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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