Physio Control Lifepak CR2 LIFELINKcentral User manual

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This document is electronically signed in the Physio-Control, Inc. Product Lifecycle Management
(PLM) System. Approvals can be obtained from the PLM system which displays the selected
approvers, their approval roles, and approval dates.
PROPRIETARY AND CONFIDENTIAL DOCUMENT FOR PHYSIO-CONTROL, INC. USE ONLY. This
document is property of Physio-Control and may not be used, reproduced, published or
disclosed to others without authorization from Physio-Control.
Owner
Corporate
Attachments (Optional):
Qty
Pages
Page Sequencing
Change Description
1. Added supported Wi-Fi frequency, 2.4 GHz and noted 5 GHz is not a supported frequency.
2. Added Warranty Void Letter template PNs for Tire 2 countries.

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Table of Contents
Table of Contents............................................................................................................................................................... 2
Preface ............................................................................................................................................................................... 5
Disclaimer....................................................................................................................................................................... 5
Trademarks .................................................................................................................................................................... 5
Definitions, Acronyms, and Abbreviations..................................................................................................................... 5
Contacting Physic-Control.............................................................................................................................................. 7
Service Personnel Qualifications.................................................................................................................................... 8
Service Information........................................................................................................................................................ 8
Recycling information .................................................................................................................................................... 9
Configuration Information ............................................................................................................................................. 9
Warranty ........................................................................................................................................................................ 9
Tamper Proof Label........................................................................................................................................................ 9
Safety - Technical Description.......................................................................................................................................... 10
Serial Label Information............................................................................................................................................... 10
Symbols ........................................................................................................................................................................ 10
General Danger and Warnings Statements ................................................................................................................. 12
LIFEPAK CR2 Defibrillator Description.......................................................................................................................... 15
LIFEPAK CR2 Defibrillator Specifications...................................................................................................................... 15
CR2 Device Description .................................................................................................................................................... 20
Physical Description and Features ............................................................................................................................... 20
Functional Descriptions................................................................................................................................................ 21
Modes of Operation..................................................................................................................................................... 22
Battery and Time.......................................................................................................................................................... 23
Electrodes .................................................................................................................................................................... 23
Connectivity Module.................................................................................................................................................... 24
Device Communication ................................................................................................................................................ 25
Initial Device Setup Overview ...................................................................................................................................... 30
CR2 Trainer Device Description........................................................................................................................................ 31
CR2 Trainer Device Overview....................................................................................................................................... 31

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CR2 Trainer Service ...................................................................................................................................................... 32
CR2 Trainer Parts ......................................................................................................................................................... 32
Data Management Solution............................................................................................................................................. 33
LIFELINK and LIFENET account creation....................................................................................................................... 33
LIFELINK or LIFENET Password Reset ........................................................................................................................... 33
Connectivity ..................................................................................................................................................................... 34
Download and Install Wi-Fi Configuration Tool ........................................................................................................... 34
Store Wi-Fi Settings on CR2 ......................................................................................................................................... 35
Confirm Connection to LIFELINK or LIFENET................................................................................................................ 43
Check CR2 Device Readiness Status............................................................................................................................. 44
Monthly Auto-Check-In................................................................................................................................................ 46
Change or Remove Wi-Fi Settings on the CR2 ............................................................................................................. 47
Change Setup Options or Update Software..................................................................................................................... 50
Update Setup Options or Software from LIFENET or LIFELINK.................................................................................... 50
Applying Updates with Wi-Fi or Cellular Connection................................................................................................... 54
Applying Updates with USB connection ...................................................................................................................... 54
Monitor Update Status ................................................................................................................................................ 59
View Software Version................................................................................................................................................. 61
Viewing LIFEPAK CR2 Log Files......................................................................................................................................... 63
View Log from LIFENET System.................................................................................................................................... 63
View Log from LIFELINK ............................................................................................................................................... 65
View WCT Log .............................................................................................................................................................. 68
Post AED Event Services................................................................................................................................................... 71
LIFELINK AED Event Service.......................................................................................................................................... 71
LIFENET AED Event Service for EMS customers........................................................................................................... 74
Using DT EXPRESS Data Transfer Software to download an AED Event ...................................................................... 75
Preventive Maintenance.................................................................................................................................................. 81
Device self-test............................................................................................................................................................. 81
Device Daily, Weekly, and Monthly Tests.................................................................................................................... 82
Battery Maintenance ................................................................................................................................................... 83
Performance Inspection Procedure (PIP)..................................................................................................................... 85

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Replacement Procedure .................................................................................................................................................. 85
Supply and Replacement Parts .................................................................................................................................... 85
Lid Replacement........................................................................................................................................................... 86
Handle or Carrying Case Replacement......................................................................................................................... 87
USB Cover Replacement .............................................................................................................................................. 88
Battery Replacement ................................................................................................................................................... 88
Electrode Replacement................................................................................................................................................ 88
Troubleshooting............................................................................................................................................................... 89
Readiness indicator...................................................................................................................................................... 89
No Voice Prompt.......................................................................................................................................................... 90
Unable to establish USB connection to a computer .................................................................................................... 91
Unable to establish Wi-Fi network connection............................................................................................................ 91
Connection Failed ........................................................................................................................................................ 92
Unable to change/update the device setup options ................................................................................................... 92
Using Voice Prompts for Troubleshooting................................................................................................................... 92
Error Codes .................................................................................................................................................................. 94
Tables of useful information............................................................................................................................................ 97
LIFENET System URL..................................................................................................................................................... 97
List of Declaration of Conformity Documents ............................................................................................................. 98
List of Reference Document and Tool.......................................................................................................................... 98
Wi-Fi Signal Noise Ratio (SNR) ..................................................................................................................................... 99
System Context Diagram............................................................................................................................................ 100
System Component View........................................................................................................................................... 101
Sample Warranty Void Letter .................................................................................................................................... 103

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Preface
This Service manual describes how to support the following tasks for the LIFEPAK CR2 defibrillator:
•Connecting to LIFELINK or LIFENET System
•Confirming connectivity
•Checking self-test results
•Changing device setup options
•Updating device software
•Post AED event support
•Replacement Procedure
•Troubleshooting common issues
•Preventive Maintenance
Another publication, the LIFEPAK CR2 Defibrillator Operating Instructions, is for use by physicians, clinicians, and
emergency care providers. The operating instructions provide step-by-step instructions for use, as well as operator-
level testing and maintenance.
Disclaimer
All the screenshots or pictures in this document are for the example only; they are subject to change without matching
the latest versions of software.
Trademarks
LIFEPAK, LIFENET, QUIK-STEP, LIFELINKcentral, cprCOACH, cprINSIGHT, Shock Advisory System, SAS, and
ClearVoice are trademarks of Physio-Control, Inc. CODE SUMMARY, CODE-STAT, and DT EXPRESS are
Trademarks of Physio-Control, Inc. Microsoft and Windows are registered trademarks of Microsoft Corporation in the
US and/or other countries. Specifications are subject to change without notice.
Definitions, Acronyms, and Abbreviations
802.11 Commonly known as "Wi-Fi," the IEEE 802.11 standards provide the wireless counterpart to
Ethernet, and the Wi-Fi Alliance certifies products. The versions have the suffixes 11a, 11b,
11g, 11n and 11ac; the latest being 802.11ac. The original 20 MHz channel was increased
to 40 MHz in 11n and to 80 and 160 MHz in 11ac.
AED Automated External Defibrillator
ASR Account Support Representative - a Physio-Control support team member dedicated to
supporting customers with a full AED support service contract.
CR2 LIFEPAK CR2 Defibrillator
DTx DT Express™ Data Transfer Software
FSR Field Service Representative (services products in the Field)

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LIFELINK LIFELINKcentral AED Program Manager, a user interface on the LIFENET system designed
for Workplace and Community Customers to view and manage their AED programs
including devices, maintenance, and training.
LIFENET LIFENET System including website
LDA LIFENET Device Agent,
OI Operating Instructions
PCO file Physio Case Object file, a data format for a combination of device data and user-entered
data. Data in this format can be imported and exported by Physio-Control data management
applications.
SmartDesk Data Solutions Technical Support
WCT Wireless Configuration Tool is a software Application to configure Wi-Fi connection in the
LIFEPAK CR2® Defibrillator.
Workplace
and
Community
A Physio-control customer segment that represents public access locations for Automated
External Defibrillators such as schools, government agencies, airports, health clubs, and
workplaces.

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Contacting Physic-Control
Physio-Control, Inc.
11811 Willows Road NE
Redmond, WA 98052-2003 USA
Telephone: [phone]
Toll Free (USA only): 800.442.1142
Fax: [phone]
Internet: www.physio-control.com
Physio-Control Operations Netherlands B.V.
Galjoenweg 68
6222 NV Maastricht
The Netherlands
Physio-Control Australia Pty Ltd
Suite 4.01
15 Orion Road
Lane Cove
NSW 2066
Australia
Regional Phone Number and LIFELINKcentral URLs:
Region
Phone Number
LIFELINKcentral™ AED Program Manager
website
Australia
1800 987 982
https://lifelink-au.lifenetsystems.com
Austria / Österreich
01 74040 2866
https://lifelink-at.lifenetsystems.com
Belgium / België / Belgique
0800 263 77
https://lifelink-be.lifenetsystems.com
Bulgaria / България
0800 450 0013
https://lifelink-bg.lifenetsystems.com
Canada
800 895 5896
https://lifelink-ca.lifenetsystems.com
Cyprus / Κύπρος
0800 450 0013
https://lifelink-cy.lifenetsystems.com
Czech Republic / Ceská republika
420 602 565 977
https://lifelink-cz.lifenetsystems.com
Denmark / Danmark
69 60 70 58
https://lifelink-dk.lifenetsystems.com
Estonia / Viro
0800 450 0013
https://lifelink-ee.lifenetsystems.com
Faroe Islands / Färsaaret
358 98764630
https://lifelink-fo.lifenetsystems.com
Finland / Suomi
09 876 4630
https://lifelink-fi.lifenetsystems.com
France
01 70 36 86 98
https://lifelink-fr.lifenetsystems.com
Germany / Deutschland
02131 6617 000
https://lifelink-de.lifenetsystems.com
Greece / Ελλάδα
0800 450 0013
https://lifelink-gr.lifenetsystems.com
Greenland / Grønland
0800 450 0013
https://lifelink-gl.lifenetsystems.com
Guam
61 9415 5900
https://lifelink.lifenetsystems.com
Hong Kong /
香港
65 6718 2080
Not applicable
Hungary / Magyarország
1 882 3565
https://lifelink-hu.lifenetsystems.com
Iceland
0800 450 0013
https://lifelink-is.lifenetsystems.com
Ireland
44 808 258 0094
https://lifelink-ie.lifenetsystems.com
Israel
0800 450 0013
https://lifelink-il.lifenetsystems.com
Italy / Italia
02 6602 6100
https://lifelink-it.lifenetsystems.com
Japan /
日本
0120 715 545
https://lifelink-jp.lifenetsystems.com
Korea /
대한민국
65 6718 2080
Not applicable
Latvia / Latvija
0800 450 0013
https://lifelink-lv.lifenetsystems.com
Liechtenstein
0800 450 0013
https://lifelink-li.lifenetsystems.com

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Region
Phone Number
LIFELINKcentral™ AED Program Manager
website
Lithuania / Lietuva
0800 450 0013
https://lifelink-lt.lifenetsystems.com
Luxembourg / Luxemburg
800 8 8075
https://lifelink-lu.lifenetsystems.com
Malta
0800 450 0013
https://lifelink-mt.lifenetsystems.com
Middle East and Africa
961 4 718 414
Not applicable
Netherlands / Nederland
0800 450 0013
https://lifelink-nl.lifenetsystems.com
New Zealand
0800 937 346
https://lifelink-nz.lifenetsystems.com
Norway / Norge
22 83 88 00
https://lifelink-no.lifenetsystems.com
Poland / Polska
22 56 91 210
https://lifelink-pl.lifenetsystems.com
Portugal / República Portuguesa
351 210 415 920
https://lifelink-pt.lifenetsystems.com
Puerto Rico
800 442 1142
https://lifelink.lifenetsystems.com
ﺮﻄﻗ / Qatar
31 433 68 66 70
https://qa.lifenetsystems.com
Romania / România
0800 450 0013
https://lifelink-ro.lifenetsystems.com
Singapore /
新加坡
65-6718 2080
https://sg.lifenetsystems.com
Slovak Republic / Slovenská
Republika
420 602 565 977 https://lifelink-sk.lifenetsystems.com
Slovenia / Slovenija
0800 450 0013
https://lifelink-si.lifenetsystems.com
Spain / España
091 843 1509
https://lifelink-es.lifenetsystems.com
Sweden / Sverige
0770 870 120
https://lifelink-se.lifenetsystems.com
Switzerland / Schweiz / Suisse
0800 00 66 33
https://lifelink-ch.lifenetsystems.com
United Arab Emirates
31 433 68 66 70
https://ae.lifenetsystems.com
United Kingdom
0808 258 0094
https://lifelink-gb.lifenetsystems.com
United States
800 442 1142
https://lifelink.lifenetsystems.com
US Virgin Islands
800 442 1142
https://lifelink.lifenetsystems.com
Service Personnel Qualifications
Service technicians must be properly qualified and thoroughly familiar with the operation of the LIFEPAK CR2
defibrillator. They must meet at least one of the following requirements (or the equivalent):
• Physio-Control Service Depot technicians
• Physio-Control Field Service Representatives
• 3rd Party Service Providers that have service agreements with Physio-Control
Service Information
The CR2 will not be opened for repair activities. Parts replacement is limited to the supply and replacement parts listed
in Supply and Replacement Parts
Before attempting to clean or service the device, the service technician should be familiar with the information provided
in Preventive Maintenance.
A qualified service technician (see Service Personnel Qualifications) should inspect any device that has been
dropped, damaged, tampered, or abused to verify that the device is operating within performance standards listed in
the Performance Inspection Procedures (PIP), and that the leakage current values are acceptable.
To obtain service and maintenance for your device, contact your local Physio-Control service or sales representative.
In the USA, call Physio-Control Technical Support at 1.800.442.1142. Outside the USA, contact your local Physio-
Control representative. When you call Physio-Control to request service, provide the following information:
•Model number and part number
•Serial number
•Observation of the problem that led to the call

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Recycling information
Recycle the device and its accessories at the end of their useful life.
Do not dispose of this product or its batteries in the unsorted municipal waste stream. Any batteries must be removed
from the device and disposed of separately before disposing of the device. At all times dispose of this product and its
accessories, including batteries, according to local regulations. Contact your local Physio-Control representative for
assistance, or refer to www.physio-control.com/recycling for instructions on disposing of this product.
•The device should be clean and contaminant-free prior to being recycled.
•After using disposable electrodes, follow your local clinical procedures for recycling.
•Packaging should be recycled according to national and local regulations.
Configuration Information
This service manual is relevant for the following device and options:
Unless otherwise noted, functions and features are consistent as specified throughout this manual. Differences are
noted as appropriate.
Item Number (QAD)
PN (on Serial Label)
Catalog Number (QAD)
REF (on Serial Label)
CR2-2-0000XX* 99512-0000XX*
NOTE: * XX in the PN and REF can be different on each unit depending on the order configuration of the device.
Warranty
To obtain a detailed warranty statement, contact your local Physio-Control representative or go to www.physio-
control.com
Tamper Proof Label
If the tamper-proof label shown below is broken or missing, the warranty may be void.
A customer facing warranty void letter template in different languages is available for service to use to inform
customer. See here Sample Warranty Void Letter for detail.

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Safety - Technical Description
The following information is provided to comply with Clause 7.9.3 in IEC 60601-1 (3rd Edition) for information that is
“essential for safe operation, transport and storage, and measures or conditions necessary for installing the ME
EQUIPMENT, and preparing it for use”. This information includes:
a) Explanation of information on the serial label
b) Explanation of symbols used on the device including Cl. 6 (IEC 60601-1) applicable classifications (Type BF,
IP55) and an explanation of safety signs and other symbols.
c) For reference, the general danger and warning statements from the LIFEPAK CR2 Defibrillator Operating
Instructions, 3321515.
d) A brief description of the LIFEPAK CR2 Defibrillator and its functions, and the device’s significant physical and
performance characteristics.
e) Information concerning circuit diagrams, component lists available for authorized service representatives
Serial Label Information
Symbols
The symbols in the following table may be found on the defibrillator, its accessories, or packaging.
SYMBOL
DESCRIPTION
ON/OFF button
LANGUAGE button
CHILD MODE button
SHOCK button (on semi-automatic devices)
SHOCK indicator (on fully automatic devices)

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SYMBOL
DESCRIPTION
Consult instructions for use
Warning, high voltage
General warning
Single use only
Not made with natural rubber latex
Use By date shown: YYYY-MM-DD (on electrodes)
Expiration date: YYYY-MM-DD (on battery)
Do not recharge battery
Lithium manganese dioxide battery
Defibrillation protected, type BF patient connection
Recommended storage temperature 15° to 35°C (59° to 95°F)
Keep away from sunlight
Do not place near an open flame, heat above 100°C (212°F), or
incinerate
Do not crush, puncture, or disassemble
Do not dispose of this product in the unsorted municipal waste stream.
Dispose of this product according to local regulations. See www.physio-
control.com/recycling for instructions on disposing of this product.
Enclosure ingress protection code per IEC 60529
DC voltage
Device includes RF transmitter
Indicates device is certified to applicable Japanese wireless
requirements
Complies with (USA) Federal Communications Commission regulations
China Compulsory Certification required for medical devices imported
into China
Symbol for China RoHS indicating the Environmentally Friendly Use
Period (EFUP) denoting the number of years before any substance is
likely to leak out into the environment.

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SYMBOL
DESCRIPTION
Indicates that a product complies with applicable Australian ACMA
standards
Intertek certification for Canada and the United States
Recognized component mark for Canada and the United States
Mark of conformity to applicable European Directives
Manufacturer
Date of manufacture: YYYY-MM-DD
Authorized EC representative
For USA audiences only
By prescription only
Reference number
Lot number (batch code)
Serial number
Part number
General Danger and Warnings Statements
For reference, the following are the general danger and warning statements found in the LIFEPAK CR2 Defibrillator
Operating Instructions, 3321515.
Explosion Hazard
Do not use this defibrillator in the presence of
flammable gases or anesthetics.
Possible Fire
Use care when operating this device close to oxygen
sources (such as bag-valve-mask devices or
ventilator tubing). Turn off gas source or move source
away from patient during defibrillation.
Shock Hazard
The defibrillator delivers up to 360 joules of electrical
energy. Unless used properly by following the
defibrillator's visual and audio prompts, this electrical
energy may cause serious injury or death.

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Shock or Fire Hazard
Do not immerse any portion of this defibrillator in
water or other fluids. Avoid spilling any fluids on
defibrillator or accessories. Spilled liquids may cause
the defibrillator and accessories to perform
inaccurately or fail. Do not clean with ketones or
other flammable agents. Do not autoclave or sterilize
this defibrillator or accessories unless otherwise
specified.
Possible Device Failure
Do not modify the device.
Possible Electrical Interference
This defibrillator may cause electromagnetic
interference (EMI) especially during charge and
energy transfers. EMI may affect the performance of
equipment operating in close proximity. Verify the
effects of defibrillator discharge on other equipment
prior to using the defibrillator in an emergency
situation, if possible.
Possible Electrical Interference With Device
Performance
Equipment operating in close proximity may emit
strong electromagnetic or radio frequency
interference (RFI), which could affect the
performance of this device. RFI may result in failure
to detect a shockable rhythm. If use of equipment in
close proximity is necessary, observe the device to
verify normal operation in the configuration in which
the device will be used. Avoid operating the device
near cauterizers, diathermy equipment, or other
portable and mobile RF communications equipment.
Do not rapidly key EMS radios on and off. Refer to
Separation Distances (on page Error! Bookmark
not defined.) for recommended distances of
equipment. Contact Physio-Control Technical
Support if assistance is required.
Possible Electrical Interference
This defibrillator should not be used adjacent to or
stacked with other equipment. If adjacent or stacked
use is necessary, the defibrillator should be observed
to verify normal operation in the configuration in
which it will be used.

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Possible Electrical Interference
Using cables, electrodes, or accessories not
specified for use with this defibrillator may result in
increased emissions or immunity from
electromagnetic or radio frequency interference (RFI)
which could affect the performance of this defibrillator
or of equipment in close proximity. Use only parts
and accessories specified in these operating
instructions.
Possible Improper Device Performance
Using other manufacturers’ cables, electrodes, power
adapters, or batteries may cause the device to
perform improperly and may invalidate the safety
agency certifications. Use only the accessories that
are specified in these operating instructions.
Safety Risk And Possible Equipment
Damage
MR unsafe: Keep the defibrillator away from
magnetic resonance imaging (MRI) equipment.
Shock Hazard
When instructed EVERYONE CLEAR, do not touch the
defibrillator, patient, electrode pads, or any material
or fluids in contact with the patient. Make sure no one
is touching the patient when the defibrillator shocks
the patient.
Possible Fire, Burns, and Ineffective Energy
Delivery
During defibrillation, material in contact with the
electrode pads can cause electrical sparks, skin
burns, and divert important defibrillating energy away
from the heart. Place electrode pads so that they
adhere to the skin completely. Do not allow the
electrode pads to touch each other, medication
patches, dressings, metal objects, other electrodes,
or any other material on the patient's chest.
Shock hazard
Do not touch the patient and the USB connector on
the back of the device simultaneously.

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Possible Skin Burns
During defibrillation, air pockets between the skin and
electrode pads can cause skin burns. To help prevent
air pockets, make sure electrode pads completely
adhere to the skin. Do not use damaged, expired, or
dried-out electrode pads.
Possible Skin Burns and Ineffective Energy
Delivery
Electrode pads that are dried out or damaged may
cause electrical arcing and patient skin burns during
defibrillation. Do not pull the red handle to open the
electrodes until immediately before use.
Possible Equipment Damage
Prior to using this defibrillator, disconnect from the
patient all equipment that is not defibrillator-
protected.
LIFEPAK CR2 Defibrillator Description
The LIFEPAK CR2 defibrillator is designed for indoor and outdoor use in a stationary environment. Fully automatic and
semi-automatic models are available. After the electrode pads are applied, the fully automatic model evaluates the
heart rhythm and, if a shockable rhythm is detected, delivers a shock without any responder assistance. The semi-
automatic model evaluates the heart rhythm but requires the responder to press the shock button if a shockable
rhythm is detected. Both models have voice instructions that guide the responder through the event.
The LIFEPAK CR2 defibrillator is also able to connect to the LIFELINKcentral™ AED Program Manager or LIFENET®
System account using an internet connection. The device uses either Wi-Fi, cellular, or USB to connect.
NOTE: LIFELINKcentral AED Program Manager and LIFENET System are not available in all countries.
LIFEPAK CR2 Defibrillator Specifications
All specifications are at 20°C (68°F) unless otherwise stated.
CHARACTERISTIC
DESCRIPTION
General
Classification Internally powered equipment per IEC 60601-1.
Electrical Protection Applied parts - Electrodes are defibrillation-protected, type BF patient
connection per IEC 60601-1.
Self-test When powered on, the device performs a self-test to check internal
electrical components and circuitry. The Readiness indicator stops
flashing if an error is detected.
The device also performs automatic self-tests daily, weekly, and
monthly.

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Defibrillator
Waveform Biphasic Truncated Exponential with voltage and duration
compensation for patient impedance.
Patient Impedance
Range 10 to 300 ohms. If the detected impedance is outside this range, the user is prompted to check the electrode pads and connector. The
device will not deliver a shock if impedance is outside this range.
Output Energy Configurable energy levels for Shock 1, Shock 2, and Shock 3 or
greater.
Adult mode: 150, 200, 300, or 360 joules.
Child mode: 35, 50, 75, or 90 joules.
Output Energy
Accuracy 10% of the energy setting into 50 ohms.
15% of the rated energy output into 25–175 ohms.
Rated Energy Output
Rated energy output is the nominal delivered energy based on the energy setting and patient impedance, as defined in
the following chart.
Waveform Shape and Measured Parameters

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Biphasic waveform at 200 joules, nominal
PATIENT
IMPEDANCE (
Ω
) I1 (A) I2 (A) I3 (A) I4 (A) T1
(MS) T2 (MS)
25 58.1 21.0 20.9 10.6 5.0 3.3
50 30.0 14.8 14.8 9.2 6.9 4.7
75 20.7 11.8 11.8 8.1 8.3 5.5
100 16.0 9.9 9.9 7.3 9.3 6.2
125 13.2 8.7 8.7 6.6 10.1 6.7
150 11.3 7.8 7.8 6.1 10.8 7.2
175 9.9 7.1 7.1 5.7 11.4 7.6
Biphasic waveform at 90 joules, nominal
PATIENT
IMPEDANCE (
Ω
) I1 (A) I2 (A) I3 (A) I4 (A) T1
(MS) T2 (MS)
25 33.1 12.0 11.9 6.1 5.0 3.3
50 20.1 9.9 9.9 6.2 6.9 4.6
75 13.9 7.9 7.9 5.4 8.3 5.5
100 10.7 6.7 6.7 4.9 9.3 6.2
125 8.8 5.8 5.8 4.4 10.1 6.7
150 7.6 5.2 5.2 4.1 10.8 7.2
175 6.7 4.8 4.8 3.8 11.4 7.6
Shock Advisory
System ECG analysis system used by this device. The Shock Advisory System determines whether a shock is appropriate.
Note: The fully automatic device cannot cancel delivery of a shock
after the Shock Advisory System determines a shock is advised. The
semi-automatic device cancels the shock if the SHOCK button is not
pressed within 15 seconds.
cprINSIGHT
Analysis
Technology
Additional ECG analysis system that is designed to analyze the ECG
rhythm while CPR is being performed. The cprINSIGHT Analysis
Technology can be set to be ON or OFF. When this feature is turned
on, the voice prompts change so the user is instructed to continue
CPR during analysis.
Device Capacity With new battery:
Provides 166 200-joule shocks (with 1 minute of CPR between
shocks), 103 360-joule shocks (with 1 minute of CPR between
shocks), or 900 minutes of operating time.
When device has just reached a low battery state (Readiness
indicator has stopped flashing):
Provides 39 200-joule shocks (with 1 minute of CPR between
shocks), 24 360-joule shocks (with 1 minute of CPR between
shocks), or 210 minutes of operating time.

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Shock Ready Time Note: These times apply for a device that has just reached a low
battery state (Readiness indicator has stopped flashing).
Fully automatic device:
The time to charge to 360 joules after electrode pads are applied
is 35 seconds or less.
The time to charge to 360 joules after power is turned on
is 45 seconds or less, if electrode pads are on the patient when
device is turned on.
Semi-automatic device:
The time to charge to 360 joules after electrode pads are applied
is 35 seconds or less.
The time to charge to 360 joules after power is turned on
is 45 seconds or less, if electrode pads are on the patient when
device is turned on.
cprCOACH Feedback Technology
Metronome rate 104 beats per minute
Setup options Two options are available for CPR coaching:
•Hands-Only (no rescue breaths)
•
30:2 compression to breath ratio
Communications USB, Wireless 802.11 b/g/n, or Cellular data transfer to
LIFELINKcentral AED Program Manager or LIFENET System.
USB cable type 2.0 A Male to Micro-B is required for USB
communications.
Environmental Note: All performance specifications defined assume that the device
has been stored (two hours minimum) at the operating temperature
prior to operation.
Operating
Temperature 0° to 50°C (32° to 122°F)
Long-term Storage
Temperature 15° to 35°C (59° to 95°F)
Short-term Storage
Temperature -30° to 60°C (-22° to 140°F) for a maximum of 1 week
Altitude -382 to 4572 meters (-1253 to 15,000 feet) above sea level
Relative Humidity 5 to 95% (non-condensing)
Liquid and Solid
Ingress
IP55 per IEC 60529
Physical (with handle)
Height 9.7 cm (3.8 in)
Width
22.6 cm (8.9 in)
Depth 27.4 cm (10.8 in)
Weight 2.0 kg (4.5 lb) including electrodes and battery
Battery
Type Lithium Manganese Dioxide (Li/MnO2), 12.0 V, 4.7 Ah, 55.8 Wh
Standby Life 4 years if installed in device that is not used
Weight 0.3 kg (0.7 lb)

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Battery
Operating
Temperature 0° to 50°C (32° to 122°F)
Long-term Storage
Temperature 0° to 25°C (32° to 77°F)
Short-term Storage
Temperature -30° to 60°C (-22° to 140°F) for up to 1 week
Relative Humidity 5 to 95% non-condensing
QUIK-STEP
Electrodes
Pads Pacing/ECG/defibrillation electrodes
Packaging Pre-connected tray with rapid-release cover
Shelf Life 4 years1
Electrode Shape Oval-rectangular
Electrode Size 13.34 x 8.89 cm (5.25 x 3.50 in)
Lead Wire
1.1 m (42 in)
Conductive Gel
Contact Area 82 cm2(32 in2)
Maximum Adhesion
Time 4 hours
Maximum ECG
Monitoring Time 4 hours
Maximum Number
of Defibrillation
Shocks
20 at 360 joules
Maximum Pacing
Duration 1 hour
Operating
Temperature
0° to 50°C (32° to 122°F)
Long-Term Storage
Temperature 15° to 35°C (59° to 95°F)
Short-Term Storage
Temperature -30° to 60°C (-22° to 140°F) for up to 1 week
Altitude -382 to 4572 meters (-1253 to 15,000 feet) above sea level
1Based on historical storage temperature data, the 4-year shelf life assumes a storage temperature of 25°C (77°F). Average storage temperatures
above 25°C (77°F) may decrease shelf life.

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CR2 Device Description
Physical Description and Features
Four Control