GE Medical Systems

Technical
Publications

Direction 2298380-100
Revision 9

Prestige CDROM Addendum

Copyrighte 2002, 2003, 2004 By General Electric Co.

GE MEDICAL SYSTEMS PRESTIGE CDROM ADDENDUM
REV 9 DIRECTION 2298380–100

D THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY.

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

D CE MANUEL DE MAINTENANCE N’EST DISPONIBLE QU’EN ANGLAIS.

AVERTISSEMENT D 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.
D NE PAS TENTER D’INTERVENTION SUR LES ÉQUIPEMENTS TANT QUE LE
MANUEL SERVICE N’A PAS ÉTÉ CONSULTÉ ET COMPRIS.
D 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.

D DIESES KUNDENDIENST–HANDBUCH EXISTIERT NUR IN ENGLISCHER

SPRACHE.
WARNUNG
D FALLS EIN FREMDER KUNDENDIENST EINE ANDERE SPRACHE BENÖTIGT,
IST ES AUFGABE DES KUNDEN FÜR EINE ENTSPRECHENDE ÜBERSETZUNG
ZU SORGEN.
D VERSUCHEN SIE NICHT, DAS GERÄT ZU REPARIEREN, BEVOR DIESES
KUNDENDIENST–HANDBUCH NICHT ZU RATE GEZOGEN UND VERSTANDEN
WURDE.
D 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.

D ESTE MANUAL DE SERVICIO SÓLO EXISTE EN INGLÉS.

AVISO D 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.
D NO SE DEBERÁ DAR SERVICIO TÉCNICO AL EQUIPO, SIN HABER
CONSULTADO Y COMPRENDIDO ESTE MANUAL DE SERVICIO.
D 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.

i
GE MEDICAL SYSTEMS PRESTIGE CDROM ADDENDUM
REV 9 DIRECTION 2298380–100

D ESTE MANUAL DE ASSISTÊNCIA TÉCNICA SÓ SE ENCONTRA DISPONÍVEL

EM INGLÊS.
ATENÇÃO
D 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.
D NÃO TENTE REPARAR O EQUIPAMENTO SEM TER CONSULTADO E
COMPREENDIDO ESTE MANUAL DE ASSISTÊNCIA TÉCNICA.
D O NÃO CUMPRIMENTO DESTE AVISO PODE POR EM PERIGO A SEGURANÇA
DO TÉCNICO, OPERADOR OU PACIENTE DEVIDO A‘ CHOQUES ELÉTRICOS,
MECÂNICOS OU OUTROS.

D IL PRESENTE MANUALE DI MANUTENZIONE È DISPONIBILE SOLTANTO IN

INGLESE.
AVVERTENZA
D SE UN ADDETTO ALLA MANUTENZIONE ESTERNO ALLA GEMS RICHIEDE IL
MANUALE IN UNA LINGUA DIVERSA, IL CLIENTE È TENUTO A PROVVEDERE
DIRETTAMENTE ALLA TRADUZIONE.
D SI PROCEDA ALLA MANUTENZIONE DELL’APPARECCHIATURA SOLO DOPO
AVER CONSULTATO IL PRESENTE MANUALE ED AVERNE COMPRESO IL
CONTENUTO.
D 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.

ii
GE MEDICAL SYSTEMS
REV 9
Direction 2298380-100
Revision 9
Prestige CDROM Addendum
IMPORTANT! . . . XĆRAY PROTECTION
XĆray equipment if not properly
used may cause injury. AccordĆ
ingly, the instructions herein
contained should be thoroughly
read and understood by everyĆ
one who will use the equipment
before you attempt to place this
equipment in operation. The
General Electric Company, MediĆ
cal Systems Group, will be glad
to assist and cooperate in placing
this equipment in use.
Although this apparatus incorpoĆ
rates a high degree of protection
against xĆradiation 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 everyone having
anything to do with xĆradiation be
properly trained and fully acĆ
quainted with the recommendaĆ
tions of the National Council on
Radiation Protection and MeasureĆ
ments as published in NCRP
Reports available from NCRP PubliĆ
cations, 7910 Woodmont Avenue,
Room 1016, Bethesda, Maryland
iii
PRESTIGE CDROM ADDENDUM
DIRECTION 2298380–100
20814, and of the International
Commission on Radiation ProtecĆ
tion, and take adequate steps to
protect against injury.
The equipment is sold with the
understanding that the General
Electric Company, Medical SysĆ
tems Group, its agents, and
representatives have no responsiĆ
bility for injury or damage which
may result from improper use of the
equipment.
Various protective material and
devices are available. It is urged
that such materials or devices be
used.
GE MEDICAL SYSTEMS PRESTIGE CDROM ADDENDUM
REV 9 DIRECTION 2298380–100

If you have any comments, suggestions or corrections to the information in this document,
please write them down, include the document title and document number, and send them to:
GENERAL ELECTRIC COMPANY
MEDICAL SYSTEMS
MANAGER - FIELD SERVICE DEVELOPMENT
ENGINEERING, X-RAY W-702
P.O. BOX 414
MILWAUKEE, WI 53201-0414

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 beĆ
tween 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 sophistiĆ
cated, and special engineering
competence is required. In performĆ
ing 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 elecĆ
trical codes.
The purchaser of GE equipment
shall only utilize qualified personnel
(i.e., GE's field engineers, personnel
of thirdĆparty service companies with
equivalent training, or licensed elecĆ
tricians) to perform electrical servicĆ
ing on the equipment.

DAMAGE IN TRANSPORTATION
All packages should be closely
examined at time of delivery. If
damage is apparent, have notation
damage in shipment" written on
all copies of the freight or express
bill before delivery is accepted or
signed for" by a General Electric
representative or a hospital receivĆ
ing agent. Whether noted or
concealed, damage MUST be
reported to the carrier immediately
upon discovery, or in any event,
within 14 days after receipt, and the
contents and containers held for
inspection by the carrier. A transĆ
portation 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 (262) 827-3468Ă/
8*285-3468 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 &
Procedure Bulletins.
6/17/94

iv
GE MEDICAL SYSTEMS PRESTIGE CDROM ADDENDUM
REV 9 DIRECTION 2298380–100

TABLE OF CONTENTS

SECTION TITLE PAGE

REVISION HISTORY . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . vi

1 INTRODUCTION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1–1

2 DUAL FOOTSWITCH FRU PART NUMBER . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1–1

3 ULTRANET SRI COLLIMATOR FRU PART NUMBER . . . . . . . . . . . . . . . . . . . . . 1–1

4 MODULE 2 CIRCUIT BOARDS FRU PART NUMBERS . . . . . . . . . . . . . . . . . . . . 1–2

5 FILM CASSETTE DETECTION BAR ADJUSTMENT . . . . . . . . . . . . . . . . . . . . . 1–3

6 FLEXIBLE HOSE FRU PART NUMBER . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1–6

7 INCORRECT PREINSTALLATION REFERENCE . . . . . . . . . . . . . . . . . . . . . . . . . 1–6

8 SW133 AND SW139 SETTINGS ON 2A80 CPU

BOARD FOR CONNECTING LAPTOP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1–6

9 PALPATOR SPOON FRU PART NUMBER . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1–6

10 STATOR CABLE FRU PART NUMBER . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1–7

11 FLAT PANEL DISPLAY CONNECTOR BRACKET . . . . . . . . . . . . . . . . . . . . . . . 1–7

12 TABLE TOP FRU CHANGE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1–7

13 JOB CARD VF0002 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1–8

v
GE MEDICAL SYSTEMS PRESTIGE CDROM ADDENDUM
REV 9 DIRECTION 2298380–100

REVISION HISTORY

REV DATE REASON FOR CHANGE

0 February 1, 2002
1 May 6, 2002
2 June 26, 2002
3 November 12, 2002
4 December 11, 2002
5 December 16, 2002
6 February 11, 2003
7 April 25, 2003
8 November 14, 2003
9 April 7, 2004
Initial release.
Add Flexible Hose part number.
Add correct preinstallation reference number.
Add SW133 and SW139 on 2A80 CPU board settings for laptop.
Palpator Spoon 827812P023 FRU code 1.
Added part numbers 2145653-4 and 2145653-5, stator cables.
Added instructions on replacing the Flat Panel Display Connector Bracket.
Added section 12 about new FRU for table top.
Added job card VF0002.
Revised job card VF0002 to further clarify the screws to be checked.

LIST OF EFFECTIVE PAGES

PAGE REVISION PAGE REVISION PAGE REVISION

NUMBER NUMBER NUMBER NUMBER NUMBER NUMBER

Title Page 9

i thru vi 9

1-1 thru 1-16 9

Back page

vi
GE MEDICAL SYSTEMS PRESTIGE CDROM ADDENDUM
REV 9 DIRECTION 2298380–100

SECTION 1
INTRODUCTION

The purpose of this addendum is to provide updated information to the Prestige VH/
II AK/AD CDROM 2249768-200 revision 5. This addendum supplements the inĆ
formation contained on the CDROM. When the CDROM is revised, the information
contained in this addendum will be added to the CDROM.

SECTION 2
DUAL FOOTSWITCH FRU PART NUMBER

The part number listed in the CDROM for the Prestige dual footswitch (197799P005)
is incorrect. The correct part number is 2135299 (dual footswitch EMC version with
cover).

SECTION 3
ULTRANET SRI COLLIMATOR FRU PART NUMBER

The part number listed in the CDROM for the Prestige Ultranet SRI Collimator
(861333P015) is incorrect. The correct part number is 45296713.

1-1
GE MEDICAL SYSTEMS PRESTIGE CDROM ADDENDUM
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SECTION 4
MODULE 2 CIRCUIT BOARDS FRU PART NUMBERS

Some of the part numbers listed in the CDROM for the Prestige Positioner Cabinet
Module 2 circuit boards are incorrect.

Positioner Cabinet Module 2 Incorrect FRU Part Number Correct FRU Part Number
Circuit Board
2A10 831271G015
2A38 Low Power Servo Board for 831827G035 831146G025
Collimator
2A46 On/Off Board 832907G015 2320694
831180G025 (U-Mask and Film
Marker Version)
2A80 CPU Board 831508G035 2320690

MODULE 2 – CARD RACK PWB

1-2
GE MEDICAL SYSTEMS PRESTIGE CDROM ADDENDUM
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SECTION 5
FILM CASSETTE DETECTION BAR ADJUSTMENT

The RG0012 procedure listed in the CDROM for the Prestige Film Cassette DetecĆ
tion Bar Adjustment" is incorrect. Following is the correct procedure.

1. Refer to Illustration 1-1 and follow the instructions in Illustration 1-1.

2. Refer to Illustration 1-2 and follow the instructions in Illustration 1-2.

3. Refer to Illustration 1-3 and 1-2. The microswitch on/off engagement should
be set so that, when the front cassette detection arm center piece is raised to a
distance 17.5 mm (+/- 0.5 mm) from the top surface of the cassette tray, the
switch just switches between on/off. Loosen the two screws holding the microĆ
switch to the SFD frame and retighten when the correct on/off position is
achieved.

1-3
GE MEDICAL SYSTEMS PRESTIGE CDROM ADDENDUM
REV 9 DIRECTION 2298380–100

ILLUSTRATION 1–1

15.0 mm

2 mm

15.0 mm

1-4
GE MEDICAL SYSTEMS PRESTIGE CDROM ADDENDUM
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ILLUSTRATION 1–2

CASSETTE

CASSETTE 1.0 mm

jaw

jaw

1.0 mm

1-5
GE MEDICAL SYSTEMS PRESTIGE CDROM ADDENDUM
REV 9 DIRECTION 2298380–100

ILLUSTRATION 1–3 ADJUST MICROSWITCH SET SCREWS

SET SCREW B

CASSETTE DETECTION BAR

2 SCREWS HOLDING
MICROSWITCH

ACTUATOR ARM
OF MICROSWITCH

SET SCREW A

SECTION 6
FLEXIBLE HOSE FRU PART NUMBER

There is no part number listed in the Prestige II CDROM for the "white flexible hose
on top of the tube arm." The correct part number is 853002P015. It is a FRU code 2.

SECTION 7
PREINSTALLATION DOCUMENT REFERENCE NUMBER

On the Prestige II CDROM in the Positioner Installation - Preinstallation Checks",

the wrong preinstallation document number is given. The incorrect PIM is
2133002-100 (Prestige SI Positioner PIM). The correct reference is 2119218-100
(Prestige VH/II PIM).

SECTION 8
SW133 AND SW139 SETTINGS ON 2A80CPU BOARD FOR CONNECTING LAPTOP

Add the following note to step 3 of Job Card IN0009, Tube Arm Installation:

Note: When you connect the laptop to the Prestige table using connector DB9 on
the 2A80 CPU board , you must check the settings of switches SW133 and
SW139. When using GPX cable (part number 2128821), set switches SW133
and SW139 on the 2A80 CPU board in position 2-3. When using MPG cable
(part number 2103512), set switches SW133 and SW139 on the 2A80 CPU
board in position 1-2.

SECTION 9
PALPATOR SPOON FRU PART NUMBER

The Palpator Spoon 827812P023 now has a FRU code of 1.

1-6
GE MEDICAL SYSTEMS PRESTIGE CDROM ADDENDUM
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SECTION 10
STATOR CABLE FRU PART NUMBER

The 18 meter long stator cable 2145653-2 part number has been replaced by
2145653-4, FRU 2.
The 24 meter long stator cable 2145653-3 part number has been replaced by
2145653-5, FRU 2.

SECTION 11
FLAT PANEL DISPLAY CONNECTOR BRACKET

Save this
bracket

When you replace the flat panel display (part number 2148762) on the Prestige II conĆ
sole, the cable connector bracket shown is not included. Remove the bracket and
install it onto the replacement flat panel display. The bracket is held on with rivets.
Remove the rivets carefully. Reinstall the bracket using nuts and bolts which must be
provided locally.

SECTION 12
TABLE TOP FRU CHANGE

The carbon fiber table top (model number 830948P022 manufactured by TOPKEY) is
no longer available as a FRU replacement. Instead order the phenolic table top model
number 832871P012. The reason is that the TOPKEY carbon fiber table tops may
show artifacts. FMI 10757 will replace all TOPKEY carbon fiber table tops with the
phenolic version.

1-7
GE MEDICAL SYSTEMS PRESTIGE CDROM ADDENDUM
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SECTION 13
JOB CARD VF0002

Supplies: None

Tools:

For this inspection process we will need:

1. Phillips Head Screwdriver,

2. Box Wrench for 8 mm,

3. Socket Wrench for 2.5, 3, 5, 6, & 8 mm

Safety Precautions:
Take care not to catch your fingers.

Prerequisites:
Review all screws that fasten the Foot Table. Every single screw must be torqued by
hand pressure.

Procedure:

The screw inspection must cover the foot step

of the VH Table, located at the bottom of the
Prestige System.

All screws must be checked by hand–pressure.

1-8
GE MEDICAL SYSTEMS PRESTIGE CDROM ADDENDUM
REV 9 DIRECTION 2298380–100

1. Illustration 1-4 shows the zone where the evaluation starts.

ILLUSTRATION 1–4

2. Illustration 1–5 shows a left view from Illustration. 1–4. Check the 4 square
head (6 mm) & 3 square head (5 mm) screws.

ILLUSTRATION 1–5

1-9
GE MEDICAL SYSTEMS PRESTIGE CDROM ADDENDUM
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3. Next, Illustration 1-6 shows an upper view from Illustration 1-4. Check the two
indicated 5 mm hexagonal internal head screws.

ILLUSTRATION 1–6

4. Illustration 1-7 shows the joint for Jack 2. Check the four 5 mm square head
screws.

ILLUSTRATION 1–8

1-10
GE MEDICAL SYSTEMS PRESTIGE CDROM ADDENDUM
REV 9 DIRECTION 2298380–100

5. Illustration 1-9 shows the chain pulley for Jack 2. Check the 2.5 mm square interĆ
nal head screw, taking advantage of the hole that is in front of this pulley. IllustraĆ
tion 1-10 shows how this practice must be done.

ILLUSTRATION 1–9

Refer to Illustration 1-10 for checking the screw at the Chain Pulley for Jack 2.

ILLUSTRATION 1–10

1-11
GE MEDICAL SYSTEMS PRESTIGE CDROM ADDENDUM
REV 9 DIRECTION 2298380–100

6. Illustration 1-11 shows the other end of Jack 2. Ceck the two 5 mm square interĆ
nal head screws as shown.

ILLUSTRATION 1–11

7. Illustration 1-12 shows the joint between Jack 1 and its basement. Check the
three 8 mm hexagon head screws.

ILLUSTRATION 1–12

1-12
GE MEDICAL SYSTEMS PRESTIGE CDROM ADDENDUM
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8. Illustration 1-13 shows the other end for Jack 1. Check the four 5 mm square
internal head screws.

ILLUSTRATION 1–13

9. Also, Illustration 1-14 shows three 3 mm square internal head screws that need
to be checked.

ILLUSTRATION 1–14

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GE MEDICAL SYSTEMS PRESTIGE CDROM ADDENDUM
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10. Illustration 1-15 shows four 5 mm square internal head screws to check at the
basement.

ILLUSTRATION 1–15

11. Illustration 1-16 shows six 8 mm hexagonal internal heads screws to check.

ILLUSTRATION 1–16

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GE MEDICAL SYSTEMS PRESTIGE CDROM ADDENDUM
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12. For the following Illustrations (1-17 to 1-19), use a Phillips Head Screwdriver
to check the screws. Screws to check are identified in each photo.

ILLUSTRATION 1–17 MICROSWITCH COVER

ILLUSTRATION 1–18 POTENTIOMETER COVER

ILLUSTRATION 1–19 MOTOR COVER

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GE MEDICAL SYSTEMS PRESTIGE CDROM ADDENDUM
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13. Illustration 1-20 shows four screws (left arrows) & 2 keys (right arrows) that hold
the 2 pulleys for Jack 1. Each of these need to be checked.

ILLUSTRATION 1–20 PULLEY FOR JACK 1

1-16
 GE Medical Systems

GE Medical Systems: Telex 3797371

P.O. Box 414, Milwaukee, Wisconsin 53201 U.S.A.
(Asia, Pacific, Latin America, North America)
GE Medical Systems — Europe: Telex 698626
283, rue de la Miniére, B.P. 34, 78533 Buc Cedex
France