Issued: 2018-02-27
This manual applies to the following models and trade names
Trade Names
Model Number
Lifeline/ReviveR VIEW AUTO
DDU-2200
Lifeline/ReviveR VIEW
DDU-2300
Lifeline/ReviveR ECG
DDU-2450
Lifeline/ReviveR ECG+
DDU-2475
The Lifeline/ReviveR VIEW AUTO is referred to as the DDU-2200 from this point forward in this manual.
The Lifeline/ReviveR VIEW is referred to as the DDU-2300 from this point forward in this manual.
The Lifeline/ReviveR ECG is referred to as the DDU-2450 from this point forward in this manual.
The Lifeline/ReviveR ECG+ is referred to as the DDU-2475 from this point forward in this manual.
Statements that apply to all trade names/model numbers listed above are referred to in this manual as
“DDU-2000 Series.”
Notices
Defibtech, L.L.C. shall not be liable for errors contained herein or for incidental or consequential damages in
connection with the furnishing, performance, or use of this material.
Information in this document is subject to change without notice. Names and data used in any examples are
fictitious unless otherwise noted.
Limited Warranty
The “Limited Warranty” shipped with Defibtech AED products serves as the sole and exclusive warranty provided
by Defibtech, L.L.C., with respect to the products contained herein.
Copyright
Copyright © 2018 Defibtech, L.L.C.
All rights reserved. Copyright questions should be directed to Defibtech.
For contact information, refer to Chapter 12 of this manual.
Tracking
U.S.A. federal regulations require Defibtech to maintain records for each AED it distributes (reference 21 CFR 821,
Medical Device Tracking). These requirements also apply anytime there is a change in the AED’s location, including
if you move, sell, donate, give away, export or even throw it away. We depend on AED owners/users to contact
us when these things happen to ensure the tracking information remains accurate in the event we need to share
important product notices. If your location is outside the U.S.A., we ask you share your information for exactly the
same reasons. To keep your information up to date, please visit www.defibtech.com/register.
Federal Law (USA) restricts this device
to sale by or on the order of a physician.
CAUTION
3
DAC-U2510EN-BF rev H
