Professional Documents
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Technical Bulletin
CTB Information
Title High Energy Clinac Periodic Maintenance Inspection (PMI) - Customer Version
DWG Number 100048393 CTB GE-725
Complaint No. N/A Est. Labor 6
Hrs
Purpose Provide instructions and procedures for performing PMI.
This CTB supersedes all previous versions of the High Energy Clinac PMI – Customer
Version document.
Product Code(s) Product Code: All High Energy Clinacs Product Name: High Energy Clinac
Affected This PMI procedure does not apply to TrueBeam Systems.
Prerequisites None
AN UPDATE TO THIS CTB MAY BE AVAILABLE ON MY.VARIAN.COM
Tools Information
Revision Information
A-L 2001-2010 N/A JT HE PMI- Customer version was not customer facing and was posted on internal CTB-GE-725.doc
website only.
M May 17, 2010 N/A JT Revised text in Sections ST 11, ST 12, ST14 for consistency; CTB-GE-725-M.doc
Section ST 14: added sprocket slippage inspection step and revised Figure 9;
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no representation to the qualifications of any service technicians other than its own employees. Improper or
uninformed maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including but not limited to one or more of the following: mechanical collision, electrical shock, and radiation.
Any of these hazards could cause serious injury and even death. Copyright © 2012, Varian Medical Systems, Inc. All rights reserved.
SHEET
1 OF 70
100048393 O
Format TMP-GE-CTB-R
Customer Technical Bulletin
N Mar 29, 2011 N/A RC Remove text “RapidArc Clinacs Only” and changed text from Blue 242 Loctite to CTB-GE-725-N.doc
Blue 243 loctite and P/N 88-299282-00 to 88-299626-70 in section ST-15.
O Mar 11, 2012 N/A JT / OK Reference Document box on page 1: deleted CTB-GE-726 (this CTB is now CTB-GE_725-O.doc
obsolete because the PMI Checklist is now incorporated into Appendix E in this
CTB);
Section 2.2: revised bullet list; other minor edits in Sections 2.2.1, 2.2.3, 2.2.5,
Section 3 thru 12: changed all headings to comply with new template style;
Section 3.11: new section added titled Console MU Backup Counter Battery
Replacement;
Section 4: Removed SF6 PMI requirements due to SF6 gas bleeding hazard;
Moved Counterweight Mounting Bolt Inspection task to Gantry Module Section
5.1;
Section 4.14: new section added for Gantry chain master link inspection;
Section 11.2: new section added to verify +15V Console Power Supply output;
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 2 OF 70
cause serious injury and even death. Copyright © 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
GENERAL INFORMATION
PERFORMANCE CHECK
Complete a thorough performance verification before disassembling and modifying any system. Make
a note of any operational discrepancies.
SAFETY PROCEDURES
Become familiar with Customer Support Service’s safety policies before working on Oncology
Systems Products. Ensure compliance with CSS’s safety practices and procedures while performing
this modification. Refer to the Product Users’ Manual for safety instructions.
CONTACT INFORMATION
If there are any questions, issues, or concerns contact Varian at 1.888.VARIAN.5 (1.888.827.4265) or
go to http://my.varian.com and click on Contact Us.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 3 OF 70
cause serious injury and even death. Copyright © 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 4 OF 70
cause serious injury and even death. Copyright © 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 5 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
Abstract This manual provides information about the Periodic Maintenance Inspection
procedures for the High Energy C-Series Clinac.
Manufacturer and Manufacturer: European Representative:
European
Varian Medical Systems, Inc. Ltd. Varian Medical Systems UK Ltd.
Representative
3100 Hansen Way, Bldg. 4A Gatwick Road, Crawley
Palo Alto, CA 94304-1030, U.S.A. West Sussex RH10 9RG
United Kingdom
Notice Information in this document is subject to change without notice and does not
represent a commitment on the part of Varian. Varian is not liable for errors
contained in this document or for incidental or consequential damages in
connection with the furnishing or use of this material.
This document contains proprietary information protected by copyright. No part
of this document may be reproduced, translated, or transmitted without the
express written permission of Varian Medical Systems, Inc.
Trademarks Clinac® and VMS® are registered trademarks
Enhanced Dynamic Wedge™, Exact™, Millennium™, PortalVision™ and
Silhouette™ are trademarks of Varian Medical Systems, Inc.
Updates For updates to this document, please contact PSE Las Vegas in the USA
Copyright 2012 Varian Medical Systems Inc., Oncology Systems
All rights reserved. Edited in USA.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 6 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
Table of Contents
1. Introduction ....................................................................................................................................11
1.1. Scope .....................................................................................................................................11
1.2. Conventions ...........................................................................................................................11
1.3. Abbreviations & Terminology .................................................................................................12
1.4. Safety Hazards .......................................................................................................................13
1.5. Required Tools & Equipment .................................................................................................14
2. General PMI Information ...............................................................................................................15
2.1. Usage Formats – PMI vs. MCMS ...........................................................................................15
2.2. Supporting Documents & Labels ............................................................................................15
2.2.1. PMI Checklist ..................................................................................................................16
2.2.2. PMI Data Labels..............................................................................................................16
2.2.3. PMI Label Placement Locations......................................................................................17
2.2.4. Console Cardrack Parameters Sheet .............................................................................18
2.2.5. Replacement Log Summary............................................................................................18
2.2.6. BEAM QA Guidelines ......................................................................................................18
3. Power Off & Inspections Module ...................................................................................................19
3.1. Customer Interview Regarding PROs & Optics (Quarterly) ...................................................19
3.2. Event Log Review & Initial Output Check (Quarterly) ............................................................19
3.3. Test Console Backup MU Counter (Quarterly) .......................................................................19
3.4. Machine PMI Preparation (N/A for MCMS) ............................................................................19
3.5. Test Emergency Off Switches (Quarterly) ..............................................................................20
3.6. Test Emergency Pendant (Quarterly).....................................................................................21
3.7. Test Flow Switch Operation (Quarterly) .................................................................................21
3.8. Inspect Water System & Clean Small Filter Screen(s) (Quarterly) .........................................23
3.9. Clean Air Filters (Quarterly)....................................................................................................23
3.10. Clean & Inspect Console Electronics Cabinet (Quarterly) ..................................................23
3.11. Console Backup MU Counter Battery Replacement (Annual or Once every 3 years,
depending on unit) ............................................................................................................................24
3.12. Clean & Inspect Stand (Quarterly) ......................................................................................25
3.13. Clean & Inspect Modulator (Quarterly) ...............................................................................25
3.14. Clean & Inspect Gantry (Quarterly) ....................................................................................26
3.15. Water Hose Inspection (Semiannual) .................................................................................26
3.16. Inhibited Water System - Water & Filter Replacement (Annual) .........................................26
4. Stand Module ................................................................................................................................27
4.1. Verify Cooling Fans Operation (Quarterly) .............................................................................27
4.2. Air System Inspection (Quarterly) ..........................................................................................27
4.3. Compare Water System Parameters (Quarterly) ...................................................................27
4.4. Compare BMAG Shunt Values (Quarterly) ............................................................................27
4.5. Compare VacIon Pump Current & Voltage Values (Quarterly) ..............................................28
4.6. Compare KSOL Shunt Value (Semiannual) ...........................................................................28
4.7. Compare RF Driver & Klystron Parameters (Semiannual) .....................................................28
4.8. Water Overtemp Trip Setting (Annual) ...................................................................................31
4.9. Klystron Saturation (Annual) ..................................................................................................31
4.10. Pulse Tank Oil Level Check (Annual) .................................................................................31
4.11. Gantry Chain Tension Verification (Semiannual)................................................................31
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 7 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 8 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
List of Figures
Figure 1: Emergency OFF Continuity Test Method (C3) ................................................................................. 20
Figure 2: KONA Stand Flow Pressure Switch Manifold ................................................................................... 22
Figure 3: Shorting Stick on Main Thyratron Side ............................................................................................. 25
Figure 4: Shorting Stick on PFN CAP .............................................................................................................. 25
Figure 5: Klystron Filament Measurement on Stand Motherboard (C3) .......................................................... 29
Figure 6: KLY I & V BNC Cable Patch in Stand ............................................................................................... 30
Figure 7: KLY I & V Cable Patch in Console .................................................................................................... 30
Figure 8: Gantry Chain Tension Test ............................................................................................................... 32
Figure 9: Gantry Motor Drive Sprocket ............................................................................................................ 33
Figure 10: Sprocket Inspection Guidelines (1 = Good / 2 = Worn) .................................................................. 34
Figure 11: Chain Master Link & Spring Clip ..................................................................................................... 35
Figure 12: Counterweight Bolt/Washer Inspection ........................................................................................... 36
Figure 13: MOD Interlock BNC Cable .............................................................................................................. 42
Figure 14: Modulator 3-Phase Power Measurement at HVCB Breaker .......................................................... 43
Figure 15: Modulator Thyratron Measurements (C3 Universal Modulator) ..................................................... 44
Figure 16: Interface Mount Guide Blocks and Pressure Bar............................................................................ 45
Figure 17: Tension Block Hex Nut Adjustment ................................................................................................ 48
Figure 18: Tension Block Sensor Switch Test ................................................................................................ 48
Figure 19: Exact Couch Top Mylar Finger Guard ............................................................................................ 52
Figure 20: Couch Top Pinch Hazard Labels (4 labels required) ...................................................................... 52
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 9 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
List of Tables
Table 1: PMI Target Months ............................................................................................................................. 16
Table 2: Flow Switch Measurement Locations................................................................................................. 22
Table 3: Console MU Backup Counters ........................................................................................................... 24
Table 4: Sprocket Inspection Guidelines.......................................................................................................... 34
Table 5: Modulator Measurements (see Figure 14 and Figure 15).................................................................. 43
Table 6: Output vs. Rotation Sample Table ..................................................................................................... 57
Table 7: Recommended Lubricants and Applications ...................................................................................... 62
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 10 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
1. INTRODUCTION
1.1. Scope
This manual is intended to provide the necessary procedures to perform the Periodic Maintenance
Inspection (PMI) tasks on the High Energy Clinac family. It is designed to be a universal document
for use by all VMS customers. The tasks listed are the minimum OEM recommended requirements
to satisfy PMI obligations. Some customers may desire to compliment the PMI with additional tasks
based on their unique requirements.
1.2. Conventions
This section presents the types of notes and precautionary notices used in the guide, along with
their icons. The following notational conventions are used:
STOP: Indicates any condition that must be verified and/or satisfied before
continuing.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 11 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
Bold text All command button names and keys are printed in bold text.
Courier new Screen messages are printed in Courier new.
Italics File and directory names appear in italic type.
[References] References to other documents are shown in square brackets, e.g. [1].
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 12 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
WARNING: Radiation exposure may cause serious injury or death. Never turn the beam on
when anyone is in the Clinac room, except to perform maintenance or repair work that
cannot be completed from the Control area. During such exposures, keep kV X-Ray output
as low as possible and persons in the room must wear lead aprons.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 13 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
WARNING: Misuse or malfunction of the High Energy Clinac system can expose the
operator, service technician, and/or the patient to one or more of the following hazards:
mechanical collision, electrical shock, and radiation. Any of these hazards could cause
serious injury or death. Improper maintenance procedures, as well as presenting a danger
or possible accidents leading to injury or death, could also result in poor machine
performance and/or damage to the system and other property. All persons who service or
maintain the system must read, understand and be familiar with the material in this manual
and the Safety chapter in the Users Manual.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 14 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
The PMI should not be interrupted for routine maintenance or follow-up issues. However,
serious problems may have to be resolved immediately, which could then post-pone the PMI. In
these cases, the completion of the PMI would have to be rescheduled.
The PMI Kit is shipped with all High Energy Clinacs and the labels and parameter sheet are filled
out and installed on the Clinac during installation. Replacement kits are available (PN 100013425-
XX). The kit includes the labels and documents listed above as well as permanent ink pens (to be
used on the data labels) and a folder that should be installed in the Console Cabinet for maintaining
the PMI documents.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 15 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
This is a checklist that indicates all of the required tasks of a PMI and the frequency of inspection
for each. Boxes are provided for each task that requires initials and the date of completion. During
the first PMI, target months are then listed as the intended month(s) for completion of each
quarterly task (see example below). One copy of this document is to remain on site and should be
kept in the PMI folder that should be located in the Console cabinet. Each year, a new Checklist is
started. This Checklist document is contained in Appendix E.
Example: If the first PMI was completed in May, the subsequent target months would be listed as
follows:
Q1 Q2 Q3 Q4
NOTE: All Annual tasks should not be scheduled for the same PMI period. This would result in
one long PMI each year. Instead, Annual and Semiannual tasks should be randomly performed
throughout the 4 scheduled PMI periods.
These are adhesive labels that are attached to the Clinac at various locations. They are used to
record measured values of all the sub-systems that are checked during PMI’s. All entries should be
done in permanent ink and should be clearly legible.
NOTE: First remove the clear plastic cover sheet on each label before recording values.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 16 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
During the first PMI or during installation, these labels should be installed on the Clinac within
viewing distance of the measurement point (per the recommended locations listed below). Then
the first column is filled out with a permanent ink pen. Fresh DVM batteries are required for these
first measurements. During subsequent PMI’s, the new measurement is compared. If the new
measured value is within the tolerance listed on the label, the check is complete and no data entry
is required.
However, if the new measurement exceeds the tolerances, this new value and the date is recorded
in the next column and investigated if necessary. Simple investigations can be completed during
the PMI but others may require follow-up. Some investigations may be resolved by installing fresh
batteries in the DVM. If the problem is remedied during the PMI and the original value is restored,
do not enter the “out of tolerance” value on the label, but instead, note the work in a Service Report.
When all entry boxes are full, a new label must be ordered and installed. The last entry on the
original label should be transferred to the new label. For historical purposes, the replacement label
should be placed next to the original label, if space permits.
These labels should also be updated when any repair work or upgrades are completed. In these
cases, only the measurements that change would require an update. All label value changes
should be dated.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 17 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
This form is used to record all Console parameters and waveforms. It is filled out during the first
PMI and then used for comparison during subsequent PMI’s on a semiannual frequency. All entries
should be done in pen and be clearly legible. Fresh DVM batteries should also be used for these
first measurements.
This form also includes Output vs. Gantry Rotation measurements that are compared Annual. It is
only necessary to make entries if the new value exceeds the original value tolerance. One copy of
this document is to remain on site and should be kept in the folder that is attached to the inner side
of the Console front panel. Unlike the PMI Checklist, this form is not started over each year.
Instead, it is used for comparison during subsequent years. If all entries for any item are full, a new
form should be filled out. The original document should indicate “Superseded/date” and kept in the
Console folder along with the new form. This document can be ordered or printed from SIR.
Like the labels, this form should also be updated when any repair work or upgrades are completed
that would affect the original values. The date of change should also be indicated on the form and
the reason for change should be noted in a Service Report.
This label lists all the necessary parts or items that require replacement on a routine basis, such as
water hoses, batteries, etc. Although hoses do not require replacement on an annual basis or
during PMI’s, it is the responsibility of the OEM (Varian) to inform customers when hoses or other
items should be replaced. Depending on the Service Contract, these items should be purchased
and replaced either by the customer or Varian. Columns are provided to indicate the date of
change for these items. This label should be installed on near the inside front panel of the
Modulator (within easy view of the Filament & Beam timers), or on the inside surface of the Stand
door.
This document is very important for ensuring beam quality and patient safety. As we know, many
adjustments, repairs or alignments to various subsystems may affect the beam quality. Therefore,
this guideline document is a quality assurance tool that should be used to remind us of the required
beam checks that must be verified prior to returning a Clinac to operation. This document is
available in Customer Technical Bulletin CTB-GE-681 and should be placed in the Console PMI
folder for quick referral anytime a repair or adjustment is performed that may affect beam quality.
WARNING: It is the responsibility of all customers to become familiar with and strictly
adhere to the Beam QA Guidelines to ensure adequate beam quality after maintenance.
These guidelines are available in CTB-GE-681 on MyVarian.com.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 18 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
1. Ask the responsible person / department if there are any calibration or alignment problems with
the above-mentioned features. If problems are reported, use ‘best judgment’ to determine if
these QA issues require priority over the PMI and if so, reschedule the PMI if time does not
permit completion.
1. Review event logs for any machine performance issues or frequent interlock problems.
2. Run each energy in Service mode for 100 MU in RR4 with Dose Servo OFF. This exercise is to
establish the Clinac operating condition prior to starting the PMI procedure. Dose rate should be
approximately 15-18% over the specified servo rate.
1. Mode up a 50MU SERVICE mode treatment. Verify the backup counter resets to 0 MU.
2. Complete the treatment and verify the backup counter displays 50MU. If not, the battery or
assembly may require replacement per Section 3.11.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 19 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
Collimator cover
2. Modulator Prep:
Remove screens & panels to access both sides of the PFN Deck, Plate Transformer,
Auxiliary Power Distribution PCB Backplane and Primary Power Distribution areas.
1. C3 Clinacs: Connect DVM test leads to the Auxiliary Power Distribution PCB at J6-5 and J2-3
as shown in Figure 1. Set DVM to measure resistance in the audible mode.
Sequentially cycle one Emergency Off (EMO) button at a time while listening to the DVM.
The beeping sound should stop (indicating an open) when each button is activated.
2. C1 & C2 Clinacs: Test each additional EMO switch while the machine is OFF.
Depress one switch at a time and verify the machine will not energize when pressing and
releasing the Start button in the Modulator. Remember to reset each switch before testing
the next one.
3. Verify both Stand EM OFF switches are activated by depressing the Stand door EMO. Adjust
switches if necessary.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 20 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
1. With the machine OFF, depress / toggle the red Emergency Pendant switch to provide battery
power to the Emergency Pendant.
• Depending on the Clinac Software version, Emergency Pendant power will be provided by
toggling the red switch on the Aux Electronics chassis (Ver 6 and below) or by depressing
the right Stand EMO switch (Ver 7 and higher).
2. Using the Pendant, select longitudinal and press enable. Longitudinal brake should release
and allow free floating motion of the tabletop.
3. Select vertical and press enable. Couch vertical axis should slowly descend. If the couch does
not descend OR if the HVCB circuit breaker trips while driving the couch down, schedule
replacement of the 2 emergency back-up batteries. C1 & C2 PN 74-103705 (QTY 2) or C3 PN
74-103707 (QTY 2).
4. For Clinac Console SW Version 7 or higher: verify the Emergency Pendant label (PN
100019135-xx) is installed on the EMO switch bracket below the Stand Motherboard and on the
outside of the Stand door next to the corresponding EMO actuator button.
NOTE: Flow Switch operation is verified by measuring the continuity through the switch circuit.
When there is no flow, the switch circuit is open and should measure infinite resistance.
If any flow switch is closed (minimal resistance) when the machine is off, remove the switch and
clean the switch post. For Gantry switches, position the Gantry at 270° to remove switch post.
Some KONA Stands may have the pressure switches shown in Figure 2. These switches cannot
be cleaned but can be tested per TT-ST-00985. These switches sense low or high water pressure
conditions to monitor flow rates. Defective switches must be replaced. If any of these 4 pressure
switches requires replacement, it is recommended to upgrade the switches using STB-ST-127.
NOTE: If any cooling paths are suspect, flow rates can be tested as follows:
• With the pump OFF and the Gantry rotated to 270°, disconnect the hose attached
to the Gantry flow switch and cap off the manifold with a flare cap fitting.
• Aim the return hose into a bucket or receptacle and turn on the pump for one
minute.
• Measure the amount of water collected to determine the flow rate. For higher flow
rates (such as 3 GPM) collect the water for 30 seconds and multiply the
measurement by 2 to determine the GPM rate.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 21 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
1. With the Clinac de-energized, independently measure all four Gantry flow switch circuits to
verify infinite resistance.
2. With the Clinac de-energized, independently measure both Stand flow switches and verify
infinite resistance. Only measure the LO pressure switches (S2 & S4) on KONA systems.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 22 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
3.8. Inspect Water System & Clean Small Filter Screen(s) (Quarterly)
Pre-KONA Stand
1. Visibly inspect the water tank reservoir for signs of contamination/bad smell. Schedule
replacement or water system cleaning if necessary (approximately 18 gallons).
2. Turn OFF the PUMP breaker at the Modulator and remove/clean the water filter screen at the
top of the pump manifold and inside the regulator. Newer regulators have no filter.
KONA Stand
1. Visibly inspect the water tank level sight tube for signs of contamination. Schedule water
replacement or system cleaning if necessary.
NOTE: Early versions of the sight tube discolor very quickly and make it difficult to determine the
water cleanliness. If tube discoloration is a problem, order and replace sight tube (PN 28-150101-
00, Tubing, FEP-Lined, Tygon, 3/8” I.D. X 9/16” O.D.).
NOTE: Console, Stand top and Modulator air filters have an air-flow directional arrow for correct
orientation. Install the filters correctly after cleaning.
1. Console air filters: C1 has one air filter at the rear of the console. C2 and pre EMC C3 have two
filters, one at the rear and a second on the side of the LVPS chassis. EMC electronics cabinets
have additional filters in the cabinet side panels.
2. Stand: clean both air filters on the top of Stand (N/A for KONA Stand). Clean the rear Stand
filter on KONA Stands.
1. Carefully pull out the top chassis, lubricate the rails with Tri-Flow if necessary.
2. With a clean dry air source, blow out the electronics cabinet area.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 23 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
1. Refer to Table 3 to determine the type of Backup Counter that is installed and the battery or
assembly replacement information.
2. Replace the batteries or Counter assembly per the frequency listed in the table.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 24 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
1. With a flashlight visually inspect the entire Stand area. Note any signs of water leaks.
5. With a clean dry air source, blow out the Stand area or wipe down accessible areas.
1. With a flashlight visually inspect all areas of the modulator. Look for loose connectors, poor
connections, any cable discoloration, any signs of arcing on cables or HV relay contacts.
3. Inspect PFN Cap braided cables to ensure they are firmly attached to the PFN coils and verify
none of them are sagging down against any coils.
4. With a clean dry air source, blow out modulator area or wipe down accessible areas.
Figure 3: Shorting Stick on Main Thyratron Side Figure 4: Shorting Stick on PFN CAP
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 25 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
1. Visually inspect the Gantry area (including Gun Driver) for signs of water leaks, loose
connectors, poor connections.
1. Inspect Stand and Gantry water hoses for signs of cracking or wear. Pay particular attention to
the Target hoses, Accelerator Solenoid hoses, BMAG Primary Collimator/Drift Tube hoses.
CAUTION: If replacing Energy Switch water hoses, do not remove the water hoses from the
barbed pipes on the Energy Switch. This could result in damage to the Energy Switch. Instead cut
the hoses near the switch and install in-line water fittings to add new hoses to the existing hoses.
If full removal is required, extreme care must be taken to immobilize the Energy Switch, carefully
cut off the old hoses and install the new hoses. It is extremely important to prevent any ‘twisting’
stress on the energy switch when replacing hoses. This task requires the use of an Energy Switch
post clamp and very careful hose handling during removal and installation onto the water pipes.
1. Once a year, replace the closed system water with distilled water and replace the high-flow filter
cartridge (PN 100054923-01). Dispose of the used non-hazardous filter in the trash.
2. Install the provided labels (indicating the date of change) at the following locations:
• Affix one label on the Stand frame near the water fill funnel
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 26 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
4. STAND MODULE
Restore Power to the Clinac for all of the following Sections
4.1. Verify Cooling Fans Operation (Quarterly)
1. Replace air desiccant if beads are not blue (TURN OFF the air supply to open canister!).
2. Verify that the air oiler glass reservoir is filled up to the fill line (use pneumatic tool oil or
equivalent).
1. Compare Water system parameters to the previously recorded label values for pressure,
temperature, RF driver flow and Gantry Supply Manifold pressure.
• The RF Driver flow meter was discontinued on PCSN 271217+ and 290206+ and all
Silhouettes.
• C1 & C2 Clinacs: Use black and red test points on Stand frame near the BMAG P/S
4. Compare shunt values to the previously recorded label values for all energies.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 27 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
CAUTION: If any shunts are out of tolerance, the problem must be investigated. An unintended
energy change could result in minor or moderate injury to patients. Do not attempt to adjust any
BMAG shunt values without consulting the responsible physicist.
1. At VacIon Power Supply chassis, measure the base current and KV values for the Accelerator
pump (20L), Gun pump (8L) and Klystron pump (2L). Compare values to recorded values on
PMI label.
2. On first PMI’s or during installation, use a 1000:1 HV problem and measure KV value at the HV
connectors of all VacIon pumps. This voltage measurement is only required when the PMI
labels are initially filled out. Subsequent PMI checks are made by comparing only the KV
values on the VacIon P/S.
2. Determine KSOL current value on Klystron nameplate label (typically 35.0 A) and verify KSOL
P/S output matches the specified value.
• C1 Clinacs: Verify meter indication on Shunt Meter Relay assembly (located below RF
Driver) matches the nameplate KSOL value. If not adjust current pot on P/S to exact
nameplate value. As an alternative you can use your DVM (mV scale) across meter relay
terminal strip TB-1, pins (-) 2 to (+) 5, to measure the shunt value (1mV = 1A).
• C2 and C3 Clinacs: Verify KSOL P/S current output on the front panel current meter
matches the nameplate KSOL value. Adjust current pot on P/S if required.
WARNING: Before entering the treatment room for RF measurements, configure the Clinac
for ‘Radiation Safe Beam-On’ operation. This is required to prevent exposure to radiation
that could result in serious injury or death. Refer to Appendix C for procedure.
1. Verify Klystron and RF driver recorded serial numbers on label are correct.
• Shunt Tee Clinacs: record this value from the RF Driver output power meter while beamed
on. This must be done in both A & B RFDR modes.
• KLM Clinacs: mode up each energy and compare the RF Driver output meter to the label
values for each energy. Beam-On is not required.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 28 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
3. Measure and compare Klystron filament voltage to the recorded label values. KFIL voltage
should be approximately 236 VACrms.
C3 Clinacs: Measure Klystron filament voltage at the Stand Motherboard at J3 pins 1 & 2
as shown in Figure 5. Be very careful when attaching DVM leads to connector pins to
prevent any short circuits!
C1 & C2 Clinacs: Measure the KFIL voltage through the back of the Pulse Tank connector
J7 between pins A & B – be careful not to short to pins C or D!
4. Use the following procedure to measure the actual KLYI & KLYV waveform amplitude values.
Compare values to the recorded values on PMI label.
1) C3 Clinacs: Relocate the KLYI (W83) & KLYV (W84) BNC cables at the
Stand BNC Patch Panel to the STD MON A & STD MON B BNC jacks as
shown in Figure 6. Connect scope BNC cables to the corresponding J10
& J11 BNC jacks on the Console VCR backplane as shown in Figure 7.
This technique of using the built-in spare BNC monitor cables does not
require long cables or measurements in the Treatment room. Continue
at step 3 below.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 29 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
Note for C1 & C2 Clinacs: If measuring at the Pulse Tank, the J1 (KLYI) and J2 (KLYV) BNC
connectors are located on the front wall of the tank by the Klystron on Stepped tanks or near the
pulse cable connections on the Flattop tanks.
3) Turn OFF the PFN Servo. PFN Servo must be turned OFF for accurate
measurements!
Note: Although the peak signal amplitude is entered on the parameter sheet, the value at J1 also
indicates the actual Klystron current using a 10A:1V calibration factor. For example: If KLY I peak
amplitude measures 8.2 volts, the actual KLY I is 82 amps. Likewise, the value measured at J2
also indicates the actual Klystron voltage after conversion using the KLY Voltage Calibration factor
stamped on the Pulse Tank nameplate label. However, variances between pulse tank grounding
circuits, has proven this voltage conversion to be unreliable for perveance calculations.
Figure 6: KLY I & V BNC Cable Patch in Stand Figure 7: KLY I & V Cable Patch in Console
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 30 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
1. Shut off the incoming city water supply to the Clinac. Allow the water temp to climb up and
verify a PUMP fault occurs at 48°C +/- 2°C. Do not allow machine to exceed 52°C. If not set
correctly, adjust the Overtemp switch on top of the water tank for pre-KONA systems or
program the Watflow Controller on KONA systems.
1. For Shunt Tee systems only, saturate the Klystron. For KLM systems, skip this step and enter
N/A on the Checklist.
1. Transformer Side of Tank: Verify oil level is visible approximately halfway up on the sight glass.
If you are unable to clearly determine the oil level, remove fill plug and read level by inserting a
plastic stick into the fill hole. The level should be approx 3.75" from the top of the fill hole. Add
Transformer oil if required (PN 88-299437-01).
2. Klystron Side of Tank: There is a float switch in the Klystron tank compartment that will trip a
FLOW I/L if the oil level is too low.
1. Transformer Side of Tank: Remove fill plug and read level by inserting a plastic stick into the fill
hole. The level should be approx 5" from the top of the fill tube. Add Transformer oil if required
(PN 88-299437-01).
2. Klystron Side of Tank: There is a float switch in the Klystron tank compartment that will cause a
FLOW interlock if the oil is too low.
1. For OBI systems, position both KV E-Arms to the PARK (OUT) position.
3. Rotate Gantry to gain maximum access to the Gantry chain between the Gantry main sprocket
and the Gantry motor drive sprocket.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 31 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
4. Using your thumb and forefinger, check the chain tension as shown in Figure 8. Rotate the
Gantry a few degrees in each direction and check the tension after each move.
NOTE: This verification test only applies to older Gantry Rotation Drive assemblies that have a
torque limiter/clutch assembly installed. This does not apply to the new direct-drive (clutchless)
Gantry Rotation Drive assemblies that were cut-in with the introduction of OBI.
1. For OBI systems, position both KV E-Arms to the PARK (OUT) position.
3. Visually inspect the Torque Limiter / Harmonic Drive assembly for any signs of oil leakage,
loose parts and hardware.
4. Visually verify that the key stock (rectangular metal key) is properly positioned in the groove on
the motor shaft between the shaft and the clutch/sprocket assembly.
5. Using a calibrated torque wrench, verify all 3 outer setscrews on the Torque Limiter
(clutch/sprocket assembly) are tightened to 160 inch-lbs (18 Nm).
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 32 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
1. For OBI systems, position both KV E-Arms to the PARK (OUT) position.
2. Rotate Gantry to either 90° or 270° and remove lower front Stand cover.
3. Rotate Gantry to both limits and check for roughness, binding or unexpected noise when the
chain engages and disengages from the sprocket teeth.
NOTE: The next test will verify that the drive sprocket is properly tightened on the motor drive
shaft. Even though there is a key block between the sprocket and shaft, the sprocket could still
slip a little on the shaft if the setscrews are not tight. This could cause wear to the key block.
4. Verify the drive sprocket is properly tightened and not slipping on the drive shaft.
• Verify the shaft key block is firmly seated between the drive shaft and drive
sprocket (shown circled in Figure 9).
• Draw a straight reference line on the front of the sprocket and drive shaft (shown
with a red line in Figure 9).
• Momentarily apply a short full-speed command from the pendant.
• Re-inspect the reference line to verify both halves of the line are still aligned
together and did not shift apart slightly.
• Repeat this test in the other Gantry direction.
• If there is any sprocket slippage, the two setscrews on the sprocket must be
removed (one at a time) and reinstalled with Blue 243 Loctite and tightened to 50
ft-lbs (68 Nm).
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 33 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
5. Inspect the Gantry motor drive sprocket for excessive tooth wear or damage per the guidelines
shown in Figure 10 & Table 4. Rotate the Gantry as required to inspect all teeth.
Figure 10
Condition Description
Reference
Chain pitch distance increases as chain pins and bushings wear.
A Pointed Tips With increased chain pitch, the roller contact edge will move towards
the tip of the sprocket tooth, instead of riding in the center of the root.
B Working Surface Wear Decrease tooth cross-section from repeated chain busing contact.
CAUTION: Do not operate new chain on worn sprockets or worn chain on new sprockets. These
conditions will result in rapid chain or sprocket wear which could cause the chain to break and
possibly cause minor or moderate injury to patients. If motor drive sprocket requires replacement,
order parts listed below and replace the sprocket using the instructions in CTB-ST-604.
• Gantry Motor Drive Sprocket PN 100027963-01
• Blue 243 Loctite PN 88-299626-70
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 34 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
2. Rotate the Gantry until the chain master link is visible near the Motor Drive sprocket. This
should occur with the Gantry near 270°.
3. Verify the master link is installed through the back of the chain with the spring clip facing
forward towards the Couch as shown in Figure 11.
4. Make sure the spring clip is securely fastened on both link posts.
5. Rotate the Gantry in both directions and verify the master link does not come into contact with
the Stand cover.
CAUTION: Any chain contact with the cover could result in the spring clip popping off, which could
cause the master link to disengage, which could result in a hazard. If the chain is hitting the cover,
trim the affected area of the cover with a razor knife or Dremel cutting tool, or replace the cover if
necessary.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 35 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
5. GANTRY MODULE
2. Inspect each of the four mounting bolts for looseness. Inspect all 4 washer pairs for any cracks.
[ref: Figure 12]
3. Rotate Gantry to both limits while listening for any noise created from the Counterweight area.
4. If any problems are observed, it may be necessary to replace washers or torque bolts. Contact
Varian Medical Systems for part numbers and instructions.
5.2. Inspect Cables, Rotating Water Joints & Hoses During Rotation (Quarterly)
1. Carefully observe Gantry Wind-Up hoses, cables, water joints and cable guards during rotation.
Monitor for poor dressing, water leaks and insulation / cable damage.
NOTE: If OBI option is installed, carefully inspect the PVC cable tube in the front of the Gantry
wind-up area. This tube must be securely clamped to its mount and should not move.
1. Audibly verify that each of the Humphrey air solenoid valves (used by the Energy Switch,
Target and Carrousel pin) do not leak air when they are in their constant (non-cycling) state. If
any valve constantly leaks air, schedule replacement of the valve.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 36 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
1. With Hi-X selected and the machine at 40°C, measure the sum of the voltage drop for both
BMAG coils by connecting a DVM to both BMAG fuses (F1 & F2), located on the side of the
Gantry frame next to the BMAG terminal strips. Compare this reading to the value listed on the
PMI label.
2. Also measure & compare the voltage drop across each coil (E1 to E2 & E3 to E4). Carefully
push the DVM leads through the insulation near the BMAG cable/coil connections to measure
the voltage across each coil. (E1/E2 are on the left side / E3/E4 are on the right side of the
BMAG)
1. With Hi-X selected and the machine at 40°C, measure the coil voltage drop across the short
and long Accelerator Solenoid coils. Compare values to recorded values on PMI label. Refer
to PMI label for measurement locations.
1. Verify the Energy Switch adjustment knob is tight – tighten setscrews if necessary.
3. Verify the Energy Switch cycles in & out smoothly and each stroke does not exceed
approximately 2 seconds. The switch can be cycled locally as follows:
3) Clip one end of a jumper wire onto Sled Patch Panel TB5 terminal 1.
4) While observing the Energy Switch, momentarily ground the other end of
the jumper to chassis ground. This will cycle the switch into the guide
side cavity. Removing the ground will cycle the switch back out. If either
stroke is too slow or jerky, adjust the HI (out) or LO (in) regulator valves
on the Sled Patch Panel. Large adjustments make small changes.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 37 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
3) Depress the small button on the Energy Switch air valve (located on the
Gantry inner wall) to cycle the switch in. Release the button to cycle out.
4) If motion is too slow, adjust the small gold regulator knobs on the Energy
Switch air cylinder assembly.
NOTE: If regulator adjustment does not improve the cycle speed, remove the air cylinder from the
back of the energy switch shaft and manually cycle the energy switch outward. If the shaft
movement feels smooth, schedule replacement of the two in-line air filters located after the
regulator valves on the Sled Patch Panel.
4. While cycling the Energy Switch in & out, verify the two water hoses do not cause any ‘twisting’
stress to the switch body. Both hoses should be tie-wrapped to the rear Accelerator Solenoid
on the big black retaining bolt.
1. Inspect Lead Shielding pieces around the BMAG assembly for secure mounting.
1. With the Gantry pinned @ 270°, remove lead shield side plates to access Target assembly.
2. Carefully grasp Target Drive Assembly looking for free play movement side-to-side, up down, in
& out without exerting too much force. If free play movement is detected, verify that the Target
drive shaft set screws (on both sides of BMAG) are secure and the ¼-20 locking nuts are
secure (if equipped).
CAUTION: Too much torque on these setscrews or locknuts will cause the setscrew to break
which could cause excessive rework to remove the broken screw. It will be necessary to remove
the lead shielding from the other side of the BMAG to access the second setscrew.
3. Inspect Target I/L switch block assembly and actuators for secure mounting.
4. Using Pendant Redirection, cycle through energies looking for smooth operation.
1. With the Carrousel area still exposed from previous step, inspect the cam index switches for
secure positioning.
2. Verify the pin is fully seating in the Carrousel ring recess / hole.
3. Visually inspect the BMAG Primary Collimator hoses for signs of cracking.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 38 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
4. Visually inspect the Angle T Steering Coil wires for any signs of insulation damage from
possible contact with removable pieces of side lead.
1. Remove the small lead shielding block that covers the bottom of the carrousel filters/foil ports.
This block is bolted down with two 7/16” bolts and is located directly under the tungsten
research port shielding in the front of the BMAG.
2. With the Gantry down and the shielding removed, lightly lubricate the carrousel outer bearing
ring with Tri-Flow or light machine oil (sewing machine oil) while cycling the carrousel.
1. Grease the Gantry bearing with the lubricant listed in Appendix D. To apply the grease, attach
a grease gun (through the Stand area) to each of the Gantry bearing zerk fittings and pump in 2
strokes of grease.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 39 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
1. With the two Gun Driver protective side covers removed, pull one screen interlock switch and
then toggle the screen switch on the other side. Verify both light bulbs turn on and the HV
crowbar energizes. Remember, HV is present on the hot deck side.
1. De-energize the Gun Driver by turning OFF the main power switches on the cold deck. Hang
shorting stick on hot deck
2. With a clean dry air source, blow out the Gun Driver assembly or wipe down accessible areas.
3. Visually inspect for loose hardware, loose connections and signs of arcing. Verify boards and
fiber optic cables (if applicable) are fully seated and the Crowbar & ground connections are
secure. Verify the Gun lead is tie-wrapped to the Sled to limit motion during rotation.
1. Measure and compare Gun HV in each mode (Hi & Lo) at the hot deck chassis using a 1000:1
HV probe.
2. Measure and compare Gun Filament across the yellow & black Gun leads with high voltage
OFF!
3. Measure and compare Grid Bias between the red Gun lead and hot deck chassis with high
voltage OFF!
NOTE: Grid bias should measure between -95 to -109 VDC. A lower value may indicate a
resistive path developing between the grid and cathode.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 40 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
1. Measure the Gun V value shown on the Analog Meters Display screen for each energy.
Compare values to recorded values on PMI label.
NOTE: During the following steps, if at any time while displaying values on the Digital Gun Driver
Controller PCB, the display indicates Save =>, do not press the Enter switch. Instead, rotate the
rotary switch position to any other setting to clear this display and prevent saving erroneous
values. Return to the original switch position to continue. If unintended values are saved, the
correct values must be re-entered and saved.
1. Turn OFF the Gun Driver high voltage by releasing the screen interlock switch above the cold
deck access port. This will allow the Grid setting to be displayed without having to pull the
Controller PCB and switching S2-4 to LOCAL. However, S2-4 must be set to the LOCAL
position if Grid programming is required.
2. At the Controller PCB, set the rotary switch to Position 3 (Grid Setting).
3. Select each energy and depress the Enter switch once on the Controller PCB to display the grid
default setting value. Compare displayed values to recorded values on PMI label.
1. At the Controller PCB, set the rotary switch to Position E (Monitor values).
2. Sequentially toggle the INC/DEC switch on the Controller to scroll through all the Gun Driver
monitor values. Compare values to recorded values on PMI label.
1. Turn OFF Gun Driver high voltage and hang the grounding stick to the hot deck chassis.
2. Using a DVM, measure between the Heater and Cathode test points on the face of the hot
deck chassis. Compare value to recorded value on PMI label. Ideally, the gun filament should
be operating between 5.3 to 5.5V, unless the filament was intentionally increased due to gun
current instability.
NOTE: Measure the true gun filament between the Heater test point (TP3) and the Cathode test
point (TP2). The Heater Ref test point measures approximately 0.15V higher than the actual
voltage directly across the yellow and black gun leads. The Controller will display this higher
voltage, so a nominal setting of 5.3V across the gun filament leads will actually indicate
approximately 5.5 on the Controller LED display. A 5.3 display on the Controller correlates to
5.15V on the gun filaments and this lower voltage has been known to cause emission instability.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 41 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
7. MODULATOR MODULE
1. Verify the two large cooling fans next to HVPS rectifying diodes are operating. Machine must
be in the ON mode.
2. C1 & C2 Clinacs: Verify the blue 6-pack of cooling fans just above the Aux Power Distribution
is operating properly.
3. C3: Verify the fans next to the DeQing resistors are operating properly.
1. Verify the Crowbar drops out when each Modulator door is opened.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 42 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
Point of Measurement
Measurement
C1 & C2 Modulator C3 Modulator Universal Modulator
Main Thyratron 2 blue leads on T6 2 yellow test points 2 black test points (TP1 & 2)
Filament transformer in (TP3 to TP5) on on Thyratron chassis (see
Thyratron chassis Thyratron chassis TP’s A & B in Figure 15)
(AC voltage)
DeQing Thyratron 2 yellow leads on T3 2 yellow leads on Yellow and white leads on
Filament transformer (DeQing T3 transformer T5 transformer (see location
Deck) (DeQing deck) D in Figure 15)
(AC Voltage)
Keep Alive voltage TP3 to chassis TP1 to TP4 TP3 to TP2 (see TP’s B & C
in Figure 15)
(DC Voltage)
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 43 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 44 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
8. ACCESSORIES MODULE
1. Test each Applicator for proper operation (including the ACC interlock).
2. Verify that pressing “each side” of the Applicator Touchguard trips the collision circuit. Repeat
this test for ALL applicators.
1. Visually inspect the Interface Mount, Accessory Mount and Compensator Mount guide blocks
for any damage or cracks. Pay special attention to any cracks present on the spring loaded
pressure bar.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 45 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
1. With the Gantry head down and the Collimator fiberglass cover removed, inspect all wiring, tie-
wraps and limit switches in the Collimator area.
1) Clean and lubricate the lower jaw ball screws with Tri-Flow.
2) Dual Independent Jaws: clean the 5 lower jaw drive sprockets, two at
each end of the push rods and one on the drive motor. Lubricate by
applying a thin coat of G/N Metal Paste and wipe away any excess.
3) Dual Independent Jaws: locate the lower jaw drive sprockets (PN
885485-01). There are a total of two sprockets per jaw interconnected by
one push rod. Each gear has an inner and outer thrust bearing (thrust
bearings are shaped like a flat washer with inserted needle bearings).
Flush and lubricate all lower jaw thrust bearings with Tri-Flow. See lower
Collimator assembly drawing #882855 detail “F” for additional location
information.
4) For chain driven symmetrical lower jaws, flush and lubricate the chain
with Tri-Flow.
1) Using only G/N Metal Paste, lubricate the upper jaw gears located inside
the upper jaw motor housings (gear boxes) - directly behind the primary
readout pots. Each of the motor housings has a visible opening for
lubrication. Newer assemblies have a dust cover that is held on with two
very small flat head screws. Remove one screw and swing the cover
open to access the gear. Use an applicator (tie wrap tip) to apply grease
on to the gear sprockets while driving the jaw.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 46 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
1. Rotate the Gantry down and pin it. Remove the Collimator cover and long jaw cover.
2. Remove the large front lead ring and the smaller rear lead ring to access the Collimator Bearing
retaining ring. Locate the retaining ring seams where the two half rings come together - there
should be one at the front and one at the rear of the Collimator. Rotate the Collimator to 90°,
using Tri-Flow (with the plastic tube nozzle on) inject lubricant in both seams. Repeat this step
for Collimator angles of 180° & 270°. Rotate the Collimator several times until the Tri-Flow is
distributed throughout the bearing.
1. With the Gantry head down, remove the right & left side pieces of lead shielding surrounding
the Collimator.
2. Visually verify that all Collimator chain drive assemblies are not loose or damaged, which
includes:
• Chain
• Idler Sprockets
• Wiring Harness
3. Complete the applicable step below depending on the type of Collimator Chain Tension Block
installed.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 47 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 48 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
1. Once a year, replace the lamp in the Field Light Projector assembly. This only applies to the
non-FiberOptic Field Light assemblies (PN 1106642) that were cut-in on Collimators to
accommodate the Millennium MLC system. It is recommended to replace the lamp when
performing the previous step (Collimator bearing lubrication) since this step provides easy
access to the Field Light assembly.
NOTE: Varian recommends replacement of the bulb AND bulb holder as an assembly (PN
100010122-01) for two reasons:
1. Bulb position is preset in the socket (designed to prevent any light field shifts)
2. Bulb does not require any “handling” which should maximize lamp life
CAUTION: If only the bulb is replaced (instead of the bulb & bulb holder assembly), light field
walkout will have to be checked BEFORE and AFTER replacement to ensure accurate light field
alignment. Incorrect field alignment could result in minor patient mispositioning which could result
in minor or moderate injury.
1. Remove the fiberglass RBS housing to gain access to the rails. Remove the top and bottom
fiberglass Beamstopper covers to gain access to the 4 oil tube lubrication points - these four
lubrication fittings will be clearly visible. With a small oil can gun, inject 30-weight oil until full. If
you don’t have an oil can gun use a 5/8” socket to remove the oil tubes. Rotate the Gantry to
gain access to all four. Remove the zerk fittings with a 7/16” wrench and reattach the oil tubes
into Beamstopper blocks. You can now fill the oil tubes and reassemble.
CAUTION: Do not over torque as the tubes can easily break off at the threads.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 49 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
1. Lower the Couch skirt / bellows. Raise the Couch high enough and insert the two safety braces
in the lower tracks. Clean any excess grease off the lift drive screw. If dry, spread a thin layer
of Shell Alvania EP-2 over threads.
2. Lubricate zerk fittings on the lift drive block and lift motor gear box with Shell Alvania EP-2,
Annual only.
3. Visually inspect the lift drive assemblies for any signs of wear or damage.
4. Remove safety braces and drive table to lower and upper limits. If all looks and sounds OK,
lower and re-attach the skirt.
10.2. Clean, Inspect, Lubricate Longitudinal & Lateral Carriage Ways (Quarterly)
1. ETR Couch Longitudinal & Lateral Carriage Ways (rails): If the ways (rails) are extremely
dirty, use mineral spirits to flush the bearings, then lubricate with Tri-Flow. If the ways are fairly
clean, just flush and lubricate with Tri-Flow as follows: apply a liberal amount of Tri-Flow to all
way (rail) surfaces, free float table laterally & longitudinally through all limits to distribute
lubricant. Wipe off any excess Tri-Flow.
2. ETR Couch Backlash: Measure longitudinal carriage backlash (spec is 2 mm). If backlash
exceeds spec, note as follow up. Adjust backlash as follows; Loosen the two shoulder bolts on
the telescoping drive assembly using a 5/32 Allen. The shoulder bolts are accessed through
two holes located on center of the outer longitudinal carriage next to the inner carriage
(reference drawing 876830). The shoulder bolts attach the telescoping drive to the carriage.
With the bolts loose, push assembly towards the center of the carriage and re-tighten. If
backlash cannot be minimized replace drive assembly.
3. Exact Couch Longitudinal & Lateral Carriage Ways: This Couch uses bearing blocks. Each
bearing block has a small zerk fitting. There are lubrication access holes located on the top of
the inner longitudinal carriage (4 places) and the lateral carriage (4 places) above the bearing
blocks. The uni-panel and fixed panel must be removed to access these lubrication points. Use
a needle nozzle (PN 865055-01) and apply Tri-Flow.
4. Exact Couch Backlash: Measure longitudinal backlash (spec is 2 mm). If backlash exceeds
spec, adjustment is required. There are two cam adjustments at the center/top of the inner
longitudinal carriage. Loosen the hold down screws at the center of the tightening cams and
rotate the cams to minimize the backlash. Tighten the hold down screws. The fixed panel must
be removed to access the cam tighteners (reference drawing TM53391).
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 50 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
10.3. Verify Longitudinal, Lateral & Vertical Limit Switch Operation (Quarterly)
1. Using the pendant, drive each motion to both limits and verify the limit switch stops drive motor
operation. Version 5 and above has software limits which hinder this test so use Raw scale
readouts.
NOTE: If lateral or longitude motions continue to drive after engaging a mechanical limit it may not
be a limit switch problem. The bearing ways may no longer be in the center of travel and therefore
are acting as a mechanical stop before the limit switch can be engaged. In this case the bearing
needs to be re-centered.
1. Verify motor and switch functions for both Pendants and Side Panels.
10.5. Inspect Couch Top Mylar Finger Guard – Exact Couch Top Only (Annual)
WARNING: Possible bio-hazards exist on the mylar sheet which could result in serious
injury or death. Wear protective gloves, eyeglasses and any other appropriate Personal
Protective Equipment (PPE) if cleaning is needed.
2. Float Couch top fully forward (towards Gantry) and inspect the mylar finger guard as follows:
• Outer edges of the mylar sheet are adhered to the Couch top and the adhesive corner
pieces are attached. [ref: Figure 19]
3. Float Couch top fully to the opposite end (away from Gantry) and repeat the above process (no
corner pieces).
4. If the mylar sheet is damaged or separating from any area of the Couch top, order PN
TM75182000 and install new mylar sheet. A permanent aluminum solution is also available
instead of using mylar sheets. This upgrade can be purchased through Varian.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 51 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
5. Verify 4 pinch hazard labels (PN TM53556000) are installed at locations shown in Figure 20.
The two labels on the front edge of the Couch top should not cover the outer magnets.
3. 36-inch Standard Turntable: Verify proper operation of electromagnetic rotation brake at various
Turntable angles.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 52 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
2) C2 & pre EMC C3 Clinacs: two fans, one at the back and one on the
side of the LVPS chassis.
1. In SERVICE Mode, select Display > Analog > Machine to display the power supply voltages.
2. Verify the +15V value is ≥15.0V. If lower than 15V, replace the 1.5A SLO-BLO fuse on top of
the Console Power Supply chassis.
CAUTION: If the +15V power supply fuse was replaced, inform the customer to verify Dose Cal
before resuming patient treatments. 1 to 2% changes have been observed after fuse replacement.
NOTE: Clinacs with Portal Vision systems installed may be affected by gun timing adjustments.
Do not adjust these pots unless absolutely necessary. If gun-timing pots are adjusted, the PLS
may require re-alignment.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 53 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
1. Turn OFF the PFN Servo & Dose Servo and verify each energy is running between 15-20%
above the required servoed dose rate. Small PFN-V pot (or RFDR pot for KLM systems)
adjustments may be necessary to peak the dose rate. Likewise, small GUN I pot adjustments
may be necessary to set the correct unservoed dose rate margins. If dose rate problems exist
after these basic adjustments, such as warm-up, AFC problems, etc., refer to the Beam Tuning
procedures in Appendix B.
2. For machines equipped with Portal Vision, verify that the dose rate in both X-Ray energies
reaches the required servoed dose rate value within 2-3 seconds after first beaming on. If the
dose rate remains too low or too high after this period of time, it will be necessary to adjust the
PV PLS Servo.
3. After each energy is tuned, print out the Service mode screen (Display/Analog/Machine) while
beamed on in RR3. Compare the low voltage power supply values on one of the printouts to a
previous printout sheet. Verify no significant changes. Then date and place the printouts in the
Console folder.
1. Measure and compare the Cardrack voltages and waveforms to the recorded values on the
Console Cardrack Parameters sheet. Indicate any “out of tolerance” changes in value from the
original recorded values. Record any findings for diagnosis or list follow up recommendations
on a Service Report.
2. Draw the Low-X Target and LPWR2 waveforms on the Console Cardrack Parameters sheet (if
not already drawn). These waveforms are very useful for future troubleshooting. Record any
findings for diagnosis or list follow up recommendations.
1. Perform the Output versus Gantry Rotation values for the energies listed on the Console
Cardrack Parameters sheet. [ref: Appendix A]
3. If any output problems occur, schedule a follow-up service call for further investigation.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 54 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
1. Locate original Console Software floppy disks or Compact Flash card (whichever applies). If not
available, any clean, unused, formatted diskette may also be used.
NOTE: Each Clinac has 4 personality files (manuf.cnf, physics.cnf, service.cnf & accy.cnf) which
determine the machine specific configuration. It is important to backup the configuration in Physics
Mode after any service involving PRO calibration, Physics mode configuration changes or any
upgrade.
2. Insert Console S/W disk 2 of 2 (or the Compact Flash card) into the Clinac PC.
3. From the Major Mode screen select Physics mode (password should be 8888). Select Utilities
> Backup Configuration and press enter. If the disk is not accessible or an ‘attribute’ error
appears, verify the disk write protection tab is set correctly.
1. Run Morning Checkout for each energy including arcs. If arcs are not a part of the morning
checkout, run from Clinical mode.
1. Review follow up section at the end of the PMI Checklist to schedule any required follow up
service. Also, enter any new follow-up recommendations in this section.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 55 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 56 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
NOTE: All energies should be final tuned and steering servos should be balanced and closed for
these tests.
Set-Up
2. At the console...
Hi-X Lo-X Lo e- Hi e-
001° (179 IEC)
090°
180° (000 IEC)
270°
359° (181 IEC)
Min
Max
%∆
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 57 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
Test Procedure
1. Rotate the Gantry down to 001° (179° IEC) and beam on in RR3. Allow the beam output to
stabilize and record the dose rate for this Gantry angle.
2. Using the Automatic motion control feature in the Motors pull-down window, select Gantry
Automatic and enter 359 (181 IEC) for the target position value.
3. Hold down the DKB motion enable bar and start rotating the Gantry. Record the dose rate
every 90° as the Gantry rotates.
NOTE: It is common for the output to change in small gradual amounts as the Gantry rotates.
However, if you notice a sudden large change during Gantry rotation at ANY GANTRY ANGLE,
return to that angle and resolve the problem. See Trouble shooting section at the end of this
procedure.
4. Record the minimum and maximum values in the table and determine the % of output loss,
using the formula below. Spec is ≤ 15%. If the value is greater than 15%, refer to the
Troubleshooting section below.
5. Repeat these steps for both X-Ray energies and the low & high electron energies. For CW
rotations, start at 359 (181 IEC) and select 001 (179 IEC) for target positions.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 58 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
NOTE: For Clinacs equipped with Portal Vision systems, it is necessary to disable the PLS servo
operation before making dose rate adjustments.
5. Beam on in Rep Rate 3 (X-Rays) or max Rep Rate (electrons) and peak the RFDR pot (PFN
pot for non-KLM) in each energy for maximum dose rate.
6. Verify dose rate peak is approximately 15 - 20% higher than the servoed dose rate. See
following Note for electron tuning.
NOTE: For C/D Clinacs, verify the dose rate margin percentage in Rep Rate 7 for all electron
energies (rate should be approximately 1150 MU/Min). Due to a non-linear gun PRF rate in
electrons on C/D machines, Rep Rate 3 will be approximately 28% higher than the servoed rate
while all other rep rates will be approximately 15% higher. This anomaly applies to electron
modes only. Photon gun PRF rates are linear.
7. If peak dose rate is too high or too low, adjust the GUN I pot and repeak the RFDR pot (PFN
pot for non-KLM) until the correct rate is achieved.
8. View Beam I waveform and verify that the leading edge is relatively straight. If not, it may be
necessary to adjust the gun delay timing.
9. View LPWR2 waveform in each energy and verify that the center section of the pulse is
relatively flat. If not, it may be necessary to peak the AFC pot.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 59 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
Occasionally, it is necessary to enter the treatment room while the modulator PFN pulse is being
applied to the Klystron, such as during Klystron Saturation. To prevent harmful radiation exposure,
the Clinac must be configured for Radiation Safe operation, whereas no beam output is present.
Follow the procedure to configure the Clinac for this type operation.
1) Gun Delay to ON
1) Open any screen interlock switch to disable high voltage and hang the
grounding stick on the hot deck
4. In the treatment room, rotate the Gantry so the gun is away from the area of work. For
example, if saturating the Klystron, rotate the Gantry to 315° IEC (225° Varian) since the area of
work is at the RFDR.
5. At the Console,
5) Turn OFF PFN Servo (required for accurate measurements of KLY I & V)
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 60 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
6) Set AFC switch to manual and adjust frequency knob to either limit (full
off-resonance) – This is essential to prevent acceleration of stray copper
electrons.
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 61 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
Automatic Transmission Self Purchase HE/LE Gantry (harmonic drive), HE/LE RBS (Harmonic Drive)
Fluid, Dextron II (auto)
30 Weight Motor Oil Self Purchase HE RBS (lubrication ports)
(automotive)
Roughing Pump Oil 1 ltr 88-299480-00 HE (Mechanical roughing pump)
Fel-Pro Anti-Seize Lube 88-299465-00 HE/LE (Gantry bearing bolts), PSA/ETR (toe bolts)
C5A
West Lube 88-299471 Drill and Tap Lubricant
Lamora D68 H930000500 VEO Baseframe turntable track
Mineral Spirits Self Purchase Used as a cleaning agent for heavy duty cleaning on various bearings,
such as ETR EXACT longitudinal and lateral bearings, Collimator,
Carrousel and Gantry bearings.
Shell Diala Ax, (55 gal) 88-299437-00 Pulse Transformer
Shell Diala Ax, (5 gal) 88-299437-01
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 62 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
Name
Beam Hours
PMI Q1 Q2 Q3 Q4
Ref # Task Frequency Init/Date Init/Date Init/Date Init/Date
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 63 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
PMI Q1 Q2 Q3 Q4
Ref # Task Frequency Init/Date Init/Date Init/Date Init/Date
Stand Module
Gantry Module
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 64 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
PMI Q1 Q2 Q3 Q4
Ref # Task Frequency Init/Date Init/Date Init/Date Init/Date
Modulator Module
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 65 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
PMI Q1 Q2 Q3 Q4
Ref # Task Frequency Init/Date Init/Date Init/Date Init/Date
Accessories Module
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 66 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
PMI Q1 Q2 Q3 Q4
Ref # Task Frequency Init/Date Init/Date Init/Date Init/Date
Console Module
Wrap Up Module
Comments (List any comments or follow-up items below. Use additional sheet if necessary)
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 67 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 68 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
Bill Of Materials
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 69 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.
Customer Technical Bulletin
March-2009
ATTENTION: This information is provided for use by qualified service technicians. Varian Medical Systems, Inc. makes no SHEET
representation to the qualifications of any service technicians other than its own employees. Improper or uninformed 100048393
maintenance or repair of the Product may expose a maintenance technician, operator and/ or patient to safety hazards including
but not limited to one or more of the following: mechanical collision, electrical shock, and radiation. Any of these hazards could DWG NO.
GE-725 Rev O 70 OF 70
cause serious injury and even death. Copyright 2012, Varian Medical Systems, Inc. All rights reserved.