ii LIFEPAK 12 Defibrillator/Monitor Operating Instructions
IMPORTANT INFORMATION
Rx Only
Device Tracking
The U.S. Food and Drug Administration requires defibrillator manufacturers and distributors to
track the location of their defibrillators. If the device is located somewhere other than the shipping
address or the device has been sold, donated, lost, stolen, exported, destroyed, permanently retired
from use, or if the device was not obtained directly from Physio-Control, please do one of the
following: register the device at http://www.physio-control.com, call the device tracking coordinator at
1.800.426.4448, or use one of the postage-paid address change cards located in the back of this
manual to update this vital tracking information.
Responsibility for Information
It is the responsibility of our customers to ensure that the appropriate person(s) within their organization
have access to this information, including general safety information provided in Section 1.
Version History
These operating instructions describe LIFEPAK 12 defibrillator/monitor devices with software version
3011371-065 or later. Older devices may not have all the features described in this manual. Software
version 3011371-106 or later will not work in monophasic devices.
Operating Instructions Version Operating Software Version*
PN 3010012-000 PN 3011371-018
PN 3010012-001 PN 3011371-019 and PN 3011371-022
PN 3010012-003 PN 3011371-030
PN 3010012 (-005 international; -006 USA only) PN 3011371-061
PN 3010012-007 (USA only) PN 3011371-062
PN 3012730-000 (addendum) PN 3011371-065
PN 3010012 (-008 and -009 USA only; -050 international) PN 3011371-065
PN 3010012 (-010 and -011 USA only; -051 international) PN 3011371-067, -070
PN 3010012 (-012 and -013 USA only; -052 international) PN 3011371-072
PN 3010012 (-014 USA only; -053 international) PN 3011371-072
PN 3010012 (-015 USA only; -020 international) PN 3011371-090
PN 3010012 (-016 USA only; -021 international) PN 3011371-099
MIN 3010012 (-017 USA only; -022 international) MIN 3011371-101
MIN 3010012 (-018 USA only; -023 international) MIN 3011371-106
MIN 3010012 (-019 USA only; -024 international) MIN 3011371-106
MIN 3207254 (-001 USA only; -021 international) MIN 3011371-126
MIN 3207254 (-002 USA only; -022 international) MIN 3011371-130
MIN 3207254 (-006 USA only; -026 international) MIN 3011371-134
MIN 3207254 (-007 USA only; -027 international) MIN 3011371-134
* To view the operating software version, turn on the device and note the PN after VERSION on the
opening screen.
LIFEPAK, LIFENET, FASTPAK, FAST-PATCH, QUIK-COMBO, QUIK-LOOK, and QUIK-CHARGE are registered trademarks of Physio-Control, Inc. CODE SUMMARY, Shock
Advisory System, CODE-STAT, cprMAX, and REDI-PAK are trademarks of Physio-Control, Inc. CADEX is a registered trademark of Cadex Electronics Inc. 12SL is a trademark of GE
Medical Systems. C-LOCK, Dura-Y, Durasensor, Nellcor, Oxiband, OxiCliq, and Oxisensor are registered trademarks of Nellcor. PediCheck is a trademark of Nellcor. Microstream
and FilterLine are trademarks of Oridion Medical Ltd. The Oridion medical capnography in this product is covered by one or more of the following US patents: 6,428,483; 6,997,880;
5,300,859; 6,437,316 and their foreign equivalents. Additional patent applications pending. PC Card is a trademark of the Personal Computer Memory Card International Association.
Masimo and LNOP are registered trademarks of Masimo Corporation. EDGE System Technology is a trademark of Ludlow Technical Products. UNI-LEAD is a trademark of Unilead
International, Inc. DTXPlus is a trademark of BD Medical. Specifications are subject to change without notice.
© 2008-2010 Physio-Control, Inc. All rights reserved.
MIN
3207254-010
Publication date: 07/2010
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