Important, Device tracking, Responsibility for information – Physio-Control LIFEPAK 1000 User Manual

Page 4

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Important

This instrument is to be used by authorized personnel only.

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 registration phone line 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 cautions and warnings provided throughout this manual.

!USA

!USA

LIFEPAK, LIFENET, and QUIK-COMBO are registered trademarks of Physio-Control, Inc. ADAPTIV, CODE-STAT, cprMAX, REDI-PAK, and Shock
Advisory System are trademarks of Physio-Control, Inc. Microsoft and Windows are registered trademarks of Microsoft Corporation. Ambu is a
registered trademark of the Ambu Corporation. Specifications are subject to change without notice.

©2006–2012 Physio-Control, Inc. All rights reserved.

Publication Date: 03/2012

3205213-008

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