Physio-Control LIFEPAK CR Plus - Manual (Page 4)

Responsibility for Information
It is the responsibility of our customers to ensure that the appropriate person(s) who may use this defibrillator have
access to the information in this manual, including general safety information provided in Section 1.
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.
Revision History
These operating instructions describe the LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators with software
Version 3.0 or later.
!USA
!USA
LIFEPAK, LIFEPAK CR, LIFEPAK EXPRESS, and QUIK-COMBO are registered trademarks of Physio-Control, Inc. ADAPTIV, CODE-STAT,
CHARGE-PAK, QUIK-PAK, and Shock Advisory System are trademarks of Physio-Control, Inc. IrDA is a registered trademark of Infrared Data
Association. Specifications are subject to change without notice.
©2009-2010 Physio-Control, Inc. All rights reserved.
MIN 3201686-012 Publication Date: 05/2010