Manufacturer Responsibility; General - GE Cardiolab II Plus Service Manual

Manufacturer Responsibility

General

2002938-002E
CAUTION
MINOR INJURY OR DATA LOSS — A message which
indicates a potential hazard or unsafe practice which, if
not avoided, could result in minor personal injury or
product/property damage.
NOTE
A message which provides application tips or other useful
information to assure that you get the most from your equipment.
GE Medical Systems Information Technologies is responsible for the
effects of safety, reliability, and performance only if:
Installation operations, extensions, readjustments, modifications, or
repairs are carried out by persons authorized by GE Medical Systems
Information Technologies.
The equipment is used in accordance with the instructions for use.
The user attaches only accessory equipment recommended for
interaction with the amplifier.
The CardioLab II Plus Amplifier maintains leakage currents below
medical limits with an isolation transformer, which is incorporated into
the design of the amplifier. Amplifier power should be supplied by a
dedicated power supply on an isolated circuit for proper behavior of the
amplifier.
To ensure patient safety, use only parts and accessories manufactured or
recommended by GE Medical Systems - Information Technologies.
This equipment should only be connected as specified by GE Medical
Systems - Information Technologies. Installation of the equipment
should only be performed by qualified GE Medical Systems - Information
Technologies service representatives.
Contact GE Medical Systems - Information Technologies before
connecting any device to equipment that is not recommended in this
manual. Only cables and accessory equipment purchased from GE
Medical Systems - Information Technologies should be used in
conjunction with the amplifier.
Cardiolab® II Plus Amplifier Manual
Introduction
1-5