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PREFACE
2 9650-0801-01 Rev. A
Chapter 6—Functional Description provides technical descriptions for the Propaq MD major
subassembly modules.
Appendix A—Propaq MD Electrical Hardware Interconnect Diagram and Propaq MD Signal
and Power Interconnect Schematic.
Appendix B—Contains simulators and settings that may be used to assess the performance of
the NIBP module.
Safety Considerations
The following section describes general warnings and safety considerations for operators and
patients. Service technicians should review the safety considerations prior to servicing any
equipment and read the manual carefully before attempting to disassemble the unit. Only
qualified personnel should service the Propaq MD unit.
Federal (U.S.A.) law restricts this unit for use by or on the order of a physician.
Safety and effectiveness data submitted by ZOLL Medical Corporation to the Food and Drug
Administration (FDA) under section 510(K) of the Medical Device Act to obtain approval to
market is based upon the use of ZOLL accessories such as disposable electrodes, patient cables
and batteries. The use of external pacing/defibrillation electrodes and adapter units from
sources other than ZOLL is not recommended. ZOLL makes no representations or warranties
regarding the performance or effectiveness of its products when used in conjunction with
pacing/defibrillation electrodes and adapter units from other sources. If unit failure is
attributable to pacing/defibrillation electrodes or adapter units not manufactured by ZOLL, this
may void ZOLL's warranty.
Only qualified personnel should disassemble the Propaq MD unit.
WARNING! This unit can generate up to 2775 volts with sufficient current to cause lethal shocks.
All persons near the equipment must be warned to “STAND CLEAR” prior to discharging the
defibrillator.
Do not discharge the unit’s internal defibrillator energy more than three times in one minute or
damage to the unit may result.
Do not discharge a battery pack except in a ZOLL SurePower
TM
Charging Station.
Do not use the Propaq MD in the presence of flammable agents (such as gasoline), oxygen-rich
atmospheres, or flammable anesthetics. Using the unit near the site of a gasoline spill may
cause an explosion.
Do not use the unit near or within puddles of water.
Additional Reference Material
In addition to this guide, there is a Propaq MD Operator’s Guide which is a comprehensive
reference work that describes all the user tasks needed to operate the Propaq MD.
- MD Service Manual 1
- Table of Contents 3
- Chapter 4 Life Cycle Counters 4
- Chapter 5 Replacement Parts 4
- Appendix A 4
- Appendix B 4
- Overview 5
- Safety Considerations 6
- Conventions 7
- Service Policy Warranty 7
- Technical Service 7
- 4 9650-0801-01 Rev. A 8
- Chapter 1 9
- Maintenance Tests 9
- CHAPTER 1MAINTENANCE TESTS 10
- Operational Tests 10
- Functional Verification Tests 10
- NIBP Calibration Check 11
- Procedure 13
- Calibration Check Procedure 14
- NIBP Leak Test 15
- NIBP Deflation Test 16
- NIBP Inflation Test 17
- Keypad Test 20
- LED Test 20
- Audio Test 22
- Printer Test 22
- NIBP Test 24
- Leads Test 26
- Heart Rate Display Test 27
- Heart Rate Alarm Test 28
- Leakage Current Test 30
- Shock Test 31
- Pacer Test 33
- IBP Test 37
- Temperature Test 39
- Chapter 2 41
- Troubleshooting 41
- CHAPTER 2TROUBLESHOOTING 42
- Propaq MD Error Messages 43
- Chapter 3 51
- Disassembly Procedures 51
- Safety Precautions 52
- Removing the Handle 53
- Removing the Printer Module 54
- Disassembling the Main Unit 56
- 54 9650-0801-01 Rev. A 58
- Tools Required 59
- 56 9650-0801-01 Rev. A 60
- Removing the Display Module 61
- 58 9650-0801-01 Rev. A 62
- Removing the EtCO 63
- and NIBP Modules 63
- 60 9650-0801-01 Rev. A 64
- 62 9650-0801-01 Rev. A 66
- Modules 67
- 64 9650-0801-01 Rev. A 68
- 66 9650-0801-01 Rev. A 70
- 68 9650-0801-01 Rev. A 72
- Chapter 4 73
- Life Cycle Counters 73
- CHAPTER 4LIFE CYCLE COUNTERS 74
- Defibrillator/Pacer 74
- Chapter 5 75
- Replacement Parts 75
- Replacement Parts 76
- CHAPTER 5REPLACEMENT PARTS 78
- Chapter 6 79
- Functional Description 79
- 76 9650-0801-01 Rev. A 80
- Defibrillator Pacer Module 81
- 78 9650-0801-01 Rev. A 82
- Lithium Ion Battery 83
- 80 9650-0801-01 Rev. A 84
- 82 9650-0801-01 Rev. A 86
- 84 9650-0801-01 Rev. A 88
- Bio-Tek Instruments BP Pump 90
- Bio-Tek Instruments BP Pump2 90
- DNI Nevada CuffLink 91
- Clinical Dynamics Smart Arm 91
- 88 9650-0801-01 Rev. A 92
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