Delphi VITALPOINT II DL-00035 Manuale Utente

DL-00035 Rev. 4

The information in this document is subject to change without notice.

This document contains proprietary information that is protected by copyright.

No part of this document may be reproduced in any manner, in whole or in part

(except for brief excerpts in reviews and scientific papers), without the prior written

consent of Delphi Medical Systems.

Delphi Medical Systems makes no warranty of any kind on this material, includ-

ing but not limited to, the implied warranties of merchantability and fitness for

a particular purpose. Delphi Medical Systems shall not be liable for errors con-

tained herein or for incidental or consequential damages concerning the furnishing,

performance, or use of this material.

Before using any Delphi Medical Systems product, be sure to read carefully and

understand all manuals provided with the product.

Delphi Medical Systems Remote Device Connectivity complies with the U.S.

Health Insurance Portability and Accountability Act (HIPAA) protecting the security

and privacy of health data. It is recommended that the healthcare facility ensures

that patients complete all necessary paperwork so that the facility complies with

the HIPAA requirements.

This equipment complies with Part 68 of the U.S. Federal Communications

Commission (FCC) rules and the requirements adopted by the American Council

for Terminal Attachments (ACTA). On the back of the Delphi Medical Systems

VitalPoint

™

Home Monitor is a label that contains, among other information, a

product identifier in the format US:AAAEQ##TXXXX. If requested, this number

must be provided to the telephone company.

The Universal Services Ordering Code (USOC) jack used to connect the VitalPoint

Home Monitor to the premises’ wiring and telephone network must comply with

the applicable FCC Part 68 rules and requirements adopted by the ACTA.

Manufactured by:
Delphi Medical Systems

5725 Delphi Drive

Troy, Michigan 48098-2815 U.S.A.

CE0086