5146132-100 Planned Maintenance 4
5146132-100 Planned Maintenance 4
5146132-100 Planned Maintenance 4
Technical
Publication
5146132-100
Revision 4
GE Medical Systems
Precision RXi® Planned Maintenance
LEGAL NOTES
TRADEMARKS
All other products and their name brands are the trademarks of their respective
holders.
COPYRIGHTS
All Material Copyright © 2004 by General Electric Company, Inc. All rights
reserved. The material presented and contained herein may not be reproduced in any
form or manner, without the written permission of General Electric Company, Inc.
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
DIRECTION 5146132 -100, REVISION 4
IMPORTANT PRECAUTIONS
LANGUAGE
THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY.
WARNING 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.
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
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REVISION HISTORY
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
DIRECTION 5146132 -100, REVISION 4
TABLE OF CONTENTS
1. TABLE....................................................................................... 9
1.1. MAINTENANCE SCHEDULE ..................................................................................9
2. OVERHEAD TUBE SUSPENSION ......................................... 14
MAINTENANCE SAFETY MEASURES...............................................................................15
2.1. A.2 – GENERAL MAINTENANCE RULES...............................................................15
2.1.1. A.2.1 – Necessary tools.........................................................................16
2.2. A.3 – MAINTENANCE. ......................................................................................17
2.2.1. A.3.1 – General checks. ........................................................................17
2.2.2. A.3.2 –Controls of telescope and suspension metal ropes....................20
A.3.3 – Balancing springs control. .......................................................................23
2.3. A.4 – ROOM DISINFECTION AND CLEANING ........................................................25
2.4. A.5 - EQUIPMENT DISASSEMBLY .......................................................................25
2.5. A.6 – MAINTENANCE REGISTER........................................................................26
2.5.1. A.6.1 – Every 6 months. ........................................................................26
2.5.2. A.6.2 – Every 12 months. ......................................................................27
2.5.3. A.6.3 – Every 60 months (5 years). .......................................................27
2.6. B.1 – SAFETY MEASURES FOR INSTALLATION .....................................................28
2.7. B.2 - SAFETY MEASURES FOR INSTALLATION......................................................28
3. WALLSTAND .......................................................................... 30
3.1. NECESSARY TOOLS .........................................................................................30
3.2. GENERAL CHECKS ...........................................................................................30
3.3. GENERAL CHECKS INTERVAL ............................................................................31
3.4. COMPULSORY SPARE PARTS REPLACEMENT AFTER NUMBER OF WORKING YEARS .31
3.5. GENERAL MAINTENANCE ..................................................................................31
3.6. MAINTENANCE REGISTER ................................................................................32
4. ANALOG IMAGE CHAIN 512 ................................................. 33
4.1. X-RAY AUTOMATIC DOSE CONTROL ...................................................................33
5. ANALOG IMAGE CHAIN 1K .................................................. 34
5.1. X-RAY DOSE CALIBRATION................................................................................34
5.2. X-RAY AUTOMATIC DOSE CONTROL ...................................................................34
6. GENERATOR.......................................................................... 35
6.1. ITRODUCTION..................................................................................................35
6.2.0 X-RAY GENERATOR UPDATE/SERVICE RECORD ...............................35
6.3.0 MAINTENANCE SCHEDULE....................................................................35
6.4.0 OIL FILL/LEVEL CHECK (HT TANK).........................................................39
6.5.0 CLEANING................................................................................................41
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
DIRECTION 5146132 -100, REVISION 4
1. Table
Compulsor
y
Action
Part Action replacemen
Description interval
Number required t after N° --
(months)
working
years
Elevation & tilting table
5118700 Tilting motor C E 12
5131318 Poly-v 320j10 belt D 12 5
5131317 Poly-v 220j10 belt D 12 5
5131319 Eccentric pin for extrusion A B 12 10
5131321 Eccentric pin assembly-trans. Rack A B 12
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
DIRECTION 5146132 -100, REVISION 4
Compulsor
y
Action
Part Action replacemen
Description interval
Number required t after N° --
(months)
working
years
5131438 SFD motor pinion A B 12
5131439 Chain - 247 pitches A B 12
5131442 SFD rear guide plate A B 12
5131443 SFD front guide plate A B 12
5131444 Eccentric pin ass. For SFD frame A B 12
5119059 Bearing 12x28x8 A B 12
5131446 Roller bearing A B 12
5131447 Bottom pin for frame block A B 12
5131448 Rear pin for frame block A B 12
II elevation
5118710 II elevation motor + gear box C A 12
5131507 II elevation rack A B 12
5131444 Eccentric pin ass. For SFD frame A B 12
5119059 Bearing 12x28x8 A B 12
5131510 II elevation sleeve bearings A B 12
5131511 Guide for II support A B 12
5131513 II elevation slide bar A B 12
Transversal cassette-holder
trolley
5118696 Digital motor in/out cassette tray C A 12 5
5131512 Chain - 233 pitches A B 12
5131514 Chain - 77 pitch A B 12
5131515 Guide for cassette tray sliding A B 12
5131516 Bearing 7x19x6 A B 12
5131519 Bearing 6x13x3,5 A B 12
5131520 Longitudinal guide bearing A B 12
5131521 Guide frame bearing A B 12
5131522 Longitudinal guide bearing A B 12
5131523 Longitudinal guide bearing A B 12
5118666 Spring for cassette holders kit A B D 12
Cassette holder
5145873 D 5
Longitudinal cassette-holder
trolley
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
DIRECTION 5146132 -100, REVISION 4
Compulsor
y
Action
Part Action replacemen
Description interval
Number required t after N° --
(months)
working
years
5131524 M1 rack for long.cass. Tray transm. A B 12
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
DIRECTION 5146132 -100, REVISION 4
Compulsor
y
Action
Part Action replacemen
Description interval
Number required t after N° --
(months)
working
years
5131437 Stand transmission front guide A B 12
Variable FFD
5118709 Focal distance motor + gear box C A 12
5131492 Bearing 10x35x11 A B 12
5131493 Fixed pin assembly - column A B 12
5131494 Eccentric pin assembly - column A B 12
5131495 Rack for ffd transmission A B 12
5131496 Right guide for ffd A B 12
5131497 Left guide for ffd A B 12
5131498 Tube for variable ffd bar A B 12
Compressor
5118706 Trans table/compressor motor C 12
5131499 Clutch kit for compressor D 12
5131500 Chain - 267 pitches A B 12
5131501 Compressor paddle carriage bearing A B 12
5131502 Compressor rotation cam A B 12
5131504 Bearing 6x19x6 A B 12
5131505 Chain - 31 pitches A B 12
5131506 Chain - 39 pitches A B 12
Examination table
5131537 Tabletop rack A B 12
5131538 Tabletop guide A B 12
5118706 Trans table/compressor motor C 12
5131539 Transmission gear A B 12
5131540 Eccentric pin for table top transm. A B 12
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
DIRECTION 5146132 -100, REVISION 4
Compulsor
y
Action
Part Action replacemen
Description interval
Number required t after N° --
(months)
working
years
5131546 Tabletop rear extrusion assembly A B 12
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
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9 All operations to do on the unit must be carried out when it is out of service.
The person who is responsible for the maintenance must completely disconnect
the unit from power, before the adjustment or replacement of an equipment part.
9 Keep hands, feet, dresses, jewels and hair at safe distance in order to avoid
their being caught in moving parts or part extensions.
9 Keep all parts in good condition and correctly installed. Repair damages
immediately, replacing the consumed and broken parts.
Do not change any part of the unit; changes which are not
authorized can compromise the equipment functioning and safety.
They void the manufacturer’s guarantee as well.
In particular, it is not possible to make inoperative or replace
devices and/or circuits which permit the radiations emission in
accordance with the safety laws.
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
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9 A general check of the unit and its functioning conditions must be done at
intervals no longer then 12 months. More frequent controls (al least 6 months)
must be done if the unit is subjected to heavy use or in case of restarting after a
long stop.
9 Changes, up-dates and extraordinary maintenance must be done by the
manufacturer or technical personnel authorized by them.
9 Every ordinary and extraordinary operation on the equipment must be
supported by documents; these must be findable.
IMPORTANT!
It is compulsory for the installer to act so that equipment
parts that require checks and maintenance are easily open
to inspection and readily available.
This aspect has been taken into great consideration by the
manufacturer.
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
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The user, this means the person who is responsible for the equipment, must
ask for the technical support at the foreseen dates and hold all of the units
documentation for quick reference—that means this manual and the
operators manual.
The user must always address technical personnel for the equipment
maintenance and repairing—these operations must never be done by the
user.
9 First remove all covers and clean carefully the equipment, using a damp cloth
and a common detergent that can be readily found.
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
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9 Check the functioning backlash of bearings and of guiding and braking devices.
9 Check the correct functioning of the control and braking devices as well.
9 Check the correct tightening of the nuts and bolts.
9 Check the correct functioning of the electrical parts as well, that means the
functioning of push buttons and brakes and the integrity of cables and safety
devices.
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This control must be done along all the length of the ropes, verifying that there are no
signs of deflection or strand breakage. Moreover, verify that the ropes roll up correctly
around the pulleys and their wear condition.
It is also important to check the condition of the stainless steel safety rope and of the
intervention device efficiency. This is composed by a Teflon roller, which is mounted
on a compensator kept through a spring.
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
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It is possible to ask for spare parts or updating to the manufacturer. They are at full
disposal for maintenance or extraordinary renovation interventions as well.
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
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Check, several times, carefully and all along the telescope travel that:
9 springs wind regularly around their winding wheels;
9 the springs tension is uniform and the telescope movements are free;
9 the balancing system correctly works.
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
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All materials used for the unit manufacture are not toxic or
dangerous for the operators’ health; that means they can be
used without any particular precaution.
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
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WARNING!!!
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
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3. Wallstand
1) A general check of the unit and its functioning conditions must be done at intervals
no longer then 12 months.
2) Changes, updating and extraordinary maintenance must be done by the
manufacturer or technical personnel authorized by him.
3) Every ordinary and extraordinary operation on the equipment must be supported by
documents; these must be findable.
IMPORTANT!
It is compulsory for the installer to act so that equipment parts that require checks and
maintenance are easily open to inspection and readily available. The manufacturer
has taken this aspect into great consideration.
Maintenance and documentation duties must be observed; anything contrary to the
case releases the equipments manufacturer from all responsibilities. Every technical
intervention must be recorded in the Maintenance Register (on the following pages)
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1. Remove the covers and clean the equipment with a detergent and a soft damp
cloth
2. Pay attention not to use abrasive products or substances that contain solvents,
because they can damage the unit surface. Check scrupulously if there are
possible anomalies
3. If the unit presents dents, repair them; in case of damaged painted surfaces,
touch them up using the paint issued by the manufacturer.
4. Check the functioning backlash of guide and thrust bearings.
5. Check the correct functioning of the control and braking devices
6. Check the correct torque of the nuts and bolts
7. Check the correct functions safety devices.
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Every 6/12 months it is advise to control if the x-ray beams dose is in compliance with the
requirements established by the country low directive where the TV chain equipment is
installed.
4.1. X-ray automatic dose control
The sequences of actions to be executed in order to obtain the X-ray AUTO dose control
are as follows:
1. Put at the collimator X- ray output field a copper sheet 1millimeter thick
2. Insert the AUTO dose control function
3. S start FLUOROSCOPY function and check if the nominal field of the output video
signal, measured by an oscilloscope, remains at the 400 mV (±10%) value.
4. Change the magnifying mode and control if the video signal will stay at 400 mV
(±10%) value
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
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Every 6/12 months it is advise to control if the x-ray beams dose is in compliance with the
requirements established by the country low directive where the Tv chain equipment is
installed.
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6. GENERATOR
6.1. Itroduction
The X-ray generator update / service record is stored on the inside of the upper
cabinet hood. The installation date and location should be recorded on this form at
the time of the original site installation.
Service and repairs must be recorded on the update / service record. The
record should be as thorough as possible, detailing the scope and type of work
that was performed (all service and a record of all replacement parts that were
installed). Additionally, the person performing the work should date and sign the
record.
This information will be invaluable in the future for traceability and to ensure
continued compatibility of the generator.
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
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5. Test the X-ray tube thermal switch circuits in the generator. Disconnect
the tube thermal switch(s) and verify the correct error message, and
that X-ray exposures are inhibited.
7. For units with the AK (Air Kerma) option, verify the air kerma calibration
per chapter 3F.
2. Open the generator cabinet and examine the unit for any visible
damage: missing or loose ground connections, oil leaks, damaged
cables etc.
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
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The insulating oil level in the HT tank does NOT require periodic checking under
normal conditions. However, if there is evidence of possible oil loss, the procedure
for checking the correct oil level follows.
2. With the screw sufficiently loosened, remove the rubber (neoprene) plug.
4. Use only fresh oil, type Shell DIALA AX or equivalent. It is critical that air is
not added when topping up the oil. The following procedure is strongly
recommended when adding oil.
• Use a new clean syringe to remove oil from the container. A 60 cc
catheter tip syringe is recommended. Approximately 60 cc of oil is
required to raise the oil level by one millimeter.
• Turn the syringe upright and expel any trapped air.
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
DIRECTION 5146132 -100, REVISION 4
• Place the tip of the syringe through the oil-fill plug and into the oil,
ensuring that it is below the surface of the oil.
• Gently eject the oil from the syringe into the HT tank, while making sure
that the tip of the syringe remains below the surface of the oil until all of
the oil is emptied from the syringe.
• Repeat the previous steps until the required amount of oil has been
added.
5. Replace the oil fill plug. Once the plug is installed and the screw is properly
seated, continue to tighten the screw until the neoprene plug is firmly
secured. Do not over tighten; the screw should mildly compress the
neoprene plug when tight. Wipe up any oil spills. Dispose of soiled absorber
in compliance with government requirements and ensure conformity to local
disposal regulations. THE OIL DOES NOT CONTAIN PCBs.
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
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6.5.0 CLEANING
• Never use anything other than soap and water to clean plastic surfaces. Other
cleaners may damage the plastic.
• Never use any corrosive, solvent or abrasive detergents or polishes.
• Ensure that no water or other liquid can enter any equipment. This precaution
prevents short circuits and corrosion forming on components.
• Methods of disinfection used must conform to legal regulations and guidelines
regarding disinfection and explosion protection.
• If disinfectants are used which form explosive mixtures of gases, these gases
must have dissipated before switching on the equipment again.
• Disinfection by spraying is not recommended because the disinfectant may
enter the X-ray equipment.
• If room disinfection is done with an atomizer, it is recommended that the
equipment be switched OFF, allowed to cool down and covered with a plastic
sheet. When the disinfectant mist has subsided, the plastic sheet may be
removed and the equipment be disinfected by wiping.
1. Console software for the 23 X 56 cm console and for the Rad-only console
resides in an EPROM. When the software for these consoles needs to be
field upgraded, a replacement EPROM will be supplied.
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THE RAM BACKUP BATTERY VOLTAGE, for the procedure to access the
console CPU board.
4. Locate and carefully remove the existing EPROM on the console CPU
board (refer to figure 1E-4). This does not apply if the console software
currently resides in flash memory as described in step 2.
5. Carefully insert the replacement EPROM into the socket observing the
orientation per figure 1E-4.
6. For Indico 100 with the 31 X 42 cm console:
• Ensure that JW1 on the console board is set to the EPROM BOOT
position in order to run the updated software on EPROM. Refer to
figure 1E-4. This jumper is initially set to the FLASH BOOT position in
order to boot from flash memory.
• JW1 on the console board must be set to the FLASH BOOT position
in order to run existing or upgraded console software from flash
memory.
7. Re-assemble the console as per the procedure in chapter 2.
8. Refer to 6.6.4 before re-energizing the generator.
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1. With the generator mains power switched OFF, locate and carefully remove
the existing power EPROM on the generator CPU board (U38 or U41, refer
to figure 1E-1).
2. Carefully insert the replacement EPROM into the socket observing the
orientation per figure 1E-1.
3. Refer to 6.6.4 before re-energizing the generator.
1. Switch the generator mains power OFF, AND WAIT 5 MINUTES FOR THE
DC BUS CAPACITORS TO FULLY DISCHARGE.
2. Locate and carefully remove the existing EPROM on the dual speed starter
board (U26, refer to figure 1E-6).
3. Carefully insert the replacement EPROM into the socket observing the
orientation per figure 1E-6.
If the part number (not revision) of the replacement EPROM is different from the
EPROM being replaced, then the FACTORY DEFAULT procedure(s) must be
performed as detailed below. This will initialize the CPU’s NVRAM as required by
the new software and sets the data to its factory-configured state. Note the
separate procedures for the console CPU board and for the generator CPU board.
For Indico 100 with the 31 X 42 cm console, the console software is initially
programmed into flash memory on the console board. If the console software
needs to be field-upgraded, an EPROM may be supplied containing the updated
software. As noted above, if the part number (not revision) of the replacement
firmware is different from that being replaced, then the FACTORY DEFAULT
procedure(s) must be performed as detailed below.
The part number and revision of the software in flash memory is displayed at the
password screen, below the message ENTER PASSWORD: _____, when initially
entering into programming mode. This is only displayed if running the software
from flash memory. Refer to the section EPROM REPLACEMENT, Console
EPROM for details regarding the use of flash memory vs. EPROM.
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1. With the power OFF, set switch 8 of SW1 on the console CPU board to its
ON position.
2. Power ON the generator. The console will prompt for a YES or NO to
loading defaults for two conditions (console settings and APR memory).
Select YES to both.
3. Power OFF the console. Reset switch 8 of SW1 on the console CPU board
to its OFF position.
This will initialize both the CONSOLE settings (refer to CONSOLE settings in
chapter 3C) and the APR to the factory default settings.
1. With the power OFF, set switch 8 of SW1 on the generator CPU board to its
OFF position.
2. Power ON the generator. After the initialization is complete, the console will
display the message FACTORY DEFAULTS.
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3. Power OFF the generator. Reset switch 8 of SW1 on the generator CPU
board to its ON position.
This will initialize all generator data to the factory defaults (tube selection,
generator limits, receptor setup, I/O configuration, AEC setup and calibration,
fluoro setup and calibration, tube calibration, time & date, error log and statistics).
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The “software key” activates specific options in the generator, and may need to be
installed to add certain options, or may need to be replaced if it is desired to alter
the current configuration of the generator. To install or replace the software key
follow the procedure below.
1. With the generator mains power switched OFF, locate the socket for the
“software key”, U29, on the generator CPU board. Refer to figure 6-2.
2. Remove the existing I.C. U29, if fitted. The original I.C. should be placed in
anti-static packaging, and may be set aside for future use in a generator
that requires the options that are activated by that I.C.
3. Carefully insert the replacement “software key” into the U29 socket
observing the orientation per figure 6-2.
4. Perform setup and calibration, if required, of the new features that have
been activated by the new software key. Refer to the applicable sections of
the service manual.
U29
EPROM U41
FILE: ML_CPU2.CDR
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To replace the battery on the console CPU board or on the generator CPU board,
follow the procedure below. Refer to the figure showing the location of these
batteries in chapter 2, in the section “CHECKING THE RAM BACKUP BATTERY
VOLTAGE”. Refer to that section in chapter 2 for console disassembly instructions
to gain access to the console CPU board if required.
1. Remove the battery from the holder by gently prying under the battery at the
access slot in the battery holder using a small screwdriver. Slide the battery
over the edge of the holder and remove it when it is free.
2. Check the voltage of the new battery prior to inserting it. This should be
nominally 3.0V, do not use if it is under 2.80 V.
3. Wipe the replacement battery with a clean cloth, and ensure that the holder
is clean and free of debris before inserting the battery.
4. Gently lift the spring contact on the holder and insert the replacement
battery positive (+) side up
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The generator does X-ray tube auto calibration at 50 kV, 60 kV, 70 kV, 80 kV, 100
kV and 120 kV. The tube normally needs to be seasoned before it can be operated
at the higher voltages encountered during auto calibration.
Tube seasoning is started by auto calibrating the kV stations up to and
including part of the 70 kV station. The tube is then seasoned at 70 kV.
Progressively higher kV stations are then auto calibrated and seasoned. Finally the
entire kV and mA range is auto calibrated, then the tube is seasoned at the
remaining high kV values.
Manually releasing the exposure button during auto calibration of a
particular kV station in the following procedure prevents the generator from
attempting operation beyond that kV/mA value.
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X-ray tubes that have not been used for more than 8 hours may suffer
thermal shock if operated at high mA and kV without a warm-up procedure.
A cold anode (Molybdenum) is very brittle and when suddenly heated over a
small area may experience thermal cracking of the anode surface, eventually
leading to permanent tube damage.
X-ray tube seasoning should be done on LARGE focus in order to minimize tube
wear.
The procedure below is intended for seasoning an X-ray tube prior to attempting
tube auto calibration. To season a tube that does not need to be calibrated, simply
follow steps 2, 4, 6, 8, and 9.
1. Start the tube auto calibration sequence, and manually terminate the
exposure at 70 kV and 250 mA.
3. Restart the auto calibration sequence and manually terminate the exposure
at 100 kV and 250 mA.
5. Restart the auto calibration sequence and manually terminate the exposure
at 120 kV and 160 mA.
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DIRECTION 5146132 -100, REVISION 4
7. Restart the auto calibration sequence and allow the auto calibration
sequence to complete.
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
DIRECTION 5146132 -100, REVISION 4
If the generator has completed its useful service life, local environmental
regulations must be complied with in regard to disposal of possible hazardous
materials used in the construction of the generator.
In order to assist with this determination, the noteworthy materials used in
the construction of this generator are itemized below:
ITEM
• Electrical insulating oil in HT tank. This is a mineral oil with trace additives (25 Liter,
6.5 U.S. gal).
• Solder (lead/tin).
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GE MEDICAL SYSTEMS PRECISION RXI® SYSTEM PLANNED MAINTENANCE
DIRECTION 5146132 -100, REVISION 4
6.2. NOTE
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