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LIFEPAK 20 Defibrillator/Monitor Table of Contents
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Preface
Modes of
Operation
Preventive
Maintenance
Safety
Performance
Inspection
Battery
Maintenance
Device
Description
Instrument
Calibration
Replacement
Procedures
Operating
Instructions
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LIFEPAK 20 Defibrillator/Monitor Section Contents
Preface
This service manual describes how to maintain, test, troubleshoot, and repair the
LIFEPAK 20 defibrillator/monitor. A separate publication, the LIFEPAK 20
Defibrillator/Monitor Operating Instructions, is for use by physicians,
clinicians, and emergency care providers. The operating instructions provide
step-by-step instructions as well as operator-level testing and maintenance.
Note:Hyperlinks appear in blue text. Text that indicates a control, buttons,
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ADVISORY
This section covers the following topics:
control and
EVENT
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Trademarks
Using Bookmarks
Using Thumbnails
Navigating Through the Manual
Topic Navigation
Accessing Acrobat Help
Viewing Other Medtronic Documents
Service Personnel Qualifications
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LIFEPAK 20 Defibrillator/Monitor Preface
Preface
(Continued)
Contacting Medtronic
Responsibility for Information
Device Tracking
Service Information
Warranty Information
Configuration Information
Glossary
Acronyms
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LIFEPAK 20 Defibrillator/Monitor Preface
Preface
Trademarks
1-5
PHYSIO-CONTROL, LIFEPAK, and FAST-PATCH are registered trademarks of
Medtronic Physio-Contol Corp.
QUIK-COMBO, CODE SUMMARY, REDI-PAK, PARTSLINE, Shock Advisory
System, and ADAPTIV are trademarks of Medtronic Physio-Control Corp.
Medtronic is a registered trademark of Medtronic, Inc.
MICROSOFT and WINDOWS are registered trademarks of Microsoft
Corporation in the US and/or other countries.
Pentium is a registered trademark of Intel Corporation.
Adobe and Acrobat are registered trademarks of Adobe Systems Incorporated.
Tektronix is a registered trademark of Tektronix Incorporated.
BIO-TEK is a registered trademark of Bio-Tek Instruments, Inc.
QED is a trademark of Bio-Tek Instruments, Inc.
ACCUSPLIT is a registered trademark of Accusplit Corporation.
Masimo is a registered trademark of Masimo Corporation.
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Preface
Using Bookmarks
(Continued)
1-7
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Preface
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1-8
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Preface
Navigating Through the
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1-9
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LIFEPAK 20 Defibrillator/Monitor Preface
Preface
Topic Navigation
Accessing Acrobat Help
1-10
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LIFEPAK 20 Defibrillator/Monitor Preface
Preface
Viewing Other
Medtronic Documents
1-11
The following additional online documents are included on this CD-ROM:
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LIFEPAK 20 Defibrillator/Monitor Preface
Preface
Service Personnel
Qualifications
1-12
Service personnel must be properly qualified and thoroughly familiar with the
operation of the LIFEPAK 20 defibrillator/monitor. They must meet at least one of
the following requirements (or the equivalent):
■
Associate of Applied Science, with an emphasis in biomedical electronics
■
Certificate of Technical Training, with an emphasis in biomedical electronics
■
Equivalent biomedical electronics experience
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LIFEPAK 20 Defibrillator/Monitor Preface
Preface
Contacting Medtronic
1-13
Medtronic Physio-Control
11811 Willows Road Northeast
Post Office Box 97006
Redmond, WA 98073-9706 USA
Telephone: 1.425.867.4000
Toll Free (USA only): 1.800.442.1142
Fax: 1.425.867.4121
Internet: www.physiocontrol.com
www.medtronic.com
Medtronic Europe S.A.
Medtronic Physio-Control
Rte. du Molliau 31
Case postale 84
1131 Tolochenaz
Switzerland
Telephone: 41.21.802.7000
Fax: 41.21.802.7900
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LIFEPAK 20 Defibrillator/Monitor Preface
Preface
Responsibility for
Information
1-14
This service manual describes the methods required to maintain, test, and repair
the LIFEPAK 20 defibrillator/monitor. This manual does not cover operation of
the LIFEPAK 20 defibrillator/monitor. Qualified service personnel must consult
both the LIFEPAK 20 Defibrillator/Monitor Operating Instructions and the
LIFEPAK 20 Defibrillator/Monitor Service Manual to obtain a complete
understanding of the use and maintenance of the device.
It is the responsibility of our customers to ensure that the appropriate person(s)
within their organization have access to the information in this manual, including
any warnings and cautions used throughout the LIFEPAK 20 Defibrillator/Monitor
Service Manual.
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LIFEPAK 20 Defibrillator/Monitor Preface
Preface
!USA
Device Tracking
1-15
The U.S. Food and Drug Administration requires defibrillator manufacturers and
distributors to track the location of their defibrillators. The address to which this
particular device was shipped is now listed as the current tracking location. If the
device is located somewhere other than the shipping address or the device has
been sold, donated, lost, stolen, exported, or destroyed, or if the device was not
obtained directly from Medtronic, please call the device tracking coordinator at
1.800.426.4448 to update this vital tracking information.
General information related to device tracking:
It is important to maintain accurate records of defibrillator location within your
facility or system. Maintenance of such records eases the process of locating
defibrillators should it be necessary to modify them. Defibrillators should be
tracked by both the manufacturer’s part number and serial number. Internal
asset or tracking numbers may also be useful in maintaining adequate control of
defibrillators.
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LIFEPAK 20 Defibrillator/Monitor Preface
Preface
Service Information
1-16
Before attempting to clean or repair any assembly in this device, service
personnel should be familiar with the information provided in the Preventive
Maintenance section of this manual.
Service personnel should inspect any defibrillator that has been dropped,
damaged, or abused to verify that the device is operating within the performance
standards listed in the Performance Inspection Procedure (PIP), and that the
leakage current values are acceptable.
Replacement procedures for the LIFEPAK 20 defibrillator/monitor are limited to
those items accessible at the subassembly level. Replacements and
adjustments must be made by service personnel qualified by appropriate
training and experience. Replacements at the subassembly level simplify repair
and servicing procedures, and help ensure correct device operation and
calibration.
To obtain Medtronic service and maintenance for your LIFEPAK 20 defibrillator/
monitor, contact your local service or sales representative. In the USA, call
Medtronic Technical Services at 1.800.442.1142. Outside the USA, contact your
local Medtronic representative.
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LIFEPAK 20 Defibrillator/Monitor Preface
Preface
Warranty Information
Masimo Use
Agreement
1-17
Refer to the warranty statement included in the LIFEPAK 20 Defibrillator/
Monitor Operating Instructions – Maintaining the Equipment.
No Implied License — Possession or purchase of this device does not convey
any express or implied license to use the device with replacement parts that
would, alone, or in combination with this device, fall within the scope of one or
more of the patents relating to this device.
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LIFEPAK 20 Defibrillator/Monitor Preface
Preface
Configuration
Information
1-18
This service manual covers existing LIFEPAK 20 defibrillator/monitor devices
and options through the following revisions:
■
LIFEPAK 20 defibrillator/monitor basic device with ECG
■
Pacing Option
■
SpO2 Option
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LIFEPAK 20 Defibrillator/Monitor Preface
(C
)
Preface
Glossary
The following are definitions of terms used throughout this service manual.
■
Automated External Defibrillator (AED) — The LIFEPAK 20
defibrillator/monitor uses an ECG analysis Shock Advisory System (SAS) to
advise the device operator if it detects a shockable or nonshockable rhythm.
For more information about CPSS and SAS, see the operating instructions
– Shock Advisory System.
■
Biphasic — Property of the shock waveform generated by the LIFEPAK 20
defibrillator/monitor. The biphasic waveform is characterized by a positive
current phase followed by a reverse current phase of shorter duration and
decreased magnitude. The waveform pulse characteristic is biphasic
truncated exponential (BTE).
■
CODE SUMMARY™ Report — A summary report that includes the ECG
segments associated with key events such as analysis or shock. See the
operating instructions – Data Management for a sample CODE
SUMMARY Report.
1-19
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LIFEPAK 20 Defibrillator/Monitor Preface
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)
Preface
Glossary (Continued)
■
Continuous Patient Surveillance System (CPSS) — A feature that monitors
the patient ECG in
CPSS is active when the AED Mode indicator is illuminated or the
ALARM
is selected after pressing the
LEADS
PADDLES
or
for a potentially shockable rhythm.
VF/VT
ALARMS
control (manual mode). The
CPSS operates in conjunction with the Shock Advisory System™ (SAS). For
more information about CPSS and SAS, refer to the operating instructions
– Shock Advisory System.
■
Event Log Summary — A report summarizing important events for a
particular patient record; part of the CODE SUMMARY Report.
■
FAST-PATCH disposable defibrillation/ECG electrodes — An electrode
system that allows delivery of defibrillation therapy to the patient.
■
QUIK-COMBO™ pacing/defibrillation/ECG electrodes — An electrode
system that allows delivery of pacing and defibrillation therapy to the patient.
■
QUIK-COMBO patient simulator — A combination lead tester/patient cardiac
rhythm simulator. The simulator is designed for use in training clinical
1-20
personnel in the operation of the LIFEPAK 20 defibrillator/monitor.
■
REDI-PAK™ preconnect system — A variant of the QUIK-COMBO pacing/
defibrillation/ECG electrodes system. The system allows QUIK-COMBO
pacing/defibrillation/ECG electrode cable connection without removing the
electrodes from their air-tight sealed pouch until needed.
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LIFEPAK 20 Defibrillator/Monitor Preface
Preface
Glossary (Continued)
■
Shock Advisory System™ (SAS) — A computerized ECG analysis system
for use in the detection of a shockable rhythm. For more information about
CPSS and SAS, see the operating instructions – Shock Advisory
System.
■
SpO2 — A noninvasive pulse oximeter that checks the saturation of oxygen
in arterial blood.
■
Test Load — A device that provides an external defibrillation test load for the
defibrillator/monitor. The test load connects to the patient connector on the
device.
1-21
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Preface
Acronyms
1-22
The following is a list of acronyms and abbreviations used in this manual.
TermDescription
AAMIAssociation for the Advancement of Medical Instrumentation
ADCAnalog-to-Digital Conversion
AEDAutomated External Defibrillator
AHAAmerican Heart Association
ANSIAmerican National Standards Institute
BTEBiphasic Truncated Exponential
BFElectrically isolated, external body connection
BPMBeats Per Minute
CFElectrically isolated, direct cardiac connection
CPRCardiopulmonary Resuscitation
CPUCentral Processing Unit
CPSSContinuous Patient Surveillance System
DUARTDual Universal Asynchronous Receiver/Transmitter
DMMDigital Multimeter
ECGElectrocardiogram
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LIFEPAK 20 Defibrillator/Monitor Preface
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)
Preface
Acronyms (Continued)
1-23
.Acronyms
TermDescription
EMSEmergency Medical Service
ESDElectrostatic Discharge
ESUElectrosurgical Unit
HRHeart Rate
IECInternational Electrical Commission
LCDLiquid Crystal Display
LEDLight Emitting Diode
NHAAPNational Heart Attack Alert Program
NSRNormal Sinus Rhythm
OEMOriginal Equipment Manufacturer
RRRespiration Rate
PCPersonal Computer
DSPDigital Signal Processor
PCBPrinted Circuit Board
PIPPerformance Inspection Procedure
PPMPulses Per Minute
This section describes the general safety conventions, terms, and symbols used
in this service manual or on the LIFEPAK 20 defibrillator/monitor. This
information is intended to alert service personnel to recommended precautions
in the care, use, and handling of this medical device.
Terms
General Warnings and Cautions
Symbols
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LIFEPAK 20 Defibrillator/Monitor Safety
Safety
Ter m s
2-2
The following terms are used in this service manual or on the various
configurations of the LIFEPAK 20 defibrillator/monitor. Familiarize yourself with
their definitions and significance.
Danger:Immediate hazards that will result in serious personal injury or death.
Warning:Hazards or unsafe practices that could result in serious personal
injury or death.
Caution:Hazards or unsafe practices that could result in device or property
damage.
Note:Points of particular interest for more efficient or convenient device
operation; additional information or explanation concerning the
subject under discussion.
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LIFEPAK 20 Defibrillator/Monitor Safety
Safety
General Warnings and
Cautions
2-3
The following are general warnings and cautions. Keep these warnings and
cautions in mind when working with the LIFEPAK 20 defibrillator/monitor. More
specific warnings and cautions appear throughout this service manual and the
LIFEPAK 20 defibrillator/monitor Operating Instructions.
WARNINGS!
Possible fire or explosion. Do not service this device in the presence of
flammable gases, anesthetics, or oxygen sources.
Shock or fire hazard. Do not immerse any portion of this device in water or
other fluids. Avoid spilling any fluids on the device or accessories. If the
device is ever immersed in water or other fluids, remove the batteries and
disconnect ac power until the device can be serviced.
Patient hazard. Do not mount the device directly above patient. Place the
device in a location where it cannot harm the patient should it fall from its
shelf or other mount.
Shock or fire hazard. Equipment or accessories improperly interconnected
to each other can be a source of ignition or cause a shock. Make sure that
all equipment is interconnected safely.
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LIFEPAK 20 Defibrillator/Monitor Safety
Safety
General Warnings and
Cautions (Continued)
2-4
WARNING!
Shock hazard. Servicing of this device must be performed by properly
trained individuals. This device may retain potentially lethal charges
accessible inside the device at any time – even when off. Follow
procedures carefully for discharging the A13 Energy Storage Capacitor.
CAUTION!
Possible equipment damage. This device may be damaged by mechanical
or physical abuse such as immersion in water or dropping. If the device
has been abused, remove it from use and contact qualified service
personnel.
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LIFEPAK 20 Defibrillator/Monitor Safety
Safety
Symbols
2-5
The following list includes symbols that may be used in this service
manual or on various configurations of the LIFEPAK 20 defibrillator/monitor
and accessories. Some symbols may not be relevant to your device or used in
every country.
[signal] Input
[signal] Output
ac voltage
Alarm off
Alarm on
Attention, consult accompanying documents
Biphasic defibrillator shock
Canadian Standards Association certification for Canada
and the United States
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LIFEPAK 20 Defibrillator/Monitor Safety
Safety
Symbols (Continued)
YYYY
!USA
2-6
Date of manufacture
DC voltage
Defibrillation protected, type BF patient connection
Defibrillation-proof type CF terminal
Equipotential connector
Event marker
For USA audiences only
Fragile/Breakable
Handle with care
Fuse
Greater than
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