Service Manual
154 Pages
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M Series® Service Manual
9650-0450-01 Rev R
The issue date for the M Series Service Manual (REF 9650-0450-01 Rev. R) is March, 2013. If more than 3 years have elapsed since the issue date, contact ZOLL Medical Corporation to determine if additional product information updates are available. Copyright © 2013 ZOLL Medical Corporation. All rights reserved. Rectilinear Biphasic, M Series, and ZOLL are trademarks or registered trademarks of ZOLL Medical Corporation in the United States and/or other countries. Masimo is a trademark or registered trademark of Masimo Corporation in the United States and/or other countries.
ZOLL Medical Corporation 269 Mill Road Chelmsford, MA USA 01824-4105 ZOLL International Holding B.V. Newtonweg 18 6662 PV ELST The Netherlands
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9650-0450-01 Rev R
M Series Service Manual
TABLE OF C ONTENTS PREFACE ... V Overview ...v Safety Considerations ...v Additional Reference Material ... vi Conventions ... vii Service Policy Warranty ... vii Technical Service ... vii Technical Service for International Customers ... viii
CHAPTER 1 MAINTENANCE TESTS ...1 Overview ...1 Before You Begin the Maintenance Tests ...2 Equipment that You Need to Perform the M Series Maintenance Tests ...3 Equipment You Need for the M Series Options Maintenance Tests ...4 1.0 Physical Inspection of the Unit... 5 2.0 Front Panel Button Test... 7 3.0 3, 5, and 12 Leads Test ... 10 4.0 Power Supply Test (Optional) ... 11 5.0 Leakage Current Test... 15 6.0 Paddles Test (If applicable) ... 16 7.0 Heart Rate Display Test... 18 8.0 Calibrating Pulses on Strip Chart Test ... 19 9.0 Notch Filter Test... 20 10.0 Heart Rate Alarm Test... 21 11.0 Defibrillator Self Test... 23 12.0 Synchronized Cardioversion Test... 25 13.0 Shock Test ... 26 14.0 Summary Report Test... 29 15.0 Advisory Message Test ... 30 16.0 Pacer Test ... 31
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M Series Service Manual 17.0 SpO2 Monitor Test for SpO2 Option ... 33 18.0 EtCO2 Monitor Test (for EtCO2 Option)... 36 19.0 Temperature Test... 38 20.0 IBP Monitoring Test... 39 21.0 NIBP Transducer Calibration Test ... 44 22.0 NIBP Monitor Test ... 47 23.0 NIBP Volume Leak Test with Fluke Biomedical NIBP Analyzer... 49 24.0 Bluetooth Test... 51
CHAPTER 2 TROUBLESHOOTING ...53 Overview ...53 Troubleshooting ...54 Zoll M Series Error Messages ...58
CHAPTER 3 DISASSEMBLY PROCEDURES ...75 Overview ...75 Required Equipment ...76 Parts That May Need Replacing After Disassembly ...76 Safety Precautions ...77 Overview of Modules ...78
1. Removing the ZIF Keeper ...81 2. Removing the Front Panel ...82 2A.Removing the Display ...83 2B.Removing the Control Board ...84 3. Removing the Upper Housing Assembly ...86 4. Removing the System Board Assembly ...87 5. Removing the Battery Interconnect Board Assembly ...90 6. Removing the High Voltage/Charger Assembly ...91 7. Removing the High Voltage Module Assembly ...94 8. Removing the High Voltage Capacitor Assembly ...96 9. Removing the System Interconnect Board ...98 10.Removing the Printer/Recorder Motor ...100 11.Removing the Lower Housing Assembly ...102 12.Removing the Print Head Assembly ...103 13.Removing the PCMCIA Card Slot Assembly ...104
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M Series Service Manual 14.Removing the Paddle Release Latch ...105 CHAPTER 4 REPLACEMENT PARTS ...107 Overview ...107 Replacement Parts ...108 Field Replacement Parts ...112
CHAPTER 5 FUNCTIONAL DESCRIPTION ...115 Overview ...115 Main System Board ...116 Main System Board Functions ...118 Power Supply ...120 ECG Front End ...121 Multifunction Electrode (MFE)/PADS (System Board and High Voltage Module) ...121 CPU and EPU ...121 High Voltage Module ...122 Defibrillator Charging and Discharging ...123 High Voltage Capacitor Monitor ...124 Pacer/Defibrillator Control Signals ...125 Internal Discharge Resistor Module ...127 AC/DC Charger Module ...127 System Interconnect Module ...127 Stripchart Recorder ...128 PCMCIA Slots ...128 Front Panel and Controls PWBA ...128 M Series Options ...128 Isolated Power Supply Module ...129 12 Lead Option ...129 Pulse Oximetry (SpO2) ...130 End Tidal Carbon Dioxide (EtCO2) ...130 Biphasic Waveform ...131
APPENDIX ...135 Overview ...135 Interconnect Diagram for the M Series Monophasic Unit ...136 Interconnect Diagram for the M Series Biphasic Unit ...137 Interconnect Diagram for the M Series CCT Biphasic Unit ...138
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M Series Service Manual
Preface Overview ZOLL Medical Corporation’s M Series Service Manual is intended for the service technician whose responsibility is to identify malfunctions and/or make repairs at the subassembly level. The Zoll M Series Service Manual has five main sections and one appendix. Preface-Contains safety warnings and an overview of the manual’s contents. Be sure to review this section thoroughly before attempting to use or service the M Series unit. Chapter 1-Maintenance Tests explains how to check the defibrillator’s performance using a series of recommended checkout procedures to be conducted every six months. Chapter 2-Troubleshooting provides a listing of the procedures and error messages to help the service technician detect faults and repair them. Chapter 3-Disassembly Procedures describes step-by-step procedures for removing subassemblies from the M Series unit. Chapter 4-Replacement Parts List displays a complete list of ZOLL part numbers for field replaceable parts available for the M Series unit, allowing the service person to identify and order replacement parts from ZOLL. Chapter 5-Functional Description provides technical descriptions for the M Series major subassembly modules. Appendix A-M Series Operator’s Manual.
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 M Series 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
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M Series Service Manual 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 M Series unit.
WARNING!
This unit can generate up to 4500 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 energy more than three times in one minute or damage to the unit may result. Do not discharge a battery pack except in a Base PowerCharger4x4 or compatible ZOLL Battery Charging/Testing unit. Do not use the M Series 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.
NOTE
The M Series is protected against interference from radio frequency emissions typical of two-way radios and cellular phones (digital and analog) used in emergency service/public safety activities. Users of the M Series should assess the unit’s performance in their typical environment of use for the possibility of radio frequency interference from high-power sources. Radio Frequency Interference (RFI) may be observed as shifts in monitor baseline, trace compression, or transient spikes on the display.
Additional Reference Material In addition to this guide, there are several other components to the Zoll M Series documentation. They include: • Operator’s Guide - A comprehensive reference work that describes all the user tasks needed to operate the M Series. • Configuration Guide - Describes the M Series features and functions whose operation can be customized by authorized users.
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M Series Service Manual
Conventions WARNING!
Warning statements describe conditions or actions that can result in personal injury or death.
CAUTION
Caution statements describe conditions or actions that can result in damage to the unit.
NOTE
Notes contain additional information on using the defibrillator.
Service Policy Warranty In North America: Consult your purchasing agreement for terms and conditions associated with your warranty. Outside of North America, consult ZOLL authorized representative. In order to maintain this warranty, the instructions and procedures contained in this manual must be strictly followed. For additional information, please call the ZOLL Technical Service Department 1-800-348-9011 in North America.
Technical Service If the ZOLL M Series unit requires service, contact the ZOLL Technical Service Department: Telephone: 1-978-421-9655; 1-800-348-9011 Fax 1-978-421-0010 Have the following information available for the Technical Service representative: • Unit serial number. • Description of the problem. • Department where equipment is used. • Sample chart recorder strips documenting the problem, if applicable. • Purchase Order to allow tracking of loan equipment. • Purchase Order for a unit with an expired warranty.
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M Series Service Manual If the unit needs to be sent to ZOLL Medical Corporation, obtain a service order request number from the Technical Service representative. Return the unit in its original container to: ZOLL Medical Corporation 269 Mill Road Chelmsford, Massachusetts 01824-4105 Attn: Technical Service Department Telephone: 1-800-348-9011; 1-978-421-9655 FAX: 978-421-0010
Technical Service for International Customers International customers should return the unit in its original container to the nearest authorized ZOLL Medical Corporation Service Center. To locate an authorized service center, contact the International Sales Department at ZOLL Medical at the above address. Units are available on loan while your unit is being repaired.
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M Series Service Manual
Chapter 1 Maintenance Tests Overview The M Series has two checkout procedures: the operator’s shift checklist and the extensive six-month maintenance tests checkout procedures. Because the M Series units must be maintained ready for immediate use, it is important for users to conduct the Operator’s Shift Checklist procedure at the beginning of every shift. This procedure can be completed in a few minutes and requires no additional test equipment. (See the ZOLL M Series Operator’s Guide for the Operator’s Shift Checklist.) A qualified biomedical technician must perform a more thorough maintenance test checkout every six months to ensure that the functions of the M Series unit work properly. This chapter describes the step by step procedures for performing the six month maintenance test checkout. Use the checklist at the back of this document (ZOLL M Series Maintenance Tests Checklist) to record your results of the maintenance tests. This chapter describes the following M Series maintenance tests: 1. Physical Inspection of the Unit 2. Front Panel Button 3. 3, 5, and 12 Leads 4. Power Supply 5. Leakage Current 6. Paddles 7. Heart Rate Display 8. Calibrating Pulses on Strip Chart 9. Notch Filter 10. Heart Rate Alarm
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M Series Service Manual 11. Defibrillator Self Test 12. Synchronized Cardioversion 13. Shock 14. Summary Report 15. Advisory Message 16. Pacer 17. SpO2 Monitor 18. EtCO2 Monitor 19. Temperature Test 20. IBP Monitoring Test 21. NIBP Transducer Calibration Test 22. NIBP Monitor Test 23. NIBP Volume Leak Test with Fluke Biomedical NIBP Analyzer 24. Bluetooth Test
Before You Begin the Maintenance Tests • Assemble the tools or specialized testing equipment listed in the “Equipment You Need to Perform the Maintenance Tests” section shown below. • Keep an extra fully charged ZOLL M Series compatible battery available. • Schedule an hour to conduct the entire maintenance test. • Photocopy the checklist at the back of this document and use the copy to record your results. As you conduct each step of a procedure, mark the Pass/Fail/NA check boxes on your checklist and then save it for your maintenance file. • Perform the tests in the order presented. • Perform all the steps of each test procedure. • Complete all the steps of the procedure before evaluating the test results.
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M Series Service Manual
Equipment that You Need to Perform the M Series Maintenance Tests This section lists equipment that we use to perform the maintenance tests that we describe in this chapter. You can substitute an equivalent device for a listed device; however, not all simulators and analyzers will produce the same results. Be sure to follow the manufacturer’s recommendations for conducting the maintenance tests. We recommend the use of the following equipment when performing M Series Maintenance Tests: • ZOLL Medical Electrode Adapter from Fluke Biomedical (ZOLL Part Number 3010-0378). • QED 6 Defibrillator Analyzer • MFC Test Port Connector, 1004-0053-99 • Fluke Biomedical 601 Pro Series International Safety Analyzer. • ECG Simulator; 12 Lead Simulator for 12 Lead test (e.g., Symbio CS1201). • Stop watch. • Standard series II PC flash memory cards. • 1 red miniature alligator to miniature alligator test lead. • 1 black miniature alligator to miniature alligator test lead. • DC power supply (15 amp minimum). • 0.1 ohm 1% resistor (1/4 watt or greater). • 1000 ohm 1% resistor (1/4 watt or greater). • Fluke 75 Multimeter or equivalent. • Printer Paper. • Battery. • AC line cord. • 3 lead, 5 lead and 12 lead ECG cables. (12 lead cable needed if 12 lead option is installed.
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M Series Service Manual
Equipment You Need for the M Series Options Maintenance Tests • Fluke Biomedical Index 2 SpO2 Simulator or equivalent. (For SpO2 units only.) • SpO2 cable and sensor (if option is installed). • EtCO2 cable, and CAPNOSTAT 3 Mainstream cable with airway adapter, or CAPNOSTAT 3 Sidestream cable with cannula (if option is installed). • Novametrix Capnostat Simulator Yb 1265/7100 • Paddles (if used). • ) • Fluke Biomedical BP Pump 2 NIBP Monitor Analyzer (For NIBP units only) with NIBP cable and cuff (if NIBP option is installed), or • Fluke Biomedical Cufflink Analyzer (if NIBP option is installed) • IBP Temperature Simulator 9100-0402-TF • DNI Nevada 214B Patient SImulator, with M Series interface cable NOTE The Fluke Biomedical BP Pump NIBP Monitor Analyzer and the Fluke Biomedical BP Pump NIBP Analyzer use different technologies for testing NIBP monitors and therefore, the manual provides two different procedures for performing the NIBP Volume Leak test with each of these types of test equipment.
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M Series Service Manual
1.0 Physical Inspection of the Unit Tools Needed
Battery.
Test Setup
None. Observe this...
1.1
Pass/Fail/NA
Housing
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Is the unit clean and undamaged?
1.2
Does the unit show signs of excessive wear?
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1.3
Does the handle work properly?
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1.4
Does the recorder door open and close properly?
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1.5
Are input connectors clean and undamaged?
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1.6
Are there any cracks in the housing?
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1.7
Do the front panel or selector switches have any damage or cracks?
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1.8
Are there any loose housing parts?
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1.9
Cables
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Are all cables free of cracks, cuts, exposed or broken wires?
1.10
Are all cable bend/strain reliefs undamaged and free of excessive cable wear?
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1.11
Paddles
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Do the adult and pedi plates have major scratches or show signs of damage?
1.12
Do the adult shoes slide on and off easily to expose the covered pedi plates?
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1.13
Are the paddles clean (e.g., free of gel) and undamaged? (if applicable)
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M Series Service Manual Observe this...
1.14
Pass/Fail/NA
Battery
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Place battery in battery well.
1.15
Is the battery seated in the battery well correctly?
Record your results on the Maintenance Test Checklist.
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o o
M Series Service Manual
2.0 Front Panel Button Test Tools Needed Test Setup
QED 6 Defibrillator Analyzer • Install strip chart paper into the recorder tray. • Install the battery in the unit or connect the A/C power cord to the unit and then plug the cord into an electrical outlet. • Connect the universal cable and ECG cable (3 lead, 5 lead, or 12 lead) to the QED 6 Analyzer (or equivalent). Do this...
Verify that...
Pass/Fail/ NA
Turn the selector switch to MONITOR.
The unit sounds 4 beep tones. PADS and MONITOR display on the monitor.
o o
(For AED units, turn the selector switch to ON and select Manual mode.)
Note: PADS is a factory default setting.
2.2
Set the QED 6 analyzer to NSR of 120 BPM. To check the size of the ECG waveform, press the SIZE button.
As you press the SIZE button five times (0.5, 1.0, 1.5, 2.0, 3.0), the size of the ECG waveform appropriately changes on the display.
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2.3
Press the ALARM SUSPEND button.
Alarm symbol changes from disabled to enabled. If the alarm sounds, press the ALARM SUSPEND button to turn it off. The alarm will only be suspended for 90 seconds at this point. Press and hold the ALARM SUSPEND button for 3 seconds to disable alarms.
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2.4
Press the RECORDER button.
The strip chart paper moves out of the unit from the paper tray. Check that the correct time, date, ECG lead annotation and waveform are recorded on the paper. (Set Time and Date, if necessary.)
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2.5
Open the paper compartment door, then press the RECORDER button.
The CHECK RECORDER message appears on the monitor.
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2.6
Close the paper compartment door, then press the RECORDER button.
The strip chart paper flows out of paper tray and the monitor no longer displays the CHECK RECORDER message.
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2.1
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M Series Service Manual Do this...
Verify that...
Pass/Fail/ NA
2.7
Press the RECORDER button.
The strip chart paper stops flowing out of the paper tray.
o o o
2.8
Press the VOLUME softkey.
The volume bar graph displays.
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o
o
o
o
o
o
Note: The QRS tone is on or off. There is no gradual change in volume. If equipped, voice prompts are gradual. Note: The voice volume has 5 settings. Setting 3 is in the mid-range.
2.9
Press the INC softkey.
The bar graph appears on the display, indicating an increase in volume.
Note: This action does not increase the volume of the unit’s audio prompts.
2.10
Press the DEC softkey.
The bar graph appears on the display, indicating a decrease in volume. Verify that pressing the DEC softkey until only the last bar appears silences the unit’s audio prompts, otherwise the volume of the audio prompts does not decrease.
2.11
Press the CONTRAST button.
The monitor screen displays the Contrast Menu.
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2.12
Press the INC softkey.
The screen contrast and bar graph increases on the display.
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2.13
Press the DEC softkey.
The screen contrast and bar graph decreases on the display.
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2.14
Press the SUMMARY button.
The monitor screen displays the Summary menu, showing the summary report options.
o o o
2.15
Press the CODEMARKER button.
The monitor screen displays the Code marker menu.
o o o
2.16
Connect to AC or DC current and install the battery. Turn the unit off.
The CHARGER ON indicator lights (either the Green or Amber indicator lights).
o o o
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M Series Service Manual Do this...
Verify that...
Pass/Fail/ NA
2.17
Remove the battery.
The charger light alternately flashes green and amber.
o
o
2.18
Replace the battery and the turn unit on.
The amber charger light illuminates.
o
o
2.19
Press the ANALYZE button.
The SELECT DEFIB MODE message appears on the monitor (for manual devices).
o o o
2.20
Connect the universal cable to the QED 6. Move the selector switch to DEFIB. Select 2J. Press the CHARGE button.
The display shows that the unit is charging. The SHOCK button lights when the unit is charged, and the Ready tone for DEFIB sounds.
o o o
2.21
Press and hold the ENERGY SELECT down arrow.
The unit discharges internally and selected energy decrements to 1J.
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2.22
Press and release the ENERGY SELECT up arrow 19 times.
The following selections appear: Verify the following energy amounts display incrementally:
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Biphasic:2-10, 15, 20,30, 50, 75, 100,120, 150, 200J Monophasic(DSW): 2-10, 15,20,30,50,75, 100, 150, 200, 300, 360J
2.23
Press the CHARGE button.
The display shows the unit charged up to 200J (360J monophasic) and the SHOCK button lights.
o o o
2.24
Press the SHOCK button.
The unit discharges and the SHOCK button is no longer illuminated. A 15 second strip chart automatically prints, displaying the number of joules delivered (if equipped with recorder and configured to print event).
o o o
Record your results on the Maintenance Test Checklist.
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M Series Service Manual
3.0 3, 5, and 12 Leads Test Tools Needed:
3 lead, 5 lead, and 12 lead cables. Test each cable separately. QED 6 Defibrillator Analyzer.
Test Setup:
The M Series unit must be configured to display ECG LEAD OFF message. Connect the lead wires appropriate to each test to the QED 6 Defibrillator Analyzer. Do this...
Observe this...
Pass/Fail/ NA
3.1
Turn the selector switch to MONITOR. Select leads.
The monitor displays the NO ECG LEADS OFF message.
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3.2
Disconnect one lead from the simulator.
The monitor displays the ECG LEAD OFF message within 3 seconds (if configured).
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3.3
Reconnect the lead. Repeat step 3.2 with the remaining leads.
The ECG LEAD OFF message appears when the lead is disconnected and clears the lead is reconnected.
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3.4
Repeat 3.2 and 3.3 for 5 lead and 12 lead cables.
Note: If heart rate alarm sounds, press and hold the
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ALARM SUSPEND button for 4 seconds to disable the alarms. Note: When testing the 12 lead cable, the ECG LEAD OFF message displays when you pull off a limb lead. When you pull off a V lead, the ECG VX LEAD OFF message displays, where “X” is the number between 1 and 6.
Record your results on the Maintenance Tests Checklist.
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M Series Service Manual
4.0 Power Supply Test (Optional) Tools Needed:
• 1 red miniature alligator to miniature alligator test lead. • 1 black miniature alligator to miniature alligator test lead. • DC power supply (15 Amp minimum). • 0.1 ohmresistor (¼W or greater). • 1000 ohm 1% resistor (¼W or greater). • Fluke 75 multimeter or equivalent.
Test Setup:
Make sure the unit and power supply are turned off. Connect one end of the black lead to the “-” terminal in the battery well. Connect the other end of the black lead to the “-” terminal of the power supply. Connect the red lead to “+” terminal socket of the battery well. Use the middle pin with the plastic guard around it. Connect the other end of the red lead to the “+” terminal of the power supply. Set the power supply voltage to 7V.
CAUTION
Be sure to connect the power supply properly to the M Series battery well terminals or damage to the unit may result. Do NOT raise the power supply voltage above 12V.
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