JUMONG Installation Manual-E (Dual) - Varian DIMAE
JUMONG Installation Manual-E (Dual) - Varian DIMAE
JUMONG Installation Manual-E (Dual) - Varian DIMAE
Table of Contents
Chapter 1 Introduction
Introduction
1.1 Description
1.2 Dimensions
1.3 Specifications
Chapter 2 Installation
2.1 Unpacking and Weight Locking Bolts
2.2 Room Layout
2.3 Drill Template (Fix Anchor Bolts)
2.4 Tube Stand Installation
2.4.1 Dimensions (Unit : mm)
2.4.2 Specifications
2.4.3 Category
2.4.4 Adjustment of Floor level
2.4.5 Rail Top Cover Installation
2.4.6 Rail Side Cover Installation
2.4.7 Tube Stand on Rail
2.4.8 Remove Spring Balance Locking Bolts
2.4.9 Tube Arm Installation to Tube Stand
2.5 X-Ray Tube and Collimator Installation
2.6 Connecting Cables
2.6.1 Connecting cables on Tube Arm & Tube Stand
2.6.2 Connecting cables for Tube Stand and Rail
2.6.3 Install Cable Voyeur
2.6.4 Connecting Power Cable between Table and Tube Stand
2.6.5 Connecting cables on Main Op & Tube Stand
2.7 Bucky Stand Installation
2.7.1 System Dimensions (Unit: mm)
2.7.2 Product Specification
2.7.3 Remove Hard Rubbers on Tube Stand Column
2.7.4 Remove Spring Balance Locking Bolts
2.7.5 Drill Template (Fix Anchor Bolts) (unit: mm)
2.7.6 Installation of Bucky
2.7.7 Power Cable
2.8 Table Installation
SGhealthcare 2
JUMONG Installation & Service manual
SGhealthcare 3
JUMONG Installation & Service manual
SGhealthcare 4
JUMONG Installation & Service manual
1.1.2 Features.
1.1.3 Radiographic Performance
1.1.4 Environmental Specifications
1.1.5 Applicable Standards
1.1.6 Electromagnetic Compatibility (EMC)
1.1.7 RoHS Compliance
1.2.0 SAFETY
1.2.1 Safety and Warning Symbols
1.2.2 Safety Notices and Warnings
1.2.3 Safety Warning Labels
1.3.0 PREPARING FOR INSTALLATION
1.3.1 Generator Heat Output
1.3.2 Generator Power Requirements
1.3.3 Generator Ground Requirements
1.3.4 Locating and Mounting the Generator
1.3.5 Dimensions, Cable Entrance and Seismic Center Location
1.3.6 Tools and test Equipment Required
1.3.7 Pre-Installation Checklist
1.4.0 GENERATOR LAYOUT AND MAJOR COMPONENTS
1.5.0 COMPATIBILITY LISTING
1.6.0 RUNTIME LICENSE AGREEMENT (TOUCHSCREEN CONSOLE)
INSTALLATION
2.1.0 INTRODUCTION
2.2.0 UNPACKING
2.3.0 REMOVING THE GENERATOR COVER
2.4.0 MAJOR COMPONENT LAYOUT
2.5.0 EQUIPMENT PLACEMENT
2.5.1 Main Cabinet
2.5.2 Control Console
2.5.3 Anchoring the Generator to the Floor
2.6.0 WIRING TO THE GENERATOR
2.6.1 Control Console
2.6.2 Hand Switch (Optional)
2.6.3 Stator Connections
2.6.4 Thermal Switch
2.6.5 Power Line Mains
2.6.6 High Tension Cables
2.6.7 X-Ray Tube Housing Ground
2.6.8 Room Equipment
2.6.9 Emergency Power Off / Power Distribution Relay
2.6.10 Safety Interlocks
2.7.0 LOW SPEED STARTER TUBE COMPATIBILITY
2.7.1 Setting 120 / 240 VAC Boost Voltage
2.8.0 PROGRAMMING THE DUAL-SPEED STARTER
2.8.1 EPROM type / dual speed starter
2.8.2 Setting tube type -18
2.8.3 Configuring dual speed starter 901297-15 / 901298-15
2.9.0 DIP SWITCH SETTINGS
2.10.0 INITIAL RUN-UP
2.10.1 Auxiliary Transformer Line Voltage Tap Selection
2.10.2 Initial Voltage Measurements
2.11.0 TUBE MA AUTO CALIBRATION
2.12.0 FINAL CHECKS
SGhealthcare 5
JUMONG Installation & Service manual
1.0 INTRODUCTION
2.0 LOW SPEED STARTER TUBE SELECT TABLE
3.0 DUAL SPEED STARTER TUBE SELECT TABLE
SGhealthcare 6
JUMONG Installation & Service manual
AEC CALIBRATION
3D.1.0 INTRODUCTION
3D.2.0 WIRING THE AEC PICKUP DEVICE TO THE GENERATOR
3D.2.1 AEC Board (Solid State Chambers)
3D.2.2 AEC Board (Ion Chambers)
3D.2.3 AEC Board (Ion Chambers)
3D.2.4 AEC Board (5-Field Ion Chambers)
3D.2.5 Precalibration Notes
3D.2.6 Required Test Equipment
3D.3.0 AEC CALIBRATION (TABLE BUCKY)
3D.4.0 SHORT AEC TIME COMPENSATION
3D.5.0 AEC DENSITY CALIBRATION
3D.6.0 AEC CALIBRATION (WALL BUCKY)
3D.7.0 AEC CALIBRATION (MISC)
3D.8.0 AEC OVERVIEW AND BACKGROUND INFORMATION
3D.8.1 Film/Screen Response vs. kV
3D.8.2 AEC Calibration Range
3D.9.0 PRECALIBRATION SETUP
3D.9.1 AEC SetupWorksheet
3D.9.2 AEC Precalibration Checks
3D.9.3 AEC Chamber Installation
ACCEPTANCE TESTING
4.1.0 INTRODUCTION
4.2.0 REQUIRED TEST EQUIPMENT FOR GENERATOR VERIFICATION
4.3.0 ACCEPTANCE TESTS (BASIC FUNCTIONS)
4.3.1 Console Tests
4.3.2 Low Speed Starter Verification
4.3.3 Dual Speed Starter (Optional) Verfication
4.4.0 ACCEPTANCE TESTS (KV, TIME, MA AND MAS)
4.5.0 ACCEPTANCE TESTS (AEC)
4.6.0 ACCEPTANCE TESTS (DR INTERFACE)
4.6.0 ACCEPTANCE TESTS (DAP)
4.8.0 ACCEPTANCE TESTS (HVL, LINEARITY AND REPRODUCIBILITY)
TROUBLESHOOTING
5.1.0 INTRODUCTION 5-2
5.2.0 STATUS AND ERROR CODES
5.2.1 Operator Messages
5.2.2 Limit Messages
5.2.3 Error Messages
5.3.0 MISCELLANEOUS FAULTS
5.3.1 Erratic Console Faults
5.4.0 LED INDICATORS
5.4.1 Dual Speed Starter Board
5.4.2 Generator Control Board
5.4.3 HV Auxiliary Board
SGhealthcare 7
JUMONG Installation & Service manual
REGULAR MAINTENANCE
6.1.0 INTRODUCTION
6.2.0 SERVICE RECORD
6.3.0 MAINTENANCE SCHEDULE
6.4.0 OIL FILL / LEVEL CHECK
6.5.0 CLEANING
6.6.0 FIRMWARE UPGRADE
6.6.1 Console firmware
6.6.2 Generator Firmware
6.6.3 Dual Speed Starter EPROM
6.6.4 Resetting Factory Defaults
6.7.0 BATTERY REPLACEMENT
6.8.0 AEC BOARD REMOVAL AND INSTALLATION
6.9.0 TUBE CONDITIONING / SEASONING
6.9.1 Tube Conditioning
6.10.0 END OF PRODUCT LIFE
THEORY OF OPERATION
7.1.0 INTRODUCTION
7.2.0 FUNCTIONAL THEORY OF OPERATION
7.2.1 System ON (MD-0928)
7.2.2 DC bus & power distribution (MD-0927)
7.2.3 Room interface (MD-0930)
7.2.4 X-ray exposure (MD-0931)
7.2.5 kV control and feedback (MD-0932)
7.2.6 Filament drive and mA control (MD-0934)
7.2.7 Dual-speed starter (MD-0924)
7.2.8 Low-speed starter (MD-0935)
7.2.9 DAP (MD-0938)
7.2.10 Temp sensor / programming jumpers (MD-0925)
7.2.11 Serial communications (MD-0937)
7.2.12 AEC (MD-0936)
7.2.13 Digital interface (MD-0926)
7.2.14 Interconnect diagram (MD-0939)
SPARES
8.1.0 INTRODUCTION
8.2.0 SPARE PARTS LIST
SCHEMATICS
9.1.0 INTRODUCTION
9.2.0 FUNCTIONAL SCHEMATIC INDEX
9.3.0 FUNCTIONAL DRAWINGS
SGhealthcare 8
JUMONG Installation & Service manual
Safety Information
i
Introduction
The policy of SGHealthCare is to manufacture X-Ray equipment that meets high standards
of performance and reliability. We enforce strict quality control techniques to eliminate the
potential for defects and hazards in our products.
The intended use of this equipment is to provide a sub-system for positioning an X-Ray
source and X-Ray bucky for the purpose of acquiring X-Ray images of the desired parts of a
patient’s anatomy. Use of this equipment in any other fashions may lead to serious
personal injury.
The safety guidelines provided in this section of the manual are intended to educate the
operator on all safety issues in order to operate and maintain the stand in a safe manner.
SGhealthcare 9
JUMONG Installation & Service manual
Manual Conventions
This manual uses three types of messages to emphasize information or potential risks to
personnel or equipment.
To ensure safety, read all Safety Information provided herein and observe all:
WARNINGS
CAUTIONS and
NOTES
WARNING
CAUTION
NOTE
General Safety
Numerous design features, operational safeguards and mechanical and electrical interlocks
have been incorporated into this product’s design for the safety or both the operator and
patient and to protect the equipment from damage.
NOTE
Personnel operating and maintaining this product should receive training and
be familiar with all aspects of operation and maintenance. To ensure safety,
read this SAFETY section thoroughly before using the equipment and observe
all WARNINGS, CAUTION statements and NOTE located throughout the
manual.
NOTE
SGhealthcare 10
JUMONG Installation & Service manual
NOTE
Follow all local, state and Federal guidelines and regulations on the disposal of
hazardous material(s).
A. Electrical Safety
B. Mechanical Safety
Procedural Safety
The procedures in this manual are designed for the safety of the patient, operator and the
equipment as well as ensuring the acquisition of diagnostic quality images. Failure to follow
the procedures in this manual (or warnings, cautions and notes) can result in potential
health and safety hazards and/or damage to the equipment.
Observe and follow all cautions and warnings, stated or implied, in this manual.
SGhealthcare 11
JUMONG Installation & Service manual
User Maintenance/Servicing
Unless specifically instructed herein, all maintenance and serving or the equipment should
be performed by qualified, authorized Service Providers. None of the electronic assemblies,
cables or mechanical assemblies is user serviceable.
Some cleaning solutions, disinfectants and other chemicals can be destructive to the
equipment or pose a risk of fire. The manufacturer is not responsible for damages or
injuries that may result from the use of non-authorized chemicals on or near the
equipment.
WARNING
CAUTION
Do not spray cleaning solution directly onto the equipment. Moisten a cloth
with a 70% isopropyl alcohol solution for use on plastics and enameled metal.
Apply to patient contact areas after each contact.
CAUTION
Hardware/Software Modifications
The equipment is complete as installed. The addition or subtraction of hardware or
software not authorized by the manufacturer can lead to:
WARNING
SGhealthcare 12
JUMONG Installation & Service manual
WARNING
WARNING
The following environmental conditions are appropriate for the equipment. Operation
under conditions outside of these ranges could damage the equipment.
WARNING
Operate the equipment outside of its operating environment limits may lead
to malfunction of or damage to the equipment.
PARAMETER LIMITS
Acceptable Temperature Range 5°C to 30°C or
41°F to 86°F
Acceptable Relative Humidity 10% to 75% (non-condensing)
Be sure that all personnel authorized to operate the equipment are familiar with the
established regulations of the authorities named above. All personnel should be monitored
to ensure compliance with the above.
Although X-Ray radiation is hazardous, X-Ray equipment does not pose any danger when
properly used. Be certain all operating personnel are properly educated concerning the
hazards of X-Ray radiation. Persons responsible for the equipment must understand the
safety requirements and special warnings for X-Ray operation.
SGhealthcare 13
JUMONG Installation & Service manual
Manufacturer’s Responsibility
Allow only authorized, properly trained personnel to operate the equipment.
This equipment is sold with the understanding that the manufacturer, its agents, and
representatives do not accept any responsibility for overexposure of patients or personnel
to X-Ray radiation. No responsibility is assumed for any unit that has not been serviced by
qualified authorized service personnel.
SGhealthcare 14
JUMONG Installation & Service manual
Record of Revision
ii
Revision History
SGhealthcare 15
JUMONG Installation & Service manual
Introduction
1
1.1 Introduction
This manual provides installation and service information for Jumong system.
1.2 Description
The Jumong is an X-Ray tube, collimator and bucky support subsystem integrated into a
radiographic system. This Jumong system has been designed and developed for various X-
Ray examination techniques with both Flat panel detector in proper examination
circumstances.
SGhealthcare 16
JUMONG Installation & Service manual
SGhealthcare 17
JUMONG Installation & Service manual
1.4 Specifications
Compatibility
The Jumong system is compatible with a wide variety of generators, image receptor,
and tubes. It is intended to be used in a stationary diagnostic X-Ray configuration.
Classification Class 1
SGhealthcare 18
JUMONG Installation & Service manual
Installation
2
2.1 Unpacking and Weight Locking Bolts
JUMONG system is packed with wood when it is delivered. To unpack and remove the
wood box, please use required tools.
Remove weight locking bolts which were located on back side of main tube stand column
after all installation procedures are completed.
WARNING
Weight locking bolts should be removed before connecting main power cable
for operating.
Required Tools
Standard Service engineer tool kit
Electric drill motor and assorted bits
SGhealthcare 19
JUMONG Installation & Service manual
SGhealthcare 20
JUMONG Installation & Service manual
CAUTIONS
The base plate should be locked up with a floor using anchor bolts. Otherwise,
the complete system may be fallen down to the floor due to a weight balance
problem.
SGhealthcare 21
JUMONG Installation & Service manual
SGhealthcare 22
JUMONG Installation & Service manual
2.4.2 Specifications
Circumstances
- Temperature Limits 5 ~ 40°C
- Relative Humidity Limits 10 ~ 75%
Mechanical Specification
- Weight Stand: 150 Kg (without X-ray tube and collimatior)
Floor Rail: 150 kg
- Tube Up/Down Stroke Vertical 1461 mm
Horizontal 120 mm
2.4.3 Category
Class I
Ordinary equipment (IPX0)
Equipment not suitable for use the presence of flammable anesthetic mixture with air
or with oxygen or nitrous oxide
SGhealthcare 23
JUMONG Installation & Service manual
After installation rail top cover, then you can assemble side cover like below.
Each side cover has little bit different size, so please make sure proper parts with below
picture.
SGhealthcare 24
JUMONG Installation & Service manual
SGhealthcare 25
JUMONG Installation & Service manual
Note
Please be careful to prevent failure of cabling when the tube stand is lifted on
rail.
Remove the Spring balance locking bolt which is located on left side of main tube stand
column after all installation procedures are completed.
Note
In order to secure spring balance wire during shipping and hold tube
arm, one bolt is put.
After you install tube arm, and then remove this bolt (M8x30) and
replace other proper bolt (M8x20).
SGhealthcare 26
JUMONG Installation & Service manual
Assemble Tube Arm to Tube Stand with M6x30 flat head screws.
For more details, please refer to the below figure 2-5.
Note
Please be careful to prevent failure of cabling when the tube arm is attached
on tube stand.
SGhealthcare 27
JUMONG Installation & Service manual
Note
SGhealthcare 28
JUMONG Installation & Service manual
As descripted on Section 2.4.2, please connect STAND UP/DOWN CABLE. It has to be done
during Tube Arm installation.
Figure 2-8, Connecting cable between Tube Arm and Tube Stand
For packaging and shipment, the cables packed inside of back cover like below.
SGhealthcare 29
JUMONG Installation & Service manual
Then install cable holders in proper location and connect all cables with matching each
labeling.
SGhealthcare 30
JUMONG Installation & Service manual
Install cable voyeur bracket and put cables inside like below picture.
SGhealthcare 31
JUMONG Installation & Service manual
SGhealthcare 32
JUMONG Installation & Service manual
Fan
Op
SGhealthcare 33
JUMONG Installation & Service manual
- Dimensions
SGhealthcare 34
JUMONG Installation & Service manual
Circumstances
Mechanical Specification
Hard Rubber
Remove the Spring balance locking bolt which is located on left side of main tube stand
column after all installation procedures are completed.
SGhealthcare 35
JUMONG Installation & Service manual
Note
In order to secure spring balance wire during shipping and hold tube
arm, one bolt is put.
After you install tube arm, and then remove this bolt (M8x30) and
replace other proper bolt (M8x20).
Anchor Bolts
- Floor Hole pattern of Anchor : Ø 20(4EA)
CAUTIONS
The base plate should be locked up with a floor using anchor bolts. Otherwise,
the complete system may be fallen down to the floor due to a weight balance
problem.
SGhealthcare 36
JUMONG Installation & Service manual
You can connect the power cable through the circle connector as the picture below.
* Connection power cable to table power connector.
* Power Requirement: 24VDC, 1A
SGhealthcare 37
JUMONG Installation & Service manual
Table
Table
Top
Emergency
Base
Foot
Switch Figure 2.8-1 Exterior name
SGhealthcare 38
JUMONG Installation & Service manual
SGhealthcare 39
JUMONG Installation & Service manual
Adjustment
3
3.1 Introduction
This chapter provides adjustment procedures for SS-1000.
3.2 Adjustment
After installing X-Ray detector, operator feels that weight balance needs to be required
adjustment, operator can adjust spring balance.
WARNING
SGhealthcare 40
JUMONG Installation & Service manual
To adjust, you can turn it to counter clock wise (- direction) or clock wise
(+direction).
SGhealthcare 41
JUMONG Installation & Service manual
Periodic Maintenance
4
4.1 Introduction
In order to ensure continued safe performance of the equipment, a periodic maintenance
program must be established. It is owner’s responsibility to supply or arrange for this
service.
What to do When to do it
Clean External Surfaces Every week or as required
WARNING
Ensure the power has been disconnected before starting any cleaning
operation.
SGhealthcare 42
JUMONG Installation & Service manual
What to do When to do it
SGhealthcare 43
JUMONG Installation & Service manual
Electrical Schematics
5
5.1 Introduction
This chapter provides all electrical schematics included block diagram.
SGhealthcare 44
JUMONG Installation & Service manual
SGhealthcare 45
JUMONG Installation & Service manual
5.3 Schematics
SGhealthcare 46
JUMONG Installation & Service manual
SGhealthcare 47
JUMONG Installation & Service manual
SGhealthcare 48
JUMONG Installation & Service manual
SGhealthcare 49
JUMONG Installation & Service manual
Installation to cable
6
6.1 WIRING TO THE GENERATOR
6.1.1 Power Line Mains
50kW
208~230 VAC 7 (178) 5 (127) 4.75 (121) 5 (127)
3P Configurations
SGhealthcare 50
JUMONG Installation & Service manual
SGhealthcare 51
JUMONG Installation & Service manual
Figure 6-4: Tube / thermal switch connections on H.V. auxiliary board (low speed starter)
SGhealthcare 52
JUMONG Installation & Service manual
SGhealthcare 53
JUMONG Installation & Service manual
SGhealthcare 54
JUMONG Installation & Service manual
J11
SGhealthcare 55
JUMONG Installation & Service manual
J21 : RS232 to Pc
J22 : RS232 to Pc (Service Port)
SGhealthcare 56
JUMONG Installation & Service manual
PC RS232 Port
J3 : Pc Use
J19 : Mini Console Use
SGhealthcare 57
JUMONG Installation & Service manual
Membrane Console
Use these step to access the GENERATOR SETUP menu (membrane console)
While pressing and holding the MENU button, press the power ON button on the
2
console.
SGhealthcare 58
JUMONG Installation & Service manual
6.5 Interfacing
Figure 6-8: Receptor Setup window, Receptor Properties tap (DR Mode)
SGhealthcare 59
JUMONG Installation & Service manual
J25
SGhealthcare 60
JUMONG Installation & Service manual
SGhealthcare 61
JUMONG Installation & Service manual
SGhealthcare 62
JUMONG Installation & Service manual
Step 4: Calibration is complete you see the message, Push the hand switch.
Step 5: Calibrated the same way is a large focus.
SGhealthcare 63
JUMONG Installation & Service manual
(6) About 2 sec. later, below 2 screens will be appeared one by one. And make an exposure
(7) After acquiring image, new window will be appeared as below then click “Cancel”.
(8) Put mouse cursor on the middle of image and read value of ADU.
It must be around 3100.
SGhealthcare 64
JUMONG Installation & Service manual
(9) If value of ADU is less than ± 100 then adjust KV and make exposures to get 3100.
If value of ADU is more than ± 100 then adjust mAs and make exposures to get 3100.
(2) 2 images will be acquired automatically and offset calibration will be proceed.
(No exposure is required.)
SGhealthcare 65
JUMONG Installation & Service manual
(2) Do check Offset Corrections and uncheck Gain Corrections/Pixel Defect Map/T Map Correction.
NOTE: After Gain Calibration, all check box in blue must to be checked again.
SGhealthcare 66
JUMONG Installation & Service manual
(5) About 5 sec. later, below screens will be appears one by one then make an exposure.
SGhealthcare 67
JUMONG Installation & Service manual
→ →
(6) after making an exposure below screens will be appears one by one then wait for about 3 sec.
→ →
SGhealthcare 68
JUMONG Installation & Service manual
(10) Verify value of Gain Median in Calibration Statistics is around 3000 and Click “Close”.
SGhealthcare 69
JUMONG Installation & Service manual
(12) Image acquisition is needed to make sure that calibration has been done correctly.
Click “Acquire Image”.
SGhealthcare 70
JUMONG Installation & Service manual
(13) About 2 sec. later, below screen will be appeared then make an exposure.
(14) Check image quality as Uniformity, Dead pixel, Dead line etc.
SGhealthcare 71
JUMONG Installation & Service manual
SGhealthcare 72
JUMONG Installation & Service manual
SGhealthcare 73
JUMONG Installation & Service manual
Advisory
THE FOLLOWING INSTRUCTION MANUAL MUST BE READ AND UNDERSTOOD IN ITS ENTIRETY BY THE
INSTALLER AND OPERATOR.
REPORTING
INFORMATION REGARDING ACCIDENTS THAT HAVE OCCURRED WHILE USING THIS COLLIMATOR MUST BE
REPORTED IMMEDIATELY TO RALCO, SRL.
LIMITATION OF LIABILITY
RALCO IS NOT LIABLE IF THE PROVIDED INSTRUCTIONS ARE NOT COMPLIED WITH. FURTHERMORE, RALCO
IS NOT LIABLE IF ONE OR SEVERAL OF THE FOLLOWING INSTANCES APPLY:
IF THE UNIT IS SPECIFICALLY DESIGNED PER CLIENT SPECIFICATIONS AND THE CERTIFICATION WAS THE DUTY
OF THE CLIENT;
THE COLLIMATOR WAS MODIFIED IN ANY WAY BY THE OEM OR OPERATOR;
THE COLLIMATOR WAS INSTALLED WITHOUT RESPECTING THE INSTRUCTIONS, AS PROVIDED IN THIS MANUAL;
THE COLLIMATOR WAS USED IN A WAY OUTSIDE ITS INTENDED USE;
THE COLLIMATOR WAS NOT INSTALLED BY COMPETENT PERSONNEL;
THE COLLIMATOR WAS NOT OPERATED SAFELY OR IN A WAY CONTRARY TO THE INSTRUCTIONS IN THIS
MANUAL;
THE COLLIMATOR WAS NOT SUBJECT TO ROUTINE INSPECTION AND MAINTENANCE BY COMPETENT
PERSONNEL;
THE COLLIMATOR WAS REPAIRED WITH NON-RALCO SPARE PARTS;
THE COLLIMATOR DESCRIBED HERE, IS USED ON RADIOLOGICAL SYSTEMS AND IS CLASSIFIED AS A TYPE IIB
ACCORDING TO ATTACHMENT IX. THE COLLIMATOR HAS BEEN DESIGNED AND MANUFACTURED IN
COMPLIANCE
TO ATTACHMENT II OF LEGISLATIVE DECREE, 2 FEBRUARY 1997, N. 46, IMPLEMENTATION OF DIRECTIVE
93/42/CEE OF 14 JUNE 1993 AND SUCCESSIVE MODIFICATIONS APPLYING DIRECTIVE 2007/47/CE.
LIST APPLICABLE STANDARDS AND TO WHICH RALCO ADHERES TO:
EN 60601-1:2006
EN 60601-1-2:2007
EN 60601-1-3:2008
EN 60601-2-45:2012
SGhealthcare 74
JUMONG Installation & Service manual
EN 60601-2-54:2009
EN 60825-1:2007
ISO 9001:2008
UNI ESO 13485:2004
21 CFR SUBCHAPTER J (FDA)
8750 01 & 8750 81 (CSA)
CE
*RALCO CAN PROVIDE DOCUMENTATION REGARDING ITS ADHERENCE TO ANY OF THE ABOVE STANDARDS.
EN 60601-1 par. 5
• PROTECTION AGAINST ELECTRIC HAZARDS: "CLASS I" EQUIPMENT.
• PROTECTION AGAINST DIRECT AND INDIRECT CONTACTS: TYPE B EQUIPMENT WITH APPLIED PARTS.
• PROTECTION AGAINST WATER SEE PAGE: "COMMON EQUIPMENT".
• SAFETY OF OPERATION IN THE PRESENCE OF INFLAMMABLE ANAESTHETICS WITH AIR OR OXYGEN OR
NITROUS OXIDE: EQUIPMENT NOT SUITED TO APPLICATION IN THE PRESENCE OF INFLAMMABLE
ANAESTHETIC MIXTURES CONTAINING AIR OR OXYGEN OR NITROUS OXIDE.
• OPERATION CONDITIONS: EQUIPMENT FOR CONTINUOUS OPERATION AT INTERMITTENT LOADS - SEE
CHAPTER OPERATION INSTRUCTIONS.
• SHOULD LABEL DATA ON THE COLLIMATOR NOT CORRESPOND TO THE SPECIFICATIONS HEREIN, INFORM
RALCO OF THE NON CONFORMITY.
• VERIFICATIONS OF THE SPECIFICATIONS ARE TO BE PERFORMED ACCORDING TO THE INDICATED
EQUIPMENT STANDARDS.
SYMBOLS
IN THIS MANUAL THE FOLLOWING SYMBOLS ARE USED:
THE TRIANGLE EMPHASIZES WARNINGS AND CAUTIONARY MESSAGES WHICH ARE IMPORTANT FOR YOUR
SAFETY AND/OR EFFICIENT OPERATION OF THE EQUIPMENT. THESE WARNINGS MUST BE STRICTLY COMPLIED
WITH.
INFORMATION PROVIDED WITH THE LAMP IS ADDITIONAL ADVICE FOR THE PROPER CONTROL AND PRACTICAL
USE OF THE UNIT.
SGhealthcare 75
JUMONG Installation & Service manual
SYMBOLS
SGhealthcare 76
JUMONG Installation & Service manual
SGhealthcare 77
JUMONG Installation & Service manual
DESCRIPTION
The X-ray field is defined by six pairs of shutters, four of which are lead-lined. The six pairs of
shutters move perpendicularly within the X-ray field. Two pairs of brass shutters are located
near the focus, two are located near the entrance window and two are located near the exit
window of the X-ray beam from the collimator. The latter shutters serve to accurately define the
X-ray field edges.
Shutter movements are manual, controlled by two knobs on the collimator front panel.
CHARACTERISTICS
Mounting Plane at 80 mm (3.14") from the focus.
Continuous Film Coverage from Min: 00 x 00 cm to Max: 48 x 48 cm at 100 cm (40") SID.
Maximum Radiation Leakage: 150 kVp - 4 mA.
High Luminosity provided by a quartz iodide lamp simulating the X-ray field.
Minimum Inherent Filtration: 2 mm aluminium equivalent.
Accessory Guides are used for accessories and additonal filtration.
Linear Laser to align the collimator with the Potter Bucky.
GC 338 temporizzatore che limita l’accensione della lampada da proiezione a 30 secondi
contribuendo ad una maggiore durata della lampada ed evitando il surriscaldamento.
Fig. R302 L/A - R302 L/A DHHS Front Cover with Exterior Dimensions
SGhealthcare 78
JUMONG Installation & Service manual
This collimator may have the following optional items; a detailed description is provided in the
chapter OPTIONAL ITEMS.
SGhealthcare 79
JUMONG Installation & Service manual
1. SPECIFICATIONS
Specifications of the basic version of the collimator are described here below.
SGhealthcare 80
JUMONG Installation & Service manual
SID: (optional)
Precision of Measurement with Retractable Tape < 2% SID
EN 60601-2-54
Maximum Radiation Leakage
Measured at 100 cm with X-ray Beam = 150 kVp - 4 mA < 40 mRh
EN 60601-2-54
Potentiometers
Square Field n.a.
Round Field
Maximum Load for Accessory Guides
GUIDES FOR ACCESSORIES (IF ASSEMBLED): PRIOR TO Static load: 70 N
NSERTING ACCESSORIES IN THE GUIDES CHECK ON THE
(about 7.1 Kg)
PERFECT ATTACHMENT OF THE SUPPORT WITH THE
Dynamic load: 15 Nm
MOUNTING SLOT ON THE COLLIMATOR (TOLERANCE MAX.
± 0,5 MM). A FAULTY ATTACHMENT COULD BE (approx.
DANGEROUS AND IT COULD CAUSE THE FALL OF 3.06 Kg)
ACCESSORIES
Operation Environment
10°- 40°C
• Ambient Temperature
0%- 75%
• Relative Humidity
• Atmospheric Pressure 700 - 1060 hPa
Storage
-40° - 70°C
• Temperature
10% - 95%
• Humidity
• Atmospheric Pressure 500 - 1060 hPa
Weight 9.4 Kg
Dimensions L: 268 mm
W: 195.5 mm
H: 206.5 mm
SGhealthcare 81
JUMONG Installation & Service manual
2. INSTALLATION
Using the dimensions in Fig. Tube Compatibility below, ensure the near port limiter can
be inserted in to the X-ray tube port.
• Check that the tube housing literature indicates congruent minimum inherent filtration (1
mm) and, that maximum radiation leakage is 30 mR/hour measured at 1 m from the source
when operating at its leakage technique factors (150 kVp - 4 mA).
• Source values (tube housing-collimator) must not be less than 3 mm Al for filtration and
must never exceed 100 mR/hr for radiation leakage [21 CFR sub-chapter J, part 1020.30
(m) (1)].
• The distance between the X-ray tube focus and the flange mounting plane (collimator
upper plate) must be: 80 mm (3.14"), tolerance +/- (0.04”).
SGhealthcare 82
JUMONG Installation & Service manual
IMPORTANT
TO SAFEGUARD THE OPERATOR AND PATIENT AGAINST THE
HAZARD OF A FALLING COLLIMATOR, THE FOLLOWING
INDICATIONS MUST BE RESPECTED.
• Unscrew the four mounting and centering adjustment Allen screws on the collimator until
the four tabs are withdrawn from the collimator top opening, see Fig. Mounting Flange, in
this Chapter.
• Check to see that the distance between the collimator housing and the mounting flange is
equal in all directions and that the collimator face is parallel to the axis of the table.
• Loosen the screws and adjust if required.
SGhealthcare 83
JUMONG Installation & Service manual
SGhealthcare 84
JUMONG Installation & Service manual
Supply and signals to the collimator must be to 2007/47/CE standards. Devices that supply to
the collimator must therefore feature double or reinforced insulation as provided by the General
Standard on Electro-medical Equipment CEI62-5 +A2 (EN 60601-1).
The device is electrostatic sensitive, consequently all the relating safety standards must
be complied with.
SGhealthcare 85
JUMONG Installation & Service manual
SGhealthcare 86
JUMONG Installation & Service manual
Connectors
J1 POWER SUPPLY AND OUTPUTS 1. Lamp output (max 9 A)
2. Push button input
3. Power Supply +12/24 V DC o 12-24 V AC/V DC A
4. Shared Lamp
5. Power Supply –12/24 V DC o 12-24 V AC/V DC B
6. Shared push button
J2 LASER POWER SUPPLY 5VDC 1. +Laser Power Supply (5 V)
2. GND Laser
J3 PROGRAMING CONNECTOR 1. V pp
2. +5 V
3. GND
4. PGD
5. PGC
6. NC
J4 – FAN POWER SUPPLY 12V DC 1. +Fan Power Supply (max 200 mA)
2. – Fan Power Supply
JUMPERS OFF - no jumper
ON - jumper
JP1, JP2 – LAMP TIME SELECTION JP1 JP2
OFF - 30 s OFF - 30 s
ON - 45 s OFF - 45 s
OFF - 60 s ON - 60 s
ON - 120 s ON - 120 s
JP3, JP4 – OPERATION MODE JP3 JP4
SELECTION OFF - Timer OFF - Timer
ON - Timer reset by OFF - Timer reset by pressing
pressing the button the button
OFF - Power Supply ON - Power Supply
ON - Fan ON for 90 ON - Fan ON for 90 seconds
seconds longer than the longer than the lamp
lamp
SGhealthcare 87
JUMONG Installation & Service manual
SGhealthcare 88
JUMONG Installation & Service manual
3. OPERATION INSTRUCTIONS
3.1 LIGHT/X-RAY FIELD SETTING
• Set the collimator at 100 cm SID.
• By rotating the knobs and with the knob index on the front panel, follow the tags of the
scale.
• Do not force the knobs.
• Activate the light field by pressing the related push-button on the collimator front panel.
• The collimator is ready to operate.
WARNING:
PROLONGED LIGHTING WITHOUT ALLOWING LIGHT SOURCE TO COOL
CAUSES THE COLLIMATOR TO OVERHEAT IN THE AREA NEAR THE LIGHT
SOURCE.
FOR EMERGENCIES: MAXIMUM LIMIT ADIVSED IS 5 SUCCESSIVE LIGHT
SOURCE OPERATIONS.
ALLOW THE COLLIMATOR TO COOL (ABOUT 10 MIN).
SGhealthcare 89
JUMONG Installation & Service manual
The table provides the readout of the numbers which must be set with the knobs. The exact
number to be set is obtained by crossing the SID in use (the value indicated by vertical
arrow), with the Cassette size value in cm or inches (horizontal arrow).If necessary see
Chapter- ADJUSTMENTS.
SID in Use
Format Required
Knob Index
Setting
SGhealthcare 90
JUMONG Installation & Service manual
4. CALIBRATION
THE FOLLOWING PROCEDURES REQUIRE THAT X-RADIATION BE
PRODUCED. TAKE ADEQUATE PRECAUTIONS TO MAKE CERTAIN THAT NO
PART OF THE HUMAN BODY IS EXPOSED TO X-RADIATION, DIRECT OR
INDIRECT.
SGhealthcare 91
JUMONG Installation & Service manual
THE HEEL EFFECT WILL CAUSE THE FIELD TOWARD THE CATHODE TO BE
SLIGHTLY LESS SHARP THAN ON THE OTHER THREE SIDES. THIS IS
NORMAL AND CANNOT BE CORRECTED BY ADJUSTMENT. IN ADDITION,
AN X-RAY TUBE OF 12° OR LESS TARGET ANGLE WILL PRODUCE AN
ASYMMETRICALLY SHAPED FIELD WHEN A LARGE FIELD SIZE IS USED AT
SHORT SID, BECAUSE OF ANODE CUT-OFF EFFECT. THIS IS NORMAL AND
MAY NOT BE CORRECTED BY ADJUSTMENT.
Misalignment of the light field/ X-ray field in either the X (cross table) or Y (long table) direction
must not exceed 2% of the SID. In this case, it would be less than 20 mm (0.80"). If the test film
shows that the light field (shadows of the markers) matches the X-ray field (shadow of the
collimator shutters) to within the diameter of one marker and, if the diameter is less than 20 mm
(1.80"), then alignment complies with the regulations.
Greater precision than this is possible. Recommended maximum deviation is one fourth. It is
important the greatest degree of congruency possible is achieved.
If misalignment is detected in both X and Y directions, check the spacing from the focal spot to
the collimator mounting surface is 80 mm (3.14") +/- 1 mm. If spacing needs to be adjusted,
repeat the test film exposure after the adjustment.
If the collimator mount spacing is correct, but adjustment is still necessary proceed as follows:
• Place the test film on the face of the cassette over the white paper.
• Place the cassette in the position originally marked.
• Check the correct position of the film by the shadows cast by the markers.
• Using the images of the collimator shutters as the references for the shape and size of the
X-ray field, adjust the light field to match.
• If adjustment is necessary, adjust the travel of the light source. All procedures can be found
in LIGHT FIELD ADJUSTMENTS in this chapter.
LIGHT FIELD CALIBRATION
Longitudinal Calibration (LONG)
• Remove the part of the cover necessary to access the screws, see Chapter - COVER
REMOVAL
• Remove the light source protection heatsink by unscrewing the fixing screws . This allows
you to access the light source.
• If the light-field needs to be moved laterally, loosen (not remove) the fixing screws A.
• Adjust through screw B.
• When calibration is terminated, lock the screws A.
SGhealthcare 92
JUMONG Installation & Service manual
• If the light-field is bigger than the X-ray field, raise the light source by adjusting screws D.
• Tighten the two screws C.
SGhealthcare 93
JUMONG Installation & Service manual
5. COMPLIANCE VERIFICATION
5.1 MINIMUM FILTRATION REQUIREMENT
The above HVL requirements can be met if it is demonstrated that the aluminium equivalent in
the primary beam is not less than that shown in the following table:
The information contained in the above table was extracted from the Code of Federal
Regulations FDA 21 1020.30 (m).
Type 100 Aluminium Alloy (as given in “ALUMINUM STANDARDS AND DATA” verification of
compliance).
The above HVL requirements can be met if it is demonstrated that the aluminium equivalent in
the primary beam is not less than that shown in the following Total Filtration table:
SGhealthcare 94
JUMONG Installation & Service manual
The Aluminium equivalence of each component in the primary beam (X-ray tube and housing,
beam limiting device and any additional filtration in the system) is specified on the component,
in the technical data attached to the component or can be measured. Determine the total
aluminium equivalence in the primary beam and make sure that it is equal or greater than those
specified in the above Table Total Filtration of Primary Beam in Aluminium Equivalence.
If the total inherent filtration cannot be seen, then the HVL must be obtained with the following
procedures:
The HVL in millimetres of aluminium in the system under test must be compared with those
specified in Table Minimum Filtration Requirement - Beam Quality (HVL) and must be
greater than or equal to the values shown in the table.
a) Direct the central X-ray beam perpendicular and in the center of a RAD-Check instrument.
Determine the exact distance from the X-ray tube focal spot to the window of the collimator
(273 mm - 10.75"). Place the input area of the RAD-CHECK at an equal distance from the
collimator window. Collimate the beam to an area slightly larger than the detector.
b) Make an exposure at a pre-selected technique factor of 90 kVp and appropriate mA and time
values with no added filtration in the beam; record the reading.
Using the type 1100 Aluminium Alloy, tape a total of 2.5 mm of Aluminium to the window of
the collimator. Make an exposure using the same technique factors; record the reading.
c) Verify that the radiation read with the 2.5 mm Al in the beam is greater or equal to 50% of
the radiation read with no filtration in the beam.
The HVL determination obtained from the following procedures are to be compared with those
illustrated in the Table - Minimum Filtration Requirement - Beam Quality (HVL). The HVL
in millimetres of aluminium obtained during the test must be greater or equal than the values
listed in the above mentioned table.
a) Direct the central X-ray beam perpendicular and in the center of a RAD-Check instrument.
Determine the exact distance from the X-ray tube focal spot to the window of the collimator
(273 mm - 10.75"). Place the input area of the RAD-CHECK at an equal distance from the
collimator window. Collimate the beam to an area slightly larger than the detector.
b) Select a tube potential of 100 kVp and appropriate mA and seconds, with no added filtration
in the beam make an exposure and record the reading. Using a set of several sheets of 1100
Aluminium Alloy, each having a thickness of 0.5 or 1.0 mm, tape the filtration to the window
of the collimator. Make an exposure for each increments of filtration and record the reading.
c) Plot the exposure readings (log scale) versus the total added filtration thickness on semi-log
paper; see the sample hereunder.
d) Verify that HLV values in the useful beam for the above specific tube potential is not less
than the values shown in Table - Minimum Filtration Requirement - Beam Quality (HVL).
SGhealthcare 95
JUMONG Installation & Service manual
a) When a light field simulating the X-Ray field is used the illumination provided at 100 cm.
cannot be less than: 160 lux [(21 CFR 1020.31 (d) (2) (ii)].
b) Place the Focus of the X-Ray tube at 100 cm. from the table top were the light field as been
projected. Open the collimator's shutters to assure that each quadrant of the light field is
larger than the measuring area of the photometer.
c) Check that the voltage specified by the manufacturer is applied to the lamp, make certain
that all surfaces in the light beam are clean and unobstructed.
d) Place a photometer capable of reading up to 160 lux in the centre of each of the four
quadrants of the light field.
e) Turn on the light beam and read the light intensity, subtract to it the ambient lighting,
previously determined.
f) Verify that the average illumination is higher than 160 lux.
g) Verify that the contrast ratio is performed between two points:
• The first point at 3 mm outside the edge of the light field.
• The second point at 3 mm inside the edge of the light field.
These measurements are to be performed with the probe of the lux metre set at 1 mm
aperture.
h) Record the measured values including all data regarding the instrument and voltage
employed.
SGhealthcare 96
JUMONG Installation & Service manual
The R302 L/A - R302 L/A DHHS colimator is suitable for use in the specified electromagnetic environment. The
purchaser or user of the R302 L/A - R302 L/A DHHS should assure that it is used in an electromagnetic
environment as described below:
Emissions Test Compliance Electromagnetic Environment-
Guidance
RF emissions Group 1 The Collimator R302 L/A - R302
CISPR 11 L/A DHHS uses RF energy
only for its internal function.
Therefore, its RF emissions are
very low and are not likely to
cause any interference in
nearby electronic equipment.
RF emissions Class [A] This R302 L/A - R302 L/A DHHS is
CISPR 11 suitable for use in all
Harmonic emissions [Not applicable] establishments other than
IEC 61000-3-2 domestic and those directly
Voltage fluctuations/flicker [Not applicable] connected to the low voltage
emissions power supply network which
IEC 61000-3-3 supplies buildings used for
domestic purposes.
CISPR 14 N.A. This Collimator is not suitable for
interconnection with other
equipment
CISPR 15 N.A. This Collimator is not suitable for
interconnection with other
equipment.
Collimator R302 L/A - R302 L/A DHHS is intended for use in the electromagnetic environmenmt specified
below. The customer or the user should assure that it is used in such an environment.
Immunity IEC 60601 Test Compliance Electromagnetic
Test Level Level Environment
Electrostatic 6 kV contact EN 60601-1-2 Hospital
discharge (ESD) 8 kV air test level
IEC 61000-4-2
Electronical fast 2 kV for power EN 60601-1-2 Hospital
transient/burst supply lines test level
IEC 61000-4-4 1 kV for input/output
lines
>3m
Surge 1 kV differential mode EN 60601-1-2 Hospital
IEC 61000-4-5 2 kV common mode test level
Voltage dips, short 0% Un for 0.5 cycles. EN 60601-1-2 Hospital
interruptions and 40% Unfor 5 cycles test level
voltage variations on 70% Un for 25 cycles
power supply input
0% Un for 5 s
lines
IEC 61000-4-11
Power frequency (50/ 3 A/m EN 60601-1-2 EN 60601-1-2 Hospital
60 Hz) test level test level
magnetic field
IEC 61000-4-8
SGhealthcare 97
JUMONG Installation & Service manual
SGhealthcare 98
JUMONG Installation & Service manual
Collimator R302 L/A - R302 L/A DHHS is intended for use in an electromagnetic environment in which radiated RF
disturbances are controlled. The customer or the user of the collimator can help prevent electromagnetic interference by
maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the
collimator as recommended below, according to the maximum output power of the communications equipment.
Rated Maximum Output Separation Distance According to Frequency of Transmitter
Power of Transmitter (m)
W 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2,5 GHz
d= 1.2 x √P d = 1.2 x √P d 0 2.3 x √P
0.01 0.12 0.12 0.23
0.1 0.38 0.38 0.73
1 1.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in metres
(m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output
power rating of the transmitter in watts (W) according to the transmitter manufacturer.
NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and
reflection
from structures, objects and people.
SGhealthcare 99
JUMONG Installation & Service manual
6. COVER REMOVAL
(1)
(2)
(3)
(4)
DISCONNECT THE
CONNECTOR.
(5)
IN COLLIMATORS WITH
MEASURING TAPES, REMOVE
THE TAPE STOP BY LIFTING IT
OFF WITH A SCREW DRIVER.
GENTLY EASE THE TAPE INTO
ITS CONTAINER WITHIN THE
COLLIMATOR.
(6)
(7)
SGhealthcare 100
JUMONG Installation & Service manual
(8)
(9)
Timer Board
ACCESS THE TIMER BOARD BY REMOVING THE TWO KNOBS AND/OR THE FRONT PANEL
DEPENDING ON THE COLLIMATOR MODEL.
Power Supply
SGhealthcare 101
JUMONG Installation & Service manual
Transversal Movement
SGhealthcare 102
JUMONG Installation & Service manual
7. ADJUSTMENTS
THIS IS PROVIDED AS AN AID TO THE END USER. RALCO IS NOT
LIABLE FOR ANY DAMAGES RESULTING FROM THE ALTERING
OF PRESET FACTORY CONFIGURATIONS.
ADJUSTMENTS HAVE BEEN PRESET AT THE FACTORY PRIOR TO
SHIPMENT OF THE COLLIMATOR. SHOULD ANY PROBLEM ARISE
REQUIRING THE NEED TO RECALIBRATE, PLEASE CONTACT
RALCO FOR ASSISTANCE BEFORE PROCEEDING WITH THE
ADJUSTMENT.
SGhealthcare 103
JUMONG Installation & Service manual
Friction Brake.
• If a shutter control is too tight, loosen one of the
two screws A on the U bolt that frictions the
shaft, see Fig. Friction Brake.
• Before replacing the knobs, close both shutters and mount/fix the knobs so that the field
index is set at “0” (completely closed), see paragraph Shutter Dial Adjustment in this
Chapter.
The purpose of these stops is to prevent stressing the control shafts of the shutters at the two
limits of travel. This is done by limiting rotation of the control shafts.
• Adjustment of these stops will not be required unless:
• The shutters can not be completely closed or opened to the largest size.
• Torsion is felt at one or both ends of the travel.
• The shutters themselves appear to limit the motion rather than the stops.
SGhealthcare 104
JUMONG Installation & Service manual
SGhealthcare 105
JUMONG Installation & Service manual
7.9 TROUBLESHOOTING
The use of a faulty collimator might impair the safety of the operator and patient.
Before returning the collimator to Ralco for repair, please make sure that the fault is not caused
by one of the problems listed below. If the indications provided fail to solve your fault, please
make sure that you obtain a Return number (RMA) from Ralco for the collimator, see
Chapter - GENERAL, paragraph Repairs.
Light Source
Problem Cause Solution
Collimator supplied Check: Supply/Tension/Current/
incorrectly Polarity/Fuses
Faulty light source Check item
Replace if necessary, see
The light source fails to Chapter- SUBSTITUTIONS
switch ON Faulty timer Check timer supply
Substitute if necessary, see
Chapter- SUBSTITUTIONS
Faulty ON/OFF pushbutton Check contact
Substitute if necessary
Faulty timer Substitute timer
Light source fails to
Push-button is Substitute push-button
switch OFF
shorted
Centering
Problem Cause Solution
The light field of the The mirror or light See Chapter- CALIBRATION,
collimator is not source are not paragraph Light Field to X-ray
centered positioned correctly Field Alignment
Field Size
Problem Cause Solution
Faulty field size Knobs are not Regulate, see Chapter-
indication regulated ADJUSTMENTS
Shutters
Problem Cause Solution
Shutters close Friction is loose Regulate, see Chapter-
ADJUSTMENTS
SGhealthcare 106
JUMONG Installation & Service manual
8. SUBSTITUTIONS
8.1 SUBSTITUTION OF THE HALOGEN LAMP
SGhealthcare 107
JUMONG Installation & Service manual
SGhealthcare 108
JUMONG Installation & Service manual
SGhealthcare 109
JUMONG Installation & Service manual
9. SPARE PARTS
NOTE: When ordering spare parts, the customer is requested
to specify the collimator model and serial number.
9.2 Labels
SGhealthcare 110
JUMONG Installation & Service manual
LABEL 1
LABEL 2 LABEL 3
LABEL 4
SGhealthcare 111
JUMONG Installation & Service manual
R302 L/A
SGhealthcare 112
JUMONG Installation & Service manual
10. MAINTENANCE
To ensure constantly safe performance of the collimator and its compliance with applicable
regulations, a maintenance program is indispensable.
It is the Owner's responsibility to supply or arrange for this service.
• The collimator housing must be cleaned as prescribed by the sanitary regulations followed
by the operator.
• Disconnect supply.
• Use non abrasive cleaning products.
Care must be taken to prevent liquid from entering the collimator. Please Note: The
collimator cover is not watertight.
• Do not reapply power if inflammable liquids have leaked into the collimator.
See the following Maintenance Instructions.
• Clean the varnished and aluminium surfaces with a damp cloth only, using a neutral
cleansing agent then dry the surfaces with a soft cloth.
• Clean chrome surfaces with a dry soft cloth.
Do not spray water or detergent directly over the collimator. The unit’s liquid
protection level is IPx0.
DISINFECTION
The disinfection method use must conform with the currently applicable norms and directives
covering disinfection and protection against explosion hazards.
• Disconnect supply.
• Disinfect the unit including accessories and cables with a dampened cloth.
• Do not spray the unit with the disinfectant because it could leak into the collimator.
Ralco suggests a yearly servicing program, however shorter intervals are advisable when the
collimator is subject to heavy workloads.
• Re-calibration of the collimator will be necessary whenever the X-ray tube is changed or at
each substitution of the lamp used to simulate the light field.
• Calibration procedures must be performed as described in this manual.
• Check once a week that the screws and tabs which serve to secure the collimator to the
flange/tube adapter are correctly tightened.
• Remove the covers and panels from collimator. Inspect the moving parts for signs of wear
or damage.
• Check the electric system and substitute parts that show wear.
SGhealthcare 113
JUMONG Installation & Service manual
MAKE SURE TO TIGHTEN THE ALLEN SCREWS SECURING THE COLLIMATOR OR THE CONTROL TABS.
APPROPRIATE TIGHTENING OF THE 4 ALLEN SCREWS ENSURES SECURE MOUNTING OF THE
COLLIMATOR. TIGHTENING FORCE USED MUST NOT EXCEED 0.50 NM.
SGhealthcare 114
JUMONG Installation & Service manual
11.GENERAL
11.1 REPAIRS
In the event the customer finds any noncompliance or malfunctions of the collimator, contact
Ralco via e-mail at the address: p.vescera@ralco.it (Ralco Assistance).
The information must include:
• The model and serial number of the collimator found on the label.
• A detailed description of the problem (in Italian or English).
• It is important to specify if you want a repair or a total refurbishment of the product.
Ralco will resolve the problem by either providing directions, and/or field service or by sending
replacement parts.
In the event the collimator needs to be repaired at Ralco, customer service will immediately
provide the customer with a RMA (Return Merchandise Authorization) number as your consent
to the return and provide all necessary additional information.
The shipping of the unit is at the customer’s expense if the unit is out of warranty, see
paragraph WARRANTY in this chapter.
Ralco reserves the right to decide if the collimator is to be repaired or substituted.
Your collimator contains materials which can be recycled and reused. Specialised companies
can recycle your product to increase the amount of reusable materials and to minimize the
amount of materials to be disposed of.
The product contains lead which can be highly contaminating if dispersed
incorrectly. The following symbol signifies that the product conforms to the
environmental requirements of directives 202/95/EC, 2002/96/EC, 2003/108/EC;
it must be disposed of correctly at the end of its life-cycle.
The collimator does not contain polluting materials or products with the exception
of the lead that composes the shutters - avoid direct contact with lead especially for prolonged
periods.
It is required that you observe Local Laws regulating the disposal of the collimator using
certified environmental management entities. Should this prove impossible, return the
collimator to Ralco at the purchaser's expense and Ralco will undertake its correct disposal.
If you are replacing the unit with new equipment, you may return the old collimator to Ralco.
Please contact us if you require further information.
11.3 WARRANTY
Ralco undertakes to replace and repair any collimator part during a period of 24 months from
the date of invoice and cover the labour costs involved, not including the exemptions below.
The warranty applies provided the product has been handled properly in accordance with its
operating instructions; presentation is required of the original invoice indicating the date of
purchase, the model and serial number as well as other documents originally supplied with the
set.
Exemptions:
• If unit documents have been altered in any way or made illegible;
• If the model or production number on the product has been altered, deleted, removed or
made illegible;
• If repairs or product modifications and alterations have been performed by unauthorized
and unqualified persons;
SGhealthcare 115
JUMONG Installation & Service manual
11.5 DISASSEMBLY
SGhealthcare 116
JUMONG Installation & Service manual
11.7 SAFETY/RESPONSIBILITY
The collimator has been constructed to current standards to meet the safety requisites of
directive 2007/47/CE. However, due to the presence of x-rays, the type of application implies
a residual risk derived from possible faults that could occur during operation of the unit.
The Instructions contained in the this Manual will ensure the correct use of the device and
reduce the causes of possible hazards.
The residual risks of the device are reasonable; they have been assessed and approved in the
related Risk Management Plan contained the Technical Report.
SGhealthcare 117
JUMONG Installation & Service manual
SGhealthcare 118
JUMONG Installation & Service manual
1 Pre-installation
1.1.0 INTRODUCTION
This chapter summarizes the main features of the CMP 200® and CMP 200® DR X-ray generators
(performance, regulatory and compatibility). Safety information is provided, along with environmental,
room, and installation requirements. This chapter concludes with a pre-installation checklist and a
diagram showing the major component layout.
The information in this chapter is provided in order for the installer to be able to plan the site
layout prior to installation of the generator.
1.1.2 Features
The following are the main features of and the options available for the generator:
• Integral low speed starter, compatible with X-ray tubes with type “R” stator. Optional compatibility
With GE 23/23 Ω equal impedance “E” stator.
• Optional dual-speed starter on some models of CMP 200® DR (not available on 208 / 230 VAC, 1-
phase & 3-phase units), compatible with tube types listed in chapter 2.
• Capable of interfacing with various DR imaging systems (CMP 200® DR only).
• 24 VDC, 110, or 220 VAC power source for Buckys (fused at 0.8 amps).
• 24 VAC 150 watts power source for collimator lamp.
• 24 VDC 45 watts power source for system locks.
• Optional AEC.
• Optional DAP (Dose-Area Product).
• Tomography
SGhealthcare 119
JUMONG Installation & Service manual
OPERATING
Ambient temperature range 10 to 40 °C (50 to 104 °F).
Relative humidity 20 to 80%, non-condensing.
Altitude -700 to 3000 meters (1100 to 700 hPa, 825 to 525 mm Hg).
The CMP 200® / CMP 200® DR series of X-ray generators comply with the regulatory requirements and
design standards in this section as follows:
• VZW2555 series: Only the standards marked with an asterisk * under SAFETY.
• VZW2556 series: All standards in this section.
A) SAFETY
FDA Center for Devices & Radiological Health (CDRH) - 21 CFR subchapter J (USA).
Radiation Emitting Devices Act - C34 (Canada).
Medical Devices Regulations (Canada).
EC Directive 93/42/EEC concerning Medical Devices (European Community).
EN 60601-1/IEC 60601-1, EN 60601-2-7/IEC 60601-2-7, CSA 601.1, UL60601.1.
-Type of protection against electric shock: Class I equipment.
-Degree of protection against electric shock: Not classified.
-Degree of protection against harmful ingress of water: Ordinary equipment.
-Mode of operation: Continuous operation with intermittent loading (standby - exposure).
-Equipment not suitable for use in presence of a flammable anesthetic mixture with air or
with
oxygen or nitrous oxide.
EN 60601-1-4/IEC 60601-1-4, ISO 14971, EN 60601-1-6/IEC 60601-1-6.
NOTE: All referenced standards are considered to be at the latest adopted revision.
SGhealthcare 120
JUMONG Installation & Service manual
SGhealthcare 121
JUMONG Installation & Service manual
SGhealthcare 122
JUMONG Installation & Service manual
SGhealthcare 123
JUMONG Installation & Service manual
In accordance with the intended use, some models of this series of X-ray generators comply with the
European Council Directive concerning Medical Devices. The CE marking affixed to compliant products
signifies this. One of the harmonized standards of this Directive defines the permitted levels of
electromagnetic emission from this equipment and its required immunity from the electromagnetic
emissions of other devices.
It is not possible, however, to exclude with absolute certainty the possibility that other high frequency
electronic equipment, which is fully compliant to the EMC regulations, will not adversely affect the
operation of this generator. If the other equipment has a comparatively high level of transmission power
and is in close proximity to the generator, these EMC concerns (the risk of interference) may be more
pronounced. It is therefore recommended that the operation of equipment of this type such as mobile
telephones, cordless microphones and other similar mobile radio equipment be restricted from the vicinity of
this X-ray generator.
SGhealthcare 124
JUMONG Installation & Service manual
1.2.0 SAFETY
The following advisory symbols are used on the safety warning labels, and/or on circuit boards, and/or on the
operator console.
X-ray radiation exposure may be damaging to health, with some effects being cumulative and extending
over periods of many months or even years. Operators and service personnel should avoid any
exposure to the primary beam and take protective measures to safeguard against scatter radiation.
Scatter radiation is caused by any object in the path of the primary beam and may be of equal or less
intensity than the primary beam that exposes the film
SGhealthcare 125
JUMONG Installation & Service manual
No practical design can incorporate complete protection for operators or service personnel who do not
take adequate safety precautions. Only authorized and properly trained service and operating
personnel should be allowed to work with this X-ray generator equipment. The appropriate
personnel must be made aware of the inherent dangers associated with the servicing of high voltage
equipment and the danger of excessive exposure to X-ray radiation during system operation.
SGhealthcare 126
JUMONG Installation & Service manual
SGhealthcare 127
JUMONG Installation & Service manual
This information is provided to help you establish safe operating conditions for both you and your X-ray
generator. Do not operate this X-ray generator except in accordance with these instructions, and any
additional information provided by the X-ray generator manufacturer and / or competent safety
authorities.
Weight Label
This label is attached to the main generator cabinet and to the HT tank, and states the approximate
weight of the main cabinet with the HT tank, and the weight of the HT tank separately. Do not attempt to lift
these items without proper assistance.
SGhealthcare 128
JUMONG Installation & Service manual
This label is attached to the generator cabinet and on the inside of the back cover above the HT tank.
The DC bus capacitors (approximately 300 to 670 VDC, depending on model) will remain charged for up
to 5 minutes after the AC mains is disconnected or the console is switched off.
This label is attached to the outside of the generator cabinet, the cover over the inverter assembly, the
cover over the DSS board and the fan cover. Mains voltage is present inside the cabinet whenever the
main disconnect is switched on. Additionally, the DC bus capacitors will remain charged for up to 5
minutes after the AC mains is disconnected or the console is switched off.
SGhealthcare 129
JUMONG Installation & Service manual
This notice is printed on the HT tank lid and cautions against over-tightening the nuts on the transformer
feedthrough terminals (for the primary of the HT transformers).
This notice is printed on the HT tank lid. High voltage may be present at the primary terminals on the tank lid
board, at the output high voltage connectors, and at the mA/mAs measuring jacks if the shorting link is opened
for mA/mAs measurements.
These labels are fixed on the outer face of the auxiliary transformer and indicate the presence of high
voltage taps on the primary of 120, 200, 240, 400 and 480 VAC. Ensure the main power disconnect is
switched off and appropriate documentation is consulted before attempting to service this component.
SGhealthcare 130
JUMONG Installation & Service manual
SGhealthcare 131
JUMONG Installation & Service manual
The maximum heat output of the main generator cabinet is less than 1000 BTU / hour in normal clinical
use, with a maximum of 70 BTU / hour heat output for the console. The console is convection-cooled, and the
main cabinet is fan cooled. The console and main cabinet should never be covered when the
generator is switched on, as any covering may interfere with the cooling.
The tables in this section show mains power requirements for various configurations of CMP 200® and
CMP 200® DR X-ray generators. The installer must ensure that the generator is connected to the proper
mains voltage as per the nameplate on the generator.
The table below depicts the power requirements for the 32 kW CMP 200® / CMP 200® DR X-ray
generators.
The table below depicts the power requirements for the 40 kW CMP 200® / CMP 200® DR X-ray
generators.
SGhealthcare 132
JUMONG Installation & Service manual
The table below depicts the power requirements for the 50 kW CMP 200® / CMP 200® DR X-ray
generators.
The table below depicts the power requirements for the 65 kW CMP 200® DR X-ray generators.
The table below depicts the power requirements for the 80 kW CMP 200® DR X-ray generators.
SGhealthcare 133
JUMONG Installation & Service manual
* Nominal Current = Generator standby current only. External or installer-supplied equipment connected to
the generator may increase the nominal current beyond the values shown.
The following table defines the power line requirements for the generators.
SGhealthcare 134
JUMONG Installation & Service manual
* Refer to 1.3.3 for general grounding information. Maximum wire gauge is # 2 AWG Cu (33 mm2).
** Maximum wire gauge is # 4 AWG Cu (21 mm2).
*** Maximum wire gauge is # 2 AWG Cu (33 mm2).
SGhealthcare 135
JUMONG Installation & Service manual
• A suitable ground must be connected from the disconnect switch to the main ground of the generator,
located to the right of the main fuse block, on the sub-panel. The ground wire is typically part of the
ine cord, and the current capacity of the ground conductor must normally be equal to or greater than
that of the line conductors.
• A copper ground cable, #10 AWG (6 mm2) or larger should be connected from the X-ray tube housing
to the H.T. tank ground stud (located at the top of the HT tank).
• If a neutral line is provided with the system, under no circumstances is it to be used for ground
purposes. The ground must carry fault currents only.
The main generator cabinet is self-standing and does not need to be supported. However, the installation
should meet the following requirements:
• The floor must be flat and level.
• The generator installation area must be clean and free of dirt or debris.
• The installer must supply generator hold-down brackets, if required. Alternately, mounting holes have
been provided in the base of the generator. The generator may then be anchored to the floor via
these holes.
• Sufficient room must be provided to allow access to the rear and side of the generator for installation
and service. See figure 1-1 for recommended clearances.
• A cable trough, conduit, or raceway (1 in; 2.5 mm, diameter) should be provided from the control
console to the main cabinet to allow routing of the control cable if required.
• The control console is normally freestanding on a desk or shelf. It may be anchored if necessary.
SGhealthcare 136
JUMONG Installation & Service manual
Figure 1-2 shows the dimensions of the generator cabinet, the locations of the cable access slots, the AC
mains cable entry, and the seismic center location for the CMP 200® / CMP 200® DR X-ray generator.
The dimensions and weight of the generator and control console(s) are shown in the table below.
SGhealthcare 137
JUMONG Installation & Service manual
The following is a checklist of recommended tools and test equipment for installation and calibration of
the generator.
SGhealthcare 138
JUMONG Installation & Service manual
Figure 1-3 shows the external view and dimensions of the membrane and touchscreen operator’s
consoles. Figures 1-4 and 1-5 show the major components located inside the generator cabinet. Figure
1-6 is an internal view of the console, showing the major components and cabling. Figure 1-4 does not
represent all models. This is meant to show major component layout only.
SGhealthcare 139
JUMONG Installation & Service manual
SGhealthcare 140
JUMONG Installation & Service manual
SGhealthcare 141
JUMONG Installation & Service manual
X-RAY TUBES:
Refer to the compatibility statement and to chapter 2 of this manual.
AEC DEVICES:
Refer to the compatibility statement at the front of this manual.
DR INTERFACE:
Refer to the compatibility statement at the front of this manual.
1. The Software embedded in this Product is protected by international intellectual property rights and
treaties. You may use the software in object code form only and are prohibited from distributing the
software as such. There is no grant of any of the Software’s proprietary source code. This license
does not grant you any rights to patents, copyright, trade secrets, trademarks, or any other rights
with respect to the Software. You are not authorized to modify or to create derivative works based on
this software. You are not authorized to decompile, disassemble or otherwise reverse engineer the
embedded Software. CPI reserves all rights not expressly granted herein.
2. You are authorized to copy the Software only for the following purposes.
a. If such copying is an essential step in the use of the Software and in accordance with this
agreement; or
b. To make an archival copy for back up purposes.
3. If making a copy pursuant to Section 2 above, you must ensure that all trademark, copyright and
intellectual property notices are reproduced and included on any copies that are made.
4. The Software embedded in this Product is provided to you within the same warranty terms, as those
offered for the Products, except for any third party software, which is offered “as is” and without
warranties of any kind including, but not limited to: warranties of merchantability, fitness for a
particular purpose, title and non-infringement.
5. The Software embedded in this Product is not intended for use in or with systems, devices, or
products intended to support of sustain life or for any aviation or nuclear reactor application in which
the software or its failure, malfunction, or inadequacy could directly or indirectly cause or contribute
to personal injury or death or significant property damage. It is your responsibility, as the User or End
User, to ascertain the suitability of the Software for your particular situation and / or application.
6. This agreement is effective until terminated. The agreement shall terminate immediately if you fail to
adhere to the terms and conditions set forth herein. Upon termination, you must immediately cease
all use of the Software and destroy any and all copies of the embedded Software in your possession.
SGhealthcare 142
JUMONG Installation & Service manual
7. This agreement represents the entire agreement between you and CPI with respect to the Software,
and supersedes all other agreements or representations, whether written or oral. The terms of this
agreement can only be modified by the express written consent of both parties. If any part of this
agreement is held to be unenforceable as written, it will be enforced to the maximum extent allowed
by applicable law, and without effect to the enforceability of any other part.
SGhealthcare 143
JUMONG Installation & Service manual
Chapter 2
INSTALLATION
2.1.0 INTRODUCTION
This chapter contains instructions for unpacking and installing the CMP 200® and CMP 200® DR X-ray
generators. This chapter also describes the basic wiring and setup of the generator (console, X-ray tube,
AC mains, etc), allowing for initial power-up of the generator. This is followed by tube seasoning and auto
calibration.
2.2.0 UNPACKING
4. Remove and unpack the membrane control console, if included. This is strapped to the top of the
generator. Then carefully lift the generator from the pallet.
5. Remove and unpack the optional hand switch and the optional mini-console control unit, if
included.
6. If applicable, unpack the optional touchscreen console along with the base and console cables.
7. Inspect all items for shipping damage, including loose hardware if applicable.
8. Unpack the manuals and any other paperwork that may be packed with the generator.
9. Keep the shipping packs. In case of shipping damage, place the unit(s) back in their shipping
pack(s) and notify the carrier and the customer support department as described in chapter 1 of
this manual.
1. Remove and set aside the screws and washers securing the cover to the generator chassis.
2. Carefully lift the cover off the chassis.
Refer to the section GENERATOR LAYOUT AND MAJOR COMPONENTS in chapter 1 for major
component identification and layout.
SGhealthcare 144
JUMONG Installation & Service manual
Place the generator cabinet in a location that will allow the following:
• Easy front and side access for service and sufficient clearance at the rear for room interface cables.
Refer to chapter 1.
• Air circulation: The main cabinet is fan cooled, therefore room-temperature air must be free to
circulate around the cabinet. The cooling slots in the cabinet must be unobstructed at all times.
• A stable footing.
• Close proximity to service-disconnect boxes. Cables should not be on the floor where they could be
stepped on or tripped over.
• Do not locate the X-ray generator within the patient environment of the X-ray room.
YOU MAY CHOOSE TO TEMPORARILY LOCATE THE CONSOLE NEAR THE GENERATOR FOR
INITIAL PROGRAMMING AND CALIBRATION. IF SO, PLEASE COMPLETE THE FINAL CONSOLE
INSTALLATION PER THIS SECTION WHEN THE GENERATOR INSTALLATION IS COMPLETED.
Position the control console in its intended location and ensure that it is stable.
• The control console (membrane console, touchscreen console, or mini-console) must be located
inside an X-ray shielded control booth within the X-ray room, or outside the X-ray room.
• If the console is located on a shelf, supply index pins or equivalent hardware to the base of the
console to prevent slipping.
• Ensure that the console is mounted at a height and angle to allow for easy viewing of the displays.
• If the optional CPI pedestal stand (membrane console) is to be used for the console mounting, follow
the mounting instructions supplied with the stand.
Membrane Console
Note: Some jurisdictions require that the console PREP and EXPOSE buttons be disabled if a hand
switch is used. This is done by removing JW1 and JW2 from the console board as described below.
1. Turn the console upside down and place it on a clean, non-abrasive surface.
2. Remove and set aside the screws securing the console base to the molded case, and the
hardware from the console ground stud.
3. Remove the console base (the metal bottom panel with the feet attached).
4. Locate and then remove JW1 and JW2 from the console board. Refer to the appropriate figure in
chapter 1, in the section GENERATOR LAYOUT AND MAJOR COMPONENTS.
5. Do not discard the jumpers that were removed in the previous step. These will need to be
reinstalled if the console PREP and EXPOSE buttons must be enabled in the future.
6. Reinstall the console base by reversing the previous steps.
Touchscreen Console
The touchscreen base is shipped as a separate item, and must be attached to the touchscreen console
before continuing with the installation. A Phillips screwdriver is required to attach the base to the
touchscreen console. A hex key has been included to adjust the tension on the tilt-arm mechanism.
1. Carefully unpack the touchscreen console and the desk-mount base components and set the
SGhealthcare 145
JUMONG Installation & Service manual
Position the touchscreen console in its intended location and ensure that it is stable.
• The touchscreen console must be placed on a solid and level surface. There must be no risk of it
tipping or falling, especially if raised to its maximum viewing height.
• Ensure that the display is positioned at a height and angle to allow for easy viewing.
If it is desired to anchor the generator to the floor, refer to chapter 1. This should not be done until all
cable hookups to the generator are completed.
SGhealthcare 146
JUMONG Installation & Service manual
Unless specified otherwise, all cables (except AC mains) should be routed into the generator main
cabinet through the cable access slots at the upper rear of the generator. The cables should be secured
to the lip on the inside of the cable access slots using tie-wraps or equivalent fasteners. For connections
that must be made to the H.V. auxiliary board, AEC board, or to the generator control board, route the
cables over the top of the fan-mounting bracket and over the chassis divider panel.
The AC mains cable is routed into the generator via the cable clamp on the rear of the generator,
adjacent to the main fuses.
All cables should be kept away from high voltage areas in the cabinet, and dressed neatly in
place. Cables should be cut to the correct length if possible, as excess cabling may contribute to EMI/RFI
problems. For those cables that cannot be cut to the correct length (HT cables and console cables for
example), try to minimize the area inside of any loops of excess cable, as these loops can create an
antenna.
Ferrules should be used on the ends of all stranded wires that are connected to terminal
connections in the generator. These must be supplied by the installer.
EXCESS LENGTHS OF CABLING MUST NEVER BE BUNDLED UP AND STORED INSIDE THE GENERATOR.
Membrane Console
1. Note the protective cover connected to the console cable. This is intended to protect the console
cable connectors during shipping and while routing the console cable during installation.
Disconnect the generator end of the cable (the end with the ferrite bead) from the protective
cover, and then route the end of the cable with the protective cover attached as required.
Remove and discard the protective cover when finished. After removing the protective cover,
inspect the console cable connectors for any damage. Please see figure 2-2 for an example of
such damage.
2. Route the generator end of the console cable into the generator cabinet via the cable access slot
nearest to the generator control board. The cable must be routed as per figure 2-3. Connect the
generator end of the console cable to J3 on the generator control board.
3. Connect the free end of the console cable to J8 at the rear of the console. Leave sufficient slack
in the cabling to the console to allow for future service and maintenance.
Touchscreen Console
1. Route the generator end of the console cable into the generator cabinet via the cable access slot
nearest to the generator control board. The cable must be routed as per figure 2-3. Connect the
generator end of the console cable to J20 on the generator control board.
SGhealthcare 147
JUMONG Installation & Service manual
2. Connect the free end of the console cable to GEN on the rear of the touchscreen console. Leave
sufficient slack in the cabling to the console to allow for future service and maintenance.
3. Tighten the screw locks to fully secure the “D” connectors.
4. Connect one end of the supplied ground wire to the touchscreen console ground screw, shown in
figure 2-4. Connect the other end of the ground wire to the ground connector near the main line
fuses in the generator (figure 2-8). Dress the ground wire away from high voltage areas in the
generator. This ground location may have other ground wires already connected; ensure that
these existing ground wires are not disconnected when making the X-ray tube ground connection.
Note that this ground wire is required for EMC compliance only. It has no safety impact.
5. Optional: Connect customer-supplied speakers (minimum 8 ohms) to LO (3.5 mm stereo jack) on
the rear of the touchscreen console (do not use externally amplified speakers). Use cable ties to
secure the speaker cable to the console cable for support. Pins 1 and 2 (left and right) on the 3.5
mm male stereo jack must be shorted together on the cable that plugs into the touchscreen
console.
Please note that connecting external speakers will disable one of the on-board touchscreen
speakers.
Mini-Console (optional)
1. Route the generator end of the console cable into the generator cabinet via the cable access slot
nearest to the generator control board. The cable must be routed as per figure 2-3. Connect the
generator end of the console cable to J19 on the generator control board.
2. Connect the free end of the console cable to the 15-pin male connector that is attached to the
short piece of console cable connected to the mini-console. Tighten the screw locks to fully
secure the “D” connectors on the console cable.
3. An extra cable (9-pin ‘D’ to RJ45) is included with the optional mini-console. This must be
connected from the standard serial port (9-pin ‘D’ connector) on the imaging computer to
J3 on the generator control board on any DR systems that require serial communication
with the generator.
SGhealthcare 148
JUMONG Installation & Service manual
SGhealthcare 149
JUMONG Installation & Service manual
Figure 2-4 shows the designations of the connectors on the rear panel of the membrane and touchscreen
consoles.
The optional hand switch, if ordered from CPI Canada Inc, is supplied pre-wired to a male 9 pin
subminiature “D” connector. This connects to J3 on the membrane console or to HS on the touchscreen
console. A male 9 pin subminiature “D” connector will need to be provided by the installer if the CPI
supplied hand switch is not used.
SGhealthcare 150
JUMONG Installation & Service manual
1. Route the X-ray tube stator cable to the stator terminal block J7 on the H.V. auxiliary board. This
is shown in figure 2-5.
2. Connect the X-ray tube stator and the thermal switch to J7 on the H.V. auxiliary board terminal
block as per the table below.
SGhealthcare 151
JUMONG Installation & Service manual
1. Route the X-ray tube stator cable to the stator terminal block on the back of the dual-speed
starter chassis. Refer to figure 2-6.
THE STATOR CABLE FOR THE DUAL SPEED STARTER MUST BE SHIELDED. THE SHIELD
FOR THE STATOR CABLE MUST BE PROPERLY GROUNDED AT BOTH THE TUBE END
AND THE GENERATOR END OF THE CABLE. CONNECT THE GENERATOR END OF THE
SHIELD TO THE GROUND TERMINAL ON THE STATOR TERMINAL BLOCK (FIGURE 2-6).
2. Connect the X-ray tube stator and the thermal switch as per the table below.
3. Secure the X-ray tube stator cable to the generator chassis using suitable tie-wraps or equivalent
fasteners.
The X-ray tube thermal switch is connected to J7-1 and J7-2 on the H.V. auxiliary board for both the low
speed starter and the dual-speed starter, as per section 2.6.3.
SGhealthcare 152
JUMONG Installation & Service manual
Refer to chapter 1 for generator power and generator power line requirements.
1. Temporarily disconnect the fan by unplugging the fan power-connector at the fan cover.
2. Remove and set aside the hardware securing the fan cover to the generator. Then remove the
fan cover with the fan attached.
3. Temporarily remove the safety cover from the main fuses (if fitted). This must be reinstalled after
the AC mains connections are made, before reinstalling the fan cover.
4. Prepare the AC mains cable as per figure 2-7 and the AC Mains Termination Table, and then
strip the ends of the leads to the required length.
5. Pass the AC mains cable through the cable clamp at the upper rear of the generator cabinet,
adjacent to the main fuses. Tighten the clamps to secure the cable.
6. Connect the ground wire to the chassis ground connector, and connect the mains power wires to
the terminals on the main fuse holder shown in figure 2-8. For 1 phase generators connect the
mains to F1 and F2; for 3 phase units connect the mains to L1, L2, and L3.
• Ferrules should be used on the ends of the AC mains wires. These must be supplied by the
installer.
• For China only, the power cable must be CCC approved.
7. Re-install the fan cover and reconnect the fan by reversing the previous steps.
SGhealthcare 153
JUMONG Installation & Service manual
SGhealthcare 154
JUMONG Installation & Service manual
The X-ray tube should be mounted in its normal fixture i.e. tube stand or other device.
1 Verify that the HT cable terminations are clean, in good condition, and coated with vapor proof
compound.
2. Remove the dust caps that cover the high voltage terminals on the HT tank.
3. Connect the anode and cathode cables to the HT tank. Ensure that the cables are plugged into
the proper connectors on the HT tank. Refer to figure 2-9.
4. Be sure that the HT cable connectors are tight and there is no play between the connector
insulator and the screw-down ring.
In addition to the X-ray tube manufacturers recommended tube grounding procedure, a separate ground wire
(10 AWG, 6mm2) must be connected from the X-ray tube housing to one of the ground studs on the HT tank.
Refer to figure 2-9 for the location of these ground studs. These ground locations may have other ground wires
already connected; ensure that these existing ground wires are not disconnected when making the X-ray tube
ground connection.
Failure to make this ground connection may result in intermittent operation and/or exposure errors.
Refer to chapter 3C for connection of Buckys, interlocks, room lights, the DR imaging system (if
applicable), DAP, collimator lamp and system locks power, and to chapter 3D for installation and
calibration of AEC. It is suggested that these items not be connected until the initial run-up of the
generator is complete, and the tube auto calibration routine has been performed as described near the
end of this chapter.
To connect an external emergency power-off switch, disconnect the jumper from J2-1 to J2-2 on the
generator control board. Then connect the emergency-off switch to J2-1 and J2-2. Refer to MD-0928 in
SGhealthcare 155
JUMONG Installation & Service manual
chapter 9.
For installations where installer-supplied auxiliary power distribution circuits are added to the
generator, 24 VDC is available on the generator interface board to drive the coil of the power distribution relay.
Connect the coil to J2-3 (+) and J2-4 (ground). Refer to MD-0927 in chapter 9.
The maximum current available from this source is 100 mA.
The room door interlock switch must be wired to the generator as described in Inputs in chapter 3C
before the generator is powered up. This switch must provide an open contact when the door is open.
Before continuing, note the part number of the H.V. auxiliary board in the generator. Part numbers
739442-00 / 739445-00 have 33 μF of phase-shift capacitance, and are compatible with the type “R”
stator tubes listed in Table 1 of X-Ray Tube Stator Compatibility Tables Supplement 746026-00. Part
numbers 739442-01 / 739445-01 have 45 μF of phase-shift capacitance, and are compatible with GE
23/23 Ω type stators, some Siemens and some Toshiba tubes as listed in the referenced Table 1.
Confirm that the boost voltage is set correctly for the selected tube type per the referenced Table 1 before
continuing. The procedure for setting the boost voltage is detailed in 2.7.1. The boost voltage may be
measured from F6 to F7 on the H.V. auxiliary board.
If the desired tube type is not listed, please contact CPI product support for assistance.
Confirm proper stator operation using a suitable tachometer before making any exposures.
Follow the steps below to verify and configure the low speed starter boost voltage. This is factory
configured to 240 VAC.
1 Confirm the required boost voltage for the selected tube as described above. The requirement for
the vast majority of tubes in Table 1 of the supplement is 240 V. For tubes that require 120 V
boost, this is noted in the table.
2. The boost voltage is configured via jumpers on the H.V. auxiliary board:
• E16 to E15 selects 240 V boost.
• E14 to E15 selects 120 V boost.
Swap the connection at E14 and E16 if the boost voltage needs to be changed. The jumper wire
(E16 - E15 or E14 - E15) will need to be replaced if making this change. Extra jumper wires are
attached to a bag on the lip on the inside of the cable access slot above the HT tank. Select the
shortest wire from this bag that will connect between the desired tabs on the board that has the
proper terminations on the jumpers. Do not discard the existing jumper; place it in the jumper kit
to be available for future configuration changes.
Proceed to the next step if the jumper setting is correct.
SGhealthcare 156
JUMONG Installation & Service manual
3. Confirm the proper boost voltage and proper anode rotation as described above.
This section applies only to units fitted with the dual-speed starter.
The dual-speed starter must be programmed for the X-ray tube type used at this site. This is done via DIP
switch SW1 on the dual speed starter board.
The following tube functions are set with this switch:
• High-speed start and run voltages.
• Low-speed start and run voltages.
• Brake time and brake voltage (high speed).
• Boost times.
• Boost time increments. Boost time may be increased in 100 ms steps in the range of 100 to 700 ms.
1. The dual-speed starter EPROM is different for 400 V units and for 480 V units. If a 400 V unit is
reconfigured for 480 V, or a 480 V unit is reconfigured for 400 V, the dual speed starter EPROM
will need to be changed. A spare EPROM (the complement of the EPROM that is in the dual
speed starter) is in a bag attached to the lip on the inside of the cable access slot above the HT
tank. Refer to chapter 6 for the EPROM replacement procedure, and to the table below for the
applicable EPROM part numbers.
2. If you are making the conversion as per the previous step, use an indelible marker to change the
part number of the dual-speed starter assembly (901297-XX to 901298-XX, or vice-versa). The
dual-speed starter part number is printed on a label near the top left side of the dual speed starter
chassis. Keeping the dual-speed starter part number current will maintain configuration control of
the product.
SGhealthcare 157
JUMONG Installation & Service manual
1. Select the desired tube type from Table 2 of X-Ray Tube Stator Compatibility Tables Supplement
746026-00. Record the tube type number (housing and insert) and the binary code as per the
third column in the table. Please note that the tube compatibility applies only to the housing and
inserts listed, i.e. for the specific manufacturer(s) shown.
2. If the desired tube type is not listed, please contact CPI product support for assistance.
3. The dual-speed starter used in CMP 200® DR X-ray generators will be either part number
901297-02, 12, 13, 15 or 16 (400 VAC units) or 901298-02, 12, 13, 15 or 16 (480 VAC units).
The “-02” dual-speed starter has a 60 μF low-speed capacitor, and a 20 μF high-speed capacitor.
The “-12” dual-speed starter will automatically select either a 36 μF or 37.5 μF low-speed
capacitor for low-speed operation, and will automatically select 6 μF or 7.5 μF for high-speed
operation, based on the setting of SW1.
The “-13” dual-speed starter has a 30 μF low-speed capacitor, and, will automatically select 5 μF
or 6 μF for high-speed operation.
The “-15” dual-speed starter has a jumper-selectable 15.5 μF or 28 μF low-speed capacitor, and
an automatically selected 3 μF or 6 μF high-speed capacitor.
The “-16” dual-speed starter will automatically select either a 31 μF or 37.5 μF low-speed
capacitor for low-speed operation, and will automatically select 6 μF or 12.5 μF for high-speed
operation.
The stated capacitor values are equivalent capacitor values, and are derived from several
combinations of relay-selected series / parallel discrete capacitors, depending on the part
number. Refer to MD-0924 in chapter 9 for details.
4. To determine if the dual-speed starter contained within your generator is compatible with the
desired tube as selected in step 1, note the part number of the dual-speed starter in your
generator. This is printed on a label near the top left side of the dual speed starter chassis. This
part number must appear in the last column of Table 2 in X-Ray Tube Stator Compatibility Tables
Supplement 746026-00.
5. Refer to figure 2-10. Set DIP switch SW1 with the binary code for the selected tube. The binary
code shown in the referenced Table 2 programs the tube type (housing and insert), for example
housing type Varian Sapphire with standard “R” stator and inserts per Table 2 requires SW1-1 to
be set ON, SW1-2 OFF, SW1-3 ON, SW1-4 OFF and SW1-5 OFF. This programs the voltages,
brake times, and boost times required.
Additionally, SW1-6 to SW1-8 may be set to give incremental increases in boost time over the
preselected values (i.e. to run an older tube with worn bearings). For example, binary 000 gives
zero increase, binary 001 gives 100 ms increase, binary 100 gives 400 ms increase, and binary
111 gives a 700 ms increase in boost time. SW1-6 represents bit 1, SW1-7 bit 2, and SW1-8
represents bit 3.
EXAMPLE:
Binary 100 = decimal 4 = 400 ms incremental boost time increase:
1 0 0
Bit 3 Bit 2 Bit 1
SW1-8 SW1-7 SW1-6
6. The DIP switch setting shown in figure 2-10 is for the example in step 5 with an incremental
increase in boost time of 200 ms.
7. Please confirm all settings using a suitable tachometer to ensure proper anode RPM
before making any exposures.
THE DIP SWITCH SHOWN IN FIGURE 2-10 IS REPRESENTATIVE OF ONE STYLE OF SWITCH ONLY. DEPENDING
ON MANUFACTURER, YOUR DIP SWITCH STYLE MAY VARY.
SGhealthcare 158
JUMONG Installation & Service manual
Dual speed starter part number 901297-15 / 901298-15 is a special configuration in which the low-speed
phase shift capacitors may be set to 15.5 uF or 28 uF. The 15.5 uF setting is intended for use in
installations where low-speed operation of CGR (GE) Statorix tubes is required. The high-speed
capacitance is automatically selected to either 3 uF or 6 uF according to the DIP switch setting.
Refer to figure 2-11. In configuration “A”, (28 uF) two leads are connected to the lower right capacitor.
Thus, the capacitor is in-circuit in this configuration. Configuration “B” (15.5 uF) has one of the leads
removed from the terminals of this capacitor, thus the capacitor is out of the circuit.
• To change from configuration “A” to “B”, disconnect the interconnecting lower lead from the lower
left capacitor in figure 2-11, and connect it to the same terminal on the lower right. This removes the
lower right capacitor from the circuit.
• To change from configuration “B” to “A” in figure 2-11, reconnect the lead between the two capacitors,
as shown. This connects the capacitor into the circuit.
After the phase shift capacitors are correctly configured, set the DIP switches as follows:
• Locate the desired tube in table 2 of supplement 746026, which follows Chapter 2. With dual speed
SGhealthcare 159
JUMONG Installation & Service manual
starter 901297-15 / 901298-15 set to configuration “A”, this starter is compatible with all tubes
requiring a 3 uF or 6 uF high-speed shift capacitor (unless indicated otherwise) and a 28, 30 or 31 uF
low-speed shift capacitor. When set to configuration “B”, it is only compatible with tubes requiring a 3
uF or 6 uF high-speed shift capacitor (unless indicated otherwise) and a 15.5 uF low-speed shift
capacitor.
• Note the DIP switch setting for the desired tube as per table 2.
• Set the DIP switches as per 2.8.2.
SGhealthcare 160
JUMONG Installation & Service manual
Before continuing, verify the DIP switch settings on the generator control board. These switches have
been factory set but may have been readjusted, particularly if this generator is a re-install.
GENERATOR CONTROL BOARD:
• Verify the settings on S3. Refer to the table below for the proper settings for this switch.
This section describes the procedure for auxiliary transformer line voltage tap selection, and for initial
power-on of the generator after it has first been installed.
PLEASE OBSERVE THE FOLLOWING POINTS REGARDING THE MAIN DISTRIBUTION
TRANSFORMER:
• IF USING A DISTRIBUTION TRANSFORMER WITH AN ISOLATED SECONDARY, THE
SECONDARY WINDING MUST BE A WYE (STAR) CONFIGURATION WITH THE CENTER
POINT GROUND-REFERENCED. DO NOT USE A DELTA-CONFIGURED SECONDARY, AS
THERE IS NO GROUND REFERENCE IN THIS CONFIGURATION.
• IF USING AN AUTOTRANSFORMER TYPE DISTRIBUTION TRANSFORMER, THE A.C.
INPUT TO THE TRANSFORMER MUST BE GROUND-REFERENCED.
For 208 / 230 V generators, the line voltage taps on the auxiliary transformer must be checked before
powering up the generator.
For 400 / 480 V generators, the auxiliary transformer line voltage tap is factory set to match the line
voltage that was specified at the time of the order. If these units are to be operated from other than the
rated line voltage (i.e. if a 400 V generator is to be operated from 480 V mains), the line voltage tap on
the auxiliary transformer must be changed as described below.
3. Note the line-voltage tap position on this transformer as determined by the location of the wire on
the 208V or the 240V tap on the transformer primary. This is normally set to the 240V tap. Refer
to figure 2-12.
4. Based on the nominal line voltage, set the transformer primary voltage tap as follows:
• Loosen the clamping screws for the current line-voltage tap, and for the required line-voltage
tap.
• Connect to the 208 V tap if the line voltage is 215 VAC or less.
SGhealthcare 161
JUMONG Installation & Service manual
• Connect to the 240 V tap if the line voltage is 216 VAC or higher.
• Retighten both of the clamping screws.
1. If the mains supply is compatible with the generator, switch on the main breaker and / or the
disconnect switch and check for the following voltages:
SGhealthcare 162
JUMONG Installation & Service manual
2. Measure and record the voltage across the main line fuses in the generator. Single-phase units
will only use one set of voltage measurements.
3. Are the line-to-line and line-to-ground voltages within specification for the unit? For single phase
230 V units, the line to ground voltage should be 99 – 127 V. For 3 phase units, the phase to
ground voltage should be 114 – 146 V for 208 / 230 V units, 230 V ± 10 % for 400 V units, and
277 V ± 10 % for 480 V units.
___ Check
4. Confirm that the auxiliary transformer line voltage taps are set to the appropriate position as per
the measured line voltage.
___ Check
5. If a 400 V unit with the optional dual-speed starter is reconfigured for 480 V, or a 480 V unit is
reconfigured for 400 V, the dual speed starter EPROM will need to be changed as described in
the section EPROM type / dual speed starter. Confirm that this has been done.
___ Check
It is recommended that the generator be tested at this point with only the X-ray tube and rotor / hightension
cables connected.
The generator should be able to complete an X-ray tube seasoning and calibration cycle without other
equipment connected to the generator (other than the basic interlocks asnoted below). This will allow for
easier fault isolation as each section of the system is connected and tested.
Before being able to make X-ray exposures, the room door interlock must be closed and the thermal switch
must be closed. The interlocks cannot be deprogrammed during tube mA auto calibration.
It is recommended that the tube(s) be conditioned (seasoned) before beginning tube auto calibration,
particularly if the tube has not been used for some time. Refer to chapter 6.
Before beginning tube auto calibration, the tube(s) used in this installation must be properly
selected, and the generator limits should be programmed. Refer to chapter 3C.
SGhealthcare 163
JUMONG Installation & Service manual
SGhealthcare 164
JUMONG Installation & Service manual
SUPPLEMENT
X-RAY TUBE STATOR COMPATIBILITY
TABLES
CONTENTS:
1.0 INTRODUCTION.................................................................................................................... 2
2.0 LOW SPEED STARTER TUBE SELECT TABLE.................................................................. 3
3.0 DUAL SPEED STARTER TUBE SELECT TABLE ................................................................ 9
The design and information contained in this document is proprietary to Communications & Power Industries
Canada Inc. (CPI), has been designed and developed at private expense, and is the exclusive property of CPI.
The information contained herein is loaned in confidence solely for the installation, operation, and
maintenance of CPI equipment. This document may not be duplicated in whole or in part, or be used for re-
engineering, reverse engineering, or otherwise reproducing in any form or creating or attempting to create or
permitting, allowing or assisting others to create or manufacture CPI’s product or products derived there from,
without the express written permission of CPI.
SGhealthcare 165
JUMONG Installation & Service manual
1.0 INTRODUCTION
This supplement contains the X-Ray Tube Stator Compatibility Tables for the Low Speed Starter and the
Dual Speed Starter.
The boost voltage may be set to either 240 VAC (factory default) or 120 VAC. This should be set to 240 VAC,
except where specifically noted in Table 1 below. The Low Speed Starter output is at the same frequency as
the AC line (50 Hz or 60 Hz).
The Low Speed Starter (LSS) is a separate sub-assembly within the Indico 100 Generator. The Low Speed
Starter part number corresponds to the value of phase-shift capacitors installed. The boost time is selectable
to either 1.5 seconds or 2.5 seconds, and the run voltage is selectable to any of 52 VAC, 73 VAC or 94 VAC.
The Low Speed Starter is integrated into the H.V. Auxiliary Board within the CMP 200 and CMP 200 DR
generators. The H.V. Auxiliary Board part number corresponds to the AC line voltage and the value of phase-
shift capacitors installed. These generators do not use a separate run voltage, instead cycling the boost voltage
on/off as required. The boost duty cycle is not hardware-configurable.
SGhealthcare 166
JUMONG Installation & Service manual
SGhealthcare 167
JUMONG Installation & Service manual
SGhealthcare 168
JUMONG Installation & Service manual
SGhealthcare 169
JUMONG Installation & Service manual
SGhealthcare 170
JUMONG Installation & Service manual
SGhealthcare 171
JUMONG Installation & Service manual
NOTE 1: Comet tube inserts with the prefix “DI” and “DX” are interchangeable.
NOTE 2: Complete Toshiba tube assemblies include the suffix “X, “FX”, “GX”, or “JX”, which are
Interchangeable with respect to rotor and anode characteristics.
NOTE 3: These X-ray tubes incorporate a control grid. Grid control is currently not supported by CPI
generators.
Connect the grid connection to Ground when using these tubes, and select the insert type
within the Generator software corresponding to the equivalent non-grid tube.
SGhealthcare 172
JUMONG Installation & Service manual
SGhealthcare 173
JUMONG Installation & Service manual
SGhealthcare 174
JUMONG Installation & Service manual
SGhealthcare 175
JUMONG Installation & Service manual
SGhealthcare 176
JUMONG Installation & Service manual
SGhealthcare 177
JUMONG Installation & Service manual
SGhealthcare 178
JUMONG Installation & Service manual
SGhealthcare 179
JUMONG Installation & Service manual
SGhealthcare 180
JUMONG Installation & Service manual
SGhealthcare 181
JUMONG Installation & Service manual
SGhealthcare 182
JUMONG Installation & Service manual
SGhealthcare 183
JUMONG Installation & Service manual
SGhealthcare 184
JUMONG Installation & Service manual
SGhealthcare 185
JUMONG Installation & Service manual
SGhealthcare 186
JUMONG Installation & Service manual
SGhealthcare 187
JUMONG Installation & Service manual
SGhealthcare 188
JUMONG Installation & Service manual
SGhealthcare 189
JUMONG Installation & Service manual
** Dual Speed Starter part numbers 733317-XX (Indico 100) and 901297-XX (CMP 200 DR) are used in
400 VAC 3φ generators / power supplies and in 480 VAC 3φ generators / power supplies with a line
adjusting transformer.
Dual Speed Starter part numbers 735925-XX (Indico 100) and 901298-XX (CMP 200 DR) are used in
230 VAC 1φ generators / power supplies and in 480 VAC 3φ direct input generators / power
supplies (using no line adjusting transformer).
Where more than one Dual Speed Starter part number is referenced for a particular tube type, any
of these (applicable to the generator and input voltage) is acceptable. For 2-tube systems using
different tube types, both tube types must be considered.
NOTE 1: Tube types designated as low speed only or high speed only must be programmed for low
speed only or high speed only operation. Refer to the section Tube Selection within Chapter
3 of the applicable generator service manual for details. For some tubes listed as high speed
only, the starter may be capable of low speed operation but the Manufacturer’s data sheet
for the Insert lists high speed only. In other cases, the limitation is due to operational
limitations of the Dual Speed Starter itself.
NOTE 2: Dual Speed Starters 733317-01 / 735925-01 (Indico 100 only) provide 6 μF of high speed and
31 μF of low speed shift capacitance. Dual Speed Starters 733317-13 / 735925-13 may be
used in place of Dual Speed Starter “-13” in all cases and are preferred.
Dual Speed Starters 733317-12 / 735925-12 (Indico 100) and 901297-12 / 901298-12 (CMP
200 DR) are universal configurations, providing either 6 μF or 7.5 μF of high speed and
either 36 μF or 37.5 μF of low speed shift capacitance. Capacitor selection is made
automatically by relays located on the Dual Speed Starter.
Dual Speed Starters 733317-13 / 735925-13 (Indico 100) and 901297-13 / 901298-13 (CMP
200 DR) are universal configurations, providing either 5 μF or 6 μF of high speed and 30 Μf
of low speed shift capacitance. Capacitor selection is made automatically by relays located
on the Dual Speed Starter.
Dual Speed Starters 733317-16 / 735925-16 (Indico 100) and 901297-16 / 901298-16 (CMP
200 DR) are special configurations, providing either 6 μF or 12.5 μF of high speed and either
31.5 μF or 37.5 μF of low speed shift capacitance. Capacitor selection is made
automatically by relays located on the Dual Speed Starter. These starters are intended
for used in place of Dual Speed Starter “-13” in two-tube systems that include both a
standard “R” stator (requiring 6 μF of high speed capacitance) and a tube requiring
12.5μF of high speed shift capacitance (Philips ROT 350//500).
Dual Speed Starters 733317-17 / 735925-17 (Indico 100 only) are special configurations,
providing either 5 μF or 12.5 μF of high speed and either 30μF or 37.5 μF of low speed
shift capacitance. Capacitor selection is made automatically by relays located on the
Dual Speed Starter. These starters may be used in place of Dual Speed Starter
configuration -13 in two-tube systems that include both a tube requiring 5μF of high
speed shift capacitance (typically IAE tubes) and a tube requiring 12.5μF of high speed
shift capacitance (Philips ROT350/500).
Do not use these starters with Siemens tubes due to high-speed shift capacitor
voltage limitations.
NOTE 3: Comet tube inserts with the prefix “DI” and “DX” are interchangeable.
NOTE 4: Philips ROT housing with the windings connected in series (high impedance
configuration).
NOTE 5: Philips ROT housing with the windings connected in parallel (low impedance
configuration).
NOTE 6: Dunlee tube inserts with the prefix “DU” and Philips tube inserts with the prefix “RO”
are interchangeable. Select the corresponding Philips insert type within the Generator
software when using Dunlee tubes.
SGhealthcare 190
JUMONG Installation & Service manual
NOTE 7: Complete Toshiba x-ray tube assemblies include the suffix “X, “FX”, “GX”, or “JX”, which
are interchangeable with respect to rotor and anode characteristics.
NOTE 8: These X-ray tubes incorporate a control grid. Grid control is currently not supported by
CPI generators. Connect the grid connection to Ground when using these tubes, and
select the insert type within the Generator software corresponding to the equivalent
non-grid tube.
NOTE 9: Dual Speed Starters 733317-15 / 735925-15 (Indico 100) and 901297-15 / 901298-15
(CMP 200 DR) have jumper selectable phase shift capacitance that allows selection of
15.5 μF or 28 μF low speed shift capacitors for operation with CGR (GE) Statorix or
Toshiba E7252 (XS-R/RA stator) tubes, respectively, as per table 2.
By default, this starter is factory set to the 28 μF position. Confirm proper
Configuration per the section “configuring dual speed starter 733317-15 / 735925-15”
in chapter 2 before proceeding.
These starters also support standard “R” stators that require 6 μF of high speed shift
capacitance.
(Indico 100 only): If configured for 28 μF of low speed capacitance, these Dual Speed
Starters also support tubes listed in Table 2 as requiring Dual Speed Starters 733317-
13 / 735925-13 and requiring 6 μF of high speed capacitance. For two-tube
operation, this configuration will support: a) these tubes and the Toshiba E7252/XS-
RA (high and low speed) simultaneously, or, b) these tubes and a CGR Statorix tube
(high-speed only) simultaneously. The Toshiba and CGR tubes can be supported
simultaneously if one or both of these tubes are operated in high-speed mode only.
(CMP 200 DR only): If configured for 28 μF low speed capacitance, these Dual Speed
Starters also support tubes listed in Table 2 as requiring Dual Speed Starters 901297-
13 / 901298-13 and requiring 6 μF of high speed capacitance.
SGhealthcare 191
JUMONG Installation & Service manual
Tube operating parameters for each tube type are selected by setting switches to the applicable Code, as
indicated in Table 2. For reference, operating parameters applicable to each Code are contained in Table 3
below.
SGhealthcare 192
JUMONG Installation & Service manual
NOTE 1: Tube Type codes should only be used with the applicable DSS types specified in this table.
Refer to Table 2 for DSS Part Numbers applicable to each Tube Type (Housing and Insert).
SGhealthcare 193
JUMONG Installation & Service manual
CHAPTER 3
INTERFACING, PROGRAMMING, AND
CALIBRATION
3.0.0 INTRODUCTION
3.1.0 Purpose
This chapter describes the interfacing of the CMP 200® and CMP 200® DR X-ray generators to Bucky’s,
interlocks, collimator lamp, etc, and to the AEC chambers (if the AEC option is fitted).
Generator programming and AEC calibration is also covered in this chapter.
SGhealthcare 194
JUMONG Installation & Service manual
3C.1.0 INTRODUCTION
This chapter describes the interfacing of the CMP 200® and CMP 200® DR X-ray generators to Bucky(s),
interlocks, room lights, a DR imaging system (if applicable), DAP, collimator lamp and tube stand locks, and
also describes the generator programming.
3C.2.1 Inputs
The Bucky inputs, interlock 1 and interlock 2 / tomo inputs, and room door interlock inputs are opto coupled.
This means that a relay contact, transistor, or other low-impedance switching device (≤ 100 Ω, 10 mA current
rating) must be connected across each of these inputs. Table 3C-1 defines the pin outs, polarity at the
terminals and the logic condition required for that input. If using a directional switching device, such as a
transistor, the polarity of the voltage seen by the switching device must be observed. This is shown in the table
below.
Refer also to figure 3C-1. This is a pictorial drawing of the J2, J4, and J11 inputs and outputs on the H.V.
auxiliary board.
Refer to 3C.2.4 for details on AEC connections.
SGhealthcare 195
JUMONG Installation & Service manual
* These inputs are meant for dry contacts only. Do not apply any voltage source to these inputs.
3C.2.2 Outputs
Table 3C-2 shows the Bucky and auxiliary power outputs from the generator. Refer also to figure 3C-1.
NOTE: The generator is factory configured to supply 110 VAC to drive the Buckys. The Bucky outputs
may be reconfigured to supply 24 VDC or 220 VAC if required, as described in chapter 8. Please
confirm compatibility with the Buckys used in this installation before proceeding. For tomo
operation, the applicable Bucky outputs must be programmed as necessary.
SGhealthcare 196
JUMONG Installation & Service manual
The BUCKY 1 START and TOMO / BUCKY 2 START relays K1 and K3 on the H.V. auxiliary board have
provisions for R-C snubber circuits to be connected across these relays. For older Buckys that typically
have relay inputs, the R-C snubber circuits usually need to be connected. These snubbers attenuate the
dV/dT transients that are generated when the corresponding relay in the Bucky opens.
For newer Buckys with opto-coupler inputs, the R-C snubber circuits across relays K1 and K3 on the
H.V.auxiliary board should remain disconnected, as the leakage current through the R-C snubber can be
sufficient to energize the opto-couplers in the Bucky(s) when the corresponding relays on the H.V
auxiliary board are open.
FOR OLDER BUCKYS WITH RELAY INPUTS:
• Refer to the table below and to MD-0930 in chapter 9. The required resistors (R2, R15) must be
installed to complete the R-C snubber circuit.
FOR NEWER BUCKYS WITH OPTO-COUPLER INPUTS:
• No action required. Resistors R2 and R15 are NOT factory installed, therefore the R-C snubber is
open-circuit. It is the responsibility of the installer to provide the proper interfacing circuits to the
opto coupler(s) in these types of installations.
The resistors that must be installed to complete the R-C snubber circuits across K1 and K3 on the H.V.
auxiliary board are shown below. Kits with these resistors are available from CPI Product Support. The kit part
number is 90301600.
SGhealthcare 197
JUMONG Installation & Service manual
Figure 3C-1: J2, J4, and J11 inputs and outputs (H.V. auxiliary board)
SGhealthcare 198
JUMONG Installation & Service manual
Refer to chapter 3D for an overview of AEC theory, for AEC chamber connections, and for the AEC calibration
procedure.
CMP 200® DR X-ray generators are factory-configured to interface with one or more DR imaging systems.
Refer to the compatibility statement in chapter 1 to determine which DR imaging system(s) this model of
generator is compatible with. The DR imaging system is connected to 37-pin “D” connector J25 on the
generator control board. The corresponding digital imaging supplement will be included in the front of this
manual. Refer to that supplement for the installation and setup procedure of the DR imaging system.
If you are using a membrane console, the generator may be programmed and calibrated via the control
console or via GenWare® MP (PC). When using the console for programming and calibration, all
programming / calibration menus are displayed on the LCD display window on the console. The “soft key”
buttons on the console are used to navigate through the programming screens and to select and enter values
in this section.
When using the touchscreen console, the generator must be programmed and calibrated via
GenWare® MP (touchscreen). This requires the GenWare® utility software, which can be accessed via
the GenWare® button in the System Utilities menu. Alternately, GenWare® MP (PC) may be used to
program the generator if desired.
SGhealthcare 199
JUMONG Installation & Service manual
To enter into the programming mode if using the membrane console, follow the steps below.
Use these steps to access the GENERATOR SETUP menu (membrane console).
SGhealthcare 200
JUMONG Installation & Service manual
Overview of the functions available within each of the options in the GENERATOR SETUP menu.
SGhealthcare 201
JUMONG Installation & Service manual
The UTILITY menu presents the user with the options shown below.
SGhealthcare 202
JUMONG Installation & Service manual
This utility allows display of the error messages stored in the generator’s error log. The error log storage limit is
200 messages at which point the generator will replace the oldest with the most recent.
The ERROR LOG menu for the membrane console is shown below.
SGhealthcare 203
JUMONG Installation & Service manual
3C.5.3 Statistics
This utility shows the tube exposure count and the accumulated generator exposure count. This also allows
resetting of the tube 1 exposure counter.
SGhealthcare 204
JUMONG Installation & Service manual
SGhealthcare 205
JUMONG Installation & Service manual
3C.5.4 Console
The CONSOLE CONFIG menus allow setting of specific console operating features to suit operator
preferences, and also allow resetting of the console parameters to the factory defaults.
SGhealthcare 206
JUMONG Installation & Service manual
Since the CONSOLE CONFIG setup affects the console only (setting of specific console operating features to
suit operator preferences), no equivalent function is available in GenWare®.
SGhealthcare 207
JUMONG Installation & Service manual
SGhealthcare 208
JUMONG Installation & Service manual
The APR EDITOR enables / disables the ability of the operator to make and then save changes to APR
techniques.
No equivalent function exists in GenWare®, as the APR EDITOR affects the console operation only.
SGhealthcare 209
JUMONG Installation & Service manual
The GEN CONFIGURATION menu presents the user with the selections shown below. These are described in
detail in this section.
The TUBE SELECTION function allows the desired tube type to be selected, and allows setting of the default
limits for that tube.
The first screen of the TUBE SELECTION menus for the membrane console is shown below. This is followed by
additional tube selection menus, with additional tube types. The number of tube selection menus, and the
actual tube selections, may not be exactly as shown.
SGhealthcare 210
JUMONG Installation & Service manual
The following menu is only available if additional tubes have been downloaded via a computer running
GenWare®.
The next three menus show the default tube limits. These menus appear after a
tube has been selected in the previous steps.
SGhealthcare 211
JUMONG Installation & Service manual
SGhealthcare 212
JUMONG Installation & Service manual
SGhealthcare 213
JUMONG Installation & Service manual
SGhealthcare 214
JUMONG Installation & Service manual
* The stated maximum kW limits apply at the 100 ms point on the X-ray tube load ratings curve.
Increasing or decreasing the kW limits will shift the entire curve up or down proportionately to the
percentage kW change.
Use these steps to select the desired tube type.
SGhealthcare 215
JUMONG Installation & Service manual
When the desired tube is selected, the default limits are displayed (membrane console). Please consult the
Xray tube data sheet(s) before making any changes.
The dual speed starter operates at 60 or 180 Hz (50 or 150 Hz for some tube types) independent of line
frequency.
The low speed starter operates at 50 Hz for 50 Hz mains, or 60 Hz for 60 Hz mains. The generator samples the
line frequency via a zero-crossing detector on the generator interface board. Therefore, for
units fitted with a low speed starter, the generator automatically derates the 60 Hz tube ratings for 50 Hz
operation if required.
PLEASE DO NOT CHANGE ANY DEFAULTS UNLESS THE IMPACT OF THOSE CHANGES IS CLEARLY
UNDERSTOOD. INITIAL CALIBRATION SHOULD BE PERFORMED USING THE DEFAULT VALUES.
Use these steps to set the tube limits and the associated parameters. Refer to the definitions in the previous
table.
SGhealthcare 216
JUMONG Installation & Service manual
Typically, the boost time should be between 200 and 250 msec, and the preheat time should be in the range of
700 - 800 ms.
If in doubt, monitor the filament feedback and be sure that there is no change in the signal level 5 ms. after
the start of an exposure, and that the mA starts at the selected level.
Standby current must be below the emission point.
If the maximum filament current is increased, be careful not to exceed the tube manufacturer’s
specifications.
SGhealthcare 217
JUMONG Installation & Service manual
SGhealthcare 218
JUMONG Installation & Service manual
The GENERATOR LIMITS function allows setting of the generator output limits defined below.
The GENERATOR LIMITS menu for the membrane console is shown below.
SGhealthcare 219
JUMONG Installation & Service manual
BEFORE MAKING ANY CHANGES IN THIS SECTION, CONSULT THE X-RAY TUBE DATA SHEETS TO
ENSURE THAT THE PROPOSED CHANGES DO NOT EXCEED THE MANUFACTURERS RECOMMENDED LIMITS.
THE ORIGINAL GENERATOR LIMITS SHOULD BE RECORDED IN A COPY OF TABLE 3C-3 BEFORE CONTINUING.
Use these steps to set the generator limits. Refer to the definitions in the previous table.
SGhealthcare 220
JUMONG Installation & Service manual
MENU 1
MENU 2
MENU 3
SGhealthcare 221
JUMONG Installation & Service manual
MENU 4
MENU 5
SGhealthcare 222
JUMONG Installation & Service manual
SGhealthcare 223
JUMONG Installation & Service manual
SGhealthcare 224
JUMONG Installation & Service manual
SGhealthcare 225
JUMONG Installation & Service manual
If the image receptor defaults are changed, please record the original defaults in a copy of the
following table:
SGhealthcare 226
JUMONG Installation & Service manual
SGhealthcare 227
JUMONG Installation & Service manual
Use these steps to set up the receptor parameters. Refer to the definitions in the previous table.
SGhealthcare 228
JUMONG Installation & Service manual
SGhealthcare 229
JUMONG Installation & Service manual
The I/O CONFIGURATION function allows programming the states of the exposure for the inputs and the
outputs on the room interface board.
The I/O CONFIGURATION menus for the membrane console are shown below.
SGhealthcare 230
JUMONG Installation & Service manual
SGhealthcare 231
JUMONG Installation & Service manual
The inputs and outputs defined in the previous table are programmable as follows:
• Inputs may be programmed such that the selected input is active or inactive during various states of
thegenerator. Inactive inputs are ignored; unused inputs should normally be programmed to be
inactive.
• Outputs may be programmed such that the relay connected to the selected output is energized or
Deenergized during various states of the generator. Unused outputs should normally be programmed
to be de-energized.
• The inputs and outputs must be programmed separately for each receptor. Each receptor may have its
own unique programming.
MEMBRANE CONSOLE
The STATE button on the upper right hand side of the menu selects the current state. The word STATE is
preceded by the description of the state: for example, STANDBY.
The arrow in the lower middle area points to the current level for the selected state. Moving to the next
state is accomplished by pressing the STATE button. The states are as follows.
• STANDBY Sets the state of the I/O when the generator is in standby or idle mode.
• PREP Sets the state of the I/O when the generator enters PREP mode.
• GEN RDY Sets the state of the I/O when the generator has completed PREP mode and is
Ready to expose.
• RAD EXP Sets the state of the I/O when the generator starts a radiographic exposure
of the selected state is changed by pressing the selection button again (low = off / inactive, high = on / active).
For inputs, setting the level “low” means that the input is ignored during that state. Setting the level
“high” requires that the corresponding input is satisfied before the generator will advance to that state. For
example, if the door interlock (DOOR ITLK) is set to logic “low” for all states, then an X-ray exposure may be
made without a door interlock closure.
Setting an output level “low” causes the relay associated with that output to be de-energized during
SGhealthcare 232
JUMONG Installation & Service manual
the selected state. Setting the level “high” will cause the associated relay to be energized during the selected
state. For example, the Bucky 1 “start” output will be disabled if BKY 1 START is set to “low” for all states.
GenWare®
On the Inputs and Outputs tabs, the generator states are shown above the vertical grey / white bars. For
inputs, grey indicates states where the input cannot be programmed. Only states that are shown in white can
be changed. Outputs are programmable for each of the four generator states.
The logic level of the selected state is changed by clicking in the desired state column, to the right of the
selected input or output (unchecked = off / inactive, checked = on / active).
For inputs, an unchecked state means that the input is ignored during that state. A checked state (marked with
an X) requires that the corresponding input be satisfied before the generator will advance to that state.
For outputs, an unchecked state causes the relay associated with that output to be de-energized
during the selected state. A checked state (marked with an X) will cause the associated relay to be energized
during the selected state.
Use these steps for programming the I/O functions. Refer to the definitions in the previous table.
SGhealthcare 233
JUMONG Installation & Service manual
The input and output programming should be recorded in a copy of the table below. This will provide a record
of the I/O configuration for future reference.
SGhealthcare 234
JUMONG Installation & Service manual
The AEC SETUP menus allow programming of AEC parameters for each AEC channel.
The AEC SETUP menus for the membrane console are shown below.
MENU 1
Figure 3C-17: AEC Setup & Calibration window, AEC Setup tab
• The AEC Channel display in the top right corner of the AEC Setup & Calibration window
Shows the selected AEC channel.
• The Progr. Receptors display below the AEC channel display shows which receptors are
programmed for the selected AEC channel.
SGhealthcare 235
JUMONG Installation & Service manual
Definitions of AEC SETUP menu items applicable to the initial AEC setup.
Use these steps to perform the initial AEC setup. Refer to the definitions in the previous table.
SGhealthcare 236
JUMONG Installation & Service manual
SGhealthcare 237
JUMONG Installation & Service manual
Before beginning tube auto calibration, the tube used in this installation must be properly selected, and the
generator limits should be programmed, as described earlier in this chapter.
It is recommended that the tube be conditioned (seasoned) during tube auto calibration, particularly if
the tube has not been used for some time. Refer to chapter 6.
SGhealthcare 238
JUMONG Installation & Service manual
1. Connect the DAP printer to the DATA LINK connector J4 on the rear of the console. Refer to the
Figure “Rear of control console” in chapter 2 of the CMP 200® service manual for the connector
location.
2. Follow the procedure in 3C.10.2 to set up and test the DAP printer.
The CMP 200® series generator, when equipped with the DAP option, is compatible with the DAP devices listed
in section 3C.10.2. The correct DAP device must be selected in the DAP SETUP menu as described in 3C.10.2 in
order to ensure device compatibility.
The DAP chamber, when fitted with the proper interconnect cable, plugs directly into the generator control
board in the generator. When ordering the DAP chamber from the DAP manufacturer, specify the CPI
compatible interconnect cable, if available. This is a special cable terminated with a 9-pin male “D” connector
that is designed to plug directly into the generator control board. If this cable is not available from the DAP
device manufacturer, consult CPI product support for the required cable to connect the DAP chamber to the
generator. Refer to the table below for the CPI cable assembly part numbers.
SGhealthcare 239
JUMONG Installation & Service manual
1. Switch OFF the AC line voltage to the generator at the main disconnect switch. Allow sufficient time
for all capacitors in the generator to discharge.
2. Install the DAP chamber as per the manufacturers instructions. The interconnect cable to the
generator must be as per 3C.9.1.
3. Route the DAP interconnect cable through one of the access slots at the upper rear of the generator,
and then route the cables toward the generator control board. Secure the cable to the lip on the
inside of the cable access slot using tie wraps or equivalent fasteners.
4. Plug the DAP cable into J4 on the generator control board. Tighten the screw locks on the
Connectors to secure the cables.
5. Set JW14 (near J4) on the generator control board as per the following table
6. Proceed with DAP setup and calibration as per the remainder of this procedure.
The DAP SETUP menus allow setup and calibration of the DAP device.
The DAP SETUP menus for the membrane console are shown below.
SGhealthcare 240
JUMONG Installation & Service manual
SGhealthcare 241
JUMONG Installation & Service manual
Use these steps to set up the DAP device. DAP calibration is done after DAP setup
SGhealthcare 242
JUMONG Installation & Service manual
SGhealthcare 243
JUMONG Installation & Service manual
The DAP device must be calibrated before use, and the calibration must be periodically checked as per the DAP
device manufacturers requirements, or as per local regulations.
The first step involved in calibrating the DAP meter in the generator is to carefully make a dose measurement
at a given distance from the X-ray source. The next step is to expose a test film at the same distance from the
X-ray source as the dose measurement that was just made.
The dose-area product is calculated by multiplying the measured dose, in mGy, by the exposed area
of the film, in cm2. This gives the actual dose-area product, in mGycm2.
After the reference dose-area product is determined as described above, it is compared to the DAP
reading as measured by the generator. Adjustments are made to the CAL. VALUE 1 parameter in the DAP
SETUP menu such that the consoles DAP display corresponds to the calculated dose-area product. This
procedure may need to be repeated several times until the required accuracy is obtained.
The reason the DAP device (a specialized ion chamber) is able to accurately measure the dose-area
product at its location at the bottom of the collimator is that although the radiation level falls off at a rate
inversely proportional to the square of the distance from the source, the irradiated area increases as the
square of the distance from the source. For example, by doubling the distance, the dose falls to (½ )2 = ¼ of the
previous dose BUT the area increases to 22 = 4 times the area. Therefore, the dose-area product will remain
constant at a given distance from the source. This is also the reason that care must be taken to ensure that the
area measurement is done at the same distance from the X-ray source as the dose measurement.
SGhealthcare 244
JUMONG Installation & Service manual
SGhealthcare 245
JUMONG Installation & Service manual
SGhealthcare 246
JUMONG Installation & Service manual
SGhealthcare 247
JUMONG Installation & Service manual
SGhealthcare 248
JUMONG Installation & Service manual
SGhealthcare 249
JUMONG Installation & Service manual
This is used with the CPI GenWare® MP (PC) utility software. This allows for data communication with a
computer in order to download additional tube types, transfer APR data, edit APR text, perform setup and
calibration functions, and for other minor functions. Further documentation is included with GenWare®
MP(PC).
A computer (i.e. a laptop) and a 9-pin null-modem cable with socket connectors (female) on both ends are
required to connect the computer to the generator in order to run GenWare®.
• Connect the null-modem cable from a serial port on the computer with GenWare® to the DATA
LINK connector on the rear of the control console. Refer to the figure “Rear of control console” in
chapter 2 for the location of this connector.
• From the GENERATOR SETUP menu select DATA LINK, and then select CONNECT TO GENWARE. A
DATA LINK submenu will open, indicating WAITING FOR DATA... PLEASE DO NOT TURN OFF
POWER.
• Switch on the computer and start GenWare®.
• GenWare® is ready for use when communication is established with the generator.
If the data link connector is not available, i.e. on units without a CPI supplied console, J21 on the generator
control board may be used.
This is used with the CPI GenWare® MP (PC) utility software. This allows the generator configuration (ie.
receptor setup, AEC setup and calibration, etc) to be stored on a PC hard drive or other external memory
device (ie. USB flash drive).
SGhealthcare 250
JUMONG Installation & Service manual
This is used with the CPI GenWare® MP utility software. This allows for additional features to be activated in
the generator software.
SGhealthcare 251
JUMONG Installation & Service manual
This is used with the CPI GenWare® MP (PC) utility software. This allows for the display to be toggled
between monochrome and full color.
SGhealthcare 252
JUMONG Installation & Service manual
SGhealthcare 253
JUMONG Installation & Service manual
SGhealthcare 254
JUMONG Installation & Service manual
It is strongly suggested that you review the section ANATOMICAL PROGRAMMING SELECTOR in the
operator’s manual before proceeding. A good understanding of the terminology and APR menu
structures is needed to make APR changes.
SGhealthcare 255
JUMONG Installation & Service manual
SGhealthcare 256
JUMONG Installation & Service manual
SGhealthcare 257
JUMONG Installation & Service manual
SGhealthcare 258
JUMONG Installation & Service manual
SGhealthcare 259
JUMONG Installation & Service manual
SGhealthcare 260
JUMONG Installation & Service manual
SGhealthcare 261
JUMONG Installation & Service manual
The current image receptor symbols may be replaced with predefined symbols chosen from the receptor
symbols library or downloaded from an external device.
Each image receptor button will always select a predefined image receptor (i.e. table Bucky, wall
Bucky, DR, etc.). Before changing the image receptor symbols, it must be clearly understood which image
receptors are selected by each image receptor button. Each image receptor button should then have a logical
and intuitive symbol assigned to that position.
SGhealthcare 262
JUMONG Installation & Service manual
SGhealthcare 263
JUMONG Installation & Service manual
The touchscreen setup menu accesses submenus that allow the service engineer to perform the following
functions:
• Enable or disable certain console functions (audible generator ready indication).
• Enable or disable optional digital features.
• Set up serial communication ports COM 1 and COM 2 on the touchscreen console.
• Select the language for operator and error messages and graphics (i.e. on buttons, etc).
• Select the generator type.
• Select the screen saver interval.
• Select the general and exposure volumes.
• Select the LCD brightness
• Change the operator and service password.
• Set the customer code.
• The System Code is a unique code assigned to each touchscreen on which the software is installed.
• The License is a code specifically assigned to each touchscreen. This enables options in the
features tab.
Please consult the factory to obtain a new license code if it is desired to enable new features, or to
Reinstall the existing license should the license code be accidentally overwritten.
• The Customer Code is a unique code assigned to each customer and selects the color scheme and
graphic style (skin) to be displayed on the touchscreen console.
Settings
The functions near the left side of the settings window are enabled when checked (√).
SGhealthcare 264
JUMONG Installation & Service manual
Features
Use these steps to select the digital functions.
SGhealthcare 265
JUMONG Installation & Service manual
Passwords
Use these steps to change the current operator and service passwords.
SGhealthcare 266
JUMONG Installation & Service manual
SGhealthcare 267
JUMONG Installation & Service manual
The touchscreen calibration function should be performed if touching the center of a buttons does not activate
that function, i.e. if the touch-sensitive area appears displaced from the center of the corresponding icon.
This is used with the CPI GenWare® MP (PC) utility software. This allows for data communication with a
computer in order to download additional tube types, transfer APR data, edit APR text, perform setup and
calibration functions, upgrade generator software and for other minor functions. Further documentation is
included with PC GenWare®.
A computer (i.e. laptop) and a 9 pin null modem cable with socket connectors (female) on both ends
are required to run this software and interface to the generator.
SGhealthcare 268
JUMONG Installation & Service manual
Use these steps to access the Configuration Backup and Restore function. This function backs up and
restores the image receptor symbol assignment (Receptor Symbols) and the auto-positioner symbol
assignment (Auto Position Symbols) if applicable.
SGhealthcare 269
JUMONG Installation & Service manual
SGhealthcare 270
JUMONG Installation & Service manual
This feature allows you to upgrade or restore from backup the firmware in your touchscreen console. A USB
flash drive or computer containing the upgrade / original files and a USB cable are required to perform this
upgrade.
SGhealthcare 271
JUMONG Installation & Service manual
SGhealthcare 272
JUMONG Installation & Service manual
SGhealthcare 273
JUMONG Installation & Service manual
SGhealthcare 274
JUMONG Installation & Service manual
Figure 3C-42: CPI Touch Screen Updater - Select Communication Media screen
SGhealthcare 275
JUMONG Installation & Service manual
Figure 3C-43: CPI Touch Screen Updater (after Upgrade Media is selected)
SGhealthcare 276
JUMONG Installation & Service manual
SGhealthcare 277
JUMONG Installation & Service manual
SGhealthcare 278
JUMONG Installation & Service manual
SGhealthcare 279
JUMONG Installation & Service manual
SGhealthcare 280
JUMONG Installation & Service manual
CHAPTER 3D
AEC CALIBRATION
3D.1.0 INTRODUCTION
This chapter describes interfacing and setup / calibration of the various AEC board assemblies that are used in
CMP200® and CMP200® DR X-ray generators.
A SET OF AEC COMPATIBILITY MATRIXES IS LOCATED AT THE FRONT OF THIS MANUAL. EACH
AEC BOARD HAS A CORRESPONDING AEC COMPATIBILITY MATRIX, I.E. FOR AEC BOARD 734614-
XX, USE AEC COMPATIBILITY MATRIX SUP73461400.
THE AEC COMPATIBILITY MATRIXES LIST THE AEC CHAMBERS / PREAMPLIFIERS THAT
EACH VERSION OF AEC BOARD IS COMPATIBLE WITH, AND THEY ALSO SHOW THE I/O PIN
CONNECTIONS AND THEIR FUNCTIONS, AS WELL AS RELATED NOTES.
This chapter contains background information that is relevant to AEC operation. This is located at the back of
this chapter, and should be understood before beginning AEC calibration.
1. Note the part number that is printed on the AEC board in the generator.
2. Connect the AEC device to the AEC board as per 3D.2.1 to 3D.2.4. Supplementary information is
In the AEC compatibility matrixes.
SGhealthcare 281
JUMONG Installation & Service manual
The AEC board shown below is compatible with various makes / models of solid-state chambers as per AEC
compatibility matrix SUP73799200.
This board will be fitted with 6 pin circular connectors (J1 to J4) or with 7 pin in-line connectors (J11
to J14), depending on the application.
AEC board input assignment (examples only, actual receptor assignments may vary):
• Ch 1 = J1 / J11 - Table Radiographic Bucky.
• Ch 2 = J2 / J12 - Vertical Wall Bucky.
• Ch 3 = J3 / J13 - Spot Film Device.
• Ch 4 = J4 / J14 - Aux. (Extra Bucky, Digital Acquisition, etc).
The following potentiometers are used for AEC gain adjustment:
• R1 is used for channel 1 gain adjustment.
• R2 is used for channel 2 gain adjustment.
• R3 is used for channel 3 gain adjustment.
• R4 is used for channel 4 gain adjustment.
SGhealthcare 282
JUMONG Installation & Service manual
Tables 3D-1 and 3D-2 show the pin outs for both the 6 pin circular connectors and for the 7 pin in-line
connectors on the AEC board in figure 3D-1.
Table 3D-2: Pin outs for 7 pin in-line connector J11 to J14
NOTE:
Jumpers JW1 to JW8 swap the left and right fields from J1 to J4 and J11 to J14 as per the table below.
SGhealthcare 283
JUMONG Installation & Service manual
The AEC board shown below is compatible with various makes / models of ion chambers as per AEC
compatibility matrix SUP73461400.
This board will be fitted with 9 pin D connectors (J11 to J14), or with 12 pin in-line connectors (J1 to
J4), depending on the application.
AEC board input assignment (examples only, actual receptor assignments may vary):
• Ch 1 = J1 / J11 - Table Radiographic Bucky.
• Ch 2 = J2 / J12 - Vertical Wall Bucky.
• Ch 3 = J3 / J13 - Spot Film Device.
• Ch 4 = J4 / J14 - Aux. (Extra Bucky, Digital Acquisition, etc).
The following potentiometers are used for AEC gain adjustment:
• R1 is used for channel 1 gain adjustment.
• R2 is used for channel 2 gain adjustment.
• R3 is used for channel 3 gain adjustment.
• R4 is used for channel 4 gain adjustment.
The following potentiometers are used for short AEC exposure time compensation:
• R11 is used for channel 1 short exposure time compensation.
• R12 is used for channel 2 short exposure time compensation.
• R13 is used for channel 3 short exposure time compensation.
• R14 is used for channel 4 short exposure time compensation.
R79 adjusts the output of the high voltage bias supply. This is only fitted on versions of this board intended for
use with ion chambers that require a separate high voltage bias supply. R79 adjusts the value of the +300 /
+500 VDC, and the +45 VDC outputs, and should be set as per the ion chamber manufacturer specifications.
Tables 3D-3 and 3D-4 show the pin outs for both the 9 pin D connectors and for the 12 pin in-line
SGhealthcare 284
JUMONG Installation & Service manual
connectors on the AEC board in figure 3D-2. The 9 pin connectors are compatible with most models of AID
ionization chambers. However, the installer should verify compatibility of the pin outs with the chamber(s)
being used.
Table 3D-4: Pin outs for 12 pin in-line connector (J1 to J4)
SGhealthcare 285
JUMONG Installation & Service manual
The AEC board shown below is compatible with various models of ion chambers as per AEC compatibility
matrix SUP73799800.
This board is fitted with 9 pin D connectors J1 to J4.
Table 3D-5 shows the pin outs for the 9 pin D connectors on the AEC board in figure 3D-3. The 9 pin
connectors are compatible with most models of AID ionization chambers. However, the installer should
verify compatibility of the pin outs with the chamber(s) being used.
SGhealthcare 286
JUMONG Installation & Service manual
SGhealthcare 287
JUMONG Installation & Service manual
The AEC board shown below is designed for use with various three-of-five-field ion chambers as per AEC
compatibility matrix SUP73938900.
This board is fitted with 15 pin D connectors J1 and J2.
SGhealthcare 288
JUMONG Installation & Service manual
Table 3D-6 shows the pin outs for the 15 pin D connectors on the AEC board in figure 3D-4. The 15 pin
connectors are compatible with some models of three-of-five-field AID ion chambers.
Table 3D-6: Pin outs for 15 pin D connector (J1 and J2)
NOTE:
Jumpers JW5 to JW8 swap the left and right fields on J1 and J2 as per the table below.
SGhealthcare 289
JUMONG Installation & Service manual
• When using a photo diode for AEC, there is normally no need to iterate all the kV breakpoints
During AEC calibration. It will usually suffice to use the 75 kV breakpoint calibration value at all kV
breakpoints. If doing this, the calibration values should be confirmed at all kV breakpoints using the
acquired digital images.
• For DR applications, the AEC calibration procedure uses the same potentiometers and menus as
described for film in the following sections. However, the imaging system manufacturers literature
should be consulted to determine the required dose / image brightness.
• The generator must be known to be calibrated before beginning AEC calibration.
• All components (X-ray tubes, collimators, AEC chambers, etc) used during AEC calibration must be
those that will be used during procedures, and must be positioned as they will be in actual use of
the X-ray room.
• During AEC calibration, always ensure that the central ray is centered relative to the image receptor.
• Before placing the absorbers, ensure that the collimator is opened sufficiently to irradiate ALL fields
on the AEC pickup device.
• Ensure that the absorber is positioned to fully cover the X-ray field. The absorber must extend a
minimum of 3/8 in. (10 mm) beyond the X-ray field.
• During AEC calibration, all AEC exposures should be done using mA values such that the
exposures are in the 30 to 100 ms range UNLESS STATED OTHERWISE.
• The recommended absorber is water. This should be in a plastic container of uniform thickness.
Lexan of a similar thickness is also a suitable absorber.
• Care must be exercised when using table Buckys with low kV values because most tabletops and
grids absorb considerable radiation in the 60 – 65 kV range. This will adversely affect AEC
operation.
• During AEC calibration, if exposure times do not change if the mA is varied, it may be that
the input signal level to the AEC board is too high. If this is experienced, check the ramp
voltage at the output of the first gain stage (the first operational amplifier output) on the AEC
board for the subject AEC channel. This voltage must never exceed 10 V. If this voltage does
exceed 10 V, reduce the input signal level as required.
SGhealthcare 290
JUMONG Installation & Service manual
The AEC CALIBRATION menus that relate to kV breakpoint calibration for the membrane console are
shown below.
SGhealthcare 291
JUMONG Installation & Service manual
Figure 3D-6: AEC Setup & Calibration window, Film Screen Calibration tab
SGhealthcare 292
JUMONG Installation & Service manual
SGhealthcare 293
JUMONG Installation & Service manual
The mAs values noted in the above table represent the approximate desired mAs at an SID of 40 in. (100cm),
using a grid with a 12:1 ratio. All measurements were done with HVL = 3 mm Al @ 75 kV.
SGhealthcare 294
JUMONG Installation & Service manual
SGhealthcare 295
JUMONG Installation & Service manual
SGhealthcare 296
JUMONG Installation & Service manual
Record the final measurements in a copy of the table below. The final measurements are those obtained
AFTER films have been developed to verify the correct O.D. at each breakpoint.
SGhealthcare 297
JUMONG Installation & Service manual
Use these steps to perform the short AEC exposure time compensation.
SGhealthcare 298
JUMONG Installation & Service manual
The DENS. SETUP menus for the membrane console are shown below.
SGhealthcare 299
JUMONG Installation & Service manual
Refer to table 3D-10 for two typical examples of density steps vs. calibration numbers. For 8 minus density
steps the mAs decrease is 6.25% per step, and for 8 + density steps the mAs increase is 12.5% per step as per
the example calculation above.
For 5 minus density steps the mAs decrease is 10% per step, and for 5 + density steps the mAs increase is 20%
per step.
SGhealthcare 300
JUMONG Installation & Service manual
SGhealthcare 301
JUMONG Installation & Service manual
SGhealthcare 302
JUMONG Installation & Service manual
SGhealthcare 303
JUMONG Installation & Service manual
Grid Absorption
The following information may aid in selecting a grid and / or estimating mAs if required: The percentages
listed are approximate.
A 10:1 ratio 60 in. (150 cm) focused grid will exhibit the following absorption when measured 5 in. (13 cm)
from center:
At 72 in. (180 cm) absorption = 18%
At 40 in. (100 cm) absorption = 40%
A 12:1 ratio 60 in. (150 cm) focused grid will exhibit the following absorption when measured 5 in. (13 cm)
from center:
At 72 in. (180 cm) absorption = 20%
At 40 in. (100 cm) absorption = 50%
A 10:1 ratio 72 in. (180 cm) focused grid will exhibit the following absorption when measured 5 in. (13 cm)
from center:
At 40 in. (100 cm) absorption = 65%
A 12:1 ratio 72 in. (180 cm) focused grid will exhibit the following absorption when measured 5 in. (13 cm)
from center:
At 40 in. (100 cm) absorption = 75%
A 10:1 ratio 40 in. (100 cm) focused grid will exhibit the following absorption when measured 5 in. (13 cm)
from center:
At 72 in. (180 cm) absorption = 65%
A 12:1 ratio 40 in. (100 cm) focused grid will exhibit the following absorption when measured 5 in. (13 cm)
from center:
At 72 in. (180 cm) absorption = 75%
SGhealthcare 304
JUMONG Installation & Service manual
SGhealthcare 305
JUMONG Installation & Service manual
The remaining image receptors are calibrated in a similar manner to the table Bucky receptor. Only the gain
pot for the active channel is to be adjusted at the slowest film screen used on the selected receptor. DO NOT
READJUST THE GAIN POT FOR PREVIOUSLY CALIBRATED RECEPTORS, AND DO NOT READJUST THE
CALIBRATION VALUES IN THE AEC CALIBRATION MENU FOR PREVIOUSLY CALIBRATED FILM SCREENS.
THE MEMORY FUNCTION THAT WAS TEMPORARILY CHANGED TO OFF EARLIER IN THIS
CHAPTER MAY NOW BE RESET TO THE DESIRED VALUE.
AEC exposures should normally be kept well under one second. When X-ray techniques are used that result in
longer exposures, the film density will not be correct due to failure of reciprocity of the film.
Care must be exercised when using low kV values with table Buckys because most tabletops and grids
absorb considerable radiation in the range of 60 – 65 kV. This will adversely affect AEC operation.
constant film density as kV is changed for different anatomical studies. By selecting and calibrating various kV
breakpoints, the overall system response will be compensated such as to yield a constant film density.
Up to eight breakpoints per film screen combination are available. The eight breakpoints are spread
over three kV ranges as shown below:
• Low kV: 50, 55, 65 kV.
• Knee kV: 75 kV.
• High kV: 85, 95, 110, 130 kV.
Since the CMP 200® family of X-ray generators allows for up to three separate film screen combinations to be
calibrated, the following points must be considered:
• The AEC board allows for a zero to a maximum of 10-volt ramp at the comparator input. All AEC
Signals must fit within this range (for all film / screens, densities, and techniques).
• Most X-ray film-based applications require the use of two or more different film screen combinations,
all of which will require different exposure doses.
• Using the slowest film screen combination, the required film input dose will be determined.
• Once this value is determined (during AEC calibration), the density calibration is performed to allow
100% (double the dose) and 50% (half the dose) values. These are typical values, and will determine
the maximum required range of the AEC reference voltage (the output from the D/A converter).
• Figure 3D-10 illustrates the different windows required for various film screen combinations.
SGhealthcare 306
JUMONG Installation & Service manual
Before continuing, it is suggested that a copy of the table below be filled in with all required information.
Refer to the example AEC setup worksheet on the next page.
SGhealthcare 307
JUMONG Installation & Service manual
SGhealthcare 308
JUMONG Installation & Service manual
It is recommended that a copy of the form below be filled in with the required information before attempting
AEC calibration.
Figure 3D-11 shows an installed AEC chamber. Note particularly the use of a suitable insulating material to
isolate the body of the chamber from the receptor ground. This is required for non-insulated AEC chambers.
SGhealthcare 309
JUMONG Installation & Service manual
SGhealthcare 310
JUMONG Installation & Service manual
CHAPTER 4
ACCEPTANCE TESTING
4.1.0 INTRODUCTION
This section details acceptance testing, which verifies that the generator is performing within limits. It is
recommended that this be done whenever the generator is reconfigured, or component(s) are replaced
which may affect the X-ray output. Examples of such components are the X-ray tube, HT tank, console
board, generator control board, filament supply board, and the AEC board.
ENSURE THAT THE FOLLOWING ITEMS ARE COMPLETED PRIOR TO PERFORMING THE
ACCEPTANCE TESTING:
• The generator is interfaced to compatible room equipment, as noted on the product description \
Compatibility statement in chapter 1.
• The tube auto calibration has been done as per chapter 3C.
• The receptors have been programmed as per chapter 3C.
• If the installation has AEC, verify that all receptors have been calibrated as per chapter 3D.
• Acceptance testing shall only be started after the installation is complete i.e. with the generator in
The final position and installed as per the previous chapters of this manual.
• Storage oscilloscope.
• mA / mAs meter.
• Radiation meter 0-10 mGy (0-1000 mR).
• Lead diaphragm or equivalent to collimate the beam.
• General purpose DVM.
• Strobe or reed tachometer.
• Current probe 0 to 20 amps AC.
• A set of HVL filters.
• Calculator.
SGhealthcare 311
JUMONG Installation & Service manual
For the touchscreen console, check the console functionality by pressing the equivalent switch position
on the touchscreen for the functions described in section 4.3.1 and 4.3.2. Verify the correct response on
the touchscreen console for each function that is tested.
SGhealthcare 312
JUMONG Installation & Service manual
THE GENERATOR MUST BE PROGRAMMED FOR DUAL SPEED STARTER OPERATION IN ORDER
TO BE ABLE TO VERIFY BOTH MODES OF OPERATION IN THIS SECTION. DO NOT DO SO IF A
TUBE IS USED THAT CANNOT OPERATE AT BOTH LOW AND HIGH SPEEDS.
***** PLEASE OBSERVE A MAXIMUM OF 2 HIGH SPEED BOOSTS PER MINUTE *****
SGhealthcare 313
JUMONG Installation & Service manual
SGhealthcare 314
JUMONG Installation & Service manual
IF HIGH kV EXPOSURES ARE NOT ALLOWED IN THE FOLLOWING STEPS, CHECK THE MAXIMUM kV
SETTING THAT HAS BEEN PROGRAMMED. REFER TO “TUBE SELECTION” IN CHAPTER 3.
SGhealthcare 315
JUMONG Installation & Service manual
For CMP 200® DR X-ray generators with a DR imaging system, follow the system manufacturer’s
recommendations for system test to verify the DR interface.
The procedure for performing reproducibility, linearity and HVL testing is contained in a separate
SGhealthcare 316
JUMONG Installation & Service manual
SGhealthcare 317
JUMONG Installation & Service manual
SUPPLEMENT
REPRODUCIBILTY, LINEARITY,
& HVL TESTING
PROPRIETARY AND CONFIDENTIAL
The design and information contained in this document is proprietary to Communications & Power Industries
Canada Inc. (CPI), has been designed and developed at private expense, and is the exclusive property of CPI.
The information contained herein is loaned in confidence solely for the installation, operation, and
maintenance of CPI equipment. This document may not be duplicated in whole or in part, or be used for re-
engineering, reverse engineering, or otherwise reproducing in any form or creating or attempting to create or
permitting, allowing or assisting others to create or manufacture CPI’s product or products derived therefrom,
without the express written permission of CPI.
Copyright © 2007 by Communications & Power Industries Canada Inc. All rights reserved.
1.0 INTRODUCTION
This supplement describes reproducibility, linearity, and half - value layer (HVL) tests which may be used
to verify performance of medical X-ray generators.
SGhealthcare 318
JUMONG Installation & Service manual
SGhealthcare 319
JUMONG Installation & Service manual
IN TABLES 1 TO 4, 3 POINT MEANS THAT FOR GENERATORS WHERE KV, MA, AND TIME
SELECTION IS AVAILABLE, THE KV, MA AND MS VALUES SHOWN SHOULD BE USED. FOR
GENERATORS WHERE 2 POINT OPERATION ONLY IS AVAILABLE, THE KV AND MAS VALUES
SHOWN SHOULD BE USED.
Table 1: Reproducibility
Table 2: Reproducibility
SGhealthcare 320
JUMONG Installation & Service manual
Table 3: Reproducibility
Table 4: Reproducibility
SGhealthcare 321
JUMONG Installation & Service manual
Table 5: Reproducibility
4.0 LINEARITY
1. Record two additional series of dose measurements for entry into tables 6 and 7:
• For table 6, use settings per table 3 EXCEPT use an mA (or mAs) value adjacent to the mA
(or mAs) setting used in table 3.
• For table 7, use settings per table 4 EXCEPT use an mA (or mAs) value adjacent to the mA
(or mAs) setting used in table 4.
• Record the mAs in the header of tables 6 and 7 as per 3.0 step 3.
1. Calculate and record the average dose K (kerma) in mGy for tables 6 and 7.
2. Record the preselected mAs and the average dose values taken from tables 3 and 4, and from
tables 6 and 7, at the top of the next page.
3. Using the appropriate mAs and K values, calculate X3, X4, X6, and X7 in tables 8 and 9.
4. Calculate the coefficient of linearity, L, as per tables 8 and 9.
Table 6: Linearity
SGhealthcare 322
JUMONG Installation & Service manual
Table 7: Linearity
Record the mAs and K values taken from tables 3, 4, 6, and 7 below.
Table 3 mAs3 = _____ K3 = _____
Table 4 mAs4 = _____ K4 = _____
Table 6 mAs6 = _____ K6 = _____
Table 7 mAs7 = _____ K7 = _____
Table 8: Linearity
Table 9: Linearity
SGhealthcare 323
JUMONG Installation & Service manual
1. Be sure the X-ray source assembly (X-ray tube and beam limiting device) is fully assembled and
functional.
2. Use the test setup as per figure 1.
3. Set the generator as follows: 3 point generators, 80 kV, 200 mA, 50 ms, large focus. For 2 point
generators use 80 kV, 200 mA if this can be set, and 10 mAs.
4. Take a series of three exposures and record the dose K (kerma) values in mGy in table 10.
Calculate and record the average of the three exposures.
5. Place 2 mm of Al on top of the lead diaphragm (total of 2 mm added), repeat the exposure and
record the K value in table 10.
6. Place an additional 1 mm of Al on top of the lead diaphragm (total of 3 mm added), repeat the
exposure; and record the K value in table 10.
7. Place an additional 3 mm of Al on top of the lead diaphragm (total of 6 mm added), repeat the
exposure; and record the K value in table 10.
8. The relative transmission for the average of the three K values where no Al was added is
assigned a value of 1.00. Using that base, assign relative transmission values to the remaining K
values. For example, if the average K value was 2.15 and has a relative transmission factor of
1.00, then 1.41 mGy will have a relative transmission of 1.41 / 2.15 = 0.66.
9. Plot the relative transmission values in figure 1. This should produce a straight line on the graph
since the X-axis is logarithmic.
10. Interpolate to determine the HVL. The Al thickness at a relative transmission of 0.5 will be the
required HVL value.
11. Repeat steps 4 to 10: 3 point generators, 100 kV, 200 mA, 50 ms, large focus. For 2 point
generators use 100 kV, 200 mA if this can be set, and 10 mAs. Use table 11 to record the values
and figure 2 to plot the results
12. Table 12 and figure 3 show example HVL determination.
SGhealthcare 324
JUMONG Installation & Service manual
SGhealthcare 325
JUMONG Installation & Service manual
SGhealthcare 326
JUMONG Installation & Service manual
CHAPTER 5
TROUBLESHOOTING
5.1.0 INTRODUCTION
The CMP 200® / CMP 200® DR series operator’s console will display status messages on the LCD display
during normal and abnormal operation of the generator. This chapter contains tables of those messages and
suggests actions to be taken by service personnel to correct any malfunctions that may occur.
SGhealthcare 327
JUMONG Installation & Service manual
These messages indicate that an exposure has been requested that exceeds one or more limits.
SGhealthcare 328
JUMONG Installation & Service manual
These messages indicate that an error has occurred. The errors are logged in the error log; previous errors
should be reviewed by service personnel before taking further action.
SGhealthcare 329
JUMONG Installation & Service manual
SGhealthcare 330
JUMONG Installation & Service manual
SGhealthcare 331
JUMONG Installation & Service manual
SGhealthcare 332
JUMONG Installation & Service manual
SGhealthcare 333
JUMONG Installation & Service manual
* The generator purges the existing X-ray tube auto calibration data before starting the auto
Calibration routine and saving new calibration data. Therefore, auto calibration should be a last
resort during general troubleshooting, and should only be done to recalibrate the tube. For
example, if a low mA fault is presented, you should ensure that the generator is fully functional,
and actually needs recalibration. If calibration is attempted on a partially functional generator,
the auto calibration routine may be aborted before any calibration is done, and the generator
will inhibit further exposures until the selected mA is calibrated for the selected kV.
1. For an APR MEMORY ERROR fault, the console factory defaults must be restored or the APR must
be restored via GenWare®. The procedure for resetting console factory defaults is described in
chapter 6.
SYMPTOM: In some environments that are “electrically noisy”, the console may exhibit erratic faults
i.e. RAM data error, intermittent loss of communication, or random fault messages may
be displayed.
SOLUTION: Connect a separate ground wire, #14 AWG (2.3 mm2) or larger from the ground stud on
the rear of the console (marked CONSOLE GROUND in the figure “Rear of control console”
in chapter 2) to the ground stud located beside the main input fuse block. This is marked
GROUND CONNECTION in the figure “Generator mains connection” in chapter 2.
SYMPTOM: In some situations the touchscreen console may appear “frozen”. i.e. cannot activate any
of the buttons on the touch sensitive screen. This may be a case of the touchscreen
calibration being significantly out of alignment.
SOLUTION: Connect a USB keyboard to the rear of the touchscreen and simultaneously press Alt + C.
This will activate the touchscreen calibration sequence. Refer to Chapter 3C for the
procedure to complete this sequence.
SGhealthcare 334
JUMONG Installation & Service manual
The following table describes the normal states and functions of the status and diagnostic LEDs on the circuit
boards in the generator.
A change in the state of an LED may be for a brief duration, especially during a fault or an exposure.
SGhealthcare 335
JUMONG Installation & Service manual
SGhealthcare 336
JUMONG Installation & Service manual
CHAPTER 6
REGULAR MAINTENANCE
6.1.0 INTRODUCTION
This chapter provides a recommended schedule for periodic maintenance of the CMP 200® series and the CMP
200® DR series of X-ray generators.
The initial installation date and location, and all service performed on the generator, should be
recorded in table 6-1. The record should be as thorough as possible, detailing the scope and type of work that
was performed (all service and a record of all replacement parts that were installed). Additionally, the person
performing the work should date and sign the record.
This information will be invaluable in the future for traceability and to ensure continued compatibility of
the generator.
If a major component (such as the HT oil tank or a major circuit board) is replaced, recalibration will be
needed. A separate procedure will be included with the spare in those cases, detailing the required
calibration procedure. The acceptance test procedure per Chapter 4 should then be performed prior to
placing the generator back into service.
SGhealthcare 337
JUMONG Installation & Service manual
SGhealthcare 338
JUMONG Installation & Service manual
SGhealthcare 339
JUMONG Installation & Service manual
CMP 200® / CMP 200® DR X-ray generators use different styles of HT tanks, depending on model. Refer to
figure 6-1. For the HT tank on the right side of figure 6-1, field maintenance is neither necessary nor possible.
The oil is factory-filled to the correct level and the HT tank is then sealed. An air-filled “bladder” within the
tank will expand and contract as the oil volume changes with pressure and temperature changes.
For the HT tank on the left side of figure 6-1, the oil level in the HT tank can be checked in the field and the oil
can be topped up if necessary. Refer to the steps below.
The insulating oil level in the HT tank does NOT require periodic checking under normal conditions. However, if
there is evidence of possible oil loss, the procedure for checking the correct oil level follows.
SGhealthcare 340
JUMONG Installation & Service manual
6.5.0 CLEANING
• To clean the console surfaces (without disinfecting) use soap and water. This should be applied
using a lint-free cloth as described below.
• If console surfaces need to be disinfected, use Actichlor or equivalent with a Hypochlorite
concentration of 3 to 5%.
∗ Dilute the disinfectant 50/50 with water.
∗ Spray or dampen a lint-free cloth with the diluted disinfectant. The cloth must be damp only, not
wet.
∗ Gently wipe the console surfaces with the damp cloth.
• Never use any corrosive, solvent or abrasive detergents or polishes.
• Ensure that no water or other liquid can enter any equipment. This precaution prevents short
circuits and corrosion forming on components.
• Methods of disinfection used must conform to legal regulations and guidelines regarding
disinfection and explosion protection.
• If disinfectants are used which form explosive mixtures of gases, these gases must have dissipated
Before switching on the equipment again.
• Disinfection by spraying is not recommended because the disinfectant may enter the X-ray
equipment.
• If room disinfection is done with an atomizer, it is recommended that the equipment be switched
OFF, allowed to cool down and covered with a plastic sheet. When the disinfectant mist has
subsided, the plastic sheet may be removed and the equipment be disinfected by wiping.
SGhealthcare 341
JUMONG Installation & Service manual
1. Ensure that GenWare® MP (version 1.03 or later) is installed on the computer that will be used for
The firmware upgrade. The CPI flash program utility is part of GenWare® MP.
2. Start with the console (generator) switched off.
3. Connect a null-modem cable from the serial port on the PC that will be used to do the firmware
upgrade to the DATA LINK connector on the console.
4. Copy the updated software file onto the computer’s hard drive. The updated software file may be
distributed by various means including CD, e-mail, etc. There is only one file to be copied, in the
format 123456A.cpm. Note the folder to which this file has been copied.
5. Switch the console on.
6. Enter the GENERATOR SETUP menu. Select DATA LINK, and then select CONNECT TO
GENWARE. Refer to chapter 3C. The LCD on the console will display WAITING FOR DATA….
PLEASE DO NOT TURN OFF POWER.
7. Start GenWare® MP on your PC. The LCD on the console will display GENERATOR LINK
ENABLED-PLEASE DO NOT TURN OFF POWER. This indicates that GenWare® MP is
communicating with the console.
8. If communication is not established, check the COM port setting in GenWare® MP.
• Select Communications Setup on the GenWare® MP toolbar. The Communication Setup
window will open.
• Under COM Port Selection, select the desired COM port, if known.
• Select Apply, and then Close.
• Exit GenWare® MP, then restart GenWare® MP in order for the change to take effect.
• If the required COM port is not known, you may need to select consecutive COM ports by trial and
error. Repeat the previous steps, using a different COM port for each trial.
9. Select Firmware Updater on the GenWare® MP toolbar. The CPI Generator Flash Program
Utility will open. Refer to figure 6-2.
10. Select EXIT on the console to return to the DATA LINK TYPE menu.
11. Select FIRMWARE UPDATE. The LCD on the console will display WAITING FOR
UPDATE…PLEASE DO NOT TURN OFF POWER.
12. On the CPI Generator Flash Program Utility, under CPM Format, ensure that File is selected.
This is the default setting.
SGhealthcare 342
JUMONG Installation & Service manual
13. Select Browse. A dialog box will open asking you to Choose a file to open. Select the cpm file
That was copied in step 4.
14. The file path and name will be copied into the text field under CPM Format.
15. DO NOT SWITCH OFF THE GENERATOR DURING THE NEXT THREE STEPS. IF POWER IS
LOST DURING THE UPGRADE PROCESS, THE CONSOLE WILL NEED TO BE RETURNED TO
THE FACTORY TO BE REPROGRAMMED.
16. Select Start Download.
17. If the updated software file is able to successfully download to the console, the Progress bar on
The downloader utility window will indicate the progress, and the % indicator will show the
Percent completion. The console LCD will display DOWNLOADING UPDATE… PLEASE DO NOT
TURN OFF POWER and it will also indicate the progress via a progress bar.
18. If the message Console type is not matched! is displayed, this indicates that the software file is
Not compatible with that console.
19. When the download is finished and the console’s flash memory has been updated, the console
Will display UPDATE SUCCESSFUL. The console and computer may then be switched off, and the
Nullmodem cable may be disconnected.
1. Ensure that GenWare® MP (version 1.03 or later) is installed on the computer that will be used
for the firmware upgrade. The CPI flash program utility is part of GenWare® MP.
2. tart with the generator switched off.
3. Connect a null-modem cable from the serial port on the PC that will be used to do the firmware
upgrade to J22 on the generator control board.
4. Copy the updated software file onto the computer’s hard drive. The updated software file may be
distributed by various means including CD, e-mail, etc. There is only one file to be copied, in the
format 123456A.cpm. Note the folder to which this file has been copied.
5. Switch the generator on.
6. Start GenWare® MP on your PC. Then select Firmware Updater on the GenWare® MP
toolbar. The CPI Generator Flash Program Utility will open. Refer to figure 6-2.
7. witch the generator off. Do not switch off GenWare® MP or close the CPI Generator Flash Program
Utility.
SGhealthcare 343
JUMONG Installation & Service manual
8. Locate jumper JW2 on the generator control board. Temporarily set this to the “upgrade” position
(short across pins 2-3).
9. Switch the generator on again.
10. On the CPI Generator Flash Program Utility, under CPM Format, ensure that File is selected. This
is the default setting.
11. Select Browse. A dialog box will open asking you to Choose a file to open. Select the cpm file that
was copied in step 4.
12. The file path and name will be copied into the text field under CPM Format.
13. DO NOT SWITCH OFF THE GENERATOR DURING THE NEXT THREE STEPS. IF POWER IS
LOST DURING THE UPGRADE PROCESS, THE GENERATOR CONTROL BOARD WILL NEED
TO BE RETURNED TO THE FACTORY TO BE REPROGRAMMED.
1. Switch the generator mains power OFF, AND WAIT 5 MINUTES FOR THE DC BUS CAPACITORS
TO FULLY DISCHARGE.
2. Locate and carefully remove the existing EPROM on the dual speed starter board.
3. Carefully insert the replacement EPROM into the socket observing the orientation per figure 1-6.
Resetting the factory defaults will restore the CPU’s flash memory contents to their factory-default state. This
will be required if a major firmware upgrade is done. Minor firmware upgrades, such as revision upgrades, do
not require resetting of the factory defaults.
The factory defaults should not be reset casually as this will erase all custom programming made to
the console or generator.
Note that there are separate procedures to reset the factory defaults for the console CPU and for the
generator CPU.
CONSOLE CPU FACTORY DEFAULTS:
The procedure for loading console defaults is described in chapter 3C of this manual. Refer to LOAD
CONSOLE DEFAULTS. This is described in the section UTILITY MENU, under CONSOLE.
SGhealthcare 344
JUMONG Installation & Service manual
6. Switch OFF the generator. Reset S3-1 back to the NORMAL (OFF) position.
7. Reprogram the tube selection to correspond to the connected tube AS PER Tube
Selection /Tube Setup IN CHAPTER 3C OF THIS MANUAL. This information was
initialized when the defaults were selected. This must be done before auto calibration is
started, to prevent damage to the X-Ray tube.
8. PERFORM TUBE AUTO CALIBRATION AS PER Tube Calibration IN CHAPTER 3C OF
THIS MANUAL. This must be done to ensure accuracy of the exposure parameters after
The generator factory defaults have been loaded.
Note: The tube calibration sequence must be completed in full. If tube calibration is interrupted,
The resulting mA / mAs values will be uncalibrated due to invalid calibration data.
This will initialize all generator data to the factory defaults [tube selection, generator
limits (including anode boost time), receptor setup, I/O configuration, AEC setup, AEC
calibration, tube calibration, time & date, error log, statistics and anode heat units].
1. Switch the generator OFF at the console, and disconnect the mains voltage.
2. Disconnect the AEC chamber connections at the AEC board.
3. Disconnect the AEC control cable at J7 on the generator control board.
4. Locate the four nylon standoffs that secure the AEC board to the control board.
5. Turn the head of each plunger on the nylon standoffs approximately 90° counterclockwise.
6. Gently lift the AEC board off the nylon standoffs. Set the AEC board aside until the required
components underneath are replaced. The AEC board should only be placed on a static-safe
surface.
7. Reverse the above steps to replace the AEC board.
SGhealthcare 345
JUMONG Installation & Service manual
Tube conditioning or “seasoning” is particularly important for new tubes or tubes that have not been used
forseveral days. This should be performed on each X-ray tube before attempting auto calibration, as an
unseasoned tube may not operate properly at higher kV values without arcing. Refer to the X-ray tube
manufacturer’s instructions, if available, for the tube conditioning or “seasoning” procedure. If the X-ray tube
manufacturers instructions are not available, the following procedure may be used:
The generator does X-ray tube auto calibration at 40 kV, 50 kV, 60 kV, 70 kV, 80 kV, 100 kV and 120 kV. The
tube normally needs to be seasoned before it can be operated at the higher voltages encountered during auto
calibration.
Tube seasoning is started by auto calibrating the kV stations up to and including part of the 70 kV
station. The tube is then seasoned at 70 kV. Progressively higher kV stations are then auto calibrated and
seasoned. Finally the entire kV and mA range is auto calibrated, then the tube is seasoned at the remaining
high kV values.
Manually releasing the exposure button during auto calibration of a particular kV station in the
following procedure prevents the generator from attempting operation beyond that kV/mA value.
X-ray tubes that have not been used for more than 8 hours may suffer thermal shock if operated at
high mA and kV without a warm-up procedure. A cold anode (Molybdenum) is very brittle and when
suddenly heated over a small area may experience thermal cracking of the anode surface, eventually
leading to permanent tube damage.
The procedure below is intended for seasoning an X-ray tube prior to attempting tube auto calibration.
Toseason a tube that does not need to be calibrated, follow steps 2, 4, and 6.
X-ray tube seasoning should be done on LARGE focus in order to minimize tube wear.
1. Start the tube auto calibration sequence, and manually terminate the exposure at 70 kV and 250
mA.
2. Season the tube at 70 kV by taking approximately 10 exposures of 200 mA and 100 ms. These
exposures should be taken at the rate of approximately one every 15 seconds.
3. Restart the auto calibration sequence and manually terminate the exposure at 100 kV and 250
mA.
4. Season the tube at 100 kV by taking approximately 5 exposures of 200 mA and 100 ms. These
exposures should be taken at the rate of approximately one every 15 seconds.
5. Restart the auto calibration sequence and manually terminate the exposure at 120 kV and 160
mA.
6. Season the tube at 120 kV by taking approximately 5 exposures of 160 mA and 100 ms. These
exposures should be taken at the rate of approximately one every 15 seconds.
7. Restart the auto calibration sequence and allow the auto calibration sequence to complete.
The generator’s useful life has been estimated at 10 years from point of sale. This will vary depending on use
and environmental conditions. If the generator has completed its useful service life, local environmental
regulations must be complied with in regard to disposal of possible hazardous materials used in the
construction of the generator.
In order to assist with this determination, the noteworthy materials used in the construction of this
generator are itemized below:
SGhealthcare 346
JUMONG Installation & Service manual
ITEM
• Electrical insulating oil in HT tank. This is a mineral oil with trace additives (25 Litre (6.5 U.S. gal)
• Solder (lead/tin).
• Epoxy fiberglass circuit board materials, tracks are solder on copper.
• Wire, tinned copper. Insulated with PVC, tefzel, or silicone.
• Steel and / or aluminum (generator cabinet and console chassis).
• Plastic (console enclosure and console membrane).
• Electrical and electronic components: IC’s, transistors, diodes, resistors, capacitors, etc.
SGhealthcare 347
JUMONG Installation & Service manual
Chapter 7
THEORY OF OPERATION
7.1.0 INTRODUCTION
This chapter contains the theory of operation for the CMP 200® and CMP 200® DR X-ray generators.
The theory of operation is organized by functional blocks as per the functional drawings in chapter 9.
Refer to the appropriate functional block diagram in chapter 9 in conjunction with the theory of operation in
this chapter. Waveforms and voltages at the pertinent test points are typically shown on the last page of each
functional drawing.
The generator control board on the CMP 200® series of X-ray generators includes power ON and power
OFF switches S1 and S2 that may be used to switch the generator on and off locally while working on the
equipment. These switches are connected in parallel with the generator ON and OFF switches that are
located on the consoles.
Pressing any of the power-ON switches turns on Q5 on the generator control board. This turns on Q6,
holding the collector of Q6 low. This latches Q5 in the “on” state by holding the base of Q5 low when the
ON switch is released.
The collector of Q6 is connected to K1 on the generator control board (MD-0927). K1 will be energized
when the generator is switched on, supplying +24 V to the console.
With Q6 turned on, the base of Q7 is held low, turning Q7 off. The collector of Q7 is connected to the ON / OFF
control pins on the +5 V, +12 V, and +15 V switching regulators on the generator control board
(MD-0927). With Q7 turned off, the regulator control pins will be pulled to a logic high state, enabling the low-
voltage supplies on the generator control board (MD-0927).
In normal operation, a wire jumper is connected between J2-1 and J2-2 on the generator control board.
An emergency-off switch may be connected to the generator by removing the jumper between J2-1 and
J2-2, and then wiring the emergency-off switch to J2-1 and J2-2. If the connection between J2-1 and J2-2
is open-circuit (i.e. no jumper or an open emergency-off switch), K2 will be de-energized as shown. This
holds the base of Q6 low, preventing Q6 from turning on.
A supervisory circuit (not shown) monitors the +1.2 V, +3.3 V, and +5 V DC supplies on the generator
control board. The supervisory circuit releases the CPU reset line when these low voltage DC supplies
are detected at start-up. This causes the CPU to enter its startup sequence. The CPU will initialize itself,
perform its startup diagnostics, and then output a command via U86 and U83 on the generator control
board to energize soft-start contactor K2 on the H.V auxiliary board. The CPU will then wait for
approximately 10 seconds for the output of opto-coupler U5 on the H.V auxiliary board to ramp high,
indicating that the DC bus capacitors are charged. If U5 indicates proper DC bus capacitor charging
within the allotted time, the CPU will output a command to U86 and the driver consisting of Q28, Q29, etc to
energize the main power contactor via the H.V auxiliary board. Soft-start contactor K2 will be deenergized
after a maximum of 10 seconds, as the soft-start circuit is not needed once the DC bus
capacitors are charged.
SGhealthcare 348
JUMONG Installation & Service manual
If opto-coupler U5 on the H.V auxiliary board does not indicate normal DC bus capacitor charge within the
allowed time limit, an error message will be presented and the turn-on sequence will be aborted.
Pressing any of the power-OFF switches turns on Q4 on the generator control board. This turns off Q5,
turning off Q6. This will de-energize K1 on the generator control board, removing the +24 V supply from
the console. With Q6 turned off, Q7 will turn on, taking the ON / OFF control lines on the +5 V, +12 V, and +15
V regulators low. This disables the switching regulators, shutting down the generator control
functions. The main power contactor will open, removing the AC input to the mains rectifier assembly.
SGhealthcare 349
JUMONG Installation & Service manual
+24 VDC, 120 VAC, or 240 VAC for the BUCKY DRIVE is available when K6 on the H.V. auxiliary board
is closed as described in 7.2.2. The 24 VAC and 24 VDC supplies are present at all times that the AC
mains is energized. The 24 VAC supply is fused by F11 and brought out at J11-6 and J11-5 on the H.V.
auxiliary board (maximum 150 watts for collimator use), and the 24 VDC supply is fused by F12 and
made available at J11-2 and J11-1 for system locks use (maximum 45 watts).
Bucky relays K1 and K3 on the H.V. auxiliary board are driven by U83 and U86 on the generator control
board. When K1 or K3 is energized, +24 VDC, 120 VAC, or 240 VAC is provided at J2-7 or J4-1 on the
H.V. auxiliary board to start Bucky 1 or Bucky 2.
The Bucky 1 or Bucky 2 ready signal (a contact closure is needed) will energize opto coupler U2 or U6
respectively. The Bucky-ready status from U2 / U6 is conveyed to the CPU via data buffer U89, where it is
processed to determine if the Buckys are ready to make an X-ray exposure.
During an X-ray exposure, the base of Q31 on the generator control board is pulled high via U19. This will turn
on Q31, energizing K7 on the H.V. auxiliary board. K7 provides a dry contact closure when
energized, which may be used to control the room light.
The H.V. auxiliary board also contains 4 interlock inputs. These include interlocks 1 and 2, the door
interlock, and the X-ray tube thermal switch interlock. Each of these interlock inputs requires a contact
closure to indicate a normal condition, with a closed interlock energizing the associated opto coupler U1,
U3, U4, or U9 respectively. The outputs of the opto-couplers are read by the CPU via data buffer U89 on
the generator control board, where the information is used to determine the readiness of the associated
input.
Pressing X-RAY on the membrane console will energize U17 on the console board. If U17 is energized,
or one of the X-RAY switches on the touchscreen console, X-ray mini-console, or on the associated hand
SGhealthcare 350
JUMONG Installation & Service manual
switches is pressed, U9 and U7 on the generator control board will be energized. The output of U17 on
the console board is read by the console CPU, and the output of U7 on the generator control board is
read by the generator CPU via data buffer U71. An X-ray request will be recognized if the output of U17
on the console board (membrane console only) and / or U7 on the generator control board is low. When
the generator CPU receives an X-ray request, the emitter of U9 on the generator control board will be
pulled low via U86 and driver U83, assuming that there are no errors that would prevent an exposure.
With U9 on the generator control board energized, and its emitter held low, the collector of U9 will be held
low.
Jumpers JW1 and JW2 on the console board (membrane consoles) may be removed to disable the
console PREP and X-RAY buttons. If these jumpers are removed, PREP and X-RAY requests may be
made via a hand switch connected to J3 on the membrane console.
SGhealthcare 351
JUMONG Installation & Service manual
is inversely proportional to demanded generator output power. The current sense feedback from T1
synchronizes the start of the pulses.
The gate-drive pulses from the VCO are fed to AND gates U26A and U26B. The control inputs of U26A
and U26B are held high if all logic conditions to allow an X-ray exposure are satisfied. The drive pulses
are inverted and level shifted by U27A and U27B, and then applied to the gates of the MOSFET inverter
consisting of Q16, Q17, Q19, and Q20 on the generator control board. These MOSFETS form a full
bridge inverter circuit that outputs high frequency gate pulses to the power MOSFETS on the inverter
board(s) via J5 and / or J13 on the generator control board.
The differential kV feedback voltage from the HT tank is brought to J9 on the generator control board.
This is applied to the inputs of U51A and U56B, where the kV feedback scaling is precisely set by R218.
The differential feedback signals are then summed by U51B. The output of U51B supplies a kV feedback
signal to error amplifier U25A as described earlier in this section. The kV feedback signal is also supplied
to the CPU via A/D converter U45, which monitors the output voltage during an exposure. Lastly, the kV
feedback signal is fed to the kV over-voltage comparator U55, which will send a fault pulse to the CPU via U78
if a kV over-voltage condition is detected.
The generator control board also contains circuits that guard against an inverter “shoot-through” fault. If a
shoot through fault is detected, T3 and / or T4 on the generator control board will supply a current pulse that
is detected by comparator circuits U70 and U75. The relevant comparator will then generate a fault pulse that
is passed to the CPU via U78, causing the gate drive to be inhibited immediately, thus
preventing inverter damage due to this fault.
SGhealthcare 352
JUMONG Installation & Service manual
The output of filament current sense transformer T1 on the filament supply board is rectified by D12, D13,D27,
and D28, and fed to RMS converter circuit consisting of U7 and associated components. The output of the RMS
converter drives U4A, which is a variable gain amplifier. The filament current feedback is calibrated such that 1
volt = 1 amp of filament current. The calibrated filament feedback voltage (representing actual filament
current) appears at the input of buffer U2B, at the summing input of error amplifier U4B as described earlier in
this section, and at the input of comparator U2A.
The output of U2B is brought to J2-2 on the filament supply board. The filament current feedback signal is then
converted to a digital signal by A/D converter U45 on the generator control board in order that the filament
current can be monitored by the CPU.
The output of U2A will be low if a filament fault is present, i.e. filament current less than approximately
1.7amps. This will turn Q1 on the filament supply off, taking its collector high. The output of Q1 is taken to the
CPU via U78 on the generator control board. If low filament current is detected, X-ray exposures will not be
possible, and a filament fault message will be displayed.
The generator CPU decides whether the pending exposure should be made at low-speed or high-speed
operation. Based on this determination, the CPU will output the high-speed / low-speed command via
U86 and U83 on the generator control board. The output of U83 lights DS10 on the generator control
board, and energizes U12 on the dual-speed starter board. The dual-speed starter CPU monitors the
output of U12, and sets low or high-speed operation based on the state of U12.
The prep command is also output by the generator CPU and latched by U86. Driver U83 lights DS11 on
the generator control board, and energizes U13 on the dual-speed starter board. The dual-speed starter
CPU monitors the output of U13, and starts the boost cycle when the output of this opto coupler is low.
K1 on the dual-speed starter board will close at the start of the prep cycle. K4 will close at the same time
that K1 is energized. This ensures that the high voltage is isolated from the stator terminals at all times
except during normal operation of the dual-speed starter.
SGhealthcare 353
JUMONG Installation & Service manual
The dual-speed starter contains an inverter, Q1 to Q4, which produces the required stator current at 50,
60, 150, or 180 Hz by precisely switching the 560 / 650 volt DC bus. The dual speed starter CPU controls
the switching of the inverter via the driver circuit consisting of U1-U9 and T1-T4, etc. The setting of DIP
switch SW1 determines all stator drive parameters (boost voltage and boost time, run voltage, brake
voltage and brake time, etc).
The modulated output from the inverter is fed to the common stator terminal via one leg of the inverter
and via K4. The shift and main currents are taken from the other leg of the inverter via K5 and K6. K1-A
switches the main current, and K1-B switches the shift current.
The following description applies to dual-speed starters 901297-12, 13, 16 and 901298-12, 13, 16 only.
Relay K3 is held open for high-speed operation and closed for low-speed operation. The dual-speed
starter will automatically set K7 open or closed based on the setting of DIP switch SW1, selecting one-oftwo
possible capacitor values. The available capacitor values are shown in the tables on MD-0924.
The operation of dual-speed starter 901297-15 and 901298-15 is similar, except that relay K7 is always
held open during low-speed operation, providing 28μF of low-speed capacitance. It is also possible to
configure this starter to provide 15.5μF of low-speed capacitance by removal of one of the low speed
capacitors. One-of-two possible value of high-speed capacitance is automatically selected using K7.
The operation of dual-speed starter 901297-02 and 901298-02 is similar, except that K7 is not used,
resulting in only one value each of low-speed capacitance (60μF) and high-speed capacitance (20μF).
The DC bus current is monitored by a circuit consisting of CS1, U10, U11, etc. If a problem such as a
ground fault in the stator circuit is detected, a latch in the inverter fault detector circuit will be set. This will
light DS1 and inhibit the drive pulses for the inverter Q1 to Q4.
The contacts of current sense relays K5 and K6 will be closed when the main and shift currents are above
preset limits. With K5 and K6 closed, Q5 on the dual-speed starter board is supplied with base current.
This will turn on Q5, whose output is monitored by the dual-speed starter CPU. If normal stator current is
detected, the CPU will output a logic low signal at J1-10 on the dual-speed starter board. This statorready
signal drives opto-coupler U88 on the generator control board, turning U88 on in the normal (no stator-current
fault) state. DS9 will be on at prep in low speed mode, and on after prep is finished in highspeed mode. The
generator CPU reads the output of U88 via U87 on the generator control board. A stator fault condition will
immediately remove the generator ready and drive-enable signals, inhibiting kV output. Additionally, the dual-
speed starter CPU will open K1 and K4 on the dual-speed starter board,removing the stator drive.
120 or 240 VAC is supplied to the low-speed starter via F6 and F7 on the H.V. auxiliary board. This
voltage is jumper-selectable on the H.V. auxiliary board; refer to MD-0927 for details.
The coil of K4 on the H.V auxiliary board is connected in parallel with the main power contactor, and
therefore is energized when the main power contactor is energized after completion of the generator
power-on sequence. This is described in 7.2.1.
When a Prep request is made, K5 on the H.V. auxiliary board is energized by the CPU via U86 and driver
U83 on the generator control board for the ROTOR BOOST duration that was selected in the
GENERATOR LIMITS menu (chapter 3C) in order to boost the rotor. The rotor is allowed to coast briefly,
and then boosted again for approximately 500 milliseconds every 5 seconds during Prep in order to
maintain normal anode rotation. During the boost cycles (when K5 is energized), 120 or 240 VAC is
applied directly to the main winding and to the shift winding on the stator via phase shift capacitor C12.
The main and shift currents flow through R20 and R19 on the H.V. auxiliary board, respectively,
energizing opto couplers U7 and U8 if there is sufficient stator current. Normally, the opto couplers will
only conduct during the peaks of the stator current. This is reflected in the output waveform of the opto
couplers at TP8 and TP7 as shown on page 2 of MD-0935. If there is low (or no) stator current, U8 and /
or U7 will not be energized. The output of the opto couplers at TP8 / TP7 will then be pulled high (+5 V).
This steady-state condition (+5 V) is detected by the CPU via U89 on the generator control board, where
SGhealthcare 354
JUMONG Installation & Service manual
The DAP circuits consist of switching circuits to control the outputs at J4, and circuits to feed the DAP
pulses back to the CPU. Data latch U19 and driver U20 switch the +5 V and +15 V supplies via Q2, Q3,
and Q1 as required to control and test the DAP chamber. For DAP chambers with differential outputs,
JW14 is jumpered from pins 2-3, thus connecting the differential output from the DAP chamber directly to the
input of U1. For DAP chambers with a single-ended output, JW14 must be jumpered on pins 1-2. This connects
the output of the DAP chamber to the input of opto-coupler U94. This provides increased noise immunity for
single-ended DAP chambers, as the signal must be greater than approximately 2 V in order to turn on the opto-
coupler. The single-ended output of U94 is then connected to the input of U1.
The RS-485 driver, U1, sends single-ended (not differential) pulses to the CPU via U78. The DAP pulses
are counted by, and the related calculations are performed by the generator CPU.
The inverter temperature sensor is mounted on a thermal sensor board that is mounted on one of the
inverter heat sinks. The output of the inverter temperature sensor is connected to J17-2 on the generator
control board. The temperature sensor, which has an output of 10mV / °C, is connected to the input of U79A.
The output of U79A is scaled 100mV / °C; this is divided by R162 / R163 to bring the signal within the useable
range of A to D converter U45. The digital output of U45 is read by the generator CPU, which will inhibit
further exposures if it calculates that the next exposure will exceed a safe inverter temperature.
The output of U79A is also connected to a fan voltage circuit controlled by voltage comparator U97. When the
voltage at TP34 is less than 3.5V, the output of U97 is high. The logic high is fed into the fan voltage regulator
circuit putting the voltage at J28-1 between 6.5 and 7 volts (driving the cooling fan at low speed).
If the voltage at TP34 reaches 3.5V (approx. 35°), the output of U97 goes low. The logic low is fed into
the fan voltage regulator circuit, which will drive the voltage at J28-1 to approximately 12.5 volts (driving
the cooling fan at high speed).
MD-0925 also shows programming jumpers JW12, JW2, and JW13. JW12 tells the CPU if the generator
has a cooling fan. JW-12 should be jumpered from pins 2-3 for generators with fans, and pins 1-2 if a
new-style generator control board is used to upgrade or repair older generators without fans. Note that if the
jumper is in position 1-2 (no fan), the generator duty cycle will be reduced.
JW2 is used to upgrade the generator firmware. This is set to JW2 pins 1-2 for normal operation, and pins 2-3
to upgrade the firmware. JW13 is factory-set, and should not be reconfigured in the field.
When the generator is switched on and the start-up diagnostics are finished, the console will attempt to
communicate with the generator. The console will send data to the generator, and then wait for a
response from the generator. If the console receives a response, communication may continue. If the
console CPU does not receive a response from the generator CPU, a communication error message will
be displayed.
When the membrane console is sending data to the generator, DS2 on the console board will flash. DS3
on the generator control board will flash when data is being received by the generator control board from the
membrane console or the touchscreen console. DS2 on the generator control board and DS3 on the
membrane console board (if applicable) will flash to indicate that the generator control board is sending data
to the console.
U11 on the console board (membrane consoles) is a RS-232 driver that drives serial port J4. DS5 and
DS4 on the console board will flash to indicate that data is being sent to, and received from the serial
port.
The generator control board includes two serial communications ports. These include J21, which is an
RS-232 communications port, and J22, which is used for optional features.
DS1 on the console board (membrane consoles) and on the generator control board will flash at a
SGhealthcare 355
JUMONG Installation & Service manual
The output of U2A connects to the common inputs of analog switches S2A to S2D. These analog
switches are controlled by the chamber-select signal, and the switch corresponding to the active channel will
be closed. This connects the output of U2A to the AEC gain adjustment potentiometer R1 to R4 corresponding
to the active channel. The AEC signal, which will be either a ramp or a DC voltage
depending on AEC chamber type, is now fed to the input of U2B. This will be factory configured as an
integrating amplifier by connecting C4 into the circuit for use with AEC chambers that output a DC output
voltage, or U2B will be configured as a linear amplifier by connecting R32 into the circuit for use with AEC
chambers that provide a ramp voltage. The start signal also connects to analog switch S4. This switch opens
when an AEC exposure starts, allowing U2B to start integrating or amplifying the AEC signal.
The output of U2B will be a positive going ramp regardless of the AEC chamber type in use. This ramp
SGhealthcare 356
JUMONG Installation & Service manual
voltage is processed by U4A and U4B, and also fed to the short AEC exposure time compensation circuit
consisting of R11 to R14, S3A to S3D, R53 and C11. Analog switches S3A to S3D are controlled by the
chamber-select signal. The switch corresponding to the active channel will be closed, connecting the
phase-lead network C11 / R53 to the wiper of the AEC short-time adjustment potentiometer. This circuit is
disabled when the wipers of R11 to R14 are at the ground end of the potentiometers, and maximum
short-time compensation is provided when the wipers are set to the end of the potentiometers connected to
U2B.
The AEC ramp from U4B is taken to the generator control board where it is processed as described
earlier in this section, and also fed to comparator U6 on the AEC board where it is compared to the AEC
reference voltage. The output of U6 is normally high, switching low when the magnitude of the AEC ramp
equals the reference voltage. This PT stop signal is further processed on the generator control board.
The START, and LEFT, MIDDLE, and RIGHT field select signals are brought to the AEC chambers via
J1/J11, J2/J12, J3/J13, and J4/J14. The AEC board will be factory configured to directly output the active
low signal from the generator control board to the AEC chamber if required, or to output +12 V or +24 V if the
chamber requires active high signals. For AEC chambers that require active high outputs, the start,
right, middle, or left field select signal is taken from the collector of Q1 to Q4, respectively. The active low
signals from the generator control board turn on Q1 to Q4, outputting either +12 V or +24V (depending on
factory configuration) at the collector when active.
Jumpers JW1 to JW8 swap the left and right fields on J11 to J14. Jumpering pins 2-3 of the field selector
jumpers (JW7 / JW8 for channel 1, JW5 / JW6 for channel 2, JW3 / JW4 for channel 3, JW1 / JW2 for
channel 4) connects the left field select signal to pin 6 and the right field select signal to pin 2. Jumpering
pins 1-2 of the field selector jumpers connects the left field select signal to pin 2 and the right field select signal
to pin 6.
The AEC board also contains a DC to DC converter that produces +45 V, + or - 300 V, and +500 VDC.
The converter circuit consists of U7, T1, output voltage adjustment potentiometer R79, and associated
components. The +45 V output is hard wired to all of the AEC chamber connectors, and + or - 300 V is
permanently connected to J1 to J4. Additionally, the AEC board will be factory configured to supply either + or
- 300 V or +500 V to J11 to J13, and to a second pin on J1 to J4 (in addition to the + or - 300 V fixed output).
The output of each preamplifier is connected to an analog switch used for field selection. Selecting the
desired field closes the corresponding analog switch, connecting the output of that preamplifier to the
summing node at the junction of R69, R9, R22 for channel 1, R40, R47, R55 for channel 2, R70, R11,
R23 for channel 3, and R41, R49, R56 for channel 4.
JW1 to JW8 swap the left and right fields. Jumpering pins 1-2 of the field selector jumpers (JW1, JW2 for
channel 1, JW3, JW4 for channel 2, JW5, JW6 for channel 3, JW7, JW8 for channel 4) selects the normal
left-right orientation, and jumpering pins 2-3 of the field selector jumpers reverses the left-right field
selection.
Selecting an active AEC channel closes U4D for channel 1, U14D for channel 2, U5D for channel 3, and
U15D for channel 4. The output from the selected AEC channel will then be passed on to the signal
processing circuits as shown on the next sheet of MD-0936.
SGhealthcare 357
JUMONG Installation & Service manual
the signal output from U12A constant relative to the number of fields that are selected.
The output of U12A feeds the inverting input of U11B. A sample and hold circuit is connected to the
noninverting input on U11B. This circuit samples any electrical noise at the output of U12A during standby
operation, and subtracts this noise from the AEC signal during an AEC exposure. This ensures that the output
of U11B is proportional to the AEC chamber output only, and is not influenced by noise.
The output of U11B is connected to the input of U11A via the gain adjustment pots R1 to R4 and the
analog switches for channels 1 to 4.
U11A is an integrating amplifier where C31 starts to integrate the AEC voltage when the AEC exposure
starts. This is accomplished by opening the analog switches that are in series with R35, R38, R42, and
R59 at the start of the exposure. This produces a ramp whose slope is proportional to the input voltage at
U11A.
The AEC ramp is taken to the generator control board where it is processed as described earlier in this
section, and fed to comparator U10 on the AEC board where it is compared to the AEC reference voltage.
The output of U10 is normally high, switching low when the magnitude of the AEC ramp equals the
reference voltage. This PT stop signal is further processed on the generator control board.
The chamber-select signals exit on the generator control board as per sheet 1. Only one chamber may be
active at one time, and the active channel is indicated by DS1 to DS4 on the AEC board. The chamberselect
signals are inverted by U6, and then connected to the control inputs on analog switches U4D,U14D, U5D, and
U15D (sheet 3) for AEC channel selection and to the analog switches in series with R1 to R4 to select the
required gain pot.
The field select signals from the generator control board are also active low. These signals are inverted
by U6, and then connected to the analog switches in the feedback loop of U12A, and to the analog
switches that select the fields on the previous sheet.
The start signal from the generator control board is inverted by U6 on the AEC board, and then inverted
again by Q2. The output of Q2 is connected to the analog switches in the feedback loop of U11A. The
extra inversion provided by Q2 is required to open those analog switches during an exposure.
SGhealthcare 358
JUMONG Installation & Service manual
Jumpers JW1 to JW8 swap the left and right fields on J1 to J4. Jumpering pins 2-3 of the field selector
jumpers (JW7 / JW8 for channel 1, JW5 / JW6 for channel 2, JW3 / JW4 for channel 3, JW1 / JW2 for
channel 4) connects the left field select signal to pin 6 and the right field select signal to pin 2. Jumpering
pins 1-2 of the field selector jumpers connects the left field select signal to pin 2 and the right field select signal
to pin 6.
The channel 3 and channel 4 select lines from U6 are inverted by Q6 and Q7. The outputs of Q6 and Q7
are redesignated as the PORTRAIT and INVERTED signals, respectively. These signals select four
different combinations of the L-M-R fields from the five available fields on the AEC chamber.
The start signal also exits from the generator control board. This is inverted by U6, and then inverted
again by Q4 and Q5. The output of Q5, when active, opens the analog switch that is part of the sample
and hold circuit at the input of U8A during an AEC exposure. This analog switch is closed at all other
times. The sample and hold circuit will sample any electrical noise at the output of U7A during standby
operation, and subtract this noise from the AEC signal during an AEC exposure. This ensures that the
output of U8A is proportional to the AEC chamber output voltage only, and is not influenced by noise.
The output of U8A connects to the common inputs of the analog switches that are in series with gain pots R11
and R12. These analog switches are controlled by the chamber-select signal, and the switch
corresponding to the active channel will be closed. This connects the output of U8A to the AEC gain
adjustment potentiometer R11 or R12 corresponding to the active channel. The AEC signal, which will be
a ramp, is now fed to the input of U8B. The analog switch in the feedback loop of U8B is opened during
an exposure, allowing the AEC ramp to appear at the input of U4A via a phase-lead network that provides
short time compensation.
The AEC ramp from U4A is again inverted by U4B and taken to the generator control board where it is
processed as described earlier in this section, and fed to comparator U9 on the AEC board where it is
compared to the AEC reference voltage. The output of U9 is normally high, switching low when the
magnitude of the AEC ramp equals the reference voltage. This PT stop signal is further processed on the
generator control board.
SGhealthcare 359
JUMONG Installation & Service manual
exposures. The resulting “exposure on” signal from U37C is taken to J25 via driver U4, and is inverted by Q15.
The output of U37C is also taken to differential driver U31 for imaging systems that need a differential
“exposure on” signal.
Lastly, U19 latches the commands to drive the prep / exposure indicators and LS1 and LS2 in the miniconsole.
These signals are fed to driver U20, which provides the required current gain.
This drawing shows the cabling between the major subassemblies in the CMP 200® X-ray generator.
Where applicable, this document references the appropriate functional schematics and sections of the
service manual for details on the area of interest.
SGhealthcare 360
JUMONG Installation & Service manual
CHAPTER 8
SPARES
8.1.0 INTRODUCTION
This chapter contains the list of spare parts for the CMP 200® series and CMP 200® DR series of X-ray
generators.
The matrix on the next page lists the recommended spare parts for the CMP 200® and CMP 200® DR
families of X-ray generators.
SGhealthcare 361
JUMONG Installation & Service manual
SGhealthcare 362
JUMONG Installation & Service manual
SGhealthcare 363
JUMONG Installation & Service manual
NOTE:
1. Refer to table 8-1 for the part number for the H.V. auxiliary board. Four different part numbers are
used, depending on the application:
Units with the dual speed starter option will be fitted with H.V. auxiliary board 739442-00.
Before installing a replacement H.V. auxiliary board, jumpers must be properly installed on this board
in order to select the Bucky voltage (24 VDC, 110 VAC, or 220 VAC). After determining the Bucky
drive voltage requirement, connect the appropriate pair of jumpers in accordance with table 8-2 *.
The jumpers that select the Bucky voltage must be set per table 8-2.
After determining the required rotor boost voltage, connect a wire jumper between the desired tabs on
the boards *.
* A complete set of jumpers is shipped with each new generator. Three of the jumpers are installed on
the H.V. auxiliary board, and the remaining jumpers are in a bag attached to the lip on the inside of
the cable access slot above the HT tank.
If the Bucky or low-speed starter boost voltage needs to be changed on an existing H.V. auxiliary
board, use the existing jumper(s) if they are of the correct length and have the proper connector to fit
the tab(s) on the board. Otherwise, select the shortest wires from the spare jumper set that will
connect between the desired tabs on the board and that have the proper connectors on the jumpers.
For spares boards, the jumpers will need to be removed from the “old” board and reused.
Additionally, JW1 must be set per table 8-4 before installing a replacement H.V. auxiliary board.
SGhealthcare 364
JUMONG Installation & Service manual
2. The AEC board in your generator was selected to be compatible with specific AEC devices. To
maintain full compatibility, the original part number must be ordered as a replacement. Refer to
chapter 9, section 9.2.0, for the part number of the original AEC board that was shipped in the
generator for which this manual was prepared.
3. This applies to the dual speed starter option only, spares should be stocked accordingly. The part
number shown for the dual speed starter board is for the board only, without the phase-shift
capacitors. For the complete dual speed starter subassembly, several part numbers (which are
tubestator dependent) are used in CMP 200® DR 400 / 480 VAC generators. To determine which
dual speed starter subassembly is in your generator, note the DUAL SPEED STARTER ASSY part
number on a label near the top left side of the dual speed starter chassis. This will be the part
number that must be ordered for spares usage. For reference, this will be part number 901297-XX
or 901298-XX where XX is a two digit number designating the exact configuration.
4. This generator control board is jumper configurable. Please refer to the following tables to
Configure the generator control board for your x-ray generator.
SGhealthcare 365
JUMONG Installation & Service manual
CHAPTER 9
SCHEMATICS
9.1.0 INTRODUCTION
This chapter contains the functional schematics for the CMP 200® X-ray generator. Each functional
schematic represents a major function in the generator. The functional schematics in this chapter
represent all of the major functional blocks in CMP 200® X-ray generators.
SGhealthcare 366
JUMONG Installation & Service manual
VIVA Software
9
Installation
Introduction
The PaxScan 4343R is a radiographic digital X-ray imaging device commonly referred to as a flat panel detector
(FPD). The detector together with image processing and command software called Virtual Command Processor
(VCP) is designed for integration into a complete X-ray system. The imaging system has two main system
components: The 38.3 x 42.7cm 139μm-pixel amorphous silicon FPD that houses the solid-state, flat
panel sensor and the VCP software, and the External Power Supply (I/O Box) that provides power supply.
SGhealthcare 367
JUMONG Installation & Service manual
This device is only for use on adult patients with healthy skin; for example, free of
blemishes, scars, skin rashes, irritants, disorders, discoloring and abnormal moles.
For hand held applications, the operator and end-user must take precautions to
protect themselves against dangerous X-ray exposure when using the flat panel
imager in the X-ray beam path of an X-ray source.
The 4343R is not intended to be used as a primary barrier to X-rays. The user is
responsible for insuring the safety of the operator, bystanders, and the subjects
being radiographed.
SGhealthcare 368
JUMONG Installation & Service manual
Explanation of Symbols
Alternating Current
Direct Current
Heated Surface
SGhealthcare 369
JUMONG Installation & Service manual
Getting Started
Connecting the Cables
Connect the cables as described below in Table 1-0 and shown in Figure 2-0.
Table 1-0 Cable Connection Details
STEP Action / Description
There are three (3) cable connections for the 4343R Flat Panel Receptor: (a) External Sync Cable, (b)
Power Supply Cable which is permanently connected to the power supply, and (c) Category 5 or
better Ethernet cable. The connections are described below.
1 External Sync Cable Connection
This connector is intended to provide the user with a means to synchronize the end-user system-
level application with the imager. This connector provides the connections for four opto-isolated
signals, (two outputs, and two inputs). The one output signal named “Expose OK” is intended to
signal that the receptor is ready for the generator to produce X-rays and the input named “Expose
Req” allows the user to trigger the panel readout. See Appendix A, diagram 1.0 for “Expose OK”
and “Expose Req” signal schematic. Connect this cable to the external sync connector on the
receptor.
2 Power Supply
This connection provides power to the receptor. Connect the power supply connector to
receptor then plug into the main AC supply.
3 Gigabit Ethernet Connection
Connect the Ethernet connector to a gigabit capable interface in the user’s host computer.
4 Ground Lug
Chassis ground lug to acceptable ground connection.
SGhealthcare 370
JUMONG Installation & Service manual
Caution
Accessory equipment connected to the analog and digital interfaces must be
certified to the respective IEC standards (i.e., IEC 60950-1 for data processing
equipment and IEC 60601-1 for medical equipment). Furthermore, all
configurations shall comply with the system standard IEC 60601-1-1. Anyone
connecting additional equipment to the signal inputs or signal outputs as part of a
configuration for medical equipment is therefore responsible for compliance with
the equipment standard IEC 60601-1. If in doubt, consult our technical support
personnel.
SGhealthcare 371
JUMONG Installation & Service manual
Appendix A
Interfacing Information
All the interfacing connections for the Paxscan 4343R are at the panel itself. The Gigabit Ethernet
connection carries control information to the panel and supplies image data with diagnostic
information to the customer supplied workstation. The Hardware Synchronization connection (“B”)
is a 9-pin D-sub type. Power for the panel is supplied by a medical-grade “laptop” style supply whose
dc supply cable “C” can be up to 3 meters in length.
NOTE: The maximum input voltage on the opto-couplers used in the 4343R is
5V.Refer to the TSM0505S datasheet for additional information.
SGhealthcare 372
JUMONG Installation & Service manual
Figure A.2 Schematic for “Expose Ok” and “Expose Request” Signal
The timing of the synchronization interface is shown below. The panel is maintained in an idle state,
until the asynchronous Expose_Request is received. The Expose_Request signal is detected as a level
and so the signal must be maintained for a minimum of 360 msecs. When the panel receives the
Expose_Request, the assumption is that the generator is ready to make an exposure when
Expose_OK is issued.
SGhealthcare 373
JUMONG Installation & Service manual
1.Software Installation
Begin software installation by using the run command under the Windows Start button, select
Browse, My Computer, and your DVD/CD ROM Drive that contains the PaxScan CD. Select the icon
Setup.exe or alternatively at the run command window enter drive location and file name, select
OK – will launch the PaxScan ViVA System Software Install Shield Wizard.
SGhealthcare 374
JUMONG Installation & Service manual
1.For a normal install, you may simply accept all the defaults in progressing to the Install Shield Wizard
Complete screen.
2.Ensure the Open Pleora Installation Instructions is “checked” and select the finish button at the Install Shield
Wizard Complete screen will automatically launches a README file instruction to complete the Pleora driver
installation. You may only install the iPORT™ High-Performance IP Device Driver if you have the Intel Pro/1000
adapter; this is the recommended configuration. An alternative which gives lower overall data handling
capability is the filter driver which may be installed to almost any Ethernet adapter on the computer. If the
filter driver is installed, make sure to disable it on any adapters NOT used for connection to the Pleora. See
Note below regarding drivers.
SGhealthcare 375
JUMONG Installation & Service manual
Note:
Pleora provides three options for the Ethernet driver. For fastest possible operation install
the Pleora Performance driver onto the Ethernet adapter of the host computer; but, – this is
only possible with specific Ethernet adapter – namely, the Intel Pro/1000. Other gigabit
Ethernet adapters may be used without noticeable loss of speed for radiography (single shot)
modes. Operation is possible with the native Windows driver which requires no additional
installation, however, performance will vary depending upon the computer system. The
Pleora Filter driver provides a third option that gives performance intermediate between
the other two. The filter driver solution is better than the Windows driver though still not
nearly as good as the performance driver. We strongly recommend using only the
Performance driver for medical applications. The user must validate that any configuration
used is suitable for the intended application.
Modes of Operation
The PaxScan 4343R supports the radiography mode of operation as defined in Table 2-0. In general,
there is a trade off between varying operation modes of resolution, or field of view, or cycle time, or
noise. The sensitivity of the imager is optimized to match the X-ray dose used in each mode.
The purpose of each mode is to configure the detector to achieve optimal performance during
specific imaging procedures. Modes are defined by a combination of factors, such as pixel binning,
cycle time, analog gain, and continuous versus single acquisition. Each mode requires a unique set of
calibration files. Refer to the ViVA Online help documentation for complete details.
The user can select the mode of operation based on image performance and cycle time. The
following two (2) modes are available:
For either RCT or SCT the user has the option to retrieve a preview image – which has the benefit of
having preliminary view of the target object in reduced time.
SGhealthcare 376
JUMONG Installation & Service manual
(3) If you see “Net” in Device Class as below, it means that Intel® PRO/1000 GT Desktop Adapter is not
recognized as Network card. You must change it to “PRO/1000 Grabber Device”.
SGhealthcare 377
JUMONG Installation & Service manual
(4) Click right mouse on the highlight area and select “Install High Performance IP Device Driver”.
SGhealthcare 378
JUMONG Installation & Service manual
(6) After complete installation, verify that “PRO/1000 Grabber Devices” is shown in Device.
And click “확인” to finish.
SGhealthcare 379
JUMONG Installation & Service manual
SGhealthcare 380
JUMONG Installation & Service manual
(1) Start -> Program -> Varian -> Paxscan L04 -> Run “Viva”.
(2) About 5 sec. later, detector will be recognized as below.
(“4pfg2550msRCTMSR8” will be shown in Mode for 14X17 Detector).
(3) If detector is not recognized automatically, then detector needs to be recognized manually as below.
(No Acquisition Link -> Link to Virtual CP)
SGhealthcare 381
JUMONG Installation & Service manual
SGhealthcare 382
JUMONG Installation & Service manual
5. Detector Calibration.
Offset Calibration
Offset calibration compensates for fixed pattern pixel intensity variations in the image associated with the dark
current and electronic offsets. The Offset reference image is an average of a series of frames acquired without
X-ray illumination and referred to as dark fields.
1. To perform offset calibration, click the ViVA icon launches the application
2. Ensure required receptor appears in the Mode drop down. The 4343R currently supports Rad 1x1 4pf. Click
Offset Calib. button or select from the menu bar under Acquisition.
3. An accumulating Dark Frames window appears followed by an offset calibration acquisition completion.
SGhealthcare 383
JUMONG Installation & Service manual
Gain Calibration
To compensate for non-uniformities in the Receptor, a gain reference image (flat field) is used by the
Corrections module as required to correct all images. The flat field image must be captured by the Virtual
Command Processor (VCP) prior to acquiring images. The process of capturing the flat field image is known as
Gain Calibration.
Gain calibration is based upon the linear response of the Receptor to dose. Normalization is achieved by
applying the flat field image acquired during the Gain calibration to all images corrected by the VCP.
Normalization will fail with pixels that are responding to dose in a non-linear manner. Pixels responding to
dose in a non-linear manner are usually caused by the saturation of the Receptor, or a low signal-to-noise ratio.
Note: It is critical to acquire the flat field image within a range that is large enough to be higher
than the background noise created by the X-ray source and readout electronics of the
Receptor, but lower than the saturation point of the imager.
Flat field images acquired near or exceeding the saturation point will cause normalization failures with all
images acquired until a Gain calibration with the correct dose is performed. We recommend that flat field
images be acquired with a median count of 1,600 – 3,000. This range will ensure that Gain calibration will meet
both the upper and lower dose requirements under all modes of operation. Dose requirements are
determined by the settings of the generator X-ray source.
To reduce the effects of noise, the average of each pixel in the flat field image is calculated by accumulating a
number of frames into an internal memory buffer, then dividing the sum of each pixel by the number of
frames acquired.
Note: Using larger numbers of calibration frames to capture the flat field image will result in
more accurate calibration.
The number of calibration frames used during Gain and Offset calibrations can be adjusted under the Mode
Settings pull down menu. We recommend accumulating 32 frames for gain calibration and 8 frames for offset
SGhealthcare 384
JUMONG Installation & Service manual
calibration for optimal image quality. However, the actual number of calibration frames used must be
determined solely by the system integrator depending upon their specific performance requirements.
The general procedure for Gain calibration for all modes is as follows in Table 3-0 and described below.
Detailed instructions on performing gain calibrations are covered in the ViVA Online help documentation.
Important: Gain calibration requires the production of X-rays and therefore certain precautions
must be taken by the human operator.
Step Action Results
To ensure proper warm up, the PaxScan 4343R Receptor must be operational
1 Warm Up
for a least two (2) hours prior to Gain calibration.
Software performs a new Offset calibration referred to as dark field
2 Offset Calibration acquisition.
Note: X-Rays must not be used for this part of the calibration.
A uniform flat field with no obstructions in the path of the X-Ray beam. The
radiation should ideally be at a level and technique representative of the
3 X-Ray Radiation
typical radiation dose for the Receptor during typical procedures, keeping in
mind the general consideration outlined above.
The above procedure must be repeated for each of the stored imaging
4 Repeat
modes.
A series of accumulated frames equals one radiographic X-ray exposure. Exposures are averaged to obtain the
Flat Field image used by the VCP correction module. The number of exposures acquired can be varied by
clicking the Finish button after collecting the desired number of exposures.
SGhealthcare 385
JUMONG Installation & Service manual
(6) About 2 sec. later, below 2 screens will be appeared one by one. And make an exposure
(7) After acquiring image, new window will be appeared as below then click “Cancel”.
SGhealthcare 386
JUMONG Installation & Service manual
(8) Put mouse cursor on the middle of image and read value of ADU.
It must be around 3100.
(9) If value of ADU is less than ± 100 then adjust KV and make exposures to get 3100.
If value of ADU is more than ± 100 then adjust mAs and make exposures to get 3100.
SGhealthcare 387
JUMONG Installation & Service manual
(2) 2 images will be acquired automatically and offset calibration will be proceed.
(No exposure is required.)
SGhealthcare 388
JUMONG Installation & Service manual
(2) Do check Offset Corrections and uncheck Gain Corrections/Pixel Defect Map/T Map Correction.
NOTE: After Gain Calibration, all check box in blue must to be checked again.
SGhealthcare 389
JUMONG Installation & Service manual
(5) About 5 sec. later, below screens will be appears one by one then make an exposure.
SGhealthcare 390
JUMONG Installation & Service manual
→ →
(6) after making an exposure below screens will be appears one by one then wait for about 3 sec.
→ →
SGhealthcare 391
JUMONG Installation & Service manual
(10) Verify value of Gain Median in Calibration Statistics is around 3000 and Click “Close”.
SGhealthcare 392
JUMONG Installation & Service manual
(12) Image acquisition is needed to make sure that calibration has been done correctly.
Click “Acquire Image”.
SGhealthcare 393
JUMONG Installation & Service manual
(13) About 2 sec. later, below screen will be appeared then make an exposure.
(14) Check image quality as Uniformity, Dead pixel, Dead line etc.
SGhealthcare 394
JUMONG Installation & Service manual
SGhealthcare 395
JUMONG Installation & Service manual
SGhealthcare 396
JUMONG Installation & Service manual
SG Healthcare
SG HEALTHCARE CO.,LTD.
753 ITECO, 150 JOJEONG-DAERO,
HANAM-SI, GYEONGGI-DO, KOREA 465736
www.sghealthcare.com
SGhealthcare 397