Professional Documents
Culture Documents
Startup
System
Beginning with serial number 4001, with software VD ..
The Startup Instructions, XPD3-500.815.02..., must also be used for startup of the 2nd plane
with the Ysio Fully Synchronized.
Document Version
Siemens reserves the right to change its products and services at any time.
In addition, manuals are subject to change without notice. The hardcopy documents cor‐
respond to the version at the time of system delivery and/or printout. Versions to hard‐
copy documentation are not automatically distributed.
Please contact your local Siemens office to order a current version or refer to our website
http://www.healthcare.siemens.com.
Disclaimer
Siemens provides this documentation “as is” without the assumption of any liability under
any theory of law.
The content described herein requires superior understanding of our equipment and may
only be performed by qualified personnel who are specially trained for such installation
and/or service.
Copyright
“© Siemens, 2012” refers to the copyright of a Siemens entity such as:
Siemens Healthcare GmbH - Germany
Siemens Aktiengesellschaft - Germany
Siemens Shenzhen Magnetic Resonance Ltd. - China
Siemens Shanghai Medical Equipment Ltd. - China
Siemens Medical Solutions USA Inc. - USA
Siemens Healthcare Diagnostics Inc. - USA and/or
Siemens Healthcare Diagnostics Products GmbH - Germany
1.1 Prerequisites . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
1.1.1 Startup. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
1.1.2 Required Aids and Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
1.1.3 Additionally Required Documents . . . . . . . . . . . . . . . . . . . . . . . . . 9
1.1.4 Tolerance Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
1.1.5 Maximum Torque Values. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
1.1.6 Conventions and Abbreviations . . . . . . . . . . . . . . . . . . . . . . . . . . 9
1.2 Notes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
1.2.1 Customer Solutions (CuSo) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
1.2.2 Product-specific Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
1.2.3 Notes regarding Danger . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
1.2.4 General Safety Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
1.2.5 Hazard Keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
1.2.6 General Safety Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
2 General Startup 21
3.1 Preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
3.1.1 Adaptation to the Room Environment . . . . . . . . . . . . . . . . . . . . . 31
3.1.2 Transport Sensors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
3.2 Handling the Transport Sensors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 34
3.2.1 Report with a Damaged Detector . . . . . . . . . . . . . . . . . . . . . . . . . 34
3.3 Returning a Detector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
3.4 Installation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
3.4.1 Installing the Mounting Plate . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
3.4.2 Testing Insulation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
3.4.3 Installation in the Patient Table. . . . . . . . . . . . . . . . . . . . . . . . . . . 37
3.4.4 Connecting the Detector Cables . . . . . . . . . . . . . . . . . . . . . . . . . . 39
3.4.5 Grid . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
6.1 General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53
6.1.1 Network. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53
6.1.2 Switching on . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53
6.1.3 Function . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
6.1.4 Monitors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
6.1.5 Switching Off the FL Compact. . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
6.1.6 HIPAA (Option) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
6.1.7 FL Compact Service Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
6.1.8 Adjustments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
6.1.9 Data Entry in the SSW . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
6.1.10 System Networking . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57
6.2 CS Service Files and the Online Operator Manual . . . . . . . . . . . . . . . . . . . . . 59
6.3 Final Work Steps . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60
6.3.1 Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 60
7 System Startup 61
8.1 Checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 74
8.1.1 Tomography (Option) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 74
8.1.2 Scan Technique (Option). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 74
8.1.3 Ortho Option . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 74
9 Options 81
9.1 Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 81
9.1.1 Compression (optional). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 81
9.1.2 Radiation Shield and OR Lamp . . . . . . . . . . . . . . . . . . . . . . . . . . . 82
9.1.3 Mach 130F. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 82
9.1.4 Second Footswitch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 84
9.1.5 DCS-F . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 84
9.1.6 Second Unit Control Console. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 84
9.1.7 Dicom . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 85
9.1.8 System Networking / Dicom Nodes . . . . . . . . . . . . . . . . . . . . . . . . 85
9.1.9 DICOM Attribute Configurator. . . . . . . . . . . . . . . . . . . . . . . . . . . . 85
9.1.10 HIPAA. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 85
9.1.11 Paper Printer Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 85
9.1.12 CD/DVD Recorder. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 85
9.1.13 Video recorder . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 86
9.1.14 Intercom System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 86
9.1.15 Starting the Video Manager (VM) . . . . . . . . . . . . . . . . . . . . . . . . . 86
9.1.16 Riverain Soft View . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 87
9.1.17 User Video Output (UVO) on the FL-C . . . . . . . . . . . . . . . . . . . . . . 88
9.1.18 Prognost XPE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 89
9.1.19 Finger Guard . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 89
9.2 UPS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91
9.2.1 APC 1500 Image System UPS . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91
9.2.2 Image System UPS with RPO . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91
9.2.3 Eaton 5P 850i Image System UPS . . . . . . . . . . . . . . . . . . . . . . . . . 93
9.2.4 System UPS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 96
10 Customer-specific Settings 97
10.1 Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 97
10.1.1 Fluoroscopy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 97
10.1.2 Organ Programs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 97
10.1.3 Unit Settings at the Customer's Request . . . . . . . . . . . . . . . . . . . . 97
10.1.4 DICOM Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 98
10.1.5 System Management . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 98
15 Appendix 128
19 Index 139
1.1 Prerequisites
1.1.1 Startup
n The system must be completely cabled.
n The system was prestaged, programmed and tested as a system at the factory. The
Test Certificates are filed in the binder "Technical Documents / System, Register 9".
Depending the version, the illustrations and drawings can appear slightly different from
what has been shipped.
n NOMEX
PTW DIADOS
Required only where DHHS Regulations apply for the measurement of skin dose
rate
(otherwise not needed for checks during startup, only if there is a difference to
required values and a new adjustment is required).
Limit values for over 3 mm over 6 mm over 30 over 120 over over 1000 over
the nominal to 6 mm to 30 mm mm to 120 mm to 400 400 mm to mm to 2000 mm
range mm mm 1000 mm 2000 mm to
4000 mm
Admissible tol‐ ± 0,5 mm ± 1 mm ± 1,5 mm ± 2,5 mm ± 4 mm ± 6 mm ± 8 mm
erance
OT = Overtable
DIT Detector target device (Agile)
SID = Source-image distance
FL = Fluoroscopy
FD = Flat Panel Detector
SSW = Service Software
RG = Optical resolution power
KT = Dose, dose rate measured on the tabletop
KB = Dose, dose rate measured in the image receptor plane
fK = Correction factor for dose detector
m = System attenuation factor
DN = Net optical density (D fog)
SHa = Numerically displayed tomo height on the control console
SHL = Tomo height of laser line light localizer above the tabletop
EST = Exposure steps
EP = Exposure points
IQ = Image Quality
VTX = Vertix exposure station (BWS)
BWS Bucky wall unit
XCS = X-ray Communication System
XCU = X-ray control unit
1.2 Notes
Light blue, metallic Control Console front Bumper, Spray: Part No.: 04011586
Column Cover Panel, Compres‐ Paint stick: Part No.: 04011594
sion
Medical white, C610 Unit Support, Extender Spray: Part No.: 05507467
Paint stick: Part No.: 03444403
White aluminum, RAL 9006 Column top Paint stick: Part No.: 08116431
The color RAL 7035 is used for the lifting/tilting base (there is no Siemens Material Num‐
ber available for this color).
Always observe the general safety information for medical products when performing
work steps and checks. See the RAD FLUORO Safety Information, XRPF-000.860.10.
WARNING
Shut down
Electrical safety, electrical shock, high voltage, line voltage, leakage current.
Risk of injury!
Electrical power is present after shutdown.
Service manual shows where voltage is present after shutdown: service man‐
uals include warnings showing where voltage is present after shutdown.
n hm_serv_unintended_radiation
WARNING
Maintenance
Injury of service technician.
Risk of injury!
Safety design is failing because of power failure.
Remark in service documents that by moving the X-ray tube briefly from the
centered exposure position into the parking position, radiation release can be
disabled. By doing this you can prevent unintended release of radiation, e.g.
while the patient is being transferred or positioned or while the system is be‐
ing cleaned.
n hm_serv_Trained_Technician_only
WARNING
System Operation
Loss of functionality: loss or deterioration of function, assignment of image, data,
objects, work flow and configuration, inadequate user information.
Risk of injury!
Operational hazard due to lack of knowledge of the system, e.g. safety measures
have been ignored by the technician.
Provide training to the technician.
n hm_serv_ProtectiveEarth
WARNING
System Operation
Danger from electric high voltage or line voltage, high voltage, line voltage, leak‐
age current.
Risk of injury!
Problems with protective ground: protective ground is insufficient, disconnected,
connecting screw loose.
Setup Instructions, protective ground measurements are described in the
Startup Instructions and are performed during system installation.
n hm_serv_tube_warning_label
WARNING
System Operation
Thermal energy and high temperature
Risk of injury!
Applied parts too warm, flammable materials, short circuit, defective insulation,
transformer or motor overheating.
Warning sign on the tube housing: a warning sign "Risk of burning" should be
placed on the tube housing. Make a note of this in the service document. In‐
struction in the Replacements of Parts document to place the label on the
tube assembly.
n hm_serv_DetOptLink_Eyeinjury
WARNING
System Operation
Injuries from laser radiation
Risk of injury!
Technician looks into the laser of the optical link (Pix box/ docking station /detec‐
tor).
Service documentation, technician looks into the laser, reason for CAUTION:
Technician looks into the laser of the optical link (Pix box/ docking station/ de‐
tector). Possible consequences: Risk of eye injury. Remedy: Do not look into
the laser diodes of the optical link.
n hm_serv_calibrating
WARNING
Calibration
Unwanted radiation: ionizing radiation.
Risk of injury!
Person in exam room during calibration.
Service training: service training (for service calibration).
n hm_serv_portable_detector_colored_label
WARNING
Portable detector 5500
Delayed diagnosis: inadequate identification.
Risk of injury!
Portable detector switches: portable detector switches from one room to another
(cross-over swapping).
Clear identification: the portable detector as well as the associated system
should have clear identification (e.g. a colored label) to prevent any switching
of detectors from one room to another. (Use same label as for the remote con‐
trol to avoid confusion). Make a note in the service documents (Startup In‐
structions and Replacement of Parts).
n hm_serv_detector_toxic_material
WARNING
Portable detector 5500
Contamination of persons or pollution of environment with thallium particles.
Risk of injury!
Detector is damaged: due to mechanical shock, the detector is damaged and thal‐
lium-doped particles are dispersed.
Note in service documents about toxic materials: make a note in the service
documents, Installation Instructions, Startup Instructions and Replacement of
Parts. How these parts are disposed of in an environmentally friendly manner
has to be documented in the Disposal Instructions. Cause: Toxic materials,
possible consequences: Toxic contamination if detector panel is broken by
mechanical shock. Remedy: Handle portable detector with care! If the detec‐
tor is broken, do not use it; inspect to determine whether any particles have
spilled. Leaked particles have to be collected and kept in a sealed container.
Spilled particles have to be returned to Siemens.
n hm_serv_detector_battery
WARNING
Portable detector 5500
Risk of injury or equipment damage.
Risk of injury!
Incorrect transportation, handling or storage of battery pack.
Note in instructions about the detector battery: note in Startup Instructions
and Disposal Instructions, WARNING: different causes, see manual of battery
pack can result in possible consequences: acid leakage, overheating, smoke
emission, bursting and/or ignition of battery pack.
n hm_serv_DisplayRadiationOn
WARNING
Generate images
Unwanted radiation exposure: ionizing radiation.
Risk of injury!
Accidental release of radiation.
Radiation display on: a light signal interface is provided by the generator
when X-ray is on. One or more lamps may be placed anywhere in the room.
An acoustic signal should also be provided.
n hm_serv_CollimatorAdjust
WARNING
FOV Position
Dose not as desired: ionizing radiation.
Risk of injury!
Incorrect collimator setting.
Adjustment of the collimator plate: adjustment of the collimator plate is de‐
signed so that the edge is visible in the fluoro image.
n hm_serv_ClosedHWloop
WARNING
System in service mode. SW X-ray release.
Unwanted radiation released only by SW: unwanted radiation released only by
SW (closed HW loop in service mode, e.g. during calibration).
Risk of injury!
SW or communication error.
Open HW loop after service; Service Instructions: Do not forget to open the
HW loop after service. Message during next bootup will be displayed to the
user.
n hm_serv_WarnSetUPSPowerMayBePresent
WARNING
UPS operation
Electric shock, ionizing radiation.
Risk of injury!
Power is not switched off; normal power off: Power is not switched off because
the UPS powers the image system.
Note: service note (Service): Unplug the power input connector, note in serv‐
ice manual. If the UPS is configured, unplug the power input connector in the
image system or switch off the UPS prior to beginning service work. If not ob‐
served, death or serious bodily injury can occur.
n hm_serv_Service_SW_Download
WARNING
Service software download
Delayed or no diagnosis.
Risk of injury!
Non-approved SW/HW technician loads non-approved SW or adds non-approved
HW to the system.
Use of unauthorized software: use of unauthorized software or manipulations
and alterations of the SW can cause the product to function incorrectly and
cause injury to the patient and damage to the product. Use software with the
correct version approved by Siemens.
The work sequence in the document is described so that all hazard keys can be taken
into consideration.
For this reason, make absolutely sure to observe the work sequence.
n Specialists
WARNING
Trained Specialists
If not observed, death or serious bodily injury can occur.
These work steps may be performed only by qualified technical personnel.
Qualified in this context means that the personnel have been trained accord‐
ingly or have acquired the necessary experience in practice.
Only trained specialists may performed the work steps listed in this docu‐
ment.
WARNING
Appropriate radiation safety measures must be provided while performing this
work.
If not observed, death or serious bodily injury can occur.
Checks and settings that need to be performed with X-ray radiation switched
on are identified by the radiation warning symbol x.
WARNING
Block release of radiation.
If not observed, death or serious bodily injury can occur.
To block unintentional release of radiation, press the soft button on the TUI, if
it is configured.
Or switch on the SS switch / ignition switch in the generator.
n Motorized Movements
WARNING
Block motorized movements.
If not observed, death or serious bodily injury can occur.
To block unintentional movements, press the soft button on the TUI, if it is
configured, or the EMERGENCY Stop on the unit.
WARNING
Prior to beginning work, make absolutely sure to switch off power to the particu‐
lar assembly:
If not observed, death or serious bodily injury can occur.
Completely switch power off to the entire X-ray system at the on-site on/off
switch and secure it against unintentional switch-on.
Only original screws may be used.
If not observed, cables can be damaged.
n Original Parts
WARNING
Danger caused by electrical voltage!
If a UPS is used, the system is not without power if the power source is inter‐
rupted. In a service situation, switch off the UPS or unplug the connector for
the image system power supply.
Fig. 3: AEC chamber connection Checking the CAN connection for the AEC
chamber:
n A1.JK.X1 is plugged in to CAN IN (1)
n A1.JK.X2 is plugged in to MODE SELECT
(2)
hm_serv_ProtectiveEarth
WARNING
Danger caused by electrical voltage!
If using an image system UPS without the RPO or ROO (Remote Power OFF,
ON/OFF), the FL-C is still being supplied with power.
2.1.6 Network
n Make sure from the hospital's local network administrator that the network socket for
the Luminos system is present and active.
- Luminos System
For options, e.g. X-Workplace, etc., a separate network socket is always required.
n The TCP/IP addresses (IP address, WNS, DNS) are required for the network connections
described. These data should already be available when startup is begun.
If needed, ask for the data from the hospital's local network administrator so
that unnecessary waiting can be avoided later.
To avoid disturbances in the hospital network, reconnect the network cable only after
setting up the network in the FL-C.
To achieve the full generator power, the measured internal line resistance may not ex‐
ceed the following values.
max. RLine
ULine Range
63 kW 80 kW
380 V 342 V ... 418 V 0.15 Ohm 0.09 Ohm
400 V 360 V ... 440 V 0.17 Ohm 0.11 Ohm
max. RLine
ULine Range
63 kW 80 kW
440 V 396 A ... 484 V 0.20 Ohm 0.14 Ohm
480 V 432 V ... 528 V 0.24 Ohm 0.16 Ohm
n If there is a higher internal line resistance, the generator power is automatically re‐
duced.
If the input voltages need to be changed, set the T1 jumpers in the M2 in the Luminos
dRF as follows.
Tab. 2 Input Voltage on the dRF M2 T1 (see also the Luminos dRF Basic Unit Wiring Diagram)
Variable Password
n To log into the SSW again and for remote operation, you need only the last 6 charac‐
ters of the variable password.
n If the password already generated is no longer known, this can also be read out from
the "Census Tool" by entering the system Part No. and Serial No.
2.4.2 Measuring Point for Room Dimensions and Spacing of the BWS
Fig. 7: Measuring point on the lifting base plate Measuring Point for the SSW and Spac‐
ing of the BWS
n The measuring point is located at
the intersection of the left front cor‐
ner of the lifting base floor plate.
3.1 Preparation
The current 4343F detector will be replaced by the optically identical 4343F3 detector
(for the designation, see the packing label).
With the 4343F3 detector, the Pix Box is already integrated into the detector. To connect
it in the generator, see the chapter "Generator", "Connecting the Components to the Gen‐
erator".
CAUTION
Risk of damage to the detector.
The 4343F detector must be slowly acclimatized to the temperature and humidity
in the room in the sealed transport crate.
Keep the unopened transport crate in the examination room 24 hours prior to
removing the detector.
For detectors without shock, humidity or temperature sensors, evaluation of the particu‐
lar sensor is no longer necessary.
3.1.2.1 Vibrations
3.1.2.2 Unpacking
Replacement film and a desiccant are located in the detector packaging that should be
kept in case the detector needs to be returned.
Fig. 9: Acclimitization of the detector n Open the transport crate and take
out the detector.
n Open the plastic packaging!
Fig. 11: Display for the maximum and minimum tem‐ Thermometer (if present)
perature
n Located under the detector.
n Read the max. temp. and the min.
temp. by pressing the MAX/MIN but‐
ton.
Specification for detector transport:
-25˚ to +55˚.
If the shock sensor has responded or if the value of an indicator is not within specifica‐
tions , send the information below (or a copy of this page, filled out) by e-mail or fax:
Report:
Inhalt/Contents:
Values: Specification:
Humidity max.: _______ [%] < 60%
Temp. min.: _______ [˚C] > - 25˚C
Temp. max.: _______ [˚C] < + 55˚C
Shock indicator ok [ ] nok [ ]
Function of Detector: ok [ ] nok [ ]
3.4 Installation
Fig. 12: Detector installation (1) 1. Position the Luminos dFR unit sup‐
port so it is vertical.
2. Remove the connector plate for the
Ethernet cable on the detector con‐
nector.
3. Remove the detector mount from the
detector insert on the unit support.
4. Move the unit support into the hori‐
zontal position.
5. Place the FD on the transport crate
and secure the detector mount in
place using eight M5x15 Allen screws
(1) Mounting screws
and insulation sleeves on both sides
so it is insulated (1).
6. Position the unit support at about the
20˚ position.
7. Place the FD with the mount on the
transport crate and slide it under the
table from the head end.
Prior to connecting the ground wire, check for isolated installation of the detector with
an Ohm meter. There may be no connection between the grounding stud and the detec‐
tor mount. The resistance must be infinite.
CAUTION
Injury to the eyes.
The detector transfers the data to t he Pix Box and to the FLC using a fiber optic
cable and a laser.
Under no circumstances should you look directly into a reflecting laser beam.
Under no circumstances should you look into the ends of the fiber optic ca‐
bles!
Connect the cables per the designations and secure them with cable ties.
The ground wire is connected to the machined-out grounding point.
3.4.5 Grid
Fig. 17: Inserting the grid 1. Carefully insert the grid into the top
rail (arrow) and let it snap in place.
2. To remove them, press the two
round latching studs on the right
and left.
Beginning with VD10, a D611 with Part No. 10569108 is used in the generator. The S2
switch on the D600 must be set to "ON" (left) for the function of the new D611.
4.1.3.1 Checking the Starter and the Rotating Anode of all Tube Units
n Set the SS switch to OFF (S1 on the D600 board in the generator).
n Select any "RAD" program.
n Press the exposure switch at the generator control console to prep:
The rotating anode starts with no unusual noises.
P n
Release the prep button again:
The rotating anode will be braked.
In a malfunction situation, the connections should be checked at the K7/K8 relay in the
generator.
Connection Use
Control System
D600 X223 CAN out
D611.X15 FL-C Interface
D611.X18 KermaX
D611.X19 Control Console
D612.X32, X33, X34 AEC chambers
Monitoring Devices and Displays for Radiation Safety
D612.X23, 4, 5, 6 and 7, 8 External radiation display, potential-free
WS1. D612.X14, 7/8 Workstation-related radiation display
(24 V / 5 W); WS 1 via FLC M59.X1.
WS1: D612.X14, 1/2 WS 1 oil pressure switch
WS1: D612.X14, 3/4. 24V from the gen‐ Door Contacts to Block Radiation
erator. With interventional workstations, no
door contacts may be connected!
External Connections
D612.X23, 2/3 Room light control
D611.X23, 1/2 Emergency power
D611.X21, 1/2. 24V from the generator X-ray disable
Switch
Port 5; System control console
Port 6; FLC (M59.X2)
Port 7; -
Port 8; SCU Ethernet (Uplink)
PixBox
System; M59.FDR1 (fiber optic cable, Aurora)
Front End; Detector (fiber optic cable)
Front End Power; Detector power supply
Power In; DSM (Detector Supply Module)
X n
Select SSW > Tune Up > Tube > Condition for the particular X-ray tube, or start “auto
tube conditioning” in the SSW menu under “Configuration” > “Autoinstallation” and
perform conditioning.
P n
During conditioning, the kV.act and the mA.act must be checked using the oscillo‐
scope.
- GND D600 X63 (ANA_GND)
- KV.act (D600 X96 UT_act), 1 V = 20 kV
- mA.act (D600 X67 IT_act), 1 V = 1 mA with fluoroscopy or 200 mA with exposure.
Stop the procedure if the X-ray tube tends to "arc" strongly and repeatedly or if the expo‐
sure is aborted. Then maintain a pause of 5 minutes and start the complete procedure
again. Replace the affected X-ray tube if there are two additional failed attempts.
n Again select an organ program with "free cassette exposure" for the 2nd plane at the
control console and perform conditioning as described for the system with 1 tube
unit.
Stop the procedure if the X-ray tube tends to "arc" strongly and repeatedly or if the expo‐
sure is aborted. Then maintain a pause of 5 minutes and start the complete procedure
again. Replace the affected X-ray tube if there are two additional failed attempts.
X Trigger a exposure with both the large focus and with the small focus for all connected
tube units.
P The voltage must be even during the entire exposure.
Tolerances: Small / large focus 73.15 kV - 80.85 kV
Perform this determination only if the required values for the internal power line resist‐
ance or the power line voltage are not reached (chapter "General Startup").
Procedure:
n Protect the detector. To do this, insert lead into the collimator or cover the detector
with a lead apron or move it out of the centered position.
n Select Examination, select the test organ program with free exposure.
- Large focus, 100% power.
- 100 kV
- 63 mAs (63 kW) or 80 mAs (80 kW)
-100 ms
Test points:
X n
Trigger exposure and use the oscilloscope to measure the kV and mA.
n Calculate the max. power from the measured kV and mA:
Fig. 19:
If the maximum power must be limited, this must be discussed with the Project Manag‐
er. The reduced value must be entered into the Startup Certificate and reason for the re‐
duction must be described in the Remarks regarding Checks.
The foam plastic of the switch-off strip is very sensitive and must therefore be handled
with care.
The fiber optic cables may not be sharply bent. Pressure on the fiber optic cables will
trigger the safety circuit.
Jumper J1/J2
LWL LWL
LED PWR
X1
Learn procedure:
1. Connect all fiber optic cables.
2. Interrupt the power supply by unplugging the X1 connector.
3. Establish bridges with jumpers J1 and J2.
4. Plug the X1 back in.
In the learn mode, only the red LEDs need to be observed.
After 1-2 seconds, the learn procedure is concluded.
If the routine was successful, the EXT1 and EXT2 LEDs and the INT1 and INT2 LEDs do not
go on.
Self check:
1. Interrupt the power supply by unplugging the X1 connector.
2. Connect all fiber optic cables.
3. Remove the bridges with jumpers J1 and J2 (plug them in on one side).
4. Plug the X1 power supply back in.
All switch-off elements are now switched on, one after the other, and the safety circuit is
closed. The MOS 1 to MOS 4 LEDs are on.
If not all switch-off elements are closed, installation of the switch strip must be checked
for errors (e.g. fiber optic cable crushed, ...).
The MOS 1 to MOS 4 LEDs indicate the status of switch elements 1 to 4.
n LED on = switch element closed
n LED off = switch element open.
Following the self check, problem-free function of the switch-off strip must be checked by
pressing it manually.
Take note of the park position of the 3D (option) as to whether it happens to be in the
collision zone of the Luminos.
The front and rear wall spacing do not have to be entered for fluoro systems (leave the
default values).
5.1.2.5 Adaptation
Adaptation of the system to the room dimensions is performed in the following screen.
n SSW - Configuration - Stand - Configuration of Group Room Configuration
n Make sure that the tabletop is moved in so that it always remains 12 cm above
the floor.
With the 90˚/90˚ option, also perform the check in the Trendelenburg position and with
the table on the left.
4
5
3
2
1
6.1 General
6.1.1 Network
To avoid problems in the hospital network, disconnect the LAN network cable prior to
switching on power. The cable may be plugged back in only after setting up the network
in the FL-C.
6.1.2 Switching on
With UPS: Prior to switching on the FLC, ensure that the emergency power supply is con‐
nected properly.
6.1.3 Function
n Create a new patient or an emergency patient.
n Select the Examination tab card at the FL-C.
n Place an object, e.g. the precision radiation filter, in the beam path.
n To determine the basic function, acquire several DR test exposures.
6.1.4 Monitors
Adjustment of the 19 inch monitors is described in “Replacement of Parts”
(TD00-000.814.24....) in the CB-DOC.
6.1.5.1 Normal situation: The application is started and the system is working without prob‐
lem.
The FL-C is shut down when the system is switched "OFF". Approx. 1 minute after the
computer has shut down, the FL-C switches off automatically.
The customer-specific setup and configuration of the option is performed by the custom‐
er's network administrator and the application specialist.
Use the following registration parameters for startup with HIPAA, otherwise configuration
of the FL-C will not be possible.
n Registration in HIPAA with Log-in
n User name: flcadmin
n Password: flcadmin
The variable password is administered by the "License Center” in TD HSC or by the USC in
the countries.
If the entry is accepted, the service window appears with the configuration menu:
Under Help, you will find an Online Help service that describes the individual steps. On‐
line Help has been installed at the factory.
6.1.8 Adjustments
Time and Language:
P n
The system time is set in Windows under "Start", "Settings", "System Controller", "Date
and Time".
- For automatic adjustment to daylight savings time/standard time, the “Set clock
automatically to daylight savings/standard time" box must be marked under
"Time Zone".
n Keyboard / National Language: To make the adjustment, see the Online Help, chap‐
ter “System”, “System Settings”.
Make entries in the boxes. Be very careful when filling in the numerical boxes so that the
logs will be correctly allocated in the server.
System Serial No. Please enter the Serial Number that is on the same label
here, similar to the system Part No.
5-digit, beginning with 04...
Handover Date Date on which the system was started up, e.g. 01/2003
P n
Save with <Save>.
When entering the AE title for the “Dicom Query Retrieve” function with FL-C, it must be
ensured that the names for the "Storage (SCP)" has to be different from all other local
AETs.
a) Set the network mask for the AXCS network to 255.255.255.0, if not already as‐
signed.
b) Make sure that neither the system IP address nor the IP addresses for network no‐
des to be configured (printer, PACS, etc.) or the IP address for the default gateway
are outside of the address range 10.1.1.0 to 10.1.1.255. However if this is the
case, a router with NAT (Network Addressed Translation) is required. The router
with NAT is available as a CS solution (see Note: Router with NAT).
n 10.1.x.x net mask 255.255.0.0
a) Set the network mask for the AXCS network to 255.255.255.0, if not already as‐
signed.
b) Make sure that neither the system IP address nor the IP addresses for network no‐
des to be configured (printer, PACS, etc.) or the IP address for the default gateway
are outside of the address range 10.1.1.0 to 10.1.1.255. However if this is the
case, a router with NAT (Network Addressed Translation) is required. The router
with NAT is available as a CS solution (see Note: Router with NAT).
n 10.1.1.x, net mask 255.255.255.0
a) If the hospital IP addresses in this range are being used, a router with NAT (Net‐
work Addressed Translation) is required. The router with NAT is available as a CS
solution (see Note: Router with NAT).
CS Service Files:
n The “Online Help“ CD-ROM is located in the System Binder.
n Select <Configuration> / <Local Installation> in the service mode.
- Insert the FL Compact Online help CD-ROM into the drive and wait until the LED
stops blinking.
- Select <Local Installation> and confirm with “GO”.
- When the copy routine has finished, press the space bar, remove the CD from the
drive and file it again in the System binder.
n After a new system start, the Online Help can be selected in the SSW with the Help
button.
6.3.1 Options
Perform a check for all options ordered by the customer to determine whether the license
codes have been entered.
n To do this, select "Configuration/ License” in FL-C service.
n Select the affected options and check whether a license has been entered.
A B
C D E
F G H
SSW Parameters:
n System designation ( A/Fig. 26 Page 61)
n Customer name ( B/Fig. 26 Page 61)
n Software status ( C/Fig. 26 Page 61)
n System identification number ( D/Fig. 26 Page 61)
n System Serial Number ( E/Fig. 26 Page 61)
n Change box to accept a new password. ( F/Fig. 26 Page 61)
n First 14 characters of the variable password. ( G/Fig. 26 Page 61)
1 2 3 4
5 6 7
8
n FL-C Service: FL-C configuration and service software. ( 8/Fig. 27 Page 62)
7.2 Detector
DANGER
There is voltage still present at the PixBox at the top left in the generator and at
the detector when the Luminos system is switched off.
There is no voltage present at the components when the F1 main switch in
the generator or the system switch is switched off.
For operation, the communication switch on the Pix Box front panel must be set to "Au‐
rora". Otherwise, no communication with the detector will be possible.
NOTICE
Impairment of image quality!
If the detector is recalibrated during customer startup without sufficient reason,
serious disturbances can occur in the examination images.
Under normal circumstances, do not calibrate the detector during startup! Cal‐
ibration has already been performed at the factory. The settings should be
kept.
Perform calibration only if serious disturbances occur during startup (pixel
blinking or missing columns) and only of the affected mode.
NOTICE
Incorrect calibration results.
A minimum temperature drift of the detector can skew the results.
Prior to calibrating the detector, the cover panels must be installed and the
acclimatization times (see below) must be observed.
It must be noted that prior to starting a calibration, the tube heating display may not be
more than 30% (particularly prior to calibration of the DR and RAD modes).
The detector temperature is monitored by the system. A calibration is possible only after
20 minutes at a constant temperature (the counter is reset when there is a reboot).
a) In the SSW, select <FD Calibration> under <Tune Up> <System Adjust>.
b) Select only the mode to be calibrated.
X c) Starting Calibration
d) Following as successful procedure, conclude with “Save” and “Exit”.
If several high-dose modes (DSA/RAD) are incorrect, a wait time of at least 5 hours must
be maintained between the calibrations.
a) Check the beam path for soiling (e.g. metal shavings, etc....), if needed, clean all
surfaces.
b) Check the collimator opening (must be completely opened).
c) Resetting the "not accepted" calibration:
Select only the incorrect calibration mode in the SSW (checkmark) an click on <Re‐
set> in the bottom command bar.
d) Recalibrate the mode. With the high dose mode, maintain a wait time of 5 hours.
7.3 System
For the adjustment, the column rear cover panel must be installed.
If the rear column cover panel is installed with the column laying down, it can affect cen‐
tral beam drift.
Always install the column cover panel while in an upright position.
Check:
n Remove the grid.
n Place a marker (small washer) in the center of the grid.
n Insert the grid.
n Set the SIDmin.
X n
Switch on fluoroscopy.
n Open the collimator plates horizontally and vertically just in front of the outside moni‐
tor edges.
n Save the LIH image.
n Determine the center of the radiation field with the corners of the collimator using the
graphic function.
n Set the SIDmax.
n Open the collimator plates again to the outside monitor edges.
n Repeat the marker procedure using the graphic function.
n By switching the images, determine the drift of the central beam to the center marker
at SIDmin. and at SIDmax. (Maximum drift 3mm on the screen, but not in the direc‐
tion of the operator.)
Fig. 30: Tube unit adjustment, operator's side - wall Mechanical tube unit adjustment:
side
n Slightly loosen the screws in the half
cowls (arrows).
n Adjust the tube unit by turning it in
the mounting half cowls.
n Retighten the screws.
n Check the adjustment; if needed, re‐
peat it.
Fig. 31: Tube unit base plates Tube Unit Adjustment (adjusted at the
factory)
1. Base Plate 1 (rotation)
2. Base Plate 2 (operator's side / wall
side)
1 3. Base Plate 3 (head end / foot end)
2
7.3.8.1 Fluoroscopy
n Select the tube unit.
n Reset the μGy/cm2 display with a new patient.
n Insert 2.1 mm Cu into the beam path.
n Completely open the collimator.
n Set the max. SID.
X
n
Trigger fluoro for 30 s.
n The value of the area dose product (μGy/cm2) displayed on the monitor must increase
continuously.
7.3.8.2 Exposure
n Select the tube unit.
n Reset the μGy/cm2 display be entering a new patient.
If the Dexi value is not half of what it was, check the connection and cabling of the AEC
chamber.
P Perform the check for all AEC chambers.
Deselect the physical EXI values again.
8.1 Checks
The measurement height of the stand must be set to the customer's request for the ad‐
justments under “Service" > "Configuration" > "System" > "System Config" > "Ortho Op‐
tions" (( 1/Fig. 33 Page 75))
If an Ortho position using the portable detector is saved in portrait format, an error mes‐
Start the "Pex Editor" and double-click on the desired Ortho OGP (e.g. ortho_Ta‐
ble)_SID130) in the "Examination View".
Switch to the "Param. Module" tab card and select, for example, "Table C150" under
"Stand Position". Save the current position with "Store Position" and then click on "Save"
and "Close".
1. Select the Settings tab card and start the Pex Editor by clicking on the icons (1).
Fig. 34: Service Mode, Settings tab
3. Enter the tcapmoc password (2) and confirm with <OK> (3).
Fig. 35: PEX Editor log-in page
3 2
All stand positions for Ortho with a mobile detector in the BWS and table must be saved
in the detector landscape format.
5. Insert a grid (115/150) into the detector tray and center the 3D to the table with the
Centering key.
- Enter an unused identifier that begins with “s” in the Identifier box (2). For exam‐
ple, s099.
- Enter an unused name in the Name box (3). For example “Tomo Test”.
- The Store Position button appears by selecting New (4).
- Save the stand position by selecting Store Position.
1
2
3
4
6 5
Fig. 38: Ortho start and end positions Ortho Test Procedure:
1. Open a patient and select an Ortho
OGP with the 1-pt technique.
2. Press the OGP button / Centering
button to move into the organ pro‐
gram position, or manually move
the system into the organ program
position. For the measurement, a
smaller SID than the one saved in
the OGP can be used.
3. Turn the tube unit so it points to the
left and collimate the light field so
that it does not over-expose the
travel range in the left direction.
4. Save the position on the TUI with
button 1.
5. Turn the tube unit so it points to the
right and collimate the light field so
that it does not over-expose the
travel range in the right direction.
6. Save the position on the TUI with
button 2.
7. Press and hold the pre-contact (first
pressure point) until movement into
the start position is complete. Trig‐
ger an exposure (second pressure
point) and hold until the procedure
has completed.
9.1 Components
The surface of the compression cover panel is very sensitive. Avoid mechanical damage
during installation!
If compression is configured in the software, but not connected, the unit cannot be
moved.
Adjusting Compression
1. Start "Online Help" and perform the adjustment.
2. When moving out the compression, the compression force display must be at 0.
3. Perform the check of switch-off again.
3
2
9.1.5 DCS-F
Fig. 43: Mobile control console Connect the second control console to the hub
foot and check functions.
9.1.7 Dicom
n The Dicom options are released in the SSW of the FL-C and is configured at the plant
(key required).
9.1.10 HIPAA
Setup of the option is performed by the application specialist.
n For startup, see the chapter ( HIPAA / Page 85).
For configuration and startup, also see the Installation and Startup document “BARCO
MVSP10 Video Manager” XPL5-360.814.01... in the blue binder.
Function Test:
n When the footswitch is pressed, the image fed to the FL-C via DICOM (X2-B - ETH 1)
must be displayed on the reference monitor.
Startup:
n Put the system into operation and test it using the Installation and Startup Instruc‐
tions, XPRF-RSV.814.02... (in the blue binder).
n The monitor, keyboard and mouse are needed for configuration of the system and can
be kept for later use in a nearby location.
Fig. 45: External video connection External Video Connection on the FL-C
1. Splitter
11 2. Power Supply for the Splitter
3. Fiber-optic cable, 35 m (stow excess
length carefully in the FL-C or a ca‐
ble duct)
10 4. Power supply for DVI coupler (to be
3
9 connected to customer power out‐
4 let)
5. DVI coupler with fiber-optic cable
connection for external monitors
8 6. DVI connection from the FL-C graph‐
2 ics card
Fig. 46: Prognost XPE The correct Prognost XPE power supply
(230 V/115 V) must be set using a
jumper.
The correct fuses must be inserted de‐
pending on the power supply voltage
that was selected.
1 1
Fig. 49: Fingerschutz vorn Installing the Finger Guard (front and back)
n Secure the transparent plastic deflector (1) on
the patient table with the double-stick tape.
2
n To do this, clean the entire adhesive area with
alcohol and pull the film off the adhesive sur‐
face on the aluminum profile of the finger
guard (2).
3 1 n Place the profile 3 mm inside the edge of the
table (3) and 1 mm below the top edge along
the entire length and press down on it.
9.2 UPS
WARNING
Danger caused by electrical voltage!
If a UPS is used, the system is not switched off to power automatically if the
power source is interrupted. In a service situation, switch off the UPS or un‐
plug the connector for the image system power supply.
Fig. 50: FLC UPS APC 1500V; only for the FL-C image system
n The UPS must be set up per the Project
Plan in the vicinity of the image system.
n The power supply voltage runs through
the UPS with a connection cable to the in‐
put of the image system.
1
Note!
Before startup, plug in the connector plug
of the rechargeable battery (1) and make
sure the connector is properly seated.
RPO
Fig. 52: RPO control unit UPS RPO (Remote Power Off)
n If there is no cable from the RPO contact,
Pins 2 and 5 in the connector can be jum‐
pered, but only for a function test.
n The RPO control unit (UPS Remote Power
Off Device) is secured on the UPS with
Velcro tape.
DIP switches 1 and 3 and must be point‐
ing down (on), all others must be pointing
up (off).
Test of the UPS with RPO
n Unplug the “RPO/Cascade in” connector
for the internal test of the RPO.
The UPS must switch off.
n Switch off the system power supply for
the external test of the RPO.
The UPS must maintain the power
supply to the image system.
n Press the system EMERGENCY OFF switch
for the EMERGENCY OFF test of the RPO.
The UPS must switch off.
WARNING
Danger caused by electrical voltage!
If a UPS is used, the system is not switched off from power automatically if
the power source is interrupted. In a service situation, switch off the UPS or
unplug the connector for the image system power supply.
hm_serv_SwitchOffUPS
Fig. 53: Eaton 850 Front Fig. 54: Eaton 850, back
1 2
7
3
4
2 3 4 5 6
6 7
1
7
Prior to initial startup, check for correct seating of the connector ( 1-4/Fig. 54 Page 94).
n UPS power supply ( 1/Fig. 54 Page 94) from the power strip in the FL-C.
n Power supply for the Live monitor in the control room ( 2/Fig. 54 Page 94)
n Power supply for the FL-C ( 3/Fig. 54 Page 94) at the computer
n Power supply for the DVI splitter ( 4/Fig. 54 Page 94) when the FL-C has the built-in
User Video Output option.
n ROO (Remote ON/Off) contact from the “Emergency Off” switch (opener)
- Leave the RPO jumper ( 5/Fig. 54 Page 94) on the UPS and connect the ROO con‐
tact for the “Emergency Off” switch at the two bottom terminals
( 6/Fig. 54 Page 94).
hm_serv_RemoteEmergencyPowerOffUPS
10.1 Settings
10.1.1 Fluoroscopy
P
n
If a change is made to the fluoro time, check the function.
P If due to the local conditions (view to the patient), the head and foot ends are to be
switched on the monitor, proceed as follows:
n Select Configuration > System Config > Mirrored Installation “Yes”.
P n
If Mirrored was set, check the joystick functions.
NOTICE
Disturbances in the Examination Images
Detector Calibration
If the examination image shows significant disturbances such as pixel blink‐
ing or missing columns, only the particular detector mode must be recalibra‐
ted prior to performing the Handover Test.
See the chapter “Detector Calibration”
P To check the image quality at the customer's location, work through the IQAP in the SSW
under “Quality Assurance”, “IQAP Control Functions”, “New”, “Available Inspections”,
<Handover> ( Fig. 56 Page 101).
Selecting the particular plane or stand (switch plane)
With subsequent adjustments (e.g. Detector Sharing), a "Partial Test" must be performed.
The “Basic Test” has already been performed at the factory.
n Constancy test
- The test must be performed basically with the customer's own test equipment, if
possible along with the person responsible for the system at the hospital.
- If the customer has no test equipment of his own (e.g. when in a new facility), com‐
plete the acceptance without the constancy test.
n Sign the certificates.
n Provide all documents to the specialist for the acceptance. If no final specialist test is
performed, file the certificates in the system binder.
Fig. 57: Tube unit cover panel Tube unit cover panel:
n Place on the two halves of the tube unit
cover panel (1). When doing this, snap on
the front grid (2).
Fig. 58: Cable routing to the tube unit Cable routing to the tube unit:
n Lay the cables to the cover panel as shown
on the left.
The rear column cover panel may be installed only when the unit is in the 0˚ position
and the column is vertical.
Fig. 61: Lifting base cover panel Install the cover panels on the lifting base in
the following sequence:
1. Rear wall of the lifting base (3)
1 ( Fig. 62 Page 106)
2. Side panels of the lifting base (2)
3. Cover of the lifting base (1)
When doing this, pay attention to the
length of the front mounting screws
(M4x10).
3
Fig. 62: Lifting base, rear cover panel Install the back wall on the spacer studs.
If the system is installed close to a rear wall,
install the cover panel prior to installing the
lifting base (see the chapter "Installing the
Lifting Base").
Fig. 64: Cable outlet on the lifting base Install the cable outlet (Pos. 1) according to
the position of the cable channel and the ca‐
ble guide on the lifting base. To do this, se‐
cure the mounting bracket on the floor
plate, left or right rear, and fasten the cable
outlet with 4 paneling screws. (Long holes)
1
13.1.4 Extender
Fig. 65: Crush protection on the extension n On new systems, a safety plate (arrow) is
attached to the extension. The plate pro‐
tects against crushing between the col‐
umns and extension.
3
n Secure the crush protector on the extend‐
3 er (Pos. 2) with 6 screws on the strut.
n Place on the two warning labels (Pos. 3)
(Risk of Crushing).
n Then connect the side cover panels on the
2 extender with the grounding wires and
secure the panels in place (see the illustra‐
tions below).
Fig. 68: Left extender cover Fig. 69: Right extender cover
Fig. 70: Side cover panel, head-end Install the cover panels on the extender in the
following sequence.
n Insert the head-end side cover panel.
- - Secure the cover panel in place with
the paneling screws (Pos. 2).
- Do not yet turn in the 5 mm long side
screws (Pos. 1).
Cable cover for the extender
n Remove the pins from the black plastic
dowels (not used), insert the dowels di‐
rectly into the holes of the extender.
n Place the cover panels on the plastic dow‐
els and secure them with the paneling
screws.
- Turn in the 5 mm long side screws (Pos.
1).
Fig. 71: Side cover panel, foot-end Foot-end side cover panel
n Slide the covers into each other (Pos. 2)
and secure them with paneling screws.
With all cover panels, make sure that the ground wires are connected and laid so that
they cannot be pinched.
Fig. 72: Safety cushions n Take the two safety cushions (Pos. 1) out
of the packaging and secure them in
place on the extension with double-sided
tape.
Fig. 73: Table cover panel, right Install the foot-end cover panels in the follow‐
ing sequence:
1. Side cover panel
- Install the side cover panel (Pos. 1).
2 - Secure with paneling screws.
3 2. Front cover panel
- Insert the front cover panel (Pos. 2)
from the front into the side cover panel.
1 - Secure with paneling screws.
3. As shown in the red outline, insert the pro‐
tective bracket (Pos. 3).
Fig. 75: Head-end cover panel n Install the head-end cover on the motor
controller (arrow) and secure it with panel‐
ing screws.
The rear chain cover ( 1/Fig. 78 Page 114) for the table longitudinal drive is installed
during startup (it must be possible to move the table for this). Following system installa‐
tion, keep the cover panel in a safe location that is accessible to the startup technician.
The rear chain cover ( 1/Fig. 78 Page 114) can also be installed with the compression
installed if the aluminum front panel ( 1/Fig. 77 Page 113) for the table is removed
and the cover panel ( 2/Fig. 77 Page 113) has been pulled forward.
Fig. 76: Front panel from below Fig. 77: Front panel
Fig. 78: Chain cover Installation of the chain cover without remov‐
ing the front panel:
n Move the patient table all the way for‐
ward.
1
n If a patient switch strip
( 1/Fig. 79 Page 115) that is already in‐
3 stalled, remove it (6 paneling screws),
slightly spread it open and slide it up.
n Position the cover panel as shown on the
left ((Pos. 1) arrow). When doing this, in‐
sert the edge on the table so that is it
2 completely guided.
Head and foot ends:
n Secure with the paneling screws (Pos. 2).
n Insert the 4x35 Allen screws (Pos. 3) into
the holes (arrows) and tighten them.
n Place the plastic covers (Pos. 3) over the
holes.
The edge cover panel is installed only during startup and until then should be kept in a
safe place.
Fig. 79: Switch strip without compression Install the cover panel during startup:
n The cover panel ( 2/Fig. 79 Page 115) is
attached approx. 2mm over the patient
switch strip ( 1/Fig. 79 Page 115).
When handling it and during installation, always make sure that it does not get scratch‐
ed or dented.
Fig. 83: Cable cover n Arrange the cables evenly and make sure
that any cable ties or tape have been re‐
moved from the cable bundle. (It should
be possible to move the cables freely in
the zipper hose.)
n Place on the zipper hose (Pos. 1) and se‐
cure it with cable ties at locations (Pos. 2)
and (Pos. 3).
When doing this, make sure that the
zipper is facing up (to prevent damaging
the paint finish on the lifting base)
Fig. 84: dRF body unit cover panel The bottom body unit cover panel (Pos. 1) and
the cover (Pos. 2) are installed during startup
b (following installation of the detector).
The installation team has stored the cover panel
a in a safe location in the vicinity of the system.
Following startup, install the two cover panels
with the paneling screws provided that are (a) =
5 mm, (b) = 10 mm long).
b
2 1
a b
14.1.2 Backup
P The backup (beginning with VC10) is performed in the SSW with the "local" backup medi‐
um.
n The data are saved on both internal hard disks.
n Even if CD/DVD is selected, a backup on the internal hard disk is generated parallel to
this.
Exit Service.
P
n
Deleting the "FLCompact.log" File
P Perform the measurement as described below and enter the measurement values re‐
quired in the Startup Certificate.
n Power must be switched off to the system.
n Measuring de‐ Ground wire test meter: SECUTEST SIII general purpose test meter or
vice: equivalent
Follow the instructions in the Operator Manual.
n Measurement ≤ 0.15 Ohm, +10%
value:
n Test Proce‐ Measure between all measuring points specified in the Startup
dure: Certificate, exposed conductive parts of the system and the
ground wire bus bar in the generator.
The measurement must be performed with (automatic or manual) re‐
verse poling of the measurement voltage or with current flow in both
directions.
Note: With the Secutest, there is a reverse poling button, while with
the Profitest, reverse poling takes place automatically.
Sample overview:
Fig. 85: Ground wire test with fixed power line connection
hm_serv_ProtectiveEarth
3 5
2
1
Fig. 87: Footswitch n The labels with the symbols for "Exposure"
must be placed on the left and for "Fluoro‐
scopy" must be placed on the right.
n Place the 2nd label (if present) in with the
service materials.
14.2.4 Labels
n Warning labels in the national language
If warning labels are available as adhesive labels in the national language (e.g. in the
System Owners Manual or even with the accessories), the appropriate warning label
must be placed over the existing one on the corresponding component. When dong
this, make sure that the label has proper adhesion.
n Additional labels
If required according to country-specific requirements, additional labels will be ship‐
ped in the System Owner Manual in Register 9. These labels are to be affixed, as nee‐
ded, according to the instructions in Register 9. When dong this, make sure that the
labels are clearly visible and have proper adhesion.
14.2.7 Certificates
Certificates (e.g. for China, ...) are filed in the System binder, Register 9.
For this, save the data and save them on the Internet under the following link:
https://intranet.med.siemens.com/P16/index.html
This can also be done after completing startup.
2.
15 Appendix
3.
08.15
4.
5.
XPD3-500.815.01.10.02
6.
7.
XP SCM EN
8.
10.
*1 Can be set free by the FSE for our Equipment, but must be unique within the network. For existing devices (workstations, printers etc.)
Hoste name and AE Tiltles must be questioned from the hospital IT personal.
© Siemens, 2012
Changes to Previous Version 16 129
Chapter Changes
Options Installation of the finger guard added.
Startup Certificate Company name "Healthcare GmbH" updated.
All Editorial revisions.
Training Requirements
Due to significant changes in this document / new publication of this document,
user training is required.
Due to slight changes in this document, user training is not required.
17.1.1 Notes
17.1.2 Checks
Tab. 4 Checks
2 ( Image System UPS (Option) / Page 21); battery connection jumper instal‐
Q Q Q
led.
3 ( Transport Brackets / Page 21); All transport safety devices removed Q Q
12 Conditioning the X-ray Tube; ( With High Voltage (all connected Tube
Q Q
Units) / Page 43)
13 Checking the Tube Unit Voltage (all connected tube units);
Q Q
( Checking the Tube Voltage / Page 45)
14 ( Checking the maximum Generator Power / Page 45); Q
(if necessary) ______kW
15 ( Starting Up the Patient Switch-off Strip on the Unit Column / Page 47);
Function Q Q
23 ( Checking the Image Position / Page 66); image position on the monitors
Q Q
checked.
24 ( Centered Position of the DAP Chamber in the Collimator / Page 66) Q Q
56 Final Visual Check according to IEC 62353; ( Final Visual Check / Page 127) Q Q
17.1.4 Remarks regarding the checks, problems that occurred, open items
Tab. 6 Remarks regarding the tests performed and problems that occurred
Open Points
Startup technician:
Department:
Telephone:
I hereby verify:
n performance of startup according to the technical documents provided by the manu‐
facturer,
n performance of all required measurements; the values are within the tolerance range
of manufacturer's specifications,
n successful completion of all safety and function tests and their documentation.
Tab. 10 Signature
H Hazard ID
hm_serv_ProtectiveEarth ................................................................................. 23, 123
hm_serv_RemoteEmergencyPowerOffUPS ............................................................... 95
hm_serv_SwitchOffUPS ........................................................................................... 93
healthcare.siemens.com/services
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