© 2010 by General Electric Company. All rights reserved. 2049809-001 Rev B vii
About this Manual
Before using the Mini Telemetry System with your Corometrics Fetal Monitor, read this entire manual. As with all
medical equipment, attempting to use this device without a thorough understanding of its operation may result
in patient or user injury. This device should only be operated by personnel trained in its operation and familiar
with the risks and benets of this type of device. Additional precautions specic to certain procedures are found
in the text of this manual.
User Responsibility
This Product will perform in conformity with the description contained in this Operation and Maintenance manual
and accompanying labels and/or inserts, when assembled, operated, maintained and repaired in accordance
with the instructions provided. This Product must be checked periodically. A defective Product should not be
used. Parts that are broken, missing, partially worn, distorted, or contaminated should be replaced immediately.
Should such repair or replacement become necessary, GE Healthcare recommends that a telephonic or written
request for service advice be made to the nearest GE Healthcare Regional Service Center. This Product or any of
its parts should not be repaired other than in accordance with written instructions provided by GE Healthcare
and by GE Healthcare trained personnel. The Product must not be altered without GE Healthcare’s prior written
approval. The user of this Product shall have the sole responsibility for any malfunction that results from improper
use, faulty maintenance, improper repair, damage, or alteration by anyone other than GE Healthcare. Do not
use this product without prior site survey and awareness of the standard medical frequency bands that can be
congured for this Telemetry system.
GE Healthcare has declared that this product conforms with the
European Council Directive 93/42/EEC Medical Device Directive when
used in accordance with the instructions provided in this Operation and
Maintenance Manual.
U.S. Federal law restricts this device to sale by or on the order of a licensed
medical practitioner.
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