apparatus incorporates a high degree of protection against x-radiation other than the
useful beam, no practical design of equipment can provide complete protection. Nor can any
practical design compel the operator to take adequate precautions to prevent the possibility of any
persons carelessly exposing themselves or others to radiation.
It is important that anyone having anything to do with x-radiation be properly trained and fully
acquainted with the recommendations of the National Council on Radiation Protection and
Measurements as published in NCRP Reports available from NCRP Publications, 7910 Woodmont
Avenue, Room 1016, Bethesda, Maryland 20814, and of the International Commission on
Radiation Protection, and take adequate steps to protect against injury.
The equipment is sold with the understanding that the General Electric Company, Medical Systems
Group, its agents, and representatives have no responsibility for injury or damage which may result
from improper use of the equipment.
Various protective materials and devices are available. It is urged that such materials or devices be used.
OMISSIONS & ERRORS

Customers, please contact your GE Sales or Service representatives.
GE personnel, please use the GEMS CQA Process to report all omissions, errors, and defects in
this publication.
Important Precautions Page 7

GE MEDICAL SYSTEMS
Page 8 Important Precautions

GE MEDICAL SYSTEMS
Revision History
Revision Date Reason for change
0 Nov. 6, 2002 Additions: M4 Release
Resolved: XRYge39512, XRYge39511, XRYge39510,
XRYge40945, XRYge39494, XRYge31982,
XRYge38672, XRYge41346
1 Nov. 25, 2002 Resolved: XRYge39218
Deletions: M3 Work arounds
Revisions: Error Message Sections 1 and 2, Jedi T/S for M4
2 Dec. 17, 2002 Changes: Generator Diagnostics: Inverter Gate Test, Short
Circuit Test, AEC and 2nd Tube Switch Diagnostics
updated.
3 May 21, 2003 Changes: Minor changes made.
Resolved: XRYge39062 (Text added to error code 8000022
recommended actions).
Additions: M5 Material (Broadband, Error codes)
4 July 23, 2003 Changes: Added “d” to the word close in error message
8000022.
5 Nov. 15, 2003 Additions: New acroymns.
Changes: Corrected spelling to “recommended” on error
message prefix.
6 Feb. 9, 2004 Resolved: PQR1271629 (Problem description completeness
improved and inverter added as potential cause in
error message 360-1200).
PSR13015226 - The word “NICHT” removed from
the German translation of “Do not attempt...” in
language statements.
Changes: Convention used to communicate hazards modified
to comply with ISO 3864 and ANSI Z535 standards.
7 July 21, 2004 Resolved: XRYge50435 - Three new generator error codes
added for SW release 13.x.x.
Additions: New and changed SW Error Messages for hardware
and SW release 13.x.x. ION chambers tests added to
Diagnostic User Guide for SW release 13.x.x. New
communication test screens for SW 13.x.x.
8 Feb. 11, 2005 Additions: New Digital computer (Saturn V2) information.
9 Aug. 30, 2005 Changes: ECR/ECO2012594 - New drawings showing system
with and without media converter shown, because it’s
no longer used in current systems.
10 13JAN2009 Changes: Changed title of Figure 2-85 and added additional RT
Bus Block Diagram Figure 2-86 for IUI Replacement
PC.
Revision History Page 9

GE MEDICAL SYSTEMS
Page 10 Revision History

GE MEDICAL SYSTEMS
List of Effected Pages
PAGES REVISION PAGES REVISION

1 through 660 10
List of Effected Pages Page 11

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Page 12 List of Effected Pages

GE MEDICAL SYSTEMS
Table of Contents
Preface
Publication Conventions ...................................................................................... 23
Section 1.0
Safety & Hazard Information ........................................................................... 23
1.1 Hazard Messages............................................................................................................ 23
1.2 Text Format of Signal Words ........................................................................................... 23
1.3 Symbols and Pictorials Used ........................................................................................... 24
Section 2.0
Publication Conventions ................................................................................. 25
2.1 General Paragraph and Character Styles........................................................................ 25
2.2 Page Layout..................................................................................................................... 25
2.3 Computer Screen Output/Input Text Character Styles .................................................... 26
2.4 Buttons, Switches and Keyboard Inputs (Hard & Soft Keys) ........................................... 26
Chapter 1
System Overview & Safety ................................................................................... 27
Section 1.0
Features ............................................................................................................ 27
1.1 Product Overview ............................................................................................................ 27
1.2 Acquisition Modes............................................................................................................ 27
1.2.1 Digital Record ..................................................................................................... 27
1.2.1.1 AEC ................................................................................................. 27
1.2.1.2 Fixed Time....................................................................................... 27
1.2.1.3 Subtraction (DSA) ........................................................................... 28
1.2.2 Digital Fluoro....................................................................................................... 28
1.2.2.1 Continuous ...................................................................................... 28
1.2.2.2 Pulsed ............................................................................................. 28
1.2.3 Radiography (Overhead Tube) ........................................................................... 28
1.2.3.1 AEC ................................................................................................. 28
1.2.3.2 Fixed Time....................................................................................... 28
Section 2.0
System Components........................................................................................ 28
Section 3.0
System Shutdown for Service......................................................................... 29
3.1 Before you Begin ............................................................................................................. 29
3.2 Procedure ........................................................................................................................ 30
Chapter 2
Theory of System Operation ................................................................................ 33
Section 1.0
Interactive User Interface (IUI) Subsystem .................................................... 34
Table of Contents Page 13

GE MEDICAL SYSTEMS
Section 2.0
Systems Cabinet............................................................................................... 34
2.1 Components.................................................................................................................... 34
2.2 Systems Cabinet Internal Connections ........................................................................... 35
2.3 Applications Software...................................................................................................... 35
2.4 Digital System “Saturn” ................................................................................................... 37
2.4.1 Saturn V1 (old style), 2290479........................................................................... 37
2.4.1.1 Digital System Block Diagram ........................................................ 37
2.4.1.2 Components ................................................................................... 37
2.4.1.3 PCI Interface................................................................................... 38
2.4.1.4 Image Bus....................................................................................... 38
2.4.1.5 Gitane Board................................................................................... 38
2.4.1.6 Image Correction Board (ICB) ........................................................ 38
2.4.1.7 Camera Control Unit (CCU)............................................................ 39
2.4.1.8 Image Memory Board (IMB) ........................................................... 39
2.4.1.9 Image Display Board (IDB) ............................................................. 39
2.4.1.10 Single Board Computer (SBC)........................................................ 39
2.4.1.11 Static Reference Board................................................................... 39
2.4.1.12 Scan Converter Board (SCB) ......................................................... 39
2.4.1.13 Digital Host Control Board (DHC) ................................................... 40
2.4.1.14 Passive Backplane ......................................................................... 40
2.4.1.15 Image Acquisition Board (IAB)........................................................ 40
2.4.1.16 Image Review ................................................................................. 40
2.4.1.17 Image Acquisition, Storage, and Display ........................................ 40
2.4.1.18 Real Time Fluoro Display ............................................................... 40
2.4.1.19 Digital Record/Pulsed Fluoro Acquisition and Storage ................... 40
2.4.1.20 Fluoro Loop Store ........................................................................... 40
2.4.1.21 Static Reference Display ................................................................ 40
2.4.1.22 External Device Transfer ................................................................ 41
2.4.2 Saturn V2 (new style), 2407276 ......................................................................... 41
2.4.2.1 Digital System Block Diagram ........................................................ 41
2.4.2.2 Saturn V2 Circuit Board Changes................................................... 42
Digital Acquisition Board (DAB) .................................................. 42
Digital Memory Board (DMB) ...................................................... 42
Digital Display Board (DDB)........................................................ 43
Digital Host Control Board II (DHCII) .......................................... 43
2.5 System Controller............................................................................................................ 43
2.6 Accessory Rack .............................................................................................................. 44
2.7 X-Ray “Generator”........................................................................................................... 45
2.7.1 Components....................................................................................................... 45
2.7.2 Generator Block Diagram................................................................................... 46
2.7.3 Auxiliary 1 Unit ................................................................................................... 46
2.7.3.1 Low Voltage Power Supply............................................................. 47
2.7.3.2 Filament Heater Boards................................................................. 47
2.7.4 Auxiliary 2 Unit ................................................................................................... 47
2.7.5 Power Unit.......................................................................................................... 48
2.7.6 AEC and Generic Interface Boards .................................................................... 48
2.7.7 kV Control Board................................................................................................ 49
2.8 AC/DC Unit..................................................................................................................... 50
2.9 Power Distribution Unit (PDU)......................................................................................... 50
2.9.1 “Main” supply from Hospital ............................................................................... 51
2.9.2 The Mains Switch ............................................................................................... 51
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2.9.3 Power Peak-Up .................................................................................................. 51
2.9.4 PDU.................................................................................................................... 51
2.9.5 PDU IO Logic Board........................................................................................... 51
2.9.6 Operational Power States .................................................................................. 51
2.9.6.1 Power-On........................................................................................ 52
2.9.6.2 Standby........................................................................................... 52
2.9.6.3 Shutdown........................................................................................ 53
2.9.6.4 Emergency Off................................................................................ 54
2.9.6.5 Tableside Emergency Off ............................................................... 55
2.9.6.6 Power Loss ..................................................................................... 56
2.9.6.7 Reset .............................................................................................. 57
2.9.6.8 UPS / Remaining power interlock. .................................................. 57
Section 3.0
Generator “Jedi”............................................................................................... 57
3.1 INTRODUCTION............................................................................................................. 57
3.1.1 Standard features............................................................................................... 58
3.1.2 Typical Applications ........................................................................................... 58
3.1.2.1 Rad ................................................................................................. 58
3.1.2.2 Surgery ........................................................................................... 58
3.1.2.3 RF ................................................................................................... 58
3.1.2.4 VASCULAR/CARDIAC ................................................................... 59
3.1.2.5 CT ................................................................................................... 59
3.1.3 Architecture ........................................................................................................ 59
3.2 Technology Overview...................................................................................................... 61
3.2.1 kV Control .......................................................................................................... 61
3.2.1.1 Introduction ..................................................................................... 61
3.2.1.2 CPU core ........................................................................................ 61
First generation ........................................................................... 61
Second generation:..................................................................... 61
3.2.1.3 Standard interface to system interface ........................................... 62
3.2.1.4 Control bus ..................................................................................... 62
3.2.1.5 Exposure control............................................................................. 62
CPU Core (Exposure control master) ......................................... 62
FPGA .......................................................................................... 63
CPU ............................................................................................ 63
3.2.1.6 HV power inverter control ............................................................... 63
3.2.1.7 HV chain measure and safeties...................................................... 64
3.2.2 HV power Inverter and HV Tank function........................................................... 65
3.2.2.1 Introduction ..................................................................................... 65
3.2.2.2 HV power Inverter principle ............................................................ 65
3.2.2.3 HV Tank principle ........................................................................... 66
3.2.3 System interface ................................................................................................ 66
3.2.3.1 CT interface .................................................................................... 67
3.2.3.2 RAD interface ................................................................................. 67
INTERFACE Bucky, Function principle....................................... 67
INTERFACE w/room door signals .............................................. 67
Console and service terminal communication ............................ 67
3.2.3.3 RF FUNCTION (used for PRECISION 500D)................................. 67
3.2.3.4 AEC ................................................................................................ 68
AEC FUNCTION ......................................................................... 68
AEC Function Principle: .............................................................. 68
3.2.4 Heater function ................................................................................................... 68

GE MEDICAL SYSTEMS
3.2.4.1 Introduction ..................................................................................... 68
3.2.4.2 1 Inverter Heater............................................................................. 69
3.2.5 Rotation function ................................................................................................ 70
3.2.5.1 Introduction ..................................................................................... 70
3.2.5.2 High speed rotation......................................................................... 70
Rotation Principle........................................................................ 70
Tube Cooling............................................................................... 72
3.2.6 Switching Tube Function .................................................................................... 72
3.2.7 EMC filter function .............................................................................................. 73
3.2.7.1 Introduction ..................................................................................... 73
3.2.7.2 3 phase EMC filter .......................................................................... 73
3.2.8 AC/DC ................................................................................................................ 73
3.2.8.1 Introduction ..................................................................................... 73
3.2.8.2 Single phase AC/DC....................................................................... 73
3.2.8.3 3 phases max power AC/DC .......................................................... 74
3.2.9 Low voltage power supply (standard LVPS) ...................................................... 74
3.2.10 Low Voltage power supply 400W (LVPS400) .................................................... 74
3.2.10.1 Circuits description. ........................................................................ 74
AC/DC Stage .............................................................................. 75
Auxiliary fly-back inverter ............................................................ 75
Main inverter ............................................................................... 75
Regulators................................................................................... 76
Control and Auxiliary Circuits...................................................... 76
3.2.11 Generator Software ............................................................................................ 76
3.2.11.1 System Communication.................................................................. 76
3.2.11.2 Exposure Sequencing..................................................................... 77
3.2.11.3 Tube/generator Thermal Protection................................................ 77
3.2.11.4 Calibrations..................................................................................... 77
3.2.11.5 Tube Spits Counting ....................................................................... 77
3.2.11.6 Generator Usage Tracking ............................................................. 78
3.2.11.7 Diagnostics ..................................................................................... 79
3.3 Functional Description..................................................................................................... 79
3.3.1 Power-on Sequence........................................................................................... 79
3.3.2 kV function ......................................................................................................... 80
3.3.3 mA function ........................................................................................................ 81
3.3.4 Rotation function ................................................................................................ 82
3.3.5 Power Supplies Distribution ............................................................................... 82
3.3.6 Exception Handling ........................................................................................... 82
3.3.6.1 Diagnostics ..................................................................................... 82
Power on Diagnostics ................................................................. 82
Alive Diagnostics......................................................................... 83
3.3.6.2 Error Code Structure....................................................................... 83
Simplified Error code definition ................................................... 84
Generator Phase definition ......................................................... 84
Error class definition ................................................................... 84
Error code definition.................................................................... 85
3.4 Block Diagrams ............................................................................................................... 86
3.4.1 JEDI Generator / Functional Architecture .......................................................... 86
3.4.2 JEDI Generator / Np+ Functional Architecture................................................... 88
3.4.3 JEDI Generator / Tiger Functional Architecture ................................................. 89
3.4.4 JEDI Generator / Precision Functional Architecture........................................... 90
3.4.5 JEDI Generator / 68360 kV Control ................................................................... 91
3.4.6 JEDI Generator / PPC KV Control ..................................................................... 92

GE MEDICAL SYSTEMS
3.4.7 JEDI Generator / HV Power Inverter .................................................................. 93
3.4.8 JEDI Generator / HV Tank ................................................................................. 94
3.4.9 JEDI Generator / AEC Functions ....................................................................... 95
3.4.10 JEDI Generator / Inverter Heater ....................................................................... 96
3.4.11 JEDI Generator/ Rotation Function .................................................................... 97
3.4.12 JEDI generator / high speed rotation ................................................................. 98
3.4.13 JEDI generator / 3 phase EMC filter .................................................................. 99
3.4.14 JEDI generator / 3 phase mid power AC/DC ................................................... 100
3.4.15 JEDI generator / kV function ............................................................................ 101
3.4.16 JEDI generator / mA function ........................................................................... 102
3.4.17 JEDI generator / power supplies distribution.................................................... 103
3.4.18 JEDI generator / LVPS400 function ................................................................. 104
3.4.19 JEDI generator / Switch Tube function............................................................. 105
3.4.20 JEDI generator / Interface function: CT I/F ...................................................... 106
3.4.21 JEDI generator / Interface function: RAD I/F.................................................... 107
3.4.22 JEDI generator / Interface function: Generic I/F............................................... 108
3.5 Switches, Jumpers and LEDS....................................................................................... 109
3.5.1 GEN IF board ................................................................................................... 109
3.5.2 PPC KV CONTROL board ............................................................................... 110
3.5.3 QUAD SNUB board.......................................................................................... 111
3.5.4 GATE CMD board ............................................................................................ 112
3.5.5 KV MEASURE (Two Tubes board) .................................................................. 113
3.5.6 HEATER board ................................................................................................ 114
3.5.7 Rotation Board ................................................................................................. 115
3.5.8 TWO SWITCHING TUBES Board.................................................................... 116
3.5.9 LVPS400 Board ............................................................................................... 117
3.5.10 AC/DC 3 Phase board...................................................................................... 118
3.5.11 AEC Board V2.................................................................................................. 119
Section 4.0
Imaging System .............................................................................................. 119
4.1 Overview ....................................................................................................................... 119
4.2 CCD Camera................................................................................................................. 121
4.3 Imaging Chain ............................................................................................................... 123
4.3.1 Components..................................................................................................... 123
4.3.1.1 Spectral Filters.............................................................................. 123
4.3.1.2 Anti-Scatter Grid ........................................................................... 123
4.3.1.3 Image Intensifier (II)...................................................................... 123
4.3.1.4 Image Intensifier Tube .................................................................. 123
4.3.1.5 High Voltage Power Supply (HVPS)............................................. 124
4.3.1.6 Active Distortion Correction System (ADCS) ................................ 124
4.3.1.7 Optics............................................................................................ 124
4.3.1.8 Real time light measurement ........................................................ 124
4.3.1.9 NDF .............................................................................................. 124
4.3.1.10 IRIS............................................................................................... 124
4.3.1.11 TV Lens ........................................................................................ 124
4.3.1.12 CCD Camera ................................................................................ 125
4.3.1.13 Image Correction Board (ICB) ...................................................... 125
4.3.1.14 ABD (Automatic Brightness Detection)......................................... 125
4.3.1.15 LUT ............................................................................................... 125
4.3.1.16 Image Acquisition Board / Digital Acquisition Board..................... 125
4.3.1.17 Image Display Board / Digital Display Board ................................ 126

GE MEDICAL SYSTEMS
4.3.1.18 Optics Control Board (OCB) ......................................................... 126
4.3.1.19 PhotoDiode Board (PDB).............................................................. 126
4.3.2 Digital Radiographic Mode ............................................................................... 127
4.3.3 Digital Image .................................................................................................... 127
Section 5.0
Positioning System ........................................................................................ 128
5.1 Positioner Cabinet......................................................................................................... 128
5.1.1 Component Locations ...................................................................................... 128
5.1.2 Positioner Cabinet Components ...................................................................... 129
5.2 Application (Saber) Software ........................................................................................ 131
5.3 Movement Functions..................................................................................................... 131
5.3.1 Power Assist Longitudinal ................................................................................ 132
5.3.2 Power Assist Vertical ....................................................................................... 132
5.3.3 Positioner/Table Angulation ............................................................................. 133
5.3.4 Table-Top Longitudinal/Lateral Drive ............................................................... 134
5.3.5 Longitudinal and Lateral Power Assist locks .................................................... 134
5.3.6 IDD Console Screen ........................................................................................ 135
5.3.7 Prep/ Expose Buttons on the IDD/ Fluoro foot Switch ..................................... 135
5.3.8 Prep/Expose buttons on the Venus console. ................................................... 135
5.3.9 Grid/Cone Motion ............................................................................................. 135
5.3.10 Digital Servo Controller 2 Circuit Board (Used w/Table 2403791 Only)........... 136
5.3.10.1 Original DSC Assembly Compared to the DSC2 Circuit Board .... 136
5.3.10.2 Functional Operation .................................................................... 136
5.3.10.3 High-level Architecture Description............................................... 138
5.3.10.4 Theory of Operation...................................................................... 139
Motion Control........................................................................... 139
CAN Communications............................................................... 140
Digital and Analog I/O ............................................................... 141
4.6.4. Power Assist Handle....................................................... 141
Under Table Collimator ............................................................. 142
Power Supplies ......................................................................... 142
Diagnostics ............................................................................... 142
Calibration................................................................................. 142
Reset......................................................................................... 143
5.3.11 Bucky ............................................................................................................... 143
5.3.12 Cassette Sensing Tray..................................................................................... 143
5.3.13 Ion Chamber .................................................................................................... 143
5.3.14 Collimator & Blade ........................................................................................... 144
5.3.15 Spectral Filter ................................................................................................... 144
5.4 Positioner Cabinet Interconnects .................................................................................. 145
Section 6.0
System Communications............................................................................... 146
6.1 CAN Bus ....................................................................................................................... 146
6.1.1 History .............................................................................................................. 146
6.1.2 Advantages of CAN Networks.......................................................................... 146
6.1.3 Operation ......................................................................................................... 146
6.1.4 Overview .......................................................................................................... 147
6.2 RT Bus .......................................................................................................................... 149
6.2.1 Real Time (RT) Bus (System & Local) ............................................................. 149
6.2.2 System RT Bus Signals ................................................................................... 150
6.3 Ethernet......................................................................................................................... 152

GE MEDICAL SYSTEMS
Section 7.0
System Interconnects .................................................................................... 153
7.1 System Communications .............................................................................................. 153
7.2 Power Distribution ......................................................................................................... 154
7.2.1 High Voltage Distribution.................................................................................. 154
7.2.2 UPS.................................................................................................................. 154
7.2.3 120/230V Distribution ....................................................................................... 155
7.2.4 Three Phase Power ......................................................................................... 155
Section 8.0
Overhead Tube Suspension (OTS) ............................................................... 156
8.1 Introduction ................................................................................................................... 156
8.2 Console ......................................................................................................................... 156
8.3 Carriage ........................................................................................................................ 157
8.4 Collimator ...................................................................................................................... 157
8.4.1 Block Diagram .................................................................................................. 157
8.4.2 Collimator Bulb ................................................................................................. 158
8.4.3 Collimator Laser ............................................................................................... 158
8.4.4 Collimator Fuses .............................................................................................. 158
8.5 OTS Counterpoise Theory of Operation ....................................................................... 159
Chapter 3
MX100 Tube Specifications “Jedi 80RF2T” ...................................................... 163
Section 1.0
Introduction..................................................................................................... 163
Section 2.0
Parameters ...................................................................................................... 163
Section 3.0
kW Rating - Track protection......................................................................... 163
3.1 Small Focus (0.6), High Speed (10000rpm).................................................................. 164
3.2 Large Focus (1.0), High Speed (10000rpm) ................................................................. 165
3.3 Large Focus (1.25), High Speed (10000rpm) ............................................................... 166
Section 4.0
Casing Protection ........................................................................................... 167
Section 5.0
Anode Protection............................................................................................ 167
5.1 Heat Capacity................................................................................................................ 167
5.2 Anode cooling Curve..................................................................................................... 167
Section 6.0
Filament protection ........................................................................................ 168
6.1 mA limitation at low kV .................................................................................................. 168
6.2 Max mA ......................................................................................................................... 169
6.3 Filament Drive Level ..................................................................................................... 169

GE MEDICAL SYSTEMS
Chapter 4
Error Message Listings (Software/Firmware Revision 11.x.x) ........................ 175
Section 1.0
Before You Begin............................................................................................ 175
Section 2.0
Introduction to Error codes ........................................................................... 175
2.1 What are Error Codes ................................................................................................... 175
2.1.1 Applications Software....................................................................................... 176
2.1.2 Operating System Software ............................................................................. 176
2.2 Applications and System Error Reporting ..................................................................... 176
2.2.1 Error Display Management .............................................................................. 176
2.2.2 “Quick” Error Viewer......................................................................................... 177
2.3 Service Error Log Viewer .............................................................................................. 177
Section 3.0
System Error Message Listing ..................................................................... 178
3.1 02 XRAcqSync .............................................................................................................. 179
3.2 04 XRAppDir ................................................................................................................. 186
3.3 06 XRBeamForm .......................................................................................................... 189
3.4 08 XRDataMgr .............................................................................................................. 199
3.5 10 XRImChainPos......................................................................................................... 202
3.6 1100 Athena Application ............................................................................................... 205
3.7 1101 Athena Communication........................................................................................ 219
3.8 1102 Athena Drivers ..................................................................................................... 221
3.9 1103 Athena Calibration................................................................................................ 229
3.10 1105 Athena Database ................................................................................................. 233
3.11 1106 Athena Error Management................................................................................... 237
3.12 12 XRImDet................................................................................................................... 238
3.13 16 XRImProc................................................................................................................. 241
3.14 18 XRExpSens.............................................................................................................. 244
3.15 20 XROpDesc ............................................................................................................... 247
3.16 22 XRPatPos................................................................................................................. 250
3.17 32 XRSvcMgr ................................................................................................................ 252
3.18 34 XRSysMgr ................................................................................................................ 255
3.19 36 XRTechMgr .............................................................................................................. 258
3.20 38 XRTechOpt .............................................................................................................. 334
3.21 50 ATLAS...................................................................................................................... 339
3.22 58 XRSubsysMgrVENUS.............................................................................................. 347
3.23 64 XRUserIfPOS ........................................................................................................... 349
3.24 66 XRSubsysMgrMARS................................................................................................ 351
3.25 80 XRDigitalProxy ......................................................................................................... 364
3.26 90 XRUserIFVenus ....................................................................................................... 369
3.27 Inhibit Conditions........................................................................................................... 389
3.28 IDD Advisory Messages................................................................................................ 391
3.29 DeviceComm................................................................................................................. 392

GE MEDICAL SYSTEMS
Chapter 5
Error Message Listings (SW Version 13.x.x or higher) .................................... 403
Section 1.0
Before You Begin ........................................................................................... 403
Section 2.0
Introduction to Error codes........................................................................... 403
2.1 What are Error Codes.................................................................................................... 403
2.1.1 Applications Software ....................................................................................... 403
2.1.2 Operating System Software.............................................................................. 404
2.2 Applications and System Error Reporting...................................................................... 404
2.2.1 Error Display Management ............................................................................... 404
2.2.2 “Quick” Error Viewer ......................................................................................... 405
2.3 Service Error Log Viewer............................................................................................... 405
Section 3.0
System Error Message Listing ..................................................................... 405
3.1 02 XRAcqSync............................................................................................................... 407
3.2 04 XRAppDir.................................................................................................................. 414
3.3 06 XRBeamForm ........................................................................................................... 417
3.4 08 XRDataMgr ............................................................................................................... 428
3.5 10 XRImChainPos ......................................................................................................... 431
3.6 11 00 Athena Application............................................................................................... 444
3.7 1101 Athena Communication ........................................................................................ 460
3.8 1102 Athena Drivers ...................................................................................................... 462
3.9 11 03 Athena Calibration ............................................................................................... 470
3.10 1105 Athena Database .................................................................................................. 475
3.11 1106 Athena Error Management ................................................................................... 479
3.12 12 XRImDet ................................................................................................................... 480
3.13 16 XRImProc ................................................................................................................. 483
3.14 18 XRExpSens .............................................................................................................. 486
3.15 20 XROpDesc................................................................................................................ 489
3.16 22 XRPatPos ................................................................................................................. 492
3.17 32 XRSvcMgr................................................................................................................. 497
3.18 34 XRSysMgr................................................................................................................. 500
3.19 36 XRTechMg................................................................................................................ 504
3.20 38 XRTechOpt ............................................................................................................... 581
3.21 50 ATLAS ...................................................................................................................... 586
3.22 58 XRSubsysMgrVENUS .............................................................................................. 594
3.23 64 XRUserIfPOS............................................................................................................ 598
3.24 66 XRSubsysMgrMARS ................................................................................................ 605
3.25 80 XRDigitalProxy.......................................................................................................... 618
3.26 90 XRUserIFVenus........................................................................................................ 623
3.27 Inhibit Conditions ........................................................................................................... 644
3.28 IDD Advisory Messages ................................................................................................ 646
3.29 DeviceComm ................................................................................................................. 647
Glossary of Acroymns & Their Meaning .......................................................... 655
Table of Contents Page 21

GE MEDICAL SYSTEMS

GE MEDICAL SYSTEMS
Preface
Publication Conventions
Standardized conventions for representing information is a uniform way of communicating
information to a reader in a consistent manner. Conventions are used so that the reader can easily
recognize the actions or decisions that must be made. There are a number of character and
paragraph styles used in this publication to accomplish this task. Please become familiar with them
before proceeding forward.
It’s important that you read and understand hazard statements, and not just ignore them.
Section 1.0
Safety & Hazard Information
Proper product safety labeling allows a person to safely use or service a product. The format and
style for safety communications reflected in this publication represents the harmonization of IEC/
ISO 3864 and ANSI Z535 standards.
Within this publication, different paragraph and character styles are used to indicated potential
hazards. Paragraph prefixes, such as hazard, caution, danger and warning, are used to identify
important safety information. Text (Hazard) styles are applied to the paragraph contents that are
applicable to each specific safety statement.
1.1 Hazard Messages

Any action that will, could or potentially cause personal injury will be preceded by the safety alert
symbol and an appropriate signal word. The safety alert symbol is the triangle with an exclamation
mark within it. It’s always used next to the signal word to indicate the severity of the hazard.
Together, they are used to indicate a hazard exists.
Signal words describe the severity of possible human injures that may be encountered. The alert
symbol and signal word are placed immediately before any paragraph they affect. Safety
information includes:
1.) Signal Word - The seriousness level of the hazard.
2.) Symbol or Pictorial - The consequence of interaction with the hazard.
3.) Word Message:
a.) The nature of the hazard (i.e. the type of hazard)
b.) How to avoid the hazard.
The safety alert symbol is not used when an action can only cause equipment damage.
1.2 Text Format of Signal Words

DANGER - INDICATES AN IMMINENTLY HAZARDOUS SITUATION WHICH, IF
NOT AVOIDED, WILL RESULT IN DEATH OR SERIOUS INJURY. THIS SIGNAL
WORD IS TO BE LIMITED TO THE MOST EXTREME SITUATIONS.
WARNING - INDICATES A POTENTIALLY HAZARDOUS SITUATION WHICH, IF NOT
AVOIDED, COULD RESULT IN DEATH OR SERIOUS INJURY.
Caution - Indicates a potentially hazardous situation which, if not avoided, may result in
minor or moderate injury. It may also be used to alert against unsafe practices.
Preface Page 23
GE MEDICAL SYSTEMS
NOTICE - Indicates information or a company policy that relates directly or indirectly to the
safety of personnel or protection of property. This signal word is associated directly with a
hazard or hazardous situation and is used in place of 'DANGER,' 'WARNING,' or 'CAUTION.'
It can include:
• Destruction of a disk drive
• Potential for internal mechanical damage, such as to a X-ray tube
1.3 Symbols and Pictorials Used

The following Symbols and Pictorials are be used in this publication. These graphical icons
(symbols) may be used to make you aware of specific types of hazards that could possibly cause
harm.
keep_up magnetic biohazard compressgas ppe-hearing
fragile impact corrosive heavyobject ppe-2people
static_elec heat general laser ppe-respitory
keep_dry pinch radiation poisongas ppe-loto
general explosive electrical flammable ppe-eye
torque crush/mechanical tipping Read Manual ppe-gloves
ce instuction poisonmatl entanglement instuction
Page 24 Preface
GE MEDICAL SYSTEMS
Section 2.0
Publication Conventions
2.1 General Paragraph and Character Styles
Prefixes are used to highlight important non-safety related information. Paragraph prefixes (such
as Purpose, Example, Comment or Note) are used to identify important but non-safety related
information. Text styles are also applied to text within each paragraph modified by the specific
prefix.
EXAMPLES OF PREFIXES USED FOR GENERAL INFORMATION:

Purpose: Introduces and provides meaning as to the information contained within the chapter,
section or subsection (such as used at the beginning this chapter, for example).
Note: Conveys information that should be considered important to the reader.
Example: Used to make the reader aware that the paragraph(s) that follow are examples of information
possibly stated previously.
Comment: Represents “additional” information that may or may not be relevant to your situation.
2.2 Page Layout

Publication Part Number & Revision Number Publication Title
The current section and its title The current chapter and its title
are always shown in the footer of are always shown in the footer of
the left (even) page. the right (odd) page.
An exclamation point in a triangle is used Paragraphs preceeded by a symbol
to indicate important information to the user. (e.g. bullets) contain information that
Paragraphs preceeded by Alphanumeric has no specific order.
characters (e.g. numbers) contain infor-
mation that must be followed in a specific order.
Headers and footers in this publication are designed to allow you to quickly identify your location.
The document part number and revision number appears in every header on every page. Odd
numbered page footers indicate the current chapter, its title and current page number. Even page
footers show the current section and its title, as well as the current page number.
Preface Page 25
GE MEDICAL SYSTEMS
2.3 Computer Screen Output/Input Text Character Styles
Within this publication, mono-spaced character styles (fonts) are used to indicate computer text
that’s either screen input and output. Mono-spaced fonts, such courier, are used to indicated text
direction. When you type at your keyboard, you are generating computer input. Occasionally you
will see the math operator “greater-than” and “less-than” symbols used to indicate the start and
finish of variable output. When reading text generated by the computer, you are reading it as
computer generated output. In addition to direction, characters are italicized (e.g. italics) to indicate
information specific to your system or site.
Example: This paragraph’s font represents computer generated screen “fixed” output.
Fixed Output Its output is fixed from the sense that it does not vary from application
to application. It’s the most commonly used style used to indicate
filenames, paths and text that do not change from system to system. The
character style used is a fixed width such as courier.
Example: This paragraph’s font represents computer screen output that is
Variable Output “variable”. It’s used to represent output that varies from application to
application or system to system. Variable output is sometimes found placed
between greater-than and less-than operators for clarification. For
example: <variable_ouput> or <3.45.120.3>. In both cases, the < and >
operators are not part of the actual input.
Example: This paragraph’s font represents fixed input. It’s computer input that is
Fixed Input typed-in via the keyboard. Typed input that does not vary from application
to application or system to system. Fixed text the user is required to
supply as input. For example: cd /usr/3p
Example: This paragraph’s font represents computer input that can vary from
Variable Input application to application or system to system. With variable text, the
user is required to supply system dependent input or information. Variable
input sometimes is placed between greater-than and less-than operators.
For example: <variable_input>. In these cases, the (<>) operators would
be dropped prior to input. For example: ypcat hosts | grep <3.45.120.3>
would be typed into the computer as
ypcat hosts | grep 3.45.120.3
without the greater-than and less-than operators.
2.4 Buttons, Switches and Keyboard Inputs (Hard & Soft Keys)
Different character styles are used to indicate actions requiring the reader to press either a hard or
soft button, switch or key. Physical hardware, such as buttons and switches, are called hard keys
because they are hard wired or mechanical in nature. A keyboard or on/off switch would be a hard
key. Software or computer generated buttons are called soft keys because they are software
generated. Software driven menu buttons are an example of such keys. Soft and hard keys are
represented differently in this publication.
Example: A power switch ON/OFF or a keyboard key like ENTER is indicated by applying a character style
Hard Keys that uses both over and under-lined bold text that is bold. This is a hard key.
Example: Whereas the computer MENU button that you would click with your mouse or touch with your hand
Soft Keys uses over and under-lined regular text. This is a soft key.
Page 26 Preface
GE MEDICAL SYSTEMS
Chapter 1
System Overview & Safety
Section 1.0
Features
1.1 Product Overview
The Precision 500D is a classical R/F system. The
main features of the system are:
• Touch-screen User Interface (IUI)
• Fully Automated Exposure Control
• 65kW or 80kW Jedi Generator
• Optional Overhead Tube and Wall-stand
• Digital Image Chain, comprised of:
- 32 or 40cm Image Intensifier
- High Resolution CCD Camera
- Digital Image Processor with a base storage
capacity of 4,000 images
- Hi-Bright Monitors (21in and 17in)
The system is designed to be fully serviceable from
the IUI touch screen interface, not requiring a service
laptop interface.
1.2 Acquisition Modes

The Precision 500D can acquire diagnostic images using several different modes.
1.2.1 Digital Record
1.2.1.1 AEC
Fully automated exposure control, the exposure technique (kV, mA) is selected based on a
calculated patient thickness from the previous AEC exposure or previous fluoro exposure. The
exposure is terminated when the target dose is reached, as determined by the brightness pulses.
Single Exposure or 1, 2, 3, 4, 5, 6, 7½ exposures/second.
1.2.1.2 Fixed Time

Fully automated exposure control, the exposure technique (kV, mA, time) is selected based on a
calculated patient thickness from a previous exposure or, if no previous exposure, uses a default
patient thickness value.
Single Exposure or 1, 2, 3, 3¾, 5, 6, 7½ exposures/second.
Chapter 1 - System Overview & Safety Page 27

GE MEDICAL SYSTEMS
1.2.1.3 Subtraction (DSA)
Digital Subtraction Angiography is a digital radiological procedure for the isolated visualization of
blood vessels. Several trial exposures are taken first, to calculate and confirm the patient thickness.
The calculated patient thickness is then used to set up an exposure technique for the DSA run.
1.2.2 Digital Fluoro
1.2.2.1 Continuous
Operates with continuous x-ray tube current at 30 frames/second.
1.2.2.2 Pulsed
The x-ray radiation is turned on and off several times a second. This technique is used to reduce
the dose to the patient. Available pulse rate options are 3, 7½ or 15 frames/second.
1.2.3 Radiography (Overhead Tube)
1.2.3.1 AEC
Operator selects kV and mA. The ion-chambers, in the table bucky or wall stand, are used to
terminate the exposure when the desired film density has been reached.
1.2.3.2 Fixed Time

Exposure at operator selected technique.
Section 2.0
System Components
The Precision 500D system is fully digital “state-of-the-art” Radiographic and Fluoroscopic system.
To identify the system components, see Figure 1-1.
Figure 1-1 System Components
Page 28 Section 2.0 - System Components

GE MEDICAL SYSTEMS
Dose Printer - An option that produces hardcopy records of patient dose.
Bar Code Reader - An option used for entering data
Systems Cabinet:
• Distributes power
• Generates x-ray tube voltage and filament current.
• Monitors and controls the system
• Manipulates and stores digital images
Positioner Cabinet - Controls movements (longitudinal, lateral and vertical limits)
Positioner Table - Used to position the patient. It contains a table Bucky and Ion-chamber.
Intelligent Digital Device (IDD) - Used to control position movements, locks, limit exposures and
control image chain.
Imaging System - Creates and displays images. Consists of:

• Image Intensifier
• CCD TV camera
• Optics
Overhead Tube Suspension (OTS) - An option used to make radiographic film exposures, using
the tabletop, table Bucky, or wallstand Bucky.
Monitors - Used to display patient information; live Fluoro and digital radiographic images.
Wall Stand - An option that is used primarily for chest x-rays.
Integrated User Interface (IUI)

• Touch screen control located in the console.
• Keyboard is used to manually enter patient data.
• The CD-RW is used to archive patient images. It’s also used to save and restore system
software.
Foot Switch - Activates Fluoro exposures. Also used in digital recording in conjunction with the
Prep switch.
Section 3.0
System Shutdown for Service
3.1 Before you Begin
System power must always be removed before any cover is removed.
DC BUS (UP TO 800VDC) AND AC INPUT VOLTAGES (UP TO 480VAC) ARE

HIGH PRESENT IN THE SYSTEM CABINET EVEN WHEN THE PRECISION 500 IS TURNED
VOLTAGES OFF FROM THE IUI CONSOLE!

GE MEDICAL SYSTEMS
3.2 Procedure
1.) Depending on your starting point, do the following:
Close all open Exams. See operator manual if necessary
or
Exit Service User Interface (SUIF).
2.) From the IUI GUI, select UTILITES and then SHUTDOWN buttons. The shutdown process
takes approximately 2 minutes to complete. As the system shuts down, text appears on the
monitors, indicating the system is shutting down.
3.) When the IUI power button goes “out”, verify the following:
- Monitor screens are blank
- Table IDD lights are extinguished (out)
4.) Place the hospital’s “mains” facility breaker to the “off” position.
5.) perform the ECPL procedure (Tag and lockout facility power).
6.) Visually inspect that all LEDs on the UPS are “OFF”
On/Test
Voltage Trim Power Overload Battery ON
Voltage Boost Replace Battery
Output OFF SW Battery Charge

Load (%) Status (%)
95
96
72 Percentage
67
48 Charged
50
24
33
0
17
Figure 1-2 UPS Control Panel
ALL UPS LEDS MUST BE “OFF”. IF ANY LED IS STILL ON, WAIT 5 MINUTES. IF
HIGH THE LEDS DO TURN OFF AFTER 5 MINUTES, DO NOT PROCEED ANY
VOLTAGES FURTHER. THE UPS MUST BE OFF TO SERVICE THIS SYSTEM.
7.) Turn off the Main power switch. Check incoming line voltage with a multi meter on the Main
Power switch. It’s located at the bottom of the System Cabinet. There must be no voltage
present before beginning equipment service.
Wait 1 minute before proceeding, to allow all voltages to discharge.
Page 30 Section 3.0 - System Shutdown for Service

GE MEDICAL SYSTEMS
Figure 1-3 Main Power Switch “Off”
8.) Check DC Bus Voltage with an appropriate multimeter. There must be no voltage present
before beginning equipment service. Check twice!
Figure 1-4 DC Bus Terminal Block (Generator with Door Open)

GE MEDICAL SYSTEMS
Page 32 Section 3.0 - System Shutdown for Service

GE MEDICAL SYSTEMS
Chapter 2
Theory of System Operation
In the material that follows, detailed information about the operation of this product is provided. You
will learn the following.
• System Cabinet consists of the following: Digital System, System Controller, Generator and
Power Distribution Unit (PDU).
- The Digital System processes, manipulates and stores digital image data.
- The System Controller is responsible for system and positioner control communications.
The main components include: gitane board, single board computer, CD-ROM and the
hard drive.
- The Generator supplies DC power to the x-ray tube. The main components include: AC/
DC unit, auxiliary 1 and 2 unit, power unit and the kV control board.
• Imaging System (Digital record and Fluoro mode) Radiation maybe hardened by the one
of the three spectral filters.
- Parallel light is refracted through the Objective lens (parallel light).
- The parallel light is deflected 90 degrees by a mirror towards the NDF.
- The iris controls the amount of light entering the CCD camera.
- The digital image data flows through the Digital system to the monitor.
• Imaging System (Digital record mode only) A light sample is sent to a Photodiode via a light
pipe.
- The Photodiode converts light to a voltage.
- The voltage is converted to a signal, then sent to the optics control board, which converts
the voltage to a frequency that represents the light quantity in the portion of the image.
This information is sent to the “Jedi” generator and is used to stop the x-ray exposure
(AEC mode).
- The exposure is terminated when the desired pulse count is reached.
• Positioner Cabinet controls positioner movements. The Positioner I/O board is involved in the
major movement functions of the table. The Positioner Cabinet and System Controller
communicate via the CAN Bus.
• Movement Functions includes the following: Positioner Angulation, Table-top Longitudinal,
Table-top Lateral, Vertical (SID) Power Assist, Longitudinal Power Assist, Cone, Collimator
Blade and Spectral Filter.
• Communication Routes includes the following: Real Time BUS, Image Bus, Video (hi-Res),
Video (low-Res), Internal Ethernet and CAN BUS.
• Power Distribution includes the following: High Voltage, UPS Power, 120/230 Vac and 3
Phase.
• Power States includes the following: Power On, Standby, Shutdown, Emergency Off,
Tableside Emergency Off, Power Loss and Reset.
Chapter 2 - Theory of System Operation Page 33

GE MEDICAL SYSTEMS
Section 1.0
Interactive User Interface (IUI) Subsystem
The IUI subsystem uses the Linux operating system to run application software. Venus is the name
for this application software collection. The Venus SW applications consists of a number of software
applications called Atlas Core, Calypso and the Integrated User Interface. Venus is the primary user
interface for the user. Venus SW is in charge of providing all the controls to power on, power off the
system, to start, to close an exam and to access to the maintenance and service functions.
Atlas Core software is in charge of the following modules:
• Error reporting, logging and viewer
• Communication brokerage between each subsystems and modules
• Interface the I/O CIB board to handle the I/O signal and Real time signals. I/O means Input/
Output signals. Those signals are usually the ON, RESET, Hands witch buttons (Inputs) and
the buzzer and exposure, inhibits signals (Output).
• Service communication infrastructure to exchange information between the system
components and the SUIF
• Boot, Reset and the shutdown management for all the SW applications `
• Calypso is in charge of the providing the following modules
• the Venus subsystem manager to adapt the Atlas core boot, reset and shutdown framework
to the specific H/W design of Venus (Reset Management with the CIB, interfacing the Linux
operating System for the Shutdown and reboot, monitoring the UPS)
• The Service manager which is the component to interface the SUIF request to the System to
perform any calibration, any diagnostics or calibration.
IUI is in charge of providing the following services:

• Display the Application User Interface including the Review screen, the Protocol selection, the
Protocol Edit and the utilities screens
• Interface the user interface request and the rest of the systems
• Turns on and off the X-ray ON, Inhibits and Prep lights on the console
• Provide a unique access to the image review and printings.
Section 2.0
Systems Cabinet
2.1 Components
The System Cabinet contains a Digital System, System Controller, X-ray Generator and Power
Distribution Unit (PDU), and system communication accessories.
Page 34 Section 1.0 - Interactive User Interface (IUI) Subsystem

GE MEDICAL SYSTEMS
Figure 2-1 System Cabinet Components
2.2 Systems Cabinet Internal Connections

See system cabinet drawing 2336900, located in schematics.
2.3 Applications Software

Saturn is the Digital acquisition and display computer/workstation used in the Precision 500 D
product. Figure 2-2 shows the components making up that subsystem and its interactions with the
image chain and the rest of the system.

GE MEDICAL SYSTEMS
12 bits video/camera control/image link
CCD Image chain RT bus

To Local
(Bright_Sig) To VCR Laser Printer
- NDF
- IRIS
image chain
CANbus
Saturn
- PHOTODIODE OCB
Optics Scan Serial Port(s)

Image Parallel Digital Host
ADCM Converter
-IIFOV Correction CCU Acquisition Port Board
-II Grid Board
Board 12bit Board Board (Option)
II Voltages (Option)
IIPS video
Backplane
Digital CPU Board
Trigger out PCI Bus
CAM ready
Ext sync CCD ISA Bus
Image Bus
ABS (ABD)
Memory Static 10 bits
GITANE Image storage
Board Image
SIB V3 Sync Display
Board
Board
(Option)
IDE
Floppy
system RT bus
positioner Ethernet
Ethernet
8 bit RB 170 video Media Customer’s

Router
Integrated Converter Network
UI +
In-room In-room
Handswitch
Monitor Static Image
(Live Monitor
Fluoro) (Option)
Pos/OTS/Wall Stand/ Calypso

Collimator Control (CAN)
Control
Room
Generator RT Monitor
Generator bus
Control (CAN)
Jedi
Collimator
Ion Chambers (3) Power &

Signal Cables
XRT
High Voltage Cables &

Stator
Figure 2-2 Saturn Block Diagram
The software on Saturn performs the following tasks:

• Controls the Leeloo image chain during Fluoro and Record exposures by appropriately
configuring the CCD camera, Image Correction board (ICB), Gitane system interface board,
Camera control unit (CCU) and Optics Control board (OCB) for optimal image quality and
performance.
• Supports the following acquisition modes: Continuous Fluoro at 30 fps with optional storage of
Fluoro images to disk, Pulsed Fluoro at 4 fps (3.75 actual), 7.5 fps and 15 fps, Digital Record
at 1, 2, 3, 4 (3.75 actual), 5, 6, 7.5 fps and single shot Digital Record exposures.
• Controls the processing of acquired images on the Image Acquisition board (IAB) and their
display on the image monitor using the Image Display board (IDB). Images can also be stored
on the Image Memory Board (IMB) and then transferred to disk.
• Displays exposure technique parameters and other system information received from Mars on
the image monitor, and stores them with the images.
• Acquired images can be reviewed later. Stored images can be played back and manipulated
during review.
• Interfaces with the rest of the system, by establishing local network connections with the Mars
(system control) and Venus (user interface) subsystems.
• Provides dose feedback to the Exposure management software on Mars, which is used to
compute optimal Technique values for exposures.
• Stores patient and exam data in a local database and provides external DICOM connectivity
to other DICOM-enabled severs and peripherals.
• Provides the capability to perform image chain calibrations and diagnostic tests, including
hardware and functional diagnostics, including the Image Quality Signature Test (IQST) and
Video Data Path Integrity Test.
Page 36 Section 2.0 - Systems Cabinet

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• Provides the capability to interface with other peripheral components such as the Reference
Image monitor, Video Tape Recorder, Infrared Remote and Laser printer.
2.4 Digital System “Saturn”

The Digital System hardware is occasionally referred to as Saturn. The name Saturn and Digital
System is used interchangeably to mean the same hardware in the discussion that follows.
In early 2005, some Saturn circuit boards were redesigned and consolidated. The original Saturn
(2290479) is referred to as ’old style’ or ’ Saturn V1’, the redesigned Saturn (2407276) is referred
to as ’new style’ or ’Saturn V2’.
2.4.1 Saturn V1 (old style), 2290479
2.4.1.1 Digital System Block Diagram

System
System (PDU) IR Remote
(PDU)
Control Power Transmitter
Power In-Room
Monitor Room System
Monitor Keyboard Mouse Hub System
IR Remote (UPS)
Receiver Power
Composite Composite
Video Video
Image Digital System

Power
CCD Data Camera Image
Image Correction Image Max Supply
Camera Control Display Opacification
(ICB) Acquisition
Head (CCU) (IDB) (MOB)
Power &
Control
Power
Sync Sync
Serial Port 100BaseT
Only
Ethernet
Imager Backplane
PCI Bus
Single Board Computer ISA Bus
Image Bus
CAN Bus
& RT Reset
Signals Multi-Function
OCB Connector
Image Memory
(IMB)
Sys RT
System Bus Gitane
Controller Scan Max Static Reference
Converter Opacification Hard Host Control
(SRB) CD-ROM
IUI (SCB) (MOB) Drive
Composite Control
Record On/Off Lo-Res VGA Image Data
Video Video External To
LEGEND System System VGA to BNC Router
System Hospital
VCR (PDU) (UPS) Power
Converter Customer’s
Power Power
Symbol Description Local Laser
Media Film Printer
PCI Bus Composite Converter
Customer’s Network
Image Bus Video
Between Digital System Boards System Static

(PDU) Ref
External to Digital System Monitor
Power
Customer’s Customer’s Customer’s Customer’s

DICOM DICOM DICOM DICOM
Printer Workstation Worklist Broker Archival Device
Figure 2-3 Digital System Block Diagram (Saturn V1)
2.4.1.2 Components
The Digital System processes, manipulates and stores digital image data using the components
shown in Figure 2-1.

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Figure 2-4 Digital System “Exploded View” (Saturn V1)
2.4.1.3 PCI Interface

The PCI interface allows the Saturn software to communicate with the system boards. Commands
through the PCI bus configure the boards for proper operation and transfer data from the boards to
the CPU memory. The PCI interface also provides the reset logic. Reset can come in from the
system RT Bus (initiated by the customer through the IUI) or the PCI Bus (initiated by the SBC as
part of the Saturn reset process). See Figure 2-3.
2.4.1.4 Image Bus

The Image Bus is a GEMS proprietary bus that moves data from circuit board to circuit board. The
Image bus is 1024x1024, 10 bit format at 40 MHz. See Figure 2-3.
2.4.1.5 Gitane Board

The Gitane board provides the system interface for Saturn. It provides the interface and
synchronization for the image chain timing, as well as providing the means of controlling the image
head through a CAN bus. In addition, it provides the means for Saturn to respond appropriately to
resets. RS422 Interface circuits provide the signal translation between the external and internal
signal levels for the timing signals needed to synchronize the image transfer at the CCU. Interface
circuits provide the appropriate signal translation between the external and internal signal levels for
the timing signals needed to synchronize the image transfer at the ICB. A relay contact is provided
to control record on/off for a VCR. Several types of signals exist on the RT Bus including 16 RS485
differential lines, and the system reset contact closure. This logic provides the appropriate interface
type for each of these signals. The system reset signal is sent on to the PCI interface logic, while
the other signals are used in the System Logic FPGA. This is a relay contact closure driven through
the PCI interface FPGA. This contact is connected through the PC backplane and enters the single
board computer through the multi-function connector. As such, when this contact closes, a full reset
will occur in the Saturn PC. See Figure 2-3.
2.4.1.6 Image Correction Board (ICB)

The Image Correction board is an off the shelf board from “Thales” that works together with the CCD
camera to deliver “corrected” digital images to the Saturn CCU board. See Figure 2-3.

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2.4.1.7 Camera Control Unit (CCU)
The CCU contains all the circuitry necessary to receive a 12 bit digital image from the ICB and
output a pre-processed 10-bit digital image to the Image Acquisition Board. Pre-processing is real-
time and consists in frame buffer, ABD computation is user-programmable ROI, encoding LUT, and
digital re-scaling gain. See Figure 2-3.
2.4.1.8 Image Memory Board (IMB)

The Image Memory Board interfaces to the PCI bus and to the proprietary Image Bus. The IMB
contains 128 Mb of memory packaged in memory SIMMS. The Memory board is where Image data
is temporarily stored before being sent to the Hard disk or output on the Image Bus. When Digital
Record, Fluoro Store or Fluoro Loop images are acquired they are initially stored in the IMB before
being copied out and written to the Hard Disk.
When images are being retrieved from the Hard Disk for display on the monitor they are first written
to the IMB before being placed on the Image Bus, sent to the display board, and out to the monitor.
See Figure 2-3.
2.4.1.9 Image Display Board (IDB)

The Image Display Board is responsible for displaying the images during acquisition and image
review. Mounted on the IDB is the Max. Opacification Board (MOB). The display board is the output
video board for the Saturn Digital System. It has 2 identical composite 73 Hz analog BNC video
outputs. The display board contains circuitry to carry out functions such as subtraction, edge
enhancement and Window/Level. It is connected to both the Image Bus and PCI Bus. See Figure 2-
3.
2.4.1.10 Single Board Computer (SBC)

The Single Board Computer is a standard off the shelf CPU board. It contains the following
interfaces: PCI, ISA, Ethernet, Serial, Parallel, IDE, PS/2, and multi-function.
The CPU board contains a Pentium III processor with 128 Mb of memory running at 850 MHz. The
SBC plugs into the PCI and ISA busses on the backplane. The SBC supports several data and
input/output interfaces. It supports an ethernet controller that is used for communications with other
portions of the system. The PS/2 port is utilized for the keyboard. The serial ports are used for a
serial mouse and the Infrared Remote interface. The SBC interfaces to an IDE hard drive and CD-
ROM. The multi-function connector connects to the passive backplane and transmits the CPU
Reset and Hard Drive Activity signals. See Figure 2-3.
2.4.1.11 Static Reference Board

The Static Reference Board is a PCI circuit board and provides a standard VGA output video signal
that is used for the reference image display.
The Static Reference Board is used to display a Static Image on a monitor if the user has purchased
the advanced package. It is one of the few boards in the Saturn Digital System, which connects to
the PCI Bus only and outputs SVGA video through a VGA connector. Only 3 connections are used;
Horizontal and Vertical sync, and video (green). A separate VGA to BNC converter is then used to
provide composite video to the in-room monitor. See Figure 2-3.
2.4.1.12 Scan Converter Board (SCB)

The Scan Converter Board outputs 525 line (NTSC) or 625 line (PAL) video to a VCR and/or low
resolution monitor.
The circuit configuration is identical to the Image Display board - the PCI Prom is the only physical
difference between the 2 assemblies. Software loads the appropriate FPGA software to the board
based on the board ID detected in the PCI PROM. The Max. Opacification Board (MOB) is mounted
on the SCB.

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The quantity of Graphical Text overlay is less on a displayed Scan Converter image than it is with
a conventional Display board image. See Figure 2-3.
2.4.1.13 Digital Host Control Board (DHC)

The Host Control Board is the Link in the digital system that outputs digital data to the Hardcopy
Laser. Utilizing P831 protocol there are 2 connections that facilitate the Transfer of Images. An
RS232 communication link enables hand shaking between the 2 devices while an RS422 parallel
data link provides a path to transfer the image data to the Laser printer. See Figure 2-3.
2.4.1.14 Passive Backplane

The Passive Backplane contains three buses: PCI, ISA, and Image Bus. The backplane houses 13
board slots: 3 ISA, 1 PCI/ISA, 3 PCI, 6 PCI/Image Bus. The backplane has two PCI bridges and two
power connections. See Figure 2-3.
2.4.1.15 Image Acquisition Board (IAB)

The acquisition board accepts digitized 10 bit data from the CCU and outputs data on the Image
Bus. It contains frame averaging circuits providing for both conventional and Motion Corrected
noise reduction. Recursive and non-recursive frame averaging algorithms are used. It connects to
both the PCI and the Image Bus. See Figure 2-3.
2.4.1.16 Image Review

Images are read from the hard disk by the CPU and sent out over the PCI bus and written into the
Image Memory board. The memory board then sends them out over the Image Bus where they are
picked up by the display board and sent on to the monitor. See Figure 2-3.
2.4.1.17 Image Acquisition, Storage, and Display

See Figure 2-3 for the following discussion.
2.4.1.18 Real Time Fluoro Display

Real time Fluoro data flows from the Camera head to the Image Correction Board, on to the Camera
Control Unit or CCU and then the Acquisition board. It travels from the Acquisition board to the
Image Bus flowing to the display board and finally to the monitor. If the VCR option is present, data
also flows from the Image Bus through the scan converter board and on to the VCR.
2.4.1.19 Digital Record/Pulsed Fluoro Acquisition and Storage

A Record or Fluoro Store Image flows from the Camera through the ICB, CCU and Image
Acquisition boards. Passing onto the Image Bus it is copied into the Memory and Display boards.
The Display board sends the image on to the monitor. The image data in the Memory board is
copied out by the CPU over the PCI Bus, and stored on the hard disk. If the VCR option is present,
data also flows to the scan converter board and VCR.
2.4.1.20 Fluoro Loop Store

Fluoro loop image data is captured in the memory board at the same time it is being displayed on
the monitor. The data stays in the memory board enabling immediate playback after acquisition.
The user must use the “store loop” button to send the images to the hard disk.
2.4.1.21 Static Reference Display

Static reference display data is taken from the display board and stored in RAM on the CPU. When
a static display is requested, data is sent on the PCI Bus to the Static Reference Display Board and
then out to the monitor.

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2.4.1.22 External Device Transfer
To transfer data to an external device, images are pulled from the hard disk through the CPU and
sent to the appropriate board. Image data will be sent to the Host Control board for output to a local
Laser for hardcopy, or to the Ethernet board for output to a customer network.
2.4.2 Saturn V2 (new style), 2407276
2.4.2.1 Digital System Block Diagram

System
(PDU) System Reset
(PDU) IR Remote PB
Power
VCR Control Power Transmitter
In-Room
Monitor Room Mouse System
Monitor Keyboard Hub System
IR Remote (UPS)
Receiver Power
Composite Composite Composite
Lo-Res Video Video Video
Image Digital System

Power
CCD Data
Image Correction Digital Acquisition Board Digital Display Board Supply
Camera
(ICB) (DAB) (DDB)
Head
Power &
Control
Serial
Sync Sync 100BaseT
Port Ethernet
Imager Backplane
PCI Bus
Image Bus Single Board Computer
CAN Bus
& Image Reset
Multi-Function
OCB RT Bus
Connector
Digital Memory Board
(DMB)
Sys RT
System Bus Gitane
Controller Digital Host Static Reference
(Mars) Control II (SRB) CD-ROM Hard Drive
(DHCII)
IUI
Control Image Data VGA
Record On/Off Video
External To
LEGEND Hospital System VGA to BNC Router
System
Power (UPS)
Customer’s Power
Symbol Description Local Laser
Film Printer Media
PCI Bus Composite Converter
Customer’s Network
Image Bus Video
Between Digital System Boards System Static

(PDU) Ref
External to Digital System Monitor
Power
Customer’s Customer’s Customer’s Customer’s

DICOM DICOM DICOM DICOM
Printer Workstation Worklist Broker Archival Device
Figure 2-5 Digital System Block Diagram (Saturn V2)

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Figure 2-6 Digital System “Exploded View” (Saturn V2)
2.4.2.2 Saturn V2 Circuit Board Changes

The Saturn V2 re-design incorporates the following changes:
- CCU board and IAB board combined to DAB (Digital Acquisition Board)
- IMB re-designed and is now the DMB (Digital Memory Board)
- IDB board and SCB board combined to DDB (Digital Display Board)
- DHC board re-designed and is now the DHCII (Digital Host Controller II)
Functional summaries of the new DAB, DMB, DDB and DCHII appear below. All other Saturn V2
circuit boards are the same as those used in the Saturn V1 system:
Digital Acquisition Board (DAB)

The acquisition board accepts digitized 12 bit data from the ICB and outputs data on the Image Bus.
It handles pre-processing in real-time and consists of a frame buffer, ABD computation, a user-
programmable ROI, encoding LUT, and digital re-scaling gain. It also contains frame averaging
circuits providing for both conventional and Motion Corrected noise reduction. Recursive and non-
recursive frame averaging algorithms are used. It connects to the Gitane, ICB, PCI, and the Image
Bus.
Digital Memory Board (DMB)

The Digital Memory Board interfaces to the PCI bus and to the proprietary Image Bus. The DMB
contains 256 Mb of memory. The Memory board is where Image data is temporarily stored before
being sent to the Hard disk or output on the Image Bus. When Digital Record, Fluoro Store or Fluoro
Loop images are acquired they are initially stored in the DMB before being copied out and written
to the Hard Disk.
When images are being retrieved from the Hard Disk for display on the monitor they are first written
to the DMB before being placed on the Image Bus, sent to the display board, and out to the monitor.

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Digital Display Board (DDB)

The Digital Display Board is responsible for displaying the images during acquisition and image
review. The display board is the output video board for the Saturn Digital System. It has 2 identical
composite 73 Hz analog BNC video outputs and also a configure-able output for 525 line (NTSC)
or 625 line (PAL) video to a VCR and/or low resolution monitor. The display board contains circuitry
to carry out functions such as subtraction, pixel re-registration, edge enhancement, panning/
zooming, 4-on-1 and 16-on-1 review and Window/Level. It is connected to both the Image Bus and
PCI Bus.
Digital Host Control Board II (DHCII)

The DHCII is the Link in the digital system that outputs digital data to the Hardcopy Laser. Utilizing
P831 protocol there are 2 connections that facilitate the Transfer of Images. An RS232
communication link enables hand shaking between the 2 devices while an RS422 parallel data link
provides a path to transfer the image data to the Laser printer. The DHCII is connected to the PCI
Bus.
2.5 System Controller

The System Controller hardware/PC is occasionally referred to as Mars. The name Mars and
System Controller is used interchangeably to mean the same hardware, in the discussion that
material that follows.
Figure 2-7 System Controller
The System Controller is responsible for system and positioner control communications. The
system controller is in the class of personal computers called workstations. It utilizes the VxWorks
as it’s operating system software. It contains the following hardware components:
• Gitane Board: An interface/communication board that translates various operating systems
commands between VxWorks, Windows 95 (Saturn HW) and Linux (Venus HW) operating
system environments.
• Single Board Computer (SBC): Contains the microprocessor, and memory necessary to run
VxWorks.
• CD-R Drive: Used as a bootable CD to reformat the System Controller hard drive or perform a
“load from cold” of operating system software.
Note: The CD-RW drive in the IUI is used to load System Controller operating and application
software, or backup and restore data. Not the system control CDROM.
• Hard Drive: Contains system control software.

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2.6 Accessory Rack
Figure 2-8 Accessory Rack with Media Converter
Figure 2-9 Accessory Rack without Media Converter
The Accessory Rack includes some key assemblies in the Precision system:
• VGA/BNC Converter - converts the VGA video signal from the Digital System to a single wire
co-axial signal, used for the optional Static Reference monitor.
• Ethernet Router - Used for the internal Precision Ethernet network, DICOM and broadband
services.

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• Keyboard/Mouse Extender - Used to extend the Digital Computer's mouse and keyboard to
the control console area.
• PDU I/O Board and power supply.
• 120VAC relay to PDU I/O - Used for signalling “mains” power failures.
• Media converter - Used on early systems and later eliminated. Provides fiber to RJ45 media
conversion, and transmits external network into router WAN/Internet port.
2.7 X-Ray “Generator”

Additional information on the “Jedi” generator can be found in Section 3.0.
2.7.1 Components
Figure 2-10 Generator Components
The generator (Jedi) supplies DC power to the x-ray tube. The Precision 500D comes with two
different power versions, 65kW and 80kW. The following are major components of the generator:
• AC/DC Unit
• Auxiliary 1 Unit
• Auxiliary 2 Unit
• Power Unit
• kV Control Board

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2.7.2 Generator Block Diagram
CAN Bus
to System
Controller
CAN Bus
Generic
Interface Heater Supply Voltage 160Vdc
RT Bus Phase Shift
Capacitors
Low
MAINS_DROP Large Small
Voltage Rotation
Ion AEC kV Control Fil. Fil.
Chambers Power Board
Board Heating Heating
Supply
DC Bus 400Vdc to 800Vdc

115Vac Sm. Fil Drive
Inverter kV, mA
Measurements Input Power Lg. Fil Drive Anode
Controls
Rotation
Drive
DC Bus 400Vdc to 800Vdc
AC/DC
Sm Filament Drive
Tube 1
Tube 2
Lg Filament Drive
Inverter H.V. Tank Tube 1 Tube
& Measurement Board Tube 2
Switching Bd
EMC Filter kV Switch Motor
Impedance
kV Switch Matching
Capacitors
HV Cables
Feedback
HV Cables
125A Fuses
Edward Singleton Fan

Rev.1
X-ray Tube 1 X-ray Tube 2
PR-Jedi Block
Page 1 of 6
(Undertable) (OTS)
Anode Rotation Drive
Oil Pump & Tube Temp. Fdbck (70oC)
3 Phase Input Power

(380 to 480Vac)
Figure 2-11 Generator Block Diagram
2.7.3 Auxiliary 1 Unit

The Auxiliary 1 Unit contains the following:
• Low Voltage Power Supply (LVPS)
• Large Filament/Heater Board
• Small Filament/Heater Board
Figure 2-12 Auxiliary 1 Unit

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2.7.3.1 Low Voltage Power Supply
The LVPS supplies the generator with the required low voltages. It is powered by either 115Vac or
230 Vac. There are eleven output voltages: ±15VCAN (supplies the kV Control Board, Filament
Heating and Rotation boards)
• +15VEXT (not used with Precision 500D)
• 24V (supplies the Gate Control board in the Inverter)
• 24V FAN (four outputs - supplies power to the fans)
• 160V H1 (supplies DC voltage for the filament inverter)
• 160V H2 (supplies DC voltage for the filament inverter)
• 160V EXT (not used with Precision 500D)
2.7.3.2 Filament Heater Boards

There are two filament boards for fast exposure switching from one filament to another. The filament
boards supply three levels of filament heating current: Standby, Boost (for 400ms) and Exposure.
• Small Filament: This board supplies heating current for the small filament.
• Large Filament: This board supplies heating current for the large filament.
Note: One filament is in standby preheating mode while the other is in use.
2.7.4 Auxiliary 2 Unit
Figure 2-13 Filament Heater Boards
The Auxiliary 2 Unit contains the following boards:

Rotation Board: This board generates the power to drive the anode rotation in either x-ray tube. It
can switch between a high and low speed drive by selecting the phase shift capacitors.
• Tube Switching Board: This board switches all functions between the x-ray tubes and
receives status and tube temperature feedback. The following describes the functions and
feedback:
• X-Ray Tube High Voltage Switching (sends drive voltage to motor in HV tank and receives
feedback)

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• X-Ray Tube Filament Heating Switching (switches large and small filament heating between
both tubes)
• Anode Rotation Switching
• X-Ray Tube Stator Impedance Switching (for different x-ray tube types, the system switches
capacitors to match the stator impedance.
• X-Ray Tube Temperature Feedback (interlock generated at 70°C)
Note: Tube Switching board also supplies either 115 Vac or 230 Vac to an oil pump or fan for tube cooling.
2.7.5 Power Unit

The Power Unit provides power to the x-ray tube and main control of the generator. It includes the
High Voltage Tank, Measurement Board and Inverter Assembly.
Figure 2-14 Power Unit
• High Voltage Tank: Contains the HV Transformer, rectifier, filament transformers, tube
switching motor and feedback switches.
• Measurement Board: (part of the HV Tank): Measures and monitors ±kV and mA for safety
violations, then sends this information to the kV Control board.
• Inverter Assembly: Contains four IGBT's (formed as a half bridge hypo-resonant inverter),
two fly back diodes and a resonance capacitor.
2.7.6 AEC and Generic Interface Boards

The Automatic Exposure Control (AEC) Board generates 230Vdc bias voltage for the ion chambers.
Up to four ion chambers can be connected (Precision 500D uses two of these). It also compares
the selected ion chamber output to a reference and generates a series of pulses, which are sent to
the KV control board.
The Generic Interface Board interfaces the internal CAN and RT Bus between the generator and
the system controller.

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Figure 2-15 AEC and Generic Interface Boards
2.7.7 kV Control Board

The kV Control Board is the main control of the generator. It provides CPU control of the following:
• Control and System Communication
• Exposure Control (including rotation and heater)
• mA Regulation
• Tube/Generator Thermal Protection
• Generator Configuration (stored on battery backed up NVRAM)
• Tube and AEC Calibration (NVRAM)
• Generator Diagnostics
• Inverter Control
• HV Chain Safety Interlocks and Monitoring (kV, mA, mAs, Inverter Current, Inverter Gate
Supply and DC Bus)
• Main Generator CPU
Note: It also controls the Generic I/F board and CAN interface.
Figure 2-16 kV Control Board

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2.8 AC/DC Unit
Figure 2-17 AC/DC Unit
The AC/DC Unit creates the DC Bus, which is a range of DC voltage from 400-800V. This voltage
feeds all the main generator functions including:
• Inverter
• Gate Drive Supply
• Anode Rotation
2.9 Power Distribution Unit (PDU)
Power On On
Circuit Breakers 1 to 7
Emergency Standby
Stop/Reset 230Vac
Service Outlet
Room InterfaceTerminal 120Vac

Block Service Outlet
UPS
Voltage Tap Selection
Terminal Block
(380 to 480Vac in 20V steps)
CB 8
Drawn By Edward Singleton

Circuit Breakers PR-PDU rev2
CB 1 Positioner (Table) CB 4 120Vac and 240Vac Service Outlets

Positioner CB 5 Logic Board Power Supply
CB 2 Wallstand UPS
OTS CB 6 Generator Auxiliary 1
CB 3 Monitors CB 7 Generator Auxiliary 2
Cabinet Fans CB 8 Isolation Transformer Input
VCR
Figure 2-18 PDU

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2.9.1 “Main” supply from Hospital
The hospital’s “mains” provide the 3-phase power and grounds needed by the system to operate.
A circuit breaker, customer supplied, should be placed before the power supplied to the system
cabinet. A room emergency button is used to activate the circuit breaker, using a trip mechanism.
The pre-install manual shows how such a configuration might be wired.
2.9.2 The Mains Switch

Mains power from enters the system through a switch at the bottom of the cabinet. If this switch is
turned off, the power to the system is removed. Note that there may be power coming out of the
UPS even when this is off if the system was “ON”
2.9.3 Power Peak-Up

Three phases of power go from this point to the Jedi Generator. Two phases of power and ground
go to the Power Distribution Unit (PDU).
2.9.4 PDU
The PDU provides power to the system except for the three phase power to the Generator. The
system is designed to operate either at 60Hz or 50Hz. At the power input to the PDU there are tap
settings to select the voltage that is being supplied to the PDU (380V to 480V in increments of 10V).
This is a tap setting into the isolation transformer in the PDU so that the output voltage is always
same irrespective of the input voltage. There are two voltage outputs 120V/ 220V from the PDU.
Most of the system uses 120V. The Gantry tilt drive uses 220V. There is no voltage regulation in
the PDU. Each of the subsystems which use power manages the variation in the input voltage.
The output from the transformer goes through an EMC filter to minimize the electrical noise entering
the system or going back into the main power supply.
The output from the EMC filter goes through various relays to turn On and Off the various parts of
the system depending on what the state of the system is. These relays are driven by the PDU IO
logic board located on the top left side of the system cabinet.
The PDU also has service power outlets.
2.9.5 PDU IO Logic Board

The PDU IO logic board turns on and off the various relays in the PDU based on the commands it
receives from the system controller computer called. In addition it provides the interface for the
room Emergency off and the door interlock.
This board is powered ON almost all the time. This board is powered when the system is in the
“ON”, “OFF” or in the “Standby” state. When there is a power failure, till the computers are shutdown
and the UPS is shutdown this board is powered. Then the power is removed. When the room
emergency button is pressed, the power to this board is removed. There is a relay in the PDU which
connects the power supply located next to the PDU IO board to the main input power when the UPS
is off and connects to the UPS output when the UPS is On. This power supply provides power to
the PDU IO board.
This board gets commands from the system controller computer called Mars, which is located next
to the PDU IO board. The commands comes to the board through the CAN bus.
2.9.6 Operational Power States

The In this section, the different states of operation for the system will be described:
• Power On, Section 2.9.6.1
• Standby, Section 2.9.6.2
• Shutdown, Section 2.9.6.3
• Emergency Off, Section 2.9.6.4

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• Tableside Emergency Off, Section 2.9.6.5
• Power Loss, Section 2.9.6.6
• Reset, Section 2.9.6.7
• UPS / Interlocks, Section 2.9.6.8
2.9.6.1 Power-On
There are three normal states to PDU operation: on, shutdown and standby. Pressing the ON
button (from the IUI console), sends a signal to the Logic/Relay Driver. Power (+24v) which is fed
to the user interface computer (Venus) through the RT bus. When the ON button is pressed on the
user interface computer Venus, it closes a contact and sends the 24V back to the PDU IO board,
which energizes relays K1 and K2. If the UPS is off, a “Turn On” signal is sent to the UPS. The UPS
turns on approximately two seconds later and supplies power to the computers.
The firmware in the FPGA on I.O board coordinates the activities. This device turns On power to all
the components in the system at the same time and thus allows the system comes up.
See Figure 2-19.
Figure 2-19 PDU Power-On
2.9.6.2 Standby
This is a state where computers, communication devices (like the Hub and the Modem), system
cabinet FAN and the tube fan power to the Jedi have steady power applied. The purpose of this
state is to provide remote access into the system during the night time. There is a Standby button
on the Venus console. When this button is pressed a software command is generated in the Venus
console. This command is passed to the rest of the computers. The Mars then sends a command
to the PDU IO board through the CAN bus to turn off power to the various parts of the system. The
PDU IO board in turn turns off the various relays. Pressing the Standby button de-energizes the K2
relay, removing power from the positioner, wallstand, OTS, monitors, and generator auxiliary 1.
See the block diagram to see what parts are On and Off. See Figure 2-20.

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Figure 2-20 PDU Standby
2.9.6.3 Shutdown
There is no power off hard button on this system. The system is turned off by selecting the
SHUTDOWN button in the UTILITIES menu on the User interface screen. Pressing the Shutdown
key (a soft key on the IUI) starts an orderly shutdown of the IUI, digital system and system controller.
When the shutdown is pressed on the Venus console, a message is send to all the computers. The
Mars computer first sends a command to turn on a backup watch dog timer in the PDU IO board.
During the shutdown process if the computers get hung up, this timer will expire and force a hard
shutdown of the system.
Normally the Mars then sends a command to turn off power to most of the system except for the
UPS which keeps the computers powered. The relays K1 and K2 are de-energized as a result of
the shutdown command. Thus removing power from the rest of the system.
The computers go through a shutdown process and at the end Venus sends an Off command to
the UPS through a serial connection between the Venus and the UPS. When the UPS is turned off
the watchdog timer running in the PDU IO board is cleared. See Figure 2-21.

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Figure 2-21 PDU Standby
2.9.6.4 Emergency Off

The room emergency button is a two pole two throw switch. One set of contacts is connected to the
room power supply main circuit breaker. So when this button is pressed the main circuit breaker will
trip and remove power from all components except for the ones powered by the UPS. The second
normally closed contact in the emergency switch is connected to the PDU IO board. This board
provides a 24 V to this switch and the return from the switch is monitored by this board. When the
switch opens this line, it is detected by the PDU IO board and it sends a hard-wired command to
the UPS to shut-off the UPS immediately. If there is a break in the wire in this circuit, the system
thinks that somebody pressed this button and the system will shutdown. See Figure 2-22.

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Figure 2-22 Emergency Off
2.9.6.5 Tableside Emergency Off

This button is hard wired into the PDU IO board through wires in the RT bus. When this is pressed
the power to the Gantry, OTS and the wall stand is removed immediately by turning off the relays
in the PDU which provide power to these devices. The PU IO board informs the Mars computer
regarding this action through the CAN bus. When the button is released, the power is restored to
these devices by turning on the relays in the PDU. See Figure 2-23.

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Figure 2-23 Table Side Emergency Off
2.9.6.6 Power Loss

There is a UPS in the system to provide power to the computers (IUI, Digital System and System
Controller) when there is a short duration(30 seconds approximately) main power loss from the
hospital power supply. This also provides power to the devices to keep the communication between
the computers, keyboard and the modem. See Figure 2-24.

GE MEDICAL SYSTEMS
Figure 2-24 Power Loss
2.9.6.7 Reset
When the Reset button on the IUI is pressed, the following three steps occur simultaneously:
1.) A reset signal is sent to the three computers. If the computers are operating normally, they will
undergo an orderly shutdown and reboot. If the computers are hung, a hard reset will occur
after two seconds.
2.) The generator CPU board is reset.
3.) The positioner, wallstand and OTS power is cycled. The K3 relays stays on for ten seconds,
turns off for ten seconds and finally turns on again.
2.9.6.8 UPS / Remaining power interlock.

There is a hard-wired interlock in the PDU between the UPS output and the rest of the system power
output. Through this interlock, when the UPS output power is turned off the rest of the system power
output power is removed. This is to assure that the system is turned off even if there is a failure in
the communication between the Mars and the PDU IO board.
Section 3.0
Generator “Jedi”
3.1 INTRODUCTION
Jedi is GE Medical System’s name for a family of compact high frequency X-Ray generators used
in many of its products. This generator family covers a wide range of applications from the mobile
equipment up to the vascular systems:
• JEDI 12-25KW: Mobile applications

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• JEDI 24-48KW: CT applications
• JEDI 32-50KW: RAD applications
• JEDI 50-65-80KW: R&F applications
• JEDI 100KW: VASCULAR applications
3.1.1 Standard features

• A family of 150kV generators operates from 12KW up to 100KW for all the major radio logic,
fluoroscopic and CT applications. This family handles exposures ranging from 1ms to
continuous; ranging from 0mA up to 1000mA
• These generators feature the very latest technology available:
- constant potential independent of the line voltage variations.
- power generation by a high-frequency converter (High voltage ripple: 40KHz-140KHz)
- distributed micro-processor controlled functions (CAN bus).
• Single phase, three phase or battery power source.
• Very low kV and mA ripple, excellent accuracies and dose reproducibility
• Compatible with a wide range of tubes, high speed or low speed, supplies up to 3 different
tubes. Thermal load interactive integrator ensuring optimum use of the heat protection curve
of the x-ray tube
• Serviceability: high reliability, fast installation (no generator calibration), application error
codes reported ensure fast troubleshooting
• Meets CE marking (and in particular EMC), IEC, UL, CSA, MHW regulations (if required)
• Optional pulsed fluoroscopy
3.1.2 Typical Applications
3.1.2.1 Rad
• “3 point” mode
• Automatic exposure control: AEC
• Tomography
• Automatic tomographic exposure (AET)
3.1.2.2 Surgery
• continuous or pulsed fluoroscopy
• Rad exposures
• 30 frames per second cinema
3.1.2.3 RF
• “3 points” mode
• Tomography
• Automatic tomographic exposure
Page 58 Section 3.0 - Generator “Jedi”

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• Automatic brightness control in fluoroscopy (ABC)
3.1.2.4 VASCULAR/CARDIAC
• cinema (up to 90 frames/s)
• Automatic brightness control in fluoroscopy (ABC)
3.1.2.5 CT
• variable mA scans
• low mA fluoroscopy
3.1.3 Architecture
Refer to Jedi generator functional architecture block diagrams in Section 3.4. The Jedi family is
composed of:
1.) A kernel
- High voltage chain composed of kV control, HV power inverter and HV tank
- Anode rotation function
- Tube filaments heater function
- control bus for communication between the functions
- DC bus for power distribution to each function
- Input voltage to DC conversion: AC/DC function
- Low voltage power supply
- Application software, running on the kV control board
These functions are the Jedi core. They are present in all versions of the generator. A function
can be unique for all products or can be derived in several releases based on product
specification
Example: Anode rotation function is declined in 2 releases:

- low speed rotation for applications where the tube is a 3000 rpm max tube
- high speed/low speed rotation for applications where at least one of the tubes is a 8000-
10000 rpm tube
However, control bus is unique
2.) options, depending on the application

- System Interface for:
* CT
* RAD (console interface, room interface, AEC management present or not)
* ATLAS
- EMC function

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- Grid function (RF, vascular)
- Bias function (RF, vascular)
- Tube management (2 tubes or 3 tubes option)
3.) packaging
The packaging architecture consists in a set of boxes which can be put together in several
ways to make it fit either in a cabinet or a console foot or a table foot. The boxes can also be
split in 2 units distant of several meters (example: CT gantry).
Depending on the configuration, the following modules will be found:
1 2 3 4 5
POWER AUXILIARY ACDC Optional interface Grid/Bias
(1 box) (1 or 2 boxes) (1 box) (1 box plugged in the (optional)
Power box) (1 tank)
1 tube Standard 3 Phase
• HV tank 1 tube • Low Voltage Power • EMC function • Rad interface Ingrid tank
• HV power Supply (100W) • ACDC function • AEC interface (plugged directly in
inverter • Heater function the X-ray tube)
• KV control • Rotation function
• system interface
if not (4)
• AEC function if
not (4)
2 tube 2 heaters – 1 tube 1 phase
• HV tank 2 tube 1st box • EMC function
• HV power • Low Voltage PS (optional)
inverter (400W) • ACDC function
• KV control • SF Heater function • Low Voltage
• system interface • LF Heater function Power supply
• AEC function 2nd box (100Wmono)
Rotation function
2 heaters – Two tubes
1st box
• Low Voltage Power
Supply (400W)
• SF Heater function
• LF Heater function
2nd box
• Tube switch
function
• Rotation function
1 heater – Two tubes
1st box
• Low voltage Power
supply (100W)
• Heater function
2nd box
• Tube switch
function
• Rotation function
Table 2-1 Packaging Architecture

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3.2 Technology Overview
3.2.1 kV Control
3.2.1.1 Introduction
The kV control function controls the generator. Its main functions include:
• a CPU, which runs the generator software:
- console and/or system communications
- exposure sequencing (rotation, heater, exposure control)
- mA regulation
- tube and generator thermal protection
- generator configuration management
- tube, AEC calibrations
- generator diagnostics (application background diagnostics and service diagnostics)
• a standard interface to system interface
• a Control bus interface
• exposure control
• HV power inverter control
• IGBT gate drive supply control
• HV chain measures and safeties (kV, mA, mAs, inverter currents, inverter gate supply, DC
bus)
3.2.1.2 CPU core
First generation
The CPU is a 68360. It’s micro-controller based CPU runs at 25MHz. Program memory consist of
1MBytes of flash memory, which allows the software to be downloaded through the system. Data
memory contains a 512Kbytes RAM and 8Kbytes of battery backed-up RAM used to store the
configuration/calibration/errorlog data. This memory also includes a clock used
mainly for thermal algorithm calculations.
Second generation:
CPU is a Power PC micro-controller based CPU running at 50MHz. Program memory is a 2Mbytes
flash memory which allows the software to be downloaded through the system or laptop
communication path. Data memory contains a 256Kbytes RAM and 32Kbytes battery backed-up
RAM used to store the configuration/calibration/errorlog data. This memory also
includes a clock used mainly for thermal algorithm calculation.
The generator software is based on the VxWorks operating system and divided into several tasks
and layers:
• communication tasks controls the various communication paths provided by the CPU
• application task handles the exposure state machine
• thermal management task
• device controller tasks which identifies and then drives the kV control, mA control, heater and
rotation functions

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Calibration and diagnostic functions are also part of the generator software
3.2.1.3 Standard interface to system interface

kV control provides a standard interface on which various system interfaces can be plugged
depending on the system configuration. This “standard” interface provides:
• a CAN communication line
• 5 UART lines
• 5 configure able IO lines
• 4 system interface identifier lines
3.2.1.4 Control bus

kV control is connected to the generator through the internal communication bus:
• CAN communication line used to drive heater and rotation functions
• reset line (from kV control to other functions)
• mains_drop (from LVPS board to signal without delay a drop on the main supply)
• ctrl_to_grid (from kV control to grid for pulsed modes in vascular)
• speed_cons_to_rotor (spare)
• +15V (used to create locally 5V supply)
• -15V
CAN is a network car industry standard. Its main purpose is to bring short command messages in
hostile environments over few meters up to hundreds of meters with a guaranteed latency and
without any information loss.
Defined for small systems, it does not require large amounts of software to encode and decode the
messages.
The network hardware is based on a differential line (2 wires) driven at each node by a CAN driver
(ISO/DIS 11898 standard). The length of the network define the maximum network speed: 1Mbit/s
max up to 30m length, 500Kb/s up to 100m.
The messages have a fixed length. Their structure is the following:

• an identifier field which defines at the same time the command number and the priority of the
command (smaller the command number is, higher is the priority)
• 8 bytes of data max
• checksum of the message
The CAN protocol ensures that:

• the highest priority message is send the first
• if a message is corrupted, it is resent automatically
• if more than 8 bytes of data must be transmitted, data is divided in packets of 8 bytes and
several messages are generated consecutively
3.2.1.5 Exposure control
CPU Core (Exposure control master)

• Once the system connected to the generator is known, the CPU downloads the exposure
control configuration stored in a FPGA (DSP also in the case of PPC control board).
• Then, the CPU manages the slow functions while the FPGA manages the hard real-time
functions:
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FPGA
• handles the system/generator IO lines (including exposure command lines, brightness...)
• triggers/cuts the exposure
• handles the HV power inverter safeties signals (by the DSP in case of PPC kv control board)
• handles X-ray On signal
• counts the mAs (n/a for CT applications)
• generates the 1KHz microprocessor main interrupt
CPU
• update the exposure state machine based on the signals send by the FPGA
• generates the exposure enable to the FPGA once everything is ready for the exposure
• calculates and applies kV, mA, exposure time, mAs
• counts the exposure time
• regulates mA each 1ms
• counts the brightness for AEC (n/a for CT applications)
• regulates brightness for ABC in fluoroscopy (n/a for CT applications)
• handles heater and rotation errors
• manages the event and error log
3.2.1.6 HV power inverter control

This function is controlled by the FPGA (or DSP + FPGA in the last KV control generation). It
handles the HV power inverter state machine. This state machine goes into its active states when
exposure control function triggers the exposure. Then the state machine successively drives each
IGBT gate. The delay applied between two consecutive IGBT “on” commands is calculated inside
the FPGA (or the DSP in the case of the PPC board).
This is the minimum time of the following two:

• the parallel resonance time which represents the max delay not to go over (the inverter must
not be driven below the parallel resonance frequency)
• the time calculated by the kV regulation
This second time is the result of the kV regulation loop whose role is to make the measured kV equal
to the kV demand:
• kV measure is subtracted to kV demand to create error_kV (analog or 360 kV control board
and digital for the PPC board)
• error_kV is divided in two parallel chains made of a kV error peak detection followed by a
analog to digital conversion (analog)
• the digital error then feeds a digital PI (proportional Integral) regulator which calculates the
delay to apply before triggering the next IGBT (FPGA) for the 360 kV control (computed by the
DSP in case of PPC board)
Each IGBT “off” command is triggered by the 0 Amps crossing of the serial resonant current.

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HV power inverter serial resonant
current
IGBT IGBT
diode curent
curent
IGBT
IGBT diode
curent curent
IGBT_HIGH command ON
IGBT_LOW command ON
Figure 2-25 IGBT Command Timing
In case of tube spit, the state machine goes to the “off” state, stays 100us inside it and automatically
restart if the maximum number of tube spits is not reached. This time can be longer in the case of
RAD or RF products (4 ms, for example). At the same time, the main software counts the number
of spits and informs the system with a process depending upon the application.
IGBT commands from the FPGA then goes through drivers to the inverter. The drivers can be
disabled by a mains drop or an incorrect gate supply. The IGBT gate drive supply is controlled
synchronously with the inverter state machine:
• gate supply voltage is read and compared to a reference
• each two IGBT command, the gate supply IGBT is commanded with a duration proportional to
the gate voltage error
• between two exposures, the inverter being not running, the gate supply is regulated by at a
fixed (8KHz) frequency. Constant gate supply voltage is ensured by regulating the gate supply
command pulse width.
3.2.1.7 HV chain measure and safeties

HV chain is protected by fast and slow safeties. Fast safeties are implemented in analog form and
cut the HV power inverter state machine in case of error:
• over kV
• no kV
• kV regulation error (at the 7th error in the exposure)
• anode spit (after the max number of tube spits allowed for the application/tube)
• cathode spit (after the max number of tube spits allowed for the application/tube)
• max resonant current
• gate supply ok
Slow safeties are based on measures made by the micro-controller. The following signals are
measured each 1ms:
• kV measure
• kV unbalance
• kV demand
• mA measure

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• HV tank temperature
• gate supply voltage
• DC Bus voltage
These measurements provide a second way to detect a fault condition in the HV chain and put the
generator in a safe state.
3.2.2 HV power Inverter and HV Tank function
For this section see Figure 2-33 and Figure 2-34.
The HV function involves the following sub-assemblies
• HV power Inverter
• HV power Inverter LC
• HV Tank
• Tube
The main features of the function are:

• HV power inverter principle is common for all applications. Several tierings have been defined
to cover the 12KW-100KW applications range:
- Battery powered HV power Inverter: 12KW-25KW inverter when supplied by 100VDC-
200VDC battery
- RAD/RF 32KW, 40 kW, 400mA, 640mAs inverter
- CT 36KW, 300mA max, 18720mAs max, 3KW average inverter
- RAD 50KW, 640mA, 640mAs inverter
- VASC/RF 100KW inverter
• HV Tank principle is common for all applications: 40kV-150kV, 0mA-1000mA max. Two HV
Tank types have been defined to cover battery powered generators on one side and the 1
phase or 3 phase products on the other side.
• In the case where 2 tubes are connected to the generator, a 2 tubes HV tank with commutation
capability replaces the standard HV tank to connect the HV output to the right tube.
3.2.2.2 HV power Inverter principle

See Figure 2-33 for the following discussion.
The HV power Inverter is a hypo-resonant type half-bridge inverter. Power switches used are
IGBTs. Depending on the power requirements, either 1 IGBT per polarity is installed (2 IGBTs total)
or 2 IGBTs in parallel per polarity for high power applications (4 IGBTs total). The resonant circuit
presents two resonant frequencies:
• A serial resonance frequency made by the resonant capacitor and the sum of all the circuit
serial inductors (including the HV transformer leakage inductance). Its frequency is fixed at
50KHz to 70KHz depending on the inverter tiering.
• A parallel resonance frequency made by the resonant capacitor and the parallel inductance.
Its frequency is fixed at 20KHz for all tierings
The inverter drive frequency is ranging between the parallel frequency and the serial frequency. The
inverter is producing the maximum current when it is commanded near (under) the serial frequency
(ex: CT inverter produces 300mA at <=50KHz) and produces the minimum current when it is
commanded near (above) the parallel frequency (ex: 0mA at >=20KHz). Serial and parallel current
are measured by current transformers and used by the inverter control for the HV power inverter
command (see kV control section).

GE MEDICAL SYSTEMS
The HV power inverter is composed of two FRUs:
• the inverter comprising:
• heat-sink
• IGBTs and aid circuit
• gate command board
• parallel inductor
The inverter LC composed of:

• aid and serial inductor
• filtering capacitors
• resonant capacitor
• serial and parallel current measure transformers
Each element can vary from one application to another. Some general rules can be drawn:
• 100KW requires 4 IGBTs
• 50KW and less require 2 IGBTs
• value of resonant elements vary from one application to another because they are linked to the
peak power and the average power
• gate command board is unique
With IGBTs being connected to the DC Bus, both their gate drivers and the gate drivers must be
isolated from ground. The IGBTs are controlled by the kV control board. The command is isolated
by small pulse transformers. They command a semi-power stage which drive the IGBTs gates. The
gate commands have the capability to drive up to two 400A IGBTs in parallel which is the case for
vascular power.
IGBT gate drivers supply is made by a small fly-back power supply fed by the DC Bus and regulated
by the kV control board (see kV control section). The fly-back IGBT command is made through a
pulse transformer. This supply produces +20V and -10V for IGBTs gates drives.
All inverter commands and measures (including inverter identificator) are going from and to the kV
control board through a bridge made by the HV tank kV measure board.
3.2.2.3 HV Tank principle

HV Tank is sealed by the kV measure board placed on top of it. This board must not be removed.
The HV Tank can be used in any position. A temperature measure is placed in the oil under the
cover and is used to track HV Tank temperature and to prevent overheating (max temperature
allowed is 67 degrees C).
The HV transformer presents two primary coils connected in serial and to the inverter LC. Four
secondary coils are connected in serial along with their rectifier/filter stage. The transformer ratio is
417 for 1 and 3 phase input line applications (which lead to a 400VDC-800VDC DC Bus) and is four
time higher for battery powered applications (which lead to a 100VDC-200VDC DC Bus).
Total HV filtering capacitor is 1nF inside the HV tank.
The inverter topology along with this HV filtering capacitor produces a HV ripple in the 40KHz-
140KHz range, not measurable at low mA up to a few percent at max mA.
Both cathode and anode kV are measured and reported to the kV control board for kV regulation,
kV safeties and tube spits detection. mA measure is made in the cathode side of the transformer
and transmitted to the kV control board for mA regulation and safety.
3.2.3 System interface

System interface is the FRU which adapts the generator to the system. It is declined in different
versions depending on the system.

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3.2.3.1 CT interface
Refer to Figure 2-46 in the following discussion. Interface between the generator and the OGP
consists of:
• an isolated CAN communication line to the OGP
• 3 isolated RS485 lines:
• exposure command
• X-ray on
• reset
• A RS232 line for the laptop connection
3.2.3.2 RAD interface

Refer to Figure 2-47 in the following discussion. RAD interface consists in:
• Two plugs with parallels signals for Buckys. (One for table, the second for Wall stand).
• One plug for connection with X-ray light and interlock door.
• One RS422 communication line to the console
• One RS232 line for the laptop connection
• One RS232 line for the tests
• One plug for AEC board option
INTERFACE Bucky, Function principle

The external CAN coming from kV Control board is converting in parallel signals to monitor bucky
and to receive hardware signals (hand-switch and exposure command, interlock door).
When prep and exposure signals are received by kV control board and after checking safeties the
exposure demand signal is sent to wall or table bucky (depending of technique selection).Then,
when the bucky is ready, it sends to kV control board Exposure command signal.(one hardware line
and one to CAN line). At this time the X-Ray exposure starts.
Buckies are plug on J5 for table Bucky and J6 for Wall Bucky.
Workstation signals are used to manage either Table or Wall bucky or Direct mode (exposures on
Table top)
INTERFACE w/room door signals

On plug J7 an interlock door signal is provided to inhibit exposure when room door is opened (If no
interlock door a jump as to be made in J7 pin 1 and 2). A prep switch is also provided by the
generator on plug J7 to monitor an X-Ray light (generally located above the room door).
Console and service terminal communication

Two serial links are provided on interface board to dialog with Control Console, service terminal.
The third one is for GEMS use only. One serial link RS422 type for Console in plug J9,the other
serial links are RS232 type.
3.2.3.3 RF FUNCTION (used for PRECISION 500D)

Refer to Figure 2-48 in the following discussion. RF interface consists in:
• Interface between the generator and the system consists in:
• an isolated CAN communication line to the system

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• 4 isolated RS485 lines:
- exposure command
- exposure enable
- X-ray on
- reset
• One plug for AEC board option
3.2.3.4 AEC
AEC FUNCTION
Refer to Figure 2-35 in the following discussion. AEC board is able to drive up to four GEMSE
ionization chambers.
• Two ionization chambers are used generally: One for table, the second for Wall stand.
• One analog ion chamber is used in “Uroview” generator, for the table.
• One analog ion chamber is used on Precision generator, for the Wall stand (note: a digital AEC
is used for the table digitally managed between system and Jedi)
• The ionization chambers are connected in front of the Interface Module.
• On each plugs (two) the following signals are available:
- Ionization chamber selection (1 to 4)
- Cells selection (Left, Middle or Right)
- Return voltage from ionization chamber (VAEC1 to VAEC4)
- High power supply (230Vdc) for ion chamber polarization (if necessary)
- Low voltage power supply (+/- 15Vdc)
AEC Function Principle:

During an exposure the output of an ionization chamber (VAEC1 to VAEC4) is monitored to
determine when the required density on film has been reached. This result is obtained by sending
pulses to kV control board (through Interface board). to increase the value in a software counter.
These pulses are also sent to a hardware counter followed by a DAC. The DAC output voltage is
then compared to the feedback voltage of the ionization chamber selected (AEC1 or AEC2). When
the return voltage of the ionization chamber is greater than the output voltage of the DAC, a new
pulse is generated. The exposure is cut when the software counter on kV control has reached a
calibrated value.
The value of the software counter is calibrated in service mode and it is depending of kV and
exposure time. These parameters are called: kVef and kT in calibration mode. The value VREF is
corresponding to the software counter value: VREF= kVef x kT
3.2.4 Heater function
Refer to Figure 2-36 in the following discussion. The heater function involves the following sub-
assemblies:
• Heater board
• HV tank heater transformers
• Tube filaments

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• One type of heater board is available:
- a 1 inverter heater board for applications which do not a fast exposure switch from one
filament to the other. In this case, 1 inverter powers alternatively the two filaments.
- For applications which need fast exposure switch from one filament to another (This
requires to pre-light one filament when the other is used), 2 heaters board are used in
parallel.
• Each heater board is able to drive all kind of filaments up to either 5,5A or 6,5A depending of
the filament type, and 10A in boost mode.
• Heater function includes filament protection against overheating and filament open detection
3.2.4.2 1 Inverter Heater

Refer to Figure 2-36 in the following discussion.
The heater inverter is an hyper-resonant half bridge inverter fed by a 160VDC voltage provided by
the Low voltage power supply function or the battery voltage (100VDC-200VDC) in case of a battery
powered generator.
The resonant frequency is fixed at 20KHz, and the working frequency range is between 20KHz
(maximum power) and 60KHz (minimum power around 1,5A in the filament).
Current waveform in the inverter is approximately a sine wave. The inverter working frequency
range makes it completely inaudible.
The filaments being at the cathode voltage, an isolation transformer for each filament is located in
the HV Tank. These transformers present a 1:1.25 ratio leading to a RMS current in the heater
inverter 1.25 times the filament current.
The inverter is switched to one of the two filaments by the focus selection relay.
The input voltage being referenced to ground, no isolation is required to drive the MOS switches
The heater drive mainly relies on a 16 bits, 20MHz, 32Kbyte memory micro-controller.
It is in charge of the main functions:

• Get at power-up the heater database containing all the data required to drive the filaments
(through the CAN serial line of the Control Bus):
- filament max currents
- boost duration
- inverter current safety levels
• Receive the commands (ex: go to filament=5A on small focus), and update the heater state
accordingly
• Measure the inverter current and regulate the inverter
• Simulate the filament temperature and protect it against overheating
• Give the feedbacks (ex: filament=5A, errors) to the main software, and put the heater in a safe
state in case of error
• Read the +15V, -15V (Control bus voltages), heater supply bus and inform the main software
The micro-controller commands the power bridge drive through an EPLD in charge of:
• de-multiplexing the drive frequency to command the 2 MOS
• stop the inverter in case a safeties which require a fast action: over-current, over-voltage
(=filament open detection), inverter short circuit, mains drop, tube temperature reaches 70
degrees
• drive the focus selection relay and read its position

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The filament current accuracy and reproducibility must be excellent (less than several 1/1000) to
ensure a good mA accuracy and reproducibility. Filament current being not measurable (because
at high voltage), the heater inverter current (and not the filament current) is regulated.
The heater inverter current is measured and converted to RMS. The RMS current is measured by
the micro-controller compared to the reference and the error leads to an adjustment of the inverter
drive frequency.
At the same time, the micro-controller tracks the filament temperature based on the filament current
applied and prevents overheating.
3.2.5 Rotation function
Refer to Figure 2-38 in the following discussion. The rotation function involves the following sub-
assemblies:
• Rotation board
• Rotation capacitors module
• Tube stator

• One type of rotation board is available: high speed (max speed=180Hz=10800rpm) rotation
board (with the capacity to drive the rotor in Low Speed)
• Each rotation board is capable to drive GE tubes (23Ohms/23Ohms stator), CGR tubes (50/
110) and all vendors tubes. Tube adaptation is made by selecting the right capacitors module
to adapt to the stator.
• High speed rotation is capable to drive both tri-phased stator and bi-phased stators.
• In the case where several tubes are connected to the generator, the Tube Management
module (optional module only present when several tubes are connected) manages the tube
selection. This module has the capability to mix up to 3 different tubes with different stators
• The rotation function also manages the tube thermal safeties and the tube cooling commands
3.2.5.2 High speed rotation

Rotation Principle
Since the rotation function must be able to drive either tri-phased stator or bi-phased stators, the
inverter is a three-leg inverter with six IGBTs. This module is packaged in one pack.
The inverter is feed by the DC bus generated by the AC/DC board through a small EMC filter
(voltage 400VDC-800VDC for one or three phase input line generators, or battery voltage
(100VDC-200VDC) for battery powered generators).
The inverter drive uses a PWM (Pulse Width Modulation) of the IGBTs commands.
This principle consists in applying a periodic command on the IGBTs equal to the speed selected
in order to generate a sine wave current in each phase at the anode speed frequency with the
optimum angle between the phases.
Inside this “fundamental” command frequency, the IGBTs commands duration is modulated in order
to get the right level of current in the phases.

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5 3 1
P
Common
A
6 4 2
rotation speed period (ex:180Hz)
motor current amplitude modulation

ON
IGBT_1
OFF
IGBT_3
IGBT_5
IGBT_2 / IGBT_4 / IGBT_6 = opposite of IGBT_1/ IGBT_3 / IGBT_5
inverter
phase P current
inverter
phase A current
Figure 2-26 Example of bi-phased SLEM motors high speed drive timing
Depending on the stator windings number (2 or 3), of their impedance and of the speed selected,
the main and auxiliary phases are either connected directly to the phases (example: in high speed
mode on a tri-phased low impedance stator, in low speed mode for a bi-phased stator, in high speed
brake) or through a module of shift capacitors whose role is to put the right angle between the
phases to ensure maximum efficiency in acceleration and run.
This capacitor module is defined for each stator and so different from one stator to another.
Rotation is including a relay which allow to put the capacitors in the circuit and to short-circuit it
depending of the state of the rotation drive.
As the IGBTs are connected to the DC voltage, IGBTs gates drives require isolation. This is
accomplished through opto couplers. Gates drives power supplies are generated by a small fly-
back power supply which uses the +15V of the Control Bus to generate 4 isolated +15V to power
each IGBT gate (and the 5V for all logic function).
The rotation drive mainly relies on a 16 bits, 20MHz, 32Kbyte memory micro-controller.
It is in charge of the main functions:

• Get at power-up the rotation database containing all the data required to drive the stator
(through the CAN serial line of the Control Bus):
- currents reference for each state
- acceleration and brake durations
- inverter current safety levels
• Receive the commands (go to speed=10000rpm), and update the rotation state accordingly
• Measure the inverter currents and regulate the inverter (fundamental and modulation)
• Give the feedbacks (speed=10000rpm, errors) to the main software, and put the rotation in a
safe state in case of error
• Read the tube safeties and drive the tube cooling
- The micro-controller commands the power bridge drive through an EPLD in charge of:

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- mixing fundamental and modulation commands
- de-multiplexing the PWM command to command the 6 IGBTs
- stop the inverter in case a safeties which require a fast action: inverter overload, mains
drop, tube temperature reaches 70 degrees
- drive the high speed relay
Fundamental frequency is applied so that the sine wave in the phases is at the frequency
corresponding to the desired anode speed. It is calculated by the micro-controller.
The modulation of the IGBT commands is the result of a regulation loop which ensure to reach the
right current level for the tube and the rotation state (example: high speed acceleration current = 7A
for Qj tube, high speed run current = 2A for Qj tube).
This loop ensure optimum acceleration performances in all conditions of DC bus and of stator
temperature.
The current is measured inside 2 phases, reconstructed for the third phase.
Then the measure is compared to the reference value and the error leads to an adjustment of the
modulation rate.
All rotation states are regulated except the brake. Brake includes a state where a DC current is
generated in open loop mode, the commands frequency depending only of the tube and the line
voltage.
The rotation function has capabilities which are not yet developed like:
• variable speed profiles for tri-phase motor drive
• anode speed control
Tube Cooling
The high speed rotation board handles the following functions:
• supply and reading of two tube thermo-switches (typically 40 degrees and 70 degrees). The
information is send to the main software which takes appropriate actions based on the tube
and system
• when supplied by a 1 phase 115VAC or 230VAC, capability to power permanently a tube lamp
• when supplied by a 1 phase 115VAC or 230VAC, capability to power a fan and/or pump and/
or to trigger a chiller whenever decided by the main software based on tube and system
• read-back of the cooling supply voltage to prevent tube damage in case of a no cooling
condition
Note that the tube cooling supply (115VAC or 230VAC) must be isolated from ground and protected
by a fuse at the source wherever this voltage is created.
3.2.6 Switching Tube Function

Refer to Figure 2-45 in the following discussion. This function is realized with the following sub
assemblies:
• Two Switching Tubes board
• Two tubes HV tank with motorized internal switch
The Two Switching Tubes board ensures

• the switch of the rotation stator currents (delivered by the rotation board) between tube 1 and
tube 2 with management of the shift capacitors. It may have 4 shift capacitors – 2 per tube -
used for high speed with the selected tube or shorted for low speed)
• the switch of the filament currents from the heaters board to the Two tubes HV tank
• the management of the cooling supply between tube 1 and tube 2
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• the management of the thermal security signals between tube 1 and tube 2
• the control of the motor for the High voltage switch and the management of the HV tank
position switches
• the dialog through CAN bus with the main generator software.
The two tubes HV tank contains
• the same high voltage stage than the standard single tube HV tank
• an internal mechanical switch allowing a selection between two High Voltage outputs (4 HV
receptacles)
• a motor driving the mechanical switch controlled by the Two Switching Tubes Board.
3.2.7 EMC filter function
EMC filter is designed to make the generator compliant with the EMC conducted noise and
immunity regulatory by filtering the HV power inverter noise (rotation noise is mainly filtered on
rotation board).
It is placed at the power input of the generator and mainly composed of one to several (L,C) filters
cells placed in cascade to filter common mode noise (filters referenced to ground) and differential
mode noise (filters between phases).
EMC filter is declined in:
• single phase version
• three phase version
3.2.7.2 3 phase EMC filter

3.2.8 AC/DC
AC/DC function consists in creating the DC Bus. Standard DC Bus range is 400VDC-800VDC.
This voltage is feeding all the main generator functions (inverter, gate drive supply, low voltage
power supply, rotation).
DC Bus to the auxiliary functions (gate drive supply, low voltage power supply, rotation) is protected
by a fuse rated to protect them against short circuits.
Note that the mains phases feeding the generator must be protected wherever they are created with
a rating matching generator power requirements.
AC/DC function is declined in:
• single phase version
• three phase max power version
3.2.8.2 Single phase AC/DC

This function is designed to create a DC Bus in the 400VDC-800VDC range when supplied by a
230VAC (200 to 240V) input.
The design uses a voltage doubler principle to generate the right DC Bus voltage.
If the mains is lower than 230VAC, an auto-transformer may be required to generate a 240VAC
input to the generator.
The function includes a set of storage capacitors whose role is to limit the DC voltage drop during
the exposure.

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The capacitors number required to run up to 32KW exposure being high, the generator power-up
requires a pre-load at low charging current. Once the capacitors are charged, the pre load resistor
is shunted for normal operation through a contactor.
The capacitors also require a discharge circuit to comply with a fast access to the generator once
it is powered off.
In order to protect the discharge circuit against overheating, three successive ON/OFF sequences
are allowed. After the third, the software inhibits any ON command within 15mn.
3.2.8.3 3 phases max power AC/DC

Refer to Figure 2-40 in the following discussion.The function mainly includes differential modes
filters. The main storage capacitors are designed to limit the DC Bus drop during the kV rise.
3.2.9 Low voltage power supply (standard LVPS)

This fly-back type power supply generates the +15V/-15V supplies for the generator. At the same
time it creates the heater supply voltage.
This power supplies is powered by the main DC bus. It means that all the generator is off when the
3 phases are off.
Low voltage power supply is declined in 2 versions:
• - for 3 phases application
• - for 1 phase applications:
3.2.10 Low Voltage power supply 400W (LVPS400)

• The LVPS400 board is designed to supply the various circuits of the JEDI generator with the
required low voltages. The board communicates with JEDI generator by the mean of a CAN
bus and one real time line (MAINS_DROP). It is intended to be connected to a fuse protected
230V RMS Mains. (115V RMS with a specific strap). It has 11 specific outputs:
• P15VCAN and M15VCAN to supply mainly the PPC board and the low voltage parts of
HEATER boards and ROTATION board.
• P15V EXT intended to supply mainly the low voltage circuits of the grid control tank - InGrid
tank- (If required)
• 24V GATE to supply the Gate control board of JEDI main inverter (HELIOS application) or a
ON/OFF contactor (in UROVIEW single phase system).
• Four specific outputs (24V FAN) intended to connect fans. Each output can drive two fans
connected in parallel, so depending on the considered system, up to eight fans can be used.
Each output voltage is programmable by firmware
• Two outputs 160 H1 and 160V H2 designed to supply two different HEATER boards for XL and
XS filament. (if required)
• 160V EXT to supply the INGRID tank power circuits (if required).
The board monitors the output voltage and current. Depending on the values, it may generate
warnings, which are sent to the kV control board, but the exposure is not interrupted.
Refer to the Low voltage power supply Bloc diagram in appendix:
3.2.10.1 Circuits description.

The LVPS400 board is constituted by
• A rectifier stage
• An auxiliary fly-back inverter which provides three specific voltages P15V, M15V and P7V
intended to supply the control and regulation circuits on the board
• A main regulated inverter with four separate outputs: P17V, M17V, P26V and P160V

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• Eleven separate regulators with individual ON/OFF function controlled by the LVPS micro
controller
• A control circuit
AC/DC Stage
This stage is composed by an EMI filter (L1, C19, C12), a rectifier bridge U10 and a tank capacitor
formed by C34,C43,C47,C36. The CTN U11 and U15 are used to limit the inrush current. For
115VRMS operation, pins 1 and 2 of J2 connector must be externally connected. A voltage doubler
stage is formed by two diodes of U10 and the capacitors C34 and C43 on one side, and the
capacitors C36 and C47 on the other side. The neon lamp DS8 lights as long as the capacitors C34,
C43, C47, C36 are not completely discharged.
The Mains AC input is monitored by the two signals LINE1 and LINE2. The needed isolation is
made by opto couplers U16. The DC signal, at the output of the rectification stage CR112 and
CR113, is applied to the comparator U14 which provides the signal _LINE ON to the micro controller
(needed data to generate MAINS_DROP to the JEDI generator and allow a preventive data back
up when the ac input voltage disappears)
Auxiliary fly-back inverter

It is a stand-by power supply which delivers the internal voltages needed on the LVPS400 board.
The inverter is supplied from the DC bus and protected by an internal fuse. The inverter is made
with an integrated fly-back driverU101, a switch Q16 and the transformer T1. The T1 secondary
voltages are rectified by the diodes CR24, CR128 and CR25.
Main inverter
POWER STAGE
The switches Q7 and Q12, the inductance L9 and the capacitors C52 and C53 are the main parts
of a resonant inverter working above the resonant frequency of about 20kHz. The transformer T2
provide the needed isolation and with its four secondary windings it can deliver after rectification,
the voltages P17V, M17V, P26V, P160V. The input lines of the gate switch drivers U19 are isolated
by opto couplers U20. The main inverter can be disabled by the LVPS micro controller with the
INV_ON signal (state 1 = inverter enable)
CONTROL AND FEEDBACK CIRCUIT

The switch control signals _CMD_INV_H and _CMD_INV_L are derived from a sawtooth generator
and the two comparators U17 and U18. The sawtooth generator is set up with the integrator U2
(1,2,3) and the comparator U2 (8,9,10) which drives a diodes switch CR102 to commute the voltage
of CR3 or CR4. The comparison level of U2 comparator is issued by the output 7 or 14 of U2
depending on the sawtooth polarity (diodes switch CR1). We obtain in this way a voltage /period
generator. This control voltage is derived from an inverter current measurement and a signal
_CONS_I_INV (output 14 of U5) calculated from error voltage.
The error signal is calculated from the reference voltage P10REF and the lowest voltage among
P160V, P26V and P17V (in respect to their nominal value) by the amplifiers U5 and U13 an the
diodes switches CR7 and CR8
When we start the inverter the signal _INV_ON has a transition from 1 to 0, Q3 is OFF and the
feedback reference voltage (On the Q3 drain) rise at a rate depending on R151, C10, C11 and
C118. followed by the inverter output voltages

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Regulators
P15V, M15V, 15V EXT, 24V GATE REGULATORS

These four linear regulators are the same type. They show only a slight difference in components
choice to take into account the various output power. The P15V CAN regulator, for example
includes:
• A ballast transistor Q13
• A driver stage Q123, Q124
• An error amplifier U13 which compare the output voltage to the reference voltage M10REF
• An enable /disable circuit Q117, Q5 with a rising voltage ramp R28, C23
A LED DS7 shows when the P15V CAN supply is ON.An image of the output voltage is sent to the
micro controller to measurement MEAS_V_P15_CAN
160V H1, 160V H2, 160V EXT REGULATORS

These three linear regulators are the same type that the previous one but in this case the error
amplifier and driver stage are made with a two differential transistors stage Q132 and Q133 for
160V H1 output
24V FAN1, 24V FAN2, 24V FAN3, 24V FAAN4 REGULATORS

These four regulators consist in a pulse width modulation switching stage. So each output can be
adjusted to the right value by the firmware.(taking in count temperature measurements) The PWM
signal is delivered by the micro controller. For the 24V FAN1 the switch is made by Q13 and the
MOS Q108, the output smoothing filter L5, C8, C114. An over current detection is provided with the
shunt R102 and the comparator U8 (_OVER_I_FAN1)
Control and Auxiliary Circuits

The control of LVPS400 board is made by the micro controller U7 which manage the CAN bus by
the mean of a transceiver CAN U1. A specialized circuit U6 reset the micro controller at power on.
A red LED DS5 lights when the micro is in reset state. The two LED DS3 and DS4 blink alternatively
in normal operation.
An integrated voltage reference circuit U12 and the amplifiers U9 generate the two needed
reference voltage P10REF and M10REF.
3.2.11 Generator Software

The generator software runs on the kV control CPU.
Its main function are:
• console and/or system communication
• exposure sequencing (rotation, heater, exposure control, mA regulation)
• tube/generator thermal protection
• Image quality algorithms
• tube, AEC calibrations
• Tube/generator tracking
• generator diagnostics (application background diagnostics and service diagnostics)
3.2.11.1 System Communication

The generator has some communication capabilities: CAN, RS232 (not for PPC kV control).

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Each communication path is connected to the application software through a communication driver.
This mechanism allows:
• to have the same generator behavior regardless the communication path used to drive the
generator
• to connect several interfaces at the same time on the generator
3.2.11.2 Exposure Sequencing

Refer to Figure 2-41, Figure 2-42 and Figure 2-37 in the following discussion.
3.2.11.3 Tube/generator Thermal Protection

The generator software simulates HV power inverter, HV tank and tube temperature in real time.
These algorithms are based on generator and tube models. They use the real kV and mA applied
to the tube.
They are used to protect the generator and tube against overloads.
They are also used to predict the exposure parameters/number of exposures allowed based on the
current generator and tube thermal status.
The algorithms parameters are tube and generator power dependent. They are included in the tube
and generator database downloaded in the generator during manufacturing integration or
installation.
Depending on the system using the generator, the algorithms can be either active or inhibited.
For CT systems, the tube thermal algorithm included in the generator is inhibited. Tube protection
is managed at the OC level.
3.2.11.4 Calibrations
Calibrations handled by the generator software are:
• AEC calibration
• tube filament calibration
See the service manual for a description of these calibrations. These calibrations do not apply to
CT systems.
FILAMENT AGING
Tube filaments are aging during the tube life leading to mA inaccuracy. In order to get accurate mA,
the mA accuracy is tracked all over the tube life:
At the beginning of each exposure, the difference between the mA demand and the real mA is
measured
The drift is recorded. It is used with a slow time constant to correct the filament drive initial values.
During all the generator life, the software logs the drift on both focal spot in the generator saved
RAM.
3.2.11.5 Tube Spits Counting

The generator software counts the number of tube spits occurring during an exposure.
The count generates an error if:
• the number of tube spits exceeds the maximum number allowed for the medical application (X-
ray applications: 7 spits, CT applications: (100+8*T) spits where T is the exposure time in
seconds)
• the tube spits rate exceeds the maximum allowed for the medical application (CT applications:
20 spits/0,1s, X-ray applications n/a)
In both cases, the exposure is stopped and the error is reported to the system.

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If the count do not exceed the limits, the number of spits is reported to the system at the end of the
exposure.
During all the generator life, the software adds the number of tube spits detected and log it in the
generator saved RAM.
3.2.11.6 Generator Usage Tracking

During all the generator life, the software logs in the saved RAM the following parameters:
Tube Filament aging corrections for small filament
Tube Filament aging corrections for large filament
Tube Total number of spits
Tube Anode + cathode spits
Tube Anode spits
Tube Cathode spits
Tube kV regulation spits
Tube Number of anode accelerations (new)
Tube Number of exposures on small filament
Tube Number of exposures on large filament
Tube Cumulated energy on small filament
Tube Cumulated energy on large filament
Tube Cumulated Rad exposure time on small focus
Tube Cumulated Rad exposure time on large focus
Tube Cumulated Fluoro time
Tube Cumulated mAs
Generator Max Temperatures for IGBT (simulated)
Generator Max Temperatures for Diode (simulated)
Generator Max Temperatures for Snubber (simulated)
Generator Max Temperatures for Base (simulated)
Generator Max Temperatures for Base_snubber (simulated)
Generator Max Temperatures for Heat-sink (simulated)
Generator Max Temperatures for 3mF Capacitor (simulated)
Generator Max Temperatures for HV Tank
Generator Max Temperatures for Inverter board
Generator DC_bus min. in preparation
Generator DC_bus max in preparation
Generator DC_bus min. during exposure

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Generator DC_bus max during exposure
Generator Time since first power-up
Generator Cumulated Power-on time
3.2.11.7 Diagnostics
Refer to troubleshooting for diagnostics functions.
3.3 Functional Description
3.3.1 Power-on Sequence

Generator power on can be achieved by various ways depending on the system (circuit breaker,
console ON/OFF, PDU contactor).
In all the cases, generator power on starts when input phases are applied to the generator.
For three phase Generator, the DC voltage rises on the AC/DC board when this voltage reaches
200VDC, the low voltage power supply starts providing the +15V/-15V bus (Rotation Leds DS1/DS2
lighting).
The +15V rise triggers the 5V rise on the kV control, heater and rotation (Led DS3 lighting) boards.
For single phase Generator, a DC voltage (400VDC,DS2 lighting)) is provided on ACDC board to
supply the low voltage power supply (NE1) as soon the input phases are applied. The low voltage
power supply starts providing the +15V/-15V bus (Rotation Leds DS1/DS2 lighting) and the
160VDC (DS1) for Heater board.
The +15V rise triggers the 5V rise on the kV control, heater and rotation (Led DS3 lighting) boards.
At this stage, many actions take place in parallel:
• kV control:
- software starts running the PRDs (1s) (in case of error, Leds S0-S7 display an error code)
- software downloads the kV control FPGA which starts regulating the inverter gate drivers
supply (in case of error Leds S0-S7 display an error code)
- software checks the hardware configuration:
* reads inverter identification
* reads HV tank identification
* reads system Interface identification
* talks on Control Bus to identify the function present
- In case of single phase generator. The software monitor the DC Bus pre load and full load
through low voltage power supply board. The sequence is the following:
* Check the DC Voltage value=0
* Monitor pre load relay on ACDC board during 15 seconds
* Check DC Bus voltage over 400V
* Monitor load contactor for full charge
* Remove pre load Relay after 5 seconds
* Check the DC Bus voltage over 450VDC min. and under 850VDC max
* In case of a wrong sequence an error is generated.
• heater:
- micro-controller starts running the PRDs (in case of error, Led ST0/ST1 flashes)
- then goes to the idle state
- heater supply bus reaches its final value

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• rotation:
- micro-controller starts by running the PRDs (in case of error Led ST0/ST1 flashes)
- then goes to the idle state
- gates drive supply reaches its final value
- DC Bus reaches its final value
• inverter: DC Bus reaches its final value on inverter LC and on gate drive supply
Once each main function is alive, kV control:

- checks the generator configuration consistency (in case of error, error message TBD is
send)
- installs the right hardware drivers
- talks to the system or the console (in case of no system/laptop presence detected, kV
control Leds S0-S7 display an error code)
- configures the final kV control FPGA
- sends to rotation and heater their database based on the knowledge of the tube selected
At this level, if no error has been detected, the generator is ready for the exposure procedure.
3.3.2 kV function
Refer to Figure 2-41 in the following discussion. KV function is mainly controlled by the kV control
exposure control function.
After power on, the exposure control FPGA is downloaded by the main CPU (and also DSP in case
of the PPC kV control board).
The FPGA then:
• configures the real-time lines to the system
• drives the inverter gate drive supply to provide the right voltage for the IGBT gates
• monitors the DC bus voltage, the IGBT gates voltage
Then the CPU receives the kV, mA, exposure time commands.
When the CPU receives the exposure enable signal (either by a communication message or by a
real time hardware line both linked to the prep button), it drives the filament drive and anode rotation
During this preparation phase, kV reference is applied to the hardware.
Once these functions are ready, CPU informs the exposure control that the generator is ready for
an exposure.
When exposure command goes in its active state, the CPU;
• starts exposure time counter
• starts mAs and brightness counters (for AEC cut-off) (if required by the application)
• measures kV demand, kV measure, DC bus, gate voltage, HV tank temperature each 16ms
during the exposure
• calculates new kV, mA reference in RAD tomography or ABC
• applies new kV, mA reference if the system/operator changes the parameters
Exposure control:
• starts the HV power inverter by driving the IGBTs
• put X-ray on in its active state
• regulates the inverter
• monitors the hardware safeties: tube spits, no kV, over kV, HV inverter over current, kV
regulation error

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When either exposure command goes down, exposure enable goes down, a fatal safety occurs or
a timer reaches its final count, the exposure control:
• stops the inverter
• puts X-ray on in its inactive state
CPU:
• store tube spit count, exposure count, exposure parameters
• computes the generator thermal status
When a tube spit occurs, exposure control stops the inverter 100us, informs the CPU that reads and
store the error, verify if the max number of spits is not reached, and restart if authorized. If it is a
hardware failure: exposure control stops the exposure, reports the error to the CPU, which in turn
that reports the error to the system.
When a measure goes out of range, the CPU stops the exposure and reports the error to the
system. The CPU also stores the error in the generator error log.
3.3.3 mA function
Refer to Figure 2-42 in the following discussion. mA function is mainly controlled by the kV control
CPU function.
After power on, the CPU sends a preheat command to the heater function (except for application
where preheat is not used).
Then the CPU receives the kV, mA and exposure time commands.
real time hardware line both linked to the prep button), it calculates the acquisition filament drive to
apply to the filament in order to match the required tube mA.
This calculation is based on:
• the filament drive values stored in the tube database
• the interpolation to calculate the filament drive for the (kV, mA) point selected
• the filament aging correction
Then it either:
• calculates the filament boost command to apply to the filament to fasten the filament
temperature rise and send it to the heater function. In this case, the boost duration is 400ms
and is followed by the acquisition command send to the heater function.
• or do not use any boost command and directly send the acquisition command to the heater
function
When exposure command goes in its active state, the CPU:

• starts the exposure
• measures the mA each 1ms (start 5ms after exposure start), compares it to the mA demand
and calculates the filament drive to apply to reach the mA demand
• sends each 1ms, the new filament drive to the heater function
• updates mA demand if required by the system or by generator algorithm (ABC mode, falling
load mode, variable mA mode)
• checks mA accuracy
The heater function:

• gets the filament drive demand each 1ms
• measures the heater inverter RMS current two times per 1ms, compares it to the filament drive
demand and applies the inverter frequency to reach the right filament drive current
• checks inverter RMS current to avoid exceeding the max filament temperature
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• sends each 100ms the inverter RMS current measure to the kV control CPU
When exposure command goes in its inactive state, the CPU either stay with the last filament drive
demand or goes in preheat mode or stops filament drive to allow a fast filament cooling before going
preheat. The rule depends on the application.
3.3.4 Rotation function

Refer to Figure 2-37 in the following discussion. Rotation function is mainly controlled by the kV
control CPU function.
real time hardware line both linked to the prep button), it sends the anode speed reference to the
rotation function.
Upon receiving this command, the rotation drive:
• compares it to the present anode speed. If the present speed is lower:
• gets from the tube database the current required to accelerate the anode and the acceleration
time to apply
• drives the inverter with the frequency required for the speed selected
• measure the phases currents, compare them to the current demand and applies the
modulation rate to supply the right stator current
• counts the acceleration time
• monitors rotation safeties
• sends back each 100ms the speed to the kV control CPU
The speed feedback is used by the kV control CPU to authorize exposure

Once the acceleration time is complete, the rotation drive applies the inverter current required for
the anode speed maintain.
When exposure command goes in its inactive state, the CPU either:
• sends a speed=0 command to the rotation to stop the anode rotation
• applies a “hold” time to maintain the anode rotation speed before stopping it
• applies a “hold” time to maintain the anode rotation speed before going to a low speed mode
depending on the application.
3.3.5 Power Supplies Distribution

3.3.6 Exception Handling

JEDI software performs auto-test at power up and continuously monitors the correct operation of
it’s functions during application. Any miss functioning is stored in the Jedi error log and reported to
the system through a protocol that vehicles error code.
Errors found can only be reported if the generator is powered on and alive.
3.3.6.1 Diagnostics
There are different levels of diagnostics:
Power on Diagnostics
At power up, the kV control performs its own initialization, checks its memory integrity (Checksum
of program and NVRam), and starts the communication with its peripherals and the system;
Communication is permanently checked afterwards. Then it initializes the Rotation board and
Heater board with their respective Data base parameters and loads kV control FPGA.
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8 LEDs (S7.S0) on kV control board show the software status.
During power on, the Heater board and the Rotation board CPU’s initialize themselves and check
their memory integrity and hardware. If a problem is encountered, a PRD error is reported to the kV
control.
Alive Diagnostics
1.) Under application. Faults will be reported through an error code and associated message.
Some are straight forward and drive to the root cause. Refer to recommended action in the
error list.
2.) Diagnostics run separately:
- Heating without HV nor rotation
- Rotation without HV nor filament
- Inverter gate command diagnostic
- Inverter in Short circuit diagnostic
- no load HV without anode rotation nor filament heating
- AEC diagnostic
3.) Manual diagnostics: Through troubleshooting guide based on error message or when the
generator does not reply.
3.3.6.2 Error Code Structure

The error code structure described in this chapter applies to the JEDI error detection and logging.
JEDI error log file can be accessed from the system through the system console or a laptop (Jedi
error log upload functionality).
When an error is detected, it is sent to the system and is logged in parallel in the JEDI error log file.
The file contains 64 logs maximum. Each log shows the following structure:
Simplified Generat Error Error Data associated to number of Date and

error code or class code the error code occurrences time
Phase
The first four fields will be described in the following paragraphs.

The field “data associated with the error code” shows detailed information about the state of the
generator when the error occurred. Examples: rotation high speed acceleration state, small focus
preheat, tube number 1 selected
The field “number of occurrences” is used to log the same error occurring several times
consecutively. Instead of filling the error log file with the same error several times consecutively, the
first error is logged and the following errors are recorded through increasing the “number of
occurrences” field.
The field “date and time” stores the date and time when the error occurred. This is the Jedi internal
date and time which may be different of the system date and time. In case of logging several time
the same error, the field is indicating the date and time of the first occurrence.

GE MEDICAL SYSTEMS
Simplified Error code definition

The simplified error code is a grouping of the Jedi error codes. This field gives a fast understanding
of which part of Jedi is faulty.
Simplified error code Description

30 Tube Spits errors
40 Rotation errors
50 Heater errors
60 Exposure errors (HV inverter+mA measure+exposure control)
70 Power Supply errors (low voltage + DC bus)
80 Hardware errors (internal communications + cables)
90 Application errors (saved RAM+software)
100 external communications errors
110 thermal errors
120 Manipulation errors
130 Ingrid errors
140 Tube switch errors
10 rotation warnings (engineering use)
20 heater warnings (engineering use)
25 LVPS warnings (engineering use)
27 application warnings (mainly saved RAM battery change)
Table 2-2 Simplified Error code definition
Generator Phase definition

The generator phase field contains the state of the generator when the error occurred:
Generator phase Description

0 idle: entered in diagnostic mode
1 Powered-Up; Waiting for Configuration
2 Stand by: Config done. Waiting for a preparation command
3 Preparation in Progress: JEDI gets ready to take X-rays
4 Ready for exposures (Rotor at speed; Filament; HV inverter drive ready;
no errors): waiting for an exposure command
5 High voltage on
6 error detected and not yet cleared
Table 2-3 Generator Phase definition
Error class definition

There are 5 classes of errors that correspond to different levels of impact to the system.
Class of errors correspond to the seriousness of the error and the system software will manage
operations upon it.

GE MEDICAL SYSTEMS
Class Description
1 Errors which have no impact on the system operation.
Those are errors detected in background diagnostics during application. They are
referred as “Warning” errors, to monitor drifts and used for engineering tracking.
The generator phase remains unchanged.
They are stored in JEDI error log.
2 Errors which are detected by JEDI and that are recoverable automatically without
noticeable effect on the system, such as error related to recovered tube spits.
The generator phase remains unchanged.
Those errors usually occur during exposure.
3 Errors detected by JEDI during exposure. They stop the exposure and turn the generator
in a safe state.
Error will be reset on Exposure Command release. It will require another Exposure
Command to restart the sequence.
The generator phase is set to “error” until the error is cleared
4 Errors which are related to any hardware failures, software application or communication
errors.
JEDI will turn to a safe state.
If preparation is in progress, it is stopped.
They are cleared either by a reset error action from the system (for system having a reset
error mechanism) or by a prep release or by a new prep command.
The generator phase is set to “error” until the error is cleared.
Application can not work if errors is persistent.
5 Those are codes that may rise up when generator or tube temperature limits are reached.
The application waits until the thermal information disappears. The error information is
temporary.
The generator phase is set to “error” until the error is cleared.
Table 2-4 Error class definition
Error code definition

Each error code consists in two fields (which cannot be generated and used separately):
the first field describes the Jedi function which is faulty (referred to as function code)
the second field describes the error detected
Example: Error code 0306 means: 03 means high voltage generation function and 06: no kV feedback on
anode.

GE MEDICAL SYSTEMS
FUNCTION CODES LIST:
Function Code Description

01 rotation
02 heater 1
03 Kv control
04 mA control
05 power supplies
06 system interface
07 software
08 application
09 tube control
10 tube switch
11 Grid/bias
12 Heater 2
13 AEC
14 hardware
15 Operator errors
Table 2-5 Error code definition
3.4 Block Diagrams
3.4.1 JEDI Generator / Functional Architecture

GE MEDICAL SYSTEMS
3 phase power
1 phase or
System
AC/DC
input
Filter
EMC
1 phase tube
preload (1 phase)
cooling
input
Interface
System
High Voltage
Inverter
kV control
inverter controls
Control Bus
HV measures
High Voltage
Tank
fil. drives
Heater
DC Bus
tube selection
HV cables
heater supply
Grid/Bias
bus
voltage
X-Ray tube 1
Supply
Power
Low
rotation phases
+safeties+fans
Management
Rotation
X-Ray tube 2
Tube
rotation phases
rotation phases
+safeties+fans
Chiller
Figure 2-27 JEDI generator / functional architecture

GE MEDICAL SYSTEMS
3.4.2 JEDI Generator / Np+ Functional Architecture
3 phase power
System
AC/DC
input
Filter
EMC
tube cooling
1 phase
input
Interface
System
High Voltage
Inverter
kV control
inverter controls
Control Bus
HV measures
High Voltage
Tank
fil. drives
Heater
DC Bus
HV cables
heater supply
bus
voltage
X-Ray tube 1
Supply
Power
Low
rotation phases
+safeties+fans
Rotation
Figure 2-28 JEDI generator / Np+ functional architecture

GE MEDICAL SYSTEMS
3.4.3 JEDI Generator / Tiger Functional Architecture
1 phase power
System
input
AC/DC
tube cooling
preload/load
1 phase
input
Interface
System
High Voltage
Inverter
kV control
inverter controls
Control Bus
HV measures
High Voltage
Tank
fil. drives
Heater
HV cables
DC Bus
heater supply
bus
voltage
X-Ray tube 1
Supply
Power
Low
400Vdc
rotation phases
+safeties+fans
Rotation
Figure 2-29 JEDI generator / Tiger functional architecture

GE MEDICAL SYSTEMS
3.4.4 JEDI Generator / Precision Functional Architecture
System
Lap top
3 phase power
AC/DC
input
Filter
EMC
CAN Externe
serial Link
tube cooling
1 phase
input
AEC
Interface
Generic
Inverter 100kW
High Voltage
POWER PC
kV control
inverter controls
Control Bus
HV measures
High Voltage
Tank
fil.SF drives
Heater
SF
DC Bus
High Voltage
Switching
Tank
Heater
LF
heater supply
bus
HV cables
HV cables
voltage
X-Ray tube 1
Supply
Power
Low
rotation phases
+safeties+fans
Management
Tube
Rotation
X-Ray tube 2
rotation phases
+safeties+fans
Figure 2-30 JEDI generator / Precision functional architecture

Page 91
PRECISION 500D ®, R&F SYSTEM MANUAL
mAs_measure
IGBT_H_cmd
measure_controls mA/mAs mA_measure
IGBT_L_cmd
HV Tank MEASURE
GATE_PS_cmd Ilr_max INVERTER
DC_BUS_meas Ilr_threshold CURRENT I_meas
MEASURE
+
control Ilp_sign
GATES EXPOSURE SAFETIES
SUPPLY CONTROL
REGUL. (FPGA) over_kV, no_kV cathode_kV_measure
Chapter 2 - Theory of System Operation

Vgate_meas cathode_spit, anode_spit KV ERROR
MEASURE HV Tank
DCB_meas measure_controls
+ anode_kV_measure
5 configurable IO lines kV_error SAFETIES
system
Figure 2-31 JEDI generator / 68360 kV control

1 ethernet + 5 UART lines
I/F
CAN kV_demand kV_meas kV_unbalance
microprocessor exposure Ilr_moy
JEDI Generator / 68360 kV Control
bus controls mA_meas

KV kV_ref Tank_temperature
DEMAND GEN
CAN MEASURES Vgate_meas
INTERF.
DCB_meas
Tank_id CPU CAN
HV Tank
inverter_id
IDs READ CONTROL heater,
system +15V Control Bus
DIRECTION 2360588-100, REVISION 10
IF_id
BUS rotation,
I/F kV_control_id 5V -15V
INTERF. LVPS
SUPPLY
GE MEDICAL SYSTEMS
3.4.5
mAs_measure
IGBT_H_cmd
measure_controls mA/mAs mA_measure
IGBT_L_cmd
HV Tank MEASURE
GATE_PS_cmd Ilr_max
INVERTER
DC_BUS_meas CURRENT
I_meas
Ilr_threshold,Ilr_moy MEASURE
Ilp_sign +
control SAFETIES
GATES EXPOSURE
SUPPLY CONTROL
over_kV, no_kV
REGUL. (FPGA)
Section 3.0 - Generator “Jedi”

cathode_spit, anode_spit
Vgate_meas KV ERROR cathode_kV_measure
measure_controls HV Tank
MEASURE +
DCB_meas
Figure 2-32 JEDI generator / PPC KV control

EKV,ILP,VCR, SAFETIES
DCB_meas anode_kV_measure
5 configurable IO lines ADC
system
I/F DSP_D KV_meas
JEDI Generator / PPC KV Control
EKV
exposure
controls uP bus DAC KV_cons mA_meas
1 ethernet + 5 UART lines DSP
External CAN Tank_temp
CAN INTERF. GEN Inv_temp
CAN (Sys)
MEASURES Vgate_meas
(ADC) Kv_unbalanced
Ilr_threshold,Ilr_moy
Tank_id CPU
HV Tank
inverter_id CAN heater,
IDs READ rotation,
system IF_id +15V CONTROL Control Bus
LVPS
I/F kV_control_id 1.8V-3.3V-5V BUS INTERF.
-15V (internal
SUPPLY CAN)
GE MEDICAL SYSTEMS
3.4.6
Page 92
Page 93
DC Bus :
DC_BUS_M_PT FILTER
inverter_primary_2
AC/DC DC_BUS_+
HV Tank

DC_BUS_- POWER BRIDGE SERIAL inverter_primary_1
RESONANT CIRCUIT
IGBT AID
CIRCUIT
Figure 2-33 JEDI generator / HV power inverter

DC_BUS_+
JEDI Generator / HV Power Inverter
AC/DC DC_BUS_-
GATE_PS_cmd
GATES
+20V
iso
DRIVES CURRENT
la
tio
DC_BUS_meas SUPPLY -10V

n
MEASURES
GATES SHUNTS
kV IGBT_H_cmd DRIVERS
iso
control lat
ion
IGBT_L_cmd
I_meas
inverter_id
INVERTER
ID
GE MEDICAL SYSTEMS
3.4.7
Large focus current OVERVOLTAGE LF FILAMENT

PROTECTION TRANSFORMER
heater
Small focus current OVERVOLTAGE SF FILAMENT CATHODE
PROTECTION TRANSFORMER HV
PROTECTION ANODE
HV

HV CATHODE
TRANSFORMER RECTIFIER
+ FILTER MA MEASURE
Inverter_primary_1
CATHODE KV
MEASURE
Figure 2-34 JEDI generator / HV Tank

inverter LC
Inverter_primary_2
ANODE KV
MEASURE
JEDI Generator / HV Tank
ANODE mA_measure
3 phases
RECTIFIER PROTECTION
from EMC cathode_kV_measure
+ FILTER anode_kV_measure
Bridge for signals between inverter and kV control kV
inverter
control
HV TANK Tank_id
ID
HV TANK Tank_temperature
TEMPERATURE
GE MEDICAL SYSTEMS
3.4.8
Page 94
GE MEDICAL SYSTEMS
3.4.9 JEDI Generator / AEC Functions
Bright CAN
CAN ext
CAN
chip
CAN
chip
AEC
AEC bright
decoder
CLKCAP
parallel
CLRCAP
sel AEC
DAC
Counter
sel AEC
CLRCAP
CLKCAP
VAEC4
VAEC3
VAEC1
AEC sel 1,2,3,4
AEC cells L,M,R
VAEC2
230Vdc
Figure 2-35 JEDI generator / AEC functions


Heater supply bus Power bridge Focus selection
Figure 2-36 JEDI generator / 1 inverter heater

large focus
Current and voltage
current
current measure small focus
current
+5V supplies
supplies measure
JEDI Generator / Inverter Heater
current safeties
+5V Power bridge RMS current + Overvoltage
+15V drive (EPLD) safeties safety
-15V
overvoltage safety
PWM safeties
Control
control focus selection and
bus
interface readback
Heater Drive rms current
(microcontroller)
GE MEDICAL SYSTEMS
3.4.10
Page 96
Page 97
EMC+AC/DC ROTATION
(high speed)
J3
Power
Input line EMC INVERTER
High
RECTIFIER Rotation
FILTER
AND FILTER speed capacitors
J3
fuse relay

TUBE
frequency,
modulation
Figure 2-37 JEDI generator / rotation function

currents
J1 measure
speed reference J2
Rotation drive
JEDI Generator/ Rotation Function
40 / 70 degrees safeties
tube fan / pump / chiller command
cooling tube cooling voltage input
relay
KV CONTROL
J3
CPU
GE MEDICAL SYSTEMS
3.4.11
HIGH SPEED
CAPS.
common stator phases
POWER BRIDGE tube or
DC Bus EMC DC Bus tube mgt
AC/DC p,a p,a

CURRENT
FILTER MEASURE
Figure 2-38 JEDI generator / high speed rotation

isolation
HIGH SPEED
JEDI generator / high speed rotation
io n RELAY
la t
iso
ROTATION LOW +15V gates 3 PHASES
POWER BRIDGE
VOLTAGE REBUILD +
DRIVE (EPLD) current signs
POWER SUPPLY
iso SAFETY
lat
io n
+5V HS relay command
pwm
+15V controls
-15V safeties
phases current cooling command

CONTROL tube or
kV Control Bus ROTATION tube temperatures TUBE tube temperatures
BUS tube mgt
control DRIVE (MICRO) cooling command COOLING 1 phase tube cooling input
INTERF. system
GE MEDICAL SYSTEMS
3.4.12
Page 98
GE MEDICAL SYSTEMS
3.4.13 JEDI generator / 3 phase EMC filter
system
power input
3 phase
MODE FILTER 1ST
DIFFERENTIAL
STAGE
FILTER 1ST STAGE
COMMON MODE
FILTER 2ND STAGE
COMMON MODE
OVERVOLTAGE
MODE FILTER 1ST

DIFFERENTIAL
CLAMP
STAGE
3 phase to
rectifier
bridge
AC/DC
Figure 2-39 JEDI generator / 3 phase EMC filter

GE MEDICAL SYSTEMS
3.4.14 JEDI generator / 3 phase mid power AC/DC
from EMC
3 phases
RECTIFIER
BRIDGE
input voltage
Rectified
DIFFERENTIAL
MODE FILTER
FUSE
DC_BUS_M_PT
DC_BUS_+
DC_BUS_-
DC_BUS_+
DC_BUS_+
DC_BUS_-
DC_BUS_-
DC_BUS_+
DC_BUS_-
inverter LC
rotation
inverter
LVPS
Figure 2-40 JEDI generator / 3 phase mid power AC/DC

Page 101
EMC+AC/DC INVERTER
FILTER
Power INVERTER

Input line EMC
RECTIFIER
FILTER
AND FILTER J6
fuse GATES
GATES
TUBE
DRIVERS
DRIVE
SUPPLY
CATHODE KV ANODE
KV
J3
Figure 2-41 JEDI generator / kV function

KV CONTROL J1
SYSTEM I/F J2 J2 HV TANK
Gates
drivers
J1
EXPOSURE
5 configurable lines CONTROL Gates
can be : Ilr_max, Ilr_threshold supply
(FPGA)
JEDI generator / kV function
exposure command
over_kV, no_kV, spits drive
exposure enable
XRay on
brightness Current
measures RECTIFIER
reset
+ safeties AND FILTER
KV error
exposure
micro. bus
controls
conversion
KV KV
CAN measure MEASURE
RS232
KV + safeties
CPU demand
kV_ref, kV_meas,
Measures DCB_meas,
Vgate_meas, Tank_temp,
mA_meas, Ilr_moy
GE MEDICAL SYSTEMS
3.4.15
EMC+AC/DC HEATER J1
HEATER
DRIVE
J2 RMS current
DC bus J3 LVPS J1
EMC J2
RECTIFIER
FILTER
AND FILTER power HEATER
fuse module INVERTER TUBE

CATHODE ANODE
KV KV
J2
KV CONTROL J2 J2
J3 HV TANK
Figure 2-42 JEDI generator / mA function

EXPOSURE
CONTROL mAs count
JEDI generator / mA function
exposure RECTIFIER
micro. bus
controls mAs AND FILTER
measure
J3
filament drive ref. refreshed every 1ms mA

CPU : measure
mA mA
regulation MEASURE
each 1ms
Measures
GE MEDICAL SYSTEMS
3.4.16
Page 102
Page 103
EMC+AC/DC INVERTER
DC_BUS_+
DC_BUS_M_PT
FILTER
Power INVERTER
Input line EMC DC_BUS_-
RECTIFIER
Figure 2-43 JEDI generator / power supplies distribution

FILTER
AND FILTER J1,J2 J6
fuse
DC Bus
GATES
JEDI generator / power supplies distribution
DRIVE
SUPPLY
J3 DC Bus
J3
DC Bus
J1 Heater supply bus
Low Voltage
Power Supply
+15V system network supply (12V)
-15V
J2
J1, J1A J3 J1 J2 J3 J2, J3
5V+ 5V power 5V power J1 J4
gates power
supply supply -15V

supply
+15V
5V
Inverter
Inverter
HEATER kV CONTROL CT I/F
ROTATION
GE MEDICAL SYSTEMS
3.4.17
+/-15V P15V CAN

CAN M15V CAN
P17V MEASVP 15V CAN
CMD 15V CAN Regulator MEASVN 15V CAN
M17V
+15V EXT P15V EXT
Regulator
CMD 15V EXT MEASVP 15V EXT
+24V 24V GATE
MAINS GATE
Regulator MEASV 24V GATE
ACDC CMD 24V GATE

LVPS MAIN P26V
PWM fan 24V FAN1
INVERTER Regulator
Figure 2-44 JEDI generator / LVPS400 function

CMD FAN 1
1 OVER I FAN1
115V
PWM fan 24V FAN2
Regulator
2 OVER I FAN2
CMD FAN 2
JEDI generator / LVPS400 function
PWM fan 24V FAN3

P160V Regulator
CMD FAN 3
3 OVER I FAN3
PWM fan 24V FAN4
P15V Regulator
AUXILIARY CMD FAN 4 4 OVER I FAN4
FLYBACK
M15V 160V H1
INVETER 160V H1
Regulator
P7V CMD 160V H1 MEASV 160V H1
160V H2
160V H2
CONTROL Regulator
CMD 160V H2 MEASV 160V H2
M10Ref
P10Ref 160V EXT
160V EXT
CAN bus Regulator
MEASV 160V EXT
CMD 160V EXT
Mains-drop
GE MEDICAL SYSTEMS
3.4.18
Page 104
Page 105
HV switch section Rotation section

Tube Switch Bd 2 Tubes HV Tank
Tube 2 position switch Rotation bd Tube Switch bd
Tube select Tube 1 position switch
Motor
control
Tube 1 Main
+15V/-15V Main
M T1 HV + Tube 2 Main
Rotation Tube 1 Common
common
Inverter Tube 2 Common

T2 HV +
Main Tube 1 Aux
Inverter Aux Tube 2 Aux
Figure 2-45 JEDI generator / Switch Tube function

T1 HV - capa1 cmd capa2 cmd
Tube select
T2 HV -
High voltage
JEDI generator / Switch Tube function
Filaments section
Tube Switch Bd 2 tubes HV TANK
LF
LF Tube 1
SF
Tube 1
common
Heaters Bd
SF LF
Tube 2
SF
Tube select Tube 2
GE MEDICAL SYSTEMS
3.4.19
GE MEDICAL SYSTEMS
3.4.20 JEDI generator / Interface function: CT I/F
exposure_command
CAN communication
reset
External_12V
XRay_on
spare
spare
ISOLATION
ISOLATION
SUPPLY
RS485
11898
5V
1 RS232 line
4 configurable IO lines
DRIVER
DRIVER
DRIVER
RS232 2 UART lines
1 configurable
IO line
CAN
kV control
Figure 2-46 JEDI generator / Interface function: CT I/F

Page 107
To KVCTL
bd
Exposure
enable from kv Console
control board
Prep sw

Figure 2-47 JEDI generator / Interface function: RAD I/F
Exp sw
TXT_EXT_CAN
RDX_EXT_CAN CAN Parallel WORKSTATION
Decoder
JEDI generator / Interface function: RAD I/F
selection
Room light
Isolation by relays
To Buckies
Exp dem Exp dem
Exposure Exp cmd Exp cmd
From Buckies
command Start Exp.
Interlock door
External CAN to AEC
TXT_RTL_CAN
RDX_RTL_CAN CAN Bright_CAN to AEC
TX_RX4 RS232 Service Terminal

TX_RX2 driver Console Debug
TX_RX3 RS485 Console
GE MEDICAL SYSTEMS
3.4.21
Real Time
Lines
from/to system
reset from syst
RTL1
exp cmd from syst
RTL2
Xray ON to syst
RTL3 Optocoupled IO lines
Figure 2-48 JEDI generator / Interface function: Generic I/F

exp enable from syst RS485
RTL4
for Grid
RTL5
JEDI generator / Interface function: Generic I/F
AEC brightness pulse

RTL6
RS232
External
+12V +5V supply
PPC KVCTL
CAN Optocoupled
from
system
CAN
+15V
-15V
AEC brightness pulse CAN +5V +15V -15V

AEC board link
GE MEDICAL SYSTEMS
3.4.22
Page 108
GE MEDICAL SYSTEMS
3.5 Switches, Jumpers and LEDS
3.5.1 GEN IF board
Connectors Definitions
J1 Supplies for Ingrid (Not used on
Precision 500D)
J2 Control for Ingrid (Not used on
Precision 500D)
J3 Not used on Precision 500D
J4 External CAN to and from
system
J6 To AEC board (control)
J10 Digital signals from and to
KVCTL bd
DS1 - Green
External CAN
reception
Figure 2-49 GEN IF board

GE MEDICAL SYSTEMS
3.5.2 PPC KV CONTROL board
Voltage LEDs are green
Power supplies test points:

TP3: 3.3V GND: TP1, 2, 5, 9
TP4: int 1 5V DS4: -15V DS2: 3.3V
TP6: +5V DS1: Gate cmd input
TP7: int +15V OK (yellow)
TP8: +1.8V DS3: 5V
DS5: -15V
internal
DS7: +15V
internal
DS6: +15V
input
DS8 (yellow):
DSP OK DS10 (red): Reset DS19 to 26 (yellow): Error
DS11 (red): BDM (active indication.
only in manufacturing) See diagnosis document.
DS12 (yellow): R_CAN_X Blinking successively if no
Connectors used on Precision 500D DS13 (yellow): T_CAN_X
J1 From HV tank (digital&analog signals) DS14 (yellow): TX_TAV DS18: future use
DS15 (yellow): RX_TAV
J2 Internal CAN (to auxili aries units) DS16 (yellow): TX_CONS
J4 To Gen IF board (digital signals) DS17 (yellow): RX_CONS
Swit ches and Jumpers

SWITCH OR FUNCTION
JUMPER
RST RESET PUSH BUTTON
I ndicators
INDICATOR COLOR INDICATES:
CONF Re d FIELD PROGRAMMABLE GATE ARRAY
(FPGA) CONFIGURATION NOT
ACCOMPLISHED
OK Yellow INVERTER GATE POWER SUPPLY OK
TX_TAV Yellow TRANSMIT TO SERVICE LAPTOP
RX_TAV Yellow RECEIVE FROM SERVICE LAPTOP
TX_CONS Yellow TRANSMIT TO CONSOLE (IF EXISTING)
RX_CONS Yellow RECEIVE FROM CONSOLE (IF EXISTING)
T_CAN_X Yellow SYSTEM CAN BUS TRANSMIT
R_CAN_X Yellow SYSTEM CAN BUS RECEIVE
HALT Re d MICROPROCESSOR HALTED
RESET Re d BOARD BEING RESET
S0 TO S7 Yellow STATUS LED
IN APPLICATION MODE THESE LEDS
FLASH IN SEQUENCE CONTINUOUSLY
DS1 Gre en -15V SUPPLY
DS2 Gree n +15V SUPPLY
Figure 2-50 PPC KV CONTROL board

GE MEDICAL SYSTEMS
3.5.3 QUAD SNUB board
High Voltage Present: Do not go into Generator until DS1 and DS2 (Green LEDS) go out.
DS1 / DS2 :
Presence of DCBUS
Figure 2-51 QUAD SNUB board

GE MEDICAL SYSTEMS
3.5.4 GATE CMD board
The following hazards may be present

• High Voltage: Do not touch board until DS300 on this board and DS1 on the Dual Snub
Board are out
• Hot surface on transformer T300 and heat sink.
D
S3
00
J4 : DC bu s DS300 - Neon (Orange) -

Presence of voltage on DC
bu s for Fly back Conv erter to
cr eate power su ppli es for
bo th Gate Com mands
DS200 - Yello w - High

IGBT* (Q200) Gate D
S2
Command run nin g 00
DS202 - Green - Presence

DS201 - Green - Presenc e of -10 V Supp ly on high
of +20 V Supply on high D D IGBT* Gat e Comm and
IGBT* Gate Com mand S2 S2
01 02
J1 :
Inver ter ILP
cur rent
feedb ack
ILR J3 : t o KVmeas board
J5 : Paralle l
indu ctor on HV tank
temp eratu re
DS100 -Yellow -Low IGBT*
D
(Q100) Gate Com mand runn ing S1
00
DS102 - Green - Presence
D
DS101 - Green - Presence of D
S1
S1 of -10 V Sup ply o n low
02
+20 V Supply on low IGBT* 01 IGBT* Gate Comm and
Gate Comm and
* Insulat ed Gate
Bipo lar Transi stor
Figure 2-52 GATE_CMD board

GE MEDICAL SYSTEMS
3.5.5 KV MEASURE (Two Tubes board)
This board forms part of the oil seal of the High Voltage Tank. It can only be removed at the
factory. The Field Replaceable Unit (FRU) is the complete HV Tank.
r ef_mot
pos_mot_2
pos_mot_1
mot_p
mot_n
mot_n Tomot_n
Motor
mot p Supply
mot p
Connector s definition
SF II
J1 To Gate Cmd board
LF II
(Inverter control)
J2 From KV CTL board
C
J3 Filament currents
SF I
from Auxiliaries
LF I
J7 Futureuse
J9 Sw itch motor
control
Figure 2-53 KV MEASURE (Two Tubes board)

GE MEDICAL SYSTEMS
3.5.6 HEATER board
HIGH VOLTAGE: DO NOT GO INTO GENERATOR UNTIL INDICATOR DS3 GOES OUT
Non insulated
voltages
present LF SF
Common
DS3 Green
+160Vdc present
DS4 Y ell ow
160V DC Inv erter O utput
Running
0V DC
SF-LF Yellow Small ON Yellow

Focus/L arge Focus relay In verter
feedback Command ON
RST Red Boar d being

reset or powered up
DS2 Y ell ow - Status

DS1 Yellow - Status
Figure 2-54 HEATER board

GE MEDICAL SYSTEMS
3.5.7 Rotation Board
HIGH VOLTAGE: DO NOT GO INTO GENERATOR UNTIL INDICATOR DS6 AND DS7 (NEON-
Non insulated ORANGE) GO OUT.
voltages
present
Auxil iary
DC bus Comm on
Main
DS6
DC bus
I ndicators
INDICATOR COLOR INDICATES:
RESET Red BOARD BEING RESET OR POWERED UP
INV_ON Yellow THE INVERTER IS RUNNING
DS1 Green PRESENCE OF +15 V SUPPLY
DS2 Green PRESENCE OF -15 V SUPPLY
DS3 Green PRESENCE OF +5 V SUPPLY
DS4-DS5 Yellow BOARD STATUS
DS6 Neon (orange) FAN VAC POWER SUPPLY PRESENT
DS7 Neon (orange) DC BUS PRESENT
J2 Wiring
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16
115V
Sens e **
Fan, 115V AC
Li ne i nput * *
Fan*, 115V AC
Line X-ray tube
Thermal safety
* used i n appl ication wi th fa n cooli ng tube

** used i n appl ication wi th tube pump
contr ol.
Figure 2-55 ROTATION board

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3.5.8 TWO SWITCHING TUBES Board
To Rotation Board
DS5 - Red Boar d reset DS2 - Green +15V
DS3/DS4 - Yellow
Board alive if DS1 - Green -15V
blinking
TP5 Stator Main

Phasecurre nt TP3 D CBUS-N
TP6 Stator
Auxil iar y Phase TP4 DCBUS-P
curr ent
TP7 -Stator Common

Phase curre nt
Figure 2-56 TWO SWITCHING TUBES Board

GE MEDICAL SYSTEMS
3.5.9 LVPS400 Board
Be aware of the following:

• HIGH VOLTAGE: DO NOT GO INTO GENERATOR UNTIL DS8 (NEON - ORANGE) GOES
OUT.
• THE RECTIFIER BRIDGE ON THIS BOARD CAN BECOME VERY HOT.
DS6 Gr een
-15V CAN DS2 Gr een DS1 Green
DS3/DS4 Yellow DS5 Red DS7 Green 24Vgate 15Vext
Board alive if Board reset +15V CAN (Not used in Precision) (Not used in Precision)
blin ki ng
WARNING
DS9 Gr een DS8 - Orang e Neon OF
160V_ext indi cates p resence of LOCAT ION
(not used in Dcbus (A C voltage at
Precision) LVPS400 in put )
Figure 2-57 LVPS400 board

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3.5.10 AC/DC 3 Phase board
Be aware of the following

• DO NOT GO INTO GENERATOR UNTIL DS1 (NEON - ORANGE) GOES OUT.
• Some components on this board can become very hot.
DCBUS to J1 : DCBUS to Rot ation module

M ain Inverter
J2 : DCBUS to Gate Command
F1 Fuse Pr otects
(on DCBUS) :
Rotation Board,
DS1 Neon Or ange Gate CommandBoard
In dicates presence of Type : 15A , 600VDC
voltage (>70Vdc) on
DCBUS
Rectifier Bridge
Figure 2-58 AC/DC 3 Phase board

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3.5.11 AEC Board V2
AEC4 AEC3 AEC1 AEC2 N1 - Orange (neon) -

Presen ce of 230 VDC
TESTPOINT MEASUREMENT
SIGNAL RA NGE
TP1 230 VDC 230 VDC _5%
TP2 230 VDC 230 VDC _5%
TP3 230 VDC 230 VDC _5%
TP4 230 VDC 230 VDC _5%
TP5 AEC assignment reference 0 to 10 V
TP6 10 VDC (reference) 10 VDC _1%
TP7 AEC return voltage
TP8 AEC1 return voltage
Figure 2-59 AEC Board V2
Section 4.0
Imaging System
4.1 Overview
Several hardware components work together to produce diagnostic images. See Figure 2-60.

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Optics Control Board Photdiode Board
Optics Assembly
CCD Camera
Fan
Active Distortion II Power

Correction Module Supply
(ADCM)
Image
Intensifier (II)
Figure 2-60 Imaging System
The Optics Control Board sends and receives signals, to and from the Gitane board over the CAN
RT lines. The OCB provides +/- 12v power to the Photodiode Board (PDB), controls the amplifier
circuits on the PDB, sets PDB gain, and counts the pulses of the frequency signal from the PDB.
Results are sent to the Gitane through the RT line.
The OCB also controls the Image Intensifier power supply, ADCS, NDF filter position and Iris
position. Motor “over-current” detection circuits on the OCB protect the motor, and not the OCB.
The Fan operates on +24VDC and is used to cool the CCD
The ADCS measures the actual earth’s magnetic field by running current through a coil around the
II to collapse the earth’s field. A new feature, includes an integrated EFC (Earth Field
Compensation) tool. No calibration is required but the ADCS must be set to the correct II size.
Note: The ADCS has a serial link connection to the OCB. The ADCS is configured by s/w (through OCB/
Configure RS232 messaging) to be operative with 32 cm or 40 cm Image Intensifiers. This is set during
ADCS to correct manufacture or can be set by Service personnel. Service: when an ADCS is replaced this
II size parameter must be configured to match the your Image Intensifier’s size. Please Take care about
that: if the ADCS is mis-configured, the earth field compensation does not work properly!
II High Voltage Power Supply (HVPS) supplies power to the focusing and size grids for each field
of view. It also supplies high voltage for the anode. The HVPS is specific to II type.
CCD Camera contains photo sensitive semiconductor and control electronics. The CCD converts II
light output to a 12 bit digital video signal. CCD technology offers many benefits:
• Low dark current
• Little lag
• 30 frames/second at 1024 x 1024 pixels
• Progressive scanning
• High resolution and brightness uniformity
• Good quantum efficiency
The optics assembly provides an optical interface between the image intensifier and the CD
camera.
Page 120 Section 4.0 - Imaging System

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The Photodiode Board Assembly contains Photodiodes, which convert light to a voltage. The
assembly is composed of the Photodiode board, a mask, and a neutral density filter. See Figure 2-
61. A voltage to frequency (V/F) converter is used to change the voltage to a pulsed signal.
Photo-Diode Board (PDB)
Optical densities :
Part numbers: density 1 #2329489
density 0.1 #2329489- 2
Total density = 1.3 for 40cm
II
Total density = 1.6 for II 32cm
Foam gasket
Part number: #2329050
Photodiode mask (default is 64% square)

Linos/Rodenstock Optics assembly part
Optic output for photodiode

Linos/Rodenstock Optics assembly part
Figure 2-61 Photodiode Assembly
4.2 CCD Camera

Charge Coupled Devices (CCD) are not vacuum pickup tubes but integrated circuits that have a
large number of microscopic “photosites” or pixels arranged in horizontal rows and vertical columns.
The photo sites act as “wells” and are filled by light energy.
The CCD Camera uses a high dynamic range 1024x1024 CCD chip. Each pixel photosite is able
to handle up to 150 000 electrons. Together with very low noise floor, this provides a very high
dynamic range sensor for Record acquisitions.
The image information is integrated during the whole x--ray exposure time. At the end of the
exposure period, the charges are transferred into a memory area of the chip, in order to be read-
out. The transfer time is very short (less than 0.5ms). This allows starting the next image integration
right after the previous one, while the readout takes place.
The image is read off the CCD target by both analog and digital techniques. The amount of charge
at each site is an analog function of the light intensity. Digital transfer techniques are used to
transfer the well charge levels to an output terminal.
Lag is virtually nonexistent because the charge transfer is almost instantaneous. The Pick- up tube
mechanisms for lag, carrier mobility, and insufficient beam current to effect target discharge are
absent.
CCD's have very little geometric distortion (pincushion etc.) because they are not scanned by a
moving electron beam. Like “Saticon” PUT's the CCD also has very low dark current which makes
it ideal for digital record applications. During digital record exposures the image is formed on the
CCD target. The image is read off the target once the exposure has ended.

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1024 x 1024
Pixel CCD CCD Drivers
Power Supply Board
Controller
Light Image
from 12 bit ADC for Correction
Image CDS and CCD Sensor
Board
Intensifier Analog Right Side
Video 12 bit ADC for
Gain CCD Sensor Left 12 Bit
Side Image Data
CCD Camera
Figure 2-62 CCD Camera
The analog signal of the CCD chip goes through a correlated double sampling (CDS) circuit and is
amplified by a programmable gain amplifier (camera gain). It is then converted to a 12 bit digital
signal via an Analog to Digital Converter (ADC).
The camera readout has 2 modes of operation:
• Dual channel mode: the CCD chip outputs the pixel data on 2 separate outputs, at 20MHz
each. The 2 outputs are merged after ADC to provide a combined pixel rate of 40MHz. This
mode is used for fluoro where frame rate can be up to 30fps.
• Single channel mode: the CCD chip outputs the pixel data on a single output, at 20 MHz. This
mode is used in digital Record, where frame rate doesn’t exceed 7.5fps (compatible with a
pixel frequency of 20MHz). This mode provides better brightness uniformity between left and
right half of the image, which is better for digital record.
Note: In fluoro, in some occasions (first fluoro after boot or large camera gain changes), the image can
Brightness display momentarily a “split image” artifact. The left half of the image has a slight brightness offset
Differences can vs. the right half. The artifact vanishes after a few seconds of fluoro. This is due to a dynamic gain
Occur. balancing algorithm in the CCD which takes some time to converge. This is the normal behavior of
the camera, not a failure.
The digital video data is transmitted over the CCD cable in LVDS electrical format over 12 twisted
pairs (1 per bit). Pixel clock, external sync, serial link and 24V power supply are also transmitted
within the CCD cable. The total length of the CCD cable can be up to 30m.
The CCD head has no internal cooler. Heat is mostly conducted through the optics to the II
structure. In addition, a fan flows air though the camera side vents. This fan is powered by the
camera head (24V. The fan rotates whenever the camera is powered.

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4.3 Imaging Chain
4.3.1 Components
12 Bit
10 Bit Record
10 Bit
8 Bit Fluoro
10 Bit
Figure 2-63 Imaging Chain
Please refer to Figure 2-63 as needed, during the following discussion.
4.3.1.1 Spectral Filters

The X-ray radiation is hardened (low energy x-ray is attenuated) by one of three spectral filters or
no spectral filter can be selected. The spectral filters have a thickness of 0.1, 0.2 or 0.3 mm of
copper. The filter mechanism is motorized and the desired filter is automatically selected depending
on calculated patient thickness and procedure being performed.
4.3.1.2 Anti-Scatter Grid

The anti-scatter Grid is motorized and can be removed from the field by the operator to lower patient
dose. The anti-scatter Grid ratio is 10:1 and the focal distance is 80cm (useful range 69 to 96cm).
4.3.1.3 Image Intensifier (II)
4.3.1.4 Image Intensifier Tube

The Image Intensifier has 4 Fields of View (FOV) and converts x-ray radiation at the input to light
at the output. It’s available in 2 sizes: 40cm and 32cm. It uses new technology, which provides
improvements in contrast, MTF and conversion factor.

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4.3.1.5 High Voltage Power Supply (HVPS)
The HVPS supplies the image intensifier grids G1, G2 and G3 with high voltage. Each grid voltage
is programmable and is individually adjusted for each II/HVPS couple in order to optimize the image
size, focus and focus uniformity. Each II type (40 or 32cm) uses a different type of power supply.
The HVPS is controlled by the OCB through an RS232 serial link, which provides control over
magnification and grid voltage settings. The primary power of the HVPS is 24V (up to 600mA). It is
provided by the OCB.
4.3.1.6 Active Distortion Correction System (ADCS)

The Active Distortion Correction System corrects the distortion caused by the Earth magnetic field.
This distortion is known as the “S--distortion” because of the shape it will impose on straight line
objects.
The ADCS uses a field sensor that measures the axial component of the Earth magnetic field. It
uses the sensor output to drive current into a coil placed around the entrance of the II tube, which
in effect will generate a counter magnetic field compensating the axial portion of the Earth field.
The ADCS doesn’t correct II pin--cushion distortion, which is caused by the spheric shape of the II
input.
The ADCS is fully automatic, it doesn’t require any site specific calibration.
The ADCS module uses a different set of internal parameters for each II type. The II type is
configured via a software command. The ADCS is commanded through an RS232 serial link by
OCB. This link is used to setup and read back the II type setting.
The primary power of the ADCS is 24V. It is provided by the OCB.
In terms of cabling, the ADCS provides a link between the OCB and the HVPS. It is connected to
both OCB and HVPS. The ADCS passes along 24V power and RS232 communications from OCB
to HVPS.
4.3.1.7 Optics
The Optics Assembly provides an optical interface between the II and the CCD Camera. The
collimation lens focuses the light to infinity (parallel light). Then a mirror deflects the light 90
degrees, towards the NDF filter.
4.3.1.8 Real time light measurement

Samples the light in a central region of interest of the II output screen to feed a photodiode. The
photodiode signal is amplified by the photo-diode board and sent to the generator to cut--off the
exposure in AEC mode. The region of interest is defined by a mask. This mask is setup by default
to sample a square region covering 64% of the image area. Other masks are supplied, with circular
or smaller ROIs. Smaller ROI is 32%.
4.3.1.9 NDF
The NDF (Neutral Density Filter) is motorized and has a typical optical density of 1.5 +/- 10%. It is
used to attenuate the light in Record Mode. This allows the camera iris to open up more (lower f-
stop setting) and thus decreased the depth of field. In Fluoro Mode the filter is driven out of the field.
4.3.1.10 IRIS
The Iris is motorized and is used to control the amount of light entering the CCD Camera. It is set
to a fixed position for Record Mode but is variable for Fluoro Mode.
4.3.1.11 TV Lens
The TV lens focuses the parallel light onto the target of the CCD Camera.

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4.3.1.12 CCD Camera
The CCD Camera target is an array (1024 x 1024) of pixel photo sensitive wells. Each site or well
is filled with an amount of light energy depending on the intensity of the light hitting that point. The
image information is read off the target array sequentially, line by line, as an analog video voltage
signal. The analog signal is then converted to a 12 bit digital signal via an Analog to Digital
Converter (ADC).
4.3.1.13 Image Correction Board (ICB)

The 12 bit digital image data goes to the Image Correction Board in the Saturn. This board applies
offset, gain and bad pixel corrections to the image data. The CCU Board applies ABD Calculations,
Image Re-scaling and Gamma LUT’s.
The pixel offset and bad pixel correction data are factory calibrated using a temperature cycling and
burn-in process. Normally, they do not need to be updated throughout the life of the equipment. If
you experience bad pixels.
The calibration data is stored within the camera head and downloaded at boot into the ICB. This
suppresses any dependency between the camera head and the ICB. Any camera head can be
coupled with any ICB without the need for calibration or setting.
The channel gain balance and global offset are adjusted dynamically by the ICB through a closed
loop mechanism. These loops optimize left--right gain balancing and keep constant black level.
Saturn power supply provides +12VDC which is converted (DC//DC) in the ICB to generate the
+24VDC needed to power the CCD camera head.
The ICB provides a serial communication link with the camera head. All features of the camera head
can be controlled by the host PC software through the ICB PCI interface.
The ICB provides a synchronization signal to the CCD head in order to synchronize the integration,
transfer and readout phases of the CCD with the x--ray exposures and the Saturn internal timing
reference. The synchronization signal is provided to ICB by the Gitane board.
4.3.1.14 ABD (Automatic Brightness Detection)

The ABD function provides a signal representing the brightness of the image in the ROI (Region Of
Interest). There are three ROl’s selectable for both normal and pediatric studies (see page 7). The
ABD calculation incorporates a Black Level threshold manipulation, which is intended to provide a
means of shutter compensation. The threshold value is set to a level just above the shutter
amplitude on a flat field image. In this way, the effect of collimating within the ROI will not result in
an increase of average brightness. The ABD signal is used by the Exposure Management function
to calculate the Dose Feedback which is then used to calculate the Patient Size. The ABD signal is
also used for actual image brightness feedback to control camera gain.
4.3.1.15 LUT
A Gamma LUT is used to compress the white regions of the image. The purpose of this is to
produce an overall image chain gamma response of unity, thus producing the best input to output
image reproduction.
4.3.1.16 Image Acquisition Board / Digital Acquisition Board

The Image Acquisition Board (Saturn V1) or Digital Acquisition Board (Saturn V2) applies the Fluoro
Noise Reduction (FNR) filters. This reduces the amount of “noise” in the image but increases the
lag. Left to Right image reversal is also performed on this board. The image can be stored on the
hard disk or sent to the Image Display Board (Saturn V1) or Digital Display Board (Saturn V2) for
eventual display on the monitor.

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4.3.1.17 Image Display Board / Digital Display Board
The Image Display Board (Saturn V1) or Digital Display Board (Saturn V2) applies the Edge
Enhancement filters and also the monitor display LUT’s. The digital video is reduced to 8 bit and
then converted to an analog signal by a Digital to Analog Converter (DAC). It is then sent out as a
composite video signal to the monitor on a co-axial cable.
4.3.1.18 Optics Control Board (OCB)

The Optics Control Board provides control of all the optics motorized elements, all the ADCS, HVPS
functions and Photo-diode board. The Optics Control Board receives information from the Gitane
Board over the CAN Bus. The Optics Control Board controls the II Power Supply, ADCS, NDF Filter
position and Iris positions.
The iris aperture is controlled through a software (in OCB micro controller) PID loop using the iris
potentiometer feed-back. The iris is commanded in percentage of its maximum transmission (fully
open). The maximum and minimum transmission must be calibrated for each OCB/optics couple.
OCB calibrates them by moving the IRIS to max. and min. mechanical limitations. This is done
through the iris LUT calibration. This calibration also refines the precision of the law linking the
commanded aperture and the actual light transmission. The OCB embeds a first order model for
this law, which ensures coarse precision. The calibration further improves the precision.
The NDF position (in or out) is controlled through a software (in OCB micro controller) PID loop
using the NDF DC motor and feedback potentiometer.
Both iris and NDF control circuits feature an over current detection circuit in order to protect the
motors and OCB in case of failure of one of the elements. This circuit allows 3 over current events
before sending an error message to the system (iris_overcurrent, ndf_overcurrent) and
blocking the motor operation. To reset the circuit and resume operation, the OCB board must be
reset. This can be done by powering off the OCB, pressing the on--board reset button or real time
reset coming from the Gitane Board.
Both iris and NDF control circuits feature a time out mechanism which will trigger an error message
(iris_timeout or ndf_timeout) if the target position is not within tolerances after 600ms. Time
out errors will not block the iris or NDF operation but indicate a potential failure on either the optics
or the OCB.
The OCB communicates with the ADCS and HVPS through a single RS232 serial link. This link
goes first to the ADCS, then to the HVPS. The ADCS will process the RS232 message first. If this
message is for the HVPS, the will pass the message to the HVPS. If an error occurs in the
communication between OCB and ADCS/HVPS, the OCB will send an error message
(sci_communication_error).
The OCB receives 24V input power from the OCB cable connected to its J1 subD connector. It uses
this input voltage to generate internal +12V, --12V, +5V, --5Vand provides 24V on the J4 connector
to ADCS/HVPS.
The OCB communicates with the Gitane board in the Saturn PC through the OCB cable.
Communication is done through a 250kbps CANbus, a reset line (from Gitane to OCB) and the
brightness pulse line (from OCB to Gitane) coming from the PDB.
4.3.1.19 PhotoDiode Board (PDB)

The photodiode board provides a real time light measurement signal used to control the duration of
the exposure in digital Record AEC mode. The exposure cutoff is made by the generator after the
target dose has been received by the image chain.
The PDB uses a photodiode to convert light from the optics pickup into a photo current. The photo
current is converted into a voltage and amplified through a variable gain amplifier. The amplified
voltage is converted into a frequency encoded pulse signal through a voltage--to--frequency
converter. The greater the light intensity, the higher the output frequency. The brightness signal is
frequency coded so as to insure noise immunity.

GE MEDICAL SYSTEMS
The photodiode gain is set by the exposure manager for each dose setting and scaled with the II
conversion factor to provide accurate dose rate vs. frequency feedback.
The generator counts the pulses and stops the exposure when the target pulse count is reached.
The output signal from PDB is fed into OCB in TTL level. OCB converts it to CAN electrical format
and sends it to the Saturn Gitane through the OCB cable.
The ribbon cable between OCB and PDB holds the following signals:
• PDB power supply voltages from OCB to PDB.
• Gain control signals from OCB to PDB.
• Brightness pulse from PDB to OCB.
4.3.2 Digital Radiographic Mode

For the following discussion, please refer to Figure 2-63 as needed.
1.) The prism sends a light sample using the light pipe to a Photodiode located on the Photodiode
board. A Photodiode mask (square) is used (64% is the default) as a ROI. A neutral density
filter is also used for high II CF in order to reduce the light at Photodiode entrance.
2.) The Photodiode converts the light to a voltage. The voltage is converted to a frequency. The
greater the light, the greater higher the frequency.
3.) The signal arrives at the generator through the Optics control board and Gitane Board. Signal
pulses are counted and the exposure is terminated when a predefined count is reached.
4.) While counting is taking place, the Optics control board performs other functions:
- Channel exposure management signals the NDF motor and port, and Iris motor and pot.
- Channels controls signals to the II power supply for selection of a FOV.
- Supplies power to the ADCS
4.3.3 Digital Image

For the following discussion, please refer to Figure 2-63 as needed.
1.) X-ray is produced at the tube and hardened using one of three spectral filters. The filter used
is automatically selected. Selection depends on patient thickness and the procedure chosen.
2.) The objective lens focuses the light to infinity (parallel). The mirror then deflects it through the
neutral density filter (NDF) to the CCD sensor.
3.) The optical density of the NDF filter attenuates the light some. This allows the camera iris to
open wider and decrease the depth of field. During Flouro exposures, the NDF filter rotates out
of the image field.
4.) The motorized Iris then controls the amount of light entering the CCD camera.
5.) The TV lens focuses the light onto target of the CCD camera.
6.) The 12 bit image data goes to the image correction board and CCU. The CCU applies ABD
calculation, image re-scaling and Gamma lookups.
7.) The 10 bit image data now goes to the Image Acquisition board, which applies Flouro Noise
Reduction (FNR) filters.
8.) At this point, the image can be sent to hard disk or to the image display board for display. The
image display board reduces the image data to 8 bits and then to a composite video signal.
9.) Video signal goes to the monitor.

GE MEDICAL SYSTEMS
Section 5.0
Positioning System
5.1 Positioner Cabinet
5.1.1 Component Locations
Figure 2-64 Positioner Cabinet
Page 128 Section 5.0 - Positioning System

GE MEDICAL SYSTEMS
5.1.2 Positioner Cabinet Components
Figure 2-65 Table Angulation Panel, Pre-amp, SCR and Lateral Drive Board
Figure 2-66 Longitudinal Amp., CAN Bus Breakout and Relay Panel

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Figure 2-67 I/O Board, Speed Amplifier and RS422 CAN Bridge
Figure 2-68 Power Supplies, Bucky Bulkhead, Connector Bulkhead and Angulation
Transformer

GE MEDICAL SYSTEMS
Figure 2-69 120 Vout and Power Bulkhead
5.2 Application (Saber) Software

Saber, name for the application software, is the Positioner control software used in this Diagnostics
X-ray imaging system. It supports the positioning of X-ray source(s) and receptor(s), control of
collimators, patient positioning, and displays/controls for positioner and some system parameters.
In addition, it provides the capability for positioner calibrations and positioner diagnostics. In a
Precision system, positioner devices under Saber software control are OTS, IDD, Table,
Collimators, and some peripheral components such as room door and room light.
OTS positions the overhead X-ray tube, and can be moved in three axis - vertical, longitudinal, and
lateral. IDD is part of the mechanical assembly with the Image Intensifier, which also can be moved
in vertical, longitudinal, and lateral directions. Both OTS and IDD have locks to keep the devices in
place. Additionally, IDD provides two console screens for locks status and fluoro/record displays.
In fluoro/record operation mode, Saber software will display on IDD console selective system
parameters, such as techniques, FOV, II_MAG, Contrast Media etc. It also gives user the control
of some of these parameters and image acquisition functions such as fluoro store and fluoro loop
store.
There are two collimators controlled by Saber software, which adjusts the field of view size based
on user inputs or source-to-receptor distance. FOV change can be either manually or automatically
depending on the user input and operating condition. Saber software controls the table motion
based on the table side and IDD control inputs. This includes eight-way table top motions and table
angulation. Safety limits are checked by the software before and during motion to avoid collision.
5.3 Movement Functions

The motion buttons are connected to the Positioner IO board located in the positioner cabinet. This
board detects button presses and sends a message to the Mars computer. The System Controller/
Mars computer processes the request and sends a command to the CAN amps or the positioner IO
board for a specific action.

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5.3.1 Power Assist Longitudinal
Figure 2-70 Longitudinal Power Assist
When the power assist handle is pressed in the longitudinal direction, a circuitry next to it in the IDD
creates a voltage proportional to the force applied. This voltage goes to the Pos IO board located
in the positioner cabinet which routes it to the analog input of the Longitudinal Power assist CAN
amplifier in the positioner cabinet. This CAN amplifier digitizes the signal and sends a CAN
message to the Mars computer located in the system cabinet through the CAN bus. Mars processes
the information and sends a torque command to the CAN amplifier through the CAN bus. The CAN
amplifier sends a pulse width modulated current proportional to the torque demand to the
longitudinal DC motor drive. This is a 24 V DC motor.
5.3.2 Power Assist Vertical
Figure 2-71 Vertical (SID) Power Assist
When the power assist handle is pressed in the vertical direction, a circuitry next to it in the IDD
creates a voltage proportional to the force applied. This voltage goes to the Pos IO board located

GE MEDICAL SYSTEMS
in the positioner cabinet, which routes it to the analog input of the Vertical Power assist CAN
amplifier located in the positioner cabinet. This CAN amplifier digitizes the signal and sends a CAN
message to the Mars computer located in the system cabinet through the CAN bus. Mars processes
the information and sends a torque command to the CAN amplifier through the CAN bus. The CAN
amplifier sends a pulse width modulated current proportional to the torque demand to the Vertical
DC motor drive. This is a 24 V DC motor. This motor has a resistor in series. This resistor is located
next to the motor. This resistor limits the maximum current that can be driven by the CAN amp.
During calibration of the system this resistor is set to the proper value such that the max power
assist from the motor is just over the frictional force in the mechanism. This is done by setting the
time the IDD takes to go from top to bottom to be 3+/-0.5 seconds when the power assist handle is
pressed down to the maximum level but without the hand applying a net force pushing the IDD
down. This is done by pushing the bar down with the fingers while supporting the IDD with the
thump.
5.3.3 Positioner/Table Angulation
Figure 2-72 Positioner Angulation
When the table tilt button at the table side is pressed, the signal is send to the Pos IO board located
in the positioner cabinet. It converts it into a CAN bus command and sends it to the Mars computer.
It processes the information and sends a CAN message to the CAN amplifier. An analog output
from this CAN amp is connected to the tilt drive panel located in the positioner cabinet. This panel
drives the tilt drive in the Gantry. This is a 220V DC drive.
When the tilt knob on the IDD is used, an analog voltage proportional to the turn of the knob is send
to the Pos IO board. This voltage is converted to a digital value and it is send as a CAN command
to the Mars computer. The rest is similar to the table side button.
The table tilt angle is read by a potentiometer and it is send as an analog voltage to the Pos IO
board. This board converts it to digital value and it is send to the Mars computer for processing.

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5.3.4 Table-Top Longitudinal/Lateral Drive
Figure 2-73 Table-Top Longitudinal
When the table top longitudinal or the lateral drive button is pressed on the table side or using the
joystick, that switch closure is send to the Pos IO board located in the positioner cabinet. This board
detects this signal and sends a CAN message to the Mars computer in the system cabinet. It then
sends an On or Off command to the Positioner IO board as a CAN message. This board turns On
or Off relays in the Long/Lat drive board in the positioner cabinet. There is 120V AC connected to
this relay. This relay drives this 120V AC to the AC motors which drive the table top located in the
table.
Figure 2-74 Table-Top Lateral
5.3.5 Longitudinal and Lateral Power Assist locks

Depending on the protocol and the selection on the IDD screen the Mars computer decides when
the lock should be turned on and off. When the locks needs to be turned on or off the Mars computer

GE MEDICAL SYSTEMS
in the system cabinet sends a CAN message to the Pos IO board in the Positioner cabinet. This
board applies a 24 V or removes a 24 V to these locks as needed.
5.3.6 IDD Console Screen

When a button around the screen is pressed, the IDD console controller located in the IDD creates
a command and using a RS422 protocol the command is send to the CAN bridge located in the
Positioner cabinet. This CAN bridge converts the RS422 signal into a CAN message and sends it
to the Mars computer. The Mars computer processes the information and passes the necessary
information to the other computers. Once the console display changes are determined it is send as
a CAN message from the Mars computer to the CAN bridge. CAN bridge converts it into a RS422
level signal and it is send to the IDD console controller located in the IDD. The controller displays
the information on the IDD console screen.
5.3.7 Prep/ Expose Buttons on the IDD/ Fluoro foot Switch

When these buttons are pressed a switch closure signal is send from the table to the Pos IO board
located in the positioner cabinet. This board drives two separate RT bus lines (one for Prep and
another one for Expose). The RT bus is a differential bus and signals in this bus has a logic of active
low. (When the signal is in the low state, it is logically active and vice versa). This goes to the Venus
user interface console. The Venus reads this signal and the software executes the appropriate
sequence. The RT bus is also connected to the Mars computer Gitane Bd. The hardware on this
board along with software commands to this board sends hardware signals to the Jedi generator to
enable exposures. This is a hardware path from the prep expose switch to the Jedi generator. In
addition there are commands send by software to Jedi through the second CAN bus which is
connected just between the Mars and the Jedi along with the RT bus lines between the Mars and
the Jedi.
5.3.8 Prep/Expose buttons on the Venus console.

When these buttons are pressed, it drives the RT bus just like the Pos IO board. Venus reads the
RT bus change just like when it is done by the Pos IO board. The rest of the operation is same as
the sequence explained above.
5.3.9 Grid/Cone Motion
Figure 2-75 Cone

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When the Grid or Cone button is pressed on the IDD console, the micro controller in the IDD
converts it into a command and it is send as a RS422 signal to the CAN bridge in the Positioner
cabinet. This CAN bridge converts it into a CAN message and sends it as a CAN message to the
to the Mars computer in the system cabinet. Mars processes that information and sends it to the
CAN bridge as a CAN message. The CAN bridge converts it into a RS422 signal and sends it as a
RS422 signal to the DSC box in the IDD. The controller in this DSC box drives the Cone and the
grid to the appropriate position.
5.3.10 Digital Servo Controller 2 Circuit Board (Used w/Table 2403791 Only)
5.3.10.1 Original DSC Assembly Compared to the DSC2 Circuit Board

The predecessor of the DSC2 circuit board will be referred to as the DSC Assembly. As Precision
500 evolved, DSC2 was introduced to simplify and improve reliability of Precision 500 systems.
The previous DSC (2117101) assembly was implemented on the GE “Legacy R&F” systems in
1995. Its purpose was to control 6 servomotors and communicate with the Positioner cabinet over
a RS-422 serial line. It consisted of three (3) stacked printed wire assemblies.
When the Image Intensifier (II) video signal was digitized for the Precision 500, traditional spot films
were no longer necessary, as this function could be done in software. Four of the original six DSC
axes of motion were responsible for traditional mechanical spot film functions. On the DSC
assembly originally used in the Precision 500D (2117101-7), the components driving these 4 axes
were left unpopulated.
As technology evolved, a single board can be made to provide the needed functionality. The main
form of communication in the Precision 500D system is CAN, and the serial link used to talk to the
DSC assembly. Originally done with a purchased part called a CAN bridge; it is now possible to
bring this functionality into the DSC2 circuit board. DSC2 circuit board and related cable changes
make it impractical to support previous Precision 500 systems.
The DSC2 circuit board performs several main tasks:
• Control the two remaining servomotors in the IDD, the Cone and the Grid.
• Communicate with the Aretha system software via a CAN link.
• Assume the functionality of the Power Assist Handle Pre-Amp board.
• Intercept digital and analog signals from the IDD console and convert them into CAN.
• Provide the power interface to the under table collimator.
It does this with minimal wiring changes to the Positioner cabinet and table base.
5.3.10.2 Functional Operation

The previous Digital Servo Controller assembly design allowed for six (6) axes of motion to be
controlled. The hardware involved included a dedicated PC104 board, servo control board and
servo amplifier board. With the film-less products (Precision 500D), only two axes of motion (Cone
and Grid) are required. In systems with the old DSC, the power assist handles were amplified using
a pre-amplifier board (46-321188) and then converted to CAN signals by the CAN motion amplifiers
in the Positioner cabinet. In the Aretha program, RS-422 signals from the IDD were converted to
CAN using a costly off-the-shelf Bridge device.
The DSC2 circuit board incorporate a dual-axis motion control driver and CAN bridge into its design.
The need for the old external CAN bridge now eliminated. The power assist handles are amplified
and converted to CAN on the DSC2 circuit board, eliminating the old pre-amp board. Lastly, some
analog and digital I/O signal conversion to CAN is also now done on the circuit board.
Backwards compatibility with the previous 6 axis DSC assembly is not possible. Figure 2-76
shows the Precision 500D architecture with a DSC2 circuit board installed.

GE MEDICAL SYSTEMS
J30
Main Harness
ANG_VERT - 24V
ANG_TREND - 24V J5
XRAY SW - 24V 50 Pin II 24V
J4
J6 37 Sub- D Switches
PREP/RECORD - 24V PS 9 Sub- D
Sub-D
IDD_RESET - 422 DSC2
SFD_ANG_SW_OFF - 24V
J5
Encoders
J1
POS I/O
J2 J8 J3 Motors
A1 A20 CAN CAN Tru nk
9 Sub-D
ANG_SPD - Analog Collimator Out + 24V CAN Trunk In
HANDLE_LONG - 24V 9 Sub- D 9 Sub-D
HANDLE_VERT - 24V J6 25 Sub-D 37 Sub-D Rear of IDD
TOP_RIGHT - 24V 50 Pin
TOP_LEFT - 24V Sub-D CAN Trunk
TABLE_TOP_OUT - 24V + 24V
TABLE_TOP_IN - 24V 9 Pin Sub-D
CAN + 24V Pow er Assist

J1
24V Logic Power
for Coll imator Interf ace
50 Pin
24V Motor Power Sub-D
Power Motor Power/
Logic Power
J2 A1 A28
24V Logic Power Signals
24V Motor Power
37 Pin
Sub-D
Long Vert
Serial/
3 Pin 3 Pin
CAN From Signals/
Table Base Logic Power
Handle
Table Base
J27
J1
37 Sub-D
MIS11198A
J100 25 Pin
25 Sub-D
IDD Console
Motor Power
Y Adapter OR
New Harness
Precision 500D - DSC2 Architecture
J101
POS Cabinet 50 Sub-D
Signals
Figure 2-76 DSC2 Circuit Board Functions
The primary functions of the DSC2 board, as mentioned before, are:

• To control the Cone and Grid servo motors in the IDD.
• Transmit and receive commands to and from the Positioner subsystem via an internal CAN
bridge.
• Provide a way to put discrete and analog console signals onto the CAN bus.
• Facilitate serial IDD console communication via an internal CAN bridge.
• Assume the functionality of the power assist handle pre-amp, and place the result on CAN.
• Move +24VDC from the Image Intensifier power supply into unused pins in the CAN trunk for
the collimator to use.
The 2 servos controlled using a PID position loop. The output is a PWM signal, and the position is
detected via a quadrature encoder on each servomotor. High-level motion commands come from
the CAN serial link - they are not generated locally under normal operation. The exception to this is
during boot calibration, which occurs after every reset or power-up. During this calibration, the
board must locate the “home” position of the grid by checking for a stall in 2 cases - grid in and grid
out. The cone calibration is similar, but occurs during normal operation, and only when the user
requests movement.
The DSC2 is connected to the CAN bus, which the system controller uses to communicate with
various Positioner subsystems. This bus utilizes the CAN standard pin-out and communicates at
250kb/s. The DSC2 has the I/O functionality of the CAN chip utilized on the Positioner I/O board
(2293142), allowing the DSC2 to convert discrete and analog signals to CAN locally in the IDD,
instead of sending the signals back to the Positioner cabinet (as in the old DSC assembly). In
addition, the DSC2 provides a CAN to serial bridge with at least two channels; one for on board
communication and one to allow the IDD console to talk to the CAN bus.
The power assist handle contains two “Hall effect” sensors that indicate the amount of force being
applied to the handle. The old pre-amp board was originally used to condition the output of the
handle and pass the differential analog voltage all the way back to the Positioner I/O board. Now,

GE MEDICAL SYSTEMS
the DSC2 circuit board conditions the handle outputs to the proper voltage level, and converts them
to CAN. This eliminates the need for a separate pre-amp board.
The under table (u/t) collimator is the termination point for the CAN bus. In addition, the u/t
collimator needs to be supplied with +24VDC and ground from the Image Intensifier (II) power
supply. The CAN trunk from the table base comes into the DSC2, as well as the +24VDC from the
II power supply. The +24VDC power is channeled into 4 unused CAN pins, and sent out along with
the CAN trunk to the u/t collimator.
The board is powered by a dedicated +24VDC power supply from the Positioner Cabinet. This is in
turn converted on board to other voltages.
5.3.10.3 High-level Architecture Description

The DSC2 PWA resides in the IDD and performs the following major functions:
1.) Motion Control: Provide all motion control for the cone and grid servos
2.) CAN Communications: Interface to CAN in the form of a serial bridge
3.) Digital and Analog I/O: Provide a means to convert discrete and analog signals to CAN
4.) Power Assist Handle: Power the power assist handle and convert the analog return to CAN
5.) Under Table Collimator: Provide the u/t collimator with +24VDC and the CAN trunk
6.) Power Supplies: +1.5VDC, +3.3VDC, +5VDC, +12VDC
7.) Diagnostics: Visual indicators and software reporting of errors to the rest of the system
8.) Reset: Generate self-reset after fatal application errors

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5.3.10.4 Theory of Operation
The high-level architecture is described in more detail in the following sections.
24V to 5V Conversion -
To CAN Core Digital Inputs To Console J1
To POS Cabinet ANG_EN 5 ANG_EN (24V) 25 ANG_EN

ANG_VERT 6 ANG_VERT (24V) 5 ANG_VERT
J27 - Table Base 7 24
ANG_TREND ANG_TREND (24V) ANG_TREND
X-RAY_SW 18 X-RAY_SW (24V) 31 X-RAY_SW
PREP_REC 19 PREP_REC (24V) 15 PREP_REC
IDD_TOP_IN 20 IDD_TOP_IN (24V) 26 IDD_TOP_IN
IDD_TOP_OUT 21 IDD_TOP_OUT (24V) 7 IDD_TOP_OUT
TABLE_TOP_LEFT 8 TABLE_TOP_LEFT (24V) 27 TABLE_TOP_LEFT
TABLE_TOP_RIGHT 9 TABLE_TOP_RIGHT (24V) 8 TABLE_TOP_RIGHT
C24V 1 6 IDD_ANG_SW_OFF
J8 25 Pin Sub-D M
J3 37 Pin Sub-D F
C24V 2 12 C24V
C24V 3 17 C24V
14 Console 24V 33
CGND C24V
CGND 15 34 C24V
CGND 16 14 CGND
M24V 23 +24 Motor Power 16 CGND
24 Console Ground 32
M24V CGND +15 V
M24V 25 35 CGND
MGND 10 Motor Ground 11 ANG_SPD +/-15V & Ground
11 30 from IDD Console
MGND ANG_SPD_RTN
12 Digital Inputs 1
MGND +1.5V+3.3V+5V +12V from Console ANG_SPD RMT_SW_DAT_P -15 V
(Shield2) 13 (Analog) 20 RMT_SW_DAT_N
RS-422
L24V 4 24V Driver 2 RMT_LMP_DAT_P
Power Serial
LGND 17 GND 21 RMT_LMP_DAT_N
Note: Conversion 3
1.) MGND, CGND, and LGND all refer to ground. They are RS-422 CNSL_RESET_P
connected together in the POS cabinet and on the DSC2. Driver 22 CNSL_RESET_N
They have different names to show power allocation.
CAN Core Reset
M=motor, C=console, L=logic. This is also true for 24V.
2.) J2 is part of the DXR generic CAN Core and may have an
"_n" atteched to the end of it in actual implementation. CAN +12V
Stub
J2 9 Pin Sub-D M
Handle
CAN Trunk CAN_L 2 1 +12V_L GND
Long
J5 9 Pin Sub-D F
CAN_GND 3 2 GND_L
Table Base CAN_H 7 HANDLE_L 6 HANDLE_LONG Vout
(Analog)
CAN_V_POS 9 Serial 4 +12V_V +12V
5 GND_V
HANDLE_V 9 Handle
HANDLE_VERT GND
(Analog) Vert
Vout
J4 9 Pin Sub-D F
Collimator Power +24V 1

+24V 4
II Power Supply
GND 6 CAN 29 CONE_VCC
GND 8 Trunk 28 CONE_ANOD
Servo Con tro ller Cone Park 12 CONE_CATH
13 CONE_GND
30 CONE_PARK
IDD Park 11 IDD_SW_12
10 IDD_PARK
CAN Trunk & 18
+24V 1 VCC_G Grid Encoder
Collimator Power 2 37 CHB_G
CAN_L
J1 9 Pin Sub-D F
Table Base 3 Grid Encoder 14 GND_G

CAN_GND
4 36 CHA_G
+24V
6 J6 37 Pin Sub-D F 1 GRID+
GND
7 2 GRID+
CAN_H
Serial 20
GND 8 Grid GRID+ Grid
PWM, Dir, Brake 3
CAN_V_POS 9 H-Bridge GRID-
21 GRID-
22 GRID-
4 CONE+
5 CONE+
Cone 23 CONE+
PWM, Dir, Brake
J9 9 Pin Sub-D F
6 Cone
2
H-Bridge CONE-
Debug Tx 24 CONE-
3 RS-232
Rx 25 CONE-
Driver
CTS 8 34 CHA_C
RTS 7 19
Cone Encoder VCC_C
35 CHB_C
15 GND_C Cone Encoder
DSC2 Rev E 22-Jan-2004
Figure 2-77 DSC2 Circuit Board Interconnects
Motion Control
The primary output of the DSC2 is the control for the cone and grid servo-motors. This control is in
the form of variable duty cycle, pulse width modulation (PWM). The inputs to the motion controller
of the DSC are the quadrature encoded position data from each channel, the current sense
determined by A/D converters, the cone's optical home switch, and any commands from the
positioner subsystem that arrive from the internal CAN bridge. The following are the high level
specifications related to motion control:
• 3 Amps is considered “over current.”
• Current “ripple” must be < 10%

GE MEDICAL SYSTEMS
• Transfer time for the grid must be < 1500ms
• Accuracy of the cone and grid is +/- 1.5mm
The motion control functions are described below.
QUADRATURE DECODE
Quadrature pulses are two pulse trains that are 90 degrees out of phase. This method allows shaft
direction to be determined along with shaft position. The DSC2 currently interfaces with encoders
that generate 200 counts per encoder wheel revolution (CPR). In addition, the cone and grid have
a 10:1 gear reduction. This ultimately equates to 2000 CPR for the cone and grid. If signal A leads
signal B, then the direction is forward. If signal A lags behind signal B, then the direction is reverse.
This data, in the form of a count of pulses, must be presented to the software to determine if the
duty cycle must be increased or decreased. The data will be read by the motion control software at
least every 10ms.
PWM CREATION
The hardware must create a variable duty cycle pulse train based on a 16 bit command. The PWM
will run with a frequency of at least 10kHz, and it will be updated a minimum of every 10ms. These
specifications attempt to keep the motion smooth and controlled.
POWER ELECTRONICS
The DSC2 is the final interface to the cone and grid motors. It must drive them at a maximum of 3A
in either forward or reverse for a maximum of 1.5s. In practice, sustained 3A current draw for this
length of time would not be seen. The implementation of choice is an H-Bridge, which allows them
to be driven in both directions depending upon which transistors are turned on. It also allows for a
braking function.
CURRENT SENSING
In addition to position sensing through the Quadrature encoders, the motion control function needs
to determine the current flowing to each motor at any given time. This is mainly to keep the PWM
in check and to protect the motors against an overload situation. The preferred implementation is a
current sense resistor (somewhere in the power electronics) whose voltage drop is read by an A/D
converter. The current reading must be available at least every 10ms.
CONTROL ALGORITHM
The motion control algorithm shall move the cone and grid as quickly and as smoothly as possible.
Overshoot should be minimized while still meeting the specs listed in Motion Control on page 139.
CAN Communications
The Positioner subsystem communicates with various peripherals via a CAN bus that uses the
CANOpen protocol. The word “CAN” is used generically to mean “a CAN bus that uses the
CANOpen protocol.” As mentioned previously, the old DSC communicates via an asynchronous
serial protocol (RS-422). The IDD console also communicates this way, and its serial lines pass
through the DSC on the way to the Positioner cabinet.
On DSC assembly Precision 500D, the method of converting CAN messages into serial is to use
an external CAN bridge mounted in the Positioner cabinet. The CAN Bridge takes CAN packets and
converts them to the serial communication, and vice versa. The functionality of this 2 channel bridge
is moved onto the DSC2 by using the generic CAN Core (2343467) designed by GE. It essentially
relocates the bridge to a different physical location and utilize a different node address, but it
functionally operates the same way and required minimal system software changes.
The new CAN Core has two bridge channels - one will be utilized for on board DSC2
communication, and the other used for the IDD console. The console channel of the bridge requires
no discussion here and is simply a routing of existing signals.

GE MEDICAL SYSTEMS
Digital and Analog I/O

A second function of the generic CAN Core mentioned above is to provide a method of putting
digital and analog I/O onto the CAN bus. The DSC2 can utilize this functionality to convert many of
the discrete and analog signals passing through on their way to the Positioner cabinet.
Unfortunately, due to safety requirements, the need for a “motion enable” signal, and the inability
to change the Positioner I/O board, all of the discrete signals except for one must be sent back.
However, they can still be put on the CAN bus at the DSC2 to allow for future cabinet elimination
and system consolidation. As seen in Figure 2-77, the following discrete signals will pass through
the DSC2 and on to the Positioner cabinet, but will be input into the CAN core for future use:
• TABLE_TOP_LEFT - Indicates a user request to move the tabletop left.
• TABLE_TOP_RIGHT - Indicates a user request to move the tabletop right.
• IDD_TOP_IN - Indicates a user request to move the tabletop in.
• IDD_TOP_OUT - Indicates a user request to move the tabletop out.
• ANG_VERT - Indicates a user request to angulate the table in the vertical direction.
• ANG_TREND - Indicates a user request to angulate the table in the Trendelenburg direction.
• ANG_EN - Signifies that ANG_VERT or ANG_TREND is set.
• PREP_REC - Indicates that the user has pushed the Prec/Rec switch.
• X-RAY_SW - Indicates that the user has pushed the X-Ray switch.
The following signal is intercepted by the DSC2 and is NOT be sent back to the Positioner cabinet:
IDD_ANG_SW_OFF - Indicates that the angulation switch is off (no motion requested).
The CAN Core has an on-board 10-bit A/D converter with a 0-5VDC conversion range. It’s used to
intercept and convert the following signal ANG_SPD (An analog potentiometer that indicates the
desired table angulation speed. The angulation speed potentiometer is powered by the IDD console
with +/-15VDC.)
• HANDLE_LONG - An analog signal from the power assist handle pre-amp function (see that
section for details on the signal conditioning).
• HANDLE_VERT - An analog signal from the power assist handle pre-amp function (see that
section for details on the signal conditioning).
4.6.4. Power Assist Handle

The power assist handle takes mechanical commands from the operator's hand and translates it
into 2 voltages, one for the vertical direction, and one for the longitudinal direction. Previously, the
handle was powered with +/- 15VDC (0-15VDC on one axis, and -15-0VDC on the other) and the
power assist pre-amp board (46-321188) conditioned the signal to be 0-10VDC with Zener diode
clipping and a potentiometer-adjusted dead band. The signal was then passed back to the
Positioner cabinet, where it was converted to a CAN message by the Positioner I/O board.
In the DSC2, the functionality of this external pre-amp board as well as the CAN message creation
is located on-board. Instead of a +/- 15 VDC power source, the handle will be powered with 0-12
VDC. Some hardware signal conditioning will be necessary to get to the 0-5 VDC level, but the dead
band and clipping will be done by the system software and the CAN Core. In summary, the
requirements are to:
• Provide the power assist handle with 0 VDC and +12 VDC power on each handle axis.
• Condition the return signal to be linear and between 0 VDC and +5VDC. +2.5 VDC will indicate
the 'null', or handle at rest position. The polarity of the signal (which direction corresponds to
< 2.5VDC and which corresponds to > 2.5VDC) will be accounted for by the system software.
• System software does all other functions (dead band and clipping).

GE MEDICAL SYSTEMS
Under Table Collimator

In systems with the previous DSC assembly, the CAN trunk comes to the table base into a CAN
“Tee”. There, 24V comes down from the Image Intensifier (II) power supply, and is injected into the
unused pins in the CAN cable. The under table (u/t) collimator makes use of this power. Since the
trunk needs to get into the IDD for the DSC2, this “Tee” functionality can be moved on board the
DSC2. The DSC2 will have 3 CAN/Collimator related inputs - +24VDC in from the II, CAN trunk in,
and CAN trunk + 24VDC out. The routing on the DSC2 board puts the proper signals and powers
into the proper pins on the CAN bus.
Power Supplies
The DSC2 takes +24VDC and ground from the Positioner cabinet. It has been allocated 3 power
and 3 ground pins for the motors, 1 power and 1 ground for DSC2 logic power, and 3 power and 3
ground pins for the IDD console. Each pin is a 20-gauge sub-D pin and each conductor in the cable
is a 24-gauge conductor capable of carrying 1.5A continuous in the worst case. The motors (more
specifically, the H-Bridge) will take the 24VDC directly, and will only draw 3A peak (each) for a very
short time in the worst case. The PWM will take care of any voltage drops that may occur as a result
of a high current draw. The DSC2 on board components will require +1.5VDC, +3.3VDC,
+5VDC(CAN core) and +12VDC (for the handle).
Diagnostics
The DSC2, like the previous DSC assembly, does not have any stand-alone service diagnostic
routines. It reports errors in normal operating modes as they occur and responds to any system
communications to verify that it is up and running. In addition, it has diagnostics to support the CAN
Core.
The CAN core has access to the DSC2's +24VDC, +12VDC, +3.3VDC, and +1.5VDC power
sources for monitoring purposes. LEDs also show the status of these voltages. The externally
visible LED's are as follows: 12VDC(green), 5VDC(green), 3.3VDC(green), Heartbeat (green),
Normal Mode (green), Safe Mode (Yellow), and 4 Error code bits (Red).
Other LEDs are present on various input signals, but will not necessarily be visible outside of the
DSC2’s enclosure. The CAN core also has its own indicator LEDs for diagnostic purposes. There’s
an on-board RS-232 debug port that supports engineering development, as well as a Mictor-style
connector to support connection to a logic analyzer.
Calibration
The DSC2 is be able to calibrate its motion functions every time it powers up. It moves the grid
inward until it stalls, and zero out the position. This is the “in” position. It will then be moved towards
the home (out) position. The home position will be recorded and compared against an expected
count to verify the grid has a full range of motion. The cone will calibrate itself by moving towards
the direction requested by the user. If it is not parked, it will drive outward at constant speed. If it is
parked, it will assume that it has full range of motion and attempt a normal move inward. When an
inward move has been completed with a full range of motion, the calibration is considered complete,
and all further moves are made normally (not constant speed). For patient safety reasons, the cone
will not move at all until requested by the user.
The software only will calibrate the pre-amp functionality - no hardware calibration will be required.

GE MEDICAL SYSTEMS
Reset
The DSC2 is responsible for generating a reset signal for itself as well as the IDD console. The
console reset comes via a CAN message, and is separate from a DSC2 reset. The DSC2 internal
reset has four conditions that are described in further detail below. A DSC2 reset will also reset the
CAN Core module on board.
POWER-UP RESET
Upon power-up, reset circuitry will ensure the DSC2 is held in reset for a minimum of 100 ms.
CAN RESET MESSAGE

Upon receiving a CAN reset message, the CAN Core will use two digital output lines to latch a reset
signal for either the DSC2, the IDD console, or both for a minimum of 100ms.
INTERNAL SOFTWARE RESET

The DSC2 software will have the ability to trigger a reset by setting an active high reset pin. The
reset generated lasts for a minimum of 100ms.
WATCHDOG RESET
A watchdog circuit, that requires a write every 0.9 seconds, has the ability to generate a reset
condition that must last for a minimum of 100ms.
5.3.11 Bucky
When it is time for the Bucky to be operated, the Mars in the system cabinet sends a CAN message
to the Pos IO board in the positioner cabinet. The Pos IO board sends a signal to the bucky in the
table to start the oscillation. When the bucky is at speed, the bucky sends a signal to the Pos I/O
board in the positioner cabinet. The Pos IO board converts it a CAN message and sends it to the
Mars computer in the system cabinet. Mars computer communicates this message to the rest of the
system.
5.3.12 Cassette Sensing Tray

The cassette sensing tray switches and pots are connected to the Pos IO board in the positioner
cabinet. The Pos IO boards converts these signals to CAN messages and sends it to the Mars
computer. This processes the information and the appropriate actions are taken.
5.3.13 Ion Chamber

The Ion chamber is connected to the Jedi Generator in the system cabinet directly.

GE MEDICAL SYSTEMS
5.3.14 Collimator & Blade
Figure 2-78 Collimator
The collimator is connected to Mars in the system cabinet through the CAN bus.
The collimator paddles are connected to a switches. These switches are connected to the Pos IO
board in the positioner cabinet. The Pos IO board converts these switch closures into CAN
messages and they are send to the Mars computer in the system cabinet. The Mars computer
processes it and sends the appropriate CAN messages to the Collimator in the table through the
CAN bus. In addition Mars sends the appropriate messages to the IDD console display through the
CAN bridge to update the graphics on the screen.
5.3.15 Spectral Filter
Figure 2-79 Spectral Filter

5.4
GE MEDICAL SYSTEMS
Power Bulkhead
Power 120VAC 230VAC
(A1A29)
Bulk head Indicator Indicator
A29 TS1 RV1
250V
J10
From Sys PDU Mate N Lok 1 1 1 1 AC A29 TS2 A29 TS3
230VAC 1 1 Line
0VAC 4 4 2 2 2 2 Filter 1 1 1 1 1 1 1 1
PE 2 2 (20A)
120VAC 3 3 3 3 3 3 2 2 2 2 2 2 2 2 A1 A27
0VAC 6 6 J2
PE CB1
5 5 4 4 4 4 AC 3 3 3 3 3 3 3 3 Mate N Lok Mate N Lok
LN1 LD1 230VAC-A 0VAC_BKY
J11 Line 1 1 J1-1
To Wall S tand Mate N Lok 1 1
5 5 5 5 Filter 4 4 4 4 4 4 4 4 LN2 LD2 2 2 0VAC_BKY_SW
PE 230VAC-B 2 2
3 3 (20A) 15A 3 3 J1-3 120_VAC_SW

120VAC 230VAC-B 3 3
1 1 4 4 J1-17 120VAC_ACC
0VAC RV3 4 4
2 2 250V 5 5 120VAC_ACD1
Chassis GND 0VAC 5 5
J12 6 6 J1-2 120VAC_ACD3
To Image He ad P.S. Mate N Lok
CB3 -15AP 6 6
CB5 J1-23 120VAC_BKY
PE LN LD 7 7
3 3 GND 120VAC_BKY
120VAC LD LN
+15AP 8 8
1 1 STUD J1-21 120VAC_LAT
5A 5A Mate N Lok
9 9
0VAC 2 2 120VAC Lat Comm 120VAC_LAT_SW
CB2 1 1 J1-22 10 10
120VAC Lat Input 120VAC_LONG
2 2 J1-28 11 11
A1 A27 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 LN LD 120VAC Long TOP_LEFT
A1A25 Connector Mate N Lok 3 3 K1 Low 12 12
J5 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 10A 120VAC Long J1-14 TOP_RIGHT
Bulkhead 4 4 13 13
Angulation Transformer As sembly 5 5
120VAC ACD1 K1 Hi SHIELD2
J1-13 14 14
120VAC ACD3
MIS11194A (A1A27) 6 6 Fld- 15 15
0VAC BKY J1-16
7 7
J106
Table Cass Tray 0VAC LAT Fld+
8 8
15p Sub-D F
15p Sub-D M
0VAC A1 J1-15
9 9 Arm(A2)1
0VAC A2 J1-11
T1 10 10
MIS11195A 230A 1 230A 0VAC LONG1
A27 TS1 11 11 Arm(A2)2 Sub D
Table Signals 0VAC LONG2
J104
12 12 24VDC_Cabinet_Power
50p M M
50p M F
Arm(A1)1 1 1
1 1 1 1 13 13 J1-10 TOP_RT*
230B 1 Arm(A1)2 2 2
14 14 TOP_LFT*
230CT A1 A27 3 3
MIS11196A 2 2 2 2 15 15 Ang En K2_HI
230A 2 J1 J1-25 4 4
K2_LOW
J103
Table Signals (Ang, etc.) 5 5
50p M M
50p M F
24V RTN
Positioner Cabinet Interconnects
3 3 3 3 J1-26 BE1*
6 6
BE2*
230B 2 230B +5V, +/-15VDC 120VAC Acc 7 7
4 4 4 4 5V_RTN J1-19 SHIELD1
4 8 8
MIS11197A Power Supply 15V_RTN SHIELD2
CB4 GND 5 9 9
Neutral
J101
STUD J1-18
Mostly SFD Signals LD LN 3 +5V Angulation Get From 0VAC A1 Relay
50p Sub-D F
50p Sub-D M
1
(A1 A28 PS2) -15V
15A Mate N Lok 6 Panel Panel
3 3 3 +15V
LPT63 1
MIS11198A 2 2
(A1 A7) (A1 A21)
GND
J100
1 1
SFD +24VDC A, B, C, D STUD
25p Sub-D F
25p Sub-D M
A1 A27 3 2 1 Mate N Lok A1 A27
J4 3 2 1 J3 +12 VDC
+24VDC +V
A1A28 J1
MIS11235A Power Supply Power Supply
Power Supply +V
(A1 A28 PS3)
J203
Figure 2-80 Positioner Cabinet Interconnect Drawing

Assemb ly
Wall Stand I/F Signals E 12V_RTN
15p Sub-D F
15p Sub-D M
1 4
N (A1 A28 PS1) -V LPS23 +12V
(A1A28)
3 3
-V
L

MIS11236A A1A28 J2 1 2 3 4 5 6 7 8 9 A1 A28
CABINET FANS JWS-600 Mate N Lok
37p Sub-D M 50p Sub-D M
1 2 3 4 5 6 7 8 9
J210
J3
15p M F
15p M M
Bucky I/F Signals
MAIN HARNESS (See 2291839WIR)

MIS11234A
26p HD Sub-D M 9p Mat N Lk 50p Sub-D M 50p Sub-D F 7p Combicon UEGM Term
J205
7p Combicon
Wall Stand Ion Chamber
15p Sub-D F
15p Sub-D M
J1 J2 J3 J4 P1 X101 DC Power 9p Mat N Lk
Real-Time DC Power Angulation DC, Motor PWR; Motor
P1
Lock/Relays, DC, Motor PWR; Mo tor
Bus Panel I/F, J1
Digital I/O RS422 to CAN
Analog I/O
P200
RJ45
MIS11669A Positioner I/O Boa rd Long PA CAN Amp Vert PA CAN A mp Lat Drive
Bridge
J206
CAN V+ Coll +24V
WS Ion Chamber To Jedi (A1 A22)
9p Sub-D F
9p Sub-D M
(A1 A20) (A1 A23) (A1 A24) PWB
JP JP
P230
RJ45
P4 P5 P4 P5 X400 (A1 A26)

MIS11698A J7 J6 J5 44p Sub-D M 9p Sub-D F 44p Sub-D M 9p Sub-D F 5p Combicon
(Power Resistors and
J110
9p Sub-D M 9p Sub-D F 37p Sub-D M Relays formerly on A5 Brd)
26HDB-M
Atlas RTB B us
26pHDB-F
MIS11692A
J111
CANopen and C. Paulik
9p Sub-D F
9p Sub-D M
A1 A30 All Cables Are 9p Sub-D M on this end
Power to Col limator REV J
CAN Break out 9p Sub-D F 3/8/2002
9p Sub-D M
MIS11694A
J112
CANopen Bus IN
9p Sub-D F
9p Sub-D M
Page 145
GE MEDICAL SYSTEMS
Section 6.0
System Communications
6.1 CAN Bus
6.1.1 History
CAN was invented by the Robert Bosch (TM) company in Germany in the mid 1980's, as a solution
to automotive communication needs.
6.1.2 Advantages of CAN Networks

CAN is a serial data communication bus for real time applications.
• Operate in harsh environments
• Easy to Configure
• Automatically Detect Data Transmission Errors
• Cost Effective
6.1.3 Operation
Up to 1 Megabit/sec (1 Mb/s) Transmission Speed
Node 1 Node 2 ... Node n
120 Ohm Can_H 120 Ohm
Can_L
CAN Network
CAN is a two wire twisted pair bus, terminated at both
ends with 120 Ohm Resistors
Number Data Field is 0 to 64

of Bits bits or 0 to 8 bytes
Cyclic
Redundancy End of
Identifier Control Frame
Check
1 11 1 6 0 to 64 16 2 7 3
Start of Remote Data Acknowledge Intermission
Field Transmission
Request
CAN 2.0A Message Format

111 Bit Message Frame
Figure 2-81 CAN Bus
Data messages transmitted from any node do not contain addresses of either the transmitting node
or of the receiving node(s).
The content of the message is labeled by an identifier that is unique throughout the network. All the
other nodes on the network receive the message and each performs an acceptance test on the
Page 146 Section 6.0 - System Communications

GE MEDICAL SYSTEMS
identifier to see if the message is relevant for that node. If the message is relevant it will be
processed, otherwise it is ignored.
The identifier also determines the priority of the message. If two or more nodes compete for access
to the bus at the same time, the highest priority message will gain access and the lower priority
messages are automatically transmitted in the next available bus cycle, if no more higher priority
messages are waiting to be sent.
6.1.4 Overview
As the Precision 500 system has evolved, three versions of CAN bus architectures has evolved.
Two hardware changes drove this:
• OTS assembly changed from Part number 2304223 (Figure 2-82) to 2327101 (Figure 2-83)
• DSC assembly 2391475 added to IDD (Figure 2-84)
Use the block diagram that matches your system configuration in the discussions that follow.
There is one system CAN bus connecting the Positioner Cabinet, Table, System Controller, and
OTS. This is controlled through the System Controller Gitane board’s J14.
There are 2 local subsystem CAN buses, one for the Optics Control Board (OCB) and one for the
Jedi Generator. The OCB bus is controlled through the Digital Gitane board’sJ14. The Jedi bus
controlled through the System Controller Gitane board’s J17.
The System CAN Bus diagnostics checks the system ability to communicate with all the configured
CAN nodes. Individual CAN node test scan be found throughout the Positioner diagnostics.
DS7 (CAN 1) CAN Bus
The Gitane Board is the CAN Controller
DS8 (CAN 3) Not used
DS9 (CAN 2) Generator Internal CAN Bus LED DS1 On = +12V Power to CAN Bus
DS7 flashes on and off during CAN data transmission (from A1 A28 PS3 in Positioner Cabinet)
Positioner Cabinet
System Cabinet A25
System Controller J12 CAN-RS422 CANopen CANopen
Digital Bridge Amplifier Amplifier
(Node ID: 0x070) (Node ID: 0x015) (Node ID: 0x016) Positioner I/O
Gitane Opto Opto Opto DS1 (Node ID: 0x045)
Gitane J14 Isolation Isolation Isolation
J32 Opto CAN V+
DS7 DS8 DS9 Isolation Source
J30 A25
A1A25 A30 CAN Bus
J82
CAN 1
CAN 3
CAN 2
J112 Breakout
J17 J18
Local Jedi
CAN/RT bus A1A25
J31 J14
J6
J111
PDU I/O
(Node ID: 0x047) Opto
Isolation RFP3
Opto
Isolation
Local Digital/OCB
A1A1 J2
OCB Table
Jedi CAN/RT bus
J3 J4
II
A25
120 Ohm Terminator J41 IDD
J2 J1
2305473
Collimator OTS 2304223 If no OTS then the 120 Coll/OCB
Opto +24VDC
Isolation OTS I/O A3A1 Ohm terminator plugs Source
(Node ID: 0x040)
Term into A25 J41
J11
OTS J1 J8 Opto
UIF Isolation
J10 J5 Collimator J2 J1
J12
Opto J3
Isolation
CANopen
Opto
Amplifier 120 Ohm Isolation

RFP3
(Node ID: 0x010) Term
Terminator A1A2
A25
J41 Plug Notation
Figure 2-82 CAN Bus w/OTS Assembly 2304223

GE MEDICAL SYSTEMS
DS7 (CAN 1) CAN Bus The Gitane Board is the CAN Controller
DS9 (CAN 2) Generator Internal CAN Bus LED DS1 On = +12V Power to CAN Bus
DS7 flashes on and off during CAN data transmission (from A1 A28 PS3 in Positioner Cabinet)
Positioner Cabinet
System Cabinet A25
System Controller J12 CAN-RS422 CANopen CANopen
Digital Bridge Amplifier Amplifier
(Node ID: 0x070) (Node ID: 0x015) (Node ID: 0x016) Positioner I/O
Gitane Opto Opto Opto DS1 (Node ID: 0x045)
Gitane J14 Isolation Isolation Isolation
J32 Opto CAN V+
J30 A25
A1A25 A30 CAN Bus
J82
CAN 1
CAN 3
CAN 2
J112 Breakout
J17 J18
Local Jedi
CAN/RT bus
J31 J14 A1A25
PDU I/O J6
J111
Isolation RFP3
Opto
Isolation
Local Digital/OCB
A1A1 J2
OCB Table
Jedi CAN/RT bus
J3 J4
II
A25
J41 IDD
120 Ohm Terminator J2 J1
2305473
Opto +24VDC
Isolation Ohm terminator plugs Source
Term
Bulkhead into A25 J41
J11 J8 I/O A3A1
Opto
Isolation Collimator J1
J8 J6 A25 J2
OTS J1 J41 Plug Notation J3
UIF J2 Opto
Isolation
J12 Term RFP3
A1A2
120 Ohm Terminator
Figure 2-83 CAN Bus w/OTS Assembly 2327101
DS7 (CAN 1) CAN Bus The Gitane Board is the CAN Controller
DS9 (CAN 2) Generator Internal CAN Bus
DS7 flashes on and off during CAN data transmission LED DS1 On = +12V Power to CAN Bus
(from A1 A28 PS3 in Positioner Cabinet)
Positioner Cabinet
System Cabinet A25
System Controller J12 CANopen CANopen
Digital Amplifier Amplifier
(Node ID: 0x015) (Node ID: 0x016) Positioner I/O
Gitane Opto Opto DS1 (Node ID: 0x045)
Gitane J14 Isolation Isolation
J32 Opto CAN V+
J30 A25
A1A25 A30 CAN Bus
J82
CAN 1
CAN 3
CAN 2
J112 Breakout
J17 J18
Local Jedi
CAN/RT bus
J31 J14 A1A25
PDU I/O J6
J111
Isolation RFP3
Opto
Isolation
Local Digital/OCB
A1A1 J2
OCB Table
Jedi CAN/RT bus
J3 J4
II
A25
J41 IDD 2403790
120 Ohm Terminator J2 J1
DSC2
J4
2391475
J1 J2_3
Opto +24VDC
Isolation Ohm terminator plugs Source
Term
Bulkhead into A25 J41
J11 J8 I/O A3A1
Opto
Isolation Jx
J8 J6 Collimator
OTS J1
A25
UIF J41 Plug Notation
J2 Opto RFP3
Isolation
J12 Term
Jx A1
120 Ohm Terminator
Figure 2-84 CAN Bus w/DSC Assembly 2391475

GE MEDICAL SYSTEMS
6.2 RT Bus
6.2.1 Real Time (RT) Bus (System & Local)

The system RT bus is used for safety and very fast transmission of signal from one part of the
system to another part of the system. The electrical signals on these lines are differential RS485
drive. The two end of this bidirectional bus are Venus console and the Positioner IO board. These
end boards have termination resistors across the differential bus lines and biasing resistors to bias
the bus to the logically inactive state when none of the devices are driving the bus. In the RS485
driver sense this is the high state. The devices on this bus only drive the bus to the active state. It
never drives to the inactive state. When a device stops driving, the output of the drivers goes to a
high Z state. It is possible for two devices to drive at the same time to the active state and the
function will be a logical OR function.
There is one system RT bus connecting the Systems Cabinet, Positioner Cabinet, and IUI. The
system RT bus signals are “low” active. See Figure 2-85.
There are two (2) local subsystem RT buses; one for the Optics Control Board (OCB) and one for
the Jedi Generator. The OCB bus is controlled through the Digital Gitane board’s J14. The Jedi bus
is controlled through the System Controller Gitane board’s J17. Jedi bus signals are “high” active.
Local Digital/OCB CAN/RT bus
Local Jedi CAN/RT bus System Cabinet "Generation of Brt Sig for Digital Record"
"Generation of Xray ON"
J6
JEDI
A25
J82
IUI
System Controller Digital IUI
J18
Wallbox J2
Termination/
Gitane J17 J14 Gitane Biasing
J11 J11
50SC2 to
J20 26HDB
J1 converter
J3 J2
50SC2 OCB Table
to 26HDB
converter J2
J3
RFP3 II
A25 J1 A1A1 J2
PDU I/O IDD
J2 J2 J1 2305473
J1 Coll/OCB
+24VDC
A25 J13 Source
Positioner Cabinet
A1A25 System RT bus signals are active low.

Positioner I/O Jedi RT bus signals are active high.
J110
J1
Termination/
Biasing A25
J41 Plug Notation
Figure 2-85 Real Time (RT) Bus Block Diagram for Original IUI 2289299-2

GE MEDICAL SYSTEMS
Figure 2-86 Real Time (RT) Bus Block Diagram for IUI Replacement PC
6.2.2 System RT Bus Signals

The signals which are on this Bus are:
EXPOSE ENABLE
This is driven by the Pos IO board or the Venus console when the expose buttons are pressed. The
s/w has to give permission to the hardware board before this line can be driven. But s/w cannot by
itself drive this line. This signal is received by the Venus console for starting the exposure. This
signal is also used by the Mars Gitane board in the system cabinet to process the Jedi RT bus
signals.
EXPOSE COMMAND
This signal is generated by the Saturn Gitane Board when ever an exposure needs to be made and
these pulses are created in sync with the signal to the camera frame signals. This is received by
the Mars Gitane bd and processed before being sent to Jedi as an RT signal.
X-RAY ON
This signal is created by Jedi generator. It goes to the Mars Gitane Bd through the Jedi RT bus.
This signal is passed to the system RT bus. It is used by the Venus console and the Saturn to
determine when exactly the X-Rays are being turned on.

GE MEDICAL SYSTEMS
BRIGHTNESS SIGNAL
This is high frequency signal which is generated by the OCB and send to Saturn’s Gitane Bd. This
in turn sends it to Mars’ Gitane Bd. This is then send to the Jedi Generator. The Jedi integrates on
the pulse count and determines when to terminate the exposure.
MOTION ENABLE
This line is driven active when the table motions are enabled. The signal is driven by the Pos IO
board. At this point no other devices uses it. All the motion enables are handled by the Pos IO board.
In the future designs when remote consoles are present this line will be used.
PREP
This is driven by the Pos IO board and the Venus console when the prep button is pressed. This is
used by the Venus console to start the sequence and the Mars Gitane Bd to gate the signals to the
Jedi.
SYSTEM RESET
This is driven by the reset button on the Venus console. This signal goes to Mars Gitane Bd, Saturn
Gitane Bd, Positioner IO board and the PDU IO board. All these are reset when the reset button is
pressed.
The system reset RT line is analog “differential” RT line. Two positions (+/-12V or NC). The active
(i.e. reset enabled position) is +/-12V.
RT SIGNAL CHARACTERISTICS (RS485 SIGNALS)

“+5V Drivers are used and there’s 120 Ohm termination between the “-P” and “-N” leads. Biasing
in the form of 470 Ohm resistors from the “-P” to +5V and the “-N” to 5V_RTN is provided at each
end of the bus. Termination and biasing is selectable via a bus switching device (i.e. 3383).
“Transient Protection is provided for each “-P” and “-N” line. The device clamps the lines to +5V and
5V_RTN.

GE MEDICAL SYSTEMS
6.3 Ethernet
The Router is connected to the external hospital network and The Precision has three systems (System Controller (Mars), Digital
is configured for an external hospital provided IP Address. The System (Saturn) and the IUI Console (Venus)) connected, via a
router also has an internal IP address (165.100.10.100) Router, on an internal Ethernet network.
System Cabinet IUI, System Cabinet,

System Controller
Digital cables are straight
165.100.10.2 connections (no Rx/Tx
CPU crossover). IUI
Digital 165.100.10.3
165.100.10.1
Ethernet cable
A3
CPU IUI
LAN - Switch is one piece
Router Wallbox J3 from IUI to
Router/ Router
Firewall
Straight connection
165.100.10.100 (no Rx/Tx crossover). Fiber Optic There are 3 Rx/Tx crossovers in the fiber
Cable optic cable chain.
A2 Media - one between the A2 Media Convert &
WAN - Hospital Converter Bulkhead
Internet Supplied
RJ45 Fiber - one at the Bulkhead connection
IP
Optic - one between the Bulkhead and the
A25 J61
external Media Converter
The Media Converter The net result is one Rx/Tx crossover.
converts the RJ45, CAT 5 Media
cable media to fiber optic (for Converter
electrical isolation). Fiber Precision Internal Ethernet IP Addresses
RJ45 Digital System (Saturn): 165.100.10.1
Optic
Hospital System Controller (Mars): 165.100.10.2
Network Connection IUI Console (Venus): 165.100.10.3
Typically is straight Hospital Router (Internal Address): 165.100.10.100
connection (no Rx/Tx Power
crossover). A25
J41 Plug Notation
Figure 2-87 Ethernet Block Diagram with Media Converter
The Router is connected to the external hospital network and The Precision has three systems (System Controller (Mars), Digital
is configured for an external hospital provided IP Address. The System (Saturn) and the IUI Console (Venus)) connected, via a
router also has an internal IP address (165.100.10.100) Router, on an internal Ethernet network.
System Cabinet IUI, System Cabinet,

System Controller
Digital cables are straight
165.100.10.2 connections (no Rx/Tx
CPU crossover). IUI
Digital 165.100.10.3
165.100.10.1
Ethernet cable
A3
CPU IUI
LAN - Switch is one piece
Router Wallbox J3 from IUI to
Router/ Router
Firewall
165.100.10.100
Precision Internal Ethernet IP Addresses A25
A25 J62 Digital System (Saturn): 165.100.10.1 J41
WAN - Hospital
Hospital System Controller (Mars): 165.100.10.2
Internet Supplied Plug
IP Network Connection IUI Console (Venus): 165.100.10.3
Router (Internal Address): 165.100.10.100 Notation
Figure 2-88 Ethernet Block Diagram without Media Converter
The system has a broadband router with a firewall. This router is used to connect the Precision
system to external sites such as DICOM stations or the OnLine Center (OLC).
The Precision system Local Area Network (LAN) comprising the System Controller, IUI, and Digital
is also connected and switched through the router.

GE MEDICAL SYSTEMS
The Precision LAN IP addresses are as follows:
• Digital – 165.100.10.1
• System Controller – 165.100.10.2
• IUI – 165.100.10.3
• Router Internal – 165.100.10.100
An Internet IP address is also assigned to the router for use with the external sites. This address is
usually assigned by the hospital.
Section 7.0
System Interconnects
Please see the MIS map (2308534-100) for specific cable information.
7.1 System Communications
Figure 2-89 Communication Routes

GE MEDICAL SYSTEMS
7.2 Power Distribution
7.2.1 High Voltage Distribution
Figure 2-90 High Voltage Distribution
7.2.2 UPS
Figure 2-91 UPS
Page 154 Section 7.0 - System Interconnects

GE MEDICAL SYSTEMS
7.2.3 120/230V Distribution
Figure 2-92 120/230V Distribution
7.2.4 Three Phase Power
Figure 2-93 Three Phase Power

GE MEDICAL SYSTEMS
Section 8.0
Overhead Tube Suspension (OTS)
8.1 Introduction
The overhead tube suspension is the positioning device
that supports the x-ray tube and the remote console. It
includes the:
•Overhead rail system
•Carriage assembly
•Telescopic column - vertical travel of 1500 mm (59 in)
•Tube support - Precision 500D OTS includes a MX100 x-
ray tube
•Collimator
OTS
Console
8.2 Console
The OTS console allows the operator to select receptor,
kV and mAs. Positioning of the tube can be performed
with one or two hands on the OTS Console. Notice the
three indicators below the tube rotation angle display:
Manual Collimation
•Exposure Hold
•Ready
Exposure Hold indicates an exposure is not allowed.
This could be due to:
•Lateral or longitudinal detent error
•Incorrect vertical SID
•Tube angle
•No film cassette
•Room door interlock
The Collimator Display includes:
• SID
• Collimator size
• Spectral filter (0, 0.1, 0.2, or 0.3 mm Copper)
Page 156 Section 8.0 - Overhead Tube Suspension (OTS)

GE MEDICAL SYSTEMS
8.3 Carriage
Figure 2-94 OTS Carriage
8.4 Collimator
8.4.1 Block Diagram

AC Voltage
D2
User Interface Collimator
RS232 Voltage DC
D1 SM1
Voltage DC
System Basis Module
SM4
CAN Bus
Step motors: SM1 ... SM10 Voltage DC
Electronic boards: D1, D2, D3, D4

D4 SM5 D3
Light Barriers
DSA Module
e DSA Filter
SM10
Figure 2-95 Collimator Block Diagram

GE MEDICAL SYSTEMS
8.4.2 Collimator Bulb
The collimator is produced by Siemens Corporation and can be replaced as a complete assembly.
The collimator light is a halogen lamp bulb that is user replaceable. Bulb must be replaced with the
manufacturer's part number as specified in the parts manual
Figure 2-96 Collimator Bulb
8.4.3 Collimator Laser

The Laser Alignment Light is adjusted in the factory and should not need adjustment. If the laser is
received out of alignment, please notify your GE sales or Service representative.
Hardware damage may occur if you attempt to adjust the laser.

Laser Fragile
1.) Adjusting the laser while power is on could result in electrical damage to the power supply
requiring the whole collimator to be replaced.
2.) Use of conductive tools within the collimator may cause the ungrounded laser base to short
the laser power supply.
3.) Tightening of the adjustment screws too much may pierce the laser case and make the laser
not function.
Figure 2-97 Collimator Laser
8.4.4 Collimator Fuses

Fuses used in the collimator help prevent electrical damage. To inspect them:
1.) Open the collimator side panel.
2.) Locate the fuses on the circuit boards.
3.) Measure to detect an open fuse

GE MEDICAL SYSTEMS
Figure 2-98 Collimator Fuses
8.5 OTS Counterpoise Theory of Operation

The x-ray tube vertical motion is counterpoised over a 59 inch (150 cm) range.
The counterpoise assembly uses two torsion springs attached to a tapered cam. A steel
counterpoise cable is attached to the large diameter of the cam and wound in the cam grooves then
over an idler pulley and down through the telescoping columns where the cable fitting is anchored
in the pivot shaft (gooseneck) of the tube support.
The torsion springs are fastened, on the inside coil, to a shaft fitted with a worm wheel that meshes
with a worm. The springs are pre-wound by turning the worm. See Figure 2-99 and Figure 2-100.
NOTE:
COUNTERPOISE
THE OUTER END OF 2 SPRINGS SPRING
AND OUTER END OF COUNTERPOISE COUNTERPOISE
CABLE ARE FASTENED TO A COMMON CABLE WOUND
MACHINERY GROUND ON CAM
COUNTERPOISE
MAIN REEL SPRING
WORM
COUNTERPOISE
CABLE
TURN TO ADJUST
WORM COUNTERPOISE
WHEEL SPRING TENSION
MX 100
TUBE
BALL FITTING SEATED IN

TUBE SUPPORT FITTING
Figure 2-99 SCHEMATIC OF COUNTERPOISE SYSTEM

GE MEDICAL SYSTEMS
MAIN REEL COUNTERPOISE COUNTERPOISE
CABLE SPRING HOUSING
FIELD
LIGHT
LAMP
TRANS.
TAPERED
COUNTERPOISE CAM WORM
WHEEL
Figure 2-100 COUNTERPOISE ASSEMBLY
The following graph (Figure 2-101) shows the forces involved.
Figure 2-101 COUNTERPOISE FORCE GRAPH
From the curves it can be seen that the torque provided by the two springs is exactly opposite the
torque of the “load” times the radius of the tapered counterpoise cam, so that the net effect is zero
torque and a counterpoised condition. As the load is changed, the cable must be relocated on the
cam to use a different radius so that the new load times the new radius is equal (but opposite) to
the torque output of the two springs.

GE MEDICAL SYSTEMS
There are two fittings swagged onto the main cable: one at the cable end, and another located
22.64 (57.51 cm) from the end. Since the system uses a MX 100 tube, the end cable fitting is
anchored in the tube support. The second swagged cable fitting is used when a MX 75 tube is
mounted on the XT hanger.
Since the MX 100 is heavier than the MX 75, there will be more cable on the tapered cam and it will
be using the cam on the smaller radii. The cable location on the cam is determined by the load to
be applied to the counterpoise system. The various components loads as part of the system load,
are as in Table 2-6.
COMPONENT Counterpoise Cable Loads for

SIEMENS COLLIMATOR
TELESCOPING COLUMN 47 LB. (21.3 KG)1
TUBE SUPPORT 27 LB. (12.2 KG)
COLLIMATOR 22 LB. (10.0 KG)
ELECTRICAL CABLES 5 LB. (2.3 KG)
SUBTOTAL COUNTERPOISE LOAD 109 LB. (49.4 KG)
MX 100 TUBE UNIT 65 LB. (29.5 KG)
GRAND TOTAL COUNTERPOISE LOAD 174 LB. (78.9 KG)
1
This is not the weight of the telescoping column assembly, but the sum of the loads
that each of the individual column loads contribute to the counterpoise cable.
Table 2-6 COUNTERPOISE CABLE LOADS
On the face of the cam, there is a series of numbers stamped from 1 through 7. These numbers
indicate the number of the cam groove. See Figure 2-102.
The cam, which starts at the zero turn and extends to the eighth turn, has eight full turns during
which the radius of the groove is changing continuously. See Figure 2-102. After the eighth turn,
the radius remains constant and the cable groove widens out on the outside diameter to form a wide
groove in which excess cable may be stored.
ZERO POINT OR
“START” OF THE
CAM
Figure 2-102 46-177061P1 FACE OF COUNTERPOISE CAM

GE MEDICAL SYSTEMS
The start of the cam is back on turn form No. 1, but it was not stamped “0” since this face would not
be visible when the cam is in the counterpoise assembly.
CABLE IS TANGENT
TO THE 3.8 TURN ONE TURN
ON CAM WHEN TUBE ON STORAGE
MAIN
IS “UP” DIAMETER
REEL
POSITION OF MAIN CABLE ON

CAM WITH MX 100 TUBE
Figure 2-103 COUNTERPOISE

GE MEDICAL SYSTEMS
Chapter 3
MX100 Tube Specifications “Jedi 80RF2T”
Section 1.0
Introduction
The following specifications are applicable only to MX100 tubes used with a Jedi 80RF2T generator
(Precision 500D R&F System).
Tube P/N Catalog Number Insert Description Focal Spot

MX100 Fluoro 46-155500G228 D2281F 4"/12.5 degree/Metal 0.6 - 1.0
MX100 Rad 46-155400G281 D2301R 4"/12.5 degree/Metal 0.6 - 1.25
Table 3-1 Tube Identifiers
Section 2.0
Parameters
Description Fluoro Tube Rad Tube
Anode heat capacity 260 kJ (350 kHU) 260 kJ (350 kHU)
Anode continuous dissipation 925 W (75 kHU/mn) 925 W (75 kHU/mn)
Casing heat capacity 1,100 kJ (1,500 kHU) 1,100 kJ (1,500 kHU)
Casing continuous dissipation 925 W (75 kHU/mn) 740 W (60 kHU/mn)
Nominal high voltage 150 kV 150 kV
Maximum Power for fluoro exposures 825 W NA
Table 3-2 Tube Specifications
Section 3.0
kW Rating - Track protection
These charts are computed for 75% HU remaining (target temperature equivalent to 25% of
storage) and 100% of HU. They are applicable to single exposures and series of exposure. For
series of exposures, the time is the sum of pulse duration.
Chapter 3 - MX100 Tube Specifications “Jedi 80RF2T” Page 163

GE MEDICAL SYSTEMS
3.1 Small Focus (0.6), High Speed (10000rpm)
Small Focus (0,6), High Spee d (10000rpm)

100% HU
45,00
40,00
35,00
30,00
kW Rating
25,00
20,00
15,00
10,00
5,00
0,00
0,01 0,1 1 10
Maximum Exposure Time in seconds
Small Focus ( 0,6), High Speed ( 10000rpm )

75%HU
40,00
35,00
30,00
25,00
kW Ratin g
20,00
15,00
10,00
5,00
0,00
0,01 0,1 1 10
Maximum Expo sur e Time in secon ds
Figure 3-1 Small Focus (0.6), High Speed (10000rpm)
Page 164 Section 3.0 - kW Rating - Track protection

GE MEDICAL SYSTEMS
3.2 Large Focus (1.0), High Speed (10000rpm)
Large Focus ( 1.0), High Speed (10000rpm )

100% HU
100,00
90,00
80,00
70,00
60,00
kW Rating
50,00
40,00
30,00
20,00
10,00
0,00
0,01 0,1 1 10
Maximum Expos ur e Time in seconds
Large Focus ( 1.0), High Speed (10000rpm )

75% HU
90,00
80,00
70,00
60,00
kW Rating
50,00
40,00
30,00
20,00
10,00
0,00
0,01 0,1 1 10
Maxi mum Expo su re Time in se co nds
Figure 3-2 Large Focus (1.0), High Speed (10000rpm)

GE MEDICAL SYSTEMS
3.3 Large Focus (1.25), High Speed (10000rpm)
Large Focu s (1.25), High Speed (10000rpm)

100% HU
140,00
120,00
100,00
kW Rating
80,00
60,00
40,00
20,00
0,00
0,01 0,1 1 10
Maximum Expos ur e Time in seconds
Large Focu s (1.25), High Speed (10000rpm)

75% HU
120,00
100,00
80,00
kW Rating
60,00
40,00
20,00
0,00
0,01 0,1 1 10
Maxi mum Exposure Time in seconds
Figure 3-3 Large Focus (1.25), High Speed (10000rpm)
Page 166 Section 3.0 - kW Rating - Track protection

GE MEDICAL SYSTEMS
Section 4.0
Casing Protection
See service manual 46-014427, Tube rating for Maxiray 100, for Casing Heat Capacity.
Section 5.0
Anode Protection
5.1 Heat Capacity
See service manual 46-014427, Tube Rating for Maxiray 100, for Anode Heat Capacity.
5.2 Anode cooling Curve
Anode cooling curve

300,0
250,0
200,0
Cb (kJ)
150,0
100,0
50,0
0,0
0 2 4 6 8 10 12 14 16
Time (min)
Figure 3-4 Anode cooling Curve

GE MEDICAL SYSTEMS
Section 6.0
Filament protection
6.1 mA limitation at low kV
mA is limited at low kV in order to protect the filament.
KV MA MAX
FIL 0.6 FIL 1.0 FIL 1.25
40 100 397 500
45 150 466 583
50 200 533 666
55 250 599 750
60 300 666 833
65 350 733 917
70 400 799 1000
75 400 800 1000
higher kV 400 800 1000
Table 3-3 mA Limits at Low kV
mA max ver su s kV (for t=10ms)

80
Fil 0.6
75 Fil 1.0
Fil 1.25
70
65
kV
60
55
50
45
40
0
100
200
300
400
500
600
700
800
900
1000
mA
Figure 3-5 mA max versus kV (for t=10 ms)
Page 168 Section 6.0 - Filament protection

GE MEDICAL SYSTEMS
6.2 Max mA
For each Filament, there is a mA limitation, regardless the kV.
Fil 0.6 400 mA
Fil 1.0 800 mA
Fil 1.25 1000 mA
Table 3-4 Filament “mA” limitations
6.3 Filament Drive Level
State Tube Fluoro Tube Rad Duration max.

SF 0.6 LF 1.0 SF 0.6 LF 1.25
Preheat 1.9 A 1.9 A 2.5 A 2.5 A NA
Stand-By 3.2 A 3.2 A 3.2 A 3.2 A 5mn
(see comment)
Exposure (max) 5.7 A 7.1 A 5.7 A 7.1 A NA
Boost (max) 9A 9A 9A 9A 400ms
Table 3-5 Filament Drive Level
Comment: The spec of 3.2A, used for Jedi is a conservative rating. Hence it does not impact negatively tube
life.

GE MEDICAL SYSTEMS
Page 170 Section 6.0 - Filament protection

ay
Xr
GE MEDICAL SYSTEMS
172
GE Medical Systems
gemedicalsystems.com
Technical
Publication
Revision 10
Book 2
Pages 173 - 400
of 3
GE Medical Systems
Chapter 4 - Error Message Listings

(Software/Firmware Revision 11.x.x)
Copyright © 2002, 2003, 2004 and 2005

by General Electric Company, Inc.
GE MEDICAL SYSTEMS

Rick Fauska
Page 174
GE MEDICAL SYSTEMS
Chapter 4
Error Message Listings (Software/Firmware Revision 11.x.x)
Section 1.0
Before You Begin
The error message listings in this chapter are for systems with Software/Firmware Revision
11.x.x installed only. To determine the version of software installed on your system, open the
service users interface (SUIF) and read the Revision number listed for the IUI. If it’s Revision 11 or
lower, use this book.
Figure 4-1 SUIF Home Page Showing Software/Firmware Revision 11.x.x
Section 2.0
Introduction to Error codes
2.1 What are Error Codes
Applications and System error codes are messages that alert you-and the customer that system
applications or the operating system cannot perform one of their programmed tasks. Applications
and System error codes can appear on the console display at any time, whether you are running
Applications, Diagnostics, or Service Mode software.
Chapter 1 - Precision 500 Error Messages Page 175

GE MEDICAL SYSTEMS
The Error management mechanisms in the system handle of all error transmissions on the system.
All errors are stored in a single system error log, which can be viewed via the Service Error Log
Viewer.
2.1.1 Applications Software

As its name implies, Applications software controls customer X-ray applications- such as Digital
RAD, Table Top, and Fluoro.
When the customer selects the fluoro function, Applications software uses the Console (to accept
operator input), the generator module (to control the exposure and to generate X rays), the Imaging
module (to control the camera system), and the Positioner module (to position the patient).
Software controls all aspects of system operation. In this system, these software “actors” are
assigned names. You’ll see those names used in the chapters that follow. Therefore, you might
want to become familiar with them.
In Figure 4-2, you can see were these software actors live inside certain hardware subsystems,
and they’re able to communicate with each other directly or indirectly.
Saturn HW Mars HW
Software Actors
Software Actors
Athena Calypso
Saber
Atlas Atlas
Venus HW
Software Actors
IUI
Calypso
IIP
Saber
Atlas
Figure 4-2 Primary SW Applications “Actors”
2.1.2 Operating System Software

Operating System software handles:
• high-level system related functions
• initializing system hardware
• managing system resources
• downloading software to modules
• system timing functions
• handling and processing operator input from the console
• processing and displaying system output to the console, etc.
2.2 Applications and System Error Reporting
2.2.1 Error Display Management

Detailed error information is displayed in an easily visible area of the console and the live in-room
monitor.
Page 176 Section 2.0 - Introduction to Error codes

GE MEDICAL SYSTEMS
Figure 4-3 error display – In–Room Monitor
2.2.2 “Quick” Error Viewer

The console also provides the ability for the operator to access the last errors generated on the
system (maximum of 10). This allows further investigation and viewing of errors occurring in rapid
succession, so that the proper course of action can be taken.
Figure 4-4 Quick Error Viewer
2.3 Service Error Log Viewer

The console provides the ability for the service person to access the complete set (2000 maximum
entries) of system errors generated over time. The error log gives you a complete time line of all
errors that have occurred. Used together with the error message listing in Section 3.0 (System Error
Message Listing on page 178) of this chapter, the service person has needed information for more
efficient and effective troubleshooting.

GE MEDICAL SYSTEMS
Section 3.0
System Error Message Listing
In this section you'll find the system’s error code's listed in hexadecimal order by SW Module
(Process) Actor.
Sometimes the customer may easily correct an Applications software error condition, such as when
the error is caused by an unsatisfied interlock. At other times, however, the Applications software
error message only advises the customer to call service.
Whichever action you pursue, always bear in mind which module generated the error, which type
of software generated the error, and what the system was trying to do when the error occurred.
Each Error Code listed below, shows its message(s): the module that generated the error, the error
Description and the Recommended Action(s) to correct the error.
Major Function Impacted
This is the name of the actor that reported the error
Minor Function Impacted
This indicates the actor-specific function that was in progress when the error was reported. Each
actor will define a set of legal values for this field. Each error reported by the actor will be associated
with a unique minor function.
Error Recovery Classes
System error management supports various recovery classes of errors:
• Debug-only – these errors are logged in the system error log, but are not displayed
• Advisory – logging of this class of error is optional
• Warning – non-fatal failure
• Abort – causes termination of current x-ray acquisition
• Inhibit – causes termination of current x-ray and subsequently inhibits further acquisition
attempts until the error situation is cleared
• Halt – when failure is so severe that the system is no longer functional. The only operator
action allowed is a Reset or Shutdown.
• Action(s) - This field gives the recommended action.
System Error Message Listings begin on next page.
Page 178 Section 3.0 - System Error Message Listing

GE MEDICAL SYSTEMS
3.1 02 XRAcqSync
200001 Error Text: The Events are ignored.
Recovery Class: DEBUG_ONLY
Major Function Impacted: SysCntrl
Minor Function Impacted: control
View Level: opr
Root Cause: 1
Recommended Action(s): Software Problem
Description: Event is ignored because it is not applicable in the current state.
200002 Error Text: Do not know the Switch Status.

View Level: opr
Root Cause: 1
Description: The current foot/hand switch status is not know.
200003 Error Text: Failed to read AcqSync config file

Recovery Class: WARNING
View Level: opr
Root Cause: 1
Description: Fail to read the actor configuration file.
Customer Text: The system did not boot properly. Reset the system. Call service if the problem persists.
200004 Error Text: Creating config parameter of type stringList failed

View Level: opr
Root Cause: 1
Description: Fail to dynamically create a data element.
200005 Error Text: XRAcqsync failed startup

View Level: opr
Root Cause: 1
Description: Actor failed to properly initialize its data or communications.
200006 Error Text: Unexpected event Occurred.

View Level: opr
Root Cause: 1
Description: Unable to understand or process an event.
200007 Error Text: This OpModeID is not found in the List.

View Level: opr
Root Cause: 1
Description: Selected OpMode ID not found in the current list of OpMode ID's.

GE MEDICAL SYSTEMS
200008 Error Text: The configuration for this Opmode is already done.
View Level: opr
Root Cause: 1
Description: Redundant OpMode configuration request.
200009 Error Text: The configuration Configure request for this OpMode is already Received.
View Level: opr
Root Cause: 1
200010 Error Text: This is an invalid synchroniser type.
View Level: opr
Root Cause: 1
Description:
200011 Error Text: Invalid OpModeID received.

View Level: opr
Root Cause: 1
Description: Actor is not configured for the requested OpMode ID.
200012 Error Text: Time out while in WAIT_FOR_STOP_SEQ waiting for
STOP_EXPOSURE_TRIGGER_DONE.
Recovery Class: ABORT
View Level: opr
Root Cause: 1
Description: Timed out while waiting for the reply from ImDet (STOP_EXPOSURE_TRIGGER_DONE)
indicating that exposure(s) have stopped.
Customer Text: Exposure stopped. Release exposure switch and try again. Call service if problem persists.
200013 Error Text: Time out while waiting for an event or an actor to respond.
View Level: opr
Root Cause: 1
Description: Time out while waiting for an event from another actor.
Customer Text: Exposure control problem. Release switch and try again. Call service if problem persists
200014 Error Text: Time out while in STOP_SEQ waiting for PREP_OFF.
View Level: opr
Root Cause: 1
Description: Time out waiting for another actor to finish processing the Prop Off switch transition.

GE MEDICAL SYSTEMS
200015 Error Text: Failed to bind with other Actors.
View Level: opr
Root Cause: 1
Description: Unable to bind with a required actor
Customer Text: An internal communication failure has occurred. Reset the system if the problem persists.
200016 Error Text: Received startBootPhase before connecting with all Actors.
View Level: opr
Root Cause: 1
Description: Events out of order during the boot process.
200017 Error Text: Do not know the Boot Level.

View Level: opr
Root Cause: 1
Description: Current boot status is not know.
200018 Error Text: Do not know the sysmode for this ID.
View Level: opr
Root Cause: 1
Description: No Longer used.
200019 Error Text: Remote call failed while calling the method on the other actor.
View Level: opr
Root Cause: 1
Description: Unable to perform a method call on another actor.
200020 Error Text: Not Bound to the actor. The pointer is Null.
View Level: opr
Root Cause: 1
Description: Unable to communicate with another actor.
200021 Error Text: Send start or stop exposure trigger of the XRImDet failed.
View Level: opr
Root Cause: 1
Description: Unable to start or stop the exposure triggers because an event publication failed.
Customer Text: X-ray exposure has been prematurely stopped. Try again.

GE MEDICAL SYSTEMS
200022 Error Text: atlasPrepDone of the XRTitan failed.
View Level: opr
Root Cause: 1
200023 Error Text: FastAcquisition request of the XRTitan failed.

View Level: opr
Root Cause: 1
200024 Error Text: AtlasAcquisitionInhibit of the XRTitan failed.
View Level: opr
Root Cause: 1
200025 Error Text: Lost EF or Normal connection status.

View Level: opr
Root Cause: 1
Description: Connect to other actor(s) has been lost.
200026 Error Text: Failed to Send actorReady

View Level: opr
Root Cause: 1
Description: Could not send the event.
200027 Error Text: Failed to send shutdowndone.
View Level: opr
Root Cause: 1
200028 Error Text: Failed to send shutdowndone

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
200029 Error Text: AcqSync not connected to all the actors
View Level: opr
Root Cause: 1
Description: Not connected to all of the required actors.
200030 Error Text: createEvent failed for these events.

View Level: opr
Root Cause: 1
Description: Unable to create an event.
200031 Error Text: publish event failed for these events

View Level: opr
Root Cause: 1
Description: Unable to publish an event.
200032 Error Text: subscribe event failed.

View Level: opr
Root Cause: 1
Description: Unable to subscribe to a required event.
200033 Error Text: Unable to set recovery filename.

View Level: opr
Root Cause: 1
Description: Unable to create/set the recevery file.
200034 Error Text: Unable to set error message filename.

View Level: opr
Root Cause: 1
Description: Unable to set the error message file link.
200035 Error Text: Invalid recovery class type received.
View Level: opr
Root Cause: 1
Description: Recovery class for the current error is not valid.

GE MEDICAL SYSTEMS
200036 Error Text: This error is not of the Inhibit type or reported before.
View Level: opr
Root Cause: 1
Description: Recovery class for the current error is of type Inhibit, and has already been reported, or not
a valid inhibit error.
200037 Error Text: Prep is not Authorized, acquisition is inhibited.

Recovery Class: ADVISORY
View Level: opr
Root Cause: 1
Description: Prep request ignored because of an inhibit condition on that OpMode.
Customer Text: X-ray exposures are inhibited. Select the Expose Hold button for more information.
200038 Error Text: Prep on requested while soak time has not elapsed
View Level: opr
Root Cause: 1
Recommended Action(s): Wait for soak time to complete. Then prep/expose switches will become active.
Description: Prep request ignored because soak time is not completed.
Customer Text: Prep/Expose switches are disabled until tube warm-up soak time is complete.
200039 Error Text: Prep on requested while Athena is not ready, waiting for START_EXAM.
View Level: opr
Root Cause: 1
Description: Prep request ignored because of specified inhibit condition.
200040 Error Text: Prep on requested while Room Door is open.

View Level: opr
Root Cause: 1
200041 Error Text: Prep on requested while Fluoro time exceeded 10 mins.
View Level: opr
Root Cause: 1
200042 Error Text: Prep on requested while no more tube run time is available.
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
200043 Error Text: Prep on requested while remaining disk space is less than 5 seconds.
View Level: opr
Root Cause: 1
200044 Error Text: Time out while in WAIT_FOR_EXPOSE waiting for EXP_ON switch event.
View Level: opr
Root Cause: 1
Description: Time out while waiting for the Expose On switch.
Customer Text: An internal communication error occurred. Release the expose switch and try again.
200045 Error Text: Time out while in ABORT_SEQ waiting for the seq control returned from COA.
View Level: opr
Root Cause: 1
Description: Calibration system control error between AcqSync and calibration owner actor.
200046 Error Text: Script processor initialization failed

View Level: opr
Root Cause: 1
Description: Failed to initialize the script processor class for the actor.
Customer Text: This protocol is not available. Reselect the protocol or select another to continue.
200047 Error Text: X-ray unavailable, check grid position to continue.
View Level: opr
Root Cause: 1
200048 Error Text: Script Processor failed to read a config script.

View Level: opr
Root Cause: 1
Description: Failed to read the config script for a selected application.

GE MEDICAL SYSTEMS
3.2 04 XRAppDir
400001 Error Text: The setRecoveryFilename failed
Minor Function Impacted: Applicationsynchro
View Level: opr
Root Cause: 1
Recommended Action(s): 1. Reset the system.
2. If the problem persists, reload application software.
Description: The configuration file may be unavailable or corrupted. Check to see if the configuration files
are present if possible. If yes, refer to Precision Diagnostic Manual to run AMI Diagnostics on
system controller.
400002 Error Text: The setErrmsgFilename failed
View Level: opr
Root Cause: 1
system controller.
400003 Error Text: XRAppDir failed to startup

View Level: opr
Root Cause: 1
Description: Unable to allocate software resources on the computer
Customer Text: The system did not boot properly. Reset and call service if the problem persists.
400004 Error Text: Unexpected Event received
View Level: opr
Root Cause: 1
Recommended Action(s): Software error only - for engineering use only. No recommended action to be taken. System
will recover from this error.
Description: Software error only - for engineering use only. No recommended action to be taken. System
400005 Error Text: Null config string received, terminate the AppSetup
View Level: opr
Root Cause: 1
Recommended Action(s): This protocol is not available:
1. Reselect the protocol or select another to continue.
2. If problem persists, reset the system.
3. If required, reload application software.
Description: The protocol data content is null, unable to configure the system for selected procedure.

GE MEDICAL SYSTEMS
400006 Error Text: The active opmode is not found in the List of Opmodes
View Level: opr
Root Cause: 1
Recommended Action(s): 1. Reselect the protocol 2. If the problem persists reset the system.
Description: A prep or expose is requested for application that is not in the list of the selected applications
400007 Error Text: Invalid OpModeId received for OPMODE_CONFIGURE_DONE

Minor Function Impacted: Applicationseq
View Level: opr
Root Cause: 1
Recommended Action(s): 1. Reselect the protocol. 2. If the problem persists reset the system.
Description: The application being configured is not in the list of the selected applications, failed to setup
the system
400008 Error Text: Failed to read XRAppDir config file

View Level: opr
Root Cause: 1
Recommended Action(s): 1. Reset the system. 2. If the problem persists, reload application software.
system controller.
400009 Error Text: Failed to bind

View Level: opr
Root Cause: 1
Description: Error in software communication infrastructure
400010 Error Text: Failed to get the leaving actor info

View Level: opr
Root Cause: 1
400011 Error Text: Time out

View Level: opr
Root Cause: 1
Recommended Action(s): 1. Reselect the protocol.
2. If the problem persists reset the system.
Description: system failed to complete the configuration for the selected applications within the configured
protocol setup time-out period

GE MEDICAL SYSTEMS
400012 Error Text: Failed to read XRAppDir time-out values
View Level: opr
Root Cause: 1
system controller.
400013 Error Text: CreateEvent failed

View Level: opr
Root Cause: 1
400014 Error Text: PublishEvent failed

View Level: opr
Root Cause: 1
400015 Error Text: SubscribeEvent failed

View Level: opr
Root Cause: 1
400016 Error Text: The appdir configuration files not found

View Level: opr
Root Cause: 1
Description: The configuration file may be unavailable or corrupted
400017 Error Text: Failed to create PeerActorsInfo class

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
3.3 06 XRBeamForm
600000 Error Text: Could not bind to actor
Major Function Impacted: Pos
Minor Function Impacted: boot
View Level: opr
Root Cause: 0
2. If the problem persists. Reload the application software.
Description: Software Error: In boot phase, the software module (BeamForm actor) needs to connect to
other modules (actors). However, this connection did not succeed. As a result, the software
will not work properly.
Customer Text: System software error. Reset the system and call service to reload software if problem
persists.
600001 Error Text: BeamForm was not bound to actor
View Level: opr
Root Cause: 0
Description: Software Error: The software module (BeamForm actor) tried to call other modules' (actors')
function. However, the connection with the target module (actor) failed (pointer is null), i.e.
the communication is broken.
persists.
600002 Error Text: Failed to open XRBeamForm Configuration file

View Level: opr
Root Cause: 0
Description: This software module's (XRBeamForm actor's) configuration file cannot be found.
persists.
600003 Error Text: Failed to open Calibration file BeamForm.cal

View Level: opr
Root Cause: 0
Description: This software module's (XRBeamForm actor's) Calibration file cannot be found.
persists.
600004 Error Text: Over table Collimator is not configured for the application mode
View Level: opr
Root Cause: 0
Recommended Action(s): Make sure that Over Table collimator is configured for this system or application.
Description: The Over Table Collimator is not configured for this system/application.
Customer Text: Film cassette exposures are not possible. Reset and call service if the problem persists.

GE MEDICAL SYSTEMS
600005 Error Text: Under table Collimator is not configured for the application mode
View Level: opr
Root Cause: 0
Recommended Action(s): Make sure that Under Table collimator is configured for this system or application.
Description: The Under Table Collimator is not configured for this system/application.
Customer Text: Collimator error. Reset the system and call service if problem persists.
600006 Error Text: Unknown Application mode received

View Level: opr
Root Cause: 0
Description: The software module (BeamForm actor) received Application Mode value that does not exist.
Customer Text: An internal communication failure has occurred. Retry or reset. Call service if the problem
persists.
600007 Error Text: Event IMAGE_INTENSIFIER_CONFIG_CHANGED not received
View Level: opr
Root Cause: 0
2. If the problem persists. Reload the system software.
Description: This software module (XRBeamForm actor) did not receive Image Intensifier Configuration
data (event).
Customer Text: X-ray exposures are not possible. Reset and call service if the problem persists.
600008 Error Text: Failed to execute OpModeConfig script

View Level: opr
Root Cause: 0
Description: Bad scripts received for Application Setup (BeamForm actor Opmode Configure).
600009 Error Text: Failed to execute Active OpMode script

View Level: opr
Root Cause: 0
Description: Bad scripts received for Application Setup (BeamForm actor Change Active Opmode).
600010 Error Text: Invalid Spectral Filter value in Apps Setup script.
View Level: opr
Root Cause: 0
Description: Desired collimator filter could not be set. Bad spectral filter value received in Application
Setup scripts.
Customer Text: Desired collimator filter could not be set. Reselect protocol or check protocol database.

GE MEDICAL SYSTEMS
600011 Error Text: Not ready for Acquisition while setting the Spectral Filter
View Level: opr
Root Cause: 1
Recommended Action(s): 1. Retry the operation.
Description: The Collimator is setting the spectral filter while START_SEQUENCE received.
Customer Text: Retry operation. Call service if problem persists.
600100 Error Text: Overtable Collimator device-driver initialization failed

View Level: opr
Root Cause: 0
Recommended Action(s): 1. Reset the system and try again.
2. If problem persists, reload the application software.
Description: The Overtable Collimator Device software failed the initialization. It may be a software error
or because the Collimator Device software can not register events with the DeviceComm.
600101 Error Text: Undertable Collimator device-driver initialization failed

View Level: opr
Root Cause: 0
2. If problem persists, reload the application software.
Description: The Undertable Collimator Device software failed the initialization. It may be a software error
600102 Error Text: Collimator device Watchdog task received an unknown message.
View Level: opr
Root Cause: 0
600200 Error Text: OverTable collimator went offline
View Level: opr
Root Cause: 1
Recommended Action(s): 1. Check overtable collimator cable connection and power supply.
2. Reset the system.
Description: No heartbeat from the overtable collimator, indicating that it is offline.
Customer Text: Collimator error. Check connection. Reset the system.
600201 Error Text: OverTable collimator is online but not going alive
View Level: opr
Root Cause: 1
Recommended Action(s): Reset the system
Description: The overtable collimator keeps sending the Node Announcement message, but doesn't
acknowledge the Set_Node_Active message from the Saber software.

GE MEDICAL SYSTEMS
600202 Error Text: OverTable collimator is offline
View Level: opr
Root Cause: 1
Description: The overtable collimator is not sending heartbeat messages.
600203 Error Text: OverTable collimator state is unknown

View Level: opr
Root Cause: 1
Description: Software error: The positioner software failed to establish connection with the Overtable
collimator.
600204 Error Text: UnderTable collimator went offline

View Level: opr
Root Cause: 1
Recommended Action(s): 1. Check undertable collimator cable connection and power supply.
Description: No heartbeat from the undertable collimator, indicating that it is offline.
600205 Error Text: UnderTable collimator is online but not going alive
View Level: opr
Root Cause: 1
Description: The undertable collimator keeps sending the Node Announcement message, but doesn't
600206 Error Text: UnderTable collimator is offline

View Level: opr
Root Cause: 1
Description: The undertable collimator is not sending heartbeat messages.
600207 Error Text: UnderTable collimator state is unknown
View Level: opr
Root Cause: 1
Description: Software error: The positioner software failed to establish connection with the undertable
collimator.

GE MEDICAL SYSTEMS
600400 Error Text: Filter-change Error
View Level: opr
Root Cause: 1
Recommended Action(s): 1. Reselect the application protocol.
3. Despite resetting the system, if the problem still continues, replace the collimator
Description: The system made an attempt to configure the selected spectral filter. However the collimator
was unable to set the required spectral filter due to an internal software error.
Customer Text: X-ray exposures may not be possible. Reset and call service if the problem persists.
600401 Error Text: Filter-change parameter invalid

View Level: opr
Root Cause: 1
Recommended Action(s): 1. Reselect the application protocol.
3. Despite resetting the system, if the problem still continues, reload system application
software
Description: The system has incorrectly configured the spectral filter value. This is an internal software
error.
600500 Error Text: No Set_Terminal_Mode response from overtable collimator

View Level: opr
Root Cause: 1
Recommended Action(s): 1. Reset the system
2. If the problem persists change the collimator and reload the system application software.
Description: Overtable collimator could not be set into the Terminal mode. NOTE: Terminal Mode: This is
the mode that the collimator is configured for 'display only' purposes. During this mode, the
collimator does not accept any other user input.
600501 Error Text: OverTable collimator RAM-D1 error

View Level: opr
Root Cause: 1
2. If the problem persists change the collimator.
Description: Overtable collimator internal error: RAM-D1 error.
600502 Error Text: OverTable collimator EEPROM error

View Level: opr
Root Cause: 1
Description: Overtable collimator internal error: EEPROM error.
600503 Error Text: OverTable collimator CAN bus error or error overrun
View Level: opr
Root Cause: 1
2. Check for collimator cable connections and power supply.

GE MEDICAL SYSTEMS
3. Run CAN bus Diagnostics listed under Positioner module.
4. If all of the above are OK, replace the collimator
Description: Overtable collimator internal error: CAN bus error.
600504 Error Text: OverTable collimator CAN receiver overrun error

View Level: opr
Root Cause: 1
Description: Overtable collimator internal error: CAN receiver error.
600505 Error Text: OverTable Collimator has lost communication with D2

View Level: opr
Root Cause: 1
Description: Overtable collimator internal error: communication lost with required module (D2).
600506 Error Text: OverTable collimator error calculating height

View Level: opr
Root Cause: 1
Description: Overtable collimator internal error when calculating height.
Customer Text: Collimator error. Try again. Reset the system and call service if problem persists.
600507 Error Text: OverTable collimator error calculating width

View Level: opr
Root Cause: 1
Description: Overtable collimator internal error when calculating width
600508 Error Text: OverTable collimator error height stepping

View Level: opr
Root Cause: 1
Description: Overtable collimator internal error while height stepping.

GE MEDICAL SYSTEMS
600509 Error Text: OverTable collimator error width stepping
View Level: opr
Root Cause: 1
Description: Overtable collimator internal error while width stepping.
600510 Error Text: OverTable collimator error prefilter stepping

View Level: opr
Root Cause: 1
Description: Overtable collimator internal error while prefilter stepping.
600511 Error Text: OverTable collimator error height limit switch
View Level: opr
Root Cause: 1
3. If system has been just installed, check that foam shipping block is removed.
Description: Overtable collimator internal error: height limit switch. The collimator blades are possibly
stuck
Customer Text:
600512 Error Text: OverTable collimator error width limit switch

View Level: opr
Root Cause: 1
Description: Overtable collimator internal error: width limit switch. The collimator blades are possibly stuck
600513 Error Text: OverTable collimator error prefilter limit switch

View Level: opr
Root Cause: 1
Description: Overtable collimator internal error: prefilter limit switch.
600514 Error Text: UnderTable collimator RAM-D1 error

View Level: opr
Root Cause: 1
Description: Undertable collimator internal error: RAM-D1 error.

GE MEDICAL SYSTEMS
600515 Error Text: UnderTable collimator EEPROM error
View Level: opr
Root Cause: 1
Description: Undertable collimator internal error: EEPROM error.
600516 Error Text: UnderTable collimator CAN bus error or error overrun
View Level: opr
Root Cause: 1
Description: Undertable collimator internal error: CAN bus error.
600517 Error Text: UnderTable collimator CAN receiver overrun error

View Level: opr
Root Cause: 1
Description: Undertable collimator internal error: CAN receiver error.
600518 Error Text: UnderTable Collimator has lost communication with D2

View Level: opr
Root Cause: 1
Description: Undertable collimator internal error: communication lost with required module (D2).
600519 Error Text: UnderTable collimator error calculating height

View Level: opr
Root Cause: 1
Description: Undertable collimator internal error when calculating height.
600520 Error Text: UnderTable collimator error calculating width

View Level: opr
Root Cause: 1
Description: Undertable collimator internal error when calculating width

GE MEDICAL SYSTEMS
600521 Error Text: UnderTable collimator error height stepping
View Level: opr
Root Cause: 1
Description: Undertable collimator internal error while height stepping.
600522 Error Text: UnderTable collimator error width stepping

View Level: opr
Root Cause: 1
Description: Undertable collimator internal error while width stepping.
600523 Error Text: UnderTable collimator error prefilter stepping
View Level: opr
Root Cause: 1
Description: Undertable collimator internal error while prefilter stepping.
600524 Error Text: UnderTable collimator error height limit switch

View Level: opr
Root Cause: 1
Description: Undertable collimator internal error: height limit switch. The collimator blades are possibly
stuck
600525 Error Text: UnderTable collimator error width limit switch

View Level: opr
Root Cause: 1
Description: Undertable collimator internal error: width limit switch. The collimator blades are possibly
stuck
600526 Error Text: UnderTable collimator error prefilter limit switch

View Level: opr
Root Cause: 1
Description: Undertable collimator internal error: prefilter limit switch.

GE MEDICAL SYSTEMS
600527 Error Text: UnderTable collimator mechanical error D1: Limit Switch - Iris Diaphragm
View Level: opr
Root Cause: 0
Description: Undertable collimator mechanical error D1: Limit Switch - iris diaphragm

GE MEDICAL SYSTEMS
3.4 08 XRDataMgr
800000 Error Text: Event Creation Failed
View Level: opr
Root Cause: 1
Recommended Action(s): Reset the system. If the problem persists, reload the software.
800001 Error Text: Event Subscription Failed

View Level: opr
Root Cause: 1
800002 Error Text: Failed to bind to Subsystem Manager

View Level: opr
Root Cause: 1
800003 Error Text: Failed to bind to Digital Proxy Actor

View Level: opr
Root Cause: 1
800004 Error Text: Trigger Received for unknown event

View Level: opr
Root Cause: 1
Recommended Action(s): Possible configuration Issue. Reinstall software.
Description: Received a message that has not been requested
800005 Error Text: Received unknown event
View Level: opr
Root Cause: 1
Recommended Action(s): No action necessary.
Description: Received a message that has not been requested.
800006 Error Text: The opModeId is not an active opMode, default to prime one
View Level: opr
Root Cause: 1
Recommended Action(s): Reselect the protocol, if the problem persists reset the system.

GE MEDICAL SYSTEMS
800007 Error Text: XRDatMgr is not ready, it may be in PowerFailure, ShutDown or HaltError
View Level: opr
Root Cause: 1
Description: The software module is not ready, it may be in PowerFailure, ShutDown or HaltError
Customer Text: Software Error. Reset the system if problem persists.
800008 Error Text: One of opModeId in the CHANGE_ACTIVE_OPMODES event is not opMode configured
View Level: opr
Root Cause: 1
800009 Error Text: Could not call method on the actor

View Level: opr
Root Cause: 1
Recommended Action(s): Refer to Precision Diagnostic Manual and run Ethernet Diagnostic.
Description: Refer to Precision Diagnostic Manual and run Ethernet Diagnostic.
800010 Error Text: Cannot send message to Saturn

View Level: opr
Root Cause: 1
Recommended Action(s): Connection to Digital lost. Refer to Precision Diagnostic Manual and run Ethernet Diagnostic.
Description: Connection to Digital lost. Refer to Precision Diagnostic Manual and run Ethernet Diagnostic.
Customer Text: System communication error. Reset the system and call service if problem persists.
800011 Error Text: Saturn did not return ALIVE_STATUS message

View Level: opr
Root Cause: 1
Recommended Action(s): System controller did not connect to the Digital Subsystem. Refer to Precision Diagnostic
Manual and run Ethernet Diagnostic.
Description: System controller did not connect to the Digital Subsystem. Refer to Precision Diagnostic
800012 Error Text: Received unknown Saturn event

View Level: opr
Root Cause: 1
Recommended Action(s): Digital Subsystem sent a message that the System Controller could not understand. Refer to
Precision Diagnostic Manual and run Ethernet Diagnostic.
Description: Digital Subsystem sent a message that the System Controller could not understand. Refer to

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Recommended Action(s): Check to see if the configuration files are present. If yes, refer to Precision Diagnostic Manual
to run AMI Diagnostics on system controller

View Level: opr
Root Cause: 1
800015 Error Text: Failed to set the calypso environment pointer

View Level: opr
Root Cause: 1
800016 Error Text: The setStateMachineFilename failed
View Level: opr
Root Cause: 1
800017 Error Text: DataMgr calculated a dose greater than total allowed dose.
View Level: opr
Root Cause: 1
Recommended Action(s): Calculated dose value beyond upper limit. Check generator output.
Description: Calculated dose value beyond upper limit. Check generator output.
800018 Error Text: DataMgr calculated a dap greater than total allowed dap.
View Level: opr
Root Cause: 1
Recommended Action(s): Calculated dap value beyond upper limit. Check generator output.
Description: Calculated dap value beyond upper limit. Check generator output.

GE MEDICAL SYSTEMS
3.5 10 XRImChainPos
View Level: opr
Root Cause: 0
2. If the problem persists, reload system software (Load from Cold)
Description: Software Error: In boot phase, the actor (software module) needs to connect to other actors.
However, due to an internal software fault the connection could not be made. As a result, the
software will not work properly.
persists.
1000001 Error Text: Was not bound to actor
View Level: opr
Root Cause: 0
Description: Software Error: The actor (software module) tried to call other actor's method. However there
was no response from the other actor. This is a result of broken software communication.
persists.
1000002 Error Text: Failed to read config file ImChain.cfg
View Level: opr
Root Cause: 1
Description: Software Error: The actor (software module) could not find it's configuration file
persists.
1000003 Error Text: Failed to read Calibration file ImChain.cal
View Level: opr
Root Cause: 1
Description: Software Error: The actor (software module) could not find it's calibration file
persists.
1000004 Error Text: OTS not configured for RAD application modes
View Level: opr
Root Cause: 1
Recommended Action(s): Reconfigure the System to appropriately reflect the status of OTS on the system. (This could
be done from Precision Service User Interface (SUIF) on Service/Config screens)
Description: This error is due to configuration issues with OTS. This error could happen if an attempt was
made to take overhead (RAD) exposures when OTS was absent on the system.
Customer Text: System Configured for NO OTS

GE MEDICAL SYSTEMS
1000005 Error Text: Wall not configured for Wall Bucky application mode
View Level: opr
Root Cause: 1
Recommended Action(s): Reconfigure the System to appropriately reflect the status of wallstand on the system. (This
could be done from Precision Service User Interface (SUIF) on Service/Config screens)
Description: This error is due to configuration issues with Wall Stand. This error could happen if an attempt
was made to take overhead (RAD) exposures when Wallstand was absent on the system.
Customer Text: System Configured for NO WALL Stand
1000200 Error Text: State Machine Errors

View Level: opr
Root Cause: 0
Recommended Action(s): Ignore
Description: Software Error: Some unexpected actor (software module) join the system.
Customer Text: An internal communication failure has occurred. Ignore. Call service if problem persists.
1000201 Error Text: Failed to execute OpModeConfigure script
View Level: opr
Root Cause: 0
1000202 Error Text: Failed to execute Change Active OpModes script
View Level: opr
Root Cause: 0
1000203 Error Text: Cone Motion Inhibited, Table Horizontal Stop Not Selected
View Level: opr
Root Cause: 0
Recommended Action(s): Select Table Horizontal stop
Description: The Cone Motion is Inhibited, Table Horizontal Stop Not Selected
Customer Text: Cone Motion Inhibited. Table horizontal stop not selected.
1000204 Error Text: SFD Not In Expose Position

View Level: opr
Root Cause: 0
Recommended Action(s): Move the IDD to the lateral latch position
Description: SFD Not In Expose Position
Customer Text: SFD Not In Expose Position

GE MEDICAL SYSTEMS
1000205 Error Text: SFD Not In Park Position
View Level: opr
Root Cause: 0
Recommended Action(s): Move the IDD to the park position
Description: SFD Not In Park Position
Customer Text: SFD Not In Park Position
1000206 Error Text: Set Bucky ready time-out, exposure is not possible
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Reset the system and then retry the exposure.
2. Make sure that no positioner IO board errors are displayed along with this error (e.g.: Node
Guarding errors). If these errors are displayed then the problem could be at the Positioner
cabinet end and not with the bucky itself. (Refer to the error comments for these errors for
recommended actions)
3. If there are no positioner IO board errors displayed and the problem still persists after reset,
then this could be due to hardware failure at the bucky end. Check for jammed bucky (make
sure that the grid can move freely). Check for proper electrical connections and power supply.
4. If all the above does not resolve the issue, replace the bucky
Description: During an expose sequence, the system vibrates the bucky and makes sure that the required
vibration frequency (bucky speed) has been reached before the system actually takes an
exposure. However due to some reasons if the required vibration frequency is not reached in
the provided time interval, the system cannot expose and this error is reported
Customer Text: Bucky is not ready. Retry exposure or reset the system if problem persists.
1000207 Error Text: Bucky size does not match the standard one
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Retry positioning the cassette again.
2. Make sure that the cassette is centered properly.
3. Check for proper electrical connections on the cassette.
4. If the problem persists, re-calibrate the cassette sensing (Service/Calibration screens).
5. If re-calibration does not resolve the problem, replace the cassette holder.
Description: The cassette size does not match the standard one.
Customer Text: The cassette size does not match the standard one. Reposition the cassette or re-calibrate
the bucky.

GE MEDICAL SYSTEMS
3.6 1100 Athena Application
1100001 Error Text: Proxy Manager not connected
Major Function Impacted: Digital
View Level: opr
Root Cause: 1
Recommended Action(s): Check connection to Mars, Ensure Mars is up, Wait for Mars
Description: Connectivity failure with Mars or error in communication software
Customer Text: Digital communication error. Reset the system and call service if problem persists.
1100002 Error Text: Proxy Manager Init Fail

View Level: opr
Root Cause: 1
Recommended Action(s): Communication proxy Init failure, reboot.
Description: Error in communication software
1100003 Error Text: Bad OpModeId received

View Level: opr
Root Cause: 1
Recommended Action(s): Reset the system. If problem persists, perform a complete re-load of all system software
Description: The OpMode Id (application identifier) received by the Digital was invalid or unexpected. This
is due to a logic error or inconsistency between subsystem software releases.
1100004 Error Text: Creation failure of Win32 data structure

View Level: opr
Root Cause: 1
Description: Digital software encountered a severe resource allocation error. Likely cause is that the
system is running low on resources.
1100005 Error Text: Destruction failure of Win32 data structure
View Level: opr
Root Cause: 1
Recommended Action(s): This is not a severe error since it is an error condition detected during a system shutdown or
reset. If the shutdown or reset operation was successful, this error can be ignored. Otherwise,
perform a complete re-load of Digital software
Description: Failure while doing clean-up prior to shutting down.
1100006 Error Text: Unexpected event occurred

View Level: opr
Root Cause: 1
Recommended Action(s): Engineering error only; System will recover
Description: An event occurred or property value was received when it was not expected. Likely cause is
that the subsystems are out of sync.

GE MEDICAL SYSTEMS
1100007 Error Text: Unexpected message received while camera off
View Level: opr
Root Cause: 1
Recommended Action(s): Digital received an unexpected command when system is in Rad mode. Select non-rad
protocol if Digital operation is desired.
Description: The received property cannot be handled when the camera is off.
Customer Text: Reselect the protocol. Reset and call service if the problem persists.
1100010 Error Text: Unknown packet received

View Level: opr
Root Cause: 1
Recommended Action(s): Reboot the system
Description: Digital received an unexpected command from Mars. Possible cause is that the subsystem
software versions are incompatible.
1100014 Error Text: Unable to start server
View Level: opr
Root Cause: 1
Recommended Action(s): Service functions may be prevented, reboot or reinstall software.
Description: FTP or HTTP server failed to start.
Customer Text: Service functions are not available. Reset and call service if the problem persists.
1100015 Error Text: 0 opModeIds in ClearOpmodes command. Cannot change protocol
View Level: opr
Root Cause: 1
Recommended Action(s): Select different protocol
Description: There are 0 opmodes in the new protocol. This is a logical error in protocol setup. Likely cause
is an error in Mars software or a communication error.
Customer Text: This protocol is not available. Select another to continue.
1100016 Error Text: Command received in power failure

View Level: opr
Root Cause: 1
Description: Saturn is in power failure mode.
Customer Text: Digital error. Reset the system and call service if problem persists.
1100103 Error Text: Bad application identifier

View Level: opr
Root Cause:
Recommended Action(s): Reset the system. Re-install software if problem persists.
Description: The sysmode (application identifier) value received is not in the list known to Athena. Likely
cause is an inconsistency between subsystem software releases.

GE MEDICAL SYSTEMS
1100104 Error Text: Application error. Internal synchronization failed.
View Level: opr
Root Cause: 1
Description: A severe software error within Athena while synchronizing internal activities using a
semaphore. A reboot may be needed.
1100117 Error Text: Bad status received for PREP, Prep Failed
View Level: opr
Root Cause: 1
Recommended Action(s): Retry the exposure. Look for other errors that may indicate a hardware problem
Description: A Start Prep or Stop Prep command was not processed correctly. This could be because it
was unexpected, or the data in the request was incorrect.
Customer Text: Prep failed. Release the exposure switch and try again.
1100118 Error Text: Bad status received for EXPOS_TRIGGER, Expose Failed
View Level: opr
Root Cause: 1
Description: A Start Expose or Stop Expose command was not processed correctly. This could be
because it was unexpected, or because the data in the request was incorrect.
Customer Text: Release the exposure switch and try again.
1100119 Error Text: Failed to display text on the Image Monitor

View Level: opr
Root Cause: 1
Description: An error occurred while trying to display Dose or Technique information on the Image
Monitor. As a result, the displayed parameters may not be accurate.
1100121 Error Text: Unknown Mag value received

View Level: opr
Root Cause: 1
Description: Incorrect II Mag value received. Possible cause is that the subsystem software versions are
incompatible.
Customer Text: The Field of View was not changed. Try again or call service if the problem persists.
1100123 Error Text: Failed to set up Image Intensifier optics

View Level: opr
Root Cause: 1
Recommended Action(s): Check the OCB connection. Reset the system. Run the OCB diagnostics if problem persists.
Description: An error occurred while trying to set up the Iris or NDF during Prep. This may be because
there is a communication problem with the OCB or because of an internal error within OCB.
Customer Text: Imaging control error. Check the imaging connection and call service if problem persists.

GE MEDICAL SYSTEMS
1100124 Error Text: General OCB Errors
View Level: opr
Root Cause: 1
Recommended Action(s): Run OCB Diagnostics via SUIF
Description: Optics Control Board (OCB) is generating errors; see debug text for more information
Customer Text: Optics control error. Release exposure switch and try again. Call service if problem
persists.K57
1100125 Error Text: II Mag not In the Valid Range

View Level: opr
Root Cause: 1
Description: Invalid parameter value for FOV received.
1100126 Error Text: Pdb not in the Valid Range

View Level: opr
Root Cause: 1
Description: Invalid parameter value for Photodiode gain received.
1100127 Error Text: Iris Transmission Not in the Valid Range

View Level: opr
Root Cause: 1
Description: Invalid parameter value for Iris aperture received.
1100128 Error Text: Failed to create OCB driver

View Level: opr
Root Cause: 1
Recommended Action(s): Check the OCB connection. Reset the system. Run the OCB diagnostics if problem persists.
Description: During boot, the Optics Control Board (OCB) driver failed to initialize.
Customer Text: Digital initialization error. Reset and call service if problem persists.
1100129 Error Text: The fluoro frame rate does not fall in the Range between 1 to 30
View Level: opr
Root Cause: 1
Description: Invalid parameter value for fluoro frame rate received.

GE MEDICAL SYSTEMS
1100130 Error Text: Failed to configure the CCU board correctly
View Level: opr
Root Cause: 1
Recommended Action(s): Run CCU diagnostics. Re-install software if needed
Description: Failed to use the IAB/CCU driver to change a configuration setting on the CCU board. This
may be because of a board/driver failure or because some required data (such as Look-up
table data) was not found or was incorrect.
1100131 Error Text: Bad parameter value received while trying to initialize the camera.
View Level: opr
Root Cause: 1
Recommended Action(s): Check the camera driver version. Re-install software if needed
Description: Invalid parameter value received for camera initialization.
Customer Text: Reselect the protocol. Reset the system. Call service if the problem persists.
1100132 Error Text: Config data is Missing or Erroneous.
View Level: opr
Root Cause: 1
Recommended Action(s): Reinstall software
Description: A required configuration or calibration parameter was missing in the registry or in the runtime
code (e.g. FOV settings or FOV factor table), or it was found to be erroneous.
Customer Text: Digital control error. Reset system and/or call service to reinstall software if problem persists.
1100133 Error Text: Video gain settings are out of range.

View Level: opr
Root Cause: 1
Recommended Action(s): Check calibration settings, and re-run Image chain calibrations if necessary
Description: The value computed for the Camera gain or Iris transmission was outside normal range. The
acquisition can proceed with corrected settings, but this indicates a likely problem with
calibration or configuration settings.
Customer Text: Image quality may not be optimal. Call service to check the calibration settings.
1100134 Error Text: Failed to communicate with Acquisition Sequencer driver.

View Level: opr
Root Cause: 1
Recommended Action(s): Reinstall software
Description: The application software failed to communicate with the Windows driver that drives
acquisition sequencing in the Digital. This is a severe internal software error that could occur
as a result of incorrect installation of Windows on Digital Subsystem.
1100135 Error Text: Failed to compute video gain.

View Level: opr
Root Cause: 1
Description: Failed to compute a video gain (Camera gain or Iris Transmission) according to Automatic
Gain Control algorithms. The exposure will be aborted.

GE MEDICAL SYSTEMS
1100136 Error Text: Failed to compute Sensor Feedback to send to Mars for Exposure Management.
View Level: opr
Root Cause: 1
Description: Failed to compute Sensor Back based on the ABD feedback read from the CCU board, This
may be because the value could not be read correctly, or because some required calibration
or configuration data was incorrect. The exposure will be aborted.
1100137 Error Text: Failed To Store Image Loop

View Level: opr
Root Cause: 1
Description: An error occurred that prevented the successful store of the image-loop.
Customer Text: Failed to store image-loop. Retry.
1100138 Error Text: Failed To Initialize Software Component
View Level: opr
Root Cause: 1
Description: General Software Failure in a module that is essential for proper functioning of the system.
E.g. failed to create application pointers.
Customer Text: Software Error. Reset the system. Call service if problem persists.
1100139 Error Text: System cannot support the requested frame rate
View Level: opr
Root Cause: 1
Recommended Action(s): No Action
Description: The system lowered the frame rate. This may be because images were acquired faster than
the system can save them to disk, or the pulse width for the acquisition was higher than the
allowable value for the requested frame rate.
Customer Text: Frame rate decreased due to system limitation.
1100140 Error Text: System cannot support the requested frame rate.
View Level: opr
Root Cause: 1
Recommended Action(s): No Action
Description: The system lowered the frame rate. This may be because images were acquired faster than
the system can save them to disk.
Customer Text: Images being acquired faster than the system can save them. Frame rate has decreased.
1100141 Error Text: Failed to close: image-store in progress

View Level: opr
Root Cause: 1
Recommended Action(s): Retry
Description: Athena received a request to close the patient while the image-store is in progress.
Customer Text: Image store in progress. Wait, then close patient.

GE MEDICAL SYSTEMS
1100142 Error Text: Maximum Series Limit Reached
View Level: opr
Root Cause: 1
Recommended Action(s): Create a new patient entry for acquisition
Description: The maximum number of runs, 80, was reached for the patient and hence no more
acquisitions can be performed on this patient entry. A new entry needs to be created.
Customer Text: Maximum number of runs reached. Create new patient entry for acquisition.
1100143 Error Text: Failed to Proceed Further

View Level: opr
Root Cause: 1
Description: General Software Failure in a module that is essential for proper functioning of the system.
1100144 Error Text: Failed to submit image to internal print queue
View Level: opr
Root Cause: 1
Recommended Action(s): Retry Expose-submission of image
Description: Athena failed to submit the image the user wanted to expose, to Athena's internal print-queue
mechanism
Customer Text: Failure to submit image. Retry. Call service if the problem persists.
1100145 Error Text: Failed to initiate Print-queue transfer

View Level: opr
Root Cause: 1
Recommended Action(s): 1. Retry print operation. 2.If problem persists, reset the system. 3. If above does not fix the
problem, perform complete reload of system software (Load From Cold).
Description: Internal Software Error in Digital
Customer Text: Check printer connection. Retry. Call service if problem persists.
1100146 Error Text: Failed to submit image to Print-queue
View Level: opr
Root Cause: 1
Recommended Action(s): 1. Retry print operation. 2.If problem persists, reset the system. 3. If above does not fix the
problem, perform complete reload of system software (Load From Cold).
1100147 Error Text: Failed to flush print-queue.

View Level: opr
Root Cause: 1
Recommended Action(s): 1. Retry print operation.
2.Verify printer connection (cabling, power-supply, printer).3.If problem persists, reset the system.

GE MEDICAL SYSTEMS
1100148 Error Text: About to reach maximum runs for this patient
View Level: opr
Root Cause: 1
Recommended Action(s): Delete some images, or create an additional record for this patient
Customer Text: Approaching maximum limit. Delete several images or create an additional record for this
patient.
1100149 Error Text: CCU parameter out of range

View Level: opr
Root Cause: 1
Description: Invalid parameter value for Camera Control Unit received.
Customer Text: An internal communication failure has occurred. Reset the system. Call service if problem
persists.
1100150 Error Text: Selected study have no images for review

View Level: opr
Root Cause: 1
Recommended Action(s): 1. Verify selected study has images to review and retry.
Description: This error is reported when the digital determines there are no images to review for the
selected study.
Customer Text: No images are stored and available for review. Close patient file.
1100151 Error Text: Not Enough space available for image storage
View Level: opr
Root Cause: 1
Recommended Action(s): Close patient and delete some images or patients from the patient list screen
Description: This error can happen when there is not enough space available to store images on the disk
Customer Text: Not enough disk space available for storage. Close patient. Delete some images or patients
from the list screen.
1100152 Error Text: Not enough disk space for acquire loop
View Level: opr
Root Cause: 1
Recommended Action(s): Close patient and delete some images or patients from the patient list screen
Description: This error can happen when there is not enough space available to store images on the disk
1100153 Error Text: Failed to start calibration mode

View Level: opr
Root Cause: 1
Recommended Action(s): Close the patient and try again. Reboot if the problem persists
Description: This could happen if Athena is not in the proper state to start calibrating
Customer Text: Retry calibration. Reset the system if the problem persists.

GE MEDICAL SYSTEMS
1100154 Error Text: Failed to start or stop a sequence
View Level: opr
Root Cause: 1
Description: A Start Sequence or Stop Sequence command was not processed correctly. This could be
because it was unexpected, or because an error occurred while trying to change hardware
settings.
Customer Text: Retry the exposure. Call service if the problem persists.
1100155 Error Text: Rescale gain value is at maximum for several exposures
View Level: opr
Root Cause: 1
Recommended Action(s): Re-Calibrate the image chain
Description: Digital Re-scaling gain value is at maximum for several consecutive exposures. This
indicates that the system may not calibrated properly.
Customer Text: System is not calibrated properly. Re-calibrate the image chain.
1100156 Error Text: Failed to display or remove the No Radiation sign.

View Level: opr
Root Cause: 1
Recommended Action(s): Release Expose switch and try again
Description: Failed to display the No Radiation sign on the Image monitor.
Customer Text: Application error. Release exposure switch and try again.
1100157 Error Text: Unable to set desired replay rate.

View Level: opr
Root Cause: 1
Recommended Action(s): 1. Retry selecting the loop replay rate.
2.If problem persists, select a different rate.
3.If problem persists, reset the system.
Description: This happens when Digital fails to set the desired replay-rate in review mode. Digital will
default to a valid replay rate.
Customer Text: Unable to set desired replay rate. Try selecting a different rate.
1100158 Error Text: Failed to open patient for exam

View Level: opr
Root Cause: 1
Recommended Action(s): Attempt to open the study manually.
Description: This can happen when the Digital does not receive appropriate RTPP information from the
User Interface.
Customer Text: Unable to open patient for exam. Retry.

View Level: opr
Root Cause: 1
Recommended Action(s): Attempt to open the study manually.
Description: This can happen when the Digital does not receive appropriate RTPP information from the
User Interface.
Customer Text: Unable to open patient for exam. Retry.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Recommended Action(s): 1. Verify that the appropriate study is highlighted on the digital's patient list screen.
Description: This will happen when a patient is already selected and a request is made to open another
exam, or when Software fails to select a patient.
Customer Text: System cannot start exam. Verify patient selection and try again.
1100161 Error Text: Failed to open patient for review

View Level: opr
Root Cause: 1
Recommended Action(s): 1. Verify that the appropriate study is highlighted on the digital's patient list screen.
Description: This will happen when Software fails to select patient for review.
Customer Text: Unable to open patient for exam. Verify patient selection and try again.
1100162 Error Text: Partial-Send in progress, failed to close exam.

View Level: opr
Root Cause: 1
Recommended Action(s): To close the study, wait for partial-send to complete.
Description: This will happen when partial-send is in progress and the user tries to close the current exam.
Customer Text: Partial-Send in progress, please wait for completion.
1100163 Error Text: Failed to go to online review: image storage in progress.

View Level: opr
Root Cause: 1
Recommended Action(s): To go to online review, wait for completion of image storage to Hard Drive from the Image
Memory.
Description: Image storage is in progress, user is prevented from going to online review till storage is
completed.
Customer Text: Image storage in progress. Please wait, then try again to review images.
1100164 Error Text: Acquisition stopped to prevent loss of images

View Level: opr
Root Cause: 1
Recommended Action(s): Wait for the image buffers to be saved to disk. There may be a problem with the hard disk
that makes disk access too slow. Try de-fragmenting the hard disk.
Description: The image memory buffers are full. Exposure was halted to prevent image loss on the next
exposure.
Customer Text: Image buffer filled. Wait while images are stored.
1100165 Error Text: Application data not received

View Level: opr
Root Cause: 1
Recommended Action(s): Close the exam and try again. Reset the system if the problem persists.
Description: A required data item was not received from Mars during Application setup for the current
Opmode. Digital cannot start an exposure without this data.

GE MEDICAL SYSTEMS
1100166 Error Text: Cannot playback when digital in stenosis or stacking mode
View Level: opr
Root Cause: 1
Recommended Action(s): To perform loop playback, go to basic review mode (Non stenosis/stacking mode).
Description: When in stenosis or stacking mode playback is disabled.
Customer Text: Loop playback is not allowed when in stenosis or stacking mode.
1100167 Error Text: No images tagged for print.

View Level: opr
Root Cause: 1
Recommended Action(s): Verify appropriate images have been tagged.
Description: No images tagged for print
Customer Text: No images are tagged for printing.
1100168 Error Text: Print Error: Could not read data

View Level: opr
Root Cause: 1
2.If problem persists, reset the system and retry print operation. 3. If above does not fix the
problem, perform complete reload of system software (Load From Cold). NOTE: Backup
system data and archive all necessary patient studies before performing load from cold. Refer
appropriate sections in service manual to perform the above.
Description: Due to a software problem (basic application or print services) or a database problem in
Digital, had to abort print and flush created queue.
Customer Text: An error occurred during print. Try again. Call service if the problem persists.
1100169 Error Text: Print Error Encountered. Forced a premature flush to printer.
View Level: opr
Root Cause: 1
2.If problem persists, reset the system and retry print operation.
3. If above does not fix the problem, perform complete reload of system software (Load From
Cold).
NOTE: Backup system data and archive all necessary patient studies before performing load
from cold. Refer appropriate sections in service manual to perform the above.
Description: An error occurred during print. Retry if the images were not printed.
1100170 Error Text: FOV change not allowed when system is waiting to start Fluoro.
View Level: opr
Root Cause: 1
Recommended Action(s): Retry the FOV change
Description: Image intensifier magnification cannot be changed from when the system is prepped for
Fluoro till exposure starts. The user should try again to change FOV after the exposure starts.
Customer Text: The Field of View was not changed. Try again.
1100171 Error Text: Cannot change display format in stenosis mode.

View Level: opr
Root Cause: 1
Recommended Action(s): To view multiview display, exit Stenosis mode.
Description: In Stenosis mode, user cannot go to multi-view format display.
Customer Text: Multiview display is not allowed in Stenosis mode.

GE MEDICAL SYSTEMS
1100172 Error Text: CD-ROM Capacity exceeded for the archive-selection.
View Level: opr
Root Cause: 1
Recommended Action(s): Verify archive-selection can fit on CD-ROM
Description: The selection size for CD-archive exceeds CD-ROM capacity.
Customer Text: CD-R capacity is exceeded for the archive selection. Select fewer images.
1100173 Error Text: Failed to back up calibration or configuration data.

View Level: opr
Root Cause: 1
Recommended Action(s): Retry or reset the system
Description: A severe error occurred while trying to perform a backup of calibration/configuration data.
Customer Text: Backup failed.
1100174 Error Text: Failed to restore calibration or configuration data.

View Level: opr
Root Cause: 1
Description: A severe error occurred while trying to perform a restore of calibration/configuration data.
Customer Text: Restore failed.
1100175 Error Text: Failed to communicate with Laser Imager. Ensure the Imager is on or call service
View Level: opr
Root Cause: 1
Recommended Action(s): Ensure the Imager is on
Description: Athena attempts to establish communication with the printer and initialize it to print our
images. An error results if we are unable to complete the initialization
Customer Text: Printer communication error. Ensure printer is turned on or call service
1100176 Error Text: Laser Imager Failure. Please call service

View Level: opr
Root Cause: 1
Recommended Action(s): printer turned off or reset printer, printer com port failure, Saturn com port failure, check for
disconnected cable
Description: Assuming the first part is successful, Athena starts sending images to the printer. If any of the
image sends within a given patient fails, another error is reported
Customer Text: Printer communication error. Ensure printer is turned on or call service
1100177 Error Text: Failed to detect DICOM SCP Service
View Level: opr
Root Cause: 1
Recommended Action(s): If error continues, reset system
Description: Digital detected SCP service suspended
Customer Text: Network Communication Error. Reset if problem persists

GE MEDICAL SYSTEMS
1100178 Error Text: Failed to detect DICOM SCU service
View Level: opr
Root Cause: 1
Description: Digital detected SCU service suspended
1100179 Error Text: Failure to detect DICOM AutoPilot

View Level: opr
Root Cause: 1
Description: Digital detected AutoPilot service suspended

View Level: opr
Root Cause: 1
Recommended Action(s): Please try again
exam, or when Mitra fails to select a patient.

View Level: opr
Root Cause: 1
Recommended Action(s): Please try again
1100182 Error Text: Calculated Iris Transmission is too small

View Level: opr
Root Cause: 1
Recommended Action(s): “Target Entrance Dose (TED) is very large; increase magnification, change the protocol ROI
or try to collimate out raw radiation
Description: “The image is too bright because the Target Entrance Dose (TED) value is very large. In order
to achieve the Target Brightness Level (TBL), the calculated Iris transmission and camera
gain are at a minimum and cannot go any lower (the iris is almost closed). It is possible that
the patient is too small or too much raw radiation is in the image. Try to increase the
magnification, change the protocol ROI or collimate raw radiation.
Customer Text: The image is too bright. Increase magnification, change the protocol ROI or collimate raw
radiation.

GE MEDICAL SYSTEMS
1100183 Error Text: Calculated Re-scaling Gain is too low
View Level: opr
Root Cause: 1
Recommended Action(s): “Target Entrance Dose (TED) is very large; increase magnification, change the protocol ROI
Description: “The image is too bright because the Target Entrance Dose (TED) value is very large. In order
to achieve the Target Brightness Level (TBL), the calculated Iris transmission, camera gain
and re-scaling gain are at a minimum and cannot go any lower (the iris is almost closed). It is
possible that the patient is too small or too much raw radiation is in the image. Try to increase
the magnification, change the protocol ROI or collimate raw radiation.
radiation.
1100184 Error Text: Calculated Re-scaling Gain is too large

View Level: opr
Root Cause: 1
Recommended Action(s): “Target Entrance Dose (TED) is very small. Decrease magnification or increase the protocol
ROI. Try again.
Description: “The image is too dark because the Target Entrance Dose (TED) value is very small. In order
to achieve the Target Brightness Level (TBL), the calculated Iris transmission, camera gain
and re-scaling gain are at a maximum and cannot go any higher (the iris is almost full open).
It is possible that the patient is too large. Try to decrease the magnification or increase the
protocol ROI.
Customer Text: The image is too dark. Decrease magnification or increase the protocol ROI.
1100185 Error Text: Time-out waiting for ABD

View Level: opr
Root Cause: 1
Recommended Action(s): “Please try again
Description: “Automatic Brightness Detection (ABD) feedback was not received for the DSA trial
exposure. Since the trial was not successful, the DSA sequence cannot continue.
Customer Text: The trial exposure was not successful. Try again and call service if the problem persists.
1100185 Error Text: Time-out waiting for ABD

View Level: opr
Root Cause: 1
Recommended Action(s): “Ignore. If error continues, reset system and try again.
Description: “ABD was not received for an exposure.
1100186 Error Text: Calculated Camera Gain is too large

View Level: opr
Root Cause: 1
Recommended Action(s): “Target Entrance Dose (TED) is very small. Decrease magnification or increase the protocol
ROI. Try again.
Description: “The image is too dark because the Target Entrance Dose (TED) value is very small. In order
to achieve the Target Brightness Level (TBL), the calculated Iris transmission and camera
gain are at a maximum and cannot go any higher (the iris is almost full open). It is possible
that the patient is too large. Try to decrease the magnification or increase the protocol ROI.

GE MEDICAL SYSTEMS
3.7 1101 Athena Communication
1101000 Error Text: Failed to register for a command
Minor Function Impacted: MyErrorHandler
View Level: opr
Root Cause: 1
Description: This error may occur when Digital software fails to register for a message id. Digital proxy
needs to register for every message id with the ProxyMgr object in order to handle it.
1101001 Error Text: Failed to connect to other system

View Level: opr
Root Cause: 1
Recommended Action(s): Check Network Cables
Description: This error may occur when Digital software fails to connect to the other system (MARS). It
could be a bad network cable, lose connection or the registry setting for the MARS IP address
is not correct
1101002 Error Text: Packet not sent

View Level: opr
Root Cause: 1
Description: This error may occur when Digital fails to send a message to the other system. It could be
that the other system is down, or the network cable is pulled out. Plugging the cables in and
rebooting the systems would fix this problem
1101003 Error Text: Null AcceptHandler pointer.

View Level: opr
Root Cause: 1
Description: This error may happen if Digital fails to create a accept handler object that is required to listen
for listen connection requests from other subsystems. A reboot would fix this problem
1101004 Error Text: Null Input handler pointer

View Level: opr
Root Cause: 1
Description: This error may happen if Digital fails to create a input handler object that is required to listen
for receive data from other subsystems. A reboot would fix this problem
1101005 Error Text: Close socket failed

View Level: opr
Root Cause: 1
Description: This error may occur when Digital fails to close a open socket.Digital needs to close a socket
when there is a connection failure or a ShutDown or Reset happens.

GE MEDICAL SYSTEMS
1101006 Error Text: Proxy library Accept call failed.
View Level: opr
Root Cause: 1
Description: This error may occur when Digital fails to accept a socket connection request into a event
handler. Digital proxy needs to have these handlers to handle incoming messages form
MARS system. If this error occurs a reboot would fix this problem
1101007 Error Text: Open Socket failed
View Level: opr
Root Cause: 1
Recommended Action(s): Check Network Cables, Check Registry entry for MARS IP Address
Description: This error may occur when Digital fails to open a socket connection.
1101008 Error Text: Connection failure

View Level: opr
Root Cause: 1
Description: This error may occur when the other system breaks the socket connection
1101009 Error Text: A bad packet received by Digital Proxy.

View Level: opr
Root Cause: 1
Description: This error may occur when there is some page fault on either the Digital system or the Mars
system. A reboot would fix this problem. If the problem still exist a software reinstallation may
be required
1101010 Error Text: Less data received then expected.

View Level: opr
Root Cause: 1
Description: This error may occur when Digital system receives less data for a packet form the other
system. A reboot would fix this problem. This could also happen if there is mismatch of Digital
and Mars software versions
1101011 Error Text: Null default message handler pointer.

View Level: opr
Root Cause: 1
Description: This error may occur when Digital fails to create a Default Message Handler object. Digital
requires a Default Message Handler object for handling any message that Digital is not
registered for with its ProxyMgr Object

GE MEDICAL SYSTEMS
3.8 1102 Athena Drivers
1102100 Error Text: Can not contact OCB in Camera Head
Minor Function Impacted: Gitane
View Level: opr
Root Cause: 0
Recommended Action(s): Check OCB, OCB power supply, RTB cables between Athena and II.
Description: Can not contact OCB in Camera Head
Customer Text: Digital control error. Reset system and call service if problem persists.
1102101 Error Text: Reprogrammed Gitane Flash memory

View Level: opr
Root Cause: 1
Recommended Action(s): Updated FLASH as part of normal upgrade - No further action required.
Description: Reprogrammed Gitane Flash memory
- just telling you that it happened
- probably due to a software update.
Customer Text: Memory has been programmed successfully.
1102102 Error Text: Could not reprogram Gitane Flash memory - bad input file
View Level: opr
Root Cause: 1
Recommended Action(s): User error during software upgrade - bad hex file provided. Re-read software upgrade
instructions and try again.
Description: Could not reprogram Gitane Flash memory - bad input file
Customer Text: Memory programming has failed. Try again.
1102103 Error Text: Could not reprogram Gitane Flash memory - bad memory device
View Level: opr
Root Cause: 1
Recommended Action(s): Hardware error during software upgrade. Cycle power and try again. Replace Gitane board
if this is a persistent problem.
Description: Could not reprogram Gitane Flash memory - bad memory device
Customer Text: Memory programming has failed. Turn the system power off/on and try again.
1102104 Error Text: Gitane driver files missing.

View Level: opr
Root Cause: 1
Recommended Action(s): Re-install Athena software
Description: Gitane driver files missing.
1102105 Error Text: Gitane board not found.
View Level: opr
Root Cause: 1
Recommended Action(s): Re-seat Athena Gitane board. Replace Gitane if this is a persistent problem.
Description: Gitane board not found.

GE MEDICAL SYSTEMS
1102106 Error Text: Gitane sys-logic FPGA is unprogrammed.
View Level: opr
Root Cause: 1
Recommended Action(s): Re-install Athena software. Replace Gitane if this is a persistent problem.
Description: Gitane sys-logic FPGA is unprogrammed.
1102107 Error Text: OCB over temperature (+60 C)

View Level: opr
Root Cause: 1
Recommended Action(s): Remove Intensifier covers and check the CCD camera, cooling fan and Optics Control Board
for overheating.
Description: OCB over temperature (+60 C)
Customer Text: Abnormal Digital temperature. Call service to monitor if problem persists.
1102108 Error Text: Excessive OCB communication errors.

View Level: opr
Root Cause: 1
Recommended Action(s): Check RTB cables between Athena and OCB. Check for proper terminating resisters.
Description: Excessive OCB communication errors.
1102012 Error Text: IAB Error

View Level: opr
Root Cause: 1
Recommended Action(s): Check hardware boards, call service
Description: Failed to initialize the driver for the Acquisition board. May be due to a hardware issue or
incorrect driver installation
1102013 Error Text: Board creation fail

View Level: opr
Root Cause: 1
Recommended Action(s): Board may not be present, call service
Description: Failed to initialize the driver for one of the boards (e.g. IAB or Gitane). May be a hardware
issue or due to incorrect installation.
1102111 Error Text: Reprogrammed OCB Flash memory
Minor Function Impacted: ImageChain
View Level: opr
Root Cause: 1
Recommended Action(s): Updated OCB FLASH as part of normal upgrade - No further action required.
Description: Reprogrammed OCB Flash memory - just telling you that it happened - probably due to a
software update.

GE MEDICAL SYSTEMS
1102112 Error Text: Could not reprogram OCB flash memory
View Level: opr
Root Cause: 1
Recommended Action(s): Re-install Athena software.
Description: Reprogram of OCB Flash memory failed. OCB may not be functional.
1102113 Error Text: Bad Firmware config file

View Level: opr
Root Cause: 1
Description: There is a problem with <athena_dir>\xilinx\firmware_revs.txt file or one of the files it points
to.
1102400 Error Text: ICB Driver Not Found

View Level: opr
Root Cause: 1
Recommended Action(s): Check ICB board and re-install driver if needed.
Description: This is an error code returned from the ICB driver. This may be due to a hardware defect or
due to an incorrect parameter passed to the driver.
Customer Text: Digital control error. Release exposure switch and try again. Reset system and/or call service
if problem persists.
1102401 Error Text: ICB Driver Not Initialized

View Level: opr
Root Cause: 1
1102402 Error Text: ICB Board Defect

View Level: opr
Root Cause: 1
1102403 Error Text: ICB Camera Head Defect

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
1102404 Error Text: ICB/Camera board defect
View Level: opr
Root Cause: 1
1102405 Error Text: Wrong CCD Operating Mode

View Level: opr
Root Cause: 1
1102406 Error Text: Wrong Synchronisation Mode

View Level: opr
Root Cause: 1
1102407 Error Text: Wrong Image Period

View Level: opr
Root Cause: 1
1102408 Error Text: Image Period is not adjustable

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
1102409 Error Text: Wrong CCD Integration Time
View Level: opr
Root Cause: 1
1102410 Error Text: CCD Integration Time is not Adjustable

View Level: opr
Root Cause: 1
1102411 Error Text: Wrong Video Gain

View Level: opr
Root Cause: 1
1102412 Error Text: Wrong Self Test

View Level: opr
Root Cause: 1
1102413 Error Text: Wrong Test Pattern

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
1102414 Error Text: Signal Sync Polarity is Not Adjustable
View Level: opr
Root Cause: 1
1102415 Error Text: Signal Trig Polarity is not adjustable

View Level: opr
Root Cause: 1
1102416 Error Text: Correct Function is Not Implemented

View Level: opr
Root Cause: 1
1102417 Error Text: Not Available while Running Test Pattern

View Level: opr
Root Cause: 1
1102418 Error Text: General Camera Driver Error

View Level: opr
Root Cause: 1
Recommended Action(s): Check ICB board and re-install driver if needed. Check cable connection at CCD camera
head or all cables from camera to Digital module.
Description: An unspecified error occurred in the ICB driver. Check the debug message field for more
details.
Description: Possible bad cable connection to CCD camera. Check cable connection at CCD camera
head or all cables from camera to Digital module

GE MEDICAL SYSTEMS
1102419 Error Text: Camera Initialization Failed
View Level: opr
Root Cause: 1
Recommended Action(s): Check ICB board and Re-install Athena software if needed. Check cable connection at CCD
camera head or all cables from camera to Digital module.
Description: Failed to initialize Camera driver.
1102420 Error Text: Gitane board reported an EMERGENCY STOP error status
View Level: opr
Root Cause: 1
Recommended Action(s): Reboot the system, call service
Description: Gitane board detected an abnormal condition in the system due to a possible timing error or
real time bus signal error occurred
1102421 Error Text: Gitane board reported a NO VD error status

View Level: opr
Root Cause: 1
1102422 Error Text: Gitane board reported a NO X-ray error status

View Level: opr
Root Cause: 1
1102423 Error Text: Gitane board reported a FRAME RATE VIOLATION error status
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
1102424 Error Text: Gitane board reported an X-ray WINDOW TIME error status
View Level: opr
Root Cause: 1
1102425 Error Text: Gitane board reported a SYS RESET IN error status
View Level: opr
Root Cause: 1
1102426 Error Text: Gitane board did not stop an acquisition even after one second
View Level: opr
Root Cause: 1
Recommended Action(s): No action. Call service if problem persists
Description: This error is reported when we attempt to write to a Gitane register to stop acquisition. After
writing the register, we monitor a Gitane status register to make sure that the acquisition has
indeed stopped. If a correct status is not returned within 1 second, this error is reported.
Customer Text: Digital control error. Reset and call service if the problem persists.

GE MEDICAL SYSTEMS
3.9 1103 Athena Calibration
1103000 Error Text: Athena failed to create or delete Patient information
Minor Function Impacted: Calibration
View Level: opr
Root Cause: 1
Recommended Action(s): 1.Quit Calibration, then retry the operation.
2.If problem persists, reset the system.
Description: Calibration needs a patient record to be selected in the memory to acquire images. Here we
could not create the Calibration patient. Internal software error in Digital.
Customer Text: Calibration error. Quit procedure and try again.
1103001 Error Text: Calibration data is missing

View Level: opr
Root Cause: 1
Recommended Action(s): 1.Reset the system, then retry the operation.
2.If problem persists, perform complete reload of system software (Load From Cold).
Description: A required calibration parameter could not be found. Internal software error in Digital.
Customer Text: Calibration parameter could not be found. Call service to re-calibrate the system.
1103002 Error Text: Calibration data is incorrect
View Level: opr
Root Cause: 1
Recommended Action(s): 1.Reset the system, then retry the operation.
2.If problem persists, perform the Iris LUT Calibration.
Description: A required calibration parameter is incorrect. The Iris LUT file appears to be bad. Internal
software error in Digital.
Customer Text: Incorrect Calibration parameter. Call service to re-calibrate the system.
1103003 Error Text: Could not save the calibration result

View Level: opr
Root Cause: 1
Recommended Action(s): Perform required Calibration or Reinstall software
Description: Could not save the calibration result
1103004 Error Text: G2 has changed more than 5%, check if G3 needs to be changed
View Level: opr
Root Cause: 1
Recommended Action(s): This is only an advisory message. G2 has been changed by more than 5%, check if G3 needs
to be changed. If not, this message can be ignored.
Description: Either G2 or G3 has changed by more than 5%. User is advised to check if the other value
needs to be changed.
Customer Text: G2 has changed by more than 5 percent; recheck G3 value. G2 is interactive with G3.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Recommended Action(s): This is only an advisory message. G3 has changed by more than 5%, check if G2 needs to
be changed. If not, this message can be ignored.
Description: Either G2 or G3 has changed by more than 5%. User is advised to check if the other value
1103006 Error Text: Got false calibration start

View Level: opr
Root Cause: 1
Recommended Action(s): 1.Close all calibrations and retry. Reset the system if the problem persist. 2.If the problem
persists, perform complete reload of system software (Load from Cold).
Description: Start calibration could fail if the Digital system received a bad Calibration Id from the System
Controller or Digital is in a bad state itself. Internal software error on Digital or System
Controller.
Customer Text: Calibration start error. Close all calibrations and retry. Reset the system if the problem
persists.
1103007 Error Text: Got false calibration stop

View Level: opr
Root Cause: 1
Recommended Action(s): Reset the system, then retry the calibration.
Description: Stop calibration could fail if the Digital system received a bad Calibration Id from the System
Controller or Digital is in a bad state itself. Internal software error on Digital or System
Controller.
Customer Text: Calibration stop error. Close all calibrations and retry. Reset the system if the problem
persists.
1103008 Error Text: Iqst store images failed

View Level: opr
Root Cause: 1
Recommended Action(s): Acquire more images and try again
Description: Store images could fail if there are not enough images to store
Customer Text: IQST image store failure. Acquire more images and try again.
1103009 Error Text: Failed to start or stop the Iqst server

View Level: opr
Root Cause: 1
Recommended Action(s): Retry or reinstall if the problem persists
Description: This error could happen we had a bad installation
Customer Text: IQST communication failure. Retry or reinstall software if problem persists.
1103010 Error Text: Failed to copy a file
View Level: opr
Root Cause: 1
Recommended Action(s): Retry or reinstall if the problem persists
Description: This error could happen we had a bad installation or the file does not exists
Customer Text: Failed to copy a file. Retry or reinstall software if problem persists.

GE MEDICAL SYSTEMS
1103011 Error Text: Less images acquired
View Level: opr
Root Cause: 1
Recommended Action(s): Acquire more images and try again
Description: This error can happen if there are less images acquired then needed for testing, such as
IQST.
Customer Text: Acquire more images to continue.
1103012 Error Text: The ABD value did not decrease when Iris transmission was reduced
View Level: opr
Root Cause: 1
Recommended Action(s): 1.Abort the calibration, then retry.
2.If problem persists, reset the system, then retry.
3.If problem persists, check the cabling from the Digital to the Camera and OCB, and run the
ICB+CCD, and OCB diagnostics.
4.If the cabling is ok, and diagnostics pass, reload system software (Load From Cold).
5.If problem persists, replace the Digital, Camera and OCB one by one.
Description: Occurs during Iris LUT calibration. This error could happen if there is a bad camera, iris, or
Optics Control Board (OCB). Could be caused by an incorrect software installation, or by bad
hardware (ICB, Camera, OCB) or loose cabling.
Customer Text: ABD value did not decrease. Repeat the calibration.
1103013 Error Text: Attempted to update one of the CF registry values with 0
View Level: opr
Root Cause: 1
Recommended Action(s): 1.If seen during calibration, quit calibration, then retry.
2. If problem persists, reset the system, then retry.
3.If problem persists, reload system software (Load From Cold).
4.If seen when not calibrating, reset the system, then retry. Then go to Step 3.
Description: Occurs during Fluoro CF, Record CF, or Compensation CF calibration. Should not happen:
usually indicates software problem.
Customer Text: Attempted to write bad calibration value. Quit, reset the system and retry.
1103014 Error Text: Attempted to update the Photodiode Gain registry value with a number outside of 1-10000
View Level: opr
Root Cause: 1
Recommended Action(s): 1.If seen during calibration, quit calibration, then retry.
2. If problem persists, reset the system, then retry.
3.If problem persists, reload system software (Load From Cold).
4.If seen when not calibrating, reset the system, then retry. Then go to Step 3.
Description: Occurs during Record CF/Photodiode Gain calibration. Should not happen: usually indicates
software problem.
1103015 Error Text: The image file needed for this calibration is missing
View Level: opr
Root Cause: 1
Recommended Action(s): Reinstall system software.
Description: The files needed for this calibration are missing. Indicates improper installation or corrupt
hard disk. Reinstalling the software will fix the problem.
Customer Text: File required for calibration is missing.

GE MEDICAL SYSTEMS
1103016 Error Text: The value received for this configuration is not valid
Configuration
View Level: opr
Root Cause: 1
Recommended Action(s): Try again, check the config files for missing or bad entries
Description: This error could happen if Mars send athena a bad value to set for a configuration parameter.
Customer Text: Digital Configuration value is bad. Recheck configuration.
1103017 Error Text: Config parameter not initialized

Configuration
View Level: opr
Root Cause: 1
Recommended Action(s): Config the parameter and try again
Description: This error can happen if the particular config parameter is not initialized in the athena config
database
1103018 Error Text: Config parameter is corrupt

Configuration
View Level: opr
Root Cause: 1
Recommended Action(s): Config database is corrupt, config again if the problem persists reinstall software
Description: This error can happen if the athena configuration database is corrupt or unreadable
Customer Text: Dicom Auto-send destination error. Reset and Call service if problem persists.
1103019 Error Text: Config set failed

Configuration
View Level: opr
Root Cause: 1
Recommended Action(s): Could not set the config parameter, check the values and try again
Description: This can happen if athena fails to set the config value for a parameter
1103020 Error Text: The calibration did not complete after the maximum allowed exposures
View Level: opr
Root Cause: 1
Recommended Action(s): Check digital screen for error percentage. If near +/-5%, save the calibration, if greater, redo
the calibration or check hardware.
Description: The sensor feedback value did not approach the target value after maximum allowable
exposures
Customer Text: The sensor feedback value did not approach the target value after maximum allowable
exposures
1103021 Error Text: The user is not authorized for this function.
View Level: opr
Root Cause: 0
Recommended Action(s): “The current user is not authorized to perform this function. The user must log-out and re-log-
in with the appropriate access level.
Description: “The current user is not authorized to perform this function. The user must log-out and re-log-
Customer Text: The current user is not authorized to perform this function.

GE MEDICAL SYSTEMS
3.10 1105 Athena Database
1105000 Error Text: Unable to update record. NO PATIENT SELECTED
Minor Function Impacted: Database
View Level: opr
Root Cause: 0
Recommended Action(s): Select a patient from gui
Description: This error may occur when Athena software fails to update a database record because there
is no patient selected at that time.
1105001 Error Text: Current Patient can not be select for acquisition or review.
View Level: opr
Root Cause: 1
Recommended Action(s): Retry or Reboot the system
Description: Current Patient can not be select for acquisition or review.
Customer Text: Current Patient can not be selected. Reset the system. Call service if the problem persists.
1105002 Error Text: Current Patient can not be deleted.

View Level: opr
Root Cause: 1
Description: Current Patient can not be deleted.
1105003 Error Text: Given Name is not entered in Add or Edit Patient Dialogue.
View Level: opr
Root Cause: 1
Description: Given Name is not entered in Add or Edit Patient Dialogue.
Customer Text: Reset the system. Call service if the problem persists.
1105004 Error Text: Family Name is not entered in Add or Edit Patient Dialogue.
View Level: opr
Root Cause: 1
Recommended Action(s): Enter complete patient information
Description: Family Name is not entered in Add or Edit Patient Dialogue.
Customer Text: Family Name is not entered. Enter complete patent information.
1105005 Error Text: Date of Birth is not entered in Add or Edit Patient Dialogue.
View Level: opr
Root Cause: 1
Description: Date of Birth is not entered in Add or Edit Patient Dialogue.
Customer Text: Date of Birth is not entered. Enter complete patent information.

GE MEDICAL SYSTEMS
1105006 Error Text: Acquisition can not be started for the selected patient from the Work list.
View Level: opr
Root Cause: 1
Description: Acquisition can not be started for the selected patient from the Work list.
Customer Text: This patient has been selected from the Work list; start the exam from the Patient List screen.
1105007 Error Text: Acquisition can not be started for the selected patient from the Patient List.
View Level: opr
Root Cause: 1
Description: Acquisition can not be started for the selected patient from the Patient List.
Customer Text: Acquisition can't initialize. Reset the system. Call service if the problem persists.
1105008 Error Text: Review can not be started for the selected patient from the Patient List.
View Level: opr
Root Cause: 1
Description: Review can not be started for the selected patient from the Patient List.
Customer Text: Patient review is unavailable. Reset the system. Call service if the problem persists.
1105009 Error Text: Patient can not be created in the database.

View Level: opr
Root Cause: 1
Description: Patient can not be created in the database.
1105010 Error Text: IQST patient can not be loaded.
View Level: opr
Root Cause: 1
Recommended Action(s): Close patient if open and Retry or Reboot the system
Description: IQST patient can not be loaded.
Customer Text: IQST patient can not be loaded. Reset the system. Call service if the problem persists.
1105011 Error Text: Services did not start successfully.

View Level: opr
Root Cause: 1
Description: Services did not start successfully.
Customer Text: Services did not start successfully. Reset the system. Call service if the problem persists.
1105012 Error Text: Services did not shut down successfully.

View Level: opr
Root Cause: 1
Description: Services did not shut down successfully.
Customer Text: Services did not shut down successfully. Reset the system. Call service if the problem
persists.

GE MEDICAL SYSTEMS
1105013 Error Text: GUI did not start successfully.
View Level: opr
Root Cause: 1
Description: GUI did not start successfully.
Customer Text: Interface did not start successfully. Reset the system. Call service if the problem persists.
1105014 Error Text: GUI did not shut down successfully.

View Level: opr
Root Cause: 1
Description: GUI did not shut down successfully.
1105900 Error Text: General error message, process and operation are undetermined.
View Level: opr
Root Cause: 1
Description: General error message, process and operation are undetermined.
1105901 Error Text: Error generated by SCP process.

View Level: opr
Root Cause: 1
Recommended Action(s): Retry the action or Reboot the system
Description: Error generated by SCP process.
Customer Text: Problem occurred. Retry or reset the system if the problem persists.
View Level: opr
Root Cause: 1
1105903 Error Text: Error generated by MAP process.

View Level: opr
Root Cause: 1
Description: Error generated by MAP process.
1105904 Error Text: Error generated by Autopilot process.

View Level: opr
Root Cause: 1
Description: Error generated by Autopilot process.
Customer Text: Autopilot problem occurred. Retry or reset the system if the problem persists.

GE MEDICAL SYSTEMS
1105920 Error Text: Process undetermined, error involves I/O operation.
View Level: opr
Root Cause: 1
Description: Process undetermined, error involves I/O operation.
1105921 Error Text: Process undetermined, error involves authentication operation.

View Level: opr
Root Cause: 1
Description: Process undetermined, error involves authentication operation.
1105999 Error Text: Mitra test error
View Level: opr
Root Cause: 1
Description: Mitra test error
1105922 Error Text: Got invalid data from Mars

View Level: opr
Root Cause: 1
Description: Mars send some data to save on the disk which is invalid
1105923 Error Text: Mars failed to send the technique values for a frame
View Level: opr
Root Cause: 1
Recommended Action(s): Check the Generator errors
Description: Mars missed to send the technique values for a frame

GE MEDICAL SYSTEMS
3.11 1106 Athena Error Management
1106000 Error Text: Failed to read the display error text file
Minor Function Impacted: ErrorReader
View Level: opr
Root Cause: 1
Recommended Action(s): Check to see if the file c:patriot_ErrorTextList.txt exits
Description: Check to see if the file c:patriot_ErrorTextList.txt exits
1106001 Error Text: Athena got an unlisted error code to display errors
View Level: opr
Root Cause: 1
Recommended Action(s): Check to see if that error code is listed in the c:ErrorTextList.txt
Description: Check to see if that error code is listed in the c:ErrorTextList.txt

GE MEDICAL SYSTEMS
3.12 12 XRImDet
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
1200007 Error Text: XRImDet is not ready, it may be in PowerFailure, ShutDown or HaltError
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Recommended Action(s): The configuration file may be unavailable or corrupted. Check to see if the configuration files
are present. If yes, refer to Precision Diagnostic Manual to run AMI Diagnostics on system
controller.
controller.
Customer Text:

View Level: opr
Root Cause: 1
controller.
controller.

View Level: opr
Root Cause: 1
controller.
controller.

View Level: opr
Root Cause: 1
controller.
controller.
1200017 Error Text: Failed to read config parameter

View Level: opr
Root Cause: 1
controller.
controller.
Customer Text: Configuration file may be corrupted. Call service to reload software.

GE MEDICAL SYSTEMS
3.13 16 XRImProc
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
1600007 Error Text: XRImProc is not ready, it may be in PowerFailure, ShutDown or HaltError
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
controller.
controller.

View Level: opr
Root Cause: 1
controller.
controller.

View Level: opr
Root Cause: 1
controller.
controller.

View Level: opr
Root Cause: 1
controller.
controller.
1600017 Error Text: Requested Mag value could not be set.

View Level: opr
Root Cause: 1
Recommended Action(s): Digital could not set the requested Mag value. Value may be out of range.
Description: Digital could not set the requested Mag value. Value may be out of range.
Customer Text: Requested Mag value could not be set. Please select another value

GE MEDICAL SYSTEMS
3.14 18 XRExpSens
View Level: opr
Root Cause: 1
Recommended Action(s): Reset the System
Description: Unable to create a required event. The software communication bus broken

View Level: opr
Root Cause: 1
Description: Unable to subscribe to a required event. The software communication bus broken

View Level: opr
Root Cause: 1
Description: Unable to bind with a required actor.The software communication bus broken

View Level: opr
Root Cause: 1
1800004 Error Text: Trigger Received for unknown actor

View Level: opr
Root Cause: 1
Description: System notified the joining of an actor which ExpSens was not interested in. There may be
configuration issues.

View Level: opr
Root Cause: 1
Description: Unable to understand and process an event.
View Level: opr
Root Cause: 1
Description: The opModeId is not an active opMode, defaulting to prime one

GE MEDICAL SYSTEMS
1800007 Error Text: XRExpSens is not ready, it may be in PowerFailure, ShutDown or HaltError
View Level: opr
Root Cause: 1
Description: XRExpSens is not ready, it may be in PowerFailure, ShutDown or HaltError
View Level: opr
Root Cause: 1
Description: One of the OpModeIds are not configured.

View Level: opr
Root Cause: 1
Description: Unable to interact with an actor.The software communication bus broken

View Level: opr
Root Cause: 1
Recommended Action(s): Component(s) - ETHERNET Communication
Description: SATURN is not responding.

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
Description: SATURN returned an unknown event.

View Level: opr
Root Cause: 1
Recommended Action(s): Reinstall the software - Call Service
Description: Software configuration problem

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
Description: Software configuration problem/System low in resources

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
3.15 20 XROpDesc
View Level: opr
Root Cause: 1
Recommended Action(s): Refer to Precision Diagnostic Manual to run AMI Diagnostics on system controller
Description: Refer to Precision Diagnostic Manual to run AMI Diagnostics on system controller

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
2000003 Error Text: XROpDesc failed to startup

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
2000010 Error Text: The OpDesc configuration files not found

View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
2000012 Error Text: OpDesc lost a frame

View Level: opr
Root Cause: 1
Recommended Action(s): Unable to track the correct frameid, the frameid id out of sync

GE MEDICAL SYSTEMS
2000013 Error Text: OpDesc failed to read config parameter
View Level: opr
Root Cause: 1
2000014 Error Text: OpDesc received negative PPD parameter

View Level: opr
Root Cause: 1
Recommended Action(s): Dose calculation module is receiving bad values.
2000015 Error Text: OpDesc calculated a dose greater than total allowed dose.
View Level: opr
Root Cause: 1
2000016 Error Text: OpDesc calculated a dap greater than total allowed dap.
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
3.16 22 XRPatPos
View Level: opr
Root Cause: 0
2200001 Error Text: Not bound to actor

View Level: opr
Root Cause: 0
2200002 Error Text: createEvent failed

View Level: opr
Root Cause: 0
Description: Software Error: In boot phase, the actor (software module) needs to create the Events to be
published. This error indicates that the actor could not create this Event. So the software shall
not function properly.
2200003 Error Text: Failed to call method

View Level: opr
Root Cause: 0
Description: Software Error: The actor (software module) tried to call other actor's (module's) method.
However, the software call failed.
2200004 Error Text: Unknown actor Joined

View Level: opr
Root Cause: 0

GE MEDICAL SYSTEMS
2200005 Error Text: Failed to read config file patpos.cfg
View Level: opr
Root Cause: 0
Description: Software Error: the actor (software module) could not read it's configuration file.
2200006 Error Text: Cannot open Configuration file PatPos.cfg to read

View Level: opr
Root Cause: 0
Description: Software Error: the actor (software module) could not find it's configuration file.
2200007 Error Text: Creation of Table Device Failed
View Level: opr
Root Cause: 0
Description: Software Error: Failed to create a software module.
2200008 Error Text: Failed to Execute the OpMode Configure Script

View Level: opr
Root Cause: 0
Description: Software Error: the actor (software module) failed to execute some commands from a script
file.
2200009 Error Text: Failed to Execute the Active OpMode Script

View Level: opr
Root Cause: 0
Description: Software Error: the actor (software module) failed to execute some commands from a script
file.

GE MEDICAL SYSTEMS
3.17 32 XRSvcMgr
3200000 Error Text: Failed to create object:
Minor Function Impacted: Control
View Level: opr
Root Cause: 1
Description: SvcMgr failed to start
Customer Text: Service Software component did not start properly.
3200001 Error Text: Failed to bind with:

View Level: opr
Root Cause: 1
Customer Text: System communication error. Try again and reset the system if problem persists.
3200002 Error Text: Create event failed for this event:

View Level: opr
Root Cause: 1
3200003 Error Text: Publish event failed for this event:
View Level: opr
Root Cause: 1
Description: Unable to publish a required event. The software communication bus broken
3200004 Error Text: Subscribe event failed for this event:

View Level: opr
Root Cause: 1
3200005 Error Text: Unsubscribe event failed for this event:

View Level: opr
Root Cause: 1
Description: Unable to unsubscribe to a required event. The software communication bus broken

GE MEDICAL SYSTEMS
3200006 Error Text: Unable to perform the requested services:
View Level: opr
Root Cause: 1
Description: The service is not able to performed, reboot the system
Customer Text: System is unable to perform action. Reset the system.
3200007 Error Text: SII failure:

View Level: opr
Root Cause: 1
Description: SII Failure, the system need to be reboot
Customer Text: System error. Reset the system.
3200008 Error Text: UponEvent cannot be processed: PowerFailure, ShutDown or Halt error occurred
View Level: opr
Root Cause: 1
Description: Unable to process the received event. PowerFailure, ShutDown or Halt error occurred
3200009 Error Text: Unable to join actor:

View Level: opr
Root Cause: 1
Description: Actor is unable to join the system, software communication problem
3200010 Error Text: Unable to identify Application from the Tag-Values passed to siiUserRequest
View Level: opr
Root Cause: 1
Description: Unable to identify Application from the Tag-Values passed to siiUserRequest
3200011 Error Text: New Application is same as the current application. User might have pressed the same
application again!
View Level: opr
Root Cause: 1
Recommended Action(s): Operator
Description: New Application is same as the current application. User might have pressed the same
application again!
3200012 Error Text: No Application is available at this moment to service this request from SUIF.
View Level: opr
Root Cause: 1
Description: No Application is available at this moment to service this request from SUIF.

GE MEDICAL SYSTEMS
3200013 Error Text: ERROR:
View Level: opr
Root Cause: 1
Description: ERROR:
3200014 Error Text: Unable to obtain handle to peer actor

View Level: opr
Root Cause: 1
Description: Unable to obtain handle to peer actor
3200015 Error Text: SERVICE APP ERROR:
View Level: opr
Root Cause: 1
Description: SERVICE APP ERROR:
3200016 Error Text: Clearing Error

View Level: opr
Root Cause: 1
Description: Clearing Error - No customer text is desired, because this error is used as a means of clearing
(erasing) INHIBIT errors generated during service applications.
3200017 Error Text: Cancelling Calibration

View Level: opr
Root Cause: 1
Recommended Action(s): Cancelling Calibration.
Description: Calibration Canceled. - No customer text is desired because this error is used as a means of
cancelling calibrations from service applications.
Customer Text: Calibration was cancelled. Please retry from start

GE MEDICAL SYSTEMS
3.18 34 XRSysMgr
3400000 Error Text: Time-out has occurred during the boot of the system
View Level: opr
Root Cause: 1
Recommended Action(s): 1. Reset the system. 2. If the problem persists, reload the application software.
Description: System did not boot within the configured boot time-out period
3400001 Error Text: Time-out has occurred during shutdown. Shutdown will be completed.
View Level: opr
Root Cause: 1
Recommended Action(s): No recommended action to be taken. System will recover from this error.
Description: System did not complete its shutdown within the configured shutdown time-out period. The
system will continue the shutdown.
3400002 Error Text: Time-out has occurred during Reset. OS Reset will be Continued.
View Level: opr
Root Cause: 1
Recommended Action(s): No recommended action to be taken. System will recover from this error.
Description: System did not complete its reset within the configured reset time-out period. The system will
continue the OS reset.
3400003 Error Text: Unable to create event

View Level: opr
Root Cause: 1
2. If the problem persists, reload the application software.
3400004 Error Text: Unable to publish event

View Level: opr
Root Cause: 1
3400005 Error Text: The system is booting.

View Level: opr
Root Cause: 1
Recommended Action(s): No recommended action to be taken.
Description: System is starting the software boot.

GE MEDICAL SYSTEMS
3400006 Error Text: EF boot phase 0 completed. All actors have bound to the actors in their list.
View Level: opr
Root Cause: 1
Description: The system is booting. Initializing system communication.
Customer Text: The system is booting. Initializing system communication.
3400007 Error Text: EF boot phase 1 completed. Communication established with the generator and/or digital.
View Level: opr
Root Cause: 1
Description: The system is booting. Initializing system communication. Completed power up for digital and
generator. Established communication between system controller and digital/generator.
Customer Text: The system is booting. Configuring the system...
3400008 Error Text: EF boot phase 2 completed.

View Level: opr
Root Cause: 1
Description: The system is booting. Configuring the system. The IUI is starting to query the subsystems
for their configured options.
Customer Text: The system is booting. Configuring the system......
3400009 Error Text: NORMAL boot phase 0 completed.
View Level: opr
Root Cause: 1
Description: The system is booting. Configuring the system. The system passes directly through this
phase without waiting for any inputs.
Customer Text: The system is booting. Configuring the system.........

View Level: opr
Root Cause: 1
Description: The system is booting. Configuring the system. The positioner configuration is complete.
Customer Text: The system is booting. Configuring the system............
3400011 Error Text: NORMAL boot phase 2 completed. System initialization and configuration completed.
View Level: opr
Root Cause: 1
Description: The system is ready for user input. Completed all system initialization and all configuration.
System is ready.
Customer Text: The System Initialization is complete.

GE MEDICAL SYSTEMS
3400012 Error Text: The system is resetting.
View Level: opr
Root Cause: 1
Description: System is starting the reset process.
3400013 Error Text: The system is shutting down.

View Level: opr
Root Cause: 1
Description: System is starting the shutdown process
3400014 Error Text: Shutdown is occurring because power failure condition exists.
View Level: opr
Root Cause: 1
Description: The system is shutting down due to a Hospital Main power failure.
Customer Text: Hospital Main power failure. System Shutdown is in progress. Please wait...
3400015 Error Text: System restart failed

View Level: opr
Root Cause: 1
Description: System restart failed after power recovery from interruption or E-stop released
Customer Text: System Restart Failed. Reset the system. Call service if the problem persists.
3400016 Error Text: System restart successful

View Level: opr
Root Cause: 1
Description: System restart successful after power recovery from interruption or E-stop released
Customer Text: System Restart successful.
3400017 Error Text: System boot successful

View Level: opr
Root Cause: 1
Recommended Action(s): “computer”
Description: System boot successful

GE MEDICAL SYSTEMS
3.19 36 XRTechMgr
3600000 Error Text: JediIF Initiation Failure
View Level: opr
Root Cause: 1
Description: DeviceComm (for system/generator CAN bus communication) initiation by JediIF failed
3600001 Error Text: JediIF Msg Block Initiation Failure

View Level: opr
Root Cause: 1
Description: Message block initiation for incoming CAN messages from generator failed
3600002 Error Text: JediIF Msg Queue Enqueue Failure

View Level: opr
Root Cause: 1
Description: JediIf msg queue enqueue failed
3600003 Error Text: XRTechMgr construction incomplete

View Level: opr
Root Cause: 1
Description: XRTechMgr construction incomplete
3600004 Error Text: XRTechMgr failed to create event

View Level: opr
Root Cause: 1
Description: XRTechMgr failed to create event
3600005 Error Text: XRTechMgr failed to subscribe event

View Level: opr
Root Cause: 1
Description: XRTechMgr failed to subscribe event
3600006 Error Text: XRTechMgr failed to publish event

View Level: opr
Root Cause: 1
Description: XRTechMgr failed to publish event

GE MEDICAL SYSTEMS
3600007 Error Text: SetKv not allowed
View Level: opr
Root Cause: 1
Recommended Action(s): Check installed protocol. Reset the system. If the problem persists, reload the software.
Description: System request SetKv not allowed for this protocol
3600008 Error Text: GetKv not allowed

View Level: opr
Root Cause: 1
Description: System request GetKv not allowed for this protocol
3600009 Error Text: SetMa not allowed
View Level: opr
Root Cause: 1
Description: System request SetMa not allowed for this protocol
3600010 Error Text: GetMa not allowed

View Level: opr
Root Cause: 1
Description: System request GetMa not allowed for this protocol
3600011 Error Text: SetMas not allowed
View Level: opr
Root Cause: 1
Description: System request SetMas not allowed for this protocol
3600012 Error Text: GetMas not allowed

View Level: opr
Root Cause: 1
Description: System request GetMas not allowed for this protocol
3600013 Error Text: SetExposureTime not allowed

View Level: opr
Root Cause: 1
Description: System request SetExposureTime not allowed for this protocol

GE MEDICAL SYSTEMS
3600014 Error Text: GetExposureTime not allowed
View Level: opr
Root Cause: 1
Description: System request GetExposureTime not allowed for this protocol
3600015 Error Text: IncrementExposureTime not allowed

View Level: opr
Root Cause: 1
Description: System request IncrementExposureTime not allowed for this protocol
3600016 Error Text: SetFocalSpot not allowed
View Level: opr
Root Cause: 1
Description: System request SetFocalSpot not allowed for this protocol
3600017 Error Text: GetFocalSpot not allowed

View Level: opr
Root Cause: 1
Description: System request GetFocalSpot not allowed for this protocol
3600018 Error Text: Clear Opmodes config failed
View Level: opr
Root Cause: 1
Description: Unloading protocol failed
3600019 Error Text: Load appSetup scripts failed

View Level: opr
Root Cause: 1
Description: Loading protocol failed
3600020 Error Text: Execute appSetup scripts failed

View Level: opr
Root Cause: 1
Description: Loading protocol failed

GE MEDICAL SYSTEMS
3600021 Error Text: Execute activeOpmode scripts failed
View Level: opr
Root Cause: 1
Description: Configure system for requested protocol failed
3600022 Error Text: Invalid active opmode requested

View Level: opr
Root Cause: 1
Description: Invalid protocol requested
3600023 Error Text: Get Gitane set retry num failed

View Level: opr
Root Cause: 1
Recommended Action(s): Check TechMgr config file. Reset the system. If the problem persists, reload the software
Description: Get Gitane firmware register set retry number failed. Check TechMgr config file
3600024 Error Text: Jedi Power Up Failure

View Level: opr
Root Cause: 1
Description: Generator Power Up Failure
Customer Text: Communication could not be established with generator. Attempting to complete boot.
3600025 Error Text: Jedi Status in Error condition

View Level: opr
Root Cause: 1
Recommended Action(s): Generator error. Refer Generator manual for information
Description: Generator Status in Error condition
Customer Text: Generator error. Release exposure switch and try again. Call service if problem persists.
3600026 Error Text: Generator Status in Error condition class 3

View Level: opr
Root Cause: 1
Recommended Action(s): Possible generator error. Run generator diagnostics from SUIF
Description: Generator error during exposure and causing current exposure to stop

View Level: opr
Root Cause: 1
Description: Generator error occurred causing current exposure to stop

GE MEDICAL SYSTEMS
3600028 Error Text: Generator or tube temperature limits are reached.
Recovery Class: INHIBIT
View Level: opr
Root Cause: 1
Recommended Action(s): Generator error. Refer Generator manual for information
Description: Generator permanent error occurred. These errors appear when the generator or tube
temperature limits are reached.
Customer Text: Generator error occurred. Wait before retrying exposure. Call service if the problem persists.
3600029 Error Text: XRTechMgr failed to get NotifyJediId from JEDI

View Level: opr
Root Cause: 1
Description: XRTechMgr failed to get NotifyJediId from generator
3600030 Error Text: SystemId and JediId conflict
View Level: opr
Root Cause: 1
Description: SystemId and JediId conflict
3600031 Error Text: XRTechMgr failed to get ReplyJediCapabilities from JEDI

View Level: opr
Root Cause: 1
Description: XRTechMgr failed to get ReplyJediCapabilities from generator
3600032 Error Text: XRTechMgr failed to get StaticId from JEDI

View Level: opr
Root Cause: 1
Description: XRTechMgr failed to get StaticId from generator
3600033 Error Text: XRTechMgr failed to get SetLimitedParameters from JEDI

View Level: opr
Root Cause: 1
Description: XRTechMgr failed to get SetLimitedParameters from generator
3600034 Error Text: XRTechMgr failed to get ConfirmAecConfig from JEDI

View Level: opr
Root Cause: 1
Description: XRTechMgr failed to get ConfirmAecConfig from generator

GE MEDICAL SYSTEMS
3600035 Error Text: XRTechMgr failed to get ConfirmSelectTube from JEDI
View Level: opr
Root Cause: 1
Description: XRTechMgr failed to get ConfirmSelectTube from generator
Customer Text:
3600036 Error Text: XRTechMgr failed to send NotifySystemId to JEDI

View Level: opr
Root Cause: 1
Description: XRTechMgr failed to send NotifySystemId to generator
3600037 Error Text: XRTechMgr failed to send ReplySystemConfig to JEDI

View Level: opr
Root Cause: 1
Description: XRTechMgr failed to send ReplySystemConfig to generator
3600038 Error Text: Jedi technique limit reached

View Level: opr
Root Cause: 1
Recommended Action(s): Generator Problem. Refer to Generator manual for information
Description: generator technique limit reached.
3600039 Error Text: Jedi rejects old techniques

View Level: opr
Root Cause: 1
Description: generator rejects old techniques.
3600040 Error Text: Generator / tube spit error
View Level: opr
Root Cause: 1
Recommended Action(s): System will recover. Run generator No Load HV Diag if error is frequently occurring.
Description: generator spit error
Customer Text: Generator / tube kVp spit occurred; the image may be light.
3600041 Error Text: AEC backup time reached

View Level: opr
Root Cause: 1
Description: AEC backup time reached during exposure
Customer Text: AEC back-up time reached. Image quality may not be optimum.

GE MEDICAL SYSTEMS
3600042 Error Text: Jedi select tube failed
View Level: opr
Root Cause: 1
Recommended Action(s): Possible generator tube switch failure. Run second tube switch diagnostic from the SUIF
Description: generator select tube failed
3600043 Error Text: Gitane failed to set register correctly

View Level: opr
Root Cause: 1
Recommended Action(s): Possible system controller failure. Run Gitane diagnostic via SUIF
Description: Gitane failed to set register correctly
Customer Text: System control error. Release exposure switch and try again. Reset system if problem
persists.
3600044 Error Text: System Controller Gitane acquisition register is not correct.
View Level: opr
Root Cause: 1
Recommended Action(s): Possible system controller failure. Run Gitane diagnostic via SUIF
Description: The Gitane acquisition register not correct for selected acquisition mode. Reset and call
service if the problem persists.
persists.
3600045 Error Text: Jedi reject technique error

View Level: opr
Root Cause: 1
Recommended Action(s): Generator self-protection error.
Description: Generator rejects technique
Customer Text: Selected technic exceeds X-ray tube limits. Wait for tube to cool or select a lower technic.
3600046 Error Text: Maximum kVp reached
View Level: opr
Root Cause: 1
Recommended Action(s): No Action required
Description: Maximum kVp reached
Customer Text: Maximum kVp has been selected.
3600047 Error Text: Minimum kVp reached

View Level: opr
Root Cause: 1
Description: Minimum kVp reached
Customer Text: Minimum kVp has been selected.

GE MEDICAL SYSTEMS
3600048 Error Text: Maximum mA for generator kW
View Level: opr
Root Cause: 1
Description: Maximum mA for generator kW
Customer Text: Maximum mA has been selected.
3600049 Error Text: Minimum mA for generator kW

View Level: opr
Root Cause: 1
Description: Minimum mA for generator kW
Customer Text: Minimum mA has been selected.
3600050 Error Text: Maximum time for generator

View Level: opr
Root Cause: 1
Description: Maximum time for generator
Customer Text: Maximum time has been selected for mA, mAs.
3600051 Error Text: Minimum time for generator

View Level: opr
Root Cause: 1
Description: Minimum time for generator
Customer Text: Minimum time has been selected for mA, mAs.
3600052 Error Text: Maximum mA for kVp selected

View Level: opr
Root Cause: 1
Description: Maximum mA for kVp selected
Customer Text: Maximum mA for selected kVp and focal spot.
3600053 Error Text: Maximum mAs for generator

View Level: opr
Root Cause: 1
Description: Maximum mAs for generator
Customer Text: Maximum mAs for generator has been selected.
3600054 Error Text: Minimum mAs for generator

View Level: opr
Root Cause: 1
Description: Minimum mAs for generator
Customer Text: Minimum mAs for generator has been selected.

GE MEDICAL SYSTEMS
3600055 Error Text: Generator mode failed
View Level: opr
Root Cause: 1
Recommended Action(s): Hardware Problem
Description: Generator mode failed
3600056 Error Text: Generator filament selection failed

View Level: opr
Root Cause: 1
Description: Generator filament selection failed
Customer Text: Reselect protocol, change focal spot or adjust technic to continue.
3600057 Error Text: Generator kV is too low or mA/mAs is too low or the exposure time is too short
View Level: opr
Root Cause: 1
Recommended Action(s): Modify the technique by increasing kV, mA/mAs, and/or the exposure time to proceed.
Description: Generator rejected technique. Operator must select a higher kV or higher mA/mAs or longer
exposure time to proceed.
Customer Text: Increase kV, mA/mAs, and/or the exposure time to continue.
3600058 Error Text: Generator kV is too low or mA/mAs is too low or the exposure time is too long
View Level: opr
Root Cause: 1
Recommended Action(s): Generator technique error. Modify the technique by increasing kV, mA/mAs, and/or
decreasing the exposure time to proceed.
Description: Generator rejected technique. Operator must select a higher kV or higher mA/mAs or shorter
Customer Text: Increase kV, mA/mAs, and/or decrease the exposure time to continue.
3600059 Error Text: Generator kV is too low or mA/mAs is too low

View Level: opr
Root Cause: 1
Recommended Action(s): Modify the technique by increasing kV and/or mA/mAs to proceed.
Description: Generator rejected technique. Operator must select a higher kV or higher mA/mAs to
proceed.
Customer Text: Increase kV and/or mA/mAs to continue.
3600060 Error Text: Generator kV is too high or the exposure time is too short or mA/mAs is too high
View Level: opr
Root Cause: 1
Recommended Action(s): Modify the technique by increasing kV, exposure time, and/or decreasing mA/mAs to
proceed.
Description: Generator rejected technique. Operator must select a higher kV or lower mA/mAs or longer
Customer Text: Increase kV, exposure time and/or decrease mA/mAs to continue.

GE MEDICAL SYSTEMS
3600061 Error Text: Generator kV is too low or mA/mAs is too high or the exposure time is too long
View Level: opr
Root Cause: 1
Recommended Action(s): Modify the technique by increasing kV and/or decreasing mA/mAs and exposure time to
proceed.
Description: Generator rejected technique. Operator must select a higher kV or lower mA/mAs or shorter
Customer Text: Increase kV and/or decrease mA/mAs and exposure time to continue.
3600062 Error Text: Generator kV is too low or mA/mAs is too high

View Level: opr
Root Cause: 1
Recommended Action(s): Modify the technique by increasing kV and/or decreasing mA/mAs to proceed.
Description: Generator rejected technique. Operator must select a higher kV or lower mA/mAs to proceed.
Customer Text: Increase kV and/or decrease mA/mAs to continue.
3600063 Error Text: Generator kV too low or the exposure time is too short
View Level: opr
Root Cause: 1
Recommended Action(s): Modify the technique by increasing kV and/or the exposure time to proceed.
Description: Generator rejected technique. Operator must select a higher kV or longer exposure time to
proceed.
Customer Text: Increase kV and/or the exposure time to continue.
3600064 Error Text: Generator kV too low or the exposure time is too long
View Level: opr
Root Cause: 1
Recommended Action(s): Modify the technique by increasing kV and/or decreasing the exposure time to proceed.
Description: Generator rejected technique. Operator must select a higher kV or shorter exposure time to
proceed.
Customer Text: Increase kV and/or decrease the exposure time to continue.
3600065 Error Text: Generator kV too low
View Level: opr
Root Cause: 1
Recommended Action(s): Modify the technique by increasing kV to proceed.
Description: Generator rejected technique. Operator must select a higher kV to proceed.
Customer Text: Increase the kV to continue.
3600066 Error Text: Generator kV too high or the exposure time is too short or mA/mAs too low
View Level: opr
Root Cause: 1
Recommended Action(s): Modify the technique by decreasing kV and/or increasing mA/mAs and exposure time to
proceed.
Description: Generator rejected technique. Operator must select a lower kV or a higher mA/mAs or a
longer exposure time to proceed.
Customer Text: Decrease kV and/or increase mA/mAs and exposure time to continue.

GE MEDICAL SYSTEMS
3600067 Error Text: Generator kV too high or the exposure time too long or mA/mAs too low
View Level: opr
Root Cause: 1
Recommended Action(s): Modify the technique by decreasing kV and the exposure time and/or increasing the mA/mAs
to proceed.
Description: Generator rejected technique. Operator must select a lower kV or a higher mA/mAs or a
shorter exposure time to proceed.
Customer Text: Decrease kV and the exposure time and/or increase the mA/mAs to continue.
3600068 Error Text: Generator kV too high or mA/mAs too low

View Level: opr
Root Cause: 1
Recommended Action(s): Modify the technique by decreasing kV and/or increasing mA/mAs to proceed.
Description: Generator rejected technique. Operator must select a lower kV or a higher mA/mAs to
proceed.
Customer Text: Decrease kV and/or increase mA/mAs to continue.
3600069 Error Text: Generator kV and mA/mAs too high or exposure time too short
View Level: opr
Root Cause: 1
Recommended Action(s): Modify the technique by decreasing kV and mA/mAs and/or increasing the exposure time to
proceed.
Description: Generator rejected technique. Operator must select a lower kV or a lower mA/mAs or a longer
Customer Text: Decrease kV and mA/mAs and/or increase the exposure time to continue.
3600070 Error Text: Generator kV too high or mA/mAs too high

View Level: opr
Root Cause: 1
Recommended Action(s): Modify the technique by decreasing kV and/or mA/mAs to proceed.
Description: Generator rejected technique. Operator must select a lower kV or a higher mA/mAs to
proceed.
Customer Text: Decrease kV and/or mA/mAs to continue.
3600071 Error Text: Generator kV too high or exposure time too short
View Level: opr
Root Cause: 1
Recommended Action(s): Modify the technique by decreasing kV and/or increasing the exposure time to proceed.
Description: Generator rejected technique. Operator must select a lower kV or a longer exposure time to
proceed.
Customer Text: Decrease kV and/or increase the exposure time to continue.
3600072 Error Text: Generator kV too high or the exposure time too long
View Level: opr
Root Cause: 1
Recommended Action(s): Modify the technique by decreasing kV and/or the exposure time to proceed.
Description: Generator rejected technique. Operator must select a lower kV or a shorter exposure time to
proceed.
Customer Text: Decrease kV and/or the exposure time to continue.

GE MEDICAL SYSTEMS
3600073 Error Text: Generator kV too high
View Level: opr
Root Cause: 1
Recommended Action(s): Modify the technique by decreasing kV to proceed.
Description: Generator rejected technique. Operator must select a lower kV to proceed.
Customer Text: Decrease the kV to continue.
3600074 Error Text: Generator mA/mAs too low or exposure time too short
View Level: opr
Root Cause: 1
Recommended Action(s): Modify the technique by increasing the mA/mAs and/or the exposure time to proceed.
Description: Generator rejected technique. Operator must select a higher mA/mAs or a longer exposure
time to proceed.
Customer Text: Increase the mA/mAs and/or the exposure time to continue.
3600075 Error Text: Generator mA/mAs too low or exposure time too long
View Level: opr
Root Cause: 1
Recommended Action(s): Modify technique by increasing the mA/mAs and/or decreasing the to proceed.
Description: Generator rejected technique. Operator must select a higher mA/mAs or a shorter exposure
time to proceed.
Customer Text: Increase the mA/mAs and/or decrease the exposure time to continue.
3600076 Error Text: Generator mA/mAs too low
View Level: opr
Root Cause: 1
Recommended Action(s): Modify technique by increasing the mA/mAs to proceed.
Description: Generator rejected technique. Operator must select a higher mA/mAs to proceed.
Customer Text: Increase the mA/mAs to continue.
3600077 Error Text: Generator mA/mAs too high or exposure time too short
View Level: opr
Root Cause: 1
Recommended Action(s): Modify technique by decreasing the mA/mAs and/or increasing the exposure time to proceed.
Description: Generator rejected technique. Operator must select a lower mA/mAs or a longer exposure
time to proceed.
Customer Text: Decrease the mA/mAs and/or increase the exposure time to continue.
3600078 Error Text: Generator mA/mAs too high or exposure time too long
View Level: opr
Root Cause: 1
Recommended Action(s): Modify technique by decreasing the mA/mAs and/or the exposure time to proceed.
Description: Generator rejected technique. Operator must select a lower mA/mAs or shorter exposure
time to proceed.
Customer Text: Decrease the mA/mAs and/or the exposure time to continue.

GE MEDICAL SYSTEMS
3600079 Error Text: Generator mA/mAs too high
View Level: opr
Root Cause: 1
Recommended Action(s): Modify technique by decreasing the mA/mAs to proceed.
Description: Generator rejected technique. Operator must select a lower mA/mAs to proceed.
Customer Text: Decrease the mA/mAs to continue.
3600080 Error Text: Generator exposure time too short

View Level: opr
Root Cause: 1
Recommended Action(s): Modify technique by increasing the exposure time to proceed.
Description: Generator rejected technique. Operator must select a longer exposure time to proceed.
Customer Text: Increase the exposure time to continue.
3600081 Error Text: Generator exposure time too long

View Level: opr
Root Cause: 1
Recommended Action(s): Modify technique by decreasing the exposure time to proceed.
Description: Generator rejected technique. Operator must select a shorter exposure time to proceed.
Customer Text: Decrease the exposure time to continue.
3600082 Error Text: Generator thermal limit reached

View Level: opr
Root Cause: 1
Recommended Action(s): Hardware Problem. Wait for tube cool or decrease techniques
Description: Generator thermal limit reached
Customer Text: Thermal limit has been reached. Wait for tube to cool or decrease the technic.

View Level: opr
Root Cause: 1
Description: Generator filament selection failed
3600084 Error Text: mA is 0 for setMA/setMAs

View Level: opr
Root Cause: 1
Recommended Action(s): Increase mA or mAs
Description: mA is 0 for setMA/setMAs
Customer Text: Increase mA or reselect protocol to continue.
3600085 Error Text: Maximum mA reached

View Level: opr
Root Cause: 1
Description: Maximum mA reached

GE MEDICAL SYSTEMS
3600086 Error Text: Minimum mA reached
View Level: opr
Root Cause: 1
Description: Minimum mA reached
3600087 Error Text: Maximum mA for selected kVp, focal spot

View Level: opr
Root Cause: 1
Description: Maximum mA for selected kVp, focal spot
Customer Text: Maximum mA has been selected for kVp, focal spot.
3600088 Error Text: Minimum mA for selected kVp, focal spot

View Level: opr
Root Cause: 1
Description: Minimum mA for selected kVp, focal spot
Customer Text: Minimum mA has been selected for kVp, focal spot.
3600089 Error Text: Digital mode techniques rejected by generator

View Level: opr
Root Cause: 1
Recommended Action(s): Check trajectory values
Description: Digital mode techniques rejected by generator. Possibly bad trajectory. Selecting another
FOV or another protocol will select another trajectory. The user can also reduce the record
frame rate.
Customer Text: Reduce the frame rate or select another FOV or select another protocol to continue.
3600090 Error Text: Current collimator size less than ion chambers selected, center cell selected
View Level: opr
Root Cause: 1
Description: Current collimator size less than ion chambers selected, center cell selected
Customer Text: Collimator field size is less than selected ion chamber area; center area will be used.
3600091 Error Text: Wait for tube filament to stabilize

View Level: opr
Root Cause: 1
Description: Wait for tube filament to stabilize
Customer Text: Wait for X-ray tube filament to stabilize.

GE MEDICAL SYSTEMS
3600092 Error Text: setLimitedFineParameters: kV+
View Level: opr
Root Cause: 1
Recommended Action(s): Try fluoro again. Reselect the protocol.
Description: setLimitedFineParameters: kV+ During fluoro or digital record, this means the EM loop
provided a technic which was rejected by the generator. The generator will ignore this and
exposures will continue. Image Quality may not be optimal. It is possible that other related
EM loop errors may occur.
Customer Text: Desired technic was not reached; image quality may not be optimal. Restart fluoro.
3600093 Error Text: setLimitedFineParameters: kV-

View Level: opr
Root Cause: 1
Description: setLimitedFineParameters: kV- During fluoro or digital record, this means the EM loop
3600094 Error Text: setLimitedFineParameters: mA+

View Level: opr
Root Cause: 1
Description: setLimitedFineParameters: mA+ During fluoro or digital record, this means the EM loop
3600095 Error Text: setLimitedFineParameters: mA-

View Level: opr
Root Cause: 1
Description: setLimitedFineParameters: mA- During fluoro or digital record, this means the EM loop
3600096 Error Text: setLimitedFineParameters: ms+

View Level: opr
Root Cause: 1
Description: setLimitedFineParameters: ms+ During fluoro or digital record, this means the EM loop

GE MEDICAL SYSTEMS
3600097 Error Text: setLimitedFineParameters: ms-
View Level: opr
Root Cause: 1
Description: setLimitedFineParameters: ms- During fluoro or digital record, this means the EM loop
3600098 Error Text: setLimitedFineParameters: power+

View Level: opr
Root Cause: 1
Description: setLimitedFineParameters: power+ During fluoro or digital record, this means the EM loop
3600099 Error Text: setLimitedFineParameters: power-

View Level: opr
Root Cause: 1
Description: setLimitedFineParameters: power- During fluoro or digital record, this means the EM loop
3600100 Error Text: setLimitedFineParameters: mAs+

View Level: opr
Root Cause: 1
Description: setLimitedFineParameters: mAs+ During fluoro or digital record, this means the EM loop
3600101 Error Text: setLimitedFineParameters: mAs-

View Level: opr
Root Cause: 1
Description: setLimitedFineParameters: mAs- During fluoro or digital record, this means the EM loop

GE MEDICAL SYSTEMS
3600102 Error Text: setLimitedFineParameters: Thermic+
View Level: opr
Root Cause: 1
Description: setLimitedFineParameters: Thermic+ During fluoro or digital record, this means the EM loop
provided a technic which was rejected by the Generator. The generator will ignore this and
3600103 Error Text: setLimitedFineParameters: unknown reject

View Level: opr
Root Cause: 1
Description: setLimitedFineParameters: unknown reject During fluoro or digital record, this means the EM
loop provided a technic which was rejected by the generator. The generator will ignore this
and exposures will continue. Image Quality may not be optimal. It is possible that other
related EM loop errors may occur.
3600104 Error Text: setLimitedFineParameters: Thermic-

View Level: opr
Root Cause: 1
Description: setLimitedFineParameters: Thermic- During fluoro or digital record, this means the EM loop
3600105 Error Text: Config Cache error

View Level: opr
Root Cause: 1
Recommended Action(s): Check config cache value
Description: Config cache error
3600106 Error Text: Time out while expecting CAN message from generator
View Level: opr
Root Cause: 1
Recommended Action(s): Check system/Generator CAN bus cable
Description: Time out while expecting CAN message from generator. It will be reported when TechMgr
times out while waiting for CAN message from JEDI, which mostly indicates that the
TechMgr/JEDI CAN communication failed. (Ref: XRYge38512, No error reported when Jedi
fails to communicate with Techmgr)
Customer Text: Generator error. Reset system. Call service if the problem persists.
3600107 Error Text: Generator time synchronization failure

View Level: opr
Root Cause: 1
Recommended Action(s): Reset the system. If problem persists, call service
Description: Generator internal time can not be synchronized with the system time

GE MEDICAL SYSTEMS
3600108 Error Text: Generator software update failure
View Level: opr
Root Cause: 1
3600109 Error Text: Generator did not send Ready For Exposure or standby Response
View Level: opr
Root Cause: 1
3600110 Error Text: Event unscribe failed

View Level: opr
Root Cause: 1
3600111 Error Text: DSA Trial exposure AEC backup time reached
View Level: opr
Root Cause: 1
Recommended Action(s): “Possible generator error. Run generator diagnostics from SUIF
Description: “AEC backup time reached during the DSA trial exposure. The DSA sequence will not be
allowed to continue when the trial is unsuccessful.
Customer Text: The trial AEC back-up time was reached. Release the exposure switches and try again.
3600112 Error Text: Generator / tube spit error DSA trial
View Level: opr
Root Cause: 1
Recommended Action(s): “System shall recover. Run generator No Load HV Diag if error is frequently occurring.
Description: “A generator or X-ray tube spit error occurred during the DSA trial; sequence is aborted and
user must retry.
Customer Text: A generator error occurred during the DSA trial. Release the exposure switches and try again.
3600113 Error Text: setLimitedFineParameters: ms-

View Level: opr
Root Cause: 1
Recommended Action(s): “Try fluoro again. Reselect the protocol.
Description: “setLimitedFineParameters: ms-
During fluoro or digital record, this means the EM loop provided a technic which was rejected
by the generator. The generator will ignore this and exposures will continue. Image Quality
may not be optimal. It is possible that other related EM loop errors may occur.
Customer Text: “The selected technic exceeds system limits. Decrease magnification and retry.
3601000 Error Text: Generator status in error condition class 1
Major Function Impacted: Gen
View Level: opr
Root Cause: 1
Recommended Action(s): System Error is engineering use and do not indicate any hardware error failure.
Description: Generator class 1 error, debug

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
Recommended Action(s): Determine Jedi error in debug text and refer to the Precision Diagnostic Manual
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
Recommended Action(s): System Error is engineering use and do not indicate any hardware error failure.
Description: Generator class 1 error, abort

View Level: opr
Root Cause: 1
Recommended Action(s): Possible generator error. Run No Load HV and inverter diagnostics from SUIF

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Recommended Action(s): Determine Jedi error in debug text and refer to the Precision Diagnostic Manual

View Level: opr
Root Cause: 1
3601010 Error Text: Generator Error: 40-0102(4): error msg from Rotor FW; Database not correct
View Level: opr
Root Cause: 1
Recommended Action(s): Reload NVRam database. It might be necessary to replace Rotation board.
Description: The firmware of the rotation board has detected that the data base received from the kV
control board has wrong data.
Potential Cause: Wrong kV control data base. It can only happen at power up
Recommended Action:
1) Restore database.
2) Replace rotation bd.
3601011 Error Text: Generator Error 40-0107(4): error msg from Rotor FW; Inverter permanent over current
View Level: opr
Root Cause: 1
Recommended Action(s): Perform one of the three actions. Check wiring from rotation board to tube. Replace Rotation
board. Troubleshoot tube windings (replace tube).
Description: An over current has been detected and 3 restarts have been tried unsuccessfully, within a
single rotation state.
Potential Cause:
1. Rotation board
2. Tube stator winding short circuit
3. Wiring incorrect (shorted)
Recommended Action:
- Check wiring from rotation board to tube.
- Replace Rotation board.
- Troubleshoot tube windings (replace tube).
Customer Text: Critical generator error. Call Service. Do not use the system.
3601012 Error Text: Generator Error 40-0110(4): error msg from Rotor FW; PRD error (Z3 Z4 = bitmap)
View Level: opr
Root Cause: 1
Recommended Action(s): Retry or Replace Rotation board.
Description: Firmware checksum, RAM test and EPLD access are performed at power up or reset.
Potential Cause: Rotation board.
Recommended Action:
- Retry

GE MEDICAL SYSTEMS
3601013 Error Text: Generator Error 50-0201;(4): Heater 0: no CAN message received within 5 secs
View Level: opr
Root Cause: 1
Recommended Action(s): Unlikely to happen. This is a debug error. Re-initialize and retry. Run CAN communication
diag.
Description: The Heater board has not received any command from the kV control main software for the
last 5 seconds. This is interpreted as a loss of communication.
Potential Cause:
1. kV Control main software lost.
2. kV control or Heater board driver failure.
3. Bad contact on one of the pin on the CAN bus line connector.
Recommended Action:
- Retry
- Reset and retry.
3601014 Error Text: Generator Error 50-0202;(4): Heater 0: database not correct
View Level: opr
Root Cause: 1
Recommended Action(s): Run Jedi diagnostic from SUIF
Description: Heater 0: database not correct. Generator error occurred causing current exposure to stop
3601015 Error Text: Generator Error 50-0213;(4): Heater 0: PRD error (Z3 Z4 = bitmap)
View Level: opr
Root Cause: 1
Recommended Action(s): Try again. If the error persists, replace the heater board.
Potential Cause: Heater board.
Recommended Action: Try again. If the error persists, replace the heater board.
3601016 Error Text: Generator Error 50-0221;(4): Heater 0: filaments database tube1 err (Z3= LF Z4=SF)
View Level: opr
Root Cause: 1
Recommended Action(s): Reload NVRam data base. It might be necessary to replace Heater board. (large focus)
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
3601018 Error Text: Generator Error 50-0223(4): Heater 0: filaments database tube3 err (Z3= LF Z4=SF)
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
Description: The firmware of the heater board has detected that the Received Data base from kV control
contains erroneous data for Tube 1, 2, 3, or 4.
3601020 Error Text: Generator Error 50-1202 (4): Heater 1: database not correct
View Level: opr
Root Cause: 1
Recommended Action(s): Run TBD Jedi diagnostic from SUIF
Description: Heater 1: database not correct. Generator error occurred causing current exposure to stop.
View Level: opr
Root Cause: 1
Recommended Action(s): Try again. If the error persists, replace the heater board.
View Level: opr
Root Cause: 1
Recommended Action(s): Reload NVRam data base. It might be necessary to replace Heater board. (small focus)
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
3601026 Error Text: Generator Error 60-0802;(3): Exposure backup time exceeded
View Level: opr
Root Cause: 1
Recommended Action(s): Retry, changing parameters and duration0. disconnect system-Generator cable in different
places and check exposure command line voltage
Description: The exposure command last longer than the duration that was loaded by the system (Backup
time + 5%.).
Potential Causes:
1. System
2. System-Generator cable
3. I/F board: exposure line stuck to the active state
Recommended Action:
- Retry, changing parameters and duration.
- Disconnect system-Generator cable in different places and check exposure command line
voltage
3601027 Error Text: Generator Error 60-0803;(3): Exp cmd while generator not ready
View Level: opr
Root Cause: 1
Recommended Action(s): If problem is persistent, check heater, anode rotation and system to Generator preparation
command to find the root cause for the Generator not to be ready
Description: Generator received an exposure command while not in ready state.
Potential Cause:
0. Software bug/problem.
1. Cable / communication problem.
2. External cause (Spikes).
Recommended Action: If problem is persistent, check heater, anode rotation and system to
Generator preparation command to find the root cause for the Generator not to be ready.

GE MEDICAL SYSTEMS
3601028 Error Text: Generator Error 60-1408;(3): AEC does not count
View Level: opr
Root Cause: 1
Recommended Action(s): Run Generator AEC diagnostic
Description: If there is no AEC feedback in AEC station exposure.
Potential Cause:
1. ION chamber
2. AEC cable, connection.
3. AEC board.
Recommended Action: Run AEC diagnostics (See diagnostics)
Customer Text: Exposure stopped - No AEC brightness. Try again. Call service if problem persists.
3601029 Error Text: Generator Error 80-1000;(4): Tube Switch communication problem
View Level: opr
Root Cause: 1
Description: Tube Switch communication problem.
Potential Cause:
1. Tube Switch Board.
2. Control Bus cable.
3. KV control.
Recommended Action:
A. Check that Tube Switch firmware is running (DS3/4 Led are lit successively).If no:
1/ Verify +15V/-15V (DS1 & DS2 are lit): if they are wrong, go to +/-15V errors
troubleshooting.
2/ verify that RST Led (DS5) is not lit. If it is lit, disconnect successively the control bus cable
from rotation board and kV control to find the board which is holding the reset line and replace
it. If after disconnecting all the boards, the Led remains lit, replace Tube Switch board.
B. Verify the flat cable between kV control and auxiliary module is correctly connected until
the Tube Switch board C, else replace kV control board
Customer Text: X-ray tube selection error. Reselect tube and continue.
3601030 Error Text: Generator Error 80-1010;(4): Tube Switch board has reset
View Level: opr
Root Cause: 1
Description: Tube Switch board has reset.
Potential Cause:
2. Interference (Spikes).
Recommended Action:
- Re-initialize system, retry.
- If persistent, replace board or check power and grounding.

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
3601032 Error Text: Generator error 110-804;(5): Tank Thermal sensor to high.
View Level: opr
Root Cause: 1
Recommended Action(s): Stop acquisition and wait for cooling
Description: HV tank temperature measurement has reached 67 degree c for Precision 500D.
Potential Cause:
1. HV tank too hot.
2. HV tank.
3. kV control.
Recommended Action:
- Wait for error clearance.
- If persistent while HV Tank is cool:
1/check LED DS1 on kV control (top and right of board). If it is off, change kV control.
2/check flat cable connection between HV Tank and kV control board.
3/replace HV tank.
4/replace kV control.
Customer Text: Generator temperature is too high. Allow the generator to cool and try again.
3601033 Error Text: Generator error 110-805;(5): Inverter HW temperature too high.
View Level: opr
Root Cause: 1
Description: Inverter HW temperature too high.
3601034 Error Text: Generator error 110-806;(5): Lp temperature too high.

View Level: opr
Root Cause: 1
3601035 Error Text: Generator error 110-903;(5): Tube exceeded 70degC.

View Level: opr
Root Cause: 1
Description: Tube exceeded 70degC
Customer Text: Tube temperature exceeded limits. Stop acquisition and wait for tube to cool.
3601036 Error Text: Generator error 110-904;(5): HW signal from Rotor board; HEMIT Error.
View Level: opr
Root Cause: 1
3601037 Error Text: Generator error 110-905;(5): Tube thermal protection.

View Level: opr
Root Cause: 1
Description: Tube thermal protection

GE MEDICAL SYSTEMS
3601050 Error Text: Generator error class 1: error msg from Rotor FW, CAN Domain command number error
View Level: opr
Root Cause: 1
Description: error msg from Rotor FW, CAN Domain command number error
3601051 Error Text: Generator error class 1: error msg from Rotor FW, CAN Domain request with no transfer init
View Level: opr
Root Cause: 1
Description: error msg from Rotor FW, CAN Domain request with no transfer init
3601052 Error Text: Generator error class 1: error msg from Rotor FW, CAN Domain Toggle bit error
View Level: opr
Root Cause: 1
Description: error msg from Rotor FW, CAN Domain Toggle bit error
3601053 Error Text: Generator error class 1: error msg from Rotor FW, CAN Domain: less than 2 data to download
View Level: opr
Root Cause: 1
Description: error msg from Rotor FW, CAN Domain: less than 2 data to download
3601054 Error Text: Generator error class 1: error msg from Rotor FW, CAN Domain Abort received & applied
View Level: opr
Root Cause: 1
Description: error msg from Rotor FW, CAN Domain Abort received & applied
3601055 Error Text: Generator error class 1: error msg from Rotor FW, Bad index in config upload
View Level: opr
Root Cause: 1
Description: error msg from Rotor FW, Bad index in config upload
3601056 Error Text: Generator error class 1: error msg from Rotor FW, Tube switch while rotor not off
View Level: opr
Root Cause: 1
Description: error msg from Rotor FW, Tube switch while rotor not off

GE MEDICAL SYSTEMS
3601057 Error Text: Generator error class 1: error msg from Rotor FW, Acceleration cmd while no tube selected
View Level: opr
Root Cause: 1
Description: error msg from Rotor FW, Acceleration cmd while no tube selected
3601058 Error Text: Generator error class 1: error msg from Rotor FW, Acceleration cmd while database not OK
View Level: opr
Root Cause: 1
Description: error msg from Rotor FW, Acceleration cmd while database not OK
3601059 Error Text: Generator error class 1: error msg from Rotor FW, Database download while rotor speeding
View Level: opr
Root Cause: 1
Description: error msg from Rotor FW, Database download while rotor speeding
3601060 Error Text: Generator error class 1: error msg from Rotor FW, Acceleration command not OK
View Level: opr
Root Cause: 1
Description: error msg from Rotor FW, Acceleration command not OK
3601061 Error Text: Generator error class 1: error msg from Rotor FW, Acceleration while in error
View Level: opr
Root Cause: 1
Description: error msg from Rotor FW, Acceleration while in error
3601062 Error Text: Generator error class 1: error msg from Rotor FW, No CAN message received within 4 sec.
View Level: opr
Root Cause: 1
Description: error msg from Rotor FW, No CAN message received within 4 sec.
3601063 Error Text: Generator error class 1: error msg from Rotor FW, Inverter over current (< 3 times)
View Level: opr
Root Cause: 1
Description: error msg from Rotor FW, Inverter over current (< 3 times)

GE MEDICAL SYSTEMS
3601064 Error Text: Generator error class 1: error msg from Rotor FW, Unknown warning
View Level: opr
Root Cause: 1
Description: error msg from Rotor FW, Unknown warning
3601065 Error Text: Generator error class 1: Heater 0: received command is not OK
View Level: opr
Root Cause: 1
Description: Heater 0: received command is not OK
3601066 Error Text: Generator error class 1: Heater 0: command not OK
View Level: opr
Root Cause: 1
Description: Heater 0: command not OK
3601067 Error Text: Generator error class 1: Heater 0: inverter over current (inverter1) (<3 times)
View Level: opr
Root Cause: 1
Description: Heater 0: inverter over current (inverter1) (<3 times)
3601068 Error Text: Generator error class 1: Heater 0: filament open circuit (inverter1) (<3 times)
View Level: opr
Root Cause: 1
Description: Heater 0: filament open circuit (inverter1) (<3 times)
3601069 Error Text: Generator error class 1: Heater 0: inverter short circuit (inverter1) (<3times)
View Level: opr
Root Cause: 1
Description: Heater 0: inverter short circuit (inverter1) (<3times)
3601070 Error Text: Generator error class 1: Heater 0: tube switch while filaments not OFF
View Level: opr
Root Cause: 1
Description: Heater 0: tube switch while filaments not OFF

GE MEDICAL SYSTEMS
3601071 Error Text: Generator error class 1: Heater 0: CAN Domain command number error
View Level: opr
Root Cause: 1
Description: Heater 0: CAN Domain command number error
3601072 Error Text: Generator error class 1: Heater 0: CAN Domain request with no transfer init
View Level: opr
Root Cause: 1
Description: Heater 0: CAN Domain request with no transfer init
3601073 Error Text: Generator error class 1: Heater 0: CAN Domain Toggle bit error
View Level: opr
Root Cause: 1
Description: Heater 0: CAN Domain Toggle bit error
3601074 Error Text: Generator error class 1: Heater 0: CAN Domain less than 2 data to download
View Level: opr
Root Cause: 1
Description: Heater 0: CAN Domain less than 2 data to download
3601075 Error Text: Generator error class 1: Heater 0: unknown warning
View Level: opr
Root Cause: 1
Description: Heater 0: unknown warning
View Level: opr
Root Cause: 1
Description: Heater 1: received command is not OK

View Level: opr
Root Cause: 1
Description: Heater 1: command not OK

GE MEDICAL SYSTEMS
3601078 Error Text: Generator error class 1: Heater 1: no CAN message received within 4 secs
View Level: opr
Root Cause: 1
Description: Heater 1: no CAN message received within 4 secs
3601079 Error Text: Generator error class 1: Heater 1: inverter over current (inverter1) (<3 times)
View Level: opr
Root Cause: 1
Description: Heater 1: inverter over current (inverter1) (<3 times)
3601080 Error Text: Generator error class 1: Heater 1: Filament open circuit (inverter1) (<3 times)
View Level: opr
Root Cause: 1
Description: Heater 1: Filament open circuit (inverter1) (<3 times)
View Level: opr
Root Cause: 1
Description: Heater 1: inverter short circuit (inverter1) (<3times)
View Level: opr
Root Cause: 1
Description: Heater 1: tube switch while filaments not OFF
View Level: opr
Root Cause: 1
Description: Heater 1: CAN Domain command number error
View Level: opr
Root Cause: 1
Description: Heater 1: CAN Domain request with no transfer init

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: Heater 1: CAN Domain Toggle bit error
3601086 Error Text: Generator error class 1: Heater 1: CAN Domain: less than 2 data to download
View Level: opr
Root Cause: 1
Description: Heater 1: CAN Domain: less than 2 data to download
3601087 Error Text: Generator error class 1: Heater 1: CAN Domain Abort received & applied
View Level: opr
Root Cause: 1
Description: Heater 1: CAN Domain Abort received & applied
3601088 Error Text: Generator error class 1: Heater 1: database download while heater not cut
View Level: opr
Root Cause: 1
Description: Heater 1: database download while heater not cut
View Level: opr
Root Cause: 1
Description: Heater 1: unknown warning
3601090 Error Text: Generator error class 1: DC Bus Warning Over voltage > 755VDC
View Level: opr
Root Cause: 1
Description: DC Bux Warning Over voltage > 755VDC. dcbus measures > 380V and < 680V
3601091 Error Text: Generator error class 1: DC Bus Warning Under voltage < 320VDC
View Level: opr
Root Cause: 1
Description: DC Bus Warning Under voltage < 320VDC. dcbus measures > 380V and < 680V

GE MEDICAL SYSTEMS
3601092 Error Text: Generator error class 1: LVPS 400: received command is not OK
View Level: opr
Root Cause: 1
Description: LVPS 400: received command is not OK
3601093 Error Text: Generator error class 1: LVPS 400: external +15V too high
View Level: opr
Root Cause: 1
Description: LVPS 400: external +15V too high
3601094 Error Text: Generator error class 1: LVPS 400: external +15V too low
View Level: opr
Root Cause: 1
Description: LVPS 400: external +15V too low
View Level: opr
Root Cause: 1
Description: LVPS 400: external +160V too high
View Level: opr
Root Cause: 1
Description: LVPS 400: external +160V too low
3601097 Error Text: Generator error class 1: LVPS 400: gate +24V too high
View Level: opr
Root Cause: 1
Description: LVPS 400: gate +24V too high
3601098 Error Text: Generator error class 1: LVPS 400: gate +24V too low
View Level: opr
Root Cause: 1
Description: LVPS 400: gate +24V too low

GE MEDICAL SYSTEMS
3601099 Error Text: Generator error class 1: LVPS 400: CAN +15V too high
View Level: opr
Root Cause: 1
Description: LVPS 400: CAN +15V too high
3601100 Error Text: Generator error class 1: LVPS 400: CAN +15V too low
View Level: opr
Root Cause: 1
Description: LVPS 400: CAN +15V too low
3601101 Error Text: Generator error class 1: LVPS 400: CAN -15V too high
View Level: opr
Root Cause: 1
Description: LVPS 400: CAN -15V too high
3601102 Error Text: Generator error class 1: LVPS 400: CAN -15V too low
View Level: opr
Root Cause: 1
Description: LVPS 400: CAN -15V too low
3601103 Error Text: Generator error class 1: LVPS 400: heater 0 +160V too high
View Level: opr
Root Cause: 1
Description: LVPS 400: heater 0 +160V too high
3601104 Error Text: Generator error class 1: LVPS 400: heater 0 +160V too low
View Level: opr
Root Cause: 1
Description: LVPS 400: heater 0 +160V too low
View Level: opr
Root Cause: 1
Description: LVPS 400: heater 1 +160V too high

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: LVPS 400: heater 1 +160V too low
3601107 Error Text: Generator error class 1: LVPS 400: main inverter +17V too high
View Level: opr
Root Cause: 1
Description: LVPS 400: main inverter +17V too high
3601108 Error Text: Generator error class 1: LVPS 400: main inverter +17V too low
View Level: opr
Root Cause: 1
Description: LVPS 400: main inverter +17V too low
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
3601113 Error Text: Generator error class 1: LVPS 400: FAN 0 over current
View Level: opr
Root Cause: 1
Description: LVPS 400: FAN 0 over current
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
3601117 Error Text: Generator error class 1: LVPS TRI: no more warn +160V
View Level: opr
Root Cause: 1
Description: LVPS TRI: no more warn +160V
3601118 Error Text: Generator error class 1: LVPS TRI: detected +160V too high
View Level: opr
Root Cause: 1
Description: LVPS TRI: detected +160V too high
3601119 Error Text: Generator error class 1: LVPS TRI: detected +160V too low
View Level: opr
Root Cause: 1
Description: LVPS TRI: detected +160V too low

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: LVPS TRI: no more warn +15V
View Level: opr
Root Cause: 1
Description: LVPS TRI: detected +15V too high
View Level: opr
Root Cause: 1
Description: LVPS TRI: detected +15V too low
3601123 Error Text: Generator error class 1: LVPS TRI: no more warn -15V
View Level: opr
Root Cause: 1
Description: LVPS TRI: no more warn -15V
3601124 Error Text: Generator error class 1: LVPS TRI: detected -15V too strong
View Level: opr
Root Cause: 1
Description: LVPS TRI: detected -15V too strong
3601125 Error Text: Generator error class 1: LVPS TRI: detected -15V too weak
View Level: opr
Root Cause: 1
Description: LVPS TRI: detected -15V too weak
3601126 Error Text: Generator error class 1: LVPS 400: communication error
View Level: opr
Root Cause: 1
Description: LVPS 400: communication error

GE MEDICAL SYSTEMS
3601127 Error Text: Generator error class 1: LVPS 400: unknown error
View Level: opr
Root Cause: 1
Description: LVPS 400: unknown error
3601128 Error Text: Generator error class 1: LVPS TRI: unknown warning
View Level: opr
Root Cause: 1
Description: LVPS TRI: unknown warning
3601129 Error Text: Generator error class 1: PPC kV Control - Watchdog reset has just occurred (MSB)
View Level: opr
Root Cause: 1
Description: PPC kV Control - Watchdog reset has just occurred (MSB)
3601130 Error Text: Generator error class 1: PPC kV Control - Watchdog reset has just occurred (LSB)
View Level: opr
Root Cause: 1
Description: PPC kV Control - Watchdog reset has just occurred (LSB)
3601131 Error Text: Generator error class 1: Saved RAM Battery life time limit reached
View Level: opr
Root Cause: 1
Description: Saved RAM Battery life time limit reached
3601132 Error Text: Generator error class 2: Tube spit (kV+ and kV- dropped)
View Level: opr
Root Cause: 1
Description: Tube spit (kV+ and kV- dropped)
3601133 Error Text: Generator error class 2: Tube spit (kV+ has dropped)
View Level: opr
Root Cause: 1
Description: Tube spit (kV+ has dropped)

GE MEDICAL SYSTEMS
3601134 Error Text: Generator error class 2: Tube spit (kV- has dropped)
View Level: opr
Root Cause: 1
Description: Tube spit (kV- has dropped)
3601135 Error Text: Generator error class 2: Tube spit (kV regulation error)
View Level: opr
Root Cause: 1
Description: Tube spit (kV regulation error)
3601136 Error Text: Generator error class 2: FPGA problem (restarting safety signal)
View Level: opr
Root Cause: 1
Description: FPGA problem (restarting safety signal)
3601137 Error Text: Generator error class 2: Tube spit (all kV drop/regulation errors)
View Level: opr
Root Cause: 1
Description: Tube spit (all kV drop/regulation errors)
3601138 Error Text: Generator error class 1: Warning, spit counter overflow
View Level: opr
Root Cause: 1
Description: Warning, spit counter overflow
3601139 Error Text: Generator error class 2: Tube Current max detected
View Level: opr
Root Cause: 1
Description: Tube Current max detected
3601140 Error Text: Generator error 40-0101(4): error msg from Rotor FW; No CAN message received within 5
sec.
View Level: opr
Root Cause: 1
Recommended Action(s): If trying to take exposure, release the switch and try again. Reset system if problem persists.
Description: The rotation bd has not received any signal from the kV control bd. for the last 5 sec.,
interpreted as loss of communication.
Potential cause:
2. kV control or Rotation board driver failure.
Recommended Action: Reset system, check connections, replace rotation bd.
Customer Text: Generator error. Try again. Call service if the problem persists.

GE MEDICAL SYSTEMS
3601141 Error Text: Generator error 40-0103;(4): error msg from Rotor FW; Current overload
View Level: opr
Root Cause: 1
Description: Rotation board has detected Main or auxiliary Rotation current too high compared to the max.
tube motor current.
Potential Cause:
1. Rotation board.
2. Rotation board phase capacitor short circuit.
3. Wrong data base (improbable).
Recommended Action: Check wiring from rotation board to tube. Check the rotation
capacitors. If no cabling problem, run Rotation diagnostic test to differentiate between rotation
board and phase shift capacitors.
3601142 Error Text: Generator error 40-0104;(4):error msg from Rotor FW; Open load
View Level: opr
Root Cause: 1
Description: Rotation board detected that no current is flowing to the motor.
Potential Cause:
1. Tube stator winding is open circuit.
2. Incorrect wiring (Open).
3. No DC bus on Rotation board.
4. Rotation board.
5. Rotation board phase capacitor not connected.
Recommended Action:
- Check wiring from rotation board to tube.
- Check DC bus cables from AC-DC board to rotation board.
- Check that phases capacitors are correctly connected
- If no cabling problem, run Rotation diagnostic to differentiate between rotation board and
phase shift capacitors.
3601143 Error Text: Generator error 40-0105;(4): error msg from Rotor FW; Phases unbalanced
View Level: opr
Root Cause: 1
Description: The amplitude difference of the current between main and auxiliary is too large.
Potential Cause:
1. One Rotation wire missing.
2. Rotation board.
3. Rotation board phase capacitors inverted or wrong value or not connected.
4. Wrong tube configuration data base.
5. Tube problem (stator).
Recommended Action: Check wiring from rotation board to tube (See Rotation diagnosis).
Check that phases capacitors are correctly connected.If no cabling problem, run Rotation
diagnostic to differentiate between rotation board and phase shift capacitors.

GE MEDICAL SYSTEMS
3601144 Error Text: Generator error 40-0106;(4): error msg from Rotor FW; Phases error
View Level: opr
Root Cause: 1
Description: The Rotation board has detected that the current in the anode stator does not show the
correct phase shift between main and auxiliary.
Potential Cause:
1. Rotation board.
2. Tube problem (stator).
3. Rotation board phase capacitors inverted or wrong value.
Recommended Action: Check wiring from rotation board to tube. Check that phase capacitors
are correctly connected Verify none is in short circuit.If no wiring problem, Run Rotation
diagnostic.
3601145 Error Text: Generator error 40-0108;(4): error msg from Rotor FW; Command error
View Level: opr
Root Cause: 1
Description: error msg from Rotor FW; Command error.
3601146 Error Text: Generator error 40-0109;(4): error msg from Rotor FW; MAINS_DROP has failed
View Level: opr
Root Cause: 1
Description: The firmware of the rotation board has detected the mains_drop signal activation and
transmitted error to kV control.
Potential Cause:
1. Interference (spikes).
2. Mains has dropped.
3. Cable or connector contact in DC bus between power unit and auxiliary unit.
4. Rotation board.
Recommended Action:
- Do a power and grounding check.
- If systematic, replace Rotation board.
3601147 Error Text: Generator error 40-0111;(4): error msg from Rotor FW; F0 main frequency problem
View Level: opr
Root Cause: 1
Description: EPLD has not applied the inverter start command.
Recommended Action:
- Retry.

GE MEDICAL SYSTEMS
3601148 Error Text: Generator error 40-0112;(4): error msg from Rotor FW; HW/FW config error
View Level: opr
Root Cause: 1
Description: HW/FW config error.
Recommended Action:
- Download official data base.
- If the problem persists, change rotation board.
3601149 Error Text: Generator error 40-0113;(4):error msg from Rotor FW; IUVW short circuit error
View Level: opr
Root Cause: 1
Description: error msg from Rotor FW; IUVW short circuit error
3601150 Error Text: Generator error 40-0114;(4): error msg from Rotor FW; HV cable short circuit error
View Level: opr
Root Cause: 1
Description: error msg from Rotor FW; HV cable short circuit error
3601151 Error Text: Generator error 40-0115;(4): error msg from Rotor FW; HV cable open error
View Level: opr
Root Cause: 1
Description: error msg from Rotor FW; HV cable open error
3601152 Error Text: Generator error 40-0149;(4): error msg from Rotor FW; Unknown error
View Level: opr
Root Cause: 1
Description: The main software received an error from rotation board with no error code associated.
Potential Cause: Software problem.
Recommended Action: Reset
3601153 Error Text: Generator error 40-0162;(4): error msg from Rotor FW; Acceleration while in error
View Level: opr
Root Cause: 1
Description: error msg from Rotor FW; Acceleration while in error

GE MEDICAL SYSTEMS
3601154 Error Text: Generator error 40-0163;(4): error msg from Rotor FW; No CAN message received within 4
sec.
View Level: opr
Root Cause: 1
Description: error msg from Rotor FW; No CAN message received within 4 sec.
3601155 Error Text: Generator error 50-0203;(4): Heater 0: inverter permanent over current
View Level: opr
Root Cause: 1
Description: Issued by the heater board when an over current has been detected and 3 restarts have been
tried without success within 100 ms.
Recommended Action:
- Check cabling of heater.
- Restart.
- If persistent, replace Heater board.
3601156 Error Text: Generator error 50-0204;(4): Heater 0: filament permanent open circuit
View Level: opr
Root Cause: 1
Description: Issued by the heater board when an open has been detected and 3 restarts have been tried
without success within 100 ms
Potential Cause:
1. X-ray tube filament open.
2. Heater to HV tank cable.
3. Cathode HV cable or pin contacts.
4. Open circuit in filament transformer inside HV Tank.
5- Two Switching Board cable.
Recommended Action:
- Switch on the other filaments, if no error is reported, heater board is working properly.
- Check heater board to HV Tank to tube connections. If OK, test with Ohm-meter HV Tank
heater transformers (primary and secondary) and filament impedance. Order accordingly. If
the same error is reported, check the connections as above. If all are right, replace heater
board
3601157 Error Text: Generator error 50-0205;(4): Heater 0: inverter permanent short circuit
View Level: opr
Root Cause: 1
Description: Issued by the heater board when a short circuit has been detected and 3 restarts have been
Recommended Action:
- Reset.
- If persistent, replace Heater board

GE MEDICAL SYSTEMS
3601158 Error Text: Generator error 50-0206;(4): Heater 0: filament Overload Pre-heat
View Level: opr
Root Cause: 1
Description: This is the result of an integrated value of the RMS current measurement on Heater board
comparison with max. Tube value in data base.
Potential Cause:
1. Tube data base or filament calibration.
2. Heater board.
Recommended Action:
- It’s unlikely, but reload NVRam database.
- Replace heater board.
3601159 Error Text: Generator error 50-0207;(4): Heater 0: filament Overload Boost
View Level: opr
Root Cause: 1
Potential Cause:
2. Heater board.
Recommended Action:
3601160 Error Text: Generator error 50-0208;(4): Heater 0: filament Overload Heat
View Level: opr
Root Cause: 1
Potential Cause:
2. Heater board.
Recommended Action:
3601161 Error Text: Generator error 50-0209;(4): Heater 0: command error

View Level: opr
Root Cause: 1
Description: Heater 0: command error.

GE MEDICAL SYSTEMS
3601162 Error Text: Generator error 50-0210;(4): Heater 0: PWM rate too low
View Level: opr
Root Cause: 1
Description: RMS filament current measurement (every 0.5 m sec.) on heater board is too low.
Potential Cause:
1. short circuit.
2. Heater board.
Recommended Action:
- Switch on the other filament: if no error is reported, heater board is working properly.
heater transformers (primary and secondary) and filament impedance. Order accordingly.
- If the same error is reported, check the connections as above. If all are right, change heater
board.
3601163 Error Text: Generator error 50-0211;(4): Heater 0: PWM rate too high
View Level: opr
Root Cause: 1
Description: RMS filament current measurement (every 0.5 m sec.) on heater board is too high
Potential Cause:
1. Open circuit.
2. Heater board.
Recommended Action: Replace heater board.
3601164 Error Text: Generator error 50-0212;(4): Heater 0: MAINS_DROP has failed
View Level: opr
Root Cause: 1
Description: The firmware of the Heater board has detected the mains_drop signal activation and has
transmitted error to kV control
Potential Cause:
2. Mains drop.
4. Heater board.
Recommended Action:
- If systematic, replace heater board.
3601165 Error Text: Generator error 50-0214;(4): Heater 0: boost too long
View Level: opr
Root Cause: 1
Description: Boost command stayed longer than 400ms.
Potential Cause: May be a loss of communication during boost.
Recommended Action: Retry.It will probably be followed by another communication code.

GE MEDICAL SYSTEMS
3601166 Error Text: Generator error 50-0215;(4): Heater 0: filament selection error
View Level: opr
Root Cause: 1
Description: The relay on the Heater board selecting the filament is in the wrong position with respect to
the selection.
3601167 Error Text: Generator error 50-0216;(4): Heater 0: current feedback not nul when inverter off
View Level: opr
Root Cause: 1
the selection.
3601168 Error Text: Generator error 50-0248;(4): Heater large focus error
View Level: opr
Root Cause: 1
Description: The main software received an error from heater board with no error code associated.
Potential Cause: software problem.
Recommended Action: No action.
3601169 Error Text: Generator error 50-0249;(4): Heater small focus error
View Level: opr
Root Cause: 1
Description: The main software received an error from heater board with no error code associated.
Potential Cause: software problem.
Recommended Action: No action.
3601170 Error Text: Generator error 50-1201;(4): Heater 1: no CAN message received within 5 secs
View Level: opr
Root Cause: 1
Description: The Heater board has not received any command from the kV control main software for the
last 5 sec., interpreted as a loss of communication.
Potential Cause:
2. kV control or Heater board driver failure.
Recommended Action:
- Retry.
- Reset and retry.

GE MEDICAL SYSTEMS
3601171 Error Text: Generator error 50-1203;(4): Heater 1: inverter permanent over current
View Level: opr
Root Cause: 1
Description: Issued by the heater board when an over current has been detected and 3 restarts have been
Recommended Action:
- Check cabling of heater.
- Restart.
View Level: opr
Root Cause: 1
Description: Issued by the heater board when an open has been detected and 3 restarts have been tried
without success within 100 ms
Potential Cause:
1. X-ray tube filament open.
2. Heater to HV tank cable.
3. Cathode HV cable or pin contacts.
4. Open circuit in filament transformer inside HV Tank.
5- Two Switching Board cable.
Recommended Action:
heater transformers (primary and secondary) and filament impedance. Order accordingly. If
the same error is reported, check the connections as above. If all are right, replace heater
board.
View Level: opr
Root Cause: 1
Description: Issued by the heater board when a short circuit has been detected and 3 restarts have been
Recommended Action:
- Reset.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Potential Cause:
2. Heater board.
Recommended Action:
View Level: opr
Root Cause: 1
Potential Cause:
2. Heater board.
Recommended Action:
View Level: opr
Root Cause: 1
Potential Cause:
2. Heater board.
Recommended Action:

View Level: opr
Root Cause: 1
Description: Heater 1: command error

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: RMS filament current measurement (every 0.5 m sec.) on heater board is too low.
Potential Cause: 1. short circuit. J2832. Heater board.
Recommended Action:
heater transformers (primary and secondary) and filament impedance. Order accordingly.
- If the same error is reported, check the connections as above. If all are right, change heater
board.
View Level: opr
Root Cause: 1
Description: RMS filament current measurement (every 0.5 m sec.) on heater board is too high.
Potential Cause:
1. Open circuit.
2. Heater board.
View Level: opr
Root Cause: 1
Description: The firmware of the Heater board has detected the mains_drop signal activation and has
transmitted error to kV control
Potential Cause:
2. Mains drop.
4. Heater board.
Recommended Action:
- If systematic, replace heater board.
View Level: opr
Root Cause: 1
Description: Boost command stayed longer than 400ms.
Potential Cause: May be a loss of communication during boost.
Recommended Action: Retry.It will probably be followed by another communication code.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
the selection.
View Level: opr
Root Cause: 1
the selection.
3601184 Error Text: Generator error 60-0306; (3): No kV Feedback on anode

View Level: opr
Root Cause: 1
Recommended Action(s): Release the switch and try again. Reset system if problem persists.
Description: kv measured <12kV 0,5ms after start of exposure on anode side only.
Potential Cause:
1. HV cable short circuit.
2. HV tank.
3. kV control board (less probable).
Recommended Action:
-Troubleshoot HV cables: run no load kV diagnostic along with inverting HV cables.
- If HV cables are right, replace HV Tank.
3601185 Error Text: Generator error 60-0307; (3): No kV Feedback on cathode

View Level: opr
Root Cause: 1
Description: kv measured <12kV 0,5ms after start of exposure on cathode side only.
Potential Cause:
1. HV cable short circuit.
2. HV tank.
3. kV control board (less probable).
Recommended Action:
-Troubleshoot HV cables: run no load kV diagnostic along with inverting HV cables.
- If HV cables are right, replace HV Tank.

GE MEDICAL SYSTEMS
3601186 Error Text: Generator error 60-0308; (3): No kV Feedback on anode and cathode
View Level: opr
Root Cause: 1
Description: kv measured <12kV 0,5ms after start of exposure on both anode and cathode.
Potential Cause:
1. HV tank.
2. kV control board.
Recommended Action:
- Verify flat cable connections and sitting between kV control and HV tank.
- Replace HV Tank.
3601187 Error Text: Generator error 60-0309; (3): kV detected during kV diag
View Level: opr
Root Cause: 1
Description: KV measured during inverter diagnostics while no kV must be generated.
Potential Cause: improper setup before the diagnostic is run.
Recommended Action: See generator diagnostic manual
3601188 Error Text: Generator error 60-0310; (3): kV max detected

View Level: opr
Root Cause: 1
Description: kV reached 160 kv during exposure.
Potential Cause: kV control.
Recommended Action: Replace kV control board
3601189 Error Text: Generator error 60-0311; (3): ILP current not OK
View Level: opr
Root Cause: 1
Description: The current in the parallel resonant circuit of the inverter did not rise at the beginning of the
exposure.
Potential Cause:
1. Inverter LC resonant circuit (Inverter coil assy, capa inverter assy, current transformers.).
2. Inverter.
3. kV control.
Recommended Action: run generator HV diagnostics.

GE MEDICAL SYSTEMS
3601190 Error Text: Generator error 60-0312; (3): ILR current not OK
View Level: opr
Root Cause: 1
Description: The current in the parallel resonant circuit of the inverter did not rise at the beginning of the
exposure.
Potential Cause:
1. Inverter LC resonant circuit (Inverter coil assy, capa inverter assy, current transformers.).
2. Inverter.
3. kV control.
Recommended Action: run generator HV diagnostics.
3601191 Error Text: Generator error 60-0313; (3): ILR max current detected
View Level: opr
Root Cause: 1
Description: This is a hardware detection of maximum current in serial resonant circuit.
Potential Cause:
1 Tube (it can be casing spits, error 0324H data=1 or 2).
2 HV tank. 3 kV control. 4 in LC resonant circuit.
Recommended Action: run HV power diagnostics in order to determine if it is associated to
tube, If during the test, you have kV unbalance, see error 0319H.
3601192 Error Text: Generator error 60-0314; (3): ILR current time-out
View Level: opr
Root Cause: 1
Description: The current resonant frequency is lower than expected.
Potential Cause:
1. kV control.
2. Inverter.
3. Current measurement circuit.
Recommended Action: run HV generator diagnostics.
3601193 Error Text: Generator error 60-0316; (3): Spit Max error
View Level: opr
Root Cause: 1
Description: kV control has detected the number of tube spits during exposure has reached the sw set limit
Potential Cause: x-ray tube.
Recommended Action:
-Try again at various kV/mA to confine problem.
- if it is associated to kV regul out spit detection, check mains input voltage connection. -
Troubleshoot HV section. (X-ray tube, cable, HV tank).
-Diagnose based on tube history.

GE MEDICAL SYSTEMS
3601194 Error Text: Generator error 60-0317; (3): Spit Ratio error
View Level: opr
Root Cause: 1
Description: kV control has detected the rate of tube spits during exposure has reached the limit (see
theory of operation, software section)
Potential Cause: x-ray tube.
Recommended Action:
-Try again at various kV/mA to confine problem.
- if it is associated to kV regulation out spit detection, check mains input voltage connection.
-Troubleshoot HV section. (X-ray tube, cable, HV tank).
-Diagnose based on tube history.
3601195 Error Text: Generator error 60-0318; (3): kV did not reach 75%(rad) or 95%(gridded) after 20ms
View Level: opr
Root Cause: 1
Description: Indicates that there were no HV ON signal generated for exposure time count-up.
Potential Cause:
1. kV control.
2. Tank.
3. Tube, HV cables.
Recommended Action:
- Run HV diagnosis.
- If OK, replace the kV control board.
3601196 Error Text: Generator error 60-0319; (3): kV unbalanced detected

View Level: opr
Root Cause: 1
Description: Detects that there is more than 12kV difference between kV+ and kV -.
Potential Cause: HV tank.
Recommended Action:
- Try again at various mA to confirm the problem.
- Replace HV tank.
3601197 Error Text: Generator error 60-0320; (3): FPGA problem (safety signal)
View Level: opr
Root Cause: 1
Description: No error at the inputs while checking for error source.
Potential Cause:
1. This may be due to transient interference (Spikes).
2. SW bug.
Recommended Action:
- Do a power and Grounding Check.
- Verify cabling and contacts. If permanent or too systematic, replace kV control board.
- Check the presence of the ferrite in the cable between kV control board and tank. Report to
GE Medical Systems Engineering.

GE MEDICAL SYSTEMS
3601198 Error Text: Generator error 60-0321; (3): Spit retry failed (TD computing)
View Level: opr
Root Cause: 1
3601199 Error Text: Generator error 60-0323; (3): ILR and ILP current not OK
View Level: opr
Root Cause: 1
Description: No inverter current measures at the beginning of the exposure.
Potential Cause:
1. DCBUS loss.
2. Inverter LC resonant circuit. (Inverter coil assy, capa inverter assy, current transformers.).
3. Inverter.
Recommended Action:
- check main DCBUS voltage on inverter.
- run HV power diagnostics.
3601200 Error Text: Generator error 60-0325; (3): DSP overload

View Level: opr
Root Cause: 1
Description: DSP overload. Error in timing between the FPGA and the DSP located on the kVp control
board during an exposure. Start of next pulse defined by DSP to the FPGA did not occur in
the required time-out period and an error has been reported by the FPGA to the kVp control
bd processor. Value may have been delayed due to measurement issues in Inverter currents.
Potential Cause:
1. Main supply.
2. KV control board.
3. Inverter Module
Recommended Action:
1. Check “mains” fuses and AC voltage on ACDC module.
2. If error repeats, replace the kV control board.
3. If error repeats, replace the Inverter Module
3601201 Error Text: Generator error 60-0326; (3): DSP exposure stop
View Level: opr
Root Cause: 1
Description: DSP exposure stop.
Potential Cause: KV control board.
Recommended Action: Try again. If error repeated, replace the kV control board.

GE MEDICAL SYSTEMS
3601202 Error Text: Generator error 60-0327; (3): DSP regulation out of range
View Level: opr
Root Cause: 1
Description: DSP regulation out of range
3601203 Error Text: Generator error 60-0329; (3): wrong HV capacitance measure
View Level: opr
Root Cause: 1
Recommended Action(s): Release the switch and try again. Reselect the X-ray tube. Reset system if problem persists.
Description: Wrong HV capacitance measure. Generator measures the HV cable capacitance
automatically after a tube switch.
Potential Cause:
1. HV cable problem
2. HV tank switch problem
3. Tube.
Recommended Action:
- Check HV cables connections
- run 2nd tube capability diagnostic- Replace HV tank
3601204 Error Text: Generator error 60-0350; (3): TMax 10s Overflow
View Level: opr
Root Cause: 1
Description: TMax 10s Overflow
3601205 Error Text: Generator error 60-0351; (3): Repetitive Error
View Level: opr
Root Cause: 1
Description: Repetitive Error

GE MEDICAL SYSTEMS
3601206 Error Text: Generator error 60-0401; (3): No mA feedback
View Level: opr
Root Cause: 1
Description: mA measurement function: kV control has detected no mA feedback 20 ms after the
beginning of the exposure.
Potential Cause:
1. HV tank5. kV control board6. X-ray tube (filament open or short circuit)
2. Cathode HV cable short-circuit. 8. Mis-connection between HV+ and HV- after a tank
replacement
3. heater function.
Recommended Action:
- run 2nd tube capability diagnostic.
- Verify filament impedance. Replace tube if necessary.
- Verify filament drive (heater).
- Replace kV control board.
- After a tank replacement, verify the HV cable connection.
- Disconnect HV Tank to kV control flat cable and verify with an Ohm-meter the accuracy of
the 5 Ohms resistor on the HV Tank mA measure. If it is far out of range, (4.9 to 5.1 Ohm,
including DVM accuracy) replace HV Tank.
3601207 Error Text: Generator error 60-0402; (3): mA scale error
View Level: opr
Root Cause: 1
Description: mA has been measured to be either too low or too high with respect to mA demand 20 ms
after the beginning of the exposure.
Potential Cause:
2. default filament currents not correctly adjusted.
3. HV Tank (improbable).
Recommended Action:
- If the tube has just been replaced or installed, run many exposures until the filament
correction adjusts the default filament drive values.
- If the error occurs after a while on a system: Disconnect HV Tank to kV control flat cable
and verify with an Ohm-meter the accuracy of the 5 Ohms resistor on the HV Tank mA
measure. If it is out of range, replace HV Tank else replace kV control board.
3601208 Error Text: Generator error class 2: mA out of range

View Level: opr
Root Cause: 1
Recommended Action(s): No system action. IQ may be affected
Description: mA out of range.
3601209 Error Text: Generator error class 2: No Pulse Warning

View Level: opr
Root Cause: 1
Recommended Action(s): No system action. IQ may be affected
Description: No Pulse Warning.

GE MEDICAL SYSTEMS
3601210 Error Text: Generator error 60-0451; (3): mA meter saturated
View Level: opr
Root Cause: 1
Description: mA meter saturated.
3601211 Error Text: Generator error 60-0504; (3): Inverter Gate Power Supply error
View Level: opr
Root Cause: 1
Description: Gate supply voltage has dropped below the level required to drive the IGBTs properly.
Potential Cause:
1. Generator input voltage too low or line impedance too high.
2. Inverter (gate command board).
Recommended Action:
- check main AC fuses and DCBUS voltage.
- run HV power diagnostics.
3601212 Error Text: Generator error 60-0801; (3): Exposure backup mAs exceeded
View Level: opr
Root Cause: 1
Description: The exposure command last so long that the maximum mAs allowed has been reached.
Potential Cause: Exposure command line stuck to the active state.
Recommended Action: Try again. If repeated, reset system and retry.
-disconnect system.
-Generator cable in different places and check exposure command line voltage.
3601213 Error Text: Generator error 60-1181; (3): mA between pulses

View Level: opr
Root Cause: 1
Recommended Action(s): Release the switch and try again. Reset system if problem persists. If persistent check Grid
Description: mA between pulses.
3601214 Error Text: Generator error 60-1406; (3): Time counter problem
View Level: opr
Root Cause: 1
Description: Time counter problem.

GE MEDICAL SYSTEMS
3601215 Error Text: Generator error 60-1407; (3): mAs counter problem
View Level: opr
Root Cause: 1
Description: Error found in verifying the counter normal operation.
Recommended Action: Replace kV control Board
3601216 Error Text: Generator error 60-1409; (3): mAs meter saturated
View Level: opr
Root Cause: 1
Description: A check is done on mAs counter operation at the beginning of exposure and found the mAs
meter with unrealistic value.
Potential Cause: kV Control.
Recommended Action: Replace kV control
3601217 Error Text: Generator error 60-1410; (3): FPGA locked

View Level: opr
Root Cause: 1
Description: FPGA detected an error and did not allow start exposure after exposure command signal was
received.
Potential Cause:
1. software bug.
2. kV control.
Recommended Action: If persistent replace kV control
View Level: opr
Root Cause: 1
Description: Error found in verifying the counter normal operation.
Potential Cause: kV control.
3601219 Error Text: Generator error 60-1420; (3): Tomo cut too early
View Level: opr
Root Cause: 1
3601220 Error Text: Generator error 60-1421; (3): Tomo cut by generator
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
3601221 Error Text: Generator error 60-1454; (3): Inverter thermal error
View Level: opr
Root Cause: 1
Description: Inverter thermal error
3601222 Error Text: Generator error 70-0501;(4): DC bus out of range

View Level: opr
Root Cause: 1
Description: DC bus out if range (<400 or >850).
Potential Cause:
1. mains problem (Too low or too high).
2. One phase missing at Generator input.
Recommended Action: Check mains line 3 phases incoming voltage. Verify line impedance
if mains is low.
3601223 Error Text: Generator error 70-0502;(4): Error Over voltage > 780 VDC
View Level: opr
Root Cause: 1
3601224 Error Text: Generator error 70-0503;(4): Inverter Gate Power Supply error
View Level: opr
Root Cause: 1
Description: Inverter Gate Power Supply error (checked at prep).
Potential Cause:
1. Mains.
2. Cable pb.
3. Gate command board (Inverter).
4. kV control.
Recommended Action: run HV power diagnostics
3601225 Error Text: Generator error 70-0505;(4): Mains power supply has dropped during exposure
View Level: opr
Root Cause: 1
Description: Mains power supply has dropped During exposure.
Potential Cause: unknown.
Recommended Action: none

GE MEDICAL SYSTEMS
3601226 Error Text: Generator error 70-0506;(4): DC bus 1 phase pre charge error
View Level: opr
Root Cause: 1
3601227 Error Text: Generator error 70-0507;(4): DC bus 1 phase discharge error
View Level: opr
Root Cause: 1
3601228 Error Text: Generator error 70-0510; (3): HVPM AEC not 230V
View Level: opr
Root Cause: 1
Description: HVPM AEC not 230V
3601229 Error Text: Generator error 70-0549;(4): LVPS TRI: unknown error
View Level: opr
Root Cause: 1
Description: LVPS TRI: unknown error
3601230 Error Text: Generator error 70-0553;(4): LVPS TRI: detected +160V too high (Z6 Z7 = value)
View Level: opr
Root Cause: 1
Description: LVPS TRI: detected +160V too high (Z6 Z7 = value)
3601231 Error Text: Generator error 70-0557;(4): LVPS TRI: detected +160V too low (Z6 Z7 = value)
View Level: opr
Root Cause: 1
Description: LVPS TRI: detected +160V too low (Z6 Z7 = value)
View Level: opr
Root Cause: 1
Description: LVPS TRI: detected +15V too high (Z6 Z7 = value)

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: LVPS TRI: detected +15V too low (Z6 Z7 = value)
3601234 Error Text: Generator error 70-0573;(4): LVPS TRI: detected -15V too strong
View Level: opr
Root Cause: 1
Description: LVPS TRI: detected -15V too strong
3601235 Error Text: Generator error 70-0577;(4): LVPS TRI: detected -15V too weak
View Level: opr
Root Cause: 1
Description: LVPS TRI: detected -15V too weak
3601236 Error Text: Generator error 80-0180;(4): Rotor board com pb

View Level: opr
Root Cause: 1
Description: kV control board communication Watch Dog with Rotation board popped up because it did
not get reply from Rotation board.
Potential Cause:
1. Rotation board.
2. Control bus cable.
3. kV control.
Recommended Action:
A. Check that rotation firmware is running (DS5 Led is blinking).
If no:
1/verify rotation board 5V: Led DS3 is lit. If no: verify DS1/DS2 Leds: if they are lit, replace
rotation board, else go to +/-15V errors troubleshooting.
2/ verify that RESET Led is not lit. If it is lit, disconnect successively the control bus cable from
heater and kV control to find the board which is holding the reset line and replace it. If after
disconnecting all the boards, the Led remains lit, replace rotation board.
3/ else replace rotation board.
B. Verify the flat cable between kV control and auxiliary module is correctly connected to the
Rotation board C/else replace kV control

GE MEDICAL SYSTEMS
3601237 Error Text: Generator error 80-0181;(4): Rotor board has reset
View Level: opr
Root Cause: 1
Description: kV control has detected the Rotation board has reset. KV control will reload Rotation data
base.
Potential Cause:
1. Rotation board.
Recommended Action:
- Re initialize system, retry.
- If persistent, replace Rotation board or check power and grounding.
3601238 Error Text: Generator error 80-0280;(4): Heater 0 board com pb

View Level: opr
Root Cause: 1
Description: kV control board communication Watch Dog with Heater board popped up because it did not
get reply from Heater board.
Potential Cause:
1. Heater 0 board
2. Control bus cable
3. kV control.
Recommended Action:
A. Check that heater firmware is running (DS1/2 Led are lit successively). If no:
1/ verify heater board 5V: J3/pin2. If wrong: verify +15V/-15V (J3, pin3,4): if they are right,
change rotation board, else go to +/-15V errors troubleshooting.
2/ verify that RST Led is not lit. If it is lit, disconnect successively the control bus cable from
LVPS to rotation and kV control to find the board which is holding the reset line and replace
it. If after disconnecting all the boards, the Led remains lit, replace heater board.
3/ else replace heater boar.
B. Verify the flat cable between kV control and auxiliary module is correctly connected until
the heater board C/else replace kV control board
3601239 Error Text: Generator error 80-0281;(4): Heater 0 board has reset
View Level: opr
Root Cause: 1
Description: KV control has detected the heater board has reset. KV ctrl will reload Rotation data base.
Potential Cause:
1. Heater board.
2. Interference. Spikes).
Recommended Action:

GE MEDICAL SYSTEMS
3601240 Error Text: Generator error 80-0322;(4): kV ref ADC / DAC failed
View Level: opr
Root Cause: 1
Description: kV control DAC and ADC capability are permanently tested for coherency.
Recommended Action: Only if this error is repetitive and comes alone (Not following other
errors), replace kV control board.
3601241 Error Text: Generator error 80-03A0;(4): DSP error

View Level: opr
Root Cause: 1
Description: DSP program corrupted.
Recommended Action:
- If persistent, change KV control board.
3601242 Error Text: Generator error 80-0601;(4): RTL error (Z6 Z7 = bitmap)
View Level: opr
Root Cause: 1
Description: Real Time Lines show a wrong state. RTL’s are tested on a regular basis in stand by.
Potential Cause:
1. system communication power supply (for isolated communications).
2. system communication cable.
3. system interface board.
4. system interface to kV control flat cable.
Recommended Action:
- Check communication cable.
- Check system communication power supply (if any).
- Check system interface to kV control flat cable.
- replace system interface board.
- replace kV control board.

GE MEDICAL SYSTEMS
3601243 Error Text: Generator error 80-0602;(4): External CAN bus off
View Level: opr
Root Cause: 1
Description: External CAN bus off.
Potential Cause:
1. system communication power supply (for isolated communications).
2. system communication cable.
3. system interface board.
4. system interface to kV control flat cable.
Recommended Action:
- Check communication cable.
- Check system communication power supply (if any).
-Check system interface to kV control flat cable.
-replace system interface board-replace kV control board.
3601244 Error Text: Generator error 80-0902;(4): tube cooling supply error
View Level: opr
Root Cause: 1
Check undertable X-ray tube fan power.
Description: Rotation board has detected that a wrong voltage is applied to the tube fan.
Potential Cause:
1. No 115V tube cooling supply.
2. Cabling.
3. Rotation board.
Recommended Action:
- Check presence of the AC voltage (DS6 neon) at the input of the Rotation board.
- Check the cables. If ok, replace the rotation board
3601245 Error Text: Generator error 80-1006;(4): HV switch select error

View Level: opr
Root Cause: 1
Recommended Action(s): If trying to take exposure, release the switch and try again. Try re-selecting the X-ray tube.
Reset system if problem persists.
Description: HV switch sel error
3601246 Error Text: Generator error 80-1007;(4): Rotor switch sel error
View Level: opr
Root Cause: 1
Description: Rotor switch sel error

GE MEDICAL SYSTEMS
3601247 Error Text: Generator error 80-1008;(4): Heater switch sel error
View Level: opr
Root Cause: 1
Description: Heater switch sel error
3601248 Error Text: Generator error 80-1180;(4): Ingrid not active

View Level: opr
Root Cause: 1
Description: Ingrid not active
3601249 Error Text: Generator error 80-1182;(4): Ingrid CAN bus off
View Level: opr
Root Cause: 1
Description: Ingrid CAN bus off

View Level: opr
Root Cause: 1
Description: Heater 1 board com pb.
Potential Cause:
1. Heater 1 board.
3. kV control.
Recommended Action:
A/Check that heater firmware is running (DS1/2 Led are lit successively). If no:
1/ Verify heater board 5V: J3/pin2. If wrong: verify +15V/-15V (J3, pin3,4): if they are right,
change rotation board, else go to +/-15V errors troubleshooting.
2/ Verify that RST Led is not lit. If it is lit, disconnect successively the control bus cable from
it. If after disconnecting all the boards, the Led remains lit, replace heater board.
3/ Else replace heater board. B/Verify the flat cable between kV control and auxiliary module
is correctly connected until the heater board C/else replace kV control board

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: KV control has detected the heater board has reset. KV ctrl will reload Rotation data base.
Potential Cause:
1. Heater 1 board.
Recommended Action:
- Re-initialize system, retry.
3601252 Error Text: Generator error 80-1402;(4): Internal CAN bus off
View Level: opr
Root Cause: 1
Description: Can device on kV control board detected abnormal level on it’s 2 line and sent error to the
CPU.
Potential Cause:
1. kV control.
3. Heater or Rotation.
Recommended Action: Check a short circuit on CAN lines, pins 5 & 6, of the control bus
cable. Short circuit may be either on Boards or connector/ cable. If no fault detected, replace
kV control
3601253 Error Text: Generator error 80-1403;(4): Connectic Fault

View Level: opr
Root Cause: 1
Check kV control board cables
Description: One of the flat cable connector is not connected in Generator.
Potential Cause: Multiple, but likely improbable.
Recommended Action: Check connection of the following cables: kV control to system I/F
board, kV control to HV tank, HV tank to inverter.
3601254 Error Text: Generator error 80-1404;(4): FPGA configuration problem

View Level: opr
Root Cause: 1
Description: Detected during power up. The kV control main software cannot load the FPGA.
Potential Cause: kV control board.
Recommended Action: Replace kV control board.

GE MEDICAL SYSTEMS
3601255 Error Text: Generator error 80-1450;(4): Hardware Inverter Error
View Level: opr
Root Cause: 1
Description: Hardware Inverter Error.:
3601256 Error Text: Generator error 80-1452;(4): Incorrect KVmA Test Sel
View Level: opr
Root Cause: 1
Description: Incorrect KVmA Test Sel.
3601257 Error Text: Generator error 90-0701;(4): Saved RAM checksum pb

View Level: opr
Root Cause: 1
Need maintenance on database
Description: Saved RAM checksum pb.
3601258 Error Text: Generator error 90-0702;(4): Software problem

View Level: opr
Root Cause: 1
Description: Software problem.
3601259 Error Text: Generator error 90-0704;(4): Heater / Rotor hold too long
View Level: opr
Root Cause: 1
Description: Heater / Rotor hold too long.
3601260 Error Text: Generator error 90-0705;(4): Configuration error

View Level: opr
Root Cause: 1
Check generator config.
Description: Configuration error.

GE MEDICAL SYSTEMS
3601261 Error Text: Generator error 90-0706;(4): Wrong DSP version
View Level: opr
Root Cause: 1
Reload generator software
Description: Wrong DSP version.
3601262 Error Text: Generator error 90-0707;(4): Wrong FPGA version

View Level: opr
Root Cause: 1
Description: Wrong FPGA version.
3601263 Error Text: Generator error 90-1001;(4): Wrong tube number sel
View Level: opr
Root Cause: 1
Description: Wrong tube number sel
3601264 Error Text: Generator error 90-1003;(4): Tube Sel While Rotor On
View Level: opr
Root Cause: 1
Description: Tube Sel While Rotor On
3601265 Error Text: Generator error 90-1004;(4): Tube Sel While Heat On
View Level: opr
Root Cause: 1
Description: Tube Sel While Heat On
3601266 Error Text: Generator error 90-1005;(4): Tube Sel While KV On

View Level: opr
Root Cause: 1
Description: Tube Sel While KV On

GE MEDICAL SYSTEMS
3601267 Error Text: Generator error 90-1011;(4): Unexpected tube switch board
View Level: opr
Root Cause: 1
Reset system if problem persists. Check generator configuration.
Description: Unexpected tube switch board.
3601268 Error Text: Generator error 90-1012;(4): Exposure preparation while tube not ready
View Level: opr
Root Cause: 1
Description: Exposure preparation while tube not ready.
3601269 Error Text: Generator error 100-0603;(4): Debug screen com error
View Level: opr
Root Cause: 1
Description: Debug screen com error.
3601270 Error Text: Generator error 100-0603;(4): Database download error

View Level: opr
Root Cause: 1
Description: Database download error.
3601271 Error Text: Generator error 100-0605;(4): TAV com error

View Level: opr
Root Cause: 1
Description: TAV com error.
3601272 Error Text: Generator error 100-0606;(4): MPC/Madrid com pb

View Level: opr
Root Cause: 1
Description: MPC/Madrid com pb

GE MEDICAL SYSTEMS
3601273 Error Text: Generator error 100-0607;(4): room SLIO com problem
View Level: opr
Root Cause: 1
Description: room SLIO com problem!
3601274 Error Text: Generator error 100-0650;(4): ETHERNET com. error

View Level: opr
Root Cause: 1
Description: ETHERNET com. Error
3601275 Error Text: Generator error 100-0651;(4): HDLC com. error

View Level: opr
Root Cause: 1
Description: HDLC com. error:
3601276 Error Text: Generator error 100-0652;(4): APR com. error

View Level: opr
Root Cause: 1
Description: APR com. Error
3601277 Error Text: Generator error 100-1301;(4): AEC Board com problem
View Level: opr
Root Cause: 1
Description: AEC Board com problem.
3601278 Error Text: Generator error 110-111; (5): Rotor Thermal error
View Level: opr
Root Cause: 1
Recommended Action(s): If trying to take exposure, release the switch and wait for the rotation circuit to cool.
Description: Rotor Thermal error

GE MEDICAL SYSTEMS
3601279 Error Text: Generator error 110-1405;(5: Tank temp measurement too low
View Level: opr
Root Cause: 1
Wait for temperature higher, or repair sensor.
Description: Means that t° value of the HV tank is < 3°C. Potential Cause: kV control. HV tank.
Recommended Action: Replace kV control. Replace HV Tank
3601280 Error Text: Generator error 110-1406;(5): Inverter Temp measurement too low
View Level: opr
Root Cause: 1
Description: Parallel inductor is 3°C.
Potential Cause: Fan of the inverter (most probable) kV control Sensor of parallel inductor.
Recommended Action: Check the activity of the fan of the power module. If it is not working,
check the voltage of the fan. If it is >14Vdc and the fan is not running, replace the fan. If the
voltage is OK check the connection of the sensor cable on J5 on Gate_cmd board. If all is
OK, replace kV control. If the problem persists, replace the inverter.
3601281 Error Text: Generator error 110-1412;(5): Lp Temp measurement too low
View Level: opr
Root Cause: 1
3601282 Error Text: Generator error 110-1453;(5): Rotor Thermal error
View Level: opr
Root Cause: 1
Description: Rotor Thermal error
3601283 Error Text: Generator error 120-1500; (3): Tomo brightness not good
View Level: opr
Root Cause: 1
3601284 Error Text: Generator error 120-1501; (3): Exposure switch release
View Level: opr
Root Cause: 1
Description: Release exposure switch (RAD-RF).
Potential Cause: during exposure switch is released.
Recommended Action: no action
Customer Text: The expose switch was released by the user before the exposure was completed.

GE MEDICAL SYSTEMS
3601285 Error Text: Generator error 120-1502; (3): AEC does not cut exposure
View Level: opr
Root Cause: 1
Description: AEC does not cut exposure (RAD-RF).
Potential Cause: backup parameters (mAs,...) cut exposure.
Recommended Action:
- change parameters (kV, mAs)
- change AEC.
3601286 Error Text: Generator error 130-1100;(4): Ingrid communication watchdog error
View Level: opr
Root Cause: 1
Description: Ingrid communication watchdog error
3601287 Error Text: Generator error 130-1101;(4): Ingrid repetition rate higher than 100 fps
View Level: opr
Root Cause: 1
Description: Ingrid repetition rate higher than 100 fps
3601288 Error Text: Generator error 130-1102;(4): Inter grid CMD time shorter than 0.5ms
View Level: opr
Root Cause: 1
Description: Inter grid CMD time shorter than 0.5ms
3601289 Error Text: Generator error 130-1103;(4): Ingrid power supply voltage lower than 130V
View Level: opr
Root Cause: 1
Description: Ingrid power supply voltage lower than 130V
3601290 Error Text: Generator error 130-1104;(4): Ingrid power supply voltage higher than 200V
View Level: opr
Root Cause: 1
Description: Ingrid power supply voltage higher than 200V

GE MEDICAL SYSTEMS
3601291 Error Text: Generator error 130-1105;(4): Ingrid feedback error
View Level: opr
Root Cause: 1
Description: Ingrid feedback error
3601292 Error Text: Generator error 130-1107;(4): Grid feedback voltage too High
View Level: opr
Root Cause: 1
Description: Grid feedback voltage too High
3601293 Error Text: Generator error 130-1109;(4): Bias feedback voltage too High
View Level: opr
Root Cause: 1
Description: Bias feedback voltage too High
3601294 Error Text: Generator error 130-1110;(4): Ingrid target DAC voltage feedback fault
View Level: opr
Root Cause: 1
Description: Ingrid target DAC voltage feedback fault
3601295 Error Text: Generator error 130-1199;(4): Ingrid error

View Level: opr
Root Cause: 1
Description: Ingrid error
3601296 Error Text: Generator error 140-1020;(4): Tube switch status error.
View Level: opr
Root Cause: 1
Description: Tube Switch status error.
Potential Cause: Tube Switch Board.
Recommended Action: Replace Tube Switch Board
Customer Text: X-ray tube selection error. Reselect tube and continue. Call service if the problem persists.

GE MEDICAL SYSTEMS
3601297 Error Text: Generator error 140-1021;(4): Tube switch state machine error
View Level: opr
Root Cause: 1
Description: Tube Switch State Machine error. Tube Switch Board.
3601298 Error Text: Generator error 140-1022;(4): Tube switch lamp relay feedback error
View Level: opr
Root Cause: 1
Description: Tube Switch lamp relay feedback error.
3601299 Error Text: Generator error 140-1023;(4): Tube Switch heater SF feedback error
View Level: opr
Root Cause: 1
Description: Tube Switch heater SF feedback error.
3601300 Error Text: Generator error 140-1024;(4): Tube switch heater LF feedback error
View Level: opr
Root Cause: 1
Description: Tube Switch heater LF feedback error.
3601301 Error Text: Generator error 140-1025;(4): Tube switch rotation relay feedback error
View Level: opr
Root Cause: 1
Description: Tube Switch rotation relay feedback error.

GE MEDICAL SYSTEMS
3601302 Error Text: Generator error 140-1026;(4): Tube switch motor position error
View Level: opr
Root Cause: 1
Description: (Motor is in intermediate position).
Potential Cause:
1. Cabling problem.
2. Two Tube HV Tank.
Recommended Action:
- check the cabling between J8I of Tube Switching board and DJ4 of Inverter module and J9
on kV measurement board on HV Tank
- if no improvement change HV Tank -if no improvement change Tube Switch board
3601303 Error Text: Generator error 140-1027;(4): Tube switch motor feedback error
View Level: opr
Root Cause: 1
Description: Tube switch motor feedback error (Switching Time out).
Potential Cause:
1. Cabling problem.
2. Two Tube HV Tank
3. Tube Switch Board
Recommended Action:
- Check the cabling between J8I of Tube Switching board and DJ4 of Inverter module and J9
on kV measurement board on HV Tank -if no improvement change HV Tank.
- If no improvement change Tube Switch board
3601304 Error Text: Generator error 140-1028;(4): Tube switch motor is in the opposite position
View Level: opr
Root Cause: 1
Description: Tube Switch Motor is in the opposite position.
Potential Cause:
1. Cabling problem.
2. Two Tube HV Tank.
3. Tube Switch Board
Recommended Action:
- Check the cabling between J8I of Tube Switching board and DJ4 of Inverter module and J9
on kV measurement board on HV Tank -if no improvement change HV Tank.
- If no improvement change Tube Switch board
3601305 Error Text: Generator error 140-1030;(4): Tube switch config reply error
View Level: opr
Root Cause: 1
Description: Tube switch config reply error

GE MEDICAL SYSTEMS
3601306 Error Text: Generator error 140-1031;(4): Tube switch status reply error
View Level: opr
Root Cause: 1
Description: Tube switch status reply error
3601307 Error Text: Generator error 140-1032;(4): Tube switch motor move refused
View Level: opr
Root Cause: 1
Description: Tube switch motor move refused
3601308 Error Text: Generator error 140-1033;(4): Tube switch rotor capa activation error
View Level: opr
Root Cause: 1
Description: Tube switch rotor capa activation error
3601309 Error Text: Generator error 110-906;(5): Tube track protection.

View Level: opr
Root Cause: 1
Description: Tube track protection
3601310 Error Text: Generator error 80-1413;(4): Internal CAN bus Txo
View Level: opr
Root Cause: 1
Description: Internal CAN bus Txo, Tx messages lost in internal Bus
3601311 Error Text: Generator error 80-1414;(4): Internal LD CAN bus Txo
View Level: opr
Root Cause: 1
Description: Internal LD CAN bus Txo; Tx messages lost in Ld internal Bus

GE MEDICAL SYSTEMS
3601312 Error Text: Generator error 80-1415;(4): External CAN bus Txo
View Level: opr
Root Cause: 1
Description: External CAN bus Txo; Tx messages lost in External Bus
3601313 Error Text: Generator error 80-1416;(4): Internal CAN RTL2 error
View Level: opr
Root Cause: 1
Description: Internal CAN RTL2 error; RTL2 - MAX485 chip failure
3601314 Error Text: Generator error 80-1417;(4):DC disch. when inhib

View Level: opr
Root Cause: 1
Description: DC disch. when inhib; Error in the DC Discharge loop
3601315 Error Text: Generator error 80-1418;(4): No DC disch. on request

View Level: opr
Root Cause: 1
Description: No DC disch. on request; Error in the DC Discharge loop

GE MEDICAL SYSTEMS
3.20 38 XRTechOpt
View Level: opr
Root Cause: 1
2. If the problem persists reload the application software.

View Level: opr
Root Cause: 1
3800002 Error Text: Failed to bind with actor

View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
Recommended Action(s): No action necessary

View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
2. If protocol is not available, reset the system and select the protocol again.
3. If problem persists, reload application software.

GE MEDICAL SYSTEMS
3800006 Error Text: Actor not ready
View Level: opr
Root Cause: 1
3800007 Error Text: Manual mode disabled

View Level: opr
Root Cause: 1
Description: An incorrect function call is made on the module
Customer Text: Set manual override to continue.
3800008 Error Text: Incorrect active OpMode

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
2. If the problem persists, Run Ethernet and Real Time Diagnostics.
Description: Unable to interact with an actor.The software communication bus may be broken
Customer Text: An internal communication error has occurred. Reset the system if the problem persists.
3800101 Error Text: Failed to publish event
View Level: opr
Root Cause: 1
3800102 Error Text: Incorrect bytes read for message queue
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
3800103 Error Text: msgQSend failed
View Level: opr
Root Cause: 1
3800104 Error Text: Actuals not received from Jedi

View Level: opr
Root Cause: 1
Recommended Action(s): 1. Release the exposure switch and retry.
Description: The module did not receive techniques used for the exposure from the generator
Customer Text: System did not receive generator techniques. Continue or release exposure switch and try
again.
3800105 Error Text: Sensor feedback not received

View Level: opr
Root Cause: 1
Recommended Action(s): 1. Release the exposure switch and retry.
Description: The module did not receive the image feedback from the digital subsystem
Customer Text: Digital control error. Release exposure switch and try again.
View Level: opr
Root Cause: 1
Description: Configuration parameter could not be read
Customer Text: Configuration file may be corrupted. Call service
3800107 Error Text: Actuals not received from Jedi during trial exposure
View Level: opr
Root Cause: 1
Recommended Action(s): “Software or hardware error - retry the sequence.
Description: “Actual techniques were not received from jedi during the DSA trial exposure”
3800300 Error Text: Unable to instantiate EM Server

View Level: opr
Root Cause: 1
Recommended Action(s): 1. Reset the system. 2. If the problem persists reload the application software.

GE MEDICAL SYSTEMS
3800301 Error Text: Unable to open EM file, defaults will be used
View Level: opr
Root Cause: 1
3800400 Error Text: Cannot open the trajectory file

View Level: opr
Root Cause: 1
Description: The trajectory file may be unavailable or corrupted
Customer Text: This protocol is not available. Call service.
3800401 Error Text: The trajectory file may be corrupted

View Level: opr
Root Cause: 1
Description: Data on the disk on system controller may be corrupted
3800402 Error Text: Incorrect FOV

View Level: opr
Root Cause: 1
Recommended Action(s): Check the system configuration (image intensifier size) and make sure the right size is
selected. If the problem persists, application software needs to be reloaded.
Description: The selected mag (field of view) is not usable
Customer Text: Field of View value is incorrect. Reselect the desired value.
3800403 Error Text: Incorrect Grid position

View Level: opr
Root Cause: 1
Recommended Action(s): System is stable if occurrence frequency is low and system will default to grid being in.
Frequent occurrence of this error means that the grid cone device is not operating properly
Description: Incorrect grid setting received from the positioner subsystem
Customer Text: The grid must be in the Field of View.
3800404 Error Text: The Focal Spot could not be set

View Level: opr
Root Cause: 1
Recommended Action(s): System is stable if occurrence frequency is low and system will default focal spot (small).
Frequent occurrence of this error could indicate a failure of the generator or the filament. Run
Generator and Tube diagnostics
Description: The desired focal spot could not be selected

GE MEDICAL SYSTEMS
3800405 Error Text: Incorrect Spectral Filter
View Level: opr
Root Cause: 1
Recommended Action(s): System is stable if occurrence frequency is low and system will default to 0.3 mm. Frequent
occurrence of this error could indicate collimator failure. Run collimator diagnostics.
Description: The desired spectral filter could not be selected
3800406 Error Text: The EPT limits are corrupted

View Level: opr
Root Cause: 1
Description: Data on the disk on system controller may be corrupted
3800407 Error Text: EPT out of bounds

View Level: opr
Root Cause: 1
Description: EPT value is out of bounds so limiting to the bounded value

GE MEDICAL SYSTEMS
3.21 50 ATLAS
5000001 Error Text: No request from the subsys manager in the default time interval
Minor Function Impacted: Heartbeat
View Level: opr
Root Cause: 0
Description: Actor Communication lost after boot. Actor is dead or is hung.
5000002 Error Text: No request from the subsys manager - Not Alive
Recovery Class: HALT
Minor Function Impacted: HeartbeatReceive
View Level: opr
Root Cause: 0
Description: Actor Communication lost after boot.Actor is dead or is hung.
Customer Text: A system failure has occurred. Reset the system to continue.
5000003 Error Text: No response from the actor in the default time interval
Minor Function Impacted: HeartBeatSend
View Level: opr
Root Cause: 0
5000004 Error Text: No response from the actor - Actor not alive
View Level: opr
Root Cause: 0
Customer Text: A critical system failure has occurred. Reset the system to continue.
5000005 Error Text: No request from system manager in the default time interval
Minor Function Impacted: HeartBeatRecieve
View Level: opr
Root Cause: 0
5000006 Error Text: No request from system manager - Not Alive?

Minor Function Impacted: HeartBeatReceive
View Level: opr
Root Cause: 0

GE MEDICAL SYSTEMS
5000007 Error Text: Beat Mechanism has gone wrong
View Level: opr
Root Cause: 0
5000008 Error Text: An incorrect actor ready was received by subsysmgr

Minor Function Impacted: Startup
View Level: opr
Root Cause: 0
Recommended Action(s): SoftWare Problem
Description: Actor not in the subsystem Manager list. An Actor has created trigger for Subsystem Manager
and the subsystem Manager does not know about it. Also the actor has sent an invalid
parameters in the actor ready if the actor is in the boot up list.
5000009 Error Text: An incorrect state for request

View Level: opr
Root Cause: 0
Description: Actor / SubsysMgr Synchronization is lost. Actor is not following the boot/Reset/Shutdown
protocol or the subsystem Manager state machine is invalid.
5000010 Error Text: Config file has actor on start diag shutdown and reset list
View Level: opr
Root Cause: 1
Recommended Action(s): File Corruption - Application
Description: Config File problem
5000011 Error Text: Timed Out waiting for boot to complete, the system has to be Reset
View Level: opr
Root Cause: 0
Description: The boot did not complete. Time out waiting for some actor to respond. The system cannot
be used without a reset. Some actor did not respond back within the time-out value.
5000012 Error Text: Timed Out waiting for Shut Down complete from all Actors, system shutdown will be
continued
View Level: opr
Root Cause: 0
Description: Some actor did not reply with a shutDownDone
Customer Text: System configuration error. System will continue with shutdown.

GE MEDICAL SYSTEMS
5000013 Error Text: Timed Out waiting for Reset complete from all actors, system reset will be continued
View Level: opr
Root Cause: 0
Description: Some actor did not reply with a reset
Customer Text: System configuration error. System will continue with reset.
5000014 Error Text: Timed Out waiting for complete shutdown from system manager, system will be turned off
View Level: opr
Root Cause: 0
Description: System Manager did not send a complete shutdown to the subsystem Manager levels
5000015 Error Text: Unable to disable error mgr for start diagnostics
Minor Function Impacted: Start_diag
View Level: opr
Root Cause: 0
Recommended Action(s): computer
Description: enableErrorMgr API returned Status = BAD.
Customer Text: A problem occurred during system configuration for diagnostics. Continue with care.
5000016 Error Text: Unable to disable heartbeat for start diagnostics

View Level: opr
Root Cause: 0
Description: Heartbeat was not disabled during diagnostics, can cause the system to shut down.
5000017 Error Text: Timed Out waiting for Start Diag shut down complete from actors, will be continued
View Level: opr
Root Cause: 0
Description: actor not following a proper protocol for Diagnostics as dictated by the subsystem Manager.
5000018 Error Text: Timed Out waiting for Start Diag reset complete from actors, will be continued
View Level: opr
Root Cause: 0
Description: actor not following a proper protocol for reset as dictated by the subsystem Manager.

GE MEDICAL SYSTEMS
5000019 Error Text: Error in Communication Infrastructure
Minor Function Impacted: subsysmgr
View Level: opr
Root Cause: 0
Description: Some actor has left the system and the system is unusable. An sequencing in process will be
aborted.
Customer Text: An internal communication failure has occurred. Retry or reset if the problem persists.

Minor Function Impacted: uponCommunicationError
View Level: opr
Root Cause: 0
Description: An actor has left the system. The system is unusable.
5000021 Error Text: Unable to create an instance of an object

Minor Function Impacted: genericactor
View Level: opr
Root Cause: 1
Description: Running low on memory or the initialization of the object failed.
5000022 Error Text: Unable to create an event

View Level: opr
Root Cause: 1
Description: CF Problem. Router dead or not responding.
5000023 Error Text: Bind to a CORBA Object Failed

Minor Function Impacted: connectToActor
View Level: opr
Root Cause: 1
Description: Unable to bind to an object. CORBA Related problems.
5000024 Error Text: CORBA Exception during a CORBA activity

Minor Function Impacted: corba
View Level: opr
Root Cause: 1
Description: An Exception occurred during a method call to some other actor.

GE MEDICAL SYSTEMS
5000025 Error Text: Failed to subscribe to an event
View Level: opr
Root Cause: 1
5000026 Error Text: Error Manager failed to startup

View Level: opr
Root Cause: 1
Description: Error Manager instantiation failed or Low on memory
5000027 Error Text: An actor has not overridden a method of GA

View Level: opr
Root Cause: 0
Description: The method should be overridden by the actor. Actor is not complaint to ATLAS Standards.
5000028 Error Text: Unable to create a trigger

Minor Function Impacted: addActorTrigger
View Level: opr
Root Cause: 1
Description: CF Problem.
5000029 Error Text: Unable to narrow an object reference to an actor reference

View Level: opr
Root Cause: 1
Description: CORBA Problems.
5000030 Error Text: An FTP Error has occurred

Minor Function Impacted: backupandrestore
View Level: opr
Root Cause: 1
Description: Failed to FTP a file successfully.
5000031 Error Text: Unable to load a dynamic library

View Level: opr
Root Cause: 1
Description: The dynamic library does not exist.

GE MEDICAL SYSTEMS
5000032 Error Text: Thread spawn failed
Minor Function Impacted: processTriggerEvents
View Level: opr
Root Cause: 1
Description: Unable to spawn a thread. Incorrect parameters to thread or OS has ran out of critical
resources.
5000033 Error Text: A System call returned invalid value or failed

Minor Function Impacted: OS
View Level: opr
Root Cause: 0
Description: System Call Made with invalid parameters or the OS has ran out of resources.
5000034 Error Text: Not bound to the actor to call a method

Minor Function Impacted: atlascomponents
View Level: opr
Root Cause: 1
Description: A Method call within GA failed to call a method on some other object. (actor)
5000035 Error Text: An environment variable required for proper startup is not set
Minor Function Impacted: user
View Level: opr
Root Cause: 0
Description: An Environment Variable that is required for proper functioning of the ATLAS Systems is not
set. The system is not able to default the value of this variable.
5000036 Error Text: This actor name or id is not known to the system or is invalid
View Level: opr
Root Cause: 0
Description: The actor is not a valid actor. It's entry does not exist in the ActorIdNames.h. If this actor is
required, a formal request to the ATLAS Core team needs to be made.
View Level: opr
Root Cause: 0
Description: Self explanatory error text

GE MEDICAL SYSTEMS
5000038 Error Text: No response from the subsys manager - Not Alive
Minor Function Impacted: HeartbeatSend
View Level: opr
Root Cause: 0
5000039 Error Text: Duplicate Actor Joining System detected in the BootState Machine
Minor Function Impacted: uponActorJoiningSystem
View Level: opr
Root Cause: 0
5000040 Error Text: The startBootPhase was received for an incorrect bootPhase
Minor Function Impacted: startBootPhase
View Level: opr
Root Cause: 0
5000041 Error Text: Timed out waiting for startBootPhase from sysmgr.
View Level: opr
Root Cause: 0
5000042 Error Text: Unable to read file

View Level: opr
Root Cause: 0
5000043 Error Text: An unexpected request was received in the sysmgr, and was not processed
Minor Function Impacted: defaultHandler
View Level: opr
Root Cause: 0
5000044 Error Text: SubsysReady was not expected at this stage

Minor Function Impacted: subsysReady
View Level: opr
Root Cause: 0

GE MEDICAL SYSTEMS
5000045 Error Text: A duplicate subsysmgr seems to exist
Minor Function Impacted: actorJoiningSystem
View Level: opr
Root Cause: 0
5000046 Error Text: could not make the remote method call
Minor Function Impacted: sendMethods
View Level: opr
Root Cause: 1
5000047 Error Text: BootTimed out
View Level: opr
Root Cause: 0
5000048 Error Text: ResetTimed out

View Level: opr
Root Cause: 0
5000049 Error Text: ShutdownTimed out
View Level: opr
Root Cause: 0
5000050 Error Text: Power Failure Timed out - Shutting Down

View Level: opr
Root Cause: 0
Customer Text: Main Power off for more than 30 seconds. Shutdown in progress.

GE MEDICAL SYSTEMS
3.22 58 XRSubsysMgrVENUS
5800001 Error Text: Unable to create a process! The system may be low in resources!
Minor Function Impacted: time-out
View Level: opr
Root Cause: 1
Customer Text: The reset or shutdown failed. Turn the system power off/on to continue.
5800002 Error Text: Unable to communicate with UPS! Check if power to UPS is ON or the communication link to
UPS is present.
Minor Function Impacted: communication
View Level: opr
Root Cause: 1
Recommended Action(s): 1. Make sure that serial connection between IUI and UPS is properly connected.
2. Run UPS and serial communication diagnostics.
Description: System was unable to connect to the UPS due to either a bad connection or the UPS not
being ON
Customer Text: Communication with UPS has failed. Continue and call service.
5800003 Error Text: Unable to subscribe to event

View Level: opr
Root Cause: 1
Customer Text: The system did not boot properly. Reset the system to continue.
5800004 Error Text: Unexpected shutdown of the Venus started by UPS daemon
View Level: opr
Root Cause: 1
Description: UPS daemon started a shutdown of the Operating system.
Customer Text: UPS started a shutdown of the system.
5800005 Error Text: Communication with UPS has been restored.

View Level: opr
Root Cause: 1
Description: System was able to connect to the UPS.
Customer Text: System communication with the UPS has been restored.
5800006 Error Text: A power failure has occurred.

Minor Function Impacted: power
View Level: opr
Root Cause: 1
Description: The UPS has switched to battery operation.
Customer Text: A Hospital Main power failure has occurred. Please wait...

GE MEDICAL SYSTEMS
5800007 Error Text: Normal power had been restored.
View Level: opr
Root Cause: 1
Description: The UPS has switched to line operation.
Customer Text: Hospital Main power has been restored. Please wait for system re-initialization.
5800008 Error Text: Shutdown is occurring because power failure condition exists.
View Level: opr
Root Cause: 1
Customer Text: Hospital Main power failure. System Shutdown is in progress. Please wait...
5800009 Error Text: Unable to send reset message to System Controller because reference was not valid.
View Level: opr
Root Cause: 1
5800010 Error Text: User time-out on Boot

View Level: opr
Root Cause: 0
Description: The System boot has failed

GE MEDICAL SYSTEMS
3.23 64 XRUserIfPOS
View Level: opr
Root Cause: 1
6400001 Error Text: UserIfPOS was not bound to actor

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
Description: Software Error: In boot phase, the actor (software module) needs to create the Events to be
published. This error indicates that the actor could not create this Event. So the software shall
not function properly.

View Level: opr
Root Cause: 0
Description: Software Error: The actor (software module) tried to call other actor's (module's) method.
However, the software call failed.
6400004 Error Text: Unknown actor

View Level: opr
Root Cause: 0
Customer Text:

GE MEDICAL SYSTEMS
6400005 Error Text: Failed to read config file UifPos.cfg
View Level: opr
Root Cause: 1
Description: Software Error: the actor (software module) could not find one of it's configuration files
(UifPOS.cfg).
Customer Text: System software error. Call service to reload software.
6400006 Error Text: Failed to read advisory message file AdvMsg.cfg

View Level: opr
Root Cause: 1
Description: Software Error: the actor (software module) could not find one of it's configuration files
(AdMsgEng.cfg).
Customer Text: System software error. Call service to reload software.
6400100 Error Text: OTS UIF heartbeat failed

View Level: opr
Root Cause: 0
2. If problem persists, check cable connections and power supply to the OTS User Interface.
Description: Software was not able to communicate to the OTS User Interface.
Customer Text: OTS communication error. Reset the system and call service if problem persists.
6400101 Error Text: Room Door Open

View Level: opr
Root Cause: 0
Recommended Action(s): 1. Close room door and try again.
2. If problem persists, check the following:
a) Room door interlock connections;
b) PDU I/O cable connections (check for PDU I/O node guarding error);
c) Power supplies for the above components.
Description: Room Door is open. Exposure inhibited.
Customer Text: Room Door is open. Exposures are inhibited. Close door to resume.

GE MEDICAL SYSTEMS
3.24 66 XRSubsysMgrMARS
View Level: opr
Root Cause: 0
Description: SubsysMgr MARS reboot failed
6600001 Error Text: User time-out on Restart

Minor Function Impacted: restart
View Level: opr
Root Cause: 0
6600002 Error Text: Not connected to System Manager

View Level: opr
Root Cause: 0
Description: Software Error: It cannot connect to System Manager.
Customer Text: X-ray exposures are not possible. Reset the system. Call service if the problem persists.
6600003 Error Text: Time-out waiting for userRestart call from SysMgr
View Level: opr
Root Cause: 0

View Level: opr
Root Cause: 1
Recommended Action(s): Shutdown the Console.
Description: Main Power Failure has been detected.

View Level: opr
Root Cause: 1
Recommended Action(s): none
Description: Main Power Failure has been recovered.
6600006 Error Text: Hospital Main power failure. System Shutdown is in progress.
View Level: opr
Root Cause: 1
Description: Main Power Failure has been detected in boot time. The system will shutdown.
Customer Text: Hospital Main power failure, System shutdown in progress. Please wait...

GE MEDICAL SYSTEMS
6600007 Error Text: Emergency stop switch at triggered position (Power is off)
View Level: opr
Root Cause: 0
Recommended Action(s): Emergency Stop Switch at the table side is triggered. Release it when it is safe
Description: The Emergency Stop Switch at the table side is triggered.
Customer Text: Emergency Stop Switch triggered. Release it.
6600008 Error Text: Emergency stop switch at released position (Power is on)
Minor Function Impacted: no
View Level: opr
Description: Indicates the table side Emergency Stop Switch is released. For debug purpose only.
Customer Text: Emergency Stop Switch at released position (Power is ON)
6608002 Error Text: CAN Bridge Initialization Error

Minor Function Impacted: DeviceGroup
View Level: opr
Root Cause: 1
Description: CAN bridge initialization failed. Possible errors in CAN-RS422 communication. Possible Boot
problem. May indicate a CAN device or bus problem. Refer to the CAN bus block diagram.
- If a single device is reporting an error, check that device, its power, and its cabling/
connections.
- If multiple devices are reporting errors, check common cabling/connections and common
power. For example, if the CAN bridge, Pos I/O, and CAN amps in the Pos cab are reporting
errors, check the external CAN cable from Sys Cab to Pos Cab and check for power to those
nodes in the Pos Cab.
- If all CAN devices are reporting errors, check common cabling/connections. Also check/
replace the System Controller.
6608003 Error Text: CAN Bridge Node Guarding Error
View Level: opr
Root Cause: 1
Recommended Action(s): Check CAN bridge connection, or reset the system
Description: CAN bridge is not sending the heartbeat messages. Indicates a CAN device or bus problem.
Refer to the CAN bus block diagram.
connections.
- If multiple device are reporting errors, check common cabling/connections and common
devices in the Pos Cab.
6608004 Error Text: IddDevice Constructor Failed

View Level: opr
Root Cause: 1
Description: Software error: failure in IddDevice constructor.
Customer Text: Software error. Reset the system and call service if problem persists.

GE MEDICAL SYSTEMS
6608005 Error Text: IddDevice Initialization Error
View Level: opr
Root Cause: 1
Description: IddDevice initialization failed.
Customer Text: IDD initialization error. Reset the system and call service if problem persists.
6608006 Error Text: IDD Vertical Amplifier Node Guarding Error

View Level: opr
Root Cause: 1
Description: IDD Power Assist Vertical CAN amp initialization failed or is not responding. Indicates a CAN
device or bus problem. Refer to the CAN bus block diagram.
connections.
6608007 Error Text: IDD Vertical Motion Control Error

View Level: opr
Root Cause: 1
Description: IDD vertical motion control error.
Customer Text: Power-assisted motion has failed at the imaging device. Continue and call service if problem
persists.
6608008 Error Text: IDD Longitudinal Amplifier Node Guarding Error

View Level: opr
Root Cause: 1
Description: IDD Power Assist Longitudinal CAN amp initialization failed or is not responding. Indicates a
CAN device or bus problem. Refer to the CAN bus block diagram.
connections.

GE MEDICAL SYSTEMS
6608009 Error Text: IDD Longitudinal Motion Control Error
View Level: opr
Root Cause: 1
Description: IDD longitudinal motion control error.
persists.
6608010 Error Text: IDD Positioning Error

View Level: opr
Root Cause: 1
Description: IDD positioning error. No SID feedback.
Customer Text: IDD error. Retry or reset the system if problem persists.
6608011 Error Text: IDD Console Node Guarding Error

View Level: opr
Root Cause: 1
Description: IDD console is not responding. The IDD console communications go through the CAN-RS422
bridge. Possibly a problem with the IDD console or cabling from the bridge out to the IDD
console. Possibly indicates a CAN device or bus problem. Refer to the CAN bus block
diagram.
connections.
-If all CAN devices are reporting errors, check common cabling/connections. Also check/
6608012 Error Text: IDD Goldbox Node Guarding Error

View Level: opr
Root Cause: 1
Description: IDD grid/cone controller (goldbox) is not responding. The IDD grid/cone controller (gold box)
communications go through the CAN-RS422 bridge. Possibly a problem with the IDD grid/
cone controller or cabling from the bridge out to the IDD grid/cone controller. Possibly
indicates a CAN device or bus problem. Refer to the CAN bus block diagram.
connections.

GE MEDICAL SYSTEMS
6608013 Error Text: RfTableDevice Constructor Failed
View Level: opr
Root Cause: 1
Description: Software error: failure in RfTableDevice constructor.
6608014 Error Text: RfTableDevice Initialization Error

View Level: opr
Root Cause: 1
Description: RfTableDevice initialization failure.
Customer Text: Table initialization error. Reset the system and call service if problem persists.
6608015 Error Text: Rf Table Angulation Control Error

View Level: opr
Root Cause: 1
Description: Table angulation control error.
Customer Text: Tilting motion has failed at the table. Continue and call service if problem persists.
6608016 Error Text: Rf Table Positioning Error

View Level: opr
Root Cause: 1
Description: Table positioning error.
Customer Text: Table motion is not functional. Continue and call service if problem persists.
6608017 Error Text: PDU IO Alive Time-out

View Level: opr
Root Cause: 1
Description: PDU I/O initialization problem or device is not responding. Possible boot problem. May
indicate a CAN device or bus problem. Refer to the CAN bus block diagram.
connections.

GE MEDICAL SYSTEMS
6608018 Error Text: PDUIODevice Initialization Error
View Level: opr
Root Cause: 1
connections.
6608019 Error Text: PDU IO Node Guarding Error

View Level: opr
Root Cause: 1
Description: PDU I/O device is not responding. Indicates a CAN device or bus problem. Refer to the CAN
bus block diagram.
connections.
6608020 Error Text: IOAdapter Constructor Failed
View Level: opr
Root Cause: 1
Description: Software error: failure in IOAdapter constructor.
6608021 Error Text: POS cabinet IO Initialization Error

View Level: opr
Root Cause: 1
Description: POS cabinet IO initialization failure.
Customer Text: System initialization error. Reset the system and call service if problem persists.

GE MEDICAL SYSTEMS
6608022 Error Text: POS cabinet IO Node Guarding Error
View Level: opr
Root Cause: 1
Description: POS cabinet IO is not responding. Indicates a CAN device or bus problem. Refer to the CAN
bus block diagram.
connections.
6609001 Error Text: OTS Device Constructor Failed

View Level: opr
Root Cause: 1
Description: OTS Device Constructor Failed
Customer Text: OTS communication error. Reset the system.
6609002 Error Text: OTS Device Initialization Failed.

View Level: opr
Root Cause: 1
Description: OTS Device Initialization Failed. Possible boot problem. May indicate a CAN device or bus
problem. Refer to the CAN bus block diagram.
connections.
Customer Text: OTS initialization failed. Reset and try again.
6609003 Error Text: OTS Register Call Back error.

View Level: opr
Root Cause: 1
Description: OTS Register Call Back error.
6609004 Error Text: OTS wrong call back data type error.
View Level: opr
Root Cause: 1
Description: OTS wrong call back data type error.

GE MEDICAL SYSTEMS
6609005 Error Text: OTS motion control error.
View Level: opr
Root Cause: 1
Description: OTS motion control error.
Customer Text: OTS motion control problem. Retry or reset the system.
6609006 Error Text: OTS positioning error.

View Level: opr
Root Cause: 1
Description: OTS positioning error.
Customer Text: OTS positioning problem. Reset the system. Call service if the problem persists.
6609007 Error Text: OTS locks control error.

View Level: opr
Root Cause: 1
Description: OTS locks control error. This error may occur during a hospital 480 VAC mains power failure,
and should not be cause for alarm. If you see this error immediately following an error
6600004:”A power failure has occurred.”, then please ignore it.
6609008 Error Text: OTS 30 VAC error.

View Level: opr
Root Cause: 1
Description: OTS 30 VAC error. This error may occur during a hospital 480 VAC mains power failure, and
should not be cause for alarm. If you see this error immediately following an error 6600004:”A
power failure has occurred.”, then please ignore it.
Customer Text: OTS voltage check error. Reset system or call service.
6609009 Error Text: OTS 10 VDC error.

View Level: opr
Root Cause: 1
Description: OTS 10 VDC error.

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
6609011 Error Text: OTS 24 VDC lock logic error.
View Level: opr
Root Cause: 1
Description: OTS 24 VDC lock logic error.

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
6609014 Error Text: OTS IO CAN warning limit error.

View Level: opr
Root Cause: 1
Description: OTS IO CAN warning limit error.
6609015 Error Text: OTS IO CAN overrun error.
View Level: opr
Root Cause: 1
Description: OTS IO CAN overrun error.
6609016 Error Text: OTS IO node guarding error.

View Level: opr
Root Cause: 1
Description: OTS IO is not responding. Indicates a CAN device or bus problem. Refer to the CAN bus
block diagram.
connections.
Customer Text: OTS I/O not alive. Retry or reset the system.

GE MEDICAL SYSTEMS
6609017 Error Text: OTS IO receiving buffer overrun error
View Level: opr
Root Cause: 1
Description: OTS IO receiving buffer overrun error
6609018 Error Text: OTS Amplifier node guarding error.

View Level: opr
Root Cause: 1
Description: OTS Amplifier is not responding. Indicates a CAN device or bus problem. Refer to the CAN
bus block diagram.
connections.
Customer Text: OTS Amplifier not alive. Retry or reset the system.
6609019 Error Text: OTS amplifier over voltage error.

View Level: opr
Root Cause: 1
Description: OTS amplifier over voltage error.
Customer Text: OTS amplifier over voltage error. Retry or reset the system.
6609020 Error Text: OTS amplifier under voltage error.

View Level: opr
Root Cause: 1
Description: OTS amplifier under voltage error.
Customer Text: OTS amplifier under voltage error. Retry or reset the system.
6609021 Error Text: OTS amplifier over current error.
View Level: opr
Root Cause: 1
Description: OTS amplifier over current error.
Customer Text: OTS amplifier over current error. Retry or reset the system.
6609022 Error Text: OTS amplifier over temperature error.

View Level: opr
Root Cause: 1
Description: OTS amplifier over temperature error.
Customer Text: OTS amplifier over temperature error. Retry or reset the system.

GE MEDICAL SYSTEMS
6609023 Error Text: OTS amplifier over load error.
View Level: opr
Root Cause: 1
Description: OTS amplifier over load error.
Customer Text: OTS amplifier over load error. Retry or reset the system.
6609024 Error Text: OTS amplifier over speed error.

View Level: opr
Root Cause: 1
Description: OTS amplifier over speed error.
Customer Text: OTS amplifier over speed error. Retry or reset the system.
6609025 Error Text: OTS amplifier over position error.

View Level: opr
Root Cause: 1
Description: OTS amplifier over position error.
6609026 Error Text: OTS amplifier position following error.

View Level: opr
Root Cause: 1
Description: OTS amplifier position following error.
6609027 Error Text: OTS amplifier velocity following error.

View Level: opr
Root Cause: 1
Description: OTS amplifier velocity following error.
6609028 Error Text: OTS amplifier motor over temperature error.
View Level: opr
Root Cause: 1
Description: OTS amplifier motor over temperature error.
Customer Text: OTS amplifier motor over temperature error. Retry or reset the system.
6609029 Error Text: OTS amplifier encoder error.

View Level: opr
Root Cause: 1
Description: OTS amplifier encoder error.

GE MEDICAL SYSTEMS
6609030 Error Text: OTS amplifier auxiliary encoder error.
View Level: opr
Root Cause: 1
Description: OTS amplifier auxiliary encoder error.
6609031 Error Text: OTS amplifier warning.

View Level: opr
Root Cause: 1
Description: OTS amplifier warning.
6609032 Error Text: OTS amplifier fault.
View Level: opr
Root Cause: 1
Description: OTS amplifier fault.
6609033 Error Text: OTS amplifier fatal error.

View Level: opr
Root Cause: 1
Description: OTS amplifier fatal error.
Customer Text: OTS amplifier fatal error. Retry or reset the system.
6609034 Error Text: OTS amplifier homing error.

View Level: opr
Root Cause: 1
Description: OTS amplifier homing error.
Customer Text: OTS amplifier homing error. Retry or reset the system.
View Level: opr
Root Cause: 1
6609036 Error Text: OTS longitudinal pot failure.

View Level: opr
Root Cause: 1
Description: OTS longitudinal pot failure.
Customer Text: OTS longitudinal pot failure. Retry or reset the system.

GE MEDICAL SYSTEMS
6609037 Error Text: OTS lateral pot failure.
View Level: opr
Root Cause: 1
Description: OTS lateral pot failure.
Customer Text: OTS lateral pot failure. Retry or reset the system.
6609038 Error Text: OTS vertical pot failure.

View Level: opr
Root Cause: 1
Description: OTS vertical pot failure.
Customer Text: OTS vertical pot failure. Retry or reset the system.

GE MEDICAL SYSTEMS
3.25 80 XRDigitalProxy
View Level: opr
Root Cause: 1
controller.
controller.

View Level: opr
Root Cause: 1
controller.
controller.
8000003 Error Text: Init ProxyMgr Failed.

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
8000005 Error Text: Failed to read the Digital Proxy config file.
View Level: opr
Root Cause: 1
controller.
controller.
8000006 Error Text: Digital Proxy failed to startup.

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
8000008 Error Text: publish event failed for these events.

View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
8000011 Error Text: The actor is not a hybrid actor.
View Level: opr
Root Cause: 1
8000012 Error Text: Lost connections with Hybrid actors.

View Level: opr
Root Cause: 1
Recommended Action(s): Connection to System Controller Lost. Refer to Precision Diagnostic Manual and run Ethernet
Diagnostic.
Description: Connection to System Controller Lost. Refer to Precision Diagnostic Manual and run Ethernet
Diagnostic.
8000013 Error Text: Digital Proxy not connected to all the actors.
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
8000014 Error Text: Proxy Library failed to register the message and message handler.
View Level: opr
Root Cause: 1
8000015 Error Text: Proxy Library failed to deliver the packet to server.
View Level: opr
Root Cause: 1
Recommended Action(s): Connection to System Controller lost. Refer to Precision Diagnostic Manual and run Ethernet
Diagnostic.
Diagnostic.
8000016 Error Text: Failed to connect to the other system.

View Level: opr
Root Cause: 1
Recommended Action(s): Connection to System Controller or Digital Subsystem lost. Refer to Precision Diagnostic
Description: Connection to System Controller or Digital Subsystem lost. Refer to Precision Diagnostic

View Level: opr
Root Cause: 1
Description: Unable to allocate software resources on the computer. Reset the system. If the problem
persists, reload the software.
8000018 Error Text: Null InputHandler pointer

View Level: opr
Root Cause: 1
8000019 Error Text: Failed to close the socket.

View Level: opr
Root Cause: 1
Recommended Action(s): Cannot close the connection to System Controller or Digital Subsystem. Refer to Precision
Diagnostic Manual and run Ethernet Diagnostic.
Description: Cannot close the connection to System Controller or Digital Subsystem. Refer to Precision

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Recommended Action(s): Failed to accept the connection request by the System Controller or Digital Subsystem. Refer
to Precision Diagnostic Manual and run Ethernet Diagnostic.
Description: Failed to accept the connection request by the System Controller or Digital Subsystem. Refer
8000021 Error Text: Failed to open the socket.
View Level: opr
Root Cause: 1
Recommended Action(s): Failed to open the connection by the System Controller or Digital Subsystem. Refer to
Description: Failed to open the connection by the System Controller or Digital Subsystem. Refer to
8000022 Error Text: Peer closed the socket connection, system has to be reset
View Level: opr
Root Cause: 1
Recommended Action(s): Note that the reporting of this error is an expected part of a normal system shutdown process.
Connection to the Digital System was closed by the Digital Subsystem. Reset the system.
Refer to Precision Diagnostic Manual and run Ethernet Diagnostic.
Description: Connection to the Digital System was close by the Digital Subsystem. Reset the system.
View Level: opr
Root Cause: 1
Recommended Action(s): System Controller received corrupted message. Reset the system. Refer to Precision
Description: System Controller received corrupted message. Reset the system. Refer to Precision

View Level: opr
Root Cause: 1
Recommended Action(s): System Controller did not receive the correct data length. Reset the system. Refer to
Description: System Controller did not receive the correct data length. Reset the system. Refer to
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
8000026 Error Text: Failed to create the PeerActorsInfo Class
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
3.26 90 XRUserIFVenus
9000001 Error Text: Actor Configuration file does not exist.
Major Function Impacted: IUI
Minor Function Impacted: STARTUP
View Level: opr
Root Cause: 1
Description: Software Error:-The required config file to start the IUI actor (software module) is not present
in the required directories.
Customer Text: System configuration error. Call service.
9000002 Error Text: SubSystemMgr not requested for the BOOT in the specified Interval
Minor Function Impacted: BOOT
View Level: opr
Root Cause: 0
Description: Ignore
9000003 Error Text: No request from the subsys manager for start boot phase- Not Alive
View Level: opr
Root Cause: 0
Description: Ignore
View Level: opr
Root Cause: 0
Description: Software Error.The required actor (software module) is not responding. The reason could be
the actor is down/ bad software installation.
View Level: opr
Root Cause: 1
Description: Software Error. The required actor (software module) is not responding. The reason could be
the actor is down/ bad software installation.
9000006 Error Text: The start Boot Phase was received for an incorrect boot Phase
View Level: opr
Root Cause: 0
Description: Ignore

GE MEDICAL SYSTEMS
9000007 Error Text: The system has not booted
View Level: opr
Root Cause: 1
Description: Software Error. This communication error may be due to the bad installation of application sw.
9000008 Error Text: IUI Config File not found

Minor Function Impacted: APPSETUP
View Level: opr
Root Cause: 1
Description: Software Error. The file containing application initialization information is missing/corrupted.
The reason could be bad s/w install.
9000009 Error Text: protocol DB file corrupted

View Level: opr
Root Cause: 1
Recommended Action(s): Reload the protocol database from the CD
Description: Software Error. The protocol files/protocol db (database) is corrupted due to save failures or
configuration mismatches
9000010 Error Text: The IUI config file is corrupted
View Level: opr
Root Cause: 1
Description: Software Error. Due to the bad installation / upgrade the protocol db root could be found.
9000011 Error Text: No Response from AppDir in the required time interval
View Level: opr
Root Cause: 0
Description: Ignore
9000012 Error Text: Unable to Publish event

View Level: opr
Root Cause: 1
Description: Software Error. Failure in creating events. The required configuration files is corrupted or
missing details.

GE MEDICAL SYSTEMS
9000013 Error Text: IUI Config File is corrupted.
View Level: opr
Root Cause: 0
Description: Software Error. The configuration files are bad. The reason could be s/w install or cal/config
retrieve from CD.
9000014 Error Text: OpMode Configuration failed, please try select protocol again.
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Try selecting protocol again.
2. If the problem persists, reset the system.
Description: Software Error. The application initialization failed due to some failure in the system.
9000015 Error Text: Active opMode Configuration failed, please try select another protocol or opmode again.
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Try selecting protocol again.
2. If the problem persists, reset the system.
Description: Software Error. The application initialization failed due to some failure in the system. The
could be any of the following.
1. Any of the software modules are not responding to the application initialization events.
2. The technic values for the protocol may be incorrect.
3. The Jedi generator may be in a wrong state to handle the exposure.
4. Digital failed to initialize.
5. Communication between One box to another box is broken (H/W modules like IUI/Sys
Control).
View Level: opr
Root Cause: 0
Description: Ignore
9000017 Error Text: Request failed please try again

Minor Function Impacted: GENERAL
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Please try the operation again.
2. If the problem persists, reboot the system
Description: Software Error. Any request to change the protocol/ frame rate/ FOV/ start record failed. The
reason for this is a communication between MARS (Hardware Box), Venus (Another H/W box
where User Interface is running) is broken.
9000018 Error Text: Appsetup cannot proceed because of bad parameters for Application Initialization.
View Level: opr
Root Cause: 0
Description: Ignore

GE MEDICAL SYSTEMS
9000020 Error Text: Invalid protocol, Tech values are not proper.
View Level: opr
Root Cause: 0
Description: Ignore
9000021 Error Text: File RTPPFile not found. Cannot return to previous protocol
Minor Function Impacted: RTPP
View Level: opr
Root Cause: 0
Recommended Action(s): Start exam and reselect the previous protocols.
Description: Software Error. RTPP(Return To Previous Protocol) information file is missing. Cannot return
to previous protocol.
Customer Text: Protocol error occurred. Reselect the protocol to continue. Call service if the problem persists.
9000022 Error Text: Protocol Database is changed. Restore old database or close exam
View Level: opr
Root Cause: 0
Recommended Action(s): Start exam and reselect the previous protocols.
Description: Software Error. The protocol database is changed when an RTPP is done. The RTPP
Information and the current protocol file doesn't match
Customer Text: Protocol Database has been modified. Restore previous database.
9000023 Error Text: Error in detecting RTPP status. Please check if config file is present or not
View Level: opr
Root Cause: 0
Recommended Action(s): Start exam and reselect the previous protocols manually.
Description: Software Error. The file which maintains the information about RTPP status is not present.
So the system couldn't return to previous protocol.
Customer Text: Protocol error occurred. Call service if the problem occurs again.
9000024 Error Text: Error in writing to file RTPPFile.conf
View Level: opr
Root Cause: 0
Description: Software Error. Cannot write information to a file which stores RTPP information
Customer Text: Protocol error occurred. Reset and call service if the problem occurs again.
9000025 Error Text: Error in reading file RTPPFile.conf

View Level: opr
Root Cause: 0
Description: Software Error. Cannot read information to a file which stores RTPP information

GE MEDICAL SYSTEMS
9000026 Error Text: Error in writing RTPP status to config file
View Level: opr
Root Cause: 0
Description: Software Error. Cannot write information to a file which stores RTPP information
9000027 Error Text: Error in doing RTPP

View Level: opr
Root Cause: 0
Description: Software Error. Cannot do RTPP because of internal software error.
9000028 Error Text: Error getting display Status for tube warm-up
Minor Function Impacted: TUBEWARMUP
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Close tube warm-up and start again.
2. Reset the system
Description: Cannot get the status of Tube warm-up. Internal software error.
9000029 Error Text: Error reading all opmodes needing current opmode for exposure
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Close tube warm-up and start again.
2. If error occurs, reload the software
Description: Software error. All the information needed to initialize the current tube cannot be found in
protocol database.
9000030 Error Text: Error getting current opmodes
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Close Exam and start again. 2. If error occurs, restart the system
Description: Software Error. A internal error occurred in reading the protocol information
9000031 Error Text: Appsetup not complete. Cannot configure new opmodes
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Close Exam and start again.
2. If error occurs, restart the system
Description: Software Error. A internal error occurred in reading the protocol information
Customer Text: An internal communication failure has occurred. Close Exam. Restart Application Setup.

GE MEDICAL SYSTEMS
9000032 Error Text: Invalid or Bad Opmode ID received for Optimization factors Display
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Try doing fluoro/ digital again.
2. If the problem persists, Reset the system.
Description: Software Error. Bad operational mode parameter was received for displaying technic
information.
9000033 Error Text: Invalid or Bad Opmode ID received for Dose Display
Minor Function Impacted: FLUORO_ACQUISITION
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Try doing fluoro/ digital again.
2. If the problem persists, Reset the system.
Description: Software Error. Bad operational mode parameter was received for displaying dose
information.
9000034 Error Text: Bad Reply received from Athena. Verify athena is functional or not
View Level: opr
Root Cause: 0
Description: Ignore
9000035 Error Text: System is not ready. Please reboot the system
View Level: opr
Root Cause: 0
Description: Ignore
9000036 Error Text: IUI is not in Acquire Screen. Only Tube Warm-up Exposure can be taken
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Please select a protocol and press accept
2. If the problem persist close exam and start exam again.
Description: Acquisitor can be done only from acquisition screen. Please switch to the acquisition screen.
Customer Text: Acquisition can only be taken from the Acquisition screen.
9000037 Error Text: IUIApp is sending bad contrast. System is ignoring this
View Level: opr
Root Cause: 0
Description: Ignore

GE MEDICAL SYSTEMS
9000038 Error Text: Fluoro is inhibited. Please reset the timer to remove the inhibit condition
View Level: opr
Root Cause: 0
Recommended Action(s): Fluoro is stopped because the patient was exposed to fluoro radiation for more than 10
minutes. If you still want to continue with the exposures, please reset the fluoro timer.
Description: After 10 minutes exposure cannot continue. Timer needs to be reset
Customer Text: Fluoro is inhibited, touch timer reset to continue.
9000039 Error Text: Reading the opmode script file from the disk failed
View Level: opr
Root Cause: 0
Description: The protocol database is corrupted. Reload the protocol database again from the CD
Customer Text: Error reading disk. Cannot complete application setup. Reset system. Call service if problem
persists.
9000040 Error Text: Replacing the tags in the scripts failed

View Level: opr
Root Cause: 0
Recommended Action(s): Close exam and start exam again.
Description: Software Error. The reading and processing some of the script files failed.
Customer Text: Application error occurred. Close Exam. Restart Application Setup.
9000041 Error Text: Cannot handle prep/expose switch

Minor Function Impacted: ACQUISITION
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Please make sure you have selected a protocol before starting exposures.
2. When you switch to a different protocol, please wait until application initialization is
complete and try again.
3. If the problem persists, close exam and try again.
4. If the problem still exists, reset the system
Description: The system is not reached to a state where it can take a exposure.
Customer Text: The Expose switches are not enabled yet. Wait a few seconds and try again.
9000042 Error Text: Cannot close exam while in sequence
View Level: opr
Root Cause: 0
Description: Ignore
9000043 Error Text: Cannot go to review screen

View Level: opr
Root Cause: 0
Recommended Action(s): 1. Please verify the selected patient has some images to view.
2. Reset the system if the problem persists
Description: Digital failed to open the patient for review. The reason could be a operator error due
improper selection of the patient from the patient list screen. Or some software failures.

GE MEDICAL SYSTEMS
9000044 Error Text: Cannot come back from review screen
View Level: opr
Root Cause: 0
Recommended Action(s): Make sure that you don’t attempt to start another acquisition while image printing is going on.
Description: Make sure that you don’t attempt to start another acquisition while image printing is going on.
9000045 Error Text: Athena failed to close exam

View Level: opr
Root Cause: 0
Description: Digital failed to close the patient. The reason may be some software failures.
9000046 Error Text: Cannot open exam. Athena returned failure
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Please make sure that the patient selection is proper. Try selecting a patient and start
exam.
2. If the problem persists, restart the system.
Description: The patient selection is not proper.
9000047 Error Text: Cannot add patient. Athena returned failure

View Level: opr
Root Cause: 0
Recommended Action(s): 1. Please make sure that the patient data entry is made proper.
2. If problem persists, reset the system and try again
Description: Software error. A software module failed to respond.
9000048 Error Text: Cannot edit patient. Athena returned failure
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Please make sure that the patient data entry is made proper
Recommended Action(s): 2. If problem persists, reset the system and try again
Description: Software error. A software module failed to respond.
9000049 Error Text: Exposures may resume all inhibit conditions resolved.
Minor Function Impacted: INHIBIT
View Level: opr
Root Cause: 0
Description: Ignore
Customer Text: Exposures may be resumed. All error conditions have been corrected.
9000051 Error Text: The requested mode is not present in the current Protocol.
Minor Function Impacted: APPLICATION_MODE
View Level: opr
Root Cause: 0
Recommended Action(s): Select a different protocol which has the requested mode and try again.
Description: Ignore
Customer Text: This mode is not configured for the current protocol.

GE MEDICAL SYSTEMS
9000052 Error Text: RTPP File is corrupted, Cannot return to Previous protocol.
View Level: opr
Root Cause: 0
Description: Software Error. The file which maintains the information about RTPP status is corrupted. So
system couldn't return to previous protocol.
Customer Text: Protocol error. Please select the same patient to Continue the Exam
9000053 Error Text: There was an error while create the event.
View Level: opr
Root Cause: 0
Description: Software Error. Unable initialize actor (software module).
9000054 Error Text: Invalid Character value

View Level: opr
Root Cause: 0
Description: Ignore
9000055 Error Text: Error in transition to review screen.

Minor Function Impacted: REVIEW
View Level: opr
Root Cause: 0
Recommended Action(s): Make sure the patient selection is made properly before starting a review.
Description: Operator Error: If user hasn't selected a patient, this error will be reported. Software Error:
Second reason could be communication/ component failures.
9000056 Error Text: Review option not set.

View Level: opr
Root Cause: 0
Description: Ignore
9000057 Error Text: Cannot change display format.

View Level: opr
Root Cause: 0
Description: Ignore
9000058 Error Text: Cannot move to next image.

View Level: opr
Root Cause: 0
Description: Ignore

GE MEDICAL SYSTEMS
9000059 Error Text: Cannot move to next screen
View Level: opr
Root Cause: 0
Description: Ignore
9000060 Error Text: Cannot move to next run.

View Level: opr
Root Cause: 0
Description: Ignore
9000061 Error Text: Error in playing.
View Level: opr
Root Cause: 0
Description: Ignore
9000062 Error Text: Error in image tagging.

View Level: opr
Root Cause: 0
Description: Ignore
9000063 Error Text: Cannot Tag image.
View Level: opr
Root Cause: 0
Description: Ignore
9000064 Error Text: Error in filming images.

View Level: opr
Root Cause: 0
Description: Ignore
9000065 Error Text: Error in printing images.

View Level: opr
Root Cause: 0
Description: Ignore

GE MEDICAL SYSTEMS
9000066 Error Text: Error in changing replay rate.
View Level: opr
Root Cause: 0
Description: Ignore
9000067 Error Text: Error in changing film format.

View Level: opr
Root Cause: 0
Description: Ignore
9000068 Error Text: Error in tagging all images.
View Level: opr
Root Cause: 0
Description: Ignore
9000069 Error Text: Error in un-tagging all images.

View Level: opr
Root Cause: 0
Description: Ignore
9000070 Error Text: Error while opening Serial Port
Minor Function Impacted: DOSE_PRINT
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Run Serial port diagnostic.
2. Check/replace dose printer and cable.
Description: Check if the dose printer cable is connected properly to the COM port of the venus.
Customer Text: Dose print error. Check cable connection to the COM port.
9000071 Error Text: Error Dose Print Config parameter is set to NULL
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Please configure dose printer properly and try again.
2. If the problem persists, reload the software
Description: Software Error. Due to upgrade failures, the file has been corrupted.
9000072 Error Text: Could not write to Serial port, Failed to print dose.
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Make sure that the dose printer is connected to correct serial port.
2. Run Serial port diagnostic.
3. Check/replace dose printer and cable.
Description: Configuration Error. Due to connection mismatch of the dose printer cable, software is unable
to write data on to the printer.
Customer Text: Dose print error. Check to see if the serial port is working properly.

GE MEDICAL SYSTEMS
9000073 Error Text: Could not add a Category with the same name of the already existing Category.
Minor Function Impacted: PROTOCOL_EDIT
View Level: opr
Root Cause: 0
Recommended Action(s): Add Category with different Name.
Description: Operator Error. The user tries to add a category with the name of an already existing category
Customer Text: Category name already exists. Create different Category Name.
9000074 Error Text: Could not add a Protocol with the same name of the already existing Protocol under the same
Category.
View Level: opr
Root Cause: 0
Recommended Action(s): Add Protocol with different Name.
Description: Operator Error. The user tries to add a protocol with the name of an already existing protocol
under the same category
Customer Text: Protocol Name already exists. Create different Protocol Name.
9000075 Error Text: Could not add a Exam Step with the same name of the already existing Exam Step under the
same Protocol.
View Level: opr
Root Cause: 0
Recommended Action(s): Add Exam step with different Name.
Description: Operator Error. The user tries to add an exam step with the name of an already existing exam
step under the same protocol
Customer Text: Exam Step Name already exists. Create different Exam Step Name.
9000076 Error Text: Could not add more than 12 characters in a Category Name.
View Level: opr
Root Cause: 0
Recommended Action(s): Add only 12 or less characters in a Category name.
Description: Operator Error. The user exceeds the maximum allowable length for Category name.
Customer Text: Maximum length allowed. 12 or less characters in Category Name.
9000077 Error Text: Could not add more than 12 characters in a Protocol Name.
View Level: opr
Root Cause: 0
Recommended Action(s): Add only 12 or less characters in a Protocol name.
Description: Operator Error. The user exceeds the maximum allowable length for Protocol name.
Customer Text: Maximum length allowed. 12 or less characters in Protocol Name.
9000078 Error Text: Could not add more than 10 characters in a Exam Step Name.
View Level: opr
Root Cause: 0
Recommended Action(s): Add only 10 or less characters in a Exam Step name.
Description: Operator Error. The user exceeds the maximum allowable length for Exam Step name.
Customer Text: Maximum length allowed. 10 or less characters in Exam Step Name.

GE MEDICAL SYSTEMS
9000079 Error Text: Could not enter invalid characters in the Category name.
View Level: opr
Root Cause: 0
Recommended Action(s): This is an Invalid Character. Please delete it using back-space.
Description: Operator Error. The user enters invalid characters in the Category name.
Customer Text: Invalid character selected. Delete using backspace.
9000080 Error Text: Could not enter invalid characters in the Protocol name.
View Level: opr
Root Cause: 0
Description: Operator Error. The user enters invalid characters in the Protocol name.
9000081 Error Text: Could not enter invalid characters in the Exam Step name.
View Level: opr
Root Cause: 0
Description: Operator Error. The user enters invalid characters in the Exam Step name.
9000082 Error Text: Could not save, since the protocol database size exceeds the space available on the CD
during CD backup.
View Level: opr
Root Cause: 0
Recommended Action(s): Since protocol database size is bigger than the space available on CD, Please insert blank
new CD.
Description: System Error. The protocol database size exceeds the space available on the CD during CD
backup.
Customer Text: Protocol database exceeds space available on CD. Insert new CD.
9000083 Error Text: No CD is available in the CD drive during CD backup.

View Level: opr
Root Cause: 0
Recommended Action(s): Please insert a blank CD.
Description: Operator Error. No CD is available in the CD drive for protocol backup.
Customer Text: CD is not available in drive. Insert blank CD.
9000084 Error Text: No CD is available in the CD drive during CD retrieve.

View Level: opr
Root Cause: 0
Recommended Action(s): Please insert a CD, containing Protocol Database.
Description: Operator Error. No CD is available in the CD drive during CD retrieve.
Customer Text: CD is not available in drive. Insert backup CD.

GE MEDICAL SYSTEMS
9000085 Error Text: CD does not contain a valid database for retrieval.
View Level: opr
Root Cause: 0
Recommended Action(s): Please insert a CD with a valid Protocol Database. 2. Please insert a CD with a valid protocol
database.
Description: Operator Error. The CD does not contain a protocol database that can be retrieved for this
system.
Description: Please insert a CD with a valid protocol database.
Customer Text: CD does not contain valid database for system restore. Insert CD with valid protocol
database.
9000086 Error Text: CD already contains information while Backup.

View Level: opr
Root Cause: 0
Recommended Action(s): Please insert a blank CD, to backup the protocol database.
Description: Operator Error. The CD inserted is not blank. Need to insert blank CD.
Customer Text: CD is full. Insert blank CD.
9000087 Error Text: Error has occurred in writing Protocol Database, while Retrieve.
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Try to retrieve again.
2. Reset and try again.
Description: Software Error. Error in writing Protocol Database, while Retrieve due to the hard disk space
limitation.
Customer Text: Error occurred restoring Protocol Database. Reset the system. Call Service if problem
persists.
9000088 Error Text: CD does not contain Protocol Database.
View Level: opr
Root Cause: 0
Recommended Action(s): Please insert a CD, containing Protocol Database.
Description: Operator Error. The CD does not contain Protocol Database. Need to insert CD with Protocol
Database.
Customer Text: CD does not contain the system's protocol database. Insert CD with valid protocol database.
9000089 Error Text: Save operation failed. Check file permission.

Minor Function Impacted: PROCEDURE_EDIT
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Reload the protocol database to the system.
Description: Software Error. The permissions for the protocol file or directory may not be right and save
operation is failed due to that.
Customer Text: Changes could not be saved to the database. Retry and call service if problem persists.
9000090 Error Text: SYSTEM IS SHUTING DOWN

Minor Function Impacted: SHUTDOWN
View Level: opr
Root Cause: 0
Description: Ignore

GE MEDICAL SYSTEMS
9000091 Error Text: System shutdown is in progress.Please wait.
View Level: opr
Root Cause: 0
Description: Ignore
Customer Text: System Shutdown is in progress. This may require 2 minutes to complete. Please wait.
9000092 Error Text: Protocol database is corrupted during load operation

View Level: opr
Root Cause: 0
Recommended Action(s): Reload the protocol database to the system
Description: Software Error. Protocol database is corrupted during load operation
Customer Text: The protocol database could not be loaded. Check/replace CD and try again.
9000093 Error Text: Protocol database validation failed during retrieve

View Level: opr
Root Cause: 0
Recommended Action(s): Reload the protocol database to the system
Description: Software Error. Protocol database validation failed during retrieve
9000094 Error Text: Protocol database validation failed during system validation
View Level: opr
Root Cause: 0
Recommended Action(s): Restore a valid protocol database to continue.
Description: Operator Error. The protocol database is not valid.
9000095 Error Text: Invalid Login User type

View Level: opr
Root Cause: 0
Recommended Action(s): Log-out and try log-in with one of these types, Administrator, Technician or Service
Description: Operator Error. Invalid Login User type
Customer Text: User login has failed. Log out and try again.
9000096 Error Text: accessing config parameters through config cache failed
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Please configure the system again or reload the configuration data. 2. Reset the system
and try again.
Description: Software Error. Some of the configuration is not correct. Getting configuration parameters
from ConfigCache (a database of the configuration) failed

GE MEDICAL SYSTEMS
9000097 Error Text: Invalid Config Parameter set in config file
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Restore a system configuration.
2. Reset the system and try again.
Description: Software Error. Some of the configuration is not correct. Getting configuration parameters
from ConfigCache (a database of the configuration) failed
9000098 Error Text: IUIApp fails to receive Config parameters from XRUserIfVenus actor
View Level: opr
Root Cause: 0
Recommended Action(s): Reset the system.
Description: Software Error. Some of the configuration is not correct. Getting configuration info failed.
Customer Text: System configuration error. Reset and call service if the problem persists.
9000099 Error Text: The environment variable CDRW_COMMAND is not set for backup operation
Minor Function Impacted: BACKUP
View Level: opr
Root Cause: 0
Description: Ignore
Customer Text: Protocol database backup operation has failed. Call service.
9000100 Error Text: The environment variable CDRW_COMMAND is not set for retrieve operation
Minor Function Impacted: RETRIEVE
View Level: opr
Root Cause: 0
Description: Ignore
Customer Text: Protocol database retrieve operation has failed. Call service.
9000101 Error Text: ACE Process cannot be created

Minor Function Impacted: BACKUP_RETRIEVE
View Level: opr
Root Cause: 0
Recommended Action(s): Reset the system and try again.
Description: ACE Process (application) cannot be created due to operating system limitation.
9000102 Error Text: The mkisofs utility is not installed

View Level: opr
Root Cause: 0
Description: The mkisofs utility (cd writer software) is not installed properly

GE MEDICAL SYSTEMS
9000103 Error Text: The cdrecord utility is not installed
View Level: opr
Root Cause: 0
Description: The cdrecord utility is not installed
9000104 Error Text: The cdrecord.conf file does not exist

View Level: opr
Root Cause: 0
Description: The CD record application is not configured properly during installation.
9000105 Error Text: The cdrecord.conf file has errors

View Level: opr
Root Cause: 0
Customer Text: The CDWriter cannot be accessed. Call service.
9000106 Error Text: A hardware configuration error has been detected
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Check the hardware configuration for CDWriter.
Description: A hardware configuration error has been detected for the CDWriter
9000107 Error Text: No drivers are installed for the CDWriter
View Level: opr
Root Cause: 0
Description: No drivers are installed for the CDWriter
9000108 Error Text: Insufficient space on the local disk while retrieve
View Level: opr
Root Cause: 0
Description: The local venus (hardware box for IUI) disk has insufficient space to hold the retrieved
protocol database
Customer Text: There is insufficient space to hold the retrieved information. Call service.

GE MEDICAL SYSTEMS
9000109 Error Text: The system does not support multi-session CD write operation
View Level: opr
Root Cause: 0
Recommended Action(s): Use a blank CD to backup the protocol database.
Description: Protocol database cannot be backed into an already burnt CD as the system does not support
multi-session CD write operation
Customer Text: The CD has already been used for backup. Use a blank CD.
9000110 Error Text: CDWriter cannot be mounted due to no mount permissions

View Level: opr
Root Cause: 0
9000111 Error Text: Error in mounting the CDWriter
View Level: opr
Root Cause: 0
Recommended Action(s): 1. Make sure that a cd is present in the drive.
2. Check if the error is Not able to recognize device. Do following:
A. Check if device is inserted properly.
B. Check the connectivity for the device, check cable and other connector to the drive.
C. Check if CD is readable and writable, if not try another CD.
Description: Software Error. The CDWriter cannot be mounted due to the software failure or system
limitation.
9000112 Error Text: Target specified for retrieve operation not found
View Level: opr
Root Cause: 0
Description: Software Error. Target specified for retrieve operation not found due to software component
failures.
9000113 Error Text: Backup operation successful

View Level: opr
Root Cause: 0
Description: Ignore
Customer Text: The protocol database backup operation is successful.
9000114 Error Text: Retrieve operation successful

View Level: opr
Root Cause: 0
Description: Ignore
Customer Text: The protocol database retrieve operation is successful.

GE MEDICAL SYSTEMS
9000115 Error Text: Cannot change Application Mode from online review screen
View Level: opr
Root Cause: 0
Recommended Action(s): Go to acquisition screen and change application mode.
Description: When user has moved to online review screen and he tries to change application mode
(presses digital on IDD for e.g.) which is not allowed.
Customer Text: Application mode changes are not allowed when in the View/Film screen.
9000116 Error Text: Saving Changes To Protocol Database

Minor Function Impacted: SAVE_PROTOCOL
View Level: opr
Root Cause: 0
Description: Ignore
Customer Text: Saving changes to the Protocol Database. Please wait.
9000117 Error Text: Validating Protocol Database

View Level: opr
Root Cause: 0
Description: Ignore
Customer Text: Protocol Database validation is in progress. It may take up to 20 sec. to complete
9000118 Error Text: System is Ready

Minor Function Impacted: SYSTEM_BOOT
View Level: opr
Root Cause: 1
Description: Ignore
Customer Text: The system is ready for user input.
9000119 Error Text: Invalid Object Reference.

Minor Function Impacted: SYSTEM
View Level: opr
Root Cause: 1
Recommended Action(s): Reset the system.
Description: Software Error. Some of the system actors (software component) failed to establish the
communication.
9000120 Error Text: System failed to complete boot

View Level: opr
Root Cause: 0
Recommended Action(s): “Reset the system
Description: “System did not complete boot in the allocated time. Check system error log for other boot
related errors.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 0
Recommended Action(s): “The current user is not authorized to perform this function. The user must log-out and re-log-
Description: “The current user is not authorized to perform this function. The user must log-out and re-log-

GE MEDICAL SYSTEMS
3.27 Inhibit Conditions
# Inhibit Condition ID Comments Customer Text

0 SYSTEM_NOT_CONFIGURED System is not configured for any opmode. System is not configured. Select protocol to
continue.
1 DISK_FULL The disk is full. Free up disk space to continue.
2 NEW_EXAM There is no Exam Open. To start Acquisition, Start a new exam.
first need to start a Exam
3 TW_SOAK_TIME After TW, for next 30 exposure should not be Tube is warming. Please wait.
allowed.
4 FLUORO_TIMER Maximum fluoro time reached. Touch timer Maximum fluoro time reached. Touch timer
reset to continue reset to continue.
5 CDRH_CONTROL Collimator error. If problem persists reset
system.
6 HEAT_UNIT_LIMIT_REACHED Heat units exceeded. Tube is cooling. Please
wait.
7 ROOM_DOOR_OPEN Room door is open. Close door to continue.
8 EMERGENCY_SWITCH_TRIPPED This is the table side emergency stop switch. Emergency switch is tripped. Reset switch and
system to continue.
9 SID_OUT_OF_RANGE Source to image distance out of range. Adjust
tube position.
10 NOT_IN_LATERAL_DETENT Align the overhead X-ray tube to the image
receptor.
11 TUBE_PIVOT Align the overhead X-ray tube to the image
receptor.
12 TUBE_ANGLE_OUT_OF_RANGE Rotate the overhead X-ray tube to the image
receptor.
13 CASSETTE_NOT_IN_PLACE Insert cassette to continue.
14 TABLE_CASSETTE_INSERTED Remove table cassette to continue.
15 WALLSTAND_CASSETTE_INSERT Remove wall cassette to continue.
ED
16 SFD_NOT_IN_EXPOSE_POSITION Lock imaging device in forward position.
17 SFD_NOT_IN_PARK_POSITION Move imaging device to park position.
18 COLL_NOT_ALIVE System error. Reset system. (Coll)
19 COLL_MALFUNCTION System error. Reset system. (Coll)
20 BAD_IDD_SID_POT System error. Reset system. (IDD SID)
21 PDU_IO_NOT_ALIVE The PDU I/O is located in the Systems System error. Reset system. (PDU IO)
Cabinet.
22 POS_IO_NOT_ALIVE The Pos I/O is located in the Positioner System error. Reset system. (Pos IO)
Cabinet.
23 DIGITAL_NOT_READY IUI/Digital are in image review mode. Fluoro and Digital Record not ready. Please
wait.
24 NOT_IN_ACQ_SCREEN Only from Acquire screen, exposure is Enter the Acquire mode to continue.
allowed.
25 FLUORO_LOOP_STORE X-rays are not allowed during loop storage.
26 RUN_LIMIT_REACHED Series limit reached. Start new exam to
continue.
27 DIGITAL_IS_BUSY Enter the Acquire mode to continue.
28 IUI_NOT_IN_ACQUIRE_SCREEN Only from Acquire screen, exposure is Enter the Acquire mode to continue.
allowed.
29 BACKUP_TIME_REACHED AEC backup time has reached. To continue AEC Backup time reached. Reselect technique
the exposure, Reset msec.
30 TECHNIQUES_REJECTED Select another technique to continue.
31 CASSETTE_SIZE_NOT_DETERMI Remove and replace cassette.
NED
32 IDD_GOLDBOX_NOT_ALIVE Goldbox is the grid/cone controller mounted System error. Reset system. (Goldbox)
inside rear of IDD.
33 CAN_BRIDGE_NOT_ALIVE CAN bridge is in Positioner cabinet, it is the System error. Reset system. (CAN bridge)
CAN interface to the IDD Goldbox and IDD
console.

GE MEDICAL SYSTEMS
34 OTS_UIF_NOT_ALIVE OTS UIF is the control console on the OTS. System error. Reset system. (OTS UIF)
35 OTS_AMP_NOT_ALIVE The CAN Amp on the OTS. System error. Reset system. (OTS Amp)
36 BAD_OTS_LONG_POT The longitudinal position feedback pot on the System error. Reset system. (OTS Long Pot)
OTS.
37 BAD_OTS_LAT_POT The lateral position feedback pot on the System error. Reset system. (OTS Lat Pot)
OTS.
38 BAD_OTS_VERT_POT The vertical position feedback pot on the System error. Reset system. (OTS Vert Pot)
OTS.
39 ANODE_HEAT_LIMIT_REACHED X-ray tube overheat. Wait and continue.
40 CASING_HEAT_LIMIT_REACHED X-ray tube overheat. Wait and continue.
41 TRACK_LIMIT_REACHED X-ray tube track limit. Wait or reduce technic.
42 JEDI_UNRECOVERABLE_ERROR Generator error. Reset system and try again.
43 TUBE_SWITCH_IN_PROGRESS Tube switch in progress. Exposure is Exposures disabled due to tube switch, please
inhibited wait

GE MEDICAL SYSTEMS
3.28 IDD Advisory Messages
# Message ID Customer Text

0 PATIENT_STEP_INHIBIT Patient step is not, parked. Push in prior, to tilting table.
1 CONE_MOTION_INHIBIT Cone transfer not, allowed when horizontal, stop is off.
2 TABLE_ANGULATION_WARNING Table angulating-Watch, patient and beware of, obstructions in room.
3 TABLE_TOP_MOTION_WARNING Tabletop moving -, Watch patient.
4 CONFLICTING_MOTION_COMMANDS Motion stopped -, Use only one control.
5 CONE_TABLE_TOP_INTERLOCK Powered motion not, allowed when cone in, and comp lock on.
6 FL_LOOP_STORE_IN_PROGRESS X-rays are not allowed, during loop storage.
7 FL_LOOP_FAIL_IMAGE_STORE Fluoro Loop not allowed, during image transfer., Please wait.
8 FL_LOOP_FAIL_DIGITAL_ERROR Cannot acquire Fluoro, Loop. Try again.
9 IDD_CALIBRATION_INSTRUCTIONS
10 LOW_PRI_ADVISORY_TEXT
11 MED_PRI_ADVISORY_TEXT
12 HI_PRI_ADVISORY_TEXT

GE MEDICAL SYSTEMS
3.29 DeviceComm
Error Error Text Recovery Major Minor Function View Root Action Detailed Description Customer Text
Code Class Function Level Cause
6663001 EM_INVALID_PARAM Debug SysCntr DeviceComm opr 0 Ignore "EM_INVALID_PARAM EM_INVALID_PARAM
Only l
6663002 EM_CAN_CONSTRUCTOR_MSG Debug SysCntr DeviceComm opr 0 Ignore "EM_CAN_CONSTRUCTOR_MS EM_CAN_CONSTRUCTOR_MSG_
_Q_CREATION_FAILED Only l G_Q_CREATION_FAILED Q_CREATION_FAILED
6663003 EM_CAN_CONSTRUCTOR_FAI Debug SysCntr DeviceComm opr 0 Ignore "EM_CAN_CONSTRUCTOR_FA EM_CAN_CONSTRUCTOR_FAIL

LED_TO_CREATE_RXSTART_ Only l ILED_TO_CREATE_RXSTART ED_TO_CREATE_RXSTART_TA
TASK_SEMAPHORE _TASK_SEMAPHORE SK_SEMAPHORE

LED_TO_CREATE_RXSEMID_ Only l ILED_TO_CREATE_RXSEMID ED_TO_CREATE_RXSEMID_SE
SEMAPHORE _SEMAPHORE MAPHORE

LED_TO_CREATE_TXSEMID_ Only l ILED_TO_CREATE_TXSEMID ED_TO_CREATE_TXSEMID_SE

LED_TO_CREATE_CAN_TX_T Only l ILED_TO_CREATE_CAN_TX_ ED_TO_CREATE_CAN_TX_TAS
ASK TASK K
6663007 EM_CAN_SEARCH_ID_REQUE Debug SysCntr DeviceComm opr 0 Ignore "EM_CAN_SEARCH_ID_REQU EM_CAN_SEARCH_ID_REQUES

STER_SEM_TAKE_FAILED Only l ESTER_SEM_TAKE_FAILED TER_SEM_TAKE_FAILED

STER_NO_RECEIVERS Only l ESTER_NO_RECEIVERS TER_NO_RECEIVERS

STER_ID_NOT_REGISTERED Only l ESTER_ID_NOT_REGISTERE TER_ID_NOT_REGISTERED
D

STER_SEM_GIVE_FAILED Only l ESTER_SEM_GIVE_FAILED TER_SEM_GIVE_FAILED
6663011 EM_CAN_ADD_ID_SEM_TAKE Debug SysCntr CanComm opr 0 Ignore "EM_CAN_ADD_ID_SEM_TAK EM_CAN_ADD_ID_SEM_TAKE_

_FAILED Only l E_FAILED FAILED
6663012 EM_CAN_ADD_ID_RXTASK_S Debug SysCntr CanComm opr 0 Ignore "EM_CAN_ADD_ID_RXTASK_ EM_CAN_ADD_ID_RXTASK_SP

PAWN_FAILED Only l SPAWN_FAILED AWN_FAILED
6663013 EM_CAN_ADD_ID_ADDING_D Debug SysCntr CanComm opr 0 Ignore "EM_CAN_ADD_ID_ADDING_ EM_CAN_ADD_ID_ADDING_DE

EVICE_FAILED Only l DEVICE_FAILED VICE_FAILED
6663014 EM_CAN_ADD_ID_ID_LIST_ Debug SysCntr CanComm opr 0 Ignore "EM_CAN_ADD_ID_ID_LIST EM_CAN_ADD_ID_ID_LIST_E

EXCEEDS_LIMIT Only l _EXCEEDS_LIMIT XCEEDS_LIMIT
6663015 EM_CAN_ADD_ID_ID_DUPLI Debug SysCntr CanComm opr 0 Ignore "EM_CAN_ADD_ID_ID_DUPL EM_CAN_ADD_ID_ID_DUPLIC

CATION Only l ICATION ATION
6663016 EM_CAN_ADD_ID_MSGQ_CRE Debug SysCntr CanComm opr 0 Ignore "EM_CAN_ADD_ID_MSGQ_CR EM_CAN_ADD_ID_MSGQ_CREA

ATE_FAILED Only l EATE_FAILED TE_FAILED
6663017 EM_CAN_ADD_ID_CANIFTAS Debug SysCntr CanComm opr 0 Ignore "EM_CAN_ADD_ID_CANIFTA EM_CAN_ADD_ID_CANIFTASK

K_SPAWN_FAILED Only l SK_SPAWN_FAILED _SPAWN_FAILED
6663018 EM_CAN_ADD_ID_RXSTARTT Debug SysCntr CanComm opr 0 Ignore "EM_CAN_ADD_ID_RXSTART EM_CAN_ADD_ID_RXSTARTTA

ASKSEM_GIVE_FAILED Only l TASKSEM_GIVE_FAILED SKSEM_GIVE_FAILED
6663019 EM_CAN_ADD_ID_RXSEM_GI Debug SysCntr CanComm opr 0 Ignore "EM_CAN_ADD_ID_RXSEM_G EM_CAN_ADD_ID_RXSEM_GIV

VE_FAILED Only l IVE_FAILED E_FAILED
6663020 EM_CAN_CANTXTASK_READ_ Debug SysCntr CanComm opr 0 Ignore "EM_CAN_CANTXTASK_READ EM_CAN_CANTXTASK_READ_F

FROM_MSGQ_FAILED Only l _FROM_MSGQ_FAILED ROM_MSGQ_FAILED
6663021 EM_CAN_CANRXTASK_SEM_T Debug SysCntr CanComm opr 0 Ignore "EM_CAN_CANRXTASK_SEM_ EM_CAN_CANRXTASK_SEM_TA

AKE_FAILED Only l TAKE_FAILED KE_FAILED
6663022 EM_CAN_CANRXTASK_SEM_G Debug SysCntr CanComm opr 0 Ignore "EM_CAN_CANRXTASK_SEM_ EM_CAN_CANRXTASK_SEM_GI

IVE_FAILED Only l GIVE_FAILED VE_FAILED
6663023 EM_CAN_CANRXTASK_MEM_A Debug SysCntr CanComm opr 0 Ignore "EM_CAN_CANRXTASK_MEM_ EM_CAN_CANRXTASK_MEM_AL

LLOC_FAILED Only l ALLOC_FAILED LOC_FAILED
6663024 EM_CAN_CANRXTASK_SEND_ Debug SysCntr CanComm opr 0 Ignore "EM_CAN_CANRXTASK_SEND EM_CAN_CANRXTASK_SEND_T

TO_MSGQ_FAILED Only l _TO_MSGQ_FAILED O_MSGQ_FAILED
6663025 EM_CAN_CANIFTASK_READ_ Debug SysCntr CanComm opr 0 Ignore "EM_CAN_CANIFTASK_READ EM_CAN_CANIFTASK_READ_F

FROM_MSG_Q_FAILED Only l _FROM_MSG_Q_FAILED ROM_MSG_Q_FAILED
6663026 EM_CAN_WRITE_MEM_ALLOC Debug SysCntr CanComm opr 0 Ignore "EM_CAN_WRITE_MEM_ALLO EM_CAN_WRITE_MEM_ALLOC_

_FAILED Only l C_FAILED FAILED
6663027 EM_CAN_WRITE_SEND_TO_M Debug SysCntr CanComm opr 0 Ignore "EM_CAN_WRITE_SEND_TO_ EM_CAN_WRITE_SEND_TO_MS

SG_Q_FAILED Only l MSG_Q_FAILED G_Q_FAILED
6663028 EM_CAN_RX_TIMEDOUT Debug SysCntr CanComm opr 0 Ignore "EM_CAN_RX_TIMEDOUT EM_CAN_RX_TIMEDOUT

Only l

GE MEDICAL SYSTEMS
6663029 EM_CAN_TX_TIMEDOUT Debug SysCntr CanComm opr 0 Ignore "EM_CAN_TX_TIMEDOUT EM_CAN_TX_TIMEDOUT
Only l
6663030 EM_CAN_TX_ERROR Debug SysCntr CanComm opr 0 Ignore "EM_CAN_TX_ERROR EM_CAN_TX_ERROR
Only l
6663031 EM_CAN_CONTR_OFF_BUS Debug SysCntr CanComm opr 0 Ignore "EM_CAN_CONTR_OFF_BUS EM_CAN_CONTR_OFF_BUS
Only l
6663032 EM_CAN_CONTR_BUSY Debug SysCntr CanComm opr 0 Ignore "EM_CAN_CONTR_BUSY EM_CAN_CONTR_BUSY
Only l
6663033 EM_CAN_CONTR_WARN Debug SysCntr CanComm opr 0 Ignore "EM_CAN_CONTR_WARN EM_CAN_CONTR_WARN
Only l
6663034 EM_CAN_NO_ID_ENABLED Debug SysCntr CanComm opr 0 Ignore "EM_CAN_NO_ID_ENABLED EM_CAN_NO_ID_ENABLED
Only l
6663035 EM_CAN_ID_ALREADY_ENAB Debug SysCntr CanComm opr 0 Ignore "EM_CAN_ID_ALREADY_ENA EM_CAN_ID_ALREADY_ENABL
LED Only l BLED ED
6663036 EM_CAN_ID_NOT_ENABLED Debug SysCntr CanComm opr 0 Ignore "EM_CAN_ID_NOT_ENABLED EM_CAN_ID_NOT_ENABLED

Only l
6663037 EM_CAN_INVALID_FIRMWAR Debug SysCntr CanComm opr 0 Ignore "EM_CAN_INVALID_FIRMWA EM_CAN_INVALID_FIRMWARE
E Only l RE
6663038 EM_CAN_MESSAGE_LOST Debug SysCntr CanComm opr 0 Ignore "EM_CAN_MESSAGE_LOST EM_CAN_MESSAGE_LOST

Only l
6663039 EM_CAN_INVALID_HARDWAR Debug SysCntr CanComm opr 0 Ignore "EM_CAN_INVALID_HARDWA EM_CAN_INVALID_HARDWARE
E Only l RE
6663040 EM_CAN_INVALID_PARAMET Debug SysCntr CanComm opr 0 Ignore "EM_CAN_INVALID_PARAME EM_CAN_INVALID_PARAMETE

ER Only l TER R
6663041 EM_CAN_INVALID_HANDLE Debug SysCntr CanComm opr 0 Ignore "EM_CAN_INVALID_HANDLE EM_CAN_INVALID_HANDLE

Only l
6663042 EM_CAN_NET_NOT_FOUND Debug SysCntr CanComm opr 0 Ignore "EM_CAN_NET_NOT_FOUND EM_CAN_NET_NOT_FOUND
Only l
6664001 EM_CANOPENCOMM_CONSTRU Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPENCOMM_CONSTR EM_CANOPENCOMM_CONSTRUC
CTOR_FAILED Only UCTOR_FAILED TOR_FAILED
6664002 EM_CANOPEN_CONSTRUCTOR Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_CONSTRUCTO EM_CANOPEN_CONSTRUCTOR_

_RECEIVER_TABLE_CREATI Only R_RECEIVER_TABLE_CREAT RECEIVER_TABLE_CREATION
ON_FAILED ION_FAILED _FAILED

_FAILED_TO_CREATE_SLAV Only R_FAILED_TO_CREATE_SLA FAILED_TO_CREATE_SLAVE_
E_NODE VE_NODE NODE

_SLAVE_INITIALIZATION_ Only R_SLAVE_INITIALIZATION SLAVE_INITIALIZATION_FA
FAILED _FAILED ILED

_MSG_Q_CREATION_FAILED Only R_MSG_Q_CREATION_FAILE MSG_Q_CREATION_FAILED
D

_FAILED_TO_CREATE_TXSE Only R_FAILED_TO_CREATE_TXS FAILED_TO_CREATE_TXSEMI
MID_SEMAPHORE EMID_SEMAPHORE D_SEMAPHORE

_FAILED_TO_CREATE_CO_L Only R_FAILED_TO_CREATE_CO_ FAILED_TO_CREATE_CO_LKU
KUP_TABLE_SEMAPHORE LKUP_TABLE_SEMAPHORE P_TABLE_SEMAPHORE

_FAILED_TO_CREATE_CANO Only R_FAILED_TO_CREATE_CAN FAILED_TO_CREATE_CANOPE
PEN_TX_TASK OPEN_TX_TASK N_TX_TASK
6664009 EM_CANOPEN_SEARCH_NODE Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SEARCH_NOD EM_CANOPEN_SEARCH_NODE_

_MSG_Q_SEM_TAKE_FAILED Only E_MSG_Q_SEM_TAKE_FAILE MSG_Q_SEM_TAKE_FAILED
D

_MSG_Q_NO_RECEIVERS Only E_MSG_Q_NO_RECEIVERS MSG_Q_NO_RECEIVERS

_MSG_Q_ID_NOT_REGISTER Only E_MSG_Q_ID_NOT_REGISTE MSG_Q_ID_NOT_REGISTERED
ED RED

_MSG_Q_SEM_GIVE_FAILED Only E_MSG_Q_SEM_GIVE_FAILE MSG_Q_SEM_GIVE_FAILED
D
6664013 EM_CANOPEN_ADD_ID_ADDI Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_ADD_ID_ADD EM_CANOPEN_ADD_ID_ADDIN

NG_MULTIPLE_NODES Only ING_MULTIPLE_NODES G_MULTIPLE_NODES
6664014 EM_CANOPEN_ADD_ID_SEM_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_ADD_ID_SEM EM_CANOPEN_ADD_ID_SEM_T

TAKE_FAILED Only _TAKE_FAILED AKE_FAILED

GE MEDICAL SYSTEMS
NG_DEVICE_FAILED Only ING_DEVICE_FAILED G_DEVICE_FAILED
6664016 EM_CANOPEN_ADD_ID_ID_L Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_ADD_ID_ID_ EM_CANOPEN_ADD_ID_ID_LI

IST_EXCEEDS_LIMIT Only LIST_EXCEEDS_LIMIT ST_EXCEEDS_LIMIT
6664017 EM_CANOPEN_ADD_ID_ID_D Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_ADD_ID_ID_ EM_CANOPEN_ADD_ID_ID_DU

UPLICATION Only DUPLICATION PLICATION
6664018 EM_CANOPEN_ADD_ID_MSGQ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_ADD_ID_MSG EM_CANOPEN_ADD_ID_MSGQ_

_CREATE_FAILED Only Q_CREATE_FAILED CREATE_FAILED
6664019 EM_CANOPEN_ADD_ID_CANO Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_ADD_ID_CAN EM_CANOPEN_ADD_ID_CANOP

PEN_IF_TASK_SPAWN_FAIL Only OPEN_IF_TASK_SPAWN_FAI EN_IF_TASK_SPAWN_FAILED
ED LED
6664020 EM_CANOPEN_ADD_ID_SEM_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_ADD_ID_SEM EM_CANOPEN_ADD_ID_SEM_G

GIVE_FAILED Only _GIVE_FAILED IVE_FAILED
6664021 EM_CANOPEN_DELETE_ID_N Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DELETE_ID_ EM_CANOPEN_DELETE_ID_NO

O_ID_REGISTERED Only NO_ID_REGISTERED _ID_REGISTERED
6664022 EM_CANOPEN_DELETE_ID_S Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DELETE_ID_ EM_CANOPEN_DELETE_ID_SE

EM_TAKE_FAILED Only SEM_TAKE_FAILED M_TAKE_FAILED

EM_GIVE_FAILED Only SEM_GIVE_FAILED M_GIVE_FAILED
6664024 EM_CANOPEN_CMDOUTTASK_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_CMDOUTTASK EM_CANOPEN_CMDOUTTASK_R

READ_FROM_MSGQ_FAILED Only _READ_FROM_MSGQ_FAILED EAD_FROM_MSGQ_FAILED
6664025 EM_CANOPEN_CMDOUTTASK_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_CMDOUTTASK EM_CANOPEN_CMDOUTTASK_S

SEM_TAKE_FAILED Only _SEM_TAKE_FAILED EM_TAKE_FAILED
6664026 EM_CANOPEN_CMDOUTTASK_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_CMDOUTTASK EM_CANOPEN_CMDOUTTASK_U

UNKNOWN_COMMAND Only _UNKNOWN_COMMAND NKNOWN_COMMAND

SEM_GIVE_FAILED Only _SEM_GIVE_FAILED EM_GIVE_FAILED
6664028 EM_CANOPEN_RX_SEM_TAKE Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_RX_SEM_TAK EM_CANOPEN_RX_SEM_TAKE_

_FAILED Only E_FAILED FAILED
6664029 EM_CANOPEN_RX_SEM_GIVE Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_RX_SEM_GIV EM_CANOPEN_RX_SEM_GIVE_

6664030 EM_CANOPEN_CANOPENIFTA Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_CANOPENIFT EM_CANOPEN_CANOPENIFTAS

SK_MSGQ_RECEIVE_FAILED Only ASK_MSGQ_RECEIVE_FAILE K_MSGQ_RECEIVE_FAILED
D
6664031 EM_CANOPEN_WRITE_SEND_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_WRITE_SEND EM_CANOPEN_WRITE_SEND_T

TO_MSG_Q_FAILED Only _TO_MSG_Q_FAILED O_MSG_Q_FAILED
6664032 EM_CANOPEN_READ_DATA_S Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_READ_DATA_ EM_CANOPEN_READ_DATA_SI

IZE_ERROR Only SIZE_ERROR ZE_ERROR
6664033 EM_CANOPEN_READ_SDO_SE Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_READ_SDO_S EM_CANOPEN_READ_SDO_SEM

M_TAKE_FAILED Only EM_TAKE_FAILED _TAKE_FAILED

M_GIVE_FAILED Only EM_GIVE_FAILED _GIVE_FAILED
6664035 EM_CANOPEN_LOCAL_NODE_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_LOCAL_NODE EM_CANOPEN_LOCAL_NODE_T

TABLE_CREATION_FAILED Only _TABLE_CREATION_FAILED ABLE_CREATION_FAILED
6664036 EM_CANOPEN_LOCAL_NODE_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_LOCAL_NODE EM_CANOPEN_LOCAL_NODE_R

RPDOCALLBACK_SEND_TO_M Only _RPDOCALLBACK_SEND_TO_ PDOCALLBACK_SEND_TO_MSG
SGQ_FAILED MSGQ_FAILED Q_FAILED
6665001 EM_CANOPEN_MCAL_CAN_TX Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_CAN_T EM_CANOPEN_MCAL_CAN_TX_

_TIMEOUT Only X_TIMEOUT TIMEOUT

_ERROR Only X_ERROR ERROR
6665003 EM_CANOPEN_MCAL_CAN_CO Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_CAN_C EM_CANOPEN_MCAL_CAN_CON

NTR_OFF_BUS Only ONTR_OFF_BUS TR_OFF_BUS

NTR_WARN Only ONTR_WARN TR_WARN

NTR_BUSY Only ONTR_BUSY TR_BUSY
6665006 EM_CANOPEN_DCF_INIT_ER Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_INIT_E EM_CANOPEN_DCF_INIT_ERR

ROR Only RROR OR
6665007 EM_CANOPEN_DCF_OUT_OF_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_OUT_OF EM_CANOPEN_DCF_OUT_OF_M

MEMORY Only _MEMORY EMORY
6665008 EM_CANOPEN_DCF_WRONG_N Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_WRONG_ EM_CANOPEN_DCF_WRONG_NO

ODE_ID Only NODE_ID DE_ID

GE MEDICAL SYSTEMS
6665009 EM_CANOPEN_DCF_WRONG_B Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_WRONG_ EM_CANOPEN_DCF_WRONG_BA
AUDRATE Only BAUDRATE UDRATE
6665010 EM_CANOPEN_DCF_MISSING Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_MISSIN EM_CANOPEN_DCF_MISSING_

_SECTION Only G_SECTION SECTION

_ENTRY Only G_ENTRY ENTRY
6665012 EM_CANOPEN_DCF_WRONG_P Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_WRONG_ EM_CANOPEN_DCF_WRONG_PA

ARAMETER Only PARAMETER RAMETER
6665013 EM_CANOPEN_DCF_OUT_OF_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_OUT_OF EM_CANOPEN_DCF_OUT_OF_R

RANGE Only _RANGE ANGE
6665014 EM_CANOPEN_DCF_OUT_OF_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_OUT_OF EM_CANOPEN_DCF_OUT_OF_L

LIMITS Only _LIMITS IMITS
6665015 EM_CANOPEN_DCF_DOUBLE_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_DOUBLE EM_CANOPEN_DCF_DOUBLE_S

SECTION Only _SECTION ECTION
6665016 EM_CANOPEN_DCF_DOUBLE_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_DOUBLE EM_CANOPEN_DCF_DOUBLE_K

KEYWORD Only _KEYWORD EYWORD
6665017 EM_CANOPEN_DCF_UNKNOWN Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_UNKNOW EM_CANOPEN_DCF_UNKNOWN_

_KEYWORD Only N_KEYWORD KEYWORD
6665018 EM_CANOPEN_WRONG_NET_N Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_WRONG_NET_ EM_CANOPEN_WRONG_NET_NO

O Only NO
6665019 EM_CANOPEN_WRONG_MODUL Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_WRONG_MODU EM_CANOPEN_WRONG_MODULE

E_NO Only LE_NO _NO
6665020 EM_CANOPEN_MCAL_PARA_E Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_PARA_ EM_CANOPEN_MCAL_PARA_ER

RROR Only ERROR ROR
6665021 EM_CANOPEN_MCAL_SYS_ER Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_SYS_E EM_CANOPEN_MCAL_SYS_ERR

ROR Only RROR OR
6665022 EM_CANOPEN_MCAL_NO_NET Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_NO_NE EM_CANOPEN_MCAL_NO_NET

Only T
6665023 EM_CANOPEN_MCAL_OBJ_NO Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_OBJ_N EM_CANOPEN_MCAL_OBJ_NO_

_MEMORY Only O_MEMORY MEMORY
6665024 EM_CANOPEN_MCAL_DOWNLO Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_DOWNL EM_CANOPEN_MCAL_DOWNLOA

AD_ABORT_SLAVE Only OAD_ABORT_SLAVE D_ABORT_SLAVE
6665025 EM_CANOPEN_MCAL_WRONG_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_WRONG EM_CANOPEN_MCAL_WRONG_S

SLAVE_ANSWER Only _SLAVE_ANSWER LAVE_ANSWER

SERVER_ANSWER Only _SERVER_ANSWER ERVER_ANSWER
6665027 EM_CANOPEN_MCAL_TOGGLE Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_TOGGL EM_CANOPEN_MCAL_TOGGLE_

_ERROR Only E_ERROR ERROR
6665028 EM_CANOPEN_MCAL_BUFFER Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_BUFFE EM_CANOPEN_MCAL_BUFFER_

_OVERFLOW Only R_OVERFLOW OVERFLOW
6665029 EM_CANOPEN_MCAL_ABORT_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_ABORT EM_CANOPEN_MCAL_ABORT_D

DOMAIN Only _DOMAIN OMAIN
6665030 EM_CANOPEN_MCAL_NODE_N Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_NODE_ EM_CANOPEN_MCAL_NODE_NO

OT_EXISTEND Only NOT_EXISTEND T_EXISTEND
6665031 EM_CANOPEN_MCAL_WRONG_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_WRONG EM_CANOPEN_MCAL_WRONG_G

GUARD_ID Only _GUARD_ID UARD_ID
6665032 EM_CANOPEN_MCAL_NEW_GU Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_NEW_G EM_CANOPEN_MCAL_NEW_GUA

ARD_PARA Only UARD_PARA RD_PARA

OT_FREE Only NOT_FREE T_FREE
6665034 EM_CANOPEN_MCAL_NO_EVE Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_NO_EV EM_CANOPEN_MCAL_NO_EVEN

NT Only ENT T
6665035 EM_CANOPEN_MCAL_UNSUPP Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_UNSUP EM_CANOPEN_MCAL_UNSUPPO

ORTED Only PORTED RTED
6665036 EM_CANOPEN_MCAL_FILE_R Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_FILE_ EM_CANOPEN_MCAL_FILE_RE

EAD_ERR Only READ_ERR AD_ERR
6665037 EM_CANOPEN_MCAL_FILE_O Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_FILE_ EM_CANOPEN_MCAL_FILE_OP

PEN_ERR Only OPEN_ERR EN_ERR
6665038 EM_CANOPEN_DCF_WRONG_T Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_WRONG_ EM_CANOPEN_DCF_WRONG_TY

YP Only TYP P
6665039 EM_CANOPEN_DCF_WRONG_N Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_WRONG_ EM_CANOPEN_DCF_WRONG_NE

ET_ID Only NET_ID T_ID

GE MEDICAL SYSTEMS
ODE_NAME Only NODE_NAME DE_NAME
6665041 EM_CANOPEN_MCAL_EXERR Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_EXERR EM_CANOPEN_MCAL_EXERR

Only
6665042 EM_CANOPEN_MCAL_CAN_RX Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_CAN_R EM_CANOPEN_MCAL_CAN_RX_
6665043 EM_CANOPEN_MCAL_WRONG_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_WRONG EM_CANOPEN_MCAL_WRONG_N

NODE_STATE Only _NODE_STATE ODE_STATE
6665044 EM_CANOPEN_MCAL_CONSIS Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_CONSI EM_CANOPEN_MCAL_CONSIST

TENCY_ERROR Only STENCY_ERROR ENCY_ERROR
6666001 EM_CANOPEN_SCANOPEN_PA Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_P EM_CANOPEN_SCANOPEN_PAR

RA_ERROR Only ARA_ERROR A_ERROR
6666002 EM_CANOPEN_SCANOPEN_SY Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_S EM_CANOPEN_SCANOPEN_SYS

S_ERROR Only YS_ERROR _ERROR
6666003 EM_CANOPEN_SCANOPEN_CA Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_C EM_CANOPEN_SCANOPEN_CAN

N_RX_TIMEOUT Only AN_RX_TIMEOUT _RX_TIMEOUT

N_TX_TIMEOUT Only AN_TX_TIMEOUT _TX_TIMEOUT

N_TX_ERROR Only AN_TX_ERROR _TX_ERROR

N_CONTR_OFF_BUS Only AN_CONTR_OFF_BUS _CONTR_OFF_BUS

N_CONTR_BUSY Only AN_CONTR_BUSY _CONTR_BUSY

N_CONTR_WAIT Only AN_CONTR_WAIT _CONTR_WAIT
6666009 EM_CANOPEN_SCANOPEN_PR Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_P EM_CANOPEN_SCANOPEN_PRO

OTOCOL_ERROR Only ROTOCOL_ERROR TOCOL_ERROR
6666010 EM_CANOPEN_SCANOPEN_NO Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_N EM_CANOPEN_SCANOPEN_NO_

_SLAVE_NET Only O_SLAVE_NET SLAVE_NET
6666011 EM_CANOPEN_SCANOPEN_NE Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_N EM_CANOPEN_SCANOPEN_NET

TWORK_FILE_ERROR Only ETWORK_FILE_ERROR WORK_FILE_ERROR
6666012 EM_CANOPEN_SCANOPEN_WR Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_W EM_CANOPEN_SCANOPEN_WRO

ONG_NODE_STATE Only RONG_NODE_STATE NG_NODE_STATE
6666013 EM_CANOPEN_SCANOPEN_SE Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_S EM_CANOPEN_SCANOPEN_SER

RVICE_NOT_ALLOWED Only ERVICE_NOT_ALLOWED VICE_NOT_ALLOWED
6666014 EM_CANOPEN_SCANOPEN_NO Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_N EM_CANOPEN_SCANOPEN_NOD

DE_NOT_OPERATIONAL Only ODE_NOT_OPERATIONAL E_NOT_OPERATIONAL
6666015 EM_CANOPEN_SCANOPEN_OB Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_O EM_CANOPEN_SCANOPEN_OBJ

J_NOT_EXISTS Only BJ_NOT_EXISTS _NOT_EXISTS

NNOT_START_DAEMON Only ANNOT_START_DAEMON NOT_START_DAEMON
6666017 EM_CANOPEN_SCANOPEN_UN Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_U EM_CANOPEN_SCANOPEN_UNK

KNOWN_ERROR Only NKNOWN_ERROR NOWN_ERROR
6666018 EM_CANOPEN_SCANOPEN_CH Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_C EM_CANOPEN_SCANOPEN_CHE

ECKSUM_ERROR Only HECKSUM_ERROR CKSUM_ERROR
6666019 EM_CANOPEN_SCANOPEN_VE Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_V EM_CANOPEN_SCANOPEN_VER

RIFY_ERROR Only ERIFY_ERROR IFY_ERROR
6666020 EM_CANOPEN_SCANOPEN_CO Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_C EM_CANOPEN_SCANOPEN_COB

B_DATABASE_OVERFLOW Only OB_DATABASE_OVERFLOW _DATABASE_OVERFLOW

B_DATABASE_DISABLED Only OB_DATABASE_DISABLED _DATABASE_DISABLED

B_CLASS_ERROR Only OB_CLASS_ERROR _CLASS_ERROR

B_LENGTH_ERROR Only OB_LENGTH_ERROR _LENGTH_ERROR

J_EXISTS Only BJ_EXISTS _EXISTS
6666025 EM_CANOPEN_SCANOPEN_DA Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_D EM_CANOPEN_SCANOPEN_DAT

TATYPE_TOO_LONG Only ATATYPE_TOO_LONG ATYPE_TOO_LONG

J_NO_MEMORY Only BJ_NO_MEMORY _NO_MEMORY

GE MEDICAL SYSTEMS
NNOT_OPEN_CAN Only ANNOT_OPEN_CAN NOT_OPEN_CAN
6666028 EM_CANOPEN_SCANOPEN_DO Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_D EM_CANOPEN_SCANOPEN_DOW

WNLOAD_ABORT_SLAVE Only OWNLOAD_ABORT_SLAVE NLOAD_ABORT_SLAVE

WNLOAD_ABORT_MASTER Only OWNLOAD_ABORT_MASTER NLOAD_ABORT_MASTER

J_NOT_PREPARED Only BJ_NOT_PREPARED _NOT_PREPARED

J_WRONG_ACCESS Only BJ_WRONG_ACCESS _WRONG_ACCESS

ONG_MASTER_REQUEST Only RONG_MASTER_REQUEST NG_MASTER_REQUEST

ONG_MASTER_ANSWER Only RONG_MASTER_ANSWER NG_MASTER_ANSWER

ONG_CLIENT_REQUEST Only RONG_CLIENT_REQUEST NG_CLIENT_REQUEST

ONG_CLIENT_ANSWER Only RONG_CLIENT_ANSWER NG_CLIENT_ANSWER

ONG_SERVER_REQUEST Only RONG_SERVER_REQUEST NG_SERVER_REQUEST

ONG_SERVER_ANSWER Only RONG_SERVER_ANSWER NG_SERVER_ANSWER
6666038 EM_CANOPEN_SCANOPEN_TO Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_T EM_CANOPEN_SCANOPEN_TOG

GGLE_ERROR Only OGGLE_ERROR GLE_ERROR
6666039 EM_CANOPEN_SCANOPEN_BU Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_B EM_CANOPEN_SCANOPEN_BUF

FFER_OVERFLOW Only UFFER_OVERFLOW FER_OVERFLOW
6666040 EM_CANOPEN_SCANOPEN_AB Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_A EM_CANOPEN_SCANOPEN_ABO

ORT_DOMAIN Only BORT_DOMAIN RT_DOMAIN
6666041 EM_CANOPEN_SCANOPEN_US Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_U EM_CANOPEN_SCANOPEN_USE

ER_ERROR Only SER_ERROR R_ERROR

ONG_INDEX Only RONG_INDEX NG_INDEX

ONG_SUBINDEX Only RONG_SUBINDEX NG_SUBINDEX
6666044 EM_CANOPEN_SCANOPEN_OU Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_O EM_CANOPEN_SCANOPEN_OUT

T_OF_MEMORY Only UT_OF_MEMORY _OF_MEMORY

ONG_BAUDRATE Only RONG_BAUDRATE NG_BAUDRATE

ONG_PARAMETER Only RONG_PARAMETER NG_PARAMETER
6666047 EM_CANOPEN_SCANOPEN_VA Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_V EM_CANOPEN_SCANOPEN_VAL

LUE_TOO_HIGH Only ALUE_TOO_HIGH UE_TOO_HIGH

LUE_TOO_LOW Only ALUE_TOO_LOW UE_TOO_LOW

ONG_DATA_TYPE Only RONG_DATA_TYPE NG_DATA_TYPE

ONG_OBJECT_TYPE Only RONG_OBJECT_TYPE NG_OBJECT_TYPE
6666051 EM_CANOPEN_SCANOPEN_PD Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_P EM_CANOPEN_SCANOPEN_PDO

O_MAPPING_ERROR Only DO_MAPPING_ERROR _MAPPING_ERROR
6666052 EM_CANOPEN_SCANOPEN_TO Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_T EM_CANOPEN_SCANOPEN_TOO

O_MANY_OBJECTS Only OO_MANY_OBJECTS _MANY_OBJECTS

ONG_NODESTATE Only RONG_NODESTATE NG_NODESTATE
6666054 EM_CANOPEN_SCANOPEN_LE Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_L EM_CANOPEN_SCANOPEN_LEN

NGTH_MISMATCH Only ENGTH_MISMATCH GTH_MISMATCH

O_NOT_VALID Only DO_NOT_VALID _NOT_VALID
6666056 EM_CANOPEN_SCANOPEN_IN Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_I EM_CANOPEN_SCANOPEN_INI

IT_ERROR Only NIT_ERROR T_ERROR
6666057 EM_CANOPEN_SCANOPEN_IN Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_I EM_CANOPEN_SCANOPEN_INV

VALID_HANDLE Only NVALID_HANDLE ALID_HANDLE

GE MEDICAL SYSTEMS
6666058 EM_CANOPEN_SCANOPEN_AC Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_A EM_CANOPEN_SCANOPEN_ACC
CESS_ERROR Only CCESS_ERROR ESS_ERROR

ay
Xr
GE MEDICAL SYSTEMS
400
GE Medical Systems
gemedicalsystems.com
Technical
Publication
Revision 10
Book 3
Pages 401 - 660
of 3
GE Medical Systems
Chapters 5 & 6 - Error Message Listings

( SW Version 13.x.x or higher) & Glossary
Copyright © 2002, 2003, 2004 and 2005

by General Electric Company, Inc.
GE MEDICAL SYSTEMS

Rick Fauska
Page 402
GE MEDICAL SYSTEMS
Chapter 5
Error Message Listings (SW Version 13.x.x or higher)
Section 1.0
Before You Begin
The error message listings in this chapter are for systems with Software/Firmware Revision
13.x.x or Software/Firmware Revision 14.x.x installed only. To determine the version of
software installed on your system, open the service installed only. To determine the version of
software installed on your system, open the service users interface (SUIF) and read the revision
number listed for the IUI. If it’s revision 13 or higher, use the error messages found here.
Section 2.0
Introduction to Error codes
2.1 What are Error Codes
Applications and System error codes are messages that alert you-and the customer that system
applications or the operating system cannot perform one of their programmed tasks. Applications
and System error codes can appear on the console display at any time, whether you are running
Applications, Diagnostics, or Service Mode software.
The Error management mechanisms in the system handle of all error transmissions on the system.
All errors are stored in a single system error log, which can be viewed via the Service Error Log
Viewer.
2.1.1 Applications Software

As its name implies, Applications software controls customer X-ray applications- such as Digital
RAD, Table Top, and Fluoro.
When the customer selects the fluoro function, Applications software uses the Console (to accept
operator input), the generator module (to control the exposure and to generate X rays), the Imaging
module (to control the camera system), and the Positioner module (to position the patient).
Software controls all aspects of system operation. In this system, these software “actors” are
assigned names. You’ll see those names used in the chapters that follow. Therefore, you might
want to become familiar with them.
In Figure 5-1, you can see were these software actors live inside certain hardware subsystems,
and they’re able to communicate with each other directly or indirectly.

GE MEDICAL SYSTEMS
Saturn HW Mars HW
Software Actors
Software Actors
Athena Calypso
Saber
Atlas Atlas
Venus HW
Software Actors
IUI
Calypso
IIP
Saber
Atlas
Figure 5-1 Primary SW Applications “Actors”
2.1.2 Operating System Software

Operating System software handles:
• high-level system related functions
• initializing system hardware
• managing system resources
• downloading software to modules
• system timing functions
• handling and processing operator input from the console
• processing and displaying system output to the console, etc.
2.2 Applications and System Error Reporting
2.2.1 Error Display Management

Detailed error information is displayed in an easily visible area of the console and the live in-room
monitor.
Figure 5-2 error display – In–Room Monitor
Page 404 Section 2.0 - Introduction to Error codes

GE MEDICAL SYSTEMS
2.2.2 “Quick” Error Viewer
The console also provides the ability for the operator to access the last errors generated on the
system (maximum of 10). This allows further investigation and viewing of errors occurring in rapid
succession, so that the proper course of action can be taken.
Figure 5-3 Quick Error Viewer
2.3 Service Error Log Viewer

The console provides the ability for the service person to access the complete set (2000 maximum
entries) of system errors generated over time. The error log gives you a complete time line of all
errors that have occurred. Used together with the error message listing in Section 3.0 (System Error
Message Listing on page 178) of this chapter, the service person has needed information for more
efficient and effective troubleshooting.
Section 3.0
System Error Message Listing
In this section you'll find the system’s error code's listed in hexadecimal order by SW Module
(Process) Actor.
Sometimes the customer may easily correct an Applications software error condition, such as when
the error is caused by an unsatisfied interlock. At other times, however, the Applications software
error message only advises the customer to call service.
Whichever action you pursue, always bear in mind which module generated the error, which type
of software generated the error, and what the system was trying to do when the error occurred.
Each Error Code listed below, shows its message(s): the module that generated the error, the error
Description and the Recommended Action(s) to correct the error.
Major Function Impacted
This is the name of the actor that reported the error
Minor Function Impacted
This indicates the actor-specific function that was in progress when the error was reported. Each
actor will define a set of legal values for this field. Each error reported by the actor will be associated
with a unique minor function.
Error Recovery Classes
System error management supports various recovery classes of errors:

GE MEDICAL SYSTEMS
• Debug-only – these errors are logged in the system error log, but are not displayed
• Advisory – logging of this class of error is optional
• Warning – non-fatal failure
• Abort – causes termination of current x-ray acquisition
• Inhibit – causes termination of current x-ray and subsequently inhibits further acquisition
attempts until the error situation is cleared
• Halt – when failure is so severe that the system is no longer functional. The only operator
action allowed is a Reset or Shutdown.
• Action(s) - This field gives the recommended action.
System Error Message Listings begin on next page.

GE MEDICAL SYSTEMS
3.1 02 XRAcqSync
200001 Error Text: The Events are ignored.
View Level: opr
Root Cause: 1
Description: Event is ignored because it is not applicable in the current state.
200002 Error Text: Do not know the Switch Status.

View Level: opr
Root Cause: 1
Description: The current foot/hand switch status is not know.
200003 Error Text: Failed to read AcqSync config file

View Level: opr
Root Cause: 1
Description: Fail to read the actor configuration file.
200004 Error Text: Creating config parameter of type stringList failed

View Level: opr
Root Cause: 1
Description: Fail to dynamically create a data element.
200005 Error Text: XRAcqsync failed startup

View Level: opr
Root Cause: 1
Description: Actor failed to properly initialize its data or communications.
200006 Error Text: Unexpected event Occurred.

View Level: opr
Root Cause: 1
Description: Unable to understand or process an event.
200007 Error Text: This OpModeID is not found in the List.

View Level: opr
Root Cause: 1
Description: Selected OpMode ID not found in the current list of OpMode ID's.

GE MEDICAL SYSTEMS
200008 Error Text: The configuration for this Opmode is already done.
View Level: opr
Root Cause: 1
200009 Error Text: The configuration Configure request for this OpMode is already Received.
View Level: opr
Root Cause: 1
200010 Error Text: This is an invalid synchroniser type.
View Level: opr
Root Cause: 1
Description:
200011 Error Text: Invalid OpModeID received.

View Level: opr
Root Cause: 1
Description: Actor is not configured for the requested OpMode ID.
200012 Error Text: Time out while in WAIT_FOR_STOP_SEQ waiting for
STOP_EXPOSURE_TRIGGER_DONE.
View Level: opr
Root Cause: 1
Description: Timed out while waiting for the reply from ImDet (STOP_EXPOSURE_TRIGGER_DONE)
indicating that exposure(s) have stopped.
200013 Error Text: Time out while waiting for an event or an actor to respond.
View Level: opr
Root Cause: 1
Description: Time out while waiting for an event from another actor.
Customer Text: Exposure control problem. Release switch and try again. Call service if problem persists
200014 Error Text: Time out while in STOP_SEQ waiting for PREP_OFF.
View Level: opr
Root Cause: 1
Description: Time out waiting for another actor to finish processing the Prop Off switch transition.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: Unable to bind with a required actor
200016 Error Text: Received startBootPhase before connecting with all Actors.
View Level: opr
Root Cause: 1
Description: Events out of order during the boot process.
200017 Error Text: Do not know the Boot Level.

View Level: opr
Root Cause: 1
Description: Current boot status is not know.
200018 Error Text: Do not know the sysmode for this ID.
View Level: opr
Root Cause: 1
200019 Error Text: Remote call failed while calling the method on the other actor.
View Level: opr
Root Cause: 1
Description: Unable to perform a method call on another actor.
200020 Error Text: Not Bound to the actor. The pointer is Null.
View Level: opr
Root Cause: 1
Description: Unable to communicate with another actor.
200021 Error Text: Send start or stop exposure trigger of the XRImDet failed.
View Level: opr
Root Cause: 1
Description: Unable to start or stop the exposure triggers because an event publication failed.

GE MEDICAL SYSTEMS
200022 Error Text: atlasPrepDone of the XRTitan failed.
View Level: opr
Root Cause: 1
200023 Error Text: FastAcquisition request of the XRTitan failed.

View Level: opr
Root Cause: 1
200024 Error Text: AtlasAcquisitionInhibit of the XRTitan failed.
View Level: opr
Root Cause: 1
200025 Error Text: Lost EF or Normal connection status.

View Level: opr
Root Cause: 1
Description: Connect to other actor(s) has been lost.
200026 Error Text: Failed to Send actorReady

View Level: opr
Root Cause: 1
200027 Error Text: Failed to send shutdowndone.
View Level: opr
Root Cause: 1
200028 Error Text: Failed to send shutdowndone

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
200029 Error Text: AcqSync not connected to all the actors
View Level: opr
Root Cause: 1
Description: Not connected to all of the required actors.

View Level: opr
Root Cause: 1
Description: Unable to create an event.
200031 Error Text: publish event failed for these events

View Level: opr
Root Cause: 1
Description: Unable to publish an event.

View Level: opr
Root Cause: 1
Description: Unable to subscribe to a required event.

View Level: opr
Root Cause: 1
Description: Unable to create/set the recevery file.

View Level: opr
Root Cause: 1
Description: Unable to set the error message file link.
200035 Error Text: Invalid recovery class type received.
View Level: opr
Root Cause: 1
Description: Recovery class for the current error is not valid.

GE MEDICAL SYSTEMS
200036 Error Text: This error is not of the Inhibit type or reported before.
View Level: opr
Root Cause: 1
Description: Recovery class for the current error is of type Inhibit, and has already been reported, or not
a valid inhibit error.
200037 Error Text: Prep is not Authorized, acquisition is inhibited.

View Level: opr
Root Cause: 1
Description: Prep request ignored because of an inhibit condition on that OpMode.
200038 Error Text: Prep on requested while soak time has not elapsed
View Level: opr
Root Cause: 1
Recommended Action(s): Wait for soak time to complete. Then prep/expose switches will become active.
Description: Prep request ignored because soak time is not completed.
Customer Text: Prep/Expose switches are disabled until tube warm-up soak time is complete.
200039 Error Text: Prep on requested while Athena is not ready, waiting for START_EXAM.
View Level: opr
Root Cause: 1
200040 Error Text: Prep on requested while Room Door is open.

View Level: opr
Root Cause: 1
200041 Error Text: Prep on requested while Fluoro time exceeded 10 mins.
View Level: opr
Root Cause: 1
200042 Error Text: Prep on requested while no more tube run time is available.
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
200043 Error Text: Prep on requested while remaining disk space is less than 5 seconds.
View Level: opr
Root Cause: 1
200044 Error Text: Time out while in WAIT_FOR_EXPOSE waiting for EXP_ON switch event.
View Level: opr
Root Cause: 1
Description: Time out while waiting for the Expose On switch.
Customer Text: An internal communication error occurred. Release the expose switch and try again.
200045 Error Text: Time out while in ABORT_SEQ waiting for the seq control returned from COA.
View Level: opr
Root Cause: 1
Description: Calibration system control error between AcqSync and calibration owner actor.
200046 Error Text: Script processor initialization failed

View Level: opr
Root Cause: 1
Description: Failed to initialize the script processor class for the actor.
200047 Error Text: X-ray unavailable, check grid position to continue.
View Level: opr
Root Cause: 1
200048 Error Text: Script Processor failed to read a config script.

View Level: opr
Root Cause: 1
Description: Failed to read the config script for a selected application.

GE MEDICAL SYSTEMS
3.2 04 XRAppDir
View Level: opr
Root Cause: 1
system controller.
View Level: opr
Root Cause: 1
system controller.
400003 Error Text: XRAppDir failed to startup

View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
400005 Error Text: Null config string received, terminate the AppSetup
View Level: opr
Root Cause: 1
Recommended Action(s): This protocol is not available:
1. Reselect the protocol or select another to continue.
3. If required, reload application software.
Description: The protocol data content is null, unable to configure the system for selected procedure.

GE MEDICAL SYSTEMS
400006 Error Text: The active opmode is not found in the List of Opmodes
View Level: opr
Root Cause: 1
Recommended Action(s): 1. Reselect the protocol 2. If the problem persists reset the system.
400007 Error Text: Invalid OpModeId received for OPMODE_CONFIGURE_DONE

View Level: opr
Root Cause: 1
Recommended Action(s): 1. Reselect the protocol. 2. If the problem persists reset the system.
Description: The application being configured is not in the list of the selected applications, failed to setup
the system
400008 Error Text: Failed to read XRAppDir config file

View Level: opr
Root Cause: 1
system controller.

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
400011 Error Text: Time out

View Level: opr
Root Cause: 1
Description: system failed to complete the configuration for the selected applications within the configured
protocol setup time-out period

GE MEDICAL SYSTEMS
400012 Error Text: Failed to read XRAppDir time-out values
View Level: opr
Root Cause: 1
system controller.

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
400016 Error Text: The appdir configuration files not found

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
3.3 06 XRBeamForm
View Level: opr
Root Cause: 0
Recommended Action(s): “Reset the system, Reload the software
Description: “Software Error: In boot phase, the actor needs to connect to other actors if required. For
some reason the connection cannot be built and software will not work properly.
persists.

View Level: opr
Root Cause: 0
Description: “Software Error: The actor tries call other actor's method. However, the other actor's pointer
is null. So the communication is broken.
persists.
600003 Error Text: Boot phase failed.

View Level: opr
Root Cause: 0
Description: “Software Error: The actor does not complete a boot phase. This happens when its controllers
cannot complete the boot phase.
persists.
600004 Error Text: Failed to create application controllers.

View Level: opr
Root Cause: 0
Description: “Software Error: The actor tried to initialize its controllers but failed.
persists.
600005 Error Text: Failed to read BeamForm config/cal file

View Level: opr
Root Cause: 0
Recommended Action(s): “Ignore
Description: “Software Error: Actor tried to read parameters from its cal/cfg/dyn files but could not.
persists.

GE MEDICAL SYSTEMS
600006 Error Text: Failed to set the application mode.
View Level: opr
Root Cause: 0
Description: Software Error.
600007 Error Text: Failed to execute ClearOpModesConfig script

View Level: opr
Root Cause: 0

View Level: opr
Root Cause: 0
600009 Error Text: Failed to execute ClearActiveOpModes script

View Level: opr
Root Cause: 0
600010 Error Text: Failed to execute ChangeActiveOpModes script

View Level: opr
Root Cause: 0
600011 Error Text: Failed to execute StartPrepare script

View Level: opr
Root Cause: 0

GE MEDICAL SYSTEMS
600012 Error Text: Failed to execute StopPrepare script
View Level: opr
Root Cause: 0
600013 Error Text: Failed to execute StartSequence script

View Level: opr
Root Cause: 0
600014 Error Text: Failed to execute StopSequence script

View Level: opr
Root Cause: 0
Recommended Action(s): “Ignore
Description: “Sofware Error.
600101 Error Text: Over table Collimator is not configured for the application mode
View Level: opr
Root Cause: 0
Recommended Action(s): "Make sure over table collimator exist or change BeamForm.cfg to set this configuration
Description: “The Over Table Collimator is not supposed to be there.
600102 Error Text: Under table Collimator is not configured for the application mode
View Level: opr
Root Cause: 0
Recommended Action(s): “Make sure under table collimator exist or change BeamForm.cfg to set this configuration
Description: “The Under Table Collimator is not supposed to be there
600103 Error Text: Unknown Application mode received

View Level: opr
Root Cause: 0
Recommended Action(s): “Wrong scripts/ Reload software
Description: “The actor received Application Mode that is not defined.
Customer Text: An internal communication failure has occurred. Retry or reset. Call service if the problem
persists.

GE MEDICAL SYSTEMS
600104 Error Text: Event IMAGE_INTENSIFIER_CONFIG_CHANGED not received
View Level: opr
Root Cause: 0
Recommended Action(s): “Reset the system
Description: “The XRBeamForm actor does not receive this event.
600105 Error Text: Invalid Spectral Filter value in Apps Setup script.
View Level: opr
Root Cause: 0
Recommended Action(s): “Check protocol database for SpectralFilter, the valid values shall be 0, 0.1, 0.2 and 0.3
Description: "Invalid Spectral Filter value
Customer Text: Desired collimator filter could not be set. Reselect protocol or check protocol database.
600106 Error Text: Not ready for Acquisition while setting the Spectral Filter
View Level: opr
Root Cause: 1
Recommended Action(s): "Retry
Description: "The Collimator is setting the spectral filter while START_SEQUENCE received.
Customer Text: Retry operation. Call service if problem persists.
600107 Error Text: Overtable Collimator device-driver initialization failed

View Level: opr
Root Cause: 0
Recommended Action(s): "Reset the system
Description: "The Overtable Collimator Device software failed the initialization. It may be a software error
600108 Error Text: Undertable Collimator device-driver initialization failed

View Level: opr
Root Cause: 0
Description: "The Undertable Collimator Device software failed the initialization. It may be a software error
600200 Error Text: OverTable collimator went offline

View Level: opr
Root Cause: 1
Recommended Action(s): "Check overtable collimator connection. Reset the system
Description: "No hearttbeat from the overtable collimator, indicating that it is offline.

GE MEDICAL SYSTEMS
600201 Error Text: OverTable collimator is online but not going alive
View Level: opr
Root Cause: 1
Description: "The overtable collimator keeps sending the Node Announcement message, but doesn't
600202 Error Text: OverTable collimator is offline

View Level: opr
Root Cause: 1
Recommended Action(s): "Check overtable collimator connection. Reset the system
Description: "The oevertable collimator is not sending heartbeat messages.
600203 Error Text: OverTable collimator state is unknown

View Level: opr
Root Cause: 1
Description: "Software error: The Saber software failed to establish connection with the Overtable
collimator.
600204 Error Text: UnderTable collimator went offline

View Level: opr
Root Cause: 1
Recommended Action(s): "Check undertable collimator connection. Reset the system
Description: "No hearttbeat from the undertable collimator, indicating that it is offline.
600205 Error Text: UnderTable collimator is online but not going alive
View Level: opr
Root Cause: 1
Description: "The undertable collimator keeps sending the Node Announcement message, but doesn't
600206 Error Text: UnderTable collimator is offline

View Level: opr
Root Cause: 1
Recommended Action(s): "Check undertable collimator connection. Reset the system
Description: "The undertable collimator is not sending heartbeat messages.

GE MEDICAL SYSTEMS
600207 Error Text: UnderTable collimator state is unknown
View Level: opr
Root Cause: 1
Description: "Software error: The Saber software failed to establish connection with the undertable
collimator.
600400 Error Text: Filter-change Error

View Level: opr
Root Cause: 1
Recommended Action(s): "Try again or reset the system
Description: "Error when changing the spectral filter.
Customer Text: Xray exposures may not be possible. Reset and call service if the problem persists.
600401 Error Text: Filter-change parameter invalid

View Level: opr
Root Cause: 1
Description: "Parameters for spectral filter change are not valid.
600500 Error Text: No Set_Terminal_Mode response from overtable collimator

View Level: opr
Root Cause: 1
Description: "Overtable collimator not in Terminal mode.
Customer Text: The collimator is not functioning. Reset and call service if the problem persists.
600501 Error Text: OverTable collimator RAM-D1 error

View Level: opr
Root Cause: 1
Description: "Overtable collimator internal error: RAM-D1 error.
600502 Error Text: OverTable collimator EEPROM error

View Level: opr
Root Cause: 1
Description: "Overtable collimator internal error: EEPROM error.

GE MEDICAL SYSTEMS
600503 Error Text: OverTable collimator CAN bus error or error overrun
View Level: opr
Root Cause: 1
Description: "Overtable collimator internal error: CAN bus error.
600504 Error Text: OverTable collimator CAN receiver overrun error

View Level: opr
Root Cause: 1
Description: "Overtable collimator internal error: CAN receiver error.
600505 Error Text: OverTable Collimator has lost communication with D2

View Level: opr
Root Cause: 1
Description: "Overtable collimator internal error: communication lost with D2.
600506 Error Text: OverTable collimator error calculating height

View Level: opr
Root Cause: 1
Description: "Overtable collimator internal error when calculating height.
600507 Error Text: OverTable collimator error calculating width

View Level: opr
Root Cause: 1
Description: "Overtable collimator internal error when calculating width
600508 Error Text: OverTable collimator error height stepping

View Level: opr
Root Cause: 1
Description: "Overtable collimator internal error while height stepping.

GE MEDICAL SYSTEMS
600509 Error Text: OverTable collimator error width stepping
View Level: opr
Root Cause: 1
Description: "Overtable collimator internal error while width stepping.
600510 Error Text: OverTable collimator error prefilter stepping

View Level: opr
Root Cause: 1
Description: "Overtable collimator internal error while prefilter stepping.
600511 Error Text: OverTable collimator error height limit switch

View Level: opr
Root Cause: 1
Description: "Overtable collimator internal error: height limit switch.
600512 Error Text: OverTable collimator error width limit switch

View Level: opr
Root Cause: 1
Description: "Overtable collimator internal error: width limit switch.
600513 Error Text: OverTable collimator error prefilter limit switch

View Level: opr
Root Cause: 1
Description: "Overtable collimator internal error: prefilter limit switch.
600514 Error Text: UnderTable collimator RAM-D1 error

View Level: opr
Root Cause: 1
Description: "Undertable collimator internal error: RAM-D1 error.

GE MEDICAL SYSTEMS
600515 Error Text: UnderTable collimator EEPROM error
View Level: opr
Root Cause: 1
Description: "Undertable collimator internal error: EEPROM error.
600516 Error Text: UnderTable collimator CAN bus error or error overrun
View Level: opr
Root Cause: 1
Description: "Undertable collimator internal error: CAN bus error.
600517 Error Text: UnderTable collimator CAN receiver overrun error

View Level: opr
Root Cause: 1
Description: "Undertable collimator internal error: CAN receiver error.
600518 Error Text: UnderTable Collimator has lost communication with D2

View Level: opr
Root Cause: 1
Description: "Undertable collimator internal error: communication lost with D2.
600519 Error Text: UnderTable collimator error calculating height

View Level: opr
Root Cause: 1
Description: "Undertable collimator internal error when calculating height.
600520 Error Text: UnderTable collimator error calculating width

View Level: opr
Root Cause: 1
Description: "Undertable collimator internal error when calculating width

GE MEDICAL SYSTEMS
600521 Error Text: UnderTable collimator error height stepping
View Level: opr
Root Cause: 1
Description: "Undertable collimator internal error while height stepping.
600522 Error Text: UnderTable collimator error width stepping

View Level: opr
Root Cause: 1
Description: "Undertable collimator internal error while width stepping.
600523 Error Text: UnderTable collimator error prefilter stepping

View Level: opr
Root Cause: 1
Description: "Undertable collimator internal error while prefilter stepping.
600524 Error Text: UnderTable collimator error height limit switch

View Level: opr
Root Cause: 1
Recommended Action(s): "Undertable collimator blades may be stuck. Try again or reset the system. If system just
installed, check that foam shipping block is removed.
Description: ""Undertable collimator internal error: height limit switch. The collimator blades are possibly
stuck - if system has just been installed, check that the foam shipping block has been
removed.
600525 Error Text: UnderTable collimator error width limit switch

View Level: opr
Root Cause: 1
Recommended Action(s): "Undertable collimator blades may be stuck. Try again or reset the system. If system just
installed, check that foam shipping block is removed.
Description: ""Undertable collimator internal error: height limit switch. The collimator blades are possibly
stuck - if system has just been installed, check that the foam shipping block has been
removed.
600526 Error Text: UnderTable collimator error prefilter limit switch

View Level: opr
Root Cause: 1
Description: "Undertable collimator internal error: prefilter limit switch.

GE MEDICAL SYSTEMS
600527 Error Text: UnderTable collimator mechanical error D1: Limit Switch - Iris Diaphragm
View Level: opr
Root Cause: 0
Recommended Action(s): "Reset the System
Description: "Undertable collimator mechanical error D1: Limit Switch - iris diaphragm

GE MEDICAL SYSTEMS
3.4 08 XRDataMgr
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
800007 Error Text: XRDatMgr is not ready, it may be in PowerFailure, ShutDown or HaltError
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
800017 Error Text: DataMgr calculated a dose greater than total allowed dose.
View Level: opr
Root Cause: 1
800018 Error Text: DataMgr calculated a dap greater than total allowed dap.
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
3.5 10 XRImChainPos
View Level: opr
Root Cause: 0
Recommended Action(s): "Reset the system, Reload the software
Description: "Software Error: In boot phase, the actor needs to connect to other actors if required. For
persists.

View Level: opr
Root Cause: 0
Description: "Software Error: The actor tries call other actor's method. However, the other actor's pointer
is null. So the communcation is broken.
persists.

View Level: opr
Root Cause: 0
Description: "Software Error: The actor does not complete a boot phase. This happens when its controllers
persists.

View Level: opr
Root Cause: 0
Description: "Software Error: The actor tried to initialize its controllers but failed.
persists.
1000005 Error Text: Failed to read config file

View Level: opr
Root Cause: 0
Recommended Action(s): "Ignore
Description: "Software Error: Actor tried to read parameters from its cal/cfg/dyn files but could not.
persists.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 0
Description: "Software Error.

View Level: opr
Root Cause: 0
Description: "Sofware Error.

View Level: opr
Root Cause: 0

View Level: opr
Root Cause: 0

View Level: opr
Root Cause: 0

View Level: opr
Root Cause: 0

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 0

View Level: opr
Root Cause: 0

View Level: opr
Root Cause: 0
1000101 Error Text: OTS not configured for RAD application modes
View Level: opr
Root Cause: 1
Recommended Action(s): "Reconfigure the System to make sure the OTS exist or not
Description: "Configuration Problem
Customer Text: System Configured for NO OTS
1000102 Error Text: Wall not configured for Wall Bucky application mode
View Level: opr
Root Cause: 1
Recommended Action(s): "Reconfigure the System to make sure the Wallstand exist or not
Description: "Configuration Problem
Customer Text: System Configured for NO WALL Stand
1000200 Error Text: State Machine Errors

View Level: opr
Root Cause: 0
Description: "Sofware Error: Some unexpected actor join the system.

GE MEDICAL SYSTEMS
1000203 Error Text: Cone Motion Inhibited, Table Horizontal Stop Not Selected
View Level: opr
Root Cause: 0
Recommended Action(s): "Select Table Horizontal stop
Description: "Cone Motion Inhibited, Table Horizontal Stop Not Selected
Customer Text: Cone Motion Inhibited. Table horizontal stop not selected.
1000204 Error Text: SFD Not In Expose Position

View Level: opr
Root Cause: 0
Recommended Action(s): "Move the IDD to the lateral latch position
Description: "SFD Not In Expose Position
Customer Text: SFD Not In Expose Position
1000205 Error Text: SFD Not In Park Position

View Level: opr
Root Cause: 0
Recommended Action(s): "Move the IDD to the park position
Description: "SFD Not In Park Position
Customer Text: SFD Not In Park Position
1000206 Error Text: Set Bucky ready timeout, exposure is not possible
View Level: opr
Root Cause: 0
Recommended Action(s): "Cycle the power or reset the system
Description: "Set bucky speed timeout
Customer Text: Bucky is not ready. Retry exposure or reset the system if problem persists.
1000207 Error Text: Bucky size does not match the standard one
View Level: opr
Root Cause: 0
Recommended Action(s): "Reposition the cassette or recalibrate the bucky
Description: "The cassette size does not match the standard one.
Customer Text: The cassette size does not match the standard one. Reposition the cassette or recalibrate the
bucky.
1000208 Error Text: Tracking error is beyond first threshold

View Level: opr
Root Cause: 0
Recommended Action(s): "Retry or reset the system
Description: "Tracking error is beyond the first threshold.
Customer Text: Tracking error is beyond the first threshold.

GE MEDICAL SYSTEMS
1000209 Error Text: Tracking error is beyond second threshold
View Level: opr
Root Cause: 0
Description: "Tracking error is beyond the second threshold.
Customer Text: Tracking error is beyond the second threshold.
1000210 Error Text: Detector Homing failed.

View Level: opr
Root Cause: 0
Description: "Request for Detector Homing failed.
Customer Text: Detector Homing failed.

View Level: opr
Root Cause: 1
Description: "Software error: failure in IddDevice constructor.

View Level: opr
Root Cause: 1
Description: "IddDevice initialization failed.

View Level: opr
Root Cause: 1
Description: ""IDD Power Assist Vertical CAN amp initialization failed or is not responding. Indicates a
connections.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: "IDD vertical motion control error.
persists.

View Level: opr
Root Cause: 1
Description: ""IDD Power Assist Longitudinal CAN amp initialization failed or is not responding. Indicates
a CAN device or bus problem. Refer to the CAN bus block diagram.
connections.

View Level: opr
Root Cause: 1
Description: "IDD longitudinal motion control error.
persists.

View Level: opr
Root Cause: 1
Description: "IDD positioning error. No SID feedback.

View Level: opr
Root Cause: 1
Description: "OTS Device Constructor Failed

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: ""OTS Device Initialization Failed. Possible boot problem. May indicate a CAN device or bus
connections.

View Level: opr
Root Cause: 1
Description: "OTS Register Call Back error.
Customer Text:
View Level: opr
Root Cause: 1
Description: "OTS wrong call back data type error.
Customer Text:

View Level: opr
Root Cause: 1
Description: "OTS motion control error.

View Level: opr
Root Cause: 1
Description: "OTS positioning error.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: "OTS locks control error.
Customer Text:

View Level: opr
Root Cause: 1
Description: "OTS 30 VAC error.

View Level: opr
Root Cause: 1
Description: "OTS 10 VDC error.

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
Description: "OTS 24 VDC lock logic error.

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
Description: "OTS IO CAN warning limit error.
Customer Text:

View Level: opr
Root Cause: 1
Description: "OTS IO CAN overrun error.
Customer Text:

View Level: opr
Root Cause: 1
Description: ""OTS IO is not responding. Indicates a CAN device or bus problem. Refer to the CAN bus
block diagram.
connections.
1090116 Error Text: OTS IO receiving buffer overrun errorl

View Level: opr
Root Cause: 1
Description: "OTS IO receiving buffer overrun errorl
Customer Text:

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: ""OTS Amplifier is not responding. Indicates a CAN device or bus problem. Refer to the CAN
bus block diagram.
connections.

View Level: opr
Root Cause: 1
Description: "OTS amplifier over voltage error.

View Level: opr
Root Cause: 1
Description: "OTS amplifier under voltage error.

View Level: opr
Root Cause: 1
Description: "OTS amplifier over current error.

View Level: opr
Root Cause: 1
Description: "OTS amplifier over temperature error.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: "OTS amplifier over load error.

View Level: opr
Root Cause: 1
Description: "OTS amplifier over speed error.

View Level: opr
Root Cause: 1
Description: "OTS amplifier over position error.

View Level: opr
Root Cause: 1
Description: "OTS amplifier position following error.

View Level: opr
Root Cause: 1
Description: "OTS amplifier velocity following error.

View Level: opr
Root Cause: 1
Description: "OTS amplifier motor over temperature error.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: "OTS amplifier encoder error.

View Level: opr
Root Cause: 1
Description: "OTS amplifier auxiliary encoder error.

View Level: opr
Root Cause: 1
Description: "OTS amplifier warning.
1090131 Error Text: OTS amplfier fault.

View Level: opr
Root Cause: 1
Description: "OTS amplfier fault.
1090132 Error Text: OTS amplfier fatal error.

View Level: opr
Root Cause: 1
Description: "OTS amplfier fatal error.

View Level: opr
Root Cause: 1
Description: "OTS amplifier homing error.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: "OTS amplifier position following error.

View Level: opr
Root Cause: 1
Description: "OTS longitudinal pot failure.

View Level: opr
Root Cause: 1
Description: "OTS lateral pot failure.

View Level: opr
Root Cause: 1
Description: "OTS vertical pot failure.

GE MEDICAL SYSTEMS
3.6 11 00 Athena Application
1100001 Error Text: Proxy Manager not connected
View Level: opr
Root Cause: 1
Recommended Action(s): "Check connection to Mars, Ensure Mars is up, Wait for Mars
Description: "Connectivity failure with Mars or error in communication softwrae
1100002 Error Text: Proxy Manager Init Fail

View Level: opr
Root Cause: 1
Recommended Action(s): "Communication proxy Init failure, reboot.
Description: "Error in communciation software
1100003 Error Text: Bad OpModeId received

View Level: opr
Root Cause: 1
Recommended Action(s): "Bad opModeId received in command.
Description: "The received OpMode Id was invalid or unexpected. Possible logic error in subsystem
software.
1100004 Error Text: Creation failure of Win32 data structure

View Level: opr
Root Cause: 1
Recommended Action(s): "Recommend reset.
Description: "Severe resource allocation error. Likely cause is that the system is running low on resources.
1100005 Error Text: Destruction failure of Win32 data structure

View Level: opr
Root Cause: 1
Recommended Action(s): "Reboot the system
Description: "Failure while doing clean-up prior to shutting down
1100006 Error Text: Unexpected event occurred

View Level: opr
Root Cause: 1
Recommended Action(s): "Engineering error only; System will recover
Description: "An event occurred or property value was received when it was not expected. Likely cause is
that the subsystems are out of sync.

GE MEDICAL SYSTEMS
1100007 Error Text: Unexpected messsage received while camera off
View Level: opr
Root Cause: 1
Recommended Action(s): "Property in probable Rad opmode, select non-rad protocol
Description: "The received property cannot be handled when the camera is off.
1100010 Error Text: Unknown packet received

View Level: opr
Root Cause: 1
Description: "Possible cause is that the subsystem software versions are incompatible.
1100014 Error Text: Unable to start server

View Level: opr
Root Cause: 1
Recommended Action(s): "Service functions may be prevented, reboot or reinstall software.
Description: "FTP or HTTP server failed to start.
Customer Text: Service functions are not available. Reset and call service if the problem persists.
1100015 Error Text: 0 opModeIds in ClearOpmodes command. Cannot change protocol

View Level: opr
Root Cause: 1
Recommended Action(s): "select different protocol
Description: "Logical error in protocol setup. Likely cause is an error in Mars software or a communication
error.
Customer Text: This protocol is not available. Select another to continue.
1100016 Error Text: Command received in power failure

View Level: opr
Root Cause: 1
Description: "Saturn is in power failure mode.
1100103 Error Text: Bad application identifier

View Level: opr
Description: "The sysmode value received is not in the list known to Athena.

GE MEDICAL SYSTEMS
1100104 Error Text: Application error. Internal synchrnonization failed.
View Level: opr
Root Cause: 1
Recommended Action(s): "Recommend Reset.
Description: "A severe software error within Athena while synchronizing internal activities using a
semaphore. A reboot may be needed.
1100117 Error Text: Bad status received for PREP , Prep Failed
View Level: opr
Root Cause: 1
Recommended Action(s): "Retry the exposure. Look for other errors that may indicate a hardware problem
Description: "A Start Prep or Stop Prep command was not processed correctly. This could be because it
was unexpected, or the data in the request was incorrect..
Customer Text: Prep failed. Release the exposure switch and try again.
1100118 Error Text: Bad status received for EXPOS_TRIGGER , Expose Failed
View Level: opr
Root Cause: 1
Description: "A Start Expose or Stop Expose command was not processed correctly. This could be
because it was unexpected, or because the data in the request was incorrect..
Customer Text: Release the exposure switch and try again.
1100119 Error Text: Failed to display text on the Image Monitor

View Level: opr
Root Cause: 1
Description: "An error occurred while trying to display Dose or Technique information on the Image
Monitor. As a result, the displayed parameters may not be accurate.
1100121 Error Text: Unknown Mag value received

View Level: opr
Root Cause: 1
Recommended Action(s): "Call service
Description: "Incorrect II Mag value received. Possible cause is that the subsystem softwrae versions are
incompatible.

GE MEDICAL SYSTEMS
1100123 Error Text: Failed to set up Image Intensifier optics
View Level: opr
Root Cause: 1
Recommended Action(s): "Check the OCB connection, reset the system
Description: "An error occurred while trying to set up the Iris or NDF during Prep. This may be because
there is a communication problem with the OCB or because of an internal error within OCB.
Customer Text: Imaging control error. Check the imaging connection and call service if problem persists.
1100124 Error Text: General OCB Errors

View Level: opr
Root Cause: 1
Recommended Action(s): "Run OCB Diagnostics via SUIF
Description: "Optics Control Board (OCB) is generating errors; see debug information for more information
Customer Text: Optics control error. Release exposure switch and try again. Call service if problem persists.
1100125 Error Text: II Mag not In the Valid Range

View Level: opr
Root Cause: 1
Recommended Action(s): "Check configuration
Description: "Invalid parameter value for FOV received.
1100126 Error Text: Pdb not in the Valid Range

View Level: opr
Root Cause: 1
Description: "Invalid parameter value for the Photodiode received.
1100127 Error Text: Iris Transmission Not in the Valid Range

View Level: opr
Root Cause: 1
Description: "Invalid parameter value received.
1100128 Error Text: Failed to create OCB driver

View Level: opr
Root Cause: 1
Recommended Action(s): "Check the OCB connection
Description: "During boot, the Optics Control Board (OCB) driver failed to initialize.

GE MEDICAL SYSTEMS
1100129 Error Text: The fluoro framerate does not fall in the Range between 1 to 30
View Level: opr
Root Cause: 1
Description: "Invalid parameter value for fluoro framerate received.
1100130 Error Text: Failed to configure the CCU board correctly

View Level: opr
Root Cause: 1
Recommended Action(s): "Run CCU diagnostics. Re-install software if needed
Description: "Failed to use the IAB/CCU driver to change a configuration setting on the CCU board. This
may be because of a board/driver failure or because some required data (such as Look-up
table data) was not found or was incorrect.
1100131 Error Text: Bad parameter value received while trying to initialize the camera.
View Level: opr
Root Cause: 1
Recommended Action(s): "Check the camera driver version. Re-install software if needed
Description: "Invalid parameter value received for camera initialization.
Customer Text: Reselect the protocol. Reset the system. Call service if the problem persists.
1100132 Error Text: Config data is Missing or Erroneous.

View Level: opr
Root Cause: 1
Recommended Action(s): "Reinstall software
Description: "A required configuration or calibration parameter was missing in the registry or in the runtime
code (e.g. FOV settings or FOV factor table), or it was found to be erroneous.
1100133 Error Text: Video gain settings are out of range.

View Level: opr
Root Cause: 1
Recommended Action(s): "Check calibration settings, and re-run Image chain calibrations if necessary
Description: "The value computed for the Camera gain or Iris transmission was outside normal range. The
acquisition can proceed with corrected settings, but this indicates a likely problem with
calibration or configuration settings.
Customer Text: Image quality may not be optimal. Call service to check the calibration settings.

GE MEDICAL SYSTEMS
1100134 Error Text: Failed to communicate with Acquisition Sequencer driver.
View Level: opr
Root Cause: 1
Description: "The application software failed to communicate with the Windows driver that drives
acquisition sequencing in Athena. This is a severe internal software error that could occur as
a result of incorrect installation of Windows or Athena.
1100135 Error Text: Failed to compute video gain.

View Level: opr
Root Cause: 1
Description: "Failed to compute a video gain (Camera gain or Iris Transmission) according to Automatic
Gain Control algorithms. The exposure will be aborted.
1100136 Error Text: Failed to compute Sensor Feedback to send to Mars for Exposure Management.
View Level: opr
Root Cause: 1
Description: "Failed to compute Sensor Back based on the ABD feedback read from the CCU board, This
may be because the value could not be read correctly, or because some required calibration
or configuration data was incorrect. The exposure will be aborted.
1100137 Error Text: Failed To Store Image Loop

View Level: opr
Root Cause: 1
Description: "Though the user was allowed to store an image loop, an error occurred that prevented the
successful store of the image-loop.
Customer Text: Failed to store image-loop. Retry.
1100138 Error Text: Failed To Initialize Software Component

View Level: opr
Root Cause: 1
Description: "General Software Failure in a module that is essential for proper functioning of the system.
Customer Text: Software Error. Reset the system. Call service if problem persists.

GE MEDICAL SYSTEMS
1100139 Error Text: System cannot support the requested frame rate
View Level: opr
Root Cause: 1
Recommended Action(s): "No Action
Description: "The system lowered the frame rate. This may be because images were acquired faster than
the system can save them to disk, or the pulse width for the acquisition was higher than the
allowable value for the requested frame rate.
Customer Text: Frame rate decreased due to system limitation.
1100140 Error Text: System cannot support the requested frame rate.
View Level: opr
Root Cause: 1
Recommended Action(s): "No Action
Description: "The system lowered the frame rate. This may be because images were acquired faster than
the system can save them to disk.
Customer Text: Images being acquired faster than the system can save them. Frame rate has decreased.
1100141 Error Text: Failed to close: image-store in progress

View Level: opr
Root Cause: 1
Description: "Athena received a request to close the patient while the image-store is in progress.
Customer Text: Image store in progress. Wait, then close patient.
1100142 Error Text: Maximum Series Limit Reached

View Level: opr
Root Cause: 1
Recommended Action(s): "Create a new patient entry for acquisition
Description: "The maximum number of runs, 80, was reached for the patient and hence no more
acquisitions can be performed on this patient entry. A new entry needs to be created.
Customer Text: Maximum number of runs reached. Create new patient entry for acquisition.
1100143 Error Text: Failed to Proceed Further

View Level: opr
Root Cause: 1
Description: "General Software Failure in a module that is essential for proper functioning of the system.

GE MEDICAL SYSTEMS
1100144 Error Text: Failed to submit image to internal print queue
View Level: opr
Root Cause: 1
Recommended Action(s): "Retry Expose-submission of image
Description: "Athena failed to submit the image the user wanted to expose, to Athena's internal print-
queue mechanism
Customer Text: Failure to submit image. Retry. Call service if the problem persists.
1100145 Error Text: Failed to initiate Print-queue transfer

View Level: opr
Root Cause: 1
Recommended Action(s): "Print Submit Error: May not meet expectation
Description: "Mitra Interface failed to provide a valid print-queue ID to Athena. Athena will request a new
ID when a new image is requested for expose/print.
1100146 Error Text: Failed to submit image to Print-queue

View Level: opr
Root Cause: 1
Recommended Action(s): "Print Submit Error: May not meet expectation
Description: "Mitra Interface reported a failure in accepting the print-job.
1100147 Error Text: Failed to flush print-queue.

View Level: opr
Root Cause: 1
Recommended Action(s): "Print Flush Error: Imags may not be printed; verify network queue
Description: "Mitra Interface reported a failure in flushing the opened print-queue. Images submitted in
this queue may not be printed. Athena will attempt to open a new queue when new images
come in for print/expose.
1100148 Error Text: About to reach maximum runs for this patient
View Level: opr
Root Cause: 1
Recommended Action(s): "Delete some images, or create an additional record for this patient
Description:
Customer Text: "Approaching maximum limit. Delete several images or create an additional record for this
patient.

GE MEDICAL SYSTEMS
1100149 Error Text: CCU parameter out of range
View Level: opr
Root Cause: 1
Recommended Action(s): "Reinstall the software, Reboot call service
Description: "Invalid parameter value for Camera Control Unit received.
Customer Text: An internal communication failure has occurred. Reset the system. Call service if problem
persists.
1100150 Error Text: Selected study have no images for review

View Level: opr
Root Cause: 1
Recommended Action(s): "Close patient
Description: "This happens when the tech tries to review a study which have no images stored
Customer Text: No images are stored and available for review. Close patient file.
1100151 Error Text: Not Enough space available for image storage
View Level: opr
Root Cause: 1
Recommended Action(s): "Close patient and delete some images or patients from the patient list screen
Description: "This error can happen when there is not enough space available to store images on the disk
1100152 Error Text: Not enough disk space for acquire loop
View Level: opr
Root Cause: 1
Recommended Action(s): "Close patient and delete some images or patients from the patient list screen
Description: "This error can happen when there is not enough space available to store images on the disk
1100153 Error Text: Failed to start calibration mode

View Level: opr
Root Cause: 1
Recommended Action(s): "Close the patient and try again. Reboot if the problem persists
Description: "This could happen if Athena is not in the proper state to start calibraiton
Customer Text: Retry calibration. Reset the system if the problem persists.

GE MEDICAL SYSTEMS
1100154 Error Text: Failed to start or stop a sequence
View Level: opr
Root Cause: 1
Description: "A Start Sequence or Stop Sequence command was not processed correctly. This could be
because it was unexpected, or because an error occurred while trying to change hardware
settings.
Customer Text: Retry the exposure. Call service if the problem persists.
1100155 Error Text: Rescale gain value is at maximum for several exposures
View Level: opr
Root Cause: 1
Recommended Action(s): "Re-Calibrate the image chain
Description: "Rescale gain value is at maximum for several exposures. This indicates that the system is
not calibrated properly
Customer Text: System is not calibrated properly. Recalibrate the image chain.
1100156 Error Text: Failed to display or remove the No Radiation sign.

View Level: opr
Root Cause: 1
Recommended Action(s): "Release Expose switch and try again
Description: "Failed to display the No Radiation sign on the Image monitor.
Customer Text: Application error. Release exposure switch and try again.
1100157 Error Text: Unable to set desired replay rate.

View Level: opr
Root Cause: 1
Recommended Action(s): "Please try selecting a different replay rate
Description: "This happens when Athena fails to set the desired replay-rate in review mode. Athena will
default to some known value.
Customer Text: Unable to set desired replay rate. Try selecting a different rate.

View Level: opr
Root Cause: 1
Recommended Action(s): "Please try again or open an exam
Description: "This will happen when the information provided for IUI does not match the database and
Athena fails to open the patient for RTPP.
Customer Text: The system cannot start an exam. Verify selection on the patient list and try again.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Recommended Action(s): "Please try again or open an exam
Description: "This will happen when the information provided for IUI is not correct or Athena is not in the
right mode to open a patient for RTPP

View Level: opr
Root Cause: 1
Recommended Action(s): "Please try again
Description: "This will happen when a patient is already selected and a request is made to open another
1100161 Error Text: Failed to open patient for review

View Level: opr
Root Cause: 1
Description: "This will happen when Mitra fails to select patient for review.
Customer Text: The system cannot enter review mode. Verify selection on the patient list and try again.
1100162 Error Text: Partial-Send in progress, failed to close exam.

View Level: opr
Root Cause: 1
Recommended Action(s): "Partial-Send in progress, please wait for completion.
Description: "This will happen when partial-send is in progress and the user tries to close the current
exam.
Customer Text: Partial-Send in progress, please wait for completion.
1100163 Error Text: Failed to go to online review: image storage in progress.

View Level: opr
Root Cause: 1
Recommended Action(s): "Image storage in progress, please wait then try again.
Description: "Image storage is in progress, user is prevented from going to online review till storage is
completed.
Customer Text: Image storage in progress. Please wait, then try again to review images.

GE MEDICAL SYSTEMS
1100164 Error Text: Acquisition stopped to prevent loss of images
View Level: opr
Root Cause: 1
Recommended Action(s): "Release expose switch, try again
Description: "The image memory buffers are full. Exposure was halted to prevent image loss on the next
exposure. Wait for the image buffers to be saved to disk. There may be problems with the
hard disk that makes them run too slow. Try hard disk defrag.
Customer Text: Image buffer filled. Wait while images are stored.
1100165 Error Text: Application data not received

View Level: opr
Root Cause: 1
Recommended Action(s): "Close the exam and try again. Reset the system if the problem persists
Description: "A required data item was not received from Mars during Application setup for the current
Opmode. Digital cannot start an exposure without this data.
1100166 Error Text: Cannot playback when digital in stenosis or stacking mode
View Level: opr
Root Cause: 1
Recommended Action(s): "Cannot playback when digital in stenosis or stacking mode
Description: "When in stenosis or stacking mode playback is disabled.
Customer Text: Loop playback is not allowed when in stenosis or stacking mode.
1100167 Error Text: No images tagged for print.

View Level: opr
Root Cause: 1
Recommended Action(s): "No images tagged for print
Description: "No images tagged for print
Customer Text: No images are tagged for printing.
1100168 Error Text: Print Error: Could not read data

View Level: opr
Root Cause: 1
Description: "This could happen if Athena fails to read some database field that is needed when printing.
Customer Text: An error occurred during print. Try again. Call service if the problem persists.
1100169 Error Text: Print Error Encountered. Forced a premature flush to printer.
View Level: opr
Root Cause: 1
Description: "Had to force a flush to printer prematurely due to an error.
Customer Text: An error occurred during print. Retry if the images were not printed.

GE MEDICAL SYSTEMS
1100170 Error Text: FOV change not allowed when system is waiting to start Fluoro.
View Level: opr
Root Cause: 1
Recommended Action(s): "Retry the FOV change
Description: "Image intensifier magnification cannot be changed from when the system is prepped for
Fluoro till exposure starts. The user should try again to change FOV after the exposure starts.
Customer Text: The Field of View was not changed. Try again.
1100171 Error Text: Cannot change display format in stenosis mode.

View Level: opr
Root Cause: 1
Recommended Action(s): "Cannot change display format in Stenosis mode
Description: "In Stenosis mode, user cannot go to multi-view format display.
Customer Text: Multiview display is not allowed in Stenosis mode.
1100172 Error Text: CD-ROM Capacity exceeded for the archive-selection.

View Level: opr
Root Cause: 1
Recommended Action(s): "Verify archive-selection can fit on CD-ROM
Description: "The selection size for CD-archive exceeds CD-ROM capacity.
Customer Text: CD-R capacity is exceeded for the archive selection. Select fewer images.
1100173 Error Text: Failed to back up calibration or configuration data.

View Level: opr
Root Cause: 1
Description: "A severe error occurred while trying to perform a backup of calibration/configuration data.
Customer Text: Backup failed.
1100174 Error Text: Failed to restore calibration or configuration data.

View Level: opr
Root Cause: 1
Description: "A severe error occurred while trying to perform a restore of calibration/configuration data.
Customer Text: Restore failed.
1100175 Error Text: Failed to communicate with Laser Imager. Ensure the Imager is on or call service.
View Level: opr
Root Cause: 1
Recommended Action(s): "Ensure the Imager is on
Description: "Athena attempts to establish communication with the printer and initialize it to print our
images. An error results if we are unable to complete the initialization
Customer Text: Printer communication error. Ensure printer is turned on or call service.

GE MEDICAL SYSTEMS
1100176 Error Text: Laser Imager Failure. Please call service.
View Level: opr
Root Cause: 1
Recommended Action(s): " printer turned off or reset printer, printer com port failure, Saturn comm port failure, check
for disconnected cable
Description: "Assuming the first part is successful, Athena starts sending images to the printer. If any of
the image sends within a given patient fails, another error is reported
Customer Text: Printer communication error. Ensure printer is turned on or call service.
1100177 Error Text: Failed to detect DICOM SCP Service

View Level: opr
Root Cause: 1
Recommended Action(s): "If error continues, reset system
Description: "Digital detected SCP service suspended
Customer Text: Network Communication Error. Reset if problem persists.
1100178 Error Text: Failed to detect DICOM SCU service

View Level: opr
Root Cause: 1
Description: "Digital detected SCU service suspended
1100179 Error Text: Failure to detect DICOM AutoPilot

View Level: opr
Root Cause: 1
Description: "Digital detected AutoPilot service suspended

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
1100182 Error Text: Calculated Iris Transmission is too small

View Level: opr
Root Cause: 1
Recommended Action(s): "Target Entrance Dose (TED) is very large; increase magnification, change the protocol ROI
Description: "The image is too bright because the Target Entrance Dose (TED) value is very large. In
order to achieve the Target Brightness Level (TBL), the calculated Iris transimission and
camera gain are at a minimum and cannot go any lower (the iris is almost closed). It is
possible that the patient is too small or too much raw radiation is in the image. Try to increase
the magnification, change the protocol ROI or collimate raw radiation.
radiation.
1100183 Error Text: Calculated Rescaling Gain is too low

View Level: opr
Root Cause: 1
Recommended Action(s): "Target Entrance Dose (TED) is very large; increase magnification, change the protocol ROI
Description: "The image is too bright because the Target Entrance Dose (TED) value is very large. In
order to achieve the Target Brightness Level (TBL), the calculated Iris transimission, camera
gain and rescaling gain are at a minimum and cannot go any lower (the iris is almost closed).
It is possible that the patient is too small or too much raw radiation is in the image. Try to
increase the magnification, change the protocol ROI or collimate raw radiation.
radiation.
1100184 Error Text: Calculated Rescaling Gain is too large

View Level: opr
Root Cause: 1
Recommended Action(s): "Target Entrance Dose (TED) is very small. Decrease magnification or increase the the
protocol ROI. Try again.
Description: "The image is too dark because the Target Entrance Dose (TED) value is very small. In order
to achieve the Target Brightness Level (TBL), the calculated Iris transimission, camera gain
and rescaling gain are at a maximum and cannot go any higher (the iris is almost full open).
It is possible that the patient is too large. Try to decrease the magnification or increase the
protocol ROI.

GE MEDICAL SYSTEMS
1100185 Error Text: Timeout waiting for ABD
View Level: opr
Root Cause: 1
Description: "Automatic Brightness Detection (ABD) feedback was not received for the DSA trial
exposure. Since the trial was not successful, the DSA sequence cannot continue.
1100186 Error Text: Timeout waiting for ABD

View Level: opr
Root Cause: 1
Recommended Action(s): "Ignore. If error continues, reset system and try again.
Description: "ABD was not received for an exposure.
Customer Text:
1100187 Error Text: Calculated Camera Gain is too large

View Level: opr
Root Cause: 1
Recommended Action(s): "Target Entrance Dose (TED) is very small. Decrease magnification or increase the the
protocol ROI. Try again.
Description: "The image is too dark because the Target Entrance Dose (TED) value is very small. In order
to achieve the Target Brightness Level (TBL), the calculated Iris transimission and camera
gain are at a maximum and cannot go any higher (the iris is almost full open). It is possible
that the patient is too large. Try to decrease the magnification or increase the protocol ROI.

GE MEDICAL SYSTEMS
3.7 1101 Athena Communication
1101000 Error Text: Failed to register for a command
View Level: opr
Root Cause: 1
Description: This error may occur when Digital software fails to register for a message id. Digital proxy
needs to register for every message id with the ProxyMgr object in order to handle it.
1101001 Error Text: Failed to connect to other system

View Level: opr
Root Cause: 1
Description: This error may occur when Digital software fails to connect to the other system (MARS). It
could be a bad network cable, lose connection or the registry setting for the MARS IP address
is not correct
1101002 Error Text: Packet not sent

View Level: opr
Root Cause: 1
Description: This error may occur when Digital fails to send a message to the other system. It could be
that the other system is down, or the network cable is pulled out. Plugging the cables in and
rebooting the systems would fix this problem

View Level: opr
Root Cause: 1
Description: This error may happen if Digital fails to create a accept handler object that is required to listen
for listen connection requests from other subsystems. A reboot would fix this problem
1101004 Error Text: Null Input handler pointer

View Level: opr
Root Cause: 1
Description: This error may happen if Digital fails to create a input handler object that is required to listen
for receive data from other subsystems. A reboot would fix this problem
1101005 Error Text: Close socket failed

View Level: opr
Root Cause: 1
Description: This error may occur when Digital fails to close a open socket.Digital needs to close a socket
when there is a connection failure or a ShutDown or Reset happens.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: This error may occur when Digital fails to accept a socket connection request into a event
handler. Digital proxy needs to have these handlers to handle incoming messages form
MARS system. If this error occurs a reboot would fix this problem
1101007 Error Text: Open Socket failed
View Level: opr
Root Cause: 1
Description: This error may occur when Digital fails to open a socket connection.
1101008 Error Text: Connection failure

View Level: opr
Root Cause: 1
Description: This error may occur when the other system breaks the socket connection

View Level: opr
Root Cause: 1
Description: This error may occur when there is some page fault on either the Digital system or the Mars
system. A reboot would fix this problem. If the problem still exist a software reinstallation may
be required

View Level: opr
Root Cause: 1
Description: This error may occur when Digital system receives less data for a packet form the other
system. A reboot would fix this problem. This could also happen if there is mismatch of Digital
and Mars software versions

View Level: opr
Root Cause: 1
Description: This error may occur when Digital fails to create a Default Message Handler object. Digital
requires a Default Message Handler object for handling any message that Digital is not
registered for with its ProxyMgr Object

GE MEDICAL SYSTEMS
3.8 1102 Athena Drivers
1102100 Error Text: Can not contact OCB in Camera Head
View Level: opr
Root Cause: 0
Recommended Action(s): Check OCB, OCB power supply, RTB cables between Athena and II.
Description: Can not contact OCB in Camera Head
1102101 Error Text: Reprogrammed Gitane Flash memory

View Level: opr
Root Cause: 1
Recommended Action(s): Updated FLASH as part of normal upgrade - No further action required.
Description: Reprogrammed Gitane Flash memory
- just telling you that it happened
- probably due to a software update.
1102102 Error Text: Could not reprogram Gitane Flash memory - bad input file
View Level: opr
Root Cause: 1
Recommended Action(s): User error during software upgrade - bad hex file provided. Re-read software upgrade
instructions and try again.
Description: Could not reprogram Gitane Flash memory - bad input file
Customer Text: Memory programming has failed. Try again.
1102103 Error Text: Could not reprogram Gitane Flash memory - bad memory device
View Level: opr
Root Cause: 1
Recommended Action(s): Hardware error during software upgrade. Cycle power and try again. Replace Gitane board
if this is a persistent problem.
Description: Could not reprogram Gitane Flash memory - bad memory device
Customer Text: Memory programming has failed. Turn the system power off/on and try again.
1102104 Error Text: Gitane driver files missing.

View Level: opr
Root Cause: 1
Recommended Action(s): Re-install Athena software
Description: Gitane driver files missing.
1102105 Error Text: Gitane board not found.

View Level: opr
Root Cause: 1
Recommended Action(s): Re-seat Athena Gitane board. Replace Gitane if this is a persistent problem.
Description: Gitane board not found.

GE MEDICAL SYSTEMS
1102106 Error Text: Gitane sys-logic FPGA is unprogrammed.
View Level: opr
Root Cause: 1
Recommended Action(s): Re-install Athena software. Replace Gitane if this is a persistent problem.
Description: Gitane sys-logic FPGA is unprogrammed.
1102107 Error Text: OCB over temperature (+60 C)

View Level: opr
Root Cause: 1
Recommended Action(s): Remove Intensifier covers and check the CCD camera, cooling fan and Optics Control Board
for overheating.
Description: OCB over temperature (+60 C)
Customer Text: Abnormal Digital temperature. Call service to monitor if problem persists.
1102108 Error Text: Excessive OCB communication errors.

View Level: opr
Root Cause: 1
Recommended Action(s): Check RTB cables between Athena and OCB. Check for proper terminating resisters.
Description: Excessive OCB communication errors.
1102012 Error Text: IAB Error

View Level: opr
Root Cause: 1
Recommended Action(s): Check hardware boards, call service
Description: Failed to initialize the driver for the Acquisition board. May be due to a hardware issue or
incorrect driver installation
1102013 Error Text: Board creation fail

View Level: opr
Root Cause: 1
Recommended Action(s): Board may not be present, call service
Description: Failed to initialize the driver for one of the boards (e.g. IAB or Gitane). May be a hardware
issue or due to incorrect installation.
1102111 Error Text: Reprogrammed OCB Flash memory
View Level: opr
Root Cause: 1
Recommended Action(s): Updated OCB FLASH as part of normal upgrade - No further action required.
Description: Reprogrammed OCB Flash memory - just telling you that it happened - probably due to a
software update.

GE MEDICAL SYSTEMS
1102112 Error Text: Could not reprogram OCB flash memory
View Level: opr
Root Cause: 1
Description: Reprogram of OCB Flash memory failed. OCB may not be functional.
1102113 Error Text: Bad Firmware config file

View Level: opr
Root Cause: 1
Description: There is a problem with <athena_dir>\xilinx\firmware_revs.txt file or one of the files it points
to.
1102400 Error Text: ICB Driver Not Found

View Level: opr
Root Cause: 1
1102401 Error Text: ICB Driver Not Initialized

View Level: opr
Root Cause: 1
1102402 Error Text: ICB Board Defect

View Level: opr
Root Cause: 1
1102403 Error Text: ICB Camera Head Defect

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
1102404 Error Text: ICB/Camera board defect
View Level: opr
Root Cause: 1
1102405 Error Text: Wrong CCD Operating Mode

View Level: opr
Root Cause: 1
1102406 Error Text: Wrong Synchronisation Mode

View Level: opr
Root Cause: 1
1102407 Error Text: Wrong Image Period

View Level: opr
Root Cause: 1
1102408 Error Text: Image Period is not adjustable

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
1102409 Error Text: Wrong CCD Integration Time
View Level: opr
Root Cause: 1
1102410 Error Text: CCD Integration Time is not Adjustable

View Level: opr
Root Cause: 1
1102411 Error Text: Wrong Video Gain

View Level: opr
Root Cause: 1
1102412 Error Text: Wrong Self Test

View Level: opr
Root Cause: 1
1102413 Error Text: Wrong Test Pattern

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
1102414 Error Text: Signal Sync Polarity is Not Adjustable
View Level: opr
Root Cause: 1
1102415 Error Text: Signal Trig Polarity is not adjustable

View Level: opr
Root Cause: 1
1102416 Error Text: Correct Function is Not Implemented

View Level: opr
Root Cause: 1
1102417 Error Text: Not Available while Running Test Pattern

View Level: opr
Root Cause: 1
1102418 Error Text: General Camera Driver Error

View Level: opr
Root Cause: 1
Recommended Action(s): Check ICB board and re-install driver if needed. Check cable connection at CCD camera
head or all cables from camera to Digital module.
Description: An unspecified error occurred in the ICB driver. Check the debug message field for more
details.

GE MEDICAL SYSTEMS
1102419 Error Text: Camera Initialization Failed
View Level: opr
Root Cause: 1
Recommended Action(s): Check ICB board and Re-install Athena software if needed. Check cable connection at CCD
camera head or all cables from camera to Digital module.
Description: Failed to initialize Camera driver.
1102420 Error Text: Gitane board reported an EMERGENCY STOP error status
View Level: opr
Root Cause: 1
1102421 Error Text: Gitane board reported a NO VD error status

View Level: opr
Root Cause: 1
1102422 Error Text: Gitane board reported a NO X-ray error status

View Level: opr
Root Cause: 1
1102423 Error Text: Gitane board reported a FRAME RATE VIOLATION error status
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
1102424 Error Text: Gitane board reported an X-ray WINDOW TIME error status
View Level: opr
Root Cause: 1
1102425 Error Text: Gitane board reported a SYS RESET IN error status
View Level: opr
Root Cause: 1
1102426 Error Text: Gitane board did not stop an acquisition even after one second
View Level: opr
Root Cause: 1
Recommended Action(s): No action. Call service if problem persists
Description: This error is reported when we attempt to write to a Gitane register to stop acquisition. After
writing the register, we monitor a Gitane status register to make sure that the acquisition has
indeed stopped. If a correct status is not returned within 1 second, this error is reported.
Customer Text: Digital control error. Reset and call service if the problem persists.

GE MEDICAL SYSTEMS
3.9 11 03 Athena Calibration
1103000 Error Text: Athena failed to create or delete Patient information
View Level: opr
Root Cause: 1
Recommended Action(s): "Quit Calibration
Description: "Calibration needs a patient record to be selected ion the memory to acquire images. Here
we could not create the Calibration patient
1103001 Error Text: Calibration data is missing

View Level: opr
Root Cause: 1
Recommended Action(s): "Perform required Calibration or Reinstall software
Description: "A required calibration parameter could not be found
Customer Text: Calibration parameter could not be found. Call service to recalibrate the system.
1103002 Error Text: Calibration data is incorrect

View Level: opr
Root Cause: 1
Description: "A required calibration parameter is incorrect
Customer Text: Incorrect Calibration parameter. Call service to recalibrate the system.
1103003 Error Text: Could not save the calibration result

View Level: opr
Root Cause: 1
Description: "Could not save the calibration result
View Level: opr
Root Cause: 1
Recommended Action(s): "G2 has changed by more than 5%, check if G3 needs to be changed
Description: "Either G2 or G3 has changed by more than 5%. User is advised to check if the other value

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Recommended Action(s): "G3 has changed by more than 5%, check if G2 needs to be changed
Description: "Either G2 or G3 has changed by more than 5%. User is advised to check if the other value
1103006 Error Text: Got false calibration start

View Level: opr
Root Cause: 1
Recommended Action(s): "Close all calibrations and retry. Reset the system if the problem persist
Description: "Start calibration could fail if the Athena system recevied a bad Calibration Id form the Mars
system or Athena is in a bad state it self
Customer Text: Calibration start error. Close all calibrations and retry. Reset the system if the problem
persists.
1103007 Error Text: Got false calibration stop

View Level: opr
Root Cause: 1
Recommended Action(s): "Start calibration and retry. Reset the system if the problem persist
Description: "Stop calibration could fail if the Athena system recevied a bad Calibration Id form the Mars
system or Athena is in a bad state it self
Customer Text: Calibration stop error. Close all calibrations and retry. Reset the system if the problem
persists.
1103008 Error Text: Iqst store images failed

View Level: opr
Root Cause: 1
Recommended Action(s): "Acquire more images and try again
Description: "Store images could fail if there are not enough images to store
Customer Text: IQST image store failure. Acquire more images and try again.
1103009 Error Text: Failed to start or stop the Iqst server

View Level: opr
Root Cause: 1
Recommended Action(s): "Retry or reinstall if the problem persists
Description: "This error could happen we had a bad installation
Customer Text: IQST communication failure. Retry or reinstall software if problem persists.

GE MEDICAL SYSTEMS
1103010 Error Text: Failed to copy a file
View Level: opr
Root Cause: 1
Description: "This error could happen we had a bad installation or the file does not exists
Customer Text: Failed to copy a file. Retry or reinstall software if problem persists.
1103011 Error Text: Less images acquired

View Level: opr
Root Cause: 1
Recommended Action(s): "Acquire more images and try again
Description: "This error can happen if there are less images acquired then needed for testing, such as
IQST.
Customer Text: Acquire more images to continue.
1103012 Error Text: The ABD value did not decrease when Iris transmission was reduced
View Level: opr
Root Cause: 1
Description: "Occurs during Iris LUT calibration. This error could happen if there is a bad camera, iris, or
Optics Control Board (OCB).
Customer Text: ABD value did not decrease. Repeat the calibration.
1103013 Error Text: Attempted to update one of the CF registry values with 0
View Level: opr
Root Cause: 1
Recommended Action(s): "Quit calibration, reset the system, then retry. If problem persists, reload software.
Description: "Occurs during Fluoro CF, Record CF, or Compensation CF calibration. Should not happen:
usually indicates software problem.
1103014 Error Text: Attempted to update the Photodiode Gain registry value with a number outside of 1-10000
View Level: opr
Root Cause: 1
Recommended Action(s): "Quit calibration, reset the system, then retry. If problem persists, reload software.
Description: "Occurs during Record CF/Photodiode Gain calibration. Should not happen:usually indicates
software problem.

GE MEDICAL SYSTEMS
1103015 Error Text: The image file needed for this calibration is missing
View Level: opr
Root Cause: 1
Recommended Action(s): "Quit calibration and reload software.
Description: "The files needed for this calibration are missing. Indicates improper installation or corrupt
hard disk.
Customer Text: File required for calibration is missing.
1103016 Error Text: The value received for this configuration is not valid
Minor Function Impacted: Configuration
View Level: opr
Root Cause: 1
Recommended Action(s): "Try again, check the config files for missing or bad entries
Description: "This error could happen if Mars send athena a bad value to set for a configuration parameter.
Customer Text: Digital Configuration value is bad. Recheck configuration.
1103017 Error Text: Config parmeter not initialized

View Level: opr
Root Cause: 1
Recommended Action(s): "Config the parameter and try again
Description: "This error can happen if the particular config parameter is not initialized in the athena config
database
Customer Text:
1103018 Error Text: Config parameter is corrupt

View Level: opr
Root Cause: 1
Recommended Action(s): "Config database is corrupt, config again if the problem persists reinstall software
Description: "This error can happen if the athena configuration database is corrupt or unreadable
Customer Text: DICOM Auto-send destination error. Reset and Call service if problem persists.
1103019 Error Text: Config set failed

View Level: opr
Root Cause: 1
Recommended Action(s): "Could not set the config parameter, check the values and try again
Description: "This can happen if athena fails to set the config value for a parameter
1103020 Error Text: The calibration did not complete after the maximum allowed exposures
View Level: opr
Root Cause: 1
Recommended Action(s): "Check digital screen for error percentage. If near +/-5%, save the calibration, if greater, redo
the calibration or check hardware.
Description: "The sensor feedback value did not approach the target value after maximum allowable
exposures
Customer Text: The sensor feedback value did not approach the target value after maximum allowable
exposures

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 0
Recommended Action(s): "The current user is not authorized to perform this function. The user must logout and re-login
with the appropriate access level.
Description: "The current user is not authorized to perform this function. The user must logout and re-login

GE MEDICAL SYSTEMS
3.10 1105 Athena Database
1105000 Error Text: Unable to update record. NO PATIENT SELECTED
View Level: opr
Root Cause: 0
Recommended Action(s): Select a patient from gui
Description: This error may occur when Athena software fails to update a database record because there
is no patient selected at that time.
1105001 Error Text: Current Patient can not be select for acquisition or review.
View Level: opr
Root Cause: 1
Description: Current Patient can not be select for acquisition or review.
1105002 Error Text: Current Patient can not be deleted.

View Level: opr
Root Cause: 1
Description: Current Patient can not be deleted.
1105003 Error Text: Given Name is not entered in Add or Edit Patient Dialogue.
View Level: opr
Root Cause: 1
Description: Given Name is not entered in Add or Edit Patient Dialogue.
Customer Text: Reset the system. Call service if the problem persists.
1105004 Error Text: Family Name is not entered in Add or Edit Patient Dialogue.
View Level: opr
Root Cause: 1
Description: Family Name is not entered in Add or Edit Patient Dialogue.
Customer Text: Family Name is not entered. Enter complete patent information.
1105005 Error Text: Date of Birth is not entered in Add or Edit Patient Dialogue.
View Level: opr
Root Cause: 1
Description: Date of Birth is not entered in Add or Edit Patient Dialogue.
Customer Text: Date of Birth is not entered. Enter complete patent information.

GE MEDICAL SYSTEMS
1105006 Error Text: Acquisition can not be started for the selected patient from the Work list.
View Level: opr
Root Cause: 1
Description: Acquisition can not be started for the selected patient from the Work list.
Customer Text: This patient has been selected from the Work list; start the exam from the Patient List screen.
1105007 Error Text: Acquisition can not be started for the selected patient from the Patient List.
View Level: opr
Root Cause: 1
Description: Acquisition can not be started for the selected patient from the Patient List.
Customer Text: Acquisition can't initialize. Reset the system. Call service if the problem persists.
1105008 Error Text: Review can not be started for the selected patient from the Patient List.
View Level: opr
Root Cause: 1
Description: Review can not be started for the selected patient from the Patient List.
Customer Text: Patient review is unavailable. Reset the system. Call service if the problem persists.
1105009 Error Text: Patient can not be created in the database.

View Level: opr
Root Cause: 1
Description: Patient can not be created in the database.
1105010 Error Text: IQST patient can not be loaded.
View Level: opr
Root Cause: 1
Recommended Action(s): Close patient if open and Retry or Reboot the system
Description: IQST patient can not be loaded.
Customer Text: IQST patient can not be loaded. Reset the system. Call service if the problem persists.
1105011 Error Text: Services did not start successfully.

View Level: opr
Root Cause: 1
Description: Services did not start successfully.
Customer Text: Services did not start successfully. Reset the system. Call service if the problem persists.
1105012 Error Text: Services did not shut down successfully.

View Level: opr
Root Cause: 1
Description: Services did not shut down successfully.
Customer Text: Services did not shut down successfully. Reset the system. Call service if the problem
persists.

GE MEDICAL SYSTEMS
1105013 Error Text: GUI did not start successfully.
View Level: opr
Root Cause: 1
Description: GUI did not start successfully.
1105014 Error Text: GUI did not shut down successfully.

View Level: opr
Root Cause: 1
Description: GUI did not shut down successfully.
1105900 Error Text: General error message, process and operation are undetermined.
View Level: opr
Root Cause: 1
Description: General error message, process and operation are undetermined.

View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
1105903 Error Text: Error generated by MAP process.

View Level: opr
Root Cause: 1
Description: Error generated by MAP process.
1105904 Error Text: Error generated by Autopilot process.

View Level: opr
Root Cause: 1
Description: Error generated by Autopilot process.
Customer Text: Autopilot problem occurred. Retry or reset the system if the problem persists.

GE MEDICAL SYSTEMS
1105920 Error Text: Process undetermined, error involves I/O operation.
View Level: opr
Root Cause: 1
Description: Process undetermined, error involves I/O operation.
1105921 Error Text: Process undetermined, error involves authentication operation.

View Level: opr
Root Cause: 1
Description: Process undetermined, error involves authentication operation.
1105999 Error Text: Mitra test error
View Level: opr
Root Cause: 1
Description: Mitra test error
1105922 Error Text: Got invalid data from Mars

View Level: opr
Root Cause: 1
Description: Mars send some data to save on the disk which is invalid
1105923 Error Text: Mars failed to send the technique values for a frame
View Level: opr
Root Cause: 1
Recommended Action(s): Check the Generator errors
Description: Mars missed to send the technique values for a frame

GE MEDICAL SYSTEMS
3.11 1106 Athena Error Management
1106000 Error Text: Failed to read the display error text file
View Level: opr
Root Cause: 1
Recommended Action(s): Check to see if the file c:patriot_ErrorTextList.txt exits
Description: Check to see if the file c:patriot_ErrorTextList.txt exits
1106001 Error Text: Athena got an unlisted error code to display errors
View Level: opr
Root Cause: 1
Recommended Action(s): Check to see if that error code is listed in the c:ErrorTextList.txt
Description: Check to see if that error code is listed in the c:ErrorTextList.txt

GE MEDICAL SYSTEMS
3.12 12 XRImDet
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
1200007 Error Text: XRImDet is not ready, it may be in PowerFailure, ShutDown or HaltError
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
controller.
controller.
Customer Text:

View Level: opr
Root Cause: 1
controller.
controller.

View Level: opr
Root Cause: 1
controller.
controller.

View Level: opr
Root Cause: 1
controller.
controller.

View Level: opr
Root Cause: 1
controller.
controller.
Customer Text: Configuration file may be corrupted. Call service to reload software.

GE MEDICAL SYSTEMS
3.13 16 XRImProc
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
1600007 Error Text: XRImProc is not ready, it may be in PowerFailure, ShutDown or HaltError
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
controller.
controller.

View Level: opr
Root Cause: 1
controller.
controller.

View Level: opr
Root Cause: 1
controller.
controller.

View Level: opr
Root Cause: 1
controller.
controller.
1600017 Error Text: Requested Mag value could not be set.

View Level: opr
Root Cause: 1
Recommended Action(s): Digital could not set the requested Mag value. Value may be out of range.
Description: Digital could not set the requested Mag value. Value may be out of range.
Customer Text: Requested Mag value could not be set. Please select another value

GE MEDICAL SYSTEMS
3.14 18 XRExpSens
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
Description: System notified the joining of an actor which ExpSens was not interested in. There may be
configuration issues.

View Level: opr
Root Cause: 1
Description: Unable to understand and process an event.
View Level: opr
Root Cause: 1
Description: The opModeId is not an active opMode, defaulting to prime one

GE MEDICAL SYSTEMS
1800007 Error Text: XRExpSens is not ready, it may be in PowerFailure, ShutDown or HaltError
View Level: opr
Root Cause: 1
Description: XRExpSens is not ready, it may be in PowerFailure, ShutDown or HaltError
View Level: opr
Root Cause: 1
Description: One of the OpModeIds are not configured.

View Level: opr
Root Cause: 1
Description: Unable to interact with an actor.The software communication bus broken

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
Description: SATURN returned an unknown event.

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
Description: Software configuration problem/System low in resources

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
3.15 20 XROpDesc
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
2000003 Error Text: XROpDesc failed to startup

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
2000010 Error Text: The OpDesc configuration files not found

View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
2000012 Error Text: OpDesc lost a frame

View Level: opr
Root Cause: 1
Recommended Action(s): Unable to track the correct frameid, the frameid id out of sync

GE MEDICAL SYSTEMS
2000013 Error Text: OpDesc failed to read config parameter
View Level: opr
Root Cause: 1
2000014 Error Text: OpDesc received negative PPD parameter

View Level: opr
Root Cause: 1
Recommended Action(s): Dose calculation module is receiving bad values.
2000015 Error Text: OpDesc calculated a dose greater than total allowed dose.
View Level: opr
Root Cause: 1
2000016 Error Text: OpDesc calculated a dap greater than total allowed dap.
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
3.16 22 XRPatPos
View Level: opr
Root Cause: 0
Description: "Software Error: In boot phase, the actor needs to connect to other actors if required. For
persists.

View Level: opr
Root Cause: 0
persists.

View Level: opr
Root Cause: 0
Description: "Software Error: The actor does not complete a boot phase. This happens when its controllers
persists.

View Level: opr
Root Cause: 0
Description: "Software Error: The actor tried to initialize its controllers but failed.
persists.

View Level: opr
Root Cause: 0
Description: "Software Error: Actor tried to read parameters from its cal/cfg/dyn files but could not.
persists.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 0
Description: "Software Error.

View Level: opr
Root Cause: 0

View Level: opr
Root Cause: 0

View Level: opr
Root Cause: 0

View Level: opr
Root Cause: 0

View Level: opr
Root Cause: 0

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 0

View Level: opr
Root Cause: 0

View Level: opr
Root Cause: 0

View Level: opr
Root Cause: 0
Description: "Software Error: In boot phase, the actor needs to connect to other actors if required.
However, for somehow the connection cannot be built. In this case, the software will not work
properly.
2200102 Error Text: Not bound to actor

View Level: opr
Root Cause: 0

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 0
Description: "Software Error: In boot phase, the actor needs to create the Events to be published. This
error indicates that the actor cannot create this Event. So the software not function well.
2200104 Error Text: Creation of Table Device Failed

View Level: opr
Root Cause: 0
Description: "Failed to create Table device. Software error
2200105 Error Text: Table Movement Inhibit button is on; table motion is not allowed.
View Level: opr
Root Cause: 0
Recommended Action(s): "Enable Table Motion Control Switch
Description: "The Movement Inhibit button is on; the user needs to turn it off before trying to move the
table.
Customer Text: The table control disable switch is pressed. Release it to enable table movement.

View Level: opr
Root Cause: 1
Description: "Software error: failure in RfTableDevice constructor.

View Level: opr
Root Cause: 1
Description: "RfTableDevice initialization failure.

View Level: opr
Root Cause: 1
Description: "Table angulation control error.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: "Table positioning error.

View Level: opr
Root Cause: 1
Description: "Software error: failure in IOAdapter constructor.

View Level: opr
Root Cause: 1
Description: "POS cabinet IO initialization failure.

View Level: opr
Root Cause: 1
Description: ""POS cabinet IO is not responding. Indicates a CAN device or bus problem. Refer to the
CAN bus block diagram.
connections.
2290103 Error Text: Table at angulation limit. Reverse direction and call service if error continues.
View Level: opr
Root Cause: 0
Description: "Table at angulation limit. Reverse direction and call service if error continues.
Customer Text: Table at angulation limit. Reverse direction and call service if error continues.

GE MEDICAL SYSTEMS
3.17 32 XRSvcMgr
3200000 Error Text: Failed to create object:
View Level: opr
Root Cause: 1
Description: SvcMgr failed to start
Customer Text: Service Software component did not start properly.
3200001 Error Text: Failed to bind with:

View Level: opr
Root Cause: 1
3200002 Error Text: Create event failed for this event:

View Level: opr
Root Cause: 1
3200003 Error Text: Publish event failed for this event:
View Level: opr
Root Cause: 1
Description: Unable to publish a required event. The software communication bus broken
3200004 Error Text: Subscribe event failed for this event:

View Level: opr
Root Cause: 1
3200005 Error Text: Unsubscribe event failed for this event:

View Level: opr
Root Cause: 1
Description: Unable to unsubscribe to a required event. The software communication bus broken

GE MEDICAL SYSTEMS
3200006 Error Text: Unable to perform the requested services:
View Level: opr
Root Cause: 1
Description: The service is not able to performed, reboot the system
Customer Text: System is unable to perform action. Reset the system.
3200007 Error Text: SII failure:

View Level: opr
Root Cause: 1
Description: SII Failure, the system need to be reboot
Customer Text: System error. Reset the system.
3200008 Error Text: UponEvent cannot be processed: PowerFailure, ShutDown or Halt error occurred
View Level: opr
Root Cause: 1
Description: Unable to process the received event. PowerFailure, ShutDown or Halt error occurred
3200009 Error Text: Unable to join actor:

View Level: opr
Root Cause: 1
Description: Actor is unable to join the system, software communication problem
3200010 Error Text: Unable to identify Application from the Tag-Values passed to siiUserRequest
View Level: opr
Root Cause: 1
Description: Unable to identify Application from the Tag-Values passed to siiUserRequest
3200011 Error Text: New Application is same as the current application. User might have pressed the same
application again!
View Level: opr
Root Cause: 1
Recommended Action(s): Operator
Description: New Application is same as the current application. User might have pressed the same
application again!
3200012 Error Text: No Application is available at this moment to service this request from SUIF.
View Level: opr
Root Cause: 1
Description: No Application is available at this moment to service this request from SUIF.

GE MEDICAL SYSTEMS
3200013 Error Text: ERROR:
View Level: opr
Root Cause: 1
Description: ERROR:
3200014 Error Text: Unable to obtain handle to peer actor

View Level: opr
Root Cause: 1
Description: Unable to obtain handle to peer actor
3200015 Error Text: SERVICE APP ERROR:
View Level: opr
Root Cause: 1
Description: SERVICE APP ERROR:
3200016 Error Text: Clearing Error

View Level: opr
Root Cause: 1
Description: Clearing Error - No customer text is desired, because this error is used as a means of clearing
(erasing) INHIBIT errors generated during service applications.
3200017 Error Text: Cancelling Calibration

View Level: opr
Root Cause: 1
Recommended Action(s): Cancelling Calibration.
Description: Calibration Canceled. - No customer text is desired because this error is used as a means of
cancelling calibrations from service applications.
Customer Text: Calibration was cancelled. Please retry from start

GE MEDICAL SYSTEMS
3.18 34 XRSysMgr
3400000 Error Text: Timeout has occurred during the boot of the system
View Level: opr
Root Cause: 1
Recommended Action(s): "computer
Description: "All the subsystems did not boot within the configured boot timeout period
3400001 Error Text: Timeout has occured during shutdown. Shutdown will be completed.
View Level: opr
Root Cause: 1
Description: "All the subsystems did not complete their shutdown within the configured shutdown timeout
period. The system will continue the shutdown.
3400002 Error Text: Timeout has occured during Reset. OS Reset will be Continued.
View Level: opr
Root Cause: 1
Description: "All the subsystems did not complete their shutdown within the configured shutdown timeout
period. The system will continue with the Operating System Reset
3400003 Error Text: Unable to create event

View Level: opr
Root Cause: 1
Description: "Unable to create a required event. The software comminucation bus broken
3400004 Error Text: Unable to publish event

View Level: opr
Root Cause: 1
Description: "Unable to publish a required event. The System may be low in resources
3400005 Error Text: The system is booting.

View Level: opr
Root Cause: 1
Description: "System is starting the softwre boot.

GE MEDICAL SYSTEMS
3400006 Error Text: EF boot phase 0 completed. All actors have bound to the actors in their list.
View Level: opr
Root Cause: 1
Description: "All the subsystems have completed boot level EF phase 0. All actors have bound to the
actors in their list.
Customer Text: The system is booting. Initializing system communication.
3400007 Error Text: EF boot phase 1 completed. Communication established with the generator and/or digital.
View Level: opr
Root Cause: 1
Description: "All the subsystems have completed boot level EF phase 1. Completed powerup for digital
and generator. Established communication between system controller and digital/generator.
Customer Text: The system is booting. Configuring the system. . .
3400008 Error Text: EF boot phase 2 completed.

View Level: opr
Root Cause: 1
Description: "All the subsystems have completed boot level EF phase 2. The IUI is starting to query the
subsystems for their configured options.
Customer Text: The system is booting. Configuring the system. . . . . .

View Level: opr
Root Cause: 1
Description: "All the subsystems have completed boot level NORMAL phase 0. The system passes
directly through this phase without waiting for any inputs.
Customer Text: The system is booting. Configuring the system. . . . . . . . .

View Level: opr
Root Cause: 1
Description: "All the subsystems have completed boot level NORMAL phase 1. The positioner
configuration is complete.
Customer Text: The system is booting. Configuring the system. . . . . . . . . . . .

GE MEDICAL SYSTEMS
3400011 Error Text: NORMAL boot phase 2 completed. System initialization and configuration completed.
View Level: opr
Root Cause: 1
Description: "All the subsystems have completed boot level NORMAL phase 2. Completed all system
initialization and all configuration. System is ready.
Customer Text: The System Initialization is complete.
3400012 Error Text: The system is resetting.

View Level: opr
Root Cause: 1
Description: "System is starting the reset process.
3400013 Error Text: The system is shutting down.

View Level: opr
Root Cause: 1
Description: "System is starting the shutdown process/
3400014 Error Text: Shutdown is occuring because power failure condition exists.
View Level: opr
Root Cause: 1
Description: "The system is shutting down due to a Hospital Main power failure.
Customer Text: Hospital Main power failure. System Shutdown is in progress. Please wait. . .
3400015 Error Text: System restart failed

View Level: opr
Root Cause: 1
Description: "System restart failed after power recovery from interruption or E-stop released
Customer Text: System Restart Failed. Reset the system. Call service if the problem persists.

View Level: opr
Root Cause: 1
Description: "System restart successful after power recovery from interruption or E-stop released
Customer Text: System Restart successful.

GE MEDICAL SYSTEMS
3400017 Error Text: System boot successful
View Level: opr
Root Cause: 1
Description: "System boot successful

GE MEDICAL SYSTEMS
3.19 36 XRTechMg
3600000 Error Text: JediIF Initiation Failure
View Level: opr
Root Cause: 1
Recommended Action(s): "DeviceComm Problem
Description: "DeviceComm initiation by JediIF failed
3600001 Error Text: JediIF Msg Block Initiation Failure

View Level: opr
Root Cause: 1
Recommended Action(s): "Software Problem
Description: "Message block initiation for incoming CAN messages from generator failed
3600002 Error Text: JediIF Msg Queue Enqueue Failure

View Level: opr
Root Cause: 1
Description: "JediIf msg queue enqueue failed
3600003 Error Text: XRTechMgr construction imcomplete

View Level: opr
Root Cause: 1
Description: "XRTechMgr construction imcomplete
3600004 Error Text: XRTechMgr failed to create event

View Level: opr
Root Cause: 1
Description: "XRTechMgr failed to create event
3600005 Error Text: XRTechMgr failed to subscrib event

View Level: opr
Root Cause: 1
Description: "XRTechMgr failed to subscrib event

GE MEDICAL SYSTEMS
3600006 Error Text: XRTechMgr failed to publish event
View Level: opr
Root Cause: 1
Description: "XRTechMgr failed to publish event
3600007 Error Text: SetKv not allowed

View Level: opr
Root Cause: 1
Description: "SetKv not allowed
3600008 Error Text: GetKv not allowed

View Level: opr
Root Cause: 1
Description: "GetKv not allowed
3600009 Error Text: SetMa not allowed

View Level: opr
Root Cause: 1
Description: "SetMa not allowed
3600010 Error Text: GetMa not allowed

View Level: opr
Root Cause: 1
Description: "GetMa not allowed
3600011 Error Text: SetMas not allowed

View Level: opr
Root Cause: 1
Description: "SetMas not allowed
3600012 Error Text: GetMas not allowed

View Level: opr
Root Cause: 1
Description: "GetMas not allowed

GE MEDICAL SYSTEMS
3600013 Error Text: SetExposureTime not allowed
View Level: opr
Root Cause: 1
Description: "SetExposureTime not allowed
3600014 Error Text: GetExposureTime not allowed

View Level: opr
Root Cause: 1
Description: "GetExposureTime not allowed
3600015 Error Text: IncrementExposureTime not allowed

View Level: opr
Root Cause: 1
Description: "IncrementExposureTime not allowed
3600016 Error Text: SetFocalSpot not allowed

View Level: opr
Root Cause: 1
Description: "SetFocalSpot not allowed
3600017 Error Text: GetFocalSpot not allowed

View Level: opr
Root Cause: 1
Description: "GetFocalSpot not allowed
3600018 Error Text: Clear Opmodes config failed

View Level: opr
Root Cause: 1
Description: "Clear Opmodes config failed
3600019 Error Text: Load appSetup scripts failed

View Level: opr
Root Cause: 1
Description: "Load appSetup scripts failed

GE MEDICAL SYSTEMS
3600020 Error Text: Execute appSetup scripts failed
View Level: opr
Root Cause: 1
Description: "Execute appSetup scripts failed
3600021 Error Text: Execute activeOpmode scripts failed

View Level: opr
Root Cause: 1
Recommended Action(s): "Software error only - for engineering use only. No recommended action to be taken. System
Description: "Execute activeOpmode scripts failed
3600022 Error Text: Invalid active opmode requested

View Level: opr
Root Cause: 1
Description: "Invalid active opmode requested
3600023 Error Text: Get Gitane set retry num failed

View Level: opr
Root Cause: 1
Description: "Get Gitane set retry num failed. Check TechMgr config file
3600024 Error Text: Jedi Power Up Failure

View Level: opr
Root Cause: 1
Recommended Action(s): "Software/Hardware Problem
Description: "Generator Power Up Failure
Customer Text: Communication could not be established with generator. Attempting to complete boot.
3600025 Error Text: Jedi Status in Error condition

View Level: opr
Root Cause: 1
Recommended Action(s): "Hardware Problem
Description: "Generator Status in Error condition
Customer Text: Generator error. Release exposure switch and try again. Call service if problem persists.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Recommended Action(s): "Possible generator error. Run generator diagnostics from SUIF
Description: "Generator error during exposure and causing current exposure to stop

View Level: opr
Root Cause: 1
Description: "Generator error occurred causing current exposure to stop
3600028 Error Text: Generator or tube temperature limits are reached.

View Level: opr
Root Cause: 1
Description: "Generator permanent error occurred. These errors appear when the generator or tube
temperature limits are reached.
Customer Text: Generator error occurred. Wait before retrying exposure. Call service if the problem persists.
3600029 Error Text: XRTechMgr failed to get NotifyJediId from JEDI

View Level: opr
Root Cause: 1
Description: "XRTechMgr failed to get NotifyJediId from generator
3600030 Error Text: SystemId and JediId conflict

View Level: opr
Root Cause: 1
Description: "SystemId and JediId conflict
3600031 Error Text: XRTechMgr failed to get ReplyJediCapabilities from JEDI

View Level: opr
Root Cause: 1
Description: "XRTechMgr failed to get ReplyJediCapabilities from generator

GE MEDICAL SYSTEMS
3600032 Error Text: XRTechMgr failed to get StaticId from JEDI
View Level: opr
Root Cause: 1
Description: "XRTechMgr failed to get StaticId from generator
3600033 Error Text: XRTechMgr failed to get SetLimitedParameters from JEDI

View Level: opr
Root Cause: 1
Description: "XRTechMgr failed to get SetLimitedParameters from generator
3600034 Error Text: XRTechMgr failed to get ConfirmAecConfig from JEDI

View Level: opr
Root Cause: 1
Description: "XRTechMgr failed to get ConfirmAecConfig from generator
3600035 Error Text: XRTechMgr failed to get ConfirmSelectTube from JEDI

View Level: opr
Root Cause: 1
Description: "XRTechMgr failed to get ConfirmSelectTube from generator
3600036 Error Text: XRTechMgr failed to send NotifySystemId to JEDI

View Level: opr
Root Cause: 1
Description: "XRTechMgr failed to send NotifySystemId to generator
3600037 Error Text: XRTechMgr failed to send ReplySystemConfig to JEDI

View Level: opr
Root Cause: 1
Description: "XRTechMgr failed to send ReplySystemConfig to generator

GE MEDICAL SYSTEMS
3600038 Error Text: Jedi technique limit reached
View Level: opr
Root Cause: 1
Description: "generator technique limit reached.
3600039 Error Text: Jedi rejects old techniques

View Level: opr
Root Cause: 1
Description: "generator rejects old techniques.
3600040 Error Text: Generator / tube spit error

View Level: opr
Root Cause: 1
Recommended Action(s): "System shall recover. Run generator No Load HV Diag if error is frequently occurring.
Description: "generator spit error
Customer Text: Generator / tube kVp spit occurred; the image may be light.
3600041 Error Text: AEC backup time reached

View Level: opr
Root Cause: 1
Description: "AEC backup time reached during exposure
3600042 Error Text: Jedi select tube failed

View Level: opr
Root Cause: 1
Recommended Action(s): "Possible generator tube switch failure. Run second tube switch diagnostic from the SUIF
Description: "generator select tube failed
3600043 Error Text: Gitane failed to set register correctly

View Level: opr
Root Cause: 1
Recommended Action(s): "Possible system controller failure. Run Gitane diagnostic via SUIF
Description: "Gitane failed to set register correctly
persists.

GE MEDICAL SYSTEMS
3600044 Error Text: System Controller Gitane acquisition register is not correct.
View Level: opr
Root Cause: 1
Recommended Action(s): "Possible system controller failure. Run Gitane diagnostic via SUIF
Description: "The Gitane acquisition register not correct for selected acquisition mode. Reset and call
service if the problem persists.
persists.
3600045 Error Text: Jedi reject technique error

View Level: opr
Root Cause: 1
Recommended Action(s): "Generator self-protection error.
Description: "Generator rejects technique
3600046 Error Text: Maximum kVp reached

View Level: opr
Root Cause: 1
Recommended Action(s): "No Action required
Description: "Maximum kVp reached
Customer Text: Maximum kVp has been selected.
3600047 Error Text: Minimum kVp reached

View Level: opr
Root Cause: 1
Description: "Minimum kVp reached
Customer Text: Minimum kVp has been selected.
3600048 Error Text: Maximum mA for generator kW

View Level: opr
Root Cause: 1
Description: "Maximum mA for generator kW
3600049 Error Text: Minimum mA for generator kW

View Level: opr
Root Cause: 1
Description: "Minimum mA for generator kW

GE MEDICAL SYSTEMS
3600050 Error Text: Maximum time for generator
View Level: opr
Root Cause: 1
Description: "Maximum time for generator
Customer Text: Maximum time has been selected for mA, mAs.
3600051 Error Text: Minimum time for generator

View Level: opr
Root Cause: 1
Description: "Minimum time for generator
Customer Text: Minimum time has been selected for mA, mAs.
3600052 Error Text: Maximum mA for kVp selected

View Level: opr
Root Cause: 1
Description: "Maximum mA for kVp selected
Customer Text: Maximum mA for selected kVp and focal spot.
3600053 Error Text: Maximum mAs for generator

View Level: opr
Root Cause: 1
Description: "Maximum mAs for generator
Customer Text: Maximum mAs for generator has been selected.
3600054 Error Text: Minimum mAs for generator

View Level: opr
Root Cause: 1
Description: "Minimum mAs for generator
Customer Text: Minimum mAs for generator has been selected.
3600055 Error Text: Generator mode failed

View Level: opr
Root Cause: 1
Description: "Generator mode failed

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: "Generator filament selection failed
3600057 Error Text: Generator kV is too low or mA/mAs is too low or the exposure time is too short
View Level: opr
Root Cause: 1
Recommended Action(s): "Modify the technique by increasing kV, mA/mAs, and/or the exposure time to proceed.
Description: "Generator rejected technique. Operator must select a higher kV or higher mA/mAs or longer
Customer Text: Increase kV, mA/mAs, and/or the exposure time to continue.
3600058 Error Text: Generator kV is too low or mA/mAs is too low or the exposure time is too long
View Level: opr
Root Cause: 1
Recommended Action(s): "Generator technique error. Modify the technique by increasing kV, mA/mAs, and/or
decreasing the exposure time to proceed.
Description: "Generator rejected technique. Operator must select a higher kV or higher mA/mAs or
Customer Text: Increase kV, mA/mAs, and/or decrease the exposure time to continue.
3600059 Error Text: Generator kV is too low or mA/mAs is too low

View Level: opr
Root Cause: 1
Recommended Action(s): "Modify the technique by increasing kV and/or mA/mAs to proceed.
Description: "Generator rejected technique. Operator must select a higher kV or higher mA/mAs to
proceed.
Customer Text: Increase kV and/or mA/mAs to continue.
3600060 Error Text: Generator kV is too high or the exposure time is too short or mA/mAs is too high
View Level: opr
Root Cause: 1
Recommended Action(s): "Modify the technique by increasing kV, exposure time, and/or decreasing mA/mAs to
proceed.
Description: "Generator rejected technique. Operator must select a higher kV or lower mA/mAs or longer
Customer Text: Increase kV, exposure time and/or decrease mA/mAs to continue.

GE MEDICAL SYSTEMS
3600061 Error Text: Generator kV is too low or mA/mAs is too high or the exposure time is too long
View Level: opr
Root Cause: 1
Recommended Action(s): "Modify the technique by increasing kV and/or decreasing mA/mAs and exposure time to
proceed.
Description: "Generator rejected technique. Operator must select a higher kV or lower mA/mAs or shorter
Customer Text: Increase kV and/or decrease mA/mAs and exposure time to continue.
3600062 Error Text: Generator kV is too low or mA/mAs is too high

View Level: opr
Root Cause: 1
Recommended Action(s): "Modify the technique by increasing kV and/or decreasing mA/mAs to proceed.
Description: "Generator rejected technique. Operator must select a higher kV or lower mA/mAs to
proceed.
Customer Text: Increase kV and/or decrease mA/mAs to continue.
3600063 Error Text: Generator kV too low or the exposure time is too short
View Level: opr
Root Cause: 1
Recommended Action(s): "Modify the technique by increasing kV and/or the exposure time to proceed.
Description: "Generator rejected technique. Operator must select a higher kV or longer exposure time to
proceed.
Customer Text: Increase kV and/or the exposure time to continue.
3600064 Error Text: Generator kV too low or the exposure time is too long
View Level: opr
Root Cause: 1
Recommended Action(s): "Modify the technique by increasing kV and/or decreasing the exposure time to proceed.
Description: "Generator rejected technique. Operator must select a higher kV or shorter exposure time
to proceed.
Customer Text: Increase kV and/or decrease the exposure time to continue.
3600065 Error Text: Generator kV too low

View Level: opr
Root Cause: 1
Recommended Action(s): "Modify the technique by increasing kV to proceed.
Description: "Generator rejected technique. Operator must select a higher kV to proceed.
Customer Text: Increase the kV to continue.

GE MEDICAL SYSTEMS
3600066 Error Text: Generator kV too high or the exposure time is too short or mA/mAs too low
View Level: opr
Root Cause: 1
Recommended Action(s): "Modify the technique by decreasing kV and/or increasing mA/mAs and exposure time to
proceed.
Description: "Generator rejected technique. Operator must select a lower kV or a higher mA/mAs or a
Customer Text: Decrease kV and/or increase mA/mAs and exposure time to continue.
3600067 Error Text: Generator kV too high or the exposure time too long or mA/mAs too low
View Level: opr
Root Cause: 1
Recommended Action(s): "Modify the technique by decreasing kV and the exposure time and/or increasing the mA/mAs
to proceed.
Description: "Generator rejected technique. Operator must select a lower kV or a higher mA/mAs or a
Customer Text: Decrease kV and the exposure time and/or increase the mA/mAs to continue.
3600068 Error Text: Generator kV too high or mA/mAs too low

View Level: opr
Root Cause: 1
Recommended Action(s): "Modify the technique by decreasing kV and/or increasing mA/mAs to proceed.
Description: "Generator rejected technique. Operator must select a lower kV or a higher mA/mAs to
proceed.
Customer Text: Decrease kV and/or increase mA/mAs to continue.
3600069 Error Text: Generator kV and mA/mAs too high or exposure time too short
View Level: opr
Root Cause: 1
Recommended Action(s): "Modify the technique by decreasing kV and mA/mAs and/or increasing the exposure time to
proceed.
Description: "Generator rejected technique. Operator must select a lower kV or a lower mA/mAs or a
Customer Text: Decrease kV and mA/mAs and/or increase the exposure time to continue.
3600070 Error Text: Generator kV too high or mA/mAs too high

View Level: opr
Root Cause: 1
Recommended Action(s): "Modify the technique by decreasing kV and/or mA/mAs to proceed.
Description: "Generator rejected technique. Operator must select a lower kV or a higher mA/mAs to
proceed.
Customer Text: Decrease kV and/or mA/mAs to continue.

GE MEDICAL SYSTEMS
3600071 Error Text: Generator kV too high or exposure time too short
View Level: opr
Root Cause: 1
Recommended Action(s): "Modify the technique by decreasing kV and/or increasing the exposure time to proceed.
Description: "Generator rejected technique. Operator must select a lower kV or a longer exposure time
to proceed.
Customer Text: Decrease kV and/or increase the exposure time to continue.
3600072 Error Text: Generator kV too high or the exposure time too long
View Level: opr
Root Cause: 1
Recommended Action(s): "Modify the technique by decreasing kV and/or the exposure time to proceed.
Description: "Generator rejected technique. Operator must select a lower kV or a shorter exposure time
to proceed.
Customer Text: Decrease kV and/or the exposure time to continue.
3600073 Error Text: Generator kV too high

View Level: opr
Root Cause: 1
Recommended Action(s): "Modify the technique by decreasing kV to proceed.
Description: "Generator rejected technique. Operator must select a lower kV to proceed.
Customer Text: Decrease the kV to continue.
3600074 Error Text: Generator mA/mAs too low or exposure time too short
View Level: opr
Root Cause: 1
Recommended Action(s): "Modify the technique by increasing the mA/mAs and/or the exposure time to proceed.
Description: "Generator rejected technique. Operator must select a higher mA/mAs or a longer exposure
time to proceed.
Customer Text: Increase the mA/mAs and/or the exposure time to continue.
3600075 Error Text: Generator mA/mAs too low or exposure time too long
View Level: opr
Root Cause: 1
Recommended Action(s): "Modify technique by increasing the mA/mAs and/or decreasing the to proceed.
Description: "Generator rejected technique. Operator must select a higher mA/mAs or a shorter exposure
time to proceed.
Customer Text: Increase the mA/mAs and/or decrease the exposure time to continue.

GE MEDICAL SYSTEMS
3600076 Error Text: Generator mA/mAs too low
View Level: opr
Root Cause: 1
Recommended Action(s): "Modify technique by increasing the mA/mAs to proceed.
Description: "Generator rejected technique. Operator must select a higher mA/mAs to proceed.
Customer Text: Increase the mA/mAs to continue.
3600077 Error Text: Generator mA/mAs too high or exposure time too short
View Level: opr
Root Cause: 1
Recommended Action(s): "Modify technique by decreasing the mA/mAs and/or increasing the exposure time to
proceed.
Description: "Generator rejected technique. Operator must select a lower mA/mAs or a longer exposure
time to proceed.
Customer Text: Decrease the mA/mAs and/or increase the exposure time to continue.
3600078 Error Text: Generator mA/mAs too high or exposure time too long
View Level: opr
Root Cause: 1
Recommended Action(s): "Modify technique by decreasing the mA/mAs and/or the exposure time to proceed.
Description: "Generator rejected technique. Operator must select a lower mA/mAs or shorter exposure
time to proceed.
Customer Text: Decrease the mA/mAs and/or the exposure time to continue.
3600079 Error Text: Generator mA/mAs too high

View Level: opr
Root Cause: 1
Recommended Action(s): "Modify technique by decreasing the mA/mAs to proceed.
Description: "Generator rejected technique. Operator must select a lower mA/mAs to proceed.
Customer Text: Decrease the mA/mAs to continue.
3600080 Error Text: Generator exposure time too short

View Level: opr
Root Cause: 1
Recommended Action(s): "Modify technique by increasing the exposure time to proceed.
Description: "Generator rejected technique. Operator must select a longer exposure time to proceed.
Customer Text: Increase the exposure time to continue.
3600081 Error Text: Generator exposure time too long

View Level: opr
Root Cause: 1
Recommended Action(s): "Modify technique by decreasing the exposure time to proceed.
Description: "Generator rejected technique. Operator must select a shorter exposure time to proceed.
Customer Text: Decrease the exposure time to continue.

GE MEDICAL SYSTEMS
3600082 Error Text: Generator thermal limit reached
View Level: opr
Root Cause: 1
Description: "Generator thermal limit reached
Customer Text: Thermal limit has been reached. Wait for tube to cool or decrease the technic.

View Level: opr
Root Cause: 1
Description: "Generator filament selection failed
3600084 Error Text: mA is 0 for setMA/setMAs

View Level: opr
Root Cause: 1
Description: "mA is 0 for setMA/setMAs
Customer Text: Increase mA or reselect protocol to continue.
3600085 Error Text: Maximum mA reached

View Level: opr
Root Cause: 1
Description: "Maximum mA reached
3600086 Error Text: Minimum mA reached

View Level: opr
Root Cause: 1
Description: "Minimum mA reached
3600087 Error Text: Maximum mA for selected kVp, focal spot

View Level: opr
Root Cause: 1
Description: "Maximum mA for selected kVp, focal spot
Customer Text: Maximum mA has been selected for kVp, focal spot.

GE MEDICAL SYSTEMS
3600088 Error Text: Minimum mA for selected kVp, focal spot
View Level: opr
Root Cause: 1
Description: "Minimum mA for selected kVp, focal spot
Customer Text: Minimum mA has been selected for kVp, focal spot.
3600089 Error Text: Digital mode techniques rejected by generator

View Level: opr
Root Cause: 1
Recommended Action(s): "Check trajectory values
Description: "Digital mode techniques rejected by generator. Possibly bad trajectory. Selecting another
FOV or another protocol will select another trajectory. The user can also reduce the record
frame rate.
Customer Text: Reduce the frame rate or select another FOV or select another protocol to continue.
3600090 Error Text: Current collimator size less than ion chambers selected, center cell selected
View Level: opr
Root Cause: 1
Description: ""Current collimator size less than ion chambers selected, center cell selected
Customer Text: "Collimator field size is less than selected ion chamber area; center area will be used.
3600091 Error Text: Wait for tube filament to stabilize

View Level: opr
Root Cause: 1
Description: ""Wait for tube filament to stabilize
Customer Text: "Wait for xray tube filament to stabilize.
3600092 Error Text: setLimitedFineParameters : kV+

View Level: opr
Root Cause: 1
Recommended Action(s): "Try fluoro again. Reselect the protocol.
Description: "setLimitedFineParameters : kV+ During fluoro or digital record, this means the EM loop

GE MEDICAL SYSTEMS
3600093 Error Text: setLimitedFineParameters : kV-
View Level: opr
Root Cause: 1
Description: "setLimitedFineParameters : kV- During fluoro or digital record, this means the EM loop
3600094 Error Text: setLimitedFineParameters : mA+

View Level: opr
Root Cause: 1
Description: "setLimitedFineParameters : mA+ During fluoro or digital record, this means the EM loop
3600095 Error Text: setLimitedFineParameters : mA-

View Level: opr
Root Cause: 1
Description: "setLimitedFineParameters : mA- During fluoro or digital record, this means the EM loop
3600096 Error Text: setLimitedFineParameters : ms+

View Level: opr
Root Cause: 1
Description: "setLimitedFineParameters : ms+ During fluoro or digital record, this means the EM loop
3600097 Error Text: setLimitedFineParameters : ms-

View Level: opr
Root Cause: 1
Description: "setLimitedFineParameters : ms- During fluoro or digital record, this means the EM loop

GE MEDICAL SYSTEMS
3600098 Error Text: setLimitedFineParameters : power+

View Level: opr
Root Cause: 1
Description: "setLimitedFineParameters : power+ During fluoro or digital record, this means the EM loop
3600099 Error Text: setLimitedFineParameters : power-

View Level: opr
Root Cause: 1
Description: "setLimitedFineParameters : power- During fluoro or digital record, this means the EM loop
3600100 Error Text: setLimitedFineParameters : mAs+

View Level: opr
Root Cause: 1
Description: "setLimitedFineParameters : mAs+ During fluoro or digital record, this means the EM loop
3600101 Error Text: setLimitedFineParameters : mAs-

View Level: opr
Root Cause: 1
Description: "setLimitedFineParameters : mAs- During fluoro or digital record, this means the EM loop

GE MEDICAL SYSTEMS
3600102 Error Text: setLimitedFineParameters : Thermic+
View Level: opr
Root Cause: 1
Description: "setLimitedFineParameters : Thermic+ During fluoro or digital record, this means the EM loop
3600103 Error Text: setLimitedFineParameters : unknown reject

View Level: opr
Root Cause: 1
Description: "setLimitedFineParameters : unknown reject During fluoro or digital record, this means the
EM loop provided a technic which was rejected by the generator. The generator will ignore
this and exposures will continue. Image Quality may not be optimal. It is possible that other
related EM loop errors may occur.
3600104 Error Text: setLimitedFineParameters : Thermic-

View Level: opr
Root Cause: 1
Description: "setLimitedFineParameters : Thermic- During fluoro or digital record, this means the EM loop
3600105 Error Text: Config Cache error

View Level: opr
Root Cause: 1
Recommended Action(s): "Check config cache value
Description: "Config cache error
3600106 Error Text: Time out while expecting CAN message from generator
View Level: opr
Root Cause: 1
Recommended Action(s): "Check system/Generator CAN bus cable
Description: "Time out while expecting CAN message from generator. It will be reported when TechMgr
times out while waiting for CAN message from JEDI, which mostly indicates that the
TechMgr/JEDI CAN communication failed. (Ref: XRYge38512, No error reported when Jedi
fails to communicate with Techmgr)

GE MEDICAL SYSTEMS
3600107 Error Text: Generator time synchronization failure
View Level: opr
Root Cause: 1
Recommended Action(s): "Reset the system. If problem persists, call service
Description: ""Generator internal time can not be synchronized with the system time
3600108 Error Text: Generator software update failure

View Level: opr
Root Cause: 1
Recommended Action(s): "Retry the generator softwar update. Reboot the system and repeat the generator software
update if the retry fails. If problem persists, call service
Description: ""Generator software update failed
3600109 Error Text: Generator did not send Ready For Exposure or standby Response
View Level: opr
Root Cause: 1
Recommended Action(s): "System Error is engineering use and do not indicate any hardware error failure.
Description: "System did not receive the response ReadyForExposure or standby from Generator.
3600110 Error Text: Event unscribe failed

View Level: opr
Root Cause: 1
Description: "Event unscribe failed
3600111 Error Text: DSA Trial exposure AEC backup time reached
View Level: opr
Root Cause: 1
Description: "AEC backup time reached during during the DSA trial exposure. The DSA sequence will not
be allowed to continue when the trial is unsuccessful.
Customer Text: The trial AEC back-up time was reached. Release the exposure switches and try again.
3600112 Error Text: Generator / tube spit error DSA trial

View Level: opr
Root Cause: 1
Recommended Action(s): "System shall recover. Run generator No Load HV Diag if error is frequently occurring.
Description: "A generator or xray tube spit error occurred during the DSA trial; sequence is aborted and
user must retry.
Customer Text: A generator error occurred during the DSA trial. Release the exposure switches and try again.

GE MEDICAL SYSTEMS
3600113 Error Text: setLimitedFineParameters : ms-
View Level: opr
Root Cause: 1
Description: "setLimitedFineParameters : ms- During fluoro or digital record, this means the EM loop
Customer Text: The selected technic exceeds system limits. Decrease magnification and retry.

View Level: opr
Root Cause: 1
Description: "Generator class 1 error, debug

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
Recommended Action(s): "Determine Jedi error in debug text and refer to the Precision Diagnostic Manual

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: "Generator class 1 error, abort

View Level: opr
Root Cause: 1
Recommended Action(s): "Possible generator error. Run No Load HV and inverter diagnosticss from SUIF

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
Recommended Action(s): "Determine Jedi error in debug text and refer to the Precision Diagnostic Manual

View Level: opr
Root Cause: 1
3601010 Error Text: Generator Error: 40-0102(4): error msg from Rotor FW; Database not correct
View Level: opr
Root Cause: 1
Recommended Action(s): "Reload NVRam database. It might be necessary to replace Rotation board.
Description: "The firmware of the rotation board has detected that the data base received from the kV
control board has wrong data. Potential Cause: Wrong kV control data base. It can only
happen at power up Recommended Action: Restore database. Replace rotation bd.

GE MEDICAL SYSTEMS
3601011 Error Text: Generator Error 40-0107(4): error msg from Rotor FW; Inverter permanent overcurrent
View Level: opr
Root Cause: 1
Recommended Action(s): "Perform one of the three actions. Check wiring from rotation board to tube. Replace Rotation
board. Troubleshoot tube windings (replace tube).
Description: " An overcurrent has been detected and 3 restart have been tried unsuccessfully within a
single rotation state Potential Cause: 1. Rotation board 2. Tube stator winding in short circuit
3. Wiring incorrect (shorted) Recommended Action: - Check wiring from rotation board to
tube. - Replace Rotation board. - Troubleshoot tube windings (replace tube).
Customer Text: Critical generator error. Call Service. Do not use the system.
3601012 Error Text: Generator Error 40-0110(4): error msg from Rotor FW; PRD error (Z3 Z4 = bitmap)
View Level: opr
Root Cause: 1
Recommended Action(s): "Retry or Replace Rotation board.
Description: "Firmware checksum, RAM test and EPLD access are performed at power up or reset.
Potential Cause: Rotation board Recommended Action: -Retry -Replace Rotation board.
3601013 Error Text: Generator Error 50-0201;(4): Heater 0: no CAN message received within 5 secs
View Level: opr
Root Cause: 1
Recommended Action(s): "Unlikely to happen. This is a debug error. Reinitialise and retry. Run CAN communication
diag.
Description: "The Heater board has not received any command from the kV control main software for the
last 5 sec., interpreted as a loss of communication Potential Cause: 1. kV Control main
software lost 2. kV control or Heater board driver failure 3. Bad contact on one of the pin on
the CAN bus line connector Recommended Action: -Retry -Reset and retry.
3601014 Error Text: Generator Error 50-0202;(4): Heater 0: database not correct
View Level: opr
Root Cause: 1
Recommended Action(s): "Run TBD Jedi diagnostic from SUIF
Description: "Heater 0: database not correct Generator error occurred causing current exposure to stop
Potential Cause: Recommended Action:
View Level: opr
Root Cause: 1
Recommended Action(s): "Try again. If the error persists, replace the heater board.
Potential Cause: Heater board Recommended Action: Try again. If the error persists, replace
the heater board.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Recommended Action(s): "Reload NVRam data base. It might be necessary to replace Heater board. (large focus)
the heater board.
View Level: opr
Root Cause: 1
the heater board.
View Level: opr
Root Cause: 1
the heater board.
View Level: opr
Root Cause: 1
Description: "The firmware of the heater board has detected that the Received Data base from kV control
contains erroneous data for Tube 1, 2, 3, or 4. Potential Cause: Recommended Action:
3601020 Error Text: Generator Error 50-1202 (4): Heater 1: database not correct
View Level: opr
Root Cause: 1
Recommended Action(s): "Run TBD Jedi diagnostic from SUIF
Description: "Heater 1: database not correct Generator error occurred causing current exposure to stop
Potential Cause: Recommended Action:

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Recommended Action(s): "Try again. If the error persists, replace the heater board.
the heater board.
View Level: opr
Root Cause: 1
Recommended Action(s): "Reload NVRam data base. It might be necessary to replace Heater board. (small focus)
the heater board.
View Level: opr
Root Cause: 1
the heater board.
View Level: opr
Root Cause: 1
the heater board.
View Level: opr
Root Cause: 1
the heater board.

GE MEDICAL SYSTEMS
3601026 Error Text: Generator Error 60-0802;(3): Exposure backup time exceeded
View Level: opr
Root Cause: 1
Recommended Action(s): "Retry, changing parameters and duration0. disconnect system-Generator cable in different
Description: "The exposure command last longer than the duration that was loaded by the system (Backup
time + 5%.) Potential Causes: 1. System 2. System-Generator cable 3. I/F board : exposure
line stuck to the active state Recommended Action: -Retry, changing parameters and
duration -Disconnect system-Generator cable in different places and check exposure
command line voltage
3601027 Error Text: Generator Error 60-0803;(3): Exp cmd while gene not ready
View Level: opr
Root Cause: 1
Recommended Action(s): "If problem is persistent, check heater, anode rotation and system to Generator preparation
command to find the root cause for the Generator not to be ready
Description: "Generator received an exposure command while not in ready state Potential Cause: 0.
Software bug/problem 1. Cable / communication problem 2. External cause (Spikes)
Recommended Action:If problem is persistent, check heater, anode rotation and system to
Generator preparation command to find the root cause for the Generator not to be ready
3601028 Error Text: Generator Error 60-1408;(3): AEC does not count
View Level: opr
Root Cause: 1
Recommended Action(s): "Run Generator AEC diagnostic
Description: "If there is no AEC feedback in AEC station exposure. exposure. Potential Cause: 1. ION
chamber 2. AEC cable, connection 3. AEC board Recommended Action: Run AEC
diagnostics (See diagnostic section)
Customer Text: Exposure stopped - No AEC brightness. Try again. Call service if problem persists.
3601029 Error Text: Generator Error 80-1000;(4): Tube Switch comm problem
View Level: opr
Root Cause: 1
Description: "Tube Switch comm problem Potential Cause: 1. Tube Switch Board 2. Control Bus cable 3.
KV control Recommended Action: A/Check that Tube Switch firmware is running (DS3/4 Led
are lit successively).If no : 1/ Verify +15V/-15V (DS1 & DS2 are lit) : if they are wrong, go
to +/-15V errors troubleshooting 2/ verify that RST Led (DS5) is not lit. If it is lit, disconnect
successively the control bus cable from rotation board and kV control to find the board which
is holding the reset line and replace it. If after disconnecting all the boards, the Led remains
lit, replace Tube Switch board B/Verify the flat cable between kV control and auxiliary module
is correctly connected until the Tube Switch boardC/else replace kV control board
Customer Text: Xray tube selection error. Reselect tube and continue.

GE MEDICAL SYSTEMS
3601030 Error Text: Generator Error 80-1010;(4): Tube Switch board has reset
View Level: opr
Root Cause: 1
Description: "Tube Switch board has reset Potential Cause: 1. Tube Switch Board 2. Interference (Spikes)
Recommended Action: -Reinitialize system, retry. -If persistent, replace board or check
power and grounding.

View Level: opr
Root Cause: 1
Description: "Generator class 5 error, abort Potential Cause: Recommended Action:
3601032 Error Text: Generator error 110-804;(5): Tank Thermal sensor to high.
View Level: opr
Root Cause: 1
Recommended Action(s): "Stop acquisition and wait for cooling
Description: "HV tank temperature measurement has reached 67 degree c for Precision 500D . Potential
Cause: 1. HV tank too hot 2. HV tank 3. kV control Recommended Action: -Wait for error
clearance -If persistent while HV Tank is cool : 1/check LED DS1 on kV control (top and
right of board). If it is off, change kV control 2/check flat cable connection between HV Tank
and kV control board 3/replace HV tank 4/replace kV control
3601033 Error Text: Generator error 110-805;(5): Inverter HW temperature too high.
View Level: opr
Root Cause: 1
Description: "Inverter HW temperature too high Potential Cause: Recommended Action:
3601034 Error Text: Generator error 110-806;(5): Lp temperature too high.

View Level: opr
Root Cause: 1
Customer Text: "Generator temperature is too high. Allow the generator to cool and try again.

GE MEDICAL SYSTEMS
3601035 Error Text: Generator error 110-903;(5): Tube exceeded 70degC.
View Level: opr
Root Cause: 1
Description: "Tube exceeded 70degC
Customer Text: Tube temperature exceeded limits. Stop acquisition and wait for tube to cool.
3601036 Error Text: Generator error 110-904;(5): HW signal from Rotor Brd; HEMIT Error.
View Level: opr
Root Cause: 1
Description:
Customer Text: "Generator temperature is too high. Allow the generator to cool and try again.
3601037 Error Text: Generator error 110-905;(5): Tube thermal protection.

View Level: opr
Root Cause: 1
Description: "Tube thermal protection
3601050 Error Text: Generator error class 1: error msg from Rotor FW, CAN Domain command number error
View Level: opr
Root Cause: 1
Description: "error msg from Rotor FW, CAN Domain command number error
3601051 Error Text: Generator error class 1: error msg from Rotor FW, CAN Domain request with no transfer init
View Level: opr
Root Cause: 1
Description: "error msg from Rotor FW, CAN Domain request with no transfer init
3601052 Error Text: Generator error class 1: error msg from Rotor FW, CAN Domain Toggle bit error
View Level: opr
Root Cause: 1
Description: "error msg from Rotor FW, CAN Domain Toggle bit error

GE MEDICAL SYSTEMS
3601053 Error Text: Generator error class 1: error msg from Rotor FW, CAN Domain : less than 2 data to
download
View Level: opr
Root Cause: 1
Description: "error msg from Rotor FW, CAN Domain : less than 2 data to download
3601054 Error Text: Generator error class 1: error msg from Rotor FW, CAN Domain Abort received & applied
View Level: opr
Root Cause: 1
Description: "error msg from Rotor FW, CAN Domain Abort received & applied
3601055 Error Text: Generator error class 1: error msg from Rotor FW, Bad index in config upload
View Level: opr
Root Cause: 1
Description: "error msg from Rotor FW, Bad index in config upload
3601056 Error Text: Generator error class 1: error msg from Rotor FW, Tube switch while rotor not off
View Level: opr
Root Cause: 1
Description: "error msg from Rotor FW, Tube switch while rotor not off
3601057 Error Text: Generator error class 1: error msg from Rotor FW, Acceleration cmd while no tube selected
View Level: opr
Root Cause: 1
Description: "error msg from Rotor FW, Acceleration cmd while no tube selected
3601058 Error Text: Generator error class 1: error msg from Rotor FW, Acceleration cmd while database not OK
View Level: opr
Root Cause: 1
Description: "error msg from Rotor FW, Acceleration cmd while database not OK

GE MEDICAL SYSTEMS
3601059 Error Text: Generator error class 1: error msg from Rotor FW, Database download while rotor speeding
View Level: opr
Root Cause: 1
Description: " error msg from Rotor FW, Database download while rotor speeding
3601060 Error Text: Generator error class 1: error msg from Rotor FW, Acceleration command not OK
View Level: opr
Root Cause: 1
Description: "error msg from Rotor FW, Acceleration command not OK
3601061 Error Text: Generator error class 1: error msg from Rotor FW, Acceleration while in error
View Level: opr
Root Cause: 1
Description: "error msg from Rotor FW, Acceleration while in error
3601062 Error Text: Generator error class 1: error msg from Rotor FW, No CAN message received within 4 sec
View Level: opr
Root Cause: 1
Description: "error msg from Rotor FW, No CAN message received within 4 sec
3601063 Error Text: Generator error class 1: error msg from Rotor FW, Inverter overcurrent (< 3 times)
View Level: opr
Root Cause: 1
Description: "error msg from Rotor FW, Inverter overcurrent (< 3 times)
3601064 Error Text: Generator error class 1: error msg from Rotor FW, Unknown warning
View Level: opr
Root Cause: 1
Description: "error msg from Rotor FW, Unknown warning
View Level: opr
Root Cause: 1
Description: "Heater 0: received command is not OK

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: "Heater 0: command not OK
3601067 Error Text: Generator error class 1: Heater 0: inverter overcurrent (inverter1) (<3 times)
View Level: opr
Root Cause: 1
Description: "Heater 0: inverter overcurrent (inverter1) (<3 times)
3601068 Error Text: Generator error class 1: Heater 0: filament open circuit (inverter1) (<3 times)
View Level: opr
Root Cause: 1
Description: "Heater 0: filament open circuit (inverter1) (<3 times)
View Level: opr
Root Cause: 1
Description: "Heater 0: inverter short circuit (inverter1) (<3times)
View Level: opr
Root Cause: 1
Description: "Heater 0: tube switch while filaments not OFF
View Level: opr
Root Cause: 1
Description: "Heater 0: CAN Domain command number error
View Level: opr
Root Cause: 1
Description: "Heater 0: CAN Domain request with no transfer init

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: "Heater 0: CAN Domain Toggle bit error
3601074 Error Text: Generator error class 1: Heater 0: CAN Domain less than 2 data to download
View Level: opr
Root Cause: 1
Description: "Heater 0: CAN Domain less than 2 data to download

View Level: opr
Root Cause: 1
Description: "Heater 0: unknown warning
View Level: opr
Root Cause: 1
Description: "Heater 1: received command is not OK

View Level: opr
Root Cause: 1
Description: "Heater 1: command not OK
3601078 Error Text: Generator error class 1: Heater 1: no CAN message received within 4 secs
View Level: opr
Root Cause: 1
Description: "Heater 1: no CAN message received within 4 secs
3601079 Error Text: Generator error class 1: Heater 1: inverter overcurrent (inverter1) (<3 times)
View Level: opr
Root Cause: 1
Description: "Heater 1: inverter overcurrent (inverter1) (<3 times)

GE MEDICAL SYSTEMS
3601080 Error Text: Generator error class 1: Heater 1: Filament open circuit (inverter1) (<3 times)
View Level: opr
Root Cause: 1
Description: "Heater 1: Filament open circuit (inverter1) (<3 times)
View Level: opr
Root Cause: 1
Description: "Heater 1: inverter short circuit (inverter1) (<3times)
View Level: opr
Root Cause: 1
Description: "Heater 1: tube switch while filaments not OFF
View Level: opr
Root Cause: 1
Description: "Heater 1: CAN Domain command number error
View Level: opr
Root Cause: 1
Description: "Heater 1: CAN Domain request with no transfer init
View Level: opr
Root Cause: 1
Description: "Heater 1: CAN Domain Toggle bit error
3601086 Error Text: Generator error class 1: Heater 1: CAN Domain : less than 2 data to download
View Level: opr
Root Cause: 1
Description: "Heater 1: CAN Domain : less than 2 data to download

GE MEDICAL SYSTEMS
3601087 Error Text: Generator error class 1: Heater 1: CAN Domain Abort received & applied
View Level: opr
Root Cause: 1
Description: "Heater 1: CAN Domain Abort received & applied
3601088 Error Text: Generator error class 1: Heater 1: database download while heater not cut
View Level: opr
Root Cause: 1
Description: "Heater 1: database download while heater not cut

View Level: opr
Root Cause: 1
Description: "Heater 1: unknown warning
3601090 Error Text: Generator error class 1: DC Bus Warning Overvoltage > 755VDC
View Level: opr
Root Cause: 1
Description: "DC Bux Warning Overvoltage > 755VDC dcbus meas > 380V and < 680V
3601091 Error Text: Generator error class 1: DC Bus Warning Undervoltage < 320VDC
View Level: opr
Root Cause: 1
Description: "DC Bus Warning Undervoltage < 320VDC dcbus meas > 380V and < 680V
3601092 Error Text: Generator error class 1: LVPS 400: received command is not OK
View Level: opr
Root Cause: 1
Description: "LVPS 400: received command is not OK
View Level: opr
Root Cause: 1
Description: "LVPS 400: external +15V too high

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: "LVPS 400: external +15V too low
View Level: opr
Root Cause: 1
Description: "LVPS 400: external +160V too high
View Level: opr
Root Cause: 1
Description: "LVPS 400: external +160V too low
3601097 Error Text: Generator error class 1: LVPS 400: gate +24V too high
View Level: opr
Root Cause: 1
Description: "LVPS 400: gate +24V too high
3601098 Error Text: Generator error class 1: LVPS 400: gate +24V too low
View Level: opr
Root Cause: 1
Description: "LVPS 400: gate +24V too low
3601099 Error Text: Generator error class 1: LVPS 400: CAN +15V too high
View Level: opr
Root Cause: 1
Description: "LVPS 400: CAN +15V too high
3601100 Error Text: Generator error class 1: LVPS 400: CAN +15V too low
View Level: opr
Root Cause: 1
Description: "LVPS 400: CAN +15V too low

GE MEDICAL SYSTEMS
3601101 Error Text: Generator error class 1: LVPS 400: CAN -15V too high
View Level: opr
Root Cause: 1
Description: "LVPS 400: CAN -15V too high
3601102 Error Text: Generator error class 1: LVPS 400: CAN -15V too low
View Level: opr
Root Cause: 1
Description: "LVPS 400: CAN -15V too low
View Level: opr
Root Cause: 1
Description: "LVPS 400: heater 0 +160V too high
View Level: opr
Root Cause: 1
Description: "LVPS 400: heater 0 +160V too low
View Level: opr
Root Cause: 1
Description: "LVPS 400: heater 1 +160V too high
View Level: opr
Root Cause: 1
Description: "LVPS 400: heater 1 +160V too low
View Level: opr
Root Cause: 1
Description: "LVPS 400: main inverter +17V too high

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: "LVPS 400: main inverter +17V too low
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
3601113 Error Text: Generator error class 1: LVPS 400: FAN 0 overcurrent
View Level: opr
Root Cause: 1
Description: "LVPS 400: FAN 0 overcurrent
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1
Description: "LVPS TRI: no more warn +160V
View Level: opr
Root Cause: 1
Description: "LVPS TRI: detected +160V too high
View Level: opr
Root Cause: 1
Description: "LVPS TRI: detected +160V too low
View Level: opr
Root Cause: 1
Description: "LVPS TRI: no more warn +15V
View Level: opr
Root Cause: 1
Description: "LVPS TRI: detected +15V too high

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: "LVPS TRI: detected +15V too low
3601123 Error Text: Generator error class 1: LVPS TRI: no more warn -15V
View Level: opr
Root Cause: 1
Description: "LVPS TRI: no more warn -15V
3601124 Error Text: Generator error class 1: LVPS TRI: detected -15V too strong
View Level: opr
Root Cause: 1
Description: "LVPS TRI: detected -15V too strong
3601125 Error Text: Generator error class 1: LVPS TRI: detected -15V too weak
View Level: opr
Root Cause: 1
Description: "LVPS TRI: detected -15V too weak
3601126 Error Text: Generator error class 1: LVPS 400: communication error
View Level: opr
Root Cause: 1
Description: "LVPS 400: communication error
3601127 Error Text: Generator error class 1: LVPS 400: unknown error
View Level: opr
Root Cause: 1
Description: "LVPS 400: unknown error
3601128 Error Text: Generator error class 1: LVPS TRI: unknown warning
View Level: opr
Root Cause: 1
Description: "LVPS TRI: unknown warning

GE MEDICAL SYSTEMS
3601129 Error Text: Generator error class 1: PPC kV Control - Watchdog reset has just occurred (MSB)
View Level: opr
Root Cause: 1
Description: " PPC kV Control - Watchdog reset has just occurred (MSB)
3601130 Error Text: Generator error class 1: PPC kV Control - Watchdog reset has just occurred (LSB)
View Level: opr
Root Cause: 1
Description: " PPC kV Control - Watchdog reset has just occurred (LSB)
3601131 Error Text: Generator error class 1: Saved RAM Battery life time limit reached
View Level: opr
Root Cause: 1
Description: "Saved RAM Battery life time limit reached
3601132 Error Text: Generator error class 2: Tube spit (kV+ and kV- dropped)
View Level: opr
Root Cause: 1
Description: "Tube spit (kV+ and kV- dropped)
3601133 Error Text: Generator error class 2: Tube spit (kV+ has dropped)
View Level: opr
Root Cause: 1
Description: "Tube spit (kV+ has dropped)
3601134 Error Text: Generator error class 2: Tube spit (kV- has dropped)
View Level: opr
Root Cause: 1
Description: "Tube spit (kV- has dropped)
3601135 Error Text: Generator error class 2: Tube spit (kV regulation error)
View Level: opr
Root Cause: 1
Description: "Tube spit (kV regulation error)

GE MEDICAL SYSTEMS
3601136 Error Text: Generator error class 2: FPGA problem (restarting safety signal)
View Level: opr
Root Cause: 1
Description: "FPGA problem (restarting safety signal)
3601137 Error Text: Generator error class 2: Tube spit (all kV drop/regul errors)
View Level: opr
Root Cause: 1
Description: "Tube spit (all kV drop/regul errors)
3601138 Error Text: Generator error class 1: Warning, spit counter overflow
View Level: opr
Root Cause: 1
Description: "Warning, spit counter overflow
3601139 Error Text: Generator error class 2: Tube Curr max detected
View Level: opr
Root Cause: 1
Description: "Tube Curr max detected
3601140 Error Text: Generator error 40-0101(4): error msg from Rotor FW; No CAN message received within 5
sec
View Level: opr
Root Cause: 1
Recommended Action(s): "If trying to take exposure, release the switch and try again. Reset system if problem persists.
Description: " The rotation bd has not received any signal from the kV control bd. for the last 5 sec.,
interpreted as loss of communiation Potential cause: 1. kV Control main software lost 2. kV
control or Rotation board driver failure 3. Bad contact on one of the pin on the CAN bus line
connector Recommended Action: Reset system, check connections, replace rotation bd.
3601141 Error Text: Generator error 40-0103;(4): error msg from Rotor FW; Current overload
View Level: opr
Root Cause: 1
Description: "Rotation board has detected Main or auxiliary Rotation current too high compared to the
max. tube motor current Potential Cause: 1. Rotation board 2. Rotation board phase
capacitor short circuited 3. Wrong data base (improbable) Recommended Action: Check
wiring from rotation board to tube. Check the rotation capacitors. If no cabling problem, run
Rotation diagnostic test to differentiate between rotation board and phase shift capacitors.

GE MEDICAL SYSTEMS
3601142 Error Text: Generator error 40-0104;(4):error msg from Rotor FW; Openload
View Level: opr
Root Cause: 1
Description: "Rotation board detected that no current is flowing to the motor. Potential Cause: 1. Tube
stator winding is open circuit 2. Incorrect wiring (Open) 3. No DC bus on Rotation board 4.
Rotation board 5. Rotation board phase capacitor not connected Recommended Action:
Check wiring from rotation board to tube. Check DC bus cables from AC-DC board to rotation
board Check that phases capacitors are correctly connected If no cabling problem, run
Rotation diagnostic to differentiate between rotation board and phase shift capacitors.
3601143 Error Text: Generator error 40-0105;(4): error msg from Rotor FW; Phases unbalanced
View Level: opr
Root Cause: 1
Description: "The amplitude difference of the current between main and auxiliary is too large Potential
Cause: 1. One Rotation wire missing 2. Rotation board 3. Rotation board phase capacitors
inverted or wrong value or not connected 4. Wrong tube configuration data base 5. Tube
problem (stator) Recommended Action: Check wiring from rotation board to tube (See
Rotation diagnosis). Check that phases capacitors are correctly connected.If no cabling
problem, run Rotation diagnostic to differentiate between rotation board and phase shift
capacitors.
3601144 Error Text: Generator error 40-0106;(4): error msg from Rotor FW; Phases error
View Level: opr
Root Cause: 1
Description: "The Rotation board has detected that the current in the anode stator does not show the
correct phase shift between main and auxiliary Potential Cause: 1. Rotation board 2. Tube
problem (stator) 3. Rotation board phase capacitors inverted or wrong value Recommended
Action: Check wiring from rotation board to tube Check that phase capacitors are correctly
connected Verify none is in short circuit.If no wiring problem, Run Rotation diagnostic
3601145 Error Text: Generator error 40-0108;(4): error msg from Rotor FW; Command error
View Level: opr
Root Cause: 1
Description: "error msg from Rotor FW; Command error Potential Cause: Recommended Action:

GE MEDICAL SYSTEMS
3601146 Error Text: Generator error 40-0109;(4): error msg from Rotor FW; MAINS_DROP has failed
View Level: opr
Root Cause: 1
Description: "The firmware of the rotation board has detected the mains_drop signal activation and
transmitted error to kV control Potential Cause: 1. Interference (spikes) 2. Mains has dropped
3. Cable or connector contact in DC bus between power unit and auxiliary unit 4. Rotation
board Recommended Action: - Do a power and grounding check. - If systematic, replace
Rotation board
3601147 Error Text: Generator error 40-0111;(4): error msg from Rotor FW; F0 main frequency problem
View Level: opr
Root Cause: 1
Description: "EPLD has not applied the inverter start command Potential Cause: Rotation board
Recommended Action: -Retry -Replace Rotation board.
3601148 Error Text: Generator error 40-0112;(4): error msg from Rotor FW; HW/FW config error
View Level: opr
Root Cause: 1
Description: "HW/FW config error Potential Cause: Rotation board Recommended Action: - Download
official data base - If the problem persists, change rotation board
3601149 Error Text: Generator error 40-0113;(4):error msg from Rotor FW; IUVW short circuit error
View Level: opr
Root Cause: 1
Description: "error msg from Rotor FW; IUVW short circuit error
3601150 Error Text: Generator error 40-0114;(4): error msg from Rotor FW; HV cable short circuit error
View Level: opr
Root Cause: 1
Description: "error msg from Rotor FW; HV cable short circuit error

GE MEDICAL SYSTEMS
3601151 Error Text: Generator error 40-0115;(4): error msg from Rotor FW; HV cable open error
View Level: opr
Root Cause: 1
Description: "error msg from Rotor FW; HV cable open error
3601152 Error Text: Generator error 40-0149;(4): error msg from Rotor FW; Unknown error
View Level: opr
Root Cause: 1
Description: "The main software received an error from rotation board with no error code associated
Potential Cause: Software problem Recommended Action: Reset
3601153 Error Text: Generator error 40-0162;(4): error msg from Rotor FW; Acceleration while in error
View Level: opr
Root Cause: 1
Description: "error msg from Rotor FW; Acceleration while in error Potential Cause: Recommended
Action: Reset
3601154 Error Text: Generator error 40-0163;(4): error msg from Rotor FW; No CAN message received within 4
sec
View Level: opr
Root Cause: 1
Description: "error msg from Rotor FW; No CAN message received within 4 sec Potential Cause:
Recommended Action:
3601155 Error Text: Generator error 50-0203;(4): Heater 0: inverter permanent overcurrent
View Level: opr
Root Cause: 1
Description: "Issued by the heater board when an overcurrent has been detected and 3 restarts have been
tried without success within 100 ms Potential Cause: Heater board Recommended Action: -
Check cabling of heater. -Restart. - If persistent, replace Heater board

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: "Issued by the heater board when an open has been detected and 3 restarts have been tried
without success within 100 ms Potential Cause: 1. X-ray tube filament open 2. Heater to HV
tank cable 3. Cathode HV cable or pin contacts 4. Open circuit in filament transformer inside
HV Tank. 5- Two Switching Board cable Recommended Action: - Switch on the other
filament:if no error is reported, heater board is working properly. - Check heater board to HV
Tank to tube connections. If OK, test with Ohm-meter HV Tank heater transformers (primary
and secondary) and filament impedance. Order accordingly If the same error is reported,
check the connections as above. If all are right, replace heater board
View Level: opr
Root Cause: 1
Description: "Issued by the heater board when a short circuit has been detected and 3 restarts have been
Reset. -If persistent, replace Heater board
View Level: opr
Root Cause: 1
Description: "This is the result of an integrated value of the RMS current measurement on Heater board
comparison with max. Tube value in data base Potential Cause: 1. Tube data base or
filament calibration 2. Heater board Recommended Action: - It’s unlikely, but reload NVRam
database. - Replace heater board.
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
Description: "Heater 0: command error Potential Cause: Recommended Action:
View Level: opr
Root Cause: 1
Description: "RMS filament current measurement (every 0.5 m sec.) on heater board is too low Potential
Cause: 1. short circuit 2. Heater board Recommended Action: - Switch on the other filament:
if no error is reported, heater board is working properly. - Check heater board to HV Tank to
tube connections. If OK, test with Ohm-meter HV Tank heater transformers (primary and
secondary) and filament impedance. Order accordingly - If the same error is reported, check
the connections as above. If all are right, change heater board
View Level: opr
Root Cause: 1
Description: "RMS filament current measurement (every 0.5 m sec.) on heater board is too high Potential
Cause: 1. Open circuit 2. Heater board Recommended Action: - Replace heater board
View Level: opr
Root Cause: 1
Description: "The firmware of the Heater board has detected the mains_drop signal activation and has
transmitted error to kV control Potential Cause: 1. Interference (spikes) 2. Mains drop 3.
Cable or connector contact in DC bus between power unit and auxiliary unit 4. Heater board
Recommended Action: -Do a power and grounding check. -If systematic, replace heater
board

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: "Boost command stayed longer than 400ms Potential Cause: May be a loss of
communication during boost. Recommended Action: - Retry.It will probably be followed by
another communication code.
View Level: opr
Root Cause: 1
Description: "The relay on the Heater board selecting the filament is in the wrong position with respect to
the selection Potential Cause: Heater board Recommended Action: Replace heater board
View Level: opr
Root Cause: 1
3601168 Error Text: Generator error 50-0248;(4): Heater large focus error
View Level: opr
Root Cause: 1
Description: "The main software received an error from heater board with no error code associated
Potential Cause: software problem Recommended Action: No action
3601169 Error Text: Generator error 50-0249;(4): Heater small focus error
View Level: opr
Root Cause: 1
Description: "The main software received an error from heater board with no error code associated
Potential Cause: software problem Recommended Action: No action

GE MEDICAL SYSTEMS
3601170 Error Text: Generator error 50-1201;(4): Heater 1: no CAN message received within 5 secs
View Level: opr
Root Cause: 1
Description: "The Heater board has not received any command from the kV control main software for the
last 5 sec., interpreted as a loss of communication Potential Cause: 1. kV Control main
software lost 2. kV control or Heater board driver failure 3. Bad contact on one of the pin on
the CAN bus line connector Recommended Action: -Retry -Reset and retry.
3601171 Error Text: Generator error 50-1203;(4): Heater 1: inverter permanent overcurrent
View Level: opr
Root Cause: 1
Description: "Issued by the heater board when an overcurrent has been detected and 3 restarts have been
Check cabling of heater. -Restart. - If persistent, replace Heater board
View Level: opr
Root Cause: 1
Description: "Issued by the heater board when an open has been detected and 3 restarts have been tried
without success within 100 ms Potential Cause: 1. X-ray tube filament open 2. Heater to HV
tank cable 3. Cathode HV cable or pin contacts 4. Open circuit in filament transformer inside
HV Tank. 5- Two Switching Board cable Recommended Action: - Switch on the other
filament:if no error is reported, heater board is working properly. - Check heater board to HV
Tank to tube connections. If OK, test with Ohm-meter HV Tank heater transformers (primary
and secondary) and filament impedance. Order accordingly If the same error is reported,
check the connections as above. If all are right, replace heater board
View Level: opr
Root Cause: 1
Description: "Issued by the heater board when a short circuit has been detected and 3 restarts have been
Reset. -If persistent, replace Heater board
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
Description: "Heater 1: command error Potential Cause: Recommended Action:
View Level: opr
Root Cause: 1
Description: "RMS filament current measurement (every 0.5 m sec.) on heater board is too low Potential
Cause: 1. short circuit 2. Heater board Recommended Action: - Switch on the other filament:
if no error is reported, heater board is working properly. - Check heater board to HV Tank to
tube connections. If OK, test with Ohm-meter HV Tank heater transformers (primary and
secondary) and filament impedance. Order accordingly - If the same error is reported, check
the connections as above. If all are right, change heater board

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: "RMS filament current measurement (every 0.5 m sec.) on heater board is too high Potential
Cause: 1. Open circuit 2. Heater board Recommended Action: - Replace heater board
View Level: opr
Root Cause: 1
Description: "The firmware of the Heater board has detected the mains_drop signal activation and has
transmitted error to kV control Potential Cause: 1. Interference (spikes) 2. Mains drop 3.
Cable or connector contact in DC bus between power unit and auxiliary unit 4. Heater board
Recommended Action: -Do a power and grounding check. -If systematic, replace heater
board
View Level: opr
Root Cause: 1
Description: "Boost command stayed longer than 400ms Potential Cause: May be a loss of
communication during boost. Recommended Action: - Retry.It will probably be followed by
another communication code.
View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
3601184 Error Text: Generator error 60-0306; (3): No kV Feedback on anode
View Level: opr
Root Cause: 1
Recommended Action(s): "Release the switch and try again. Reset system if problem persists.
Description: "kv measured <12kV 0,5ms after start of exposure on anode side only Potential Cause: 1.
HV cable short circuit 2. HV tank 3. kV control board (less probable) Recommended Action:
-Troubleshoot HV cables : run no load kV diagnostic along with inverting HV cables - If HV
cables are right, replace HV Tank
3601185 Error Text: Generator error 60-0307; (3): No kV Feeback on cathode

View Level: opr
Root Cause: 1
Description: "kv measured <12kV 0,5ms after start of exposure on cathode side only Potential Cause: 1.
HV cable short circuit 2. HV tank 3. kV control board (less probable) Recommended Action:
-Troubleshoot HV cables : run no load kV diagnostic along with inverting HV cables - If HV
cables are right, replace HV Tank
3601186 Error Text: Generator error 60-0308; (3): No kV Feedback on anode and cathode
View Level: opr
Root Cause: 1
Description: "kv measured <12kV 0,5ms after start of exposure on both anode and cathode. Potential
Cause: 1. HV tank 2. kV control board Recommended Action: -Verify flat cable connections
and sitting between kV control and HV tank. - Replace HV Tank
3601187 Error Text: Generator error 60-0309; (3): kV detected during kV diag
View Level: opr
Root Cause: 1
Description: "KV measured during inverter diagnostics while no kV must be generated. Potential Cause:
improper setup before the diagnostic is run. Recommended Action: See generator diagnostic
manual
3601188 Error Text: Generator error 60-0310; (3): kV max detected

View Level: opr
Root Cause: 1
Description: "kV reached 160 kv during exposure Potential Cause: kV control Recommended Action:
Replace kV control board

GE MEDICAL SYSTEMS
3601189 Error Text: Generator error 60-0311; (3): ILP current not OK
View Level: opr
Root Cause: 1
Description: "The current in the parallel resonant circuit of the inverter did not rise at the beginning of the
exposure Potential Cause: 1. Inverter LC resonant circuit (Inverter coil assy, capa inverter
assy, current transformers.) 2. Inverter 3. kV control Recommended Action: run generator HV
diagnostics
3601190 Error Text: Generator error 60-0312; (3): ILR current not OK
View Level: opr
Root Cause: 1
Description: "The current in the parallel resonant circuit of the inverter did not rise at the beginning of the
exposure Potential Cause: 1. Inverter LC resonant circuit (Inverter coil assy, capa inverter
assy, current transformers.) 2. Inverter 3. kV control Recommended Action: run generator
HV diagnostics
3601191 Error Text: Generator error 60-0313; (3): ILR max current detected
View Level: opr
Root Cause: 1
Description: "This is a hardware detection of maximum current in serial resonant circuit. Potential Cause:
1 Tube (it can be casing spits, error 0324H data=1 or 2) 2 HV tank 3 kV control 4 inv LC
resonent circuit Recommended Action: run HV power diagnostics in order to determine if it
is associated to tubeIf during the test, you have kV unbalance, see error 0319H.
3601192 Error Text: Generator error 60-0314; (3): ILR current timeout
View Level: opr
Root Cause: 1
Description: "The current resonant frequency is lower than expected Potential Cause: 1. kV control 2.
Inverter 3. Current measurement circuit. Recommended Action: run HV generator
diagnostics
3601193 Error Text: Generator error 60-0316; (3): Spit Max error
View Level: opr
Root Cause: 1
Description: "kV control has detected the number of tube spits during exposure has reached the sw set
limit Potential Cause: x-ray tube Recommended Action: -Try again at various kV/mA to
confine problem. - if it is associated to kV regul out spit detection, check mains input voltage

GE MEDICAL SYSTEMS
connection -Troubleshoot HV section. (x-ray tube, cable, HV tank) -Diagnose based on tube
history.
3601194 Error Text: Generator error 60-0317; (3): Spit Ratio error
View Level: opr
Root Cause: 1
Description: "kV control has detected the rate of tube spits during exposure has reached the limit (see
theory of operation, software section) Potential Cause: x-ray tube Recommended Action: -
Try again at various kV/mA to confine problem. - if it is associated to kV regul out spit
detection, check mains input voltage connection -Troubleshoot HV section. (x-ray tube,
cable, HV tank) -Diagnose based on tube history.
3601195 Error Text: Generator error 60-0318; (3): kV did not reach 75%(rad) or 95%(gridded) after 20ms
View Level: opr
Root Cause: 1
Description: "Indicates that there were no HV ON signal generated for exposure time count-up Potential
Cause: 1. kV control 2. Tank 3. Tube, HV cables Recommended Action: - Run HV diagnosis.
- If OK, replace the kV control board
3601196 Error Text: Generator error 60-0319; (3): kV unbalanced detected

View Level: opr
Root Cause: 1
Description: "Detects that there is more than 12kV difference between kV+ and kV - Potential Cause: HV
tank Recommended Action: - Try again at various mA to confirm the problem - Replace HV
tank
3601197 Error Text: Generator error 60-0320; (3): FPGA problem (safety signal)
View Level: opr
Root Cause: 1
Description: "No error at the inputs while checking for error source Potential Cause: 1. This may be due
to transient interference (Spikes). 2. SW bug Recommended Action: - Do a power and
Grounding Check. - Verify cabling and contacts. If permanent or too systematic, replace kV
control board. - Check the presence of the ferrite in the cable between kV control board and
tank. - Report to engineering

GE MEDICAL SYSTEMS
3601198 Error Text: Generator error 60-0321; (3): Spit retry failed (TD computing)
View Level: opr
Root Cause: 1
Customer Text: "Exposure stopped. Release exposure switch and try again. Call service if problem persists.
3601199 Error Text: Generator error 60-0323; (3): ILR and ILP current not OK
View Level: opr
Root Cause: 1
Description: "No inverter current measures at the beginning of the exposure Potential Cause: 1. DCBUS
loss 2. Inverter LC resonant circuit. (Inverter coil assy, capa inverter assy, current
transformers.) 3. Inverter 4. kV control board Recommended Action: - check main DCBUS
voltage on inverter - run HV power diagnostics
3601200 Error Text: Generator error 60-0325; (3): DSP overload

View Level: opr
Root Cause: 1
Description: "DSP overload Potential Cause: 1. Main supply 2. KV control board Recommended Action:
- check main fuses and AC voltage on ACDC module - If error repeated, replace the kV
control board.
3601201 Error Text: Generator error 60-0326; (3): DSP exposure stop
View Level: opr
Root Cause: 1
Description: "DSP exposure stop Potential Cause: KV control board Recommended Action: Try again. If
error repeated, replace the kV control board.
3601202 Error Text: Generator error 60-0327; (3): DSP regul. out of range
View Level: opr
Root Cause: 1
Description: "DSP regul. out of range Potential Cause: Recommended Action:

GE MEDICAL SYSTEMS
3601203 Error Text: Generator error 60-0329; (3): wrong HV capacitance measure
View Level: opr
Root Cause: 1
Recommended Action(s): "Release the switch and try again. Reselect the xray tube. Reset system if problem persists.
Description: "Wrong HV capacitance measure Generator measures the HV cable capacitance
automatically after a tube switch. Potential Cause:1. HV cable problem2. HV tank switch
problem3. Tube Recommended Action: - Check HV cables connections- run 2nd tube
capability diagnostic- Replace HV tank
3601204 Error Text: Generator error 60-0350; (3): TMax 10s Overflow
View Level: opr
Root Cause: 1
Description: "TMax 10s Overflow Potential Cause: Recommended Action:
3601205 Error Text: Generator error 60-0351; (3): Repetitive Error

View Level: opr
Root Cause: 1
Description: "Repetitive Error Potential Cause: Recommended Action:
3601206 Error Text: Generator error 60-0401; (3): No mA feedback

View Level: opr
Root Cause: 1
Description: "mA measurement function:kV control has detected no mA feedback 20 ms after the
beginning of the exposure. Potential Cause: 4. HV tank5. kV control board6. x-ray tube
(filament open or short circuited)7. Cathode HV cable short-circuited8. Misconnection
between HV+ and HV- after a tank replacement9. heater function Recommended Action: -
run 2nd tube capability diagnostic - Verify filament impedance. Replace tube if necessary. -
Verify filament drive (heater) - Replace kV control board - After a tank replacement, verify the
HV cable connection. - Disconnect HV Tank to kV control flat cable and verify with an Ohm-
meter the accuracy of the 5 Ohms resistor on the HV Tank mA measure. If it is far out of
range, (4.9 to 5.1 Ohm, including DVM accuracy) replace HV Tank.

GE MEDICAL SYSTEMS
3601207 Error Text: Generator error 60-0402; (3): mA scale error
View Level: opr
Root Cause: 1
Description: "mA has been measured to be either too low or too high with respect to mA demand 20 ms
after the beginning of the exposure Potential Cause: 1. kV control board 2. default filament
currents not correctly adjusted 3. HV Tank (improbable) Recommended Action: - If the tube
has just been replaced or installed, run many exposures until the filament correction adjusts
the default filament drive values. - If the error occurs after a while on a system : Disconnect
HV Tank to kV control flat cable and verify with an Ohm-meter the accuracy of the 5 Ohms
resistor on the HV Tank mA measure. If it is out of range, replace HV Tank else replace kV
control board
3601208 Error Text: Generator error class 2: mA out of range

View Level: opr
Root Cause: 1
Recommended Action(s): "No system action. IQ may be affected
Description: "mA out of range Potential Cause: Recommended Action:
3601209 Error Text: Generator error class 2: No Pulse Warning

View Level: opr
Root Cause: 1
Recommended Action(s): "No system action. IQ may be affected
Description: "No Pulse Warning Potential Cause: Recommended Action:
3601210 Error Text: Generator error 60-0451; (3): mA meter saturated

View Level: opr
Root Cause: 1
Description: "mA meter saturated Potential Cause: Recommended Action:
3601211 Error Text: Generator error 60-0504; (3): Inverter Gate Power Supply error
View Level: opr
Root Cause: 1
Description: "Gate supply voltage has dropped below the level required to drive the IGBTs properly
Potential Cause: 1. Generator input voltage too low or line impedance too high 2. Inverter
(gate command board) 3. kV control board Recommended Action: - check main AC fuses and
DCBUS voltage - run HV power diagnostics

GE MEDICAL SYSTEMS
3601212 Error Text: Generator error 60-0801; (3): Exposure backup mAs exceeded
View Level: opr
Root Cause: 1
Description: "The exposure command last so long that the maximum mAs allowed has been reached
Potential Cause:Exposure command line stuck to the active state Recommended Action: Try
again. If repeated, reset system and rentry. -disconnect system -Generator cable in different
3601213 Error Text: Generator error 60-1181; (3): mA between pulses

View Level: opr
Root Cause: 1
Recommended Action(s): "Release the switch and try again. Reset system if problem persists. If persistent check Grid
Description: "mA between pulses Potential Cause: Recommended Action:
View Level: opr
Root Cause: 1
Description: "Time counter problem Potential Cause: Recommended Action:
3601215 Error Text: Generator error 60-1407; (3): mAs counter problem
View Level: opr
Root Cause: 1
Description: "Error found in verifying the counter normal operation Potential Cause:KV control board
Recommended Action: Replace kV control Board
3601216 Error Text: Generator error 60-1409; (3): mAs meter saturated
View Level: opr
Root Cause: 1
Description: "A check is done on mAs counter operation at the beginning of exposure and found the mAs
meter with unrealistic value. Potential Cause: kV control Recommended Action: Replace kV
control

GE MEDICAL SYSTEMS
3601217 Error Text: Generator error 60-1410; (3): FPGA locked
View Level: opr
Root Cause: 1
Description: "FPGA detected an error and did not allow start exposure after exposure command signal
was received. Potential Cause: 1. software bug 2. kV control Recommended Action: If
persistent replace kV control
View Level: opr
Root Cause: 1
Description: "Error found in verifying the counter normal operation. Potential Cause: kV control
3601219 Error Text: Generator error 60-1420; (3): Tomo cut too early
View Level: opr
Root Cause: 1
3601220 Error Text: Generator error 60-1421; (3): Tomo cut by generator
View Level: opr
Root Cause: 1
3601221 Error Text: Generator error 60-1454; (3): Inverter thermal error
View Level: opr
Root Cause: 1
Description: "Inverter thermal error Potential Cause: Recommended Action:
3601222 Error Text: Generator error 70-0501;(4): DC bus out of range

View Level: opr
Root Cause: 1
Description: "DC bus out if range (<400 or >850) Potential Cause: 1. mains problem (Too low or too high)
2. One phase missing at Generator input Recommended Action: Check mains line 3 phases
incoming voltage -Verify line impedance if mains is low

GE MEDICAL SYSTEMS
3601223 Error Text: Generator error 70-0502;(4): Error Overvoltage > 780 VDC
View Level: opr
Root Cause: 1
Customer Text: "Generator error. Try again. Call service if the problem persists.
3601224 Error Text: Generator error 70-0503;(4): Inverter Gate Power Supply error
View Level: opr
Root Cause: 1
Description: "Inverter Gate Power Supply error (checked at prep) Potential Cause: 1. Mains 2. Cable pb
3. Gate command board (Inverter) 4. kV control Recommended Action:run HV power
diagnostics
3601225 Error Text: Generator error 70-0505;(4): Mains power supply has dropped during exposure
View Level: opr
Root Cause: 1
Description: "Mains power supply has dropped During exposure Potential Cause: unkonwn
Recommended Action: none
3601226 Error Text: Generator error 70-0506;(4): DC bus 1 phase precharge error
View Level: opr
Root Cause: 1
3601227 Error Text: Generator error 70-0507;(4): DC bus 1 phase discharge error
View Level: opr
Root Cause: 1
3601228 Error Text: Generator error 70-0510; (3): HVPM AEC not 230V
View Level: opr
Root Cause: 1
Description: "HVPM AEC not 230V Potential Cause: Recommended Action:

GE MEDICAL SYSTEMS
3601229 Error Text: Generator error 70-0549;(4): LVPS TRI: unknown error
View Level: opr
Root Cause: 1
Description: "LVPS TRI: unknown error
View Level: opr
Root Cause: 1
Description: "LVPS TRI: detected +160V too high (Z6 Z7 = value)
View Level: opr
Root Cause: 1
Description: "LVPS TRI: detected +160V too low (Z6 Z7 = value)
View Level: opr
Root Cause: 1
Description: "LVPS TRI: detected +15V too high (Z6 Z7 = value)
View Level: opr
Root Cause: 1
Description: "LVPS TRI: detected +15V too low (Z6 Z7 = value)
3601234 Error Text: Generator error 70-0573;(4): LVPS TRI: detected -15V too strong
View Level: opr
Root Cause: 1
Description: "LVPS TRI: detected -15V too strong

GE MEDICAL SYSTEMS
3601235 Error Text: Generator error 70-0577;(4): LVPS TRI: detected -15V too weak
View Level: opr
Root Cause: 1
Description: "LVPS TRI: detected -15V too weak
3601236 Error Text: Generator error 80-0180;(4): Rotor board com pb

View Level: opr
Root Cause: 1
Description: "kV control board communication Watch Dog with Rotation board popped up because it did
not get reply from Rotation board. Potential Cause: 1. Rotation board2. Control bus cable3.
kV control Recommended Action: A/Check that rotation firmware is running (DS5 Led is
blinking). If no : 1/verify rotation board 5V : Led DS3 is lit. If no : verify DS1/DS2 Leds : if
they are lit, replace rotation board, else go to +/-15V errors troubleshooting 2/ verify that
RESET Led is not lit. If it is lit, disconnect successively the control bus cable from heater and
kV control to find the board which is holding the reset line and replace it. If after disconnecting
all the boards, the Led remains lit, replace rotation board 3/ else replace rotation board B/
Verify the flat cable between kV control and auxiliary module is correctly connected to the
Rotation boardC/else replace kV control
3601237 Error Text: Generator error 80-0181;(4): Rotor board has reset
View Level: opr
Root Cause: 1
Description: "kV control has detected the Rotation board has reset. KV control will reload Rotation data
base Potential Cause: 1. Rotation board 2. Interference (Spikes) Recommended Action: -
Reinitialize system, retry. -If persistent, replace Rotation board or check power and grounding

View Level: opr
Root Cause: 1
Description: "kV control board communication Watch Dog with Heater board popped up because it did not
get reply from Heater board. Potential Cause:1. Heater 0 board2. Control bus cable3. kV
control Recommended Action: A/Check that heater firmware is running (DS1/2 Led are lit
successively). If no : 1/verify heater board 5V : J3/pin2. If wrong : verify +15V/-15V (J3,
pin3,4) : if they are right, change rotation board, else go to +/-15V errors troubleshooting 2/
verify that RST Led is not lit. If it is lit, disconnect successively the control bus cable from
it. If after disconnecting all the boards, the Led remains lit, replace heater board 3/ else
replace heater board B/Verify the flat cable between kV control and auxiliary module is
correctly connected until the heater boardC/else replace kV control board

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: "KV control has detected the heater board has reset. KV ctrl will reload Rotation data base
Potential Cause: 1. Heater board 2. Interference (Spikes) Recommended Action: -
Reinitialize system, retry. -If persistent, replace board or check power and grounding.
3601240 Error Text: Generator error 80-0322;(4): kV ref ADC / DAC failled
View Level: opr
Root Cause: 1
Description: "kV control DAC and ADC capability are permanently tested for coherency. Potential Cause:
KV control board Recommended Action: Only if this error is repetitive and comes alone
(Not following other errors), replace kV control board.
3601241 Error Text: Generator error 80-03A0;(4): DSP error

View Level: opr
Root Cause: 1
Description: "DSP program corrupted Potential Cause: KV control board Recommended Action: -
Reinitialize system , retry. - If persistent , change KV control board
3601242 Error Text: Generator error 80-0601;(4): RTL error (Z6 Z7 = bitmap)
View Level: opr
Root Cause: 1
Description: "Real Time Lines show a wrong state. RTL’s are tested on a regular basis in stand by.
Potential Cause: 1. system communication power supply (for isolated communications) 2.
system communication cable 3. system interface board 4. system interface to kV control flat
cable 5. kV control board Recommended Action: -Check communication cable -Check
system communication power supply (if any) -Check system interface to kV control flat cable
-replace system interface board -replace kV control board
3601243 Error Text: Generator error 80-0602;(4): External CAN bus off
View Level: opr
Root Cause: 1
Description: "External CAN bus off Potential Cause: 1. system communication power supply (for isolated
communications) 2. system communication cable 3. system interface board 4. system
interface to kV control flat cable 5. kV control board Recommended Action: -Check
communication cable -Check system communication power supply (if any) -Check system
interface to kV control flat cable -replace system interface board-replace kV control board

GE MEDICAL SYSTEMS
3601244 Error Text: Generator error 80-0902;(4): tube cooling supply error
View Level: opr
Root Cause: 1
Check undertable xray tube fan power.
Description: "Rotation board has detected that a wrong voltage is applied to the tube fan Potential Cause:
1. No 115V tube cooling supply 2. Cabling 3. Rotation board Recommended Action: -Check
presence of the AC voltage (DS6 neon) at the input of the Rotation board. -Check the cables.
If ok, replace the rotation board
3601245 Error Text: Generator error 80-1006;(4): HV switch sel error

View Level: opr
Root Cause: 1
Recommended Action(s): "If trying to take exposure, release the switch and try again. Try reselecting the xray tube.
Description: "HV switch sel error Potential Cause: Recommended Action:
3601246 Error Text: Generator error 80-1007;(4): Rotor switch sel error
View Level: opr
Root Cause: 1
Description: "Rotor switch sel error Potential Cause: Recommended Action:
3601247 Error Text: Generator error 80-1008;(4): Heater switch sel error
View Level: opr
Root Cause: 1
Description: "Heater switch sel error Potential Cause: Recommended Action:
3601248 Error Text: Generator error 80-1180;(4): Ingrid not active

View Level: opr
Root Cause: 1
Description: "Ingrid not active

GE MEDICAL SYSTEMS
3601249 Error Text: Generator error 80-1182;(4): Ingrid CAN bus off
View Level: opr
Root Cause: 1
Description: "Ingrid CAN bus off

View Level: opr
Root Cause: 1
Description: "Heater 1 board com pb Potential Cause: 1. Heater 1 board 2. Control bus cable 3. kV control
Recommended Action: A/Check that heater firmware is running (DS1/2 Led are lit
successively). If no : 1/verify heater board 5V : J3/pin2. If wrong : verify +15V/-15V (J3,
pin3,4) : if they are right, change rotation board, else go to +/-15V errors troubleshooting 2/
verify that RST Led is not lit. If it is lit, disconnect successively the control bus cable from
it. If after disconnecting all the boards, the Led remains lit, replace heater board 3/ else
replace heater board B/Verify the flat cable between kV control and auxiliary module is
correctly connected until the heater boardC/else replace kV control board
View Level: opr
Root Cause: 1
Description: "KV control has detected the heater board has reset. KV ctrl will reload Rotation data base
Potential Cause: 1. Heater 1 board 2. Interference (Spikes) Recommended Action: -
Reinitialize system, retry. -If persistent, replace board or check power and grounding.
3601252 Error Text: Generator error 80-1402;(4): Internal CAN bus off
View Level: opr
Root Cause: 1
Description: "Can device on kV control board detected abnormal level on it’s 2 line and sent error to the
CPU Potential Cause: 1. kV control 2. Control bus cable 3. Heater or Rotation
Recommended Action: Check a short circuit on CAN lines, pins 5 & 6, of the control bus
cable. Short circuit may be either on Boards or connector/ cable. If no fault detected, replace
kV control

GE MEDICAL SYSTEMS
3601253 Error Text: Generator error 80-1403;(4): Connectic Fault
View Level: opr
Root Cause: 1
Check kV control board cables
Description: "One of the flat cable connector is not connected in Generator Potential Cause: Multiple, but
likely improbable. Recommended Action: Check connection of the following cables : kV
control to system I/F board, kV control to HV tank, HV tank to inverter.
3601254 Error Text: Generator error 80-1404;(4): FPGA configuration problem

View Level: opr
Root Cause: 1
Description: "Detected during power up. The kV control main software cannot load the FPGA Potential
Cause: kV control board. Recommended Action: Replace kV control board.
3601255 Error Text: Generator error 80-1450;(4): Hardware Inverter Error

View Level: opr
Root Cause: 1
Description: "Hardware Inverter Error Potential Cause: Recommended Action:
3601256 Error Text: Generator error 80-1452;(4): Incorrect KVmA Test Sel
View Level: opr
Root Cause: 1
Description: "Incorrect KVmA Test Sel Potential Cause: Recommended Action:
3601257 Error Text: Generator error 90-0701;(4): Saved RAM checksum pb

View Level: opr
Root Cause: 1
Need maintainance on database
Description: "Saved RAM checksum pb Potential Cause: Recommended Action:

GE MEDICAL SYSTEMS
3601258 Error Text: Generator error 90-0702;(4): Software problem
View Level: opr
Root Cause: 1
Description: "Software problem Potential Cause: Recommended Action:
3601259 Error Text: Generator error 90-0704;(4): Heater / Rotor hold too long
View Level: opr
Root Cause: 1
Description: "Heater / Rotor hold too long Potential Cause: Recommended Action:
3601260 Error Text: Generator error 90-0705;(4): Configuration error

View Level: opr
Root Cause: 1
Check generator config.
Description: "Configuration error Potential Cause: Recommended Action:
3601261 Error Text: Generator error 90-0706;(4): Wrong DSP version

View Level: opr
Root Cause: 1
Description: "Wrong DSP version Potential Cause: Recommended Action:
3601262 Error Text: Generator error 90-0707;(4): Wrong FPGA version

View Level: opr
Root Cause: 1
Description: "Wrong FPGA version Potential Cause: Recommended Action:

GE MEDICAL SYSTEMS
3601263 Error Text: Generator error 90-1001;(4): Wrong tube number sel
View Level: opr
Root Cause: 1
Description: "Wrong tube number sel Potential Cause: Recommended Action:
3601264 Error Text: Generator error 90-1003;(4): Tube Sel While Rotor On
View Level: opr
Root Cause: 1
Description: "Tube Sel While Rotor On Potential Cause: Recommended Action:
3601265 Error Text: Generator error 90-1004;(4): Tube Sel While Heat On
View Level: opr
Root Cause: 1
Description: "Tube Sel While Heat On Potential Cause: Recommended Action:
3601266 Error Text: Generator error 90-1005;(4): Tube Sel While KV On

View Level: opr
Root Cause: 1
Description: "Tube Sel While KV On Potential Cause: Recommended Action:
3601267 Error Text: Generator error 90-1011;(4): Unexpected tube switch board
View Level: opr
Root Cause: 1
Reset system if problem persists. Check generator configuration.
Description: "Unexpected tube switch board Potential Cause: Recommended Action:

GE MEDICAL SYSTEMS
3601268 Error Text: Generator error 90-1012;(4): Exposure preparation while tube not ready
View Level: opr
Root Cause: 1
Description: "Exposure preparation while tube not ready Potential Cause: Recommended Action:
3601269 Error Text: Generator error 100-0603;(4): Debug screen com error
View Level: opr
Root Cause: 1
Description: "Debug screen com error Potential Cause: Recommended Action:
3601270 Error Text: Generator error 100-0603;(4): Database download error

View Level: opr
Root Cause: 1
Description: "Database download error Potential Cause: Recommended Action:
3601271 Error Text: Generator error 100-0605;(4): TAV com error

View Level: opr
Root Cause: 1
Description: "TAV com error Potential Cause: Recommended Action:
3601272 Error Text: Generator error 100-0606;(4): MPC/Madrid com pb

View Level: opr
Root Cause: 1
Description: "MPC/Madrid com pb Potential Cause: Recommended Action:
3601273 Error Text: Generator error 100-0607;(4): room SLIO com problem
View Level: opr
Root Cause: 1
Description: "room SLIO com problem ! Potential Cause: Recommended Action:

GE MEDICAL SYSTEMS
3601274 Error Text: Generator error 100-0650;(4): ETHERNET com. error
View Level: opr
Root Cause: 1
Description: "ETHERNET com. error Potential Cause: Recommended Action:
3601275 Error Text: Generator error 100-0651;(4): HDLC com. error

View Level: opr
Root Cause: 1
Description: "HDLC com. error Potential Cause: Recommended Action:
3601276 Error Text: Generator error 100-0652;(4): APR com. error

View Level: opr
Root Cause: 1
Description: "APR com. error Potential Cause: Recommended Action:
3601277 Error Text: Generator error 100-1301;(4): AEC Board com problem
View Level: opr
Root Cause: 1
Description: "AEC Board com problem Potential Cause: Recommended Action:
3601278 Error Text: Generator error 110-111; (5): Rotor Thermal error
View Level: opr
Root Cause: 1
Recommended Action(s): "If trying to take exposure, release the switch and wait for the rotation circuit to cool.
Description: "Rotor Thermal error Potential Cause: Recommended Action:
3601279 Error Text: Generator error 110-1405;(5: Tank temp meas too low
View Level: opr
Root Cause: 1
Description: "Means that t° value of the HV tank is < 3°C Potential Cause: kV control HV tank
Recommended Action: Replace kV control Replace HV Tank

GE MEDICAL SYSTEMS
3601280 Error Text: Generator error 110-1406;(5): Inverter Temp meas too low
View Level: opr
Root Cause: 1
Description: "Parallel inductor is 3°C Potential Cause: Fan of the inverter (most probable) kV control
Sensor of parallel inductor Recommended Action: Check the activity of the fan of the power
module. If it is not working, check the voltage of the fan. If it is >14Vdc and the fan is not
running, replace the fan. If the voltage is OK check the connection of the sensor cable on J5
on Gate_cmd board. If all is OK, replace kV control. If the problem persists, replace the
inverter.
3601281 Error Text: Generator error 110-1412;(5): Lp Temp meas too low
View Level: opr
Root Cause: 1
3601282 Error Text: Generator error 110-1453;(5): Rotor Thermal error

View Level: opr
Root Cause: 1
Description: "Rotor Thermal error Potential Cause: Recommended Action:
3601283 Error Text: Generator error 120-1500; (3): Tomo brightness not good
View Level: opr
Root Cause: 1
Description:
3601284 Error Text: Generator error 120-1501; (3): Exposure switch release
View Level: opr
Root Cause: 1
Description: "Release exposure switch (RAD-RF) Potential Cause: during exposure switch is released
Recommended Action: no action
Customer Text: The expose switch was released by the user before the exposure was completed.

GE MEDICAL SYSTEMS
3601285 Error Text: Generator error 120-1502; (3): AEC does not cut exposure
View Level: opr
Root Cause: 1
Description: "AEC does not cut exposure (RAD-RF) Potential Cause: backup parameters (mAs, ...) cut
exposure Recommended Action: - change parameters (kV, mAs)- change AEC
3601286 Error Text: Generator error 130-1100;(4): Ingrid communication watchdog error
View Level: opr
Root Cause: 1
Description: "Ingrid communication watchdog error
3601287 Error Text: Generator error 130-1101;(4): Ingrid repetition rate higher than 100 fps
View Level: opr
Root Cause: 1
Description: "Ingrid repetition rate higher than 100 fps
3601288 Error Text: Generator error 130-1102;(4): Inter grid CMD time shorter than 0.5ms
View Level: opr
Root Cause: 1
Description: "Inter grid CMD time shorter than 0.5ms
3601289 Error Text: Generator error 130-1103;(4): Ingrid power supply voltage lower than 130V
View Level: opr
Root Cause: 1
Description: "Ingrid power supply voltage lower than 130V
3601290 Error Text: Generator error 130-1104;(4): Ingrid power supply voltage higher than 200V
View Level: opr
Root Cause: 1
Description: "Ingrid power supply voltage higher than 200V

GE MEDICAL SYSTEMS
3601291 Error Text: Generator error 130-1105;(4): Ingrid feedback error
View Level: opr
Root Cause: 1
Description: "Ingrid feedback error
3601292 Error Text: Generator error 130-1107;(4): Grid feedback voltage too High
View Level: opr
Root Cause: 1
Description: "Grid feedback voltage too High
3601293 Error Text: Generator error 130-1109;(4): Bias feedback voltage too High
View Level: opr
Root Cause: 1
Description: "Bias feedback voltage too High
3601294 Error Text: Generator error 130-1110;(4): Ingrid target DAC voltage feedback fault
View Level: opr
Root Cause: 1
Description: "Ingrid target DAC voltage feedback fault
3601295 Error Text: Generator error 130-1199;(4): Ingrid error

View Level: opr
Root Cause: 1
Description: "Ingrid error
3601296 Error Text: Generator error 140-1020;(4): Tube switch status error.
View Level: opr
Root Cause: 1
Description: "Tube Switch status error Potential Cause: Tube Switch Board Recommended Action: -
Replace Tube Switch Board
Customer Text: Xray tube selection error. Reselect tube and continue. Call service if the problem persists.

GE MEDICAL SYSTEMS
3601297 Error Text: Generator error 140-1021;(4): Tube switch state machine error
View Level: opr
Root Cause: 1
Description: "Tube Switch State Machine error Tube Switch Board Recommended Action: - Replace
Tube Switch Board
3601298 Error Text: Generator error 140-1022;(4): Tube switch lamp relay feedback error
View Level: opr
Root Cause: 1
Description: "Tube Switch lamp relay feedback error Potential Cause: Tube Switch Board
Recommended Action: - Replace Tube Switch Board
3601299 Error Text: Generator error 140-1023;(4): Tube Switch heater SF feedback error
View Level: opr
Root Cause: 1
Description: "Tube Switch heater SF feedback error Potential Cause: Tube Switch Board Recommended
Action: - Replace Tube Switch Board
3601300 Error Text: Generator error 140-1024;(4): Tube switch heater LF feedback error
View Level: opr
Root Cause: 1
Description: "Tube Switch heater LF feedback error Potential Cause: Tube Switch Board Recommended
Action: - Replace Tube Switch Board
3601301 Error Text: Generator error 140-1025;(4): Tube switch rotation relay feedback error
View Level: opr
Root Cause: 1
Description: "Tube Switch rotation relay feedback error Potential Cause: Tube Switch Board
Recommended Action: - Replace Tube Switch Board

GE MEDICAL SYSTEMS
3601302 Error Text: Generator error 140-1026;(4): Tube switch motor position error
View Level: opr
Root Cause: 1
Description: "(Motor is in intermediate position) Potential Cause: 1. Cabling problem 2. Two Tube HV
Tank 3. Tube Switch Board Recommended Action: -check the cabling between J8I of Tube
Switching board and DJ4 of Inverter module and J9 on kVmeas board on HV Tank -if no
improvement change HV Tank -if no improvement change Tube Switch board
3601303 Error Text: Generator error 140-1027;(4): Tube switch motor feedback error
View Level: opr
Root Cause: 1
Description: "Tube switch motor feedback error (Switching Time out) Potential Cause: 1. Cabling problem
2. Two Tube HV Tank 3. Tube Switch Board Recommended Action: -check the cabling
between J8I of Tube Switching board and DJ4 of Inverter module and J9 on kVmeas board
on HV Tank -if no improvement change HV Tank -if no improvement change Tube Switch
board
3601304 Error Text: Generator error 140-1028;(4): Tube switch motor is in the opposite position
View Level: opr
Root Cause: 1
Description: "Tube Switch Motor is in the opposite position Potential Cause: 1. Cabling problem 2. Two
Tube HV Tank 3. Tube Switch Board Recommended Action: -check the cabling between J8I
of Tube Switching board and DJ4 of Inverter module and J9 on kVmeas board on HV Tank -
if no improvement change HV Tank -if no improvement change Tube Switch board
3601305 Error Text: Generator error 140-1030;(4): Tube switch config reply error
View Level: opr
Root Cause: 1
Description: "Tube switch config reply error Potential Cause: Recommended Action:

GE MEDICAL SYSTEMS
3601306 Error Text: Generator error 140-1031;(4): Tube switch status reply error
View Level: opr
Root Cause: 1
Description: "Tube switch status reply error Potential Cause: Recommended Action:
3601307 Error Text: Generator error 140-1032;(4): Tube switch motor move refused
View Level: opr
Root Cause: 1
Description: "Tube switch motor move refused Potential Cause: Recommended Action:
3601308 Error Text: Generator error 140-1033;(4): Tube switch rotor capa activation error
View Level: opr
Root Cause: 1
Description: "Tube switch rotor capa activation error Potential Cause: Recommended Action:
3601309 Error Text: Generator error 110-906;(5): Tube track protection.

View Level: opr
Root Cause: 1
Description: "Tube track protection
3601310 Error Text: Generator error 80-1413;(4): Internal CAN bus Txo
View Level: opr
Root Cause: 1
Description: "Internal CAN bus Txo, Tx messages lost in internal Bus
3601311 Error Text: Generator error 80-1414;(4): Internal LD CAN bus Txo
View Level: opr
Root Cause: 1
Description: "Internal LD CAN bus Txo; Tx messages lost in Ld internal Bus

GE MEDICAL SYSTEMS
3601312 Error Text: Generator error 80-1415;(4): External CAN bus Txo
View Level: opr
Root Cause: 1
Description: "External CAN bus Txo; Tx messages lost in External Bus
3601313 Error Text: Generator error 80-1416;(4): Internal CAN RTL2 error
View Level: opr
Root Cause: 1
Description: "Internal CAN RTL2 error; RTL2 - MAX485 chip failure
3601314 Error Text: Generator error 80-1417;(4):DC disch. when inhib

View Level: opr
Root Cause: 1
Description: "DC disch. when inhib; Error in the DC Discharge loop
3601315 Error Text: Generator error 80-1418;(4): No DC disch. on request

View Level: opr
Root Cause: 1
Description: "No DC disch. on request; Error in the DC Discharge loop
3601616 Error Text: LVPS 400: Power Supply output set to off
View Level: opr
Root Cause: 1
Recommended Action(s): "No Action required".
Description: 3 over/under voltage FW errors in the same LVPS power supply ouput
3601617 Error Text: LVPS 400: Fan output set to off

View Level: opr
Root Cause: 1
Recommended Action(s): "No Action required".
Description: 3 overcurrent FW errors in the same LVPS FAN ouput

GE MEDICAL SYSTEMS
3601618 Error Text: Generator error 60-0331; (3): Timeout on Xray ON
View Level: opr
Root Cause: 1
Description: Timeout on X-Ray on (10-20ms) after rad pluse generated by FPGA. Exposure stopped.
Customer Text: Release exposure switch and try again. Call service if problem persists.

GE MEDICAL SYSTEMS
3.20 38 XRTechOpt
View Level: opr
Root Cause: 1
Description: "Unable to create a required event.

View Level: opr
Root Cause: 1
Description: "Unable to subscribe to a required event. The software communication bus broken.
3800002 Error Text: Failed to bind with actor

View Level: opr
Root Cause: 1
Recommended Action(s): "Refer to Precision Diagnostic Manual and run Ethernet Diagnostic.
Description: " The software communication bus broken.

View Level: opr
Root Cause: 1
Description: "Unable to bind with a required actor.The software communication bus broken

View Level: opr
Root Cause: 1
Description: "Received an event, which is not supposed to be received by the actor
View Level: opr
Root Cause: 1
Description: "Opmode requested is not available

GE MEDICAL SYSTEMS
3800006 Error Text: Actor not ready
View Level: opr
Root Cause: 1
Description: "XRTechOpt is not ready, it may be in PowerFailure, ShutDown or HaltError
3800007 Error Text: Manual mode disabled

View Level: opr
Root Cause: 1
Description: "The method setTechnique() was invoked while the manual mode was disabled
Customer Text: Set manual override to continue.
3800008 Error Text: Incorrect active OpMode

View Level: opr
Root Cause: 1
Description: "One of opModeId in the CHANGE_ACTIVE_OPMODES event is not configured

View Level: opr
Root Cause: 1
Description: "Unable to interact with an actor.The software communication bus broken
Customer Text: An internal communication error has occurred. Reset the system if the problem persists.
3800101 Error Text: Failed to publish event

View Level: opr
Root Cause: 1
Description: "The system may be low in resources!!
3800102 Error Text: Incorrect bytes read for message queue

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
3800103 Error Text: msgQSend failed
View Level: opr
Root Cause: 1
3800104 Error Text: Actuals not received from Jedi

View Level: opr
Root Cause: 1
Recommended Action(s): "Software or hardware error - for engineering use only. No recommended action to be taken.
System will recover from this error.
Description: "TechMgr did not publish actuals for a frame
Customer Text: System did not receive generator techniques. Continue or release exposure switch and try
again.
3800105 Error Text: Sensor feedback not received

View Level: opr
Root Cause: 1
Recommended Action(s): "Software or hardware error - for engineering use only. No recommended action to be taken.
System will recover from this error.
Description: "Sensor feedback was not received for the last 10 frames
Customer Text: Digital control error. Release exposure switch and try again.

View Level: opr
Root Cause: 1
Recommended Action(s): "Refer to Precision Diagnostic Manual to run AMI Diagnostics on system controller
Description: "Configuration parameter could not be read
Customer Text: Configuration file may be corrupted. Call service
3800107 Error Text: Actuals not received from Jedi during trial exposure
View Level: opr
Root Cause: 1
Recommended Action(s): "Software or hardware error - retry the sequence.
Description: "Actual techniques were not received from jedi during the DSA trial exposure
3800300 Error Text: Unable to instantiate EM Server

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
3800301 Error Text: Unable to open EM file, defaults will be used
View Level: opr
Root Cause: 1
Recommended Action(s): "Call Service. Reinstall Software
Description: "The software configuration Issue
3800400 Error Text: Cannot open the trajectory file

View Level: opr
Root Cause: 1
3800401 Error Text: The trajectory file may be corrupted

View Level: opr
Root Cause: 1
3800402 Error Text: Incorrect FOV

View Level: opr
Root Cause: 1
Description: "The FOV value does not exist, seting to default
Customer Text: Field of View value is incorrect. Reselect the desired value.
3800403 Error Text: Incorrect Grid position

View Level: opr
Root Cause: 1
Description: "Grid OUT not allowed, so setting grid to IN
Customer Text: The grid must be in the Field of View.
3800404 Error Text: The Focal Spot could not be set

View Level: opr
Root Cause: 1
Recommended Action(s): "System is stable if occurance frequency is low and system will default focal spot (small).
Frequent occurance of this error could indicate a failure of the generator or the filament
Description: "The Focal Spot could not be set

GE MEDICAL SYSTEMS
3800405 Error Text: Incorrect Spectral Filter
View Level: opr
Root Cause: 1
Recommended Action(s): "System is stable if occurance frequency is low and system will default to 0.3 mm. Frequent
occurance of this error could indicate collimator failure. Run collimator diagnostics.
Description: "The Spectral Filter with current settings does not exist
3800406 Error Text: The EPT limits are corrupted

View Level: opr
Root Cause: 1
Description: "The EPT limits are corrupted
Customer Text: Xray exposure has been prematurely stopped. Try again.
3800407 Error Text: EPT out of bounds

View Level: opr
Root Cause: 1
Description: "EPT value is out of bounds so limiting to the bounded value

GE MEDICAL SYSTEMS
3.21 50 ATLAS
Minor Function Impacted: Heartbeat
View Level: opr
Root Cause: 0
Description: Actor Communication lost after boot. Actor is dead or is hung.
5000002 Error Text: No request from the subsys manager - Not Alive
View Level: opr
Root Cause: 0
Customer Text: A system failure has occurred. Reset the system to continue.
View Level: opr
Root Cause: 0
View Level: opr
Root Cause: 0
5000005 Error Text: No request from system manager in the default time interval
Minor Function Impacted: HeartBeatRecieve
View Level: opr
Root Cause: 0
5000006 Error Text: No request from system manager - Not Alive?

View Level: opr
Root Cause: 0

GE MEDICAL SYSTEMS
5000007 Error Text: Beat Mechanism has gone wrong
View Level: opr
Root Cause: 0
5000008 Error Text: An incorrect actor ready was received by subsysmgr

View Level: opr
Root Cause: 0
Description: Actor not in the subsystem Manager list. An Actor has created trigger for Subsystem Manager
and the subsystem Manager does not know about it. Also the actor has sent an invalid
parameters in the actor ready if the actor is in the boot up list.
5000009 Error Text: An incorrect state for request

View Level: opr
Root Cause: 0
Description: Actor / SubsysMgr Synchronization is lost. Actor is not following the boot/Reset/Shutdown
protocol or the subsystem Manager state machine is invalid.
5000010 Error Text: Config file has actor on start diag shutdown and reset list
View Level: opr
Root Cause: 1
Description: Config File problem
5000011 Error Text: Timed Out waiting for boot to complete, the system has to be Reset
View Level: opr
Root Cause: 0
Description: The boot did not complete. Time out waiting for some actor to respond. The system cannot
be used without a reset. Some actor did not respond back within the time-out value.
5000012 Error Text: Timed Out waiting for Shut Down complete from all Actors, system shutdown will be
continued
View Level: opr
Root Cause: 0
Description: Some actor did not reply with a shutDownDone

GE MEDICAL SYSTEMS
5000013 Error Text: Timed Out waiting for Reset complete from all actors, system reset will be continued
View Level: opr
Root Cause: 0
Description: Some actor did not reply with a reset
Customer Text: System configuration error. System will continue with reset.
5000014 Error Text: Timed Out waiting for complete shutdown from system manager, system will be turned off
View Level: opr
Root Cause: 0
Description: System Manager did not send a complete shutdown to the subsystem Manager levels
5000015 Error Text: Unable to disable error mgr for start diagnostics
View Level: opr
Root Cause: 0
Recommended Action(s): computer
Description: enableErrorMgr API returned Status = BAD.
5000016 Error Text: Unable to disable heartbeat for start diagnostics

View Level: opr
Root Cause: 0
Description: Heartbeat was not disabled during diagnostics, can cause the system to shut down.
5000017 Error Text: Timed Out waiting for Start Diag shut down complete from actors, will be continued
View Level: opr
Root Cause: 0
Description: actor not following a proper protocol for Diagnostics as dictated by the subsystem Manager.
5000018 Error Text: Timed Out waiting for Start Diag reset complete from actors, will be continued
View Level: opr
Root Cause: 0
Description: actor not following a proper protocol for reset as dictated by the subsystem Manager.

GE MEDICAL SYSTEMS
Minor Function Impacted: subsysmgr
View Level: opr
Root Cause: 0
Description: Some actor has left the system and the system is unusable. An sequencing in process will be
aborted.

Minor Function Impacted: uponCommunicationError
View Level: opr
Root Cause: 0
Description: An actor has left the system. The system is unusable.
5000021 Error Text: Unable to create an instance of an object

View Level: opr
Root Cause: 1
Description: Running low on memory or the initialization of the object failed.
5000022 Error Text: Unable to create an event

View Level: opr
Root Cause: 1
5000023 Error Text: Bind to a CORBA Object Failed

View Level: opr
Root Cause: 1
Description: Unable to bind to an object. CORBA Related problems.
5000024 Error Text: CORBA Exception during a CORBA activity

Minor Function Impacted: corba
View Level: opr
Root Cause: 1
Description: An Exception occurred during a method call to some other actor.

GE MEDICAL SYSTEMS
5000025 Error Text: Failed to subscribe to an event
View Level: opr
Root Cause: 1
5000026 Error Text: Error Manager failed to startup

View Level: opr
Root Cause: 1
Description: Error Manager instantiation failed or Low on memory
5000027 Error Text: An actor has not overridden a method of GA

View Level: opr
Root Cause: 0
Description: The method should be overridden by the actor. Actor is not complaint to ATLAS Standards.
5000028 Error Text: Unable to create a trigger

Minor Function Impacted: addActorTrigger
View Level: opr
Root Cause: 1
Description: CF Problem.
5000029 Error Text: Unable to narrow an object reference to an actor reference

View Level: opr
Root Cause: 1
Description: CORBA Problems.
5000030 Error Text: An FTP Error has occurred

Minor Function Impacted: backupandrestore
View Level: opr
Root Cause: 1
Description: Failed to FTP a file successfully.
5000031 Error Text: Unable to load a dynamic library

View Level: opr
Root Cause: 1
Description: The dynamic library does not exist.

GE MEDICAL SYSTEMS
5000032 Error Text: Thread spawn failed
Minor Function Impacted: processTriggerEvents
View Level: opr
Root Cause: 1
Description: Unable to spawn a thread. Incorrect parameters to thread or OS has ran out of critical
resources.
5000033 Error Text: A System call returned invalid value or failed

Minor Function Impacted: OS
View Level: opr
Root Cause: 0
Description: System Call Made with invalid parameters or the OS has ran out of resources.
5000034 Error Text: Not bound to the actor to call a method

View Level: opr
Root Cause: 1
Description: A Method call within GA failed to call a method on some other object. (actor)
5000035 Error Text: An environment variable required for proper startup is not set
Minor Function Impacted: user
View Level: opr
Root Cause: 0
Description: An Environment Variable that is required for proper functioning of the ATLAS Systems is not
set. The system is not able to default the value of this variable.
5000036 Error Text: This actor name or id is not known to the system or is invalid
View Level: opr
Root Cause: 0
Description: The actor is not a valid actor. It's entry does not exist in the ActorIdNames.h. If this actor is
required, a formal request to the ATLAS Core team needs to be made.
View Level: opr
Root Cause: 0

GE MEDICAL SYSTEMS
5000038 Error Text: No response from the subsys manager - Not Alive
Minor Function Impacted: HeartbeatSend
View Level: opr
Root Cause: 0
5000039 Error Text: Duplicate Actor Joining System detected in the BootState Machine
Minor Function Impacted: uponActorJoiningSystem
View Level: opr
Root Cause: 0
5000040 Error Text: The startBootPhase was received for an incorrect bootPhase
View Level: opr
Root Cause: 0
5000041 Error Text: Timed out waiting for startBootPhase from sysmgr.
View Level: opr
Root Cause: 0
5000042 Error Text: Unable to read file

View Level: opr
Root Cause: 0
5000043 Error Text: An unexpected request was received in the sysmgr, and was not processed
Minor Function Impacted: defaultHandler
View Level: opr
Root Cause: 0
5000044 Error Text: SubsysReady was not expected at this stage

Minor Function Impacted: subsysReady
View Level: opr
Root Cause: 0

GE MEDICAL SYSTEMS
5000045 Error Text: A duplicate subsysmgr seems to exist
Minor Function Impacted: actorJoiningSystem
View Level: opr
Root Cause: 0
5000046 Error Text: could not make the remote method call
View Level: opr
Root Cause: 1
5000047 Error Text: BootTimed out
View Level: opr
Root Cause: 0
5000048 Error Text: ResetTimed out

View Level: opr
Root Cause: 0
5000049 Error Text: ShutdownTimed out
View Level: opr
Root Cause: 0
5000050 Error Text: Power Failure Timed out - Shutting Down

View Level: opr
Root Cause: 0
Customer Text: Main Power off for more than 30 seconds. Shutdown in progress.

GE MEDICAL SYSTEMS
3.22 58 XRSubsysMgrVENUS
5800001 Error Text: Unable to create a process!! The system may be low in resources!!
Minor Function Impacted: timeout
View Level: opr
Root Cause: 1
Recommended Action(s): "Shutdown the Console.
Description: "The Subsystem manager failed to create a process to either shutdown the system ot reset
the system.
Customer Text: The reset or shutdown failed. Turn the system power off/on to continue.
5800002 Error Text: Unable to communicate with UPS!! Check if power to UPS is ON or the communication link
to UPS is present.
View Level: opr
Root Cause: 1
Description: The Subsystem manager was unable to connect to the UPS due to either a bad connection
or the UPS not being ON
Customer Text: Communication with UPS has failed. Continue and call service.
5800003 Error Text: Unable to subscribe to event

View Level: opr
Root Cause: 1
Recommended Action(s): "Component(s)-ETHERNET Communication
Description: "Unable to subscribe to a required event. The software communication bus broken
Customer Text: The system did not boot properly. Reset the system to continue.
5800004 Error Text: Unexpected shutdown of the Venus started by UPS daemon
View Level: opr
Root Cause: 1
Description: UPS daemon started a shutdown of the Operating system.
Customer Text: UPS started a shutdown of the system.
5800005 Error Text: Communication with UPS has been restored.

View Level: opr
Root Cause: 1
Description: The Subsystem manager was able to connect to the UPS.
Customer Text: System communication with the UPS has been restored.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Recommended Action(s): "Shutdown the Console.
Description: "The UPS has switched to battery operation.
Customer Text: A Hospital Main power failure has occurred. Please wait. . .

View Level: opr
Root Cause: 1
Description: The UPS has switched to line operation.
5800008 Error Text: Shutdown is occuring because power failure condition exists.
View Level: opr
Root Cause: 1
Customer Text: Hospital Main power failure. System Shutdown is in progress. Please wait. . .
5800009 Error Text: Unable to send reset message to System Controller because reference was not valid.
View Level: opr
Root Cause: 1
Description: This error will get logged in the event that the pointer to the SysMgr was not valid. In the case
of a reset, the Venus will still reset after a timeout.
Customer Text:
5800010 Error Text: User timeout on Boot

Minor Function Impacted: timeout
View Level: opr
Root Cause: 0
Description: "SubsysMgrVENUS boot timeout occurred.
Customer Text:
5800011 Error Text: Unable to request DUIF service

View Level: opr
Root Cause: 0
Recommended Action(s): "Component(s)-ETHERNET Communication
Description:
Customer Text: "

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: Emergency stop switch at triggered position (Power is off)
Customer Text: Emergency stop switch at triggered position (Power is off)
View Level: opr
Root Cause: 1
Description:
Customer Text:
5800014 Error Text: Hospitcal Main Power failure has occured, please wait...
View Level: opr
Root Cause: 1
Description: Hospitcal Main Power failure has occured, please wait...
Customer Text: Hospitcal Main Power failure has occured, please wait...
5800015 Error Text: Hospital Main Power failure has occured during BOOT phase,system shut down
View Level: opr
Root Cause: 1
Description: Hospital Main Power failure has occured during BOOT phase,system shut down
Customer Text: Hospital Main Power failure has occured during BOOT phase,system shut down
5800016 Error Text: System power recovery is in progress...

View Level: opr
Root Cause: 1
Description: System power recovery is in progress...
Customer Text: System power recovery is in progress...

View Level: opr
Root Cause: 1
Description: System restart successful
Customer Text: System restart successful

GE MEDICAL SYSTEMS
5800018 Error Text: System set GitaneLite Timer for Ups failed
View Level: opr
Root Cause: 1
Description: System set GitaneLite Timer for Ups failed
Customer Text:
5800019 Error Text: System disable GitaneLite Timer for Ups failed
View Level: opr
Root Cause: 1
Description: System disable GitaneLite Timer for Ups failed

GE MEDICAL SYSTEMS
3.23 64 XRUserIfPOS
View Level: opr
Root Cause: 0
Description: ""Reset the system, Reload the software
Customer Text: "System software error. Reset the system and call service to reload software if problem
persists.

View Level: opr
Root Cause: 0
persists.

View Level: opr
Root Cause: 0
persists.

View Level: opr
Root Cause: 0
persists.

View Level: opr
Root Cause: 0
Description: ""Ignore
persists.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 0
Customer Text: "An internal communication failure has occurred. Ignore. Call service if problem persists.

View Level: opr
Root Cause: 0

View Level: opr
Root Cause: 0

View Level: opr
Root Cause: 0

View Level: opr
Root Cause: 0

View Level: opr
Root Cause: 0

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 0

View Level: opr
Root Cause: 0

View Level: opr
Root Cause: 0

View Level: opr
Root Cause: 1
Customer Text: "System communication error. Reset the system and call service if problem persists.

View Level: opr
Root Cause: 0
Customer Text: "System communication error. Reset the system and call service if problem persists.
6400103 Error Text: Unknown actor

View Level: opr
Root Cause: 0

GE MEDICAL SYSTEMS
6400104 Error Text: Failed to read advisory message file AdvMsg.cfg
View Level: opr
Root Cause: 1
Recommended Action(s): "Reload the software
Description: ""Reload the software
Customer Text: "System software error. Call service to reload software.
6400105 Error Text: OTS UIF heartbeat failed

View Level: opr
Root Cause: 0
Description: ""Reset the system
Customer Text: "OTS communication error. Reset the system and call service if problem persists.
6400106 Error Text: Room Door Open

View Level: opr
Root Cause: 0
Recommended Action(s): "Close Room Door
Description: ""Close Room Door
Customer Text: "Room Door is open. Exposures are inhibited. Close door to resume.
6490000 Error Text: PDU IO Alive Timeout

View Level: opr
Root Cause: 1
Description: "PDU I/O initialization problem or device is not responding. Possible boot problem. May
indicate a CAN device or bus problem. Refer to the CAN bus block diagram. - If a single
device is reporting an error, check that device, its power, and its cabling/connections. - If
multiple device are reporting errors, check common cabling/connections and common
devices in the Pos Cab. - If all CAN devices are reporting errors, check common cabling/
connections. Also check/replace the System Controller.

View Level: opr
Root Cause: 1
Description: "PDU I/O initialization problem or device is not responding. Possible boot problem. May
indicate a CAN device or bus problem. Refer to the CAN bus block diagram. - If a single
devices in the Pos Cab. - If all CAN devices are reporting errors, check common cabling/

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: "PDU I/O device is not responding. Indicates a CAN device or bus problem. Refer to the
CAN bus block diagram. - If a single device is reporting an error, check that device, its
power, and its cabling/connections. - If multiple device are reporting errors, check common
cabling/connections and common power. For example, if the CAN bridge, Pos I/O, and CAN
amps in the Pos cab are reporting errors, check the external CAN cable from Sys Cab to Pos
Cab and check for power to those devices in the Pos Cab. - If all CAN devices are reporting
errors, check common cabling/connections. Also check/replace the System Controller.

View Level: opr
Root Cause: 1
Description: "CAN bridge initialization failed. Possible errors in CAN-RS422 communication. Possible
Boot problem. May indicate a CAN device or bus problem. Refer to the CAN bus block
diagram. - If a single device is reporting an error, check that device, its power, and its
cabling/connections. - If multiple devices are reporting errors, check common cabling/
connections and common power. For example, if the CAN bridge, Pos I/O, and CAN amps
in the Pos cab are reporting errors, check the external CAN cable from Sys Cab to Pos Cab
and check for power to those nodes in the Pos Cab. - If all CAN devices are reporting

View Level: opr
Root Cause: 1
Recommended Action(s): "Check CAN bridge connection, or reset the system
Description: "CAN bridge is not sending the heartbeat messages. Indicates a CAN device or bus problem.
Refer to the CAN bus block diagram. - If a single device is reporting an error, check that
device, its power, and its cabling/connections. - If multiple device are reporting errors,
check common cabling/connections and common power. For example, if the CAN bridge,
Pos I/O, and CAN amps in the Pos cab are reporting errors, check the external CAN cable
from Sys Cab to Pos Cab and check for power to those devices in the Pos Cab. - If all CAN
devices are reporting errors, check common cabling/connections. Also check/replace the
System Controller.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: "IDD console is not responding. The IDD console communications go through the CAN-
RS422 bridge. Possibly a problem with the IDD console or cabling from the bridge out to the
IDD console. Possibly indicates a CAN device or bus problem. Refer to the CAN bus block
diagram. - If a single device is reporting an error, check that device, its power, and its
cabling/connections. - If multiple device are reporting errors, check common cabling/
connections and common power. For example, if the CAN bridge, Pos I/O, and CAN amps
in the Pos cab are reporting errors, check the external CAN cable from Sys Cab to Pos Cab
and check for power to those devices in the Pos Cab. -If all CAN devices are reporting

View Level: opr
Root Cause: 1
Description: "IDD grid/cone controller (goldbox) is not responding. The IDD grid/cone controller (gold box)
indicates a CAN device or bus problem. Refer to the CAN bus block diagram. - If a single
devices in the Pos Cab. -If all CAN devices are reporting errors, check common cabling/
6490202 Error Text: System I/O CANopen communication failure

View Level: opr
Root Cause: 1
Recommended Action(s): "Reset system, and check CAN bus cable and connector,then check failure CAN node.
Description: "CAN bus overload, or CAN bus disconnected.
Customer Text: "System communication error. Reset system or call service.
6490301 Error Text: IDD Cancore node Guarding Error

View Level: opr
Root Cause: 1
Recommended Action(s): "Check the CAN bus connection to the DSC2, or Reset the system. Replace the DSC2 if
necessary.
Description: "The CanCore Device is not responding. Possibly indicates a CAN device or bus problem.
Refer to the CAN bus block diagram. - If a single device is reporting an error, check that
device, its power, and its cabling/connections. - If multiple device are reporting errors,
check common cabling/connections and common power. For example, if the CAN bridge,
Pos I/O, and CAN amps in the Pos cab are reporting errors, check the external CAN cable
from Sys Cab to Pos Cab and check for power to those devices in the Pos Cab. -If all CAN
devices are reporting errors, check common cabling/connections. Also check/replace the
System Controller.

GE MEDICAL SYSTEMS
6490302 Error Text: DSC2 communication Failure
View Level: opr
Root Cause: 1
Recommended Action(s): "Check the DSC2 Processor. Replace the DSC2 if necessary.
Description: "DSC2 Processor is not responding. Possibly indicates Communcation between Cancore
Device and the DSC processor. Or DSC2 Processor itself failed.
6490303 Error Text: Cancore Hardware Failure

View Level: opr
Root Cause: 1
Recommended Action(s): "Review the error log for specific failure; Check the indicated function.
Description: "The DSC2 hardware was commanded to do something, but it either did not respond or
responded with an error. Possible errors: 0x00 Boot Failure, DSC2 was unable to properly
initialize itself. 0x01 Grid Over Current, DSC2 detected an over current condition on the grid.
0x02 Cone Over Current, DSC2 detected an over current condition on the cone. 0x03 Grid
Stuck, grid is unable to move the full length of its track. 0x04 Cone Stuck, cone is unable to
move the full length of its track. 0x05 Grid H-Bridge Error, could mean over temp or over
current. 0x06 Cone H-Bridge Error, could mean over temp or over current. 0x07 Serial Error,
the UART reported an error. 0x08 A/D Converter Failure, A/D converter is not reading its
reference voltages properly. 0x09 Illegal Command, DSC2 received an illegal command from
the POS software. 0x0A Booting in Safe Mode, indicates a problem with application software.
Original functionality will be maintained, but any code upgrades since installation will be lost.
6490304 Error Text: System configured wrongly to Can Bridge.

View Level: opr
Root Cause: 1
Recommended Action(s): "Check the Positioner configuration and ensure that the proper IDD type is configured.
Description: "The system is configured for the older IDD type with the older DSC and a CAN Bridge, but
the software detects the new DSC2. The software should then automatically reconfigure the
system to the new IDD/DSC2. Check the Positioner configuration and ensure that the proper
IDD type is configured.

GE MEDICAL SYSTEMS
3.24 66 XRSubsysMgrMARS
View Level: opr
Root Cause: 0
Description: SubsysMgr MARS reboot failed
6600001 Error Text: User time-out on Restart

View Level: opr
Root Cause: 0
6600002 Error Text: Not connected to System Manager

View Level: opr
Root Cause: 0
Description: Software Error: It cannot connect to System Manager.
Customer Text: X-ray exposures are not possible. Reset the system. Call service if the problem persists.
6600003 Error Text: Time-out waiting for userRestart call from SysMgr
View Level: opr
Root Cause: 0

View Level: opr
Root Cause: 1
Description: Main Power Failure has been detected.

View Level: opr
Root Cause: 1
Description: Main Power Failure has been recovered.
6600006 Error Text: Hospital Main power failure. System Shutdown is in progress.
View Level: opr
Root Cause: 1
Description: Main Power Failure has been detected in boot time. The system will shutdown.
Customer Text: Hospital Main power failure, System shutdown in progress. Please wait...

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 0
Recommended Action(s): Emergency Stop Switch at the table side is triggered. Release it when it is safe
Description: The Emergency Stop Switch at the table side is triggered.
Customer Text: Emergency Stop Switch triggered. Release it.
Minor Function Impacted: no
View Level: opr
Description: Indicates the table side Emergency Stop Switch is released. For debug purpose only.
Customer Text: Emergency Stop Switch at released position (Power is ON)

View Level: opr
Root Cause: 1
Description: CAN bridge initialization failed. Possible errors in CAN-RS422 communication. Possible Boot
problem. May indicate a CAN device or bus problem. Refer to the CAN bus block diagram.
connections.
- If multiple devices are reporting errors, check common cabling/connections and common
nodes in the Pos Cab.
View Level: opr
Root Cause: 1
Recommended Action(s): Check CAN bridge connection, or reset the system
Description: CAN bridge is not sending the heartbeat messages. Indicates a CAN device or bus problem.
Refer to the CAN bus block diagram.
connections.

View Level: opr
Root Cause: 1
Description: Software error: failure in IddDevice constructor.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: IddDevice initialization failed.

View Level: opr
Root Cause: 1
Description: IDD Power Assist Vertical CAN amp initialization failed or is not responding. Indicates a CAN
device or bus problem. Refer to the CAN bus block diagram.
connections.

View Level: opr
Root Cause: 1
Description: IDD vertical motion control error.
persists.

View Level: opr
Root Cause: 1
Description: IDD Power Assist Longitudinal CAN amp initialization failed or is not responding. Indicates a
connections.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: IDD longitudinal motion control error.
persists.

View Level: opr
Root Cause: 1
Description: IDD positioning error. No SID feedback.

View Level: opr
Root Cause: 1
Description: IDD console is not responding. The IDD console communications go through the CAN-RS422
bridge. Possibly a problem with the IDD console or cabling from the bridge out to the IDD
console. Possibly indicates a CAN device or bus problem. Refer to the CAN bus block
diagram.
connections.

View Level: opr
Root Cause: 1
Description: IDD grid/cone controller (goldbox) is not responding. The IDD grid/cone controller (gold box)
indicates a CAN device or bus problem. Refer to the CAN bus block diagram.
connections.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: Software error: failure in RfTableDevice constructor.

View Level: opr
Root Cause: 1
Description: RfTableDevice initialization failure.

View Level: opr
Root Cause: 1
Description: Table angulation control error.

View Level: opr
Root Cause: 1
Description: Table positioning error.
6608017 Error Text: PDU IO Alive Time-out

View Level: opr
Root Cause: 1
connections.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
connections.

View Level: opr
Root Cause: 1
Description: PDU I/O device is not responding. Indicates a CAN device or bus problem. Refer to the CAN
bus block diagram.
connections.
View Level: opr
Root Cause: 1
Description: Software error: failure in IOAdapter constructor.

View Level: opr
Root Cause: 1
Description: POS cabinet IO initialization failure.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: POS cabinet IO is not responding. Indicates a CAN device or bus problem. Refer to the CAN
bus block diagram.
connections.

View Level: opr
Root Cause: 1
Description: OTS Device Constructor Failed

View Level: opr
Root Cause: 1
Description: OTS Device Initialization Failed. Possible boot problem. May indicate a CAN device or bus
connections.

View Level: opr
Root Cause: 1
Description: OTS Register Call Back error.
View Level: opr
Root Cause: 1
Description: OTS wrong call back data type error.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: OTS motion control error.

View Level: opr
Root Cause: 1
Description: OTS positioning error.

View Level: opr
Root Cause: 1
Description: OTS locks control error. This error may occur during a hospital 480 VAC mains power failure,
and should not be cause for alarm. If you see this error immediately following an error
6600004:”A power failure has occurred.”, then please ignore it.

View Level: opr
Root Cause: 1
Description: OTS 30 VAC error. This error may occur during a hospital 480 VAC mains power failure, and
should not be cause for alarm. If you see this error immediately following an error 6600004:”A
power failure has occurred.”, then please ignore it.

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: OTS 24 VDC lock logic error.

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
Description: OTS IO CAN warning limit error.
View Level: opr
Root Cause: 1
Description: OTS IO CAN overrun error.

View Level: opr
Root Cause: 1
Description: OTS IO is not responding. Indicates a CAN device or bus problem. Refer to the CAN bus
block diagram.
connections.

GE MEDICAL SYSTEMS
6609017 Error Text: OTS IO receiving buffer overrun error
View Level: opr
Root Cause: 1
Description: OTS IO receiving buffer overrun error

View Level: opr
Root Cause: 1
Description: OTS Amplifier is not responding. Indicates a CAN device or bus problem. Refer to the CAN
bus block diagram.
connections.

View Level: opr
Root Cause: 1
Description: OTS amplifier over voltage error.

View Level: opr
Root Cause: 1
Description: OTS amplifier under voltage error.
View Level: opr
Root Cause: 1
Description: OTS amplifier over current error.

View Level: opr
Root Cause: 1
Description: OTS amplifier over temperature error.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: OTS amplifier over load error.

View Level: opr
Root Cause: 1
Description: OTS amplifier over speed error.

View Level: opr
Root Cause: 1
Description: OTS amplifier over position error.

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
Description: OTS amplifier velocity following error.
View Level: opr
Root Cause: 1
Description: OTS amplifier motor over temperature error.

View Level: opr
Root Cause: 1
Description: OTS amplifier encoder error.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: OTS amplifier auxiliary encoder error.

View Level: opr
Root Cause: 1
Description: OTS amplifier warning.
6609032 Error Text: OTS amplifier fault.
View Level: opr
Root Cause: 1
Description: OTS amplifier fault.
6609033 Error Text: OTS amplifier fatal error.

View Level: opr
Root Cause: 1
Description: OTS amplifier fatal error.

View Level: opr
Root Cause: 1
Description: OTS amplifier homing error.
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
Description: OTS longitudinal pot failure.

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Description: OTS lateral pot failure.

View Level: opr
Root Cause: 1
Description: OTS vertical pot failure.

GE MEDICAL SYSTEMS
3.25 80 XRDigitalProxy
View Level: opr
Root Cause: 1
controller.
controller.

View Level: opr
Root Cause: 1
controller.
controller.

View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
8000005 Error Text: Failed to read the Digital Proxy config file.
View Level: opr
Root Cause: 1
controller.
controller.
8000006 Error Text: Digital Proxy failed to startup.

View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
8000008 Error Text: publish event failed for these events.

View Level: opr
Root Cause: 1
View Level: opr
Root Cause: 1

View Level: opr
Root Cause: 1
8000011 Error Text: The actor is not a hybrid actor.
View Level: opr
Root Cause: 1
8000012 Error Text: Lost connections with Hybrid actors.

View Level: opr
Root Cause: 1
Recommended Action(s): Connection to System Controller Lost. Refer to Precision Diagnostic Manual and run Ethernet
Diagnostic.
Diagnostic.
8000013 Error Text: Digital Proxy not connected to all the actors.
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
8000014 Error Text: Proxy Library failed to register the message and message handler.
View Level: opr
Root Cause: 1
8000015 Error Text: Proxy Library failed to deliver the packet to server.
View Level: opr
Root Cause: 1
Recommended Action(s): Connection to System Controller lost. Refer to Precision Diagnostic Manual and run Ethernet
Diagnostic.
Diagnostic.
8000016 Error Text: Failed to connect to the other system.

View Level: opr
Root Cause: 1
Recommended Action(s): Connection to System Controller or Digital Subsystem lost. Refer to Precision Diagnostic
Description: Connection to System Controller or Digital Subsystem lost. Refer to Precision Diagnostic

View Level: opr
Root Cause: 1
8000018 Error Text: Null InputHandler pointer

View Level: opr
Root Cause: 1
8000019 Error Text: Failed to close the socket.

View Level: opr
Root Cause: 1
Recommended Action(s): Cannot close the connection to System Controller or Digital Subsystem. Refer to Precision
Description: Cannot close the connection to System Controller or Digital Subsystem. Refer to Precision

GE MEDICAL SYSTEMS
View Level: opr
Root Cause: 1
Recommended Action(s): Failed to accept the connection request by the System Controller or Digital Subsystem. Refer
Description: Failed to accept the connection request by the System Controller or Digital Subsystem. Refer
8000021 Error Text: Failed to open the socket.
View Level: opr
Root Cause: 1
Recommended Action(s): Failed to open the connection by the System Controller or Digital Subsystem. Refer to
Description: Failed to open the connection by the System Controller or Digital Subsystem. Refer to
8000022 Error Text: Peer closed the socket connection, system has to be reset
View Level: opr
Root Cause: 1
Recommended Action(s): Note that the reporting of this error is an expected part of a normal system shutdown process.
Connection to the Digital System was closed by the Digital Subsystem. Reset the system.
Description: Connection to the Digital System was close by the Digital Subsystem. Reset the system.
View Level: opr
Root Cause: 1
Recommended Action(s): System Controller received corrupted message. Reset the system. Refer to Precision
Description: System Controller received corrupted message. Reset the system. Refer to Precision

View Level: opr
Root Cause: 1
Recommended Action(s): System Controller did not receive the correct data length. Reset the system. Refer to
Description: System Controller did not receive the correct data length. Reset the system. Refer to
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
8000026 Error Text: Failed to create the PeerActorsInfo Class
View Level: opr
Root Cause: 1

GE MEDICAL SYSTEMS
3.26 90 XRUserIFVenus
9000001 Error Text: Actor Configuration file does not exist.
Minor Function Impacted: STARTUP
View Level: opr
Root Cause: 1
Recommended Action(s): "Please make sure the following:Actor cofiguration file present in the XRUserIfVenus.cfg and
IUI_CONFIG_DIR enviroment is not set.
Description: "The userinterface actor's configuration file does not exist or the environment variable
IUI_CONFIG_DIR is not set to the directory path containing the configuration file.
9000002 Error Text: SubSystemMgr not requested for the BOOT in the specified Interval
View Level: opr
Root Cause: 0
Recommended Action(s): "Restart the system if this error repeats. (It not incooperated to in the first IUI release. This
will be part of the design control)
Description: "If the SubSystemManager for VENUS is malfunctioning, and not calling startBootPhase() (It
not incooperated to in the first IUI release. This will be part of the design control)
9000003 Error Text: No request from the subsys manager for start boot phase- Not Alive
View Level: opr
Root Cause: 0
Recommended Action(s): "Restart the system if this error repeats.
Description: "The Subsystem manager is malfunctioning and is not requesting for the BOOT
View Level: opr
Root Cause: 0
Description: "The actor required actor is not responding. The reason could be the actor is down.
View Level: opr
Root Cause: 1
Description: "Communication with another actor failed.

GE MEDICAL SYSTEMS
9000006 Error Text: The start Boot Phase was recieved for an incorrect boot Phase
View Level: opr
Root Cause: 0
Description: "This is because of the incorrect call made by subsysmgr. This will be ignored by
XRUserIfVENUS actor.
9000007 Error Text: The system has not booted

View Level: opr
Root Cause: 1
Recommended Action(s): "Reset and call service engr if problem persists.
Description: "This is because of IUIApp is not able to bootup and connect to system
9000008 Error Text: IUI Config File not found

View Level: opr
Root Cause: 1
Recommended Action(s): "Reset and call service engineer if problem persists. Re-install the software if this problem
repeats
Description: "The IUIConfig.txt file is not found. This file contains Appsetup information
9000009 Error Text: protocol DB file corrupted

View Level: opr
Root Cause: 1
Recommended Action(s): "Please select another protocol - the current protocol File is corrupted
Description: ""Please select another protocol - the current protocol File is corrupted
9000010 Error Text: The IUI config file is corrupted

View Level: opr
Root Cause: 1
Recommended Action(s): "A critical system failure has occurred. Call service.
Description: "ProtocolPath.txt Config File corrupted
9000011 Error Text: No Response from AppDir in the required time interval
View Level: opr
Root Cause: 0
Recommended Action(s): "Select protocols again, Reset if problem persists
Description: "No Response from AppDir in the required time interval

GE MEDICAL SYSTEMS
9000012 Error Text: Unable to Publish event
View Level: opr
Root Cause: 1
Recommended Action(s): "Reset and Call service if problem persists
Description: "Failure in creating events. The Event.cfg file is correpted or Configuration problem
9000013 Error Text: IUI Config File is corrupted.

View Level: opr
Root Cause: 0
Description: "XRUSerIfVenus.cfg file is corrupted correct this file.
9000014 Error Text: OpMode Configuration failed, please try select protocol again.
View Level: opr
Root Cause: 0
Description: "ProtocoData base file corrupted
View Level: opr
Root Cause: 0
View Level: opr
Root Cause: 0
9000017 Error Text: Request failed please try again

View Level: opr
Root Cause: 0
9000018 Error Text: Appsetup cannot proceed because of bad params for Application Initialization.
View Level: opr
Root Cause: 0

GE MEDICAL SYSTEMS
9000020 Error Text: Invalid protocol , Tech values are not proper.
View Level: opr
Root Cause: 0
9000021 Error Text: File RTPPFile not found. Cannot return to previous protocol
View Level: opr
Root Cause: 0
Recommended Action(s): "Start exam and reselect the previous protocols.
Description: "RTPP information file is missing. Cannot return to previous protocol.
Customer Text: Protocol error occurred. Reselect the protocol to continue. Call service if the problem persists.
9000022 Error Text: Protocol Database is changed. Restore old database or close exam
View Level: opr
Root Cause: 0
Recommended Action(s): "Restore previous protocol database
Description: "There protocol database is changed form the previous time system was booted
Customer Text: Protocol Database has been modified. Restore previous database.
9000023 Error Text: Error in detecting RTPP status. Please check if config file is present or not
View Level: opr
Root Cause: 0
Recommended Action(s): "Call service if problem exists next time RTPP is done
Description: "The file which maintains the information about RTPP status is not present
Customer Text: Protocol error occurred. Call service if the problem occurs again.
9000024 Error Text: Error in writing to file RTPPFile.conf

View Level: opr
Root Cause: 0
Description: "Cannot write information to a file which stores RTPP information
9000025 Error Text: Error in reading file RTPPFile.conf

View Level: opr
Root Cause: 0
Description: "Cannot read information to a file which stores RTPP information

GE MEDICAL SYSTEMS
9000026 Error Text: Error in writing RTPP status to config file
View Level: opr
Root Cause: 0
Description: "Error in writing RTPP status
9000027 Error Text: Error in doing RTPP

View Level: opr
Root Cause: 0
Description: "Cannot do RTPP because of internal error
9000028 Error Text: Error getting display Status for tubewarmup

View Level: opr
Root Cause: 0
Recommended Action(s): "Close tubewarmup and start again
Description: "Cannot get the status of Tubewarmup. Internal error. This happ
9000029 Error Text: Error reading all opmodes needing current opmode for exposure
View Level: opr
Root Cause: 0
Description: "All the opmodes for the current tube cannot be found in protocol database. Need to restart
system and check if it happens again
9000030 Error Text: Error getting current opmodes

View Level: opr
Root Cause: 0
Recommended Action(s): "Close exam and start appsetup again
Description: "Currently system is not stable. Appsetup is either not complete or not started. Need to
restart appsetup.
9000031 Error Text: Appsetup not complete. Cannot configure new opmodes
View Level: opr
Root Cause: 0
Description: "Appsetup did not go through. It should be started again after closing exam
Customer Text: An internal communication failure has occurred. Close Exam. Restart Application Setup.

GE MEDICAL SYSTEMS
9000032 Error Text: Invalid or Bad Opmode ID received for Optimization factors Display
View Level: opr
Root Cause: 0
Description: "Bad opmode was reveived for displaying optimization factors. The system is probably
unstable
9000033 Error Text: Invalid or Bad Opmode ID received for Dose Display
View Level: opr
Root Cause: 0
Description: "Bad opmode was reveived for displaying Dose display. The system is probably unstable
9000034 Error Text: Bad Reply received from Athena. Verify athena is functional or not
View Level: opr
Root Cause: 0
Description: "Athena returned a bad return value when sending an acknowledgment for a command sent
by UserIfVenus
9000035 Error Text: System is not ready. Please reboot the system
View Level: opr
Root Cause: 0
Description: "Boot is not complete
9000036 Error Text: IUI is not in Acquire Screen. Only TubeWarmup Exposure can be taken
View Level: opr
Root Cause: 0
Description: "Acquiisiton can be done only from Acquisition screen. Currently we are not in acquire
screen.
Customer Text: Acquisition can only be taken from the Acquisition screen.
9000037 Error Text: IUIApp is sending bad contrast. System is ignoring this
View Level: opr
Root Cause: 0
Description: "Internal error in IUI. Need to restart the exam

GE MEDICAL SYSTEMS
9000038 Error Text: Fluoro is inhibited. Please reset the timer to remove the inhibit condition
View Level: opr
Root Cause: 0
Description: "After 10 mins exposure cannot continue. Timer needs to be reset
Customer Text: Fluoro is inhibited, touch timer reset to continue.
9000039 Error Text: Reading the opmode script file from the disk failed
View Level: opr
Root Cause: 0
Description: "The protocol database is corrupted. Need to try reading again.
Customer Text: Error reading disk. Cannot complete application setup. Reset system. Call service if problem
persists.
9000040 Error Text: Replacing the tags in the scripts failed

View Level: opr
Root Cause: 0
Recommended Action(s): "Close exam and start appsetup again. Call service if problem persists.
Description: "The protocol database is corrupted. Need to try reading again.
Customer Text: Application error occurred. Close Exam. Restart Application Setup.
9000041 Error Text: Cannot handle prep/expose switch

View Level: opr
Root Cause: 0
Recommended Action(s): "Close exam and try again. Call service if problem persists
Description: "Received an event to start exposure but the internal state of UserIf doesn’t permit exposure.
Exam should be close and everthing should be started again
Customer Text: The Expose switches are not enabled yet. Wait a few seconds and try again.
9000042 Error Text: Cannot close exam while in sequence

View Level: opr
Root Cause: 0
Description: "Exam cannot be closed while exposure is going on
9000043 Error Text: Cannot go to review screen

View Level: opr
Root Cause: 0
Description: "Athena returned a failure when we try to go to review screen.

GE MEDICAL SYSTEMS
9000044 Error Text: Cannot come back from review screen
View Level: opr
Root Cause: 0
Recommended Action(s): "Close Exam and start appsetup again
Description: "Athena returned a failure when we try to go out of review screen. This is athena's error
9000045 Error Text: Athena failed to close exam

View Level: opr
Root Cause: 0
Description: "Closing exam failed. Athena status should be checked why this happened. But we can only
reset the system if this persists
9000046 Error Text: Cannot open exam. Athena returned failure

View Level: opr
Root Cause: 0
Description: "Starting an exam failed. Athena status should be checked as to why this happened. The
system should be reset and start exam should be tried again
9000047 Error Text: Cannot add patient. Athena returned failure

View Level: opr
Root Cause: 0
Description: "Adding patient failed. Athena returned a failure
9000048 Error Text: Cannot edit patient. Athena returned failure

View Level: opr
Root Cause: 0
Description: "Edit patient failed. All IUI knows in this case and other Athena communication, is that it failed
or succeeded. The actual status is known only to Athena. So we can only reset and try again.
If it persists we need to call service
9000049 Error Text: Exposures may resume all inhibit conditions resolved.
Minor Function Impacted: INHIBIT
View Level: opr
Root Cause: 0
Recommended Action(s): "Exposures may start as all the inhibit conditions cleared.
Description: "Exposures may start as all the inhibit conditions cleared.
Customer Text: Exposures may be resumed. All error conditions have been corrected.

GE MEDICAL SYSTEMS
9000051 Error Text: The requested mode is not present in the current Protocol.
View Level: opr
Root Cause: 0
Recommended Action(s): "Select a different protocol to get this mode
Customer Text: "This mode is not configured for the current protocol.
9000052 Error Text: RTPP File is corrupted, Cannot return to Previous protocol.
View Level: opr
Root Cause: 0
Recommended Action(s): "Close exam and start a new protocol.
Customer Text: ""Protocol error. Please select the same patient to Continue the Exam
9000053 Error Text: There was an error while create the event.
View Level: opr
Root Cause: 0
Recommended Action(s): "Event creation failed , chack for CFRTS Router or check for Venus.cfg file.Start the process
again.
9000054 Error Text: Invalid Character value

View Level: opr
Root Cause: 0
Recommended Action(s): "Invalid character entered
9000055 Error Text: Error in transitioning to review screen.

View Level: opr
Root Cause: 0
Recommended Action(s): "Ttry again. Call service if problem persists
Description: "Check if boot is complete.Check of athena is responding. In case athena is not responding .
9000056 Error Text: Review option not set.

View Level: opr
Root Cause: 0
Recommended Action(s): "none
Description: "Enablr review option in IUIApp.cfg file.
9000057 Error Text: Cannot change display format.

View Level: opr
Root Cause: 0
Description: "Check if boot is complete.Check of athena is responding. In case athena is not responding
.Close the review screen and open it again.

GE MEDICAL SYSTEMS
9000058 Error Text: Cannot move to next image.
View Level: opr
Root Cause: 0
9000059 Error Text: Cannot move to next screen

View Level: opr
Root Cause: 0
9000060 Error Text: Cannot move to next run.

View Level: opr
Root Cause: 0
9000061 Error Text: Error in playing.

View Level: opr
Root Cause: 0
9000062 Error Text: Error in image tagging.

View Level: opr
Root Cause: 0
9000063 Error Text: Cannot Tag image.

View Level: opr
Root Cause: 0

GE MEDICAL SYSTEMS
9000064 Error Text: Error in filming images.
View Level: opr
Root Cause: 0
9000065 Error Text: Error in printing images.

View Level: opr
Root Cause: 0
9000066 Error Text: Error in changing replay rate.

View Level: opr
Root Cause: 0
9000067 Error Text: Error in changing film format.

View Level: opr
Root Cause: 0
9000068 Error Text: Error in tagging all images.

View Level: opr
Root Cause: 0
9000069 Error Text: Error in untagging all images.

View Level: opr
Root Cause: 0

GE MEDICAL SYSTEMS
9000070 Error Text: Error while opening Serial Port
View Level: opr
Root Cause: 0
Recommended Action(s): "Run Serial port diagnostic. Check/replace dose printer and cable.
Description: "Check if Cabe is connected properly to the COM port
Customer Text: Dose print error. Check cable connection to the COM port.
9000071 Error Text: Error Dose Print Config parameter is set to NULL
View Level: opr
Root Cause: 0
Description: "Check the Actor Config file for the Dose Config Parameter
9000072 Error Text: Could not write to Serial port, Failed to print dose.
View Level: opr
Root Cause: 0
Recommended Action(s): "Run Serial port diagnostic. Check/replace dose printer and cable.
Description: "Check if COM port is working properly , or use some other serial prort to connect Dose
Printer.
Customer Text: Dose print error. Check to see if the serial port is working properly.
9000073 Error Text: Could not add a Category with the same name of the already exsisting Category.
View Level: opr
Root Cause: 0
Recommended Action(s): "Give different Category Name.
Description: "The user tries to add a category with the name of an already existing category
Customer Text: Category name already exists. Create different Category Name.
9000074 Error Text: Could not add a Protocol with the same name of the already exsisting Protocol under the
same Category.
View Level: opr
Root Cause: 0
Recommended Action(s): "Give different Protocol Name.
Description: "The user tries to add a protocol with the name of an already existing protocol under the same
category
Customer Text: Protocol Name already exists. Create different Protocol Name.
9000075 Error Text: Could not add a Exam Step with the same name of the already exsisting Exam Step under
the same Protocol.
View Level: opr
Root Cause: 0
Recommended Action(s): "Give different Exam Step Name.
Description: "The user tries to add an examstep with the name of an already existing examstep under the
same protocol
Customer Text: Exam Step Name already exists. Create different Exam Step Name.

GE MEDICAL SYSTEMS
9000076 Error Text: Could not add more than 12 characters in a Category Name.
View Level: opr
Root Cause: 0
Recommended Action(s): "Add only 12 or less characters in a Category name.
Description: "The user exceeds the maximum allowable length for Category name.
Customer Text: Maximum length allowed. 12 or less characters in Category Name.
9000077 Error Text: Could not add more than 12 characters in a Protocol Name.
View Level: opr
Root Cause: 0
Recommended Action(s): "Add only 12 or less characters in a Protocol name.
Description: "The user exceeds the maximum allowable length for Protocol name.
Customer Text: Maximum length allowed. 12 or less characters in Protocol Name.
9000078 Error Text: Could not add more than 10 characters in a Exam Step Name.
View Level: opr
Root Cause: 0
Recommended Action(s): "Add only 10 or less characters in a Exam Step name.
Description: "The user exceeds the maximum allowable length for Exam Step name.
Customer Text: Maximum length allowed. 10 or less characters in Exam Step Name.
9000079 Error Text: Could not enter invalid characters in the Category name.
View Level: opr
Root Cause: 0
Recommended Action(s): "This is an Invalid Character. Please delete it using back-space .
Description: "The user enters invalid characters in the Category name.
9000080 Error Text: Could not enter invalid characters in the Protocol name.
View Level: opr
Root Cause: 0
Description: "The user enters invalid characters in the Protocol name.
9000081 Error Text: Could not enter invalid characters in the Exam Step name.
View Level: opr
Root Cause: 0
Description: "The user enters invalid characters in the Exam Step name.

GE MEDICAL SYSTEMS
9000082 Error Text: Could not save, since the protocol database size exceeds the space available on the CD
during CD backup.
View Level: opr
Root Cause: 0
Recommended Action(s): "Please insert new CD .
Description: "The protocol database size exceeds the space available on the CD during CD backup.
Customer Text: Protocol database exceeds space available on CD. Insert new CD.
9000083 Error Text: No CD is available in the CD drive during CD backup.

View Level: opr
Root Cause: 0
Recommended Action(s): "Please insert a blank CD.
Description: "No CD is available in the CD drive during CD backup.
Customer Text: CD is not available in drive. Insert blank CD.
9000084 Error Text: No CD is available in the CD drive during CD retrieve.

View Level: opr
Root Cause: 0
Recommended Action(s): "Please insert a CD, containing Protocol Database.
Description: "No CD is available in the CD drive during CD retrieve.
Customer Text: CD is not available in drive. Insert backup CD.
9000085 Error Text: CD does not contain a valid database for retrieval.
View Level: opr
Root Cause: 0
Recommended Action(s): "Please insert a CD with a valid Protocol Database.
Description: ""The CD does not contain a protocol database that can be retrieved for this system. Please
insert a CD with a valid protocol database.
9000086 Error Text: CD already cvontains information while Backup.

View Level: opr
Root Cause: 0
Recommended Action(s): "Please insert an empty CD, while Backup.
Description: "The CD already cvontains information while Backup.
Customer Text: CD is full. Insert blank CD.
9000087 Error Text: Error has occurred in writing Protocol Database, while Retrieve.
View Level: opr
Root Cause: 0
Recommended Action(s): "Reset and Call service if problem persists.
Description: "Error in writing Protocol Database, while Retrieve.
Customer Text: Error occurred restoring Protocol Database. Reset the system. Call Service if problem
persists.

GE MEDICAL SYSTEMS
9000088 Error Text: CD does not contain Protocol Database.
View Level: opr
Root Cause: 0
Recommended Action(s): "Please insert a CD, containing Protocol Database.
Description: "The CD does not contain Protocol Database.
Customer Text: CD does not contain the system's protocol database. Insert CD with valid protocol database.
9000089 Error Text: Save operation failed. Check file permission.

View Level: opr
Root Cause: 0
Recommended Action(s): "Change the file permissions and and try again.
Description: "The permissions for the protocol file or directory may not be right and save operation is failed
due to that.
Customer Text: Changes could not be saved to the database. Retry and call service if problem persists.
9000090 Error Text: SYSTEM IS SHUTING DOWN

View Level: opr
Root Cause: 0
Description: "Add this error message to indicate the system is shuting down. For debug purpose only
9000091 Error Text: System shutdown is in progress.Please wait.

View Level: opr
Root Cause: 0
Description: "Add this error message to indicate the system is shuting down.
Customer Text: System Shutdown is in progress. This may require 2 minutes to complete. Please wait.
9000092 Error Text: Protocol database is corrupted during load operation

View Level: opr
Root Cause: 0
Recommended Action(s): "Replace protocol database which can be done through protocol retreive.
Description: "Protocol database is corrupted during load operation
9000093 Error Text: Protocol database validation failed during retrieve

View Level: opr
Root Cause: 0
Recommended Action(s): "Replace old protocol protocol database and revert back to previous system configuration
and reset the system.
Description: "Protocol database validation failed during retrieve

GE MEDICAL SYSTEMS
9000094 Error Text: Protocol database validation failed during system validation
View Level: opr
Root Cause: 0
Recommended Action(s): "Restore a valid protocol database to continue
Description: "Protocol database validation failed during system validation
9000095 Error Text: Invalid Login User type

View Level: opr
Root Cause: 0
Recommended Action(s): "Logout and try login with one of these types, Administrator, Technician or Service
Description: "Invalid Login User type
Customer Text: User login has failed. Log out and try again.
9000096 Error Text: accessing config parameters through config cache failed
View Level: opr
Root Cause: 0
Recommended Action(s): "Reset the system and try again.
Description: "Getting Configuration parameters from ConfigCache failed
9000097 Error Text: Invalid Config Parameter set in config file

View Level: opr
Root Cause: 0
Recommended Action(s): "Restore a valid system configuration.
Description: "If any of configuration parameter is set to junk value , then default values will be used , to set
that config parametr reset the system
9000098 Error Text: IUIApp fails to receive Config paranmeters from XRUserIfVenus actor
View Level: opr
Root Cause: 0
Recommended Action(s): "Reset the system. Call service if problem persists.
Description: "As Java application is not able to get parameters from actor , all the default params will be
used to bring up IUI Screens
Customer Text: System configuration error. Reset and call service if the problem persists.
9000099 Error Text: The environment variable CDRW_COMMAND is not set for backup operation
View Level: opr
Root Cause: 0
Recommended Action(s): "Call service to reconfigure the system to allow backup operation
Description: "Environment variable CDRW_COMMAND is not set
Customer Text: Protocol database backup operation has failed. Call service.

GE MEDICAL SYSTEMS
9000100 Error Text: The environment variable CDRW_COMMAND is not set for retrieve operation
View Level: opr
Root Cause: 0
Recommended Action(s): "Call service to reconfigure the system to allow retreive operation
Description: "Environment variable CDRW_COMMAND is not set
9000101 Error Text: ACE Process cannot be created

View Level: opr
Root Cause: 0
Recommended Action(s): "ACE process cannot be created. Reset the system and call service if problem persists.
Description: "ACE Process cannot be created
9000102 Error Text: The mkisofs utility is not installed

View Level: opr
Root Cause: 0
Description: "The mkisofs utility is not installed
9000103 Error Text: The cdrecord utility is not installed

View Level: opr
Root Cause: 0
Description: "The cdrecord utility is not installed
9000104 Error Text: The cdrecord.conf file does not exist

View Level: opr
Root Cause: 0
Recommended Action(s): "Call service to reconfigure the system to allow backup & retrieve operation
Description: "The cdrecord.conf file does not exist
9000105 Error Text: The cdrecord.conf file has errors

View Level: opr
Root Cause: 0
Recommended Action(s): "Call service to reconfigure the system to allow backup and retrieveoperation
Description: "The cdrecord .conf file may have spaces instead of tabs

GE MEDICAL SYSTEMS
9000106 Error Text: A hardware configuration error has been detected
View Level: opr
Root Cause: 0
Recommended Action(s): "Check the hardware configuration for CDWriter
Description: "A hardware configuration error has been detected for the CDWriter
9000107 Error Text: No drivers are installed for the CDWriter

View Level: opr
Root Cause: 0
Recommended Action(s): "Install the drivers for CDWriter
Description: "No drivers are installed for the CDWriter
9000108 Error Text: Insufficient space on the local disk while retrieve
View Level: opr
Root Cause: 0
Recommended Action(s): "Free some disk space on the local venus disk
Description: "The local venus disk has insufficient space to hold the retrieved protocol databas
Customer Text: There is insufficient space to hold the retrieved information. Call service.
9000109 Error Text: The system does not support multisession CD write operation
View Level: opr
Root Cause: 0
Recommended Action(s): "Use a blank CD tobackup the protocol database
Description: "Protocol database cannot be backed into an already burnt CD as the system does not
support multisession CD write operation
Customer Text: The CD has already been used for backup. Use a blank CD.
9000110 Error Text: CDWriter cannot be mounted due to no mount permissions

View Level: opr
Root Cause: 0
Recommended Action(s): "Call service to insall the CD writer
Description: "The user currently logged in does not have mount permissions for the CDWriter
9000111 Error Text: Error in mounting the CDWriter

View Level: opr
Root Cause: 0
Recommended Action(s): "Call service to insall the CD writer
Description: "The CDWriter cannot be mounted

GE MEDICAL SYSTEMS
9000112 Error Text: Target specified for retrieve operation not found
View Level: opr
Root Cause: 0
Recommended Action(s): "Call service to configure the system properly for retrieve operation
Description: "Target specified for retrieve operation not found
9000113 Error Text: Backup operation successful

View Level: opr
Root Cause: 0
Recommended Action(s): "Backup operation successful
Description: "Backup operation successful
Customer Text: The protocol database backup operation is successful.
9000114 Error Text: Retrieve operation successful

View Level: opr
Root Cause: 0
Recommended Action(s): "Retrieve operation successful
Description: "Retrieve operation successful
Customer Text: The protocol database retrieve operation is successful.
9000115 Error Text: Cannot change Application Mode from online review screen
View Level: opr
Root Cause: 0
Recommended Action(s): "Go to acquisition screen and change application mode.
Description: "When user has moved to online review screen and he tries to change application mode
(presses digital on IDD for eg) he shouldn’t be allowed to do it
Customer Text: Application mode changes are not allowed when in the View/Film screen.
9000116 Error Text: Saving Changes To Protocol Database

View Level: opr
Root Cause: 0
Recommended Action(s): "Protocol Database Save In Progress, Please Wait
Description: "The changes made are being saved to the protocol database. User has to wait for the
changes to get committed, before any other operation can be done
Customer Text: Saving changes to the Protocol Database. Please wait.
9000117 Error Text: Validating Protocol Database

View Level: opr
Root Cause: 0
Recommended Action(s): "Wait until the protocol database validation is completed, then continue.
Description: "Occurs after a system reset when the system configuration has changed; the protocol
database must be validated against the system configuration. For example, if wallstand is

GE MEDICAL SYSTEMS
deconfigured, then all wallstand exam steps are deleted. User has to wait before any other
operation can be done
Customer Text: Protocol Database validation is in progress. It may take up to 20 sec to complete
9000118 Error Text: System is Ready

Minor Function Impacted: SYSTEM_BOOT
View Level: opr
Root Cause: 0
Recommended Action(s): "System is ready to use , can select patient to start appsetup
Description: "This message is displayed when , protocol validation, login and system boot is complete and
screen is enabled on IUI.
Customer Text: The system is ready for user input.
9000119 Error Text: Invalid Object Reference.

Minor Function Impacted: SYSTEM
View Level: opr
Root Cause: 0
Description: ""Software Error. Some of the system actors ( software component) failed to establish the
communication.
9000120 Error Text: System failed to complete boot

View Level: opr
Root Cause: 0
Description: "System did not complete boot in the allocated time. Check system error log for other boot
related errors.
View Level: opr
Root Cause: 0
Recommended Action(s): "The current user is not authorized to perform this function. The user must logout and re-login
Description: "The current user is not authorized to perform this function. The user must logout and re-login
9000122 Error Text: Read data from archive media failure

Minor Function Impacted: ARCHIVE
View Level: opr
Root Cause: 0
Recommended Action(s): "1. Check the diskette. \ 2. Check diskette driver cable connetion \ 3. Replace diskette driver.
Description: "Failure to read data from archive media.
Customer Text: Read from archive media error. Retry or try another diskette. Call service if the error persists.

GE MEDICAL SYSTEMS
9000123 Error Text: Write data to archive media failure
View Level: opr
Root Cause: 0
Recommended Action(s): "1. Check the diskette. \ 2. Check diskette driver calble connetion \ 3. Replace diskette driver.
Description: "Failure to write data to archive media.
Customer Text: Write to archive media error. Retry or insert a new diskette. Call service if the error persists.
9000124 Error Text: Archive media unavailable

View Level: opr
Root Cause: 0
Recommended Action(s): "1. Check system diskette driver configration. \ 2. Check diskette driver connection. \ 3.
Replace diskette driver.
Description: "The error message displays if the destination archive media is unavailable.
Customer Text: The archive media is unavailable. Check diskette driver connection or call service.
9000125 Error Text: Not Find SID Config File

View Level: opr
Root Cause: 0
Recommended Action(s): "1. Check the SID config file directory. \ 2. Check the SID config file present in the directory.
Description: "In manual collimation mode, operator can select SID value based on the SID config file
created during installation. The error generates if system could not find the file.
Customer Text: The system could not locate the SID config file. Please make sure the file present.
9000126 Error Text: Open SID Config File Failed

View Level: opr
Root Cause: 0
Recommended Action(s): "1. Check the SID config file corrupted. \ 2. Check SID value loading procudure.
Description: "In manual collimation mode, operator can select SID value from the SID config file created
during installation. The error generates if the system could not open the config file.
Customer Text: "The system could not open the SID config file. The current File is possible corrupted. Try
again or call service.

GE MEDICAL SYSTEMS
3.27 Inhibit Conditions
0 SYSTEM_NOT_CONFIGURED System is not configured for any System is not configured. Select protocol to
opmode. continue.
1 DISK_FULL The disk is full. Free up disk space to continue.
2 NEW_EXAM There is no Exam Open. To start Start a new exam.
Acquisition , first need to start a Exam
3 TW_SOAK_TIME After TW, for next 30 exposure should Tube is warming. Please wait.
not be allowed.
4 FLUORO_TIMER Maximum fluoro time reached. Touch Maximum fluoro time reached. Touch timer
timer reset to continue reset to continue.
5 CDRH_CONTROL Collimator error. If problem persists reset
system.
6 HEAT_UNIT_LIMIT_REACHED Heat units exceeded. Tube is cooling. Please
wait.
7 ROOM_DOOR_OPEN Room door is open. Close door to continue.
8 EMERGENCY_SWITCH_TRIPPED This is the tableside emergency stop Emergency switch is tripped. Reset switch and
switch. system to continue.
9 SID_OUT_OF_RANGE Source to image distance out of range. Adjust
tube position.
10 NOT_IN_LATERAL_DETENT Align the overhead xray tube to the image
receptor.
11 TUBE_PIVOT Pivot the overhead xray tube arm to the image
receptor.
12 TUBE_ANGLE_OUT_OF_RANGE Rotate the overhead xray tube to the image
receptor.
13 CASSETTE_NOT_IN_PLACE Insert cassette to continue.
14 TABLE_CASSETTE_INSERTED Remove table cassette to continue.
15 WALLSTAND_CASSETTE_INSERTED Remove wall cassette to continue.
16 SFD_NOT_IN_EXPOSE_POSITION Lock imaging device in forward position.
17 SFD_NOT_IN_PARK_POSITION Move imaging device to park position.
18 COLL_NOT_ALIVE System error. Reset system. (Coll)
19 COLL_MALFUNCTION System error. Reset system. (Coll)
20 BAD_IDD_SID_POT System error. Reset system. (IDD SID)
21 PDU_IO_NOT_ALIVE The PDU I/O is located in the Systems System error. Reset system. (PDU IO)
Cabinet.
22 POS_IO_NOT_ALIVE The Pos I/O is located in the Positioner System error. Reset system. (Pos IO)
Cabinet.
23 DIGITAL_NOT_READY IUI/Digital are in image review mode. Fluoro and Digital Record not ready. Please
wait.
24 NOT_IN_ACQ_SCREEN Only from Acquire screen, exposure is Enter the Acquire mode to continue.
allowed.
25 FLUORO_LOOP_STORE Xrays are not allowed during loop storage.
26 RUN_LIMIT_REACHED Series limit reached. Start new exam to
continue.
27 DIGITAL_IS_BUSY Enter the Acquire mode to continue.
28 IUI_NOT_IN_ACQUIRE_SCREEN Only from Acquire screen, exposure is Enter the Acquire mode to continue.
allowed.
29 BACKUP_TIME_REACHED AEC backup time has reached. To AEC Backup time reached. Reselect technique
continue the exposure ,Reset msec.
30 TECHNIQUES_REJECTED Select another technique to continue.
31 CASSETTE_SIZE_NOT_DETERMINED Remove and replace cassette.
Table 5-1 Inhibit Conditions

GE MEDICAL SYSTEMS
32 IDD_GOLDBOX_NOT_ALIVE Goldbox /DSC2 is the grid/cone System error. Reset system. (Grid Cone Device)
controller mounted inside rear of IDD.
33 CAN_BRIDGE_NOT_ALIVE "CAN bridge is in Positioner cabinet, it is "System error. Reset system. (Can Bridge)
the CAN interface to the IDD Goldbox
and IDD console. CanCore is a can-
open device mounted inside the rear of
IDD.
34 OTS_UIF_NOT_ALIVE OTS UIF is the control console on the System error. Reset system. (OTS UIF)
OTS.
35 OTS_AMP_NOT_ALIVE Either the CAN Amp or OTS I/O on the System error. Reset system. (OTS Pos Dev)
OTS. Note, for the VCP OTS introduced
at M5, the CAN amp is no longer
present.
36 BAD_OTS_LONG_POT The longitudinal position feedback pot System error. Reset system. (OTS Long Pot)
on the OTS.
37 BAD_OTS_LAT_POT The lateral position feedback pot on the System error. Reset system. (OTS Lat Pot)
OTS.
38 BAD_OTS_VERT_POT The vertical position feedback pot on the System error. Reset system. (OTS Vert Pot)
OTS.
39 ANODE_HEAT_LIMIT_REACHED Xray tube overheat. Wait and continue.
40 CASING_HEAT_LIMIT_REACHED Xray tube overheat. Wait and continue.
41 TRACK_LIMIT_REACHED Xray tube track limit. Wait or reduce technic.
42 JEDI_UNRECOVERABLE_ERROR Generator error. Reset system and try again.
43 TUBE_SWITCH_IN_PROGRESS Tube switch in progress. Exposure is Exposures disabled due to tube switch, please
inhibited wait
44 MAIN_POWER_FAILURE
45 BAD_OTS_ANGLE_POT OTS Tube Angle feedback is bad. System error. Reset system. (OTS Ang Pot)
46 BAD_TABLE_VERT_POT Table Vertical feedback is bad. System error. Reset system. (Table Vert Pot)
47 BAD_WS_HEIGHT_POT Wallstand Height feedback is bad. System error. Reset system. (WS Height Pot)
48 BAD_WS_ANGLE_POT Wallstand Angle feedback is bad. System error. Reset system. (WS Angle Pot)
49 TABLE_RECEPTOR_POSITION Table Receptor is not in position. Table Receptor is not in position.
50 WS_TILT_POSITION WS Tilt is not in position. WS Tilt is out of range. Reposition or switch to
override.
51 GRID_NOT_POSITION Grid is not in position. Grid Position Error.
52 QAP_PHANTOM_INSERTED QAP phantom is inserted. QAP phantom is inserted.
53 COLLIMATOR_ROTATED Collimator is rotated. Collimator rotation does not match technique
setup.
54 FOV_OUTSIDE_DETECTOR Field of View is outside detector. FOV is outside detector.
55 AEC_INTERLOCK
56 TUBE_NOT_CENTER Tube is not centered. Tube is not centered.

57 AEC_CAL_TECHNIQUES_NOT_SET
58 TUBE_DETECTOR_OVERLAP Tube and Detector overlapping in Tube and Detector overlap. Move detector
Warmup mode. away.
59 TUBE_NOT_IN_0_DEGREE Tube is not at 0 deg in Warmup mode. Tube is not at 0 deg.
60 IN_OVERRIDE_MODE Override switch is on. In Override mode.
61 WS_NOT_IN_0_DEGREE WS is not at 0 deg in Warmup mode. WS is not at 0 deg.
62 DUMMY_ID_1
63 DUMMY_ID_2
64 DUMMY_ID_3
65 WAIT_FOR_RAW_IMAGE
Table 5-1 Inhibit Conditions

GE MEDICAL SYSTEMS
3.28 IDD Advisory Messages
# MESSAGE ID CUSTOMER TEXT

0 PATIENT_STEP_INHIBIT Patient step is not, parked. Push in prior, to tilting table.
1 CONE_MOTION_INHIBIT Cone transfer not, allowed when horizontal, stop is off.
2 TABLE_ANGULATION_WARNING Table angulating-Watch, patient and beware of, obstructions in room.
3 TABLE_TOP_MOTION_WARNING Tabletop moving -, Watch patient.
4 CONFLICTING_MOTION_COMMANDS Motion stopped -, Use only one control.
5 CONE_TABLE_TOP_INTERLOCK Powered motion not, allowed when cone in, and comp lock on.
6 FL_LOOP_STORE_IN_PROGRESS Xrays are not allowed, during loop storage.
7 FL_LOOP_FAIL_IMAGE_STORE Fluoro Loop not allowed, during image transfer., Please wait.
8 FL_LOOP_FAIL_DIGITAL_ERROR Cannot acquire Fluoro, Loop. Try again.
9 ROADMAP_FUNCTION_INHIBIT Selection, is not allowed, with Roadmap on.
10 ROADMAP_INHIBIT Roadmap is not allowed, with Fluoro Loop on.
11 IDD_CALIBRATION_INSTRUCTIONS
12 LOW_PRI_ADVISORY_TEXT
13 MED_PRI_ADVISORY_TEXT
14 HI_PRI_ADVISORY_TEXT
Table 5-2 IDD Advisory Messages

GE MEDICAL SYSTEMS
3.29 DeviceComm
6663001 EM_INVALID_PARAM Debug SysCntr DeviceComm opr 0 Ignore "EM_INVALID_PARAM EM_INVALID_PARAM
Only l
6663002 EM_CAN_CONSTRUCTOR_MSG Debug SysCntr DeviceComm opr 0 Ignore "EM_CAN_CONSTRUCTOR_MS EM_CAN_CONSTRUCTOR_MSG_
_Q_CREATION_FAILED Only l G_Q_CREATION_FAILED Q_CREATION_FAILED

LED_TO_CREATE_RXSTART_ Only l ILED_TO_CREATE_RXSTART ED_TO_CREATE_RXSTART_TA
TASK_SEMAPHORE _TASK_SEMAPHORE SK_SEMAPHORE

LED_TO_CREATE_RXSEMID_ Only l ILED_TO_CREATE_RXSEMID ED_TO_CREATE_RXSEMID_SE

LED_TO_CREATE_TXSEMID_ Only l ILED_TO_CREATE_TXSEMID ED_TO_CREATE_TXSEMID_SE

LED_TO_CREATE_CAN_TX_T Only l ILED_TO_CREATE_CAN_TX_ ED_TO_CREATE_CAN_TX_TAS
ASK TASK K

STER_SEM_TAKE_FAILED Only l ESTER_SEM_TAKE_FAILED TER_SEM_TAKE_FAILED

STER_NO_RECEIVERS Only l ESTER_NO_RECEIVERS TER_NO_RECEIVERS

STER_ID_NOT_REGISTERED Only l ESTER_ID_NOT_REGISTERE TER_ID_NOT_REGISTERED
D

STER_SEM_GIVE_FAILED Only l ESTER_SEM_GIVE_FAILED TER_SEM_GIVE_FAILED
6663011 EM_CAN_ADD_ID_SEM_TAKE Debug SysCntr CanComm opr 0 Ignore "EM_CAN_ADD_ID_SEM_TAK EM_CAN_ADD_ID_SEM_TAKE_

_FAILED Only l E_FAILED FAILED
6663012 EM_CAN_ADD_ID_RXTASK_S Debug SysCntr CanComm opr 0 Ignore "EM_CAN_ADD_ID_RXTASK_ EM_CAN_ADD_ID_RXTASK_SP

PAWN_FAILED Only l SPAWN_FAILED AWN_FAILED
6663013 EM_CAN_ADD_ID_ADDING_D Debug SysCntr CanComm opr 0 Ignore "EM_CAN_ADD_ID_ADDING_ EM_CAN_ADD_ID_ADDING_DE

EVICE_FAILED Only l DEVICE_FAILED VICE_FAILED
6663014 EM_CAN_ADD_ID_ID_LIST_ Debug SysCntr CanComm opr 0 Ignore "EM_CAN_ADD_ID_ID_LIST EM_CAN_ADD_ID_ID_LIST_E

EXCEEDS_LIMIT Only l _EXCEEDS_LIMIT XCEEDS_LIMIT
6663015 EM_CAN_ADD_ID_ID_DUPLI Debug SysCntr CanComm opr 0 Ignore "EM_CAN_ADD_ID_ID_DUPL EM_CAN_ADD_ID_ID_DUPLIC

CATION Only l ICATION ATION
6663016 EM_CAN_ADD_ID_MSGQ_CRE Debug SysCntr CanComm opr 0 Ignore "EM_CAN_ADD_ID_MSGQ_CR EM_CAN_ADD_ID_MSGQ_CREA

ATE_FAILED Only l EATE_FAILED TE_FAILED
6663017 EM_CAN_ADD_ID_CANIFTAS Debug SysCntr CanComm opr 0 Ignore "EM_CAN_ADD_ID_CANIFTA EM_CAN_ADD_ID_CANIFTASK

K_SPAWN_FAILED Only l SK_SPAWN_FAILED _SPAWN_FAILED
6663018 EM_CAN_ADD_ID_RXSTARTT Debug SysCntr CanComm opr 0 Ignore "EM_CAN_ADD_ID_RXSTART EM_CAN_ADD_ID_RXSTARTTA

ASKSEM_GIVE_FAILED Only l TASKSEM_GIVE_FAILED SKSEM_GIVE_FAILED
6663019 EM_CAN_ADD_ID_RXSEM_GI Debug SysCntr CanComm opr 0 Ignore "EM_CAN_ADD_ID_RXSEM_G EM_CAN_ADD_ID_RXSEM_GIV

VE_FAILED Only l IVE_FAILED E_FAILED
6663020 EM_CAN_CANTXTASK_READ_ Debug SysCntr CanComm opr 0 Ignore "EM_CAN_CANTXTASK_READ EM_CAN_CANTXTASK_READ_F

FROM_MSGQ_FAILED Only l _FROM_MSGQ_FAILED ROM_MSGQ_FAILED
6663021 EM_CAN_CANRXTASK_SEM_T Debug SysCntr CanComm opr 0 Ignore "EM_CAN_CANRXTASK_SEM_ EM_CAN_CANRXTASK_SEM_TA

AKE_FAILED Only l TAKE_FAILED KE_FAILED
6663022 EM_CAN_CANRXTASK_SEM_G Debug SysCntr CanComm opr 0 Ignore "EM_CAN_CANRXTASK_SEM_ EM_CAN_CANRXTASK_SEM_GI

IVE_FAILED Only l GIVE_FAILED VE_FAILED
6663023 EM_CAN_CANRXTASK_MEM_A Debug SysCntr CanComm opr 0 Ignore "EM_CAN_CANRXTASK_MEM_ EM_CAN_CANRXTASK_MEM_AL

LLOC_FAILED Only l ALLOC_FAILED LOC_FAILED
6663024 EM_CAN_CANRXTASK_SEND_ Debug SysCntr CanComm opr 0 Ignore "EM_CAN_CANRXTASK_SEND EM_CAN_CANRXTASK_SEND_T

TO_MSGQ_FAILED Only l _TO_MSGQ_FAILED O_MSGQ_FAILED
6663025 EM_CAN_CANIFTASK_READ_ Debug SysCntr CanComm opr 0 Ignore "EM_CAN_CANIFTASK_READ EM_CAN_CANIFTASK_READ_F

FROM_MSG_Q_FAILED Only l _FROM_MSG_Q_FAILED ROM_MSG_Q_FAILED
6663026 EM_CAN_WRITE_MEM_ALLOC Debug SysCntr CanComm opr 0 Ignore "EM_CAN_WRITE_MEM_ALLO EM_CAN_WRITE_MEM_ALLOC_

_FAILED Only l C_FAILED FAILED
6663027 EM_CAN_WRITE_SEND_TO_M Debug SysCntr CanComm opr 0 Ignore "EM_CAN_WRITE_SEND_TO_ EM_CAN_WRITE_SEND_TO_MS

SG_Q_FAILED Only l MSG_Q_FAILED G_Q_FAILED
6663028 EM_CAN_RX_TIMEDOUT Debug SysCntr CanComm opr 0 Ignore "EM_CAN_RX_TIMEDOUT EM_CAN_RX_TIMEDOUT

Only l

GE MEDICAL SYSTEMS
6663029 EM_CAN_TX_TIMEDOUT Debug SysCntr CanComm opr 0 Ignore "EM_CAN_TX_TIMEDOUT EM_CAN_TX_TIMEDOUT
Only l
6663030 EM_CAN_TX_ERROR Debug SysCntr CanComm opr 0 Ignore "EM_CAN_TX_ERROR EM_CAN_TX_ERROR
Only l
6663031 EM_CAN_CONTR_OFF_BUS Debug SysCntr CanComm opr 0 Ignore "EM_CAN_CONTR_OFF_BUS EM_CAN_CONTR_OFF_BUS
Only l
6663032 EM_CAN_CONTR_BUSY Debug SysCntr CanComm opr 0 Ignore "EM_CAN_CONTR_BUSY EM_CAN_CONTR_BUSY
Only l
6663033 EM_CAN_CONTR_WARN Debug SysCntr CanComm opr 0 Ignore "EM_CAN_CONTR_WARN EM_CAN_CONTR_WARN
Only l
6663034 EM_CAN_NO_ID_ENABLED Debug SysCntr CanComm opr 0 Ignore "EM_CAN_NO_ID_ENABLED EM_CAN_NO_ID_ENABLED
Only l
6663035 EM_CAN_ID_ALREADY_ENAB Debug SysCntr CanComm opr 0 Ignore "EM_CAN_ID_ALREADY_ENA EM_CAN_ID_ALREADY_ENABL
LED Only l BLED ED
6663036 EM_CAN_ID_NOT_ENABLED Debug SysCntr CanComm opr 0 Ignore "EM_CAN_ID_NOT_ENABLED EM_CAN_ID_NOT_ENABLED

Only l
6663037 EM_CAN_INVALID_FIRMWAR Debug SysCntr CanComm opr 0 Ignore "EM_CAN_INVALID_FIRMWA EM_CAN_INVALID_FIRMWARE
E Only l RE
6663038 EM_CAN_MESSAGE_LOST Debug SysCntr CanComm opr 0 Ignore "EM_CAN_MESSAGE_LOST EM_CAN_MESSAGE_LOST

Only l
6663039 EM_CAN_INVALID_HARDWAR Debug SysCntr CanComm opr 0 Ignore "EM_CAN_INVALID_HARDWA EM_CAN_INVALID_HARDWARE
E Only l RE
6663040 EM_CAN_INVALID_PARAMET Debug SysCntr CanComm opr 0 Ignore "EM_CAN_INVALID_PARAME EM_CAN_INVALID_PARAMETE

ER Only l TER R
6663041 EM_CAN_INVALID_HANDLE Debug SysCntr CanComm opr 0 Ignore "EM_CAN_INVALID_HANDLE EM_CAN_INVALID_HANDLE

Only l
6663042 EM_CAN_NET_NOT_FOUND Debug SysCntr CanComm opr 0 Ignore "EM_CAN_NET_NOT_FOUND EM_CAN_NET_NOT_FOUND
Only l
6664001 EM_CANOPENCOMM_CONSTRU Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPENCOMM_CONSTR EM_CANOPENCOMM_CONSTRUC
CTOR_FAILED Only UCTOR_FAILED TOR_FAILED

_RECEIVER_TABLE_CREATI Only R_RECEIVER_TABLE_CREAT RECEIVER_TABLE_CREATION
ON_FAILED ION_FAILED _FAILED

_FAILED_TO_CREATE_SLAV Only R_FAILED_TO_CREATE_SLA FAILED_TO_CREATE_SLAVE_
E_NODE VE_NODE NODE

_SLAVE_INITIALIZATION_ Only R_SLAVE_INITIALIZATION SLAVE_INITIALIZATION_FA
FAILED _FAILED ILED

_MSG_Q_CREATION_FAILED Only R_MSG_Q_CREATION_FAILE MSG_Q_CREATION_FAILED
D

_FAILED_TO_CREATE_TXSE Only R_FAILED_TO_CREATE_TXS FAILED_TO_CREATE_TXSEMI
MID_SEMAPHORE EMID_SEMAPHORE D_SEMAPHORE

_FAILED_TO_CREATE_CO_L Only R_FAILED_TO_CREATE_CO_ FAILED_TO_CREATE_CO_LKU
KUP_TABLE_SEMAPHORE LKUP_TABLE_SEMAPHORE P_TABLE_SEMAPHORE

_FAILED_TO_CREATE_CANO Only R_FAILED_TO_CREATE_CAN FAILED_TO_CREATE_CANOPE
PEN_TX_TASK OPEN_TX_TASK N_TX_TASK

_MSG_Q_SEM_TAKE_FAILED Only E_MSG_Q_SEM_TAKE_FAILE MSG_Q_SEM_TAKE_FAILED
D

_MSG_Q_NO_RECEIVERS Only E_MSG_Q_NO_RECEIVERS MSG_Q_NO_RECEIVERS

_MSG_Q_ID_NOT_REGISTER Only E_MSG_Q_ID_NOT_REGISTE MSG_Q_ID_NOT_REGISTERED
ED RED

_MSG_Q_SEM_GIVE_FAILED Only E_MSG_Q_SEM_GIVE_FAILE MSG_Q_SEM_GIVE_FAILED
D

NG_MULTIPLE_NODES Only ING_MULTIPLE_NODES G_MULTIPLE_NODES
6664014 EM_CANOPEN_ADD_ID_SEM_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_ADD_ID_SEM EM_CANOPEN_ADD_ID_SEM_T

TAKE_FAILED Only _TAKE_FAILED AKE_FAILED

GE MEDICAL SYSTEMS
NG_DEVICE_FAILED Only ING_DEVICE_FAILED G_DEVICE_FAILED
6664016 EM_CANOPEN_ADD_ID_ID_L Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_ADD_ID_ID_ EM_CANOPEN_ADD_ID_ID_LI

IST_EXCEEDS_LIMIT Only LIST_EXCEEDS_LIMIT ST_EXCEEDS_LIMIT
6664017 EM_CANOPEN_ADD_ID_ID_D Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_ADD_ID_ID_ EM_CANOPEN_ADD_ID_ID_DU

UPLICATION Only DUPLICATION PLICATION
6664018 EM_CANOPEN_ADD_ID_MSGQ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_ADD_ID_MSG EM_CANOPEN_ADD_ID_MSGQ_

_CREATE_FAILED Only Q_CREATE_FAILED CREATE_FAILED
6664019 EM_CANOPEN_ADD_ID_CANO Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_ADD_ID_CAN EM_CANOPEN_ADD_ID_CANOP

PEN_IF_TASK_SPAWN_FAIL Only OPEN_IF_TASK_SPAWN_FAI EN_IF_TASK_SPAWN_FAILED
ED LED
6664020 EM_CANOPEN_ADD_ID_SEM_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_ADD_ID_SEM EM_CANOPEN_ADD_ID_SEM_G

GIVE_FAILED Only _GIVE_FAILED IVE_FAILED
6664021 EM_CANOPEN_DELETE_ID_N Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DELETE_ID_ EM_CANOPEN_DELETE_ID_NO

O_ID_REGISTERED Only NO_ID_REGISTERED _ID_REGISTERED

EM_TAKE_FAILED Only SEM_TAKE_FAILED M_TAKE_FAILED

EM_GIVE_FAILED Only SEM_GIVE_FAILED M_GIVE_FAILED
6664024 EM_CANOPEN_CMDOUTTASK_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_CMDOUTTASK EM_CANOPEN_CMDOUTTASK_R

READ_FROM_MSGQ_FAILED Only _READ_FROM_MSGQ_FAILED EAD_FROM_MSGQ_FAILED

SEM_TAKE_FAILED Only _SEM_TAKE_FAILED EM_TAKE_FAILED
6664026 EM_CANOPEN_CMDOUTTASK_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_CMDOUTTASK EM_CANOPEN_CMDOUTTASK_U

UNKNOWN_COMMAND Only _UNKNOWN_COMMAND NKNOWN_COMMAND

SEM_GIVE_FAILED Only _SEM_GIVE_FAILED EM_GIVE_FAILED
6664028 EM_CANOPEN_RX_SEM_TAKE Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_RX_SEM_TAK EM_CANOPEN_RX_SEM_TAKE_

6664029 EM_CANOPEN_RX_SEM_GIVE Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_RX_SEM_GIV EM_CANOPEN_RX_SEM_GIVE_

6664030 EM_CANOPEN_CANOPENIFTA Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_CANOPENIFT EM_CANOPEN_CANOPENIFTAS

SK_MSGQ_RECEIVE_FAILED Only ASK_MSGQ_RECEIVE_FAILE K_MSGQ_RECEIVE_FAILED
D
6664031 EM_CANOPEN_WRITE_SEND_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_WRITE_SEND EM_CANOPEN_WRITE_SEND_T

TO_MSG_Q_FAILED Only _TO_MSG_Q_FAILED O_MSG_Q_FAILED
6664032 EM_CANOPEN_READ_DATA_S Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_READ_DATA_ EM_CANOPEN_READ_DATA_SI

IZE_ERROR Only SIZE_ERROR ZE_ERROR

M_TAKE_FAILED Only EM_TAKE_FAILED _TAKE_FAILED

M_GIVE_FAILED Only EM_GIVE_FAILED _GIVE_FAILED
6664035 EM_CANOPEN_LOCAL_NODE_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_LOCAL_NODE EM_CANOPEN_LOCAL_NODE_T

TABLE_CREATION_FAILED Only _TABLE_CREATION_FAILED ABLE_CREATION_FAILED
6664036 EM_CANOPEN_LOCAL_NODE_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_LOCAL_NODE EM_CANOPEN_LOCAL_NODE_R

RPDOCALLBACK_SEND_TO_M Only _RPDOCALLBACK_SEND_TO_ PDOCALLBACK_SEND_TO_MSG
SGQ_FAILED MSGQ_FAILED Q_FAILED


_ERROR Only X_ERROR ERROR

NTR_OFF_BUS Only ONTR_OFF_BUS TR_OFF_BUS

NTR_WARN Only ONTR_WARN TR_WARN

NTR_BUSY Only ONTR_BUSY TR_BUSY
6665006 EM_CANOPEN_DCF_INIT_ER Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_INIT_E EM_CANOPEN_DCF_INIT_ERR

ROR Only RROR OR
6665007 EM_CANOPEN_DCF_OUT_OF_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_OUT_OF EM_CANOPEN_DCF_OUT_OF_M

MEMORY Only _MEMORY EMORY

ODE_ID Only NODE_ID DE_ID

GE MEDICAL SYSTEMS
6665009 EM_CANOPEN_DCF_WRONG_B Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_WRONG_ EM_CANOPEN_DCF_WRONG_BA
AUDRATE Only BAUDRATE UDRATE

_SECTION Only G_SECTION SECTION

_ENTRY Only G_ENTRY ENTRY
6665012 EM_CANOPEN_DCF_WRONG_P Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_WRONG_ EM_CANOPEN_DCF_WRONG_PA

ARAMETER Only PARAMETER RAMETER
6665013 EM_CANOPEN_DCF_OUT_OF_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_OUT_OF EM_CANOPEN_DCF_OUT_OF_R

RANGE Only _RANGE ANGE
6665014 EM_CANOPEN_DCF_OUT_OF_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_OUT_OF EM_CANOPEN_DCF_OUT_OF_L

LIMITS Only _LIMITS IMITS
6665015 EM_CANOPEN_DCF_DOUBLE_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_DOUBLE EM_CANOPEN_DCF_DOUBLE_S

SECTION Only _SECTION ECTION
6665016 EM_CANOPEN_DCF_DOUBLE_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_DOUBLE EM_CANOPEN_DCF_DOUBLE_K

KEYWORD Only _KEYWORD EYWORD
6665017 EM_CANOPEN_DCF_UNKNOWN Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_UNKNOW EM_CANOPEN_DCF_UNKNOWN_

_KEYWORD Only N_KEYWORD KEYWORD
6665018 EM_CANOPEN_WRONG_NET_N Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_WRONG_NET_ EM_CANOPEN_WRONG_NET_NO

O Only NO
6665019 EM_CANOPEN_WRONG_MODUL Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_WRONG_MODU EM_CANOPEN_WRONG_MODULE

E_NO Only LE_NO _NO
6665020 EM_CANOPEN_MCAL_PARA_E Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_PARA_ EM_CANOPEN_MCAL_PARA_ER

RROR Only ERROR ROR
6665021 EM_CANOPEN_MCAL_SYS_ER Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_SYS_E EM_CANOPEN_MCAL_SYS_ERR

ROR Only RROR OR
6665022 EM_CANOPEN_MCAL_NO_NET Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_NO_NE EM_CANOPEN_MCAL_NO_NET

Only T
6665023 EM_CANOPEN_MCAL_OBJ_NO Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_OBJ_N EM_CANOPEN_MCAL_OBJ_NO_

_MEMORY Only O_MEMORY MEMORY
6665024 EM_CANOPEN_MCAL_DOWNLO Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_DOWNL EM_CANOPEN_MCAL_DOWNLOA

AD_ABORT_SLAVE Only OAD_ABORT_SLAVE D_ABORT_SLAVE

SLAVE_ANSWER Only _SLAVE_ANSWER LAVE_ANSWER

SERVER_ANSWER Only _SERVER_ANSWER ERVER_ANSWER
6665027 EM_CANOPEN_MCAL_TOGGLE Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_TOGGL EM_CANOPEN_MCAL_TOGGLE_

_ERROR Only E_ERROR ERROR
6665028 EM_CANOPEN_MCAL_BUFFER Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_BUFFE EM_CANOPEN_MCAL_BUFFER_

_OVERFLOW Only R_OVERFLOW OVERFLOW
6665029 EM_CANOPEN_MCAL_ABORT_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_ABORT EM_CANOPEN_MCAL_ABORT_D

DOMAIN Only _DOMAIN OMAIN

OT_EXISTEND Only NOT_EXISTEND T_EXISTEND
6665031 EM_CANOPEN_MCAL_WRONG_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_WRONG EM_CANOPEN_MCAL_WRONG_G

GUARD_ID Only _GUARD_ID UARD_ID
6665032 EM_CANOPEN_MCAL_NEW_GU Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_NEW_G EM_CANOPEN_MCAL_NEW_GUA

ARD_PARA Only UARD_PARA RD_PARA

OT_FREE Only NOT_FREE T_FREE
6665034 EM_CANOPEN_MCAL_NO_EVE Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_NO_EV EM_CANOPEN_MCAL_NO_EVEN

NT Only ENT T
6665035 EM_CANOPEN_MCAL_UNSUPP Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_UNSUP EM_CANOPEN_MCAL_UNSUPPO

ORTED Only PORTED RTED
6665036 EM_CANOPEN_MCAL_FILE_R Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_FILE_ EM_CANOPEN_MCAL_FILE_RE

EAD_ERR Only READ_ERR AD_ERR
6665037 EM_CANOPEN_MCAL_FILE_O Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_FILE_ EM_CANOPEN_MCAL_FILE_OP

PEN_ERR Only OPEN_ERR EN_ERR
6665038 EM_CANOPEN_DCF_WRONG_T Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_WRONG_ EM_CANOPEN_DCF_WRONG_TY

YP Only TYP P
6665039 EM_CANOPEN_DCF_WRONG_N Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_DCF_WRONG_ EM_CANOPEN_DCF_WRONG_NE

ET_ID Only NET_ID T_ID

GE MEDICAL SYSTEMS
ODE_NAME Only NODE_NAME DE_NAME
6665041 EM_CANOPEN_MCAL_EXERR Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_EXERR EM_CANOPEN_MCAL_EXERR

Only
6665042 EM_CANOPEN_MCAL_CAN_RX Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_CAN_R EM_CANOPEN_MCAL_CAN_RX_
6665043 EM_CANOPEN_MCAL_WRONG_ Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_WRONG EM_CANOPEN_MCAL_WRONG_N

NODE_STATE Only _NODE_STATE ODE_STATE
6665044 EM_CANOPEN_MCAL_CONSIS Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_MCAL_CONSI EM_CANOPEN_MCAL_CONSIST

TENCY_ERROR Only STENCY_ERROR ENCY_ERROR
6666001 EM_CANOPEN_SCANOPEN_PA Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_P EM_CANOPEN_SCANOPEN_PAR

RA_ERROR Only ARA_ERROR A_ERROR
6666002 EM_CANOPEN_SCANOPEN_SY Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_S EM_CANOPEN_SCANOPEN_SYS

S_ERROR Only YS_ERROR _ERROR

N_RX_TIMEOUT Only AN_RX_TIMEOUT _RX_TIMEOUT

N_TX_TIMEOUT Only AN_TX_TIMEOUT _TX_TIMEOUT

N_TX_ERROR Only AN_TX_ERROR _TX_ERROR

N_CONTR_OFF_BUS Only AN_CONTR_OFF_BUS _CONTR_OFF_BUS

N_CONTR_BUSY Only AN_CONTR_BUSY _CONTR_BUSY

N_CONTR_WAIT Only AN_CONTR_WAIT _CONTR_WAIT
6666009 EM_CANOPEN_SCANOPEN_PR Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_P EM_CANOPEN_SCANOPEN_PRO

OTOCOL_ERROR Only ROTOCOL_ERROR TOCOL_ERROR
6666010 EM_CANOPEN_SCANOPEN_NO Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_N EM_CANOPEN_SCANOPEN_NO_

_SLAVE_NET Only O_SLAVE_NET SLAVE_NET
6666011 EM_CANOPEN_SCANOPEN_NE Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_N EM_CANOPEN_SCANOPEN_NET

TWORK_FILE_ERROR Only ETWORK_FILE_ERROR WORK_FILE_ERROR

ONG_NODE_STATE Only RONG_NODE_STATE NG_NODE_STATE
6666013 EM_CANOPEN_SCANOPEN_SE Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_S EM_CANOPEN_SCANOPEN_SER

RVICE_NOT_ALLOWED Only ERVICE_NOT_ALLOWED VICE_NOT_ALLOWED
6666014 EM_CANOPEN_SCANOPEN_NO Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_N EM_CANOPEN_SCANOPEN_NOD

DE_NOT_OPERATIONAL Only ODE_NOT_OPERATIONAL E_NOT_OPERATIONAL

J_NOT_EXISTS Only BJ_NOT_EXISTS _NOT_EXISTS

NNOT_START_DAEMON Only ANNOT_START_DAEMON NOT_START_DAEMON
6666017 EM_CANOPEN_SCANOPEN_UN Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_U EM_CANOPEN_SCANOPEN_UNK

KNOWN_ERROR Only NKNOWN_ERROR NOWN_ERROR
6666018 EM_CANOPEN_SCANOPEN_CH Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_C EM_CANOPEN_SCANOPEN_CHE

ECKSUM_ERROR Only HECKSUM_ERROR CKSUM_ERROR
6666019 EM_CANOPEN_SCANOPEN_VE Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_V EM_CANOPEN_SCANOPEN_VER

RIFY_ERROR Only ERIFY_ERROR IFY_ERROR

B_DATABASE_OVERFLOW Only OB_DATABASE_OVERFLOW _DATABASE_OVERFLOW

B_DATABASE_DISABLED Only OB_DATABASE_DISABLED _DATABASE_DISABLED

B_CLASS_ERROR Only OB_CLASS_ERROR _CLASS_ERROR

B_LENGTH_ERROR Only OB_LENGTH_ERROR _LENGTH_ERROR

J_EXISTS Only BJ_EXISTS _EXISTS
6666025 EM_CANOPEN_SCANOPEN_DA Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_D EM_CANOPEN_SCANOPEN_DAT

TATYPE_TOO_LONG Only ATATYPE_TOO_LONG ATYPE_TOO_LONG

J_NO_MEMORY Only BJ_NO_MEMORY _NO_MEMORY

GE MEDICAL SYSTEMS
NNOT_OPEN_CAN Only ANNOT_OPEN_CAN NOT_OPEN_CAN

WNLOAD_ABORT_SLAVE Only OWNLOAD_ABORT_SLAVE NLOAD_ABORT_SLAVE

WNLOAD_ABORT_MASTER Only OWNLOAD_ABORT_MASTER NLOAD_ABORT_MASTER

J_NOT_PREPARED Only BJ_NOT_PREPARED _NOT_PREPARED

J_WRONG_ACCESS Only BJ_WRONG_ACCESS _WRONG_ACCESS

ONG_MASTER_REQUEST Only RONG_MASTER_REQUEST NG_MASTER_REQUEST

ONG_MASTER_ANSWER Only RONG_MASTER_ANSWER NG_MASTER_ANSWER

ONG_CLIENT_REQUEST Only RONG_CLIENT_REQUEST NG_CLIENT_REQUEST

ONG_CLIENT_ANSWER Only RONG_CLIENT_ANSWER NG_CLIENT_ANSWER

ONG_SERVER_REQUEST Only RONG_SERVER_REQUEST NG_SERVER_REQUEST

ONG_SERVER_ANSWER Only RONG_SERVER_ANSWER NG_SERVER_ANSWER
6666038 EM_CANOPEN_SCANOPEN_TO Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_T EM_CANOPEN_SCANOPEN_TOG

GGLE_ERROR Only OGGLE_ERROR GLE_ERROR
6666039 EM_CANOPEN_SCANOPEN_BU Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_B EM_CANOPEN_SCANOPEN_BUF

FFER_OVERFLOW Only UFFER_OVERFLOW FER_OVERFLOW
6666040 EM_CANOPEN_SCANOPEN_AB Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_A EM_CANOPEN_SCANOPEN_ABO

ORT_DOMAIN Only BORT_DOMAIN RT_DOMAIN
6666041 EM_CANOPEN_SCANOPEN_US Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_U EM_CANOPEN_SCANOPEN_USE

ER_ERROR Only SER_ERROR R_ERROR

ONG_INDEX Only RONG_INDEX NG_INDEX

ONG_SUBINDEX Only RONG_SUBINDEX NG_SUBINDEX
6666044 EM_CANOPEN_SCANOPEN_OU Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_O EM_CANOPEN_SCANOPEN_OUT

T_OF_MEMORY Only UT_OF_MEMORY _OF_MEMORY

ONG_BAUDRATE Only RONG_BAUDRATE NG_BAUDRATE

ONG_PARAMETER Only RONG_PARAMETER NG_PARAMETER

LUE_TOO_HIGH Only ALUE_TOO_HIGH UE_TOO_HIGH

LUE_TOO_LOW Only ALUE_TOO_LOW UE_TOO_LOW

ONG_DATA_TYPE Only RONG_DATA_TYPE NG_DATA_TYPE

ONG_OBJECT_TYPE Only RONG_OBJECT_TYPE NG_OBJECT_TYPE

O_MAPPING_ERROR Only DO_MAPPING_ERROR _MAPPING_ERROR
6666052 EM_CANOPEN_SCANOPEN_TO Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_T EM_CANOPEN_SCANOPEN_TOO

O_MANY_OBJECTS Only OO_MANY_OBJECTS _MANY_OBJECTS

ONG_NODESTATE Only RONG_NODESTATE NG_NODESTATE
6666054 EM_CANOPEN_SCANOPEN_LE Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_L EM_CANOPEN_SCANOPEN_LEN

NGTH_MISMATCH Only ENGTH_MISMATCH GTH_MISMATCH

O_NOT_VALID Only DO_NOT_VALID _NOT_VALID
6666056 EM_CANOPEN_SCANOPEN_IN Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_I EM_CANOPEN_SCANOPEN_INI

IT_ERROR Only NIT_ERROR T_ERROR
6666057 EM_CANOPEN_SCANOPEN_IN Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_I EM_CANOPEN_SCANOPEN_INV

VALID_HANDLE Only NVALID_HANDLE ALID_HANDLE

GE MEDICAL SYSTEMS
6666058 EM_CANOPEN_SCANOPEN_AC Debug Pos CanOpenComm opr 0 Ignore "EM_CANOPEN_SCANOPEN_A EM_CANOPEN_SCANOPEN_ACC
CESS_ERROR Only CCESS_ERROR ESS_ERROR

GE MEDICAL SYSTEMS

GE MEDICAL SYSTEMS
Glossary of Acroymns & Their Meaning
ACROYMN DEFINITION
ABC / (ABS) Automatic brightness control/system. Regulates brightness
ABD Automatic Brightness Detection
ACTOR A Software Module that performs some function or action
ADC or A/D Analog to Digital Converter
ADCM Active Distortion Correction Module
ADCS Active Distortion Correction System
AEC Automatic exposure control. Technique used to control brightness signal to cut exposure.
ARETHA Aretha refers to the product development name for Precision 500D. The two are
synonymous
ATHENA Digital System SW, which runs on the Windows 95 OS and on the Saturn Hardware
ATLAS CORE Operating system of the X-Ray products
CALYPSO GEMS’ engine ring name for the System control Software application
CAN Controller Area Network - A serial communication method in use on Precision 500D.
CANopen A protocol for a CAN network. Used interchangeably with CAN
CAT Collimator Alignment Tool
CCD Charge Coupled Devices
CCU Camera Control Unit
CDS Correlated Double Sampling
CIB Custom Interface Board
COTS Commercial Off The Shelf Tool
CPU Central Processing Unit
CPU Control processor unit. Microprocessor and peripherals which run the software/firmware
DAC Digital to Analog Converter
DHC Digital Host Control Board
DSA Digital Subtraction Angiography
DSC Digital Servo Controller
DSC2 Digital Servo Controller, Version 2
EFC Earth Field Compensation
FNR Fluoro Noise Reduction
FOV Field of View
FPGA Field programmable gate array. It is programmed by the CPU core after the reset and
handles all the exposure control logic including the system interface real-time lines
FPS Frames Per Second
FRU Field Replaceable Unit (Spare Part)
G1, G2, G3 Grids 1, 2 and 3
GHOST ® Software Image of the Saturn OS on CDROM. Ghost is a trademark of Symantec Inc.
GUI Graphical User Interface
Glossary Page 655

GE MEDICAL SYSTEMS
ACROYMN DEFINITION
HV RIPPLE High voltage variations due to inverter current pulses. Typically measured in percent.
HVPS High Voltage Power Supply
IAB Image Acqusition Board
ICB Image Correction Board
IDB Image Display Board
IDD Intelligent Digital Device- Equivalent to the SFD with no film functionality. Introduced with
the release of Precision 500D.
IGBT Insulated gate bipolar transistor power switch.
II Image Intensifier
Ilp HV power inverter parallel resonant current. Current in the parallel inductor
Ilr HV power inverter serial resonant current. Current in the serial inductor
IMB Image Display Board
IO or I/O Input/Output
IUI Integrated User Interface
JEDI Precision 500 High Voltage Generator
LAT Lateral
LEELO Engineering name for the Image Chain hardware; CCD, Image Intensifier,...
LFC Load from Cold
LONG Longitudinal
LOTO LockOut/Tag Out
LP Line Pair
LSL Lower Specification Limit
LUT Look Up Table
MAINS Hospital Supplied AC Power
MARS SYSTEM CONTROLLER Hardware
MITRA Software supplier for DICOM application SW
MOS Metal oxyde semiconductor. Power switch
NDF Neutral Density Filter
NVRAM Non Volatile Random Access Memory
OCB Optics Control Board
OGP On gantry processor. Unit which drives the generator in CT systems
OLC On-Line Center
OS Operating System
OTS Overhead Tube Suspension
PA Power Assist
PCI Pherperial Control Interface
PDB PhotoDiode Board
PDU Power Distribution Unit
POS Positioner
PUT Pick Up Tube
RAD Radiography
Page 656 Glossary

GE MEDICAL SYSTEMS
ACROYMN DEFINITION
R&F Radiography & Fluoroscopy
RED HAT ® SW version of Linux. Red Hat is an integrator and supplier of the Linux operating system.
ROI Region of Interest
POT Potentiometer
RPM RedHat (Linux) Package Manager software
RS422 A Serial Communications Hardware Connection Type
RT Real Time
PWA Printed Wire Board is synonymous with printed circuit board (PCB).
SABER Applications SW for positioning; run on the MARS computer
SAE Society of Automotive Engneers - International organization that sets standards for
materials and fasteners in both English and Metric units, See www.sae.org
SATURN Digital System Hardware; where the windows 95 operating system runs
SBC Single Board Computer
SCAT System Compatibility Assurance Testing performed by GE prior to deliverly.
SCB Scan Converter Board
SFD Spot Film Device - An analog filming device.
STATE MACHINE Software or hardware functions that handle the state of a computer and authorizes it to go
to the next state upon reception of specific events.
SUIF Service User Interface
SW Abbreviation for the word Software
SYSTEM CONTROLLER See MARS
SYSTEM RESET A system reset is accomplished by pressing the green button located on the IUI. Pressing
it causes all of the computer to shutdown and restart. Thus re-booting the operating
systems and system applications.
TTL Transistor to Transistor Logic
UPS Un-interruptible Power Supply
U/T Abbreviation for Under Table
USL Upper Specification Limit
VENUS IUI Hardware; where the Linux operating system executes and resides.
Glossary Page 657

GE MEDICAL SYSTEMS
Page 658 Glossary

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Xr
GE MEDICAL SYSTEMS
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GE Medical Systems

Table of Contents, Preface, Chapters 1, 2 & 3

Copyright © 2002, 2003, 2004 and 2005

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Published by GE Medical Systems

Legal Notes Page 3

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Page 4 Legal Notes

• THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY.

• CE MANUEL DE MAINTENANCE N’EST DISPONIBLE QU’EN ANGLAIS.

• DIESES KUNDENDIENST-HANDBUCH EXISTIERT NUR IN ENGLISCHER SPRACHE.

• ESTE MANUAL DE SERVICIO SÓLO EXISTE EN INGLÉS.

Important Precautions Page 5

• ESTE MANUAL DE ASSISTÊNCIA TÉCNICA SÓ SE ENCONTRA DISPONÍVEL EM

• IL PRESENTE MANUALE DI MANUTENZIONE È DISPONIBILE SOLTANTO IN INGLESE.

Page 6 Important Precautions

CERTIFIED ELECTRICAL CONTRACTOR STATEMENT

OMISSIONS & ERRORS

Important Precautions Page 7

This page left intentionally blank

Page 8 Important Precautions

Revision History Page 9

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Page 10 Revision History

List of Effected Pages

PAGES REVISION PAGES REVISION

List of Effected Pages Page 11

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Page 12 List of Effected Pages

Table of Contents Page 13

Page 14 Table of Contents

Page 15 Table of Contents

Page 16 Table of Contents

Page 17 Table of Contents

Page 18 Table of Contents

Page 19 Table of Contents

Page 20 Table of Contents

Glossary of Acroymns & Their Meaning .......................................................... 655

Table of Contents Page 21

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Page 22 Table of Contents

1.1 Hazard Messages

1.2 Text Format of Signal Words

1.3 Symbols and Pictorials Used

keep_up magnetic biohazard compressgas ppe-hearing

fragile impact corrosive heavyobject ppe-2people

static_elec heat general laser ppe-respitory

keep_dry pinch radiation poisongas ppe-loto

general explosive electrical flammable ppe-eye

torque crush/mechanical tipping Read Manual ppe-gloves

ce instuction poisonmatl entanglement instuction

EXAMPLES OF PREFIXES USED FOR GENERAL INFORMATION:

2.2 Page Layout

1.2 Acquisition Modes

1.2.1 Digital Record

1.2.1.2 Fixed Time

Chapter 1 - System Overview & Safety Page 27

1.2.2 Digital Fluoro

1.2.3 Radiography (Overhead Tube)

1.2.3.2 Fixed Time

Figure 1-1 System Components

Page 28 Section 2.0 - System Components

Bar Code Reader - An option used for entering data

Positioner Cabinet - Controls movements (longitudinal, lateral and vertical limits)