1-8 SEER Light Ambulatory Recorder/Controller Revision B
2019818-008
Introduction: Safety Information
guidelines regulating the disposal of such products. If you
have questions concerning disposal of the product, please
contact GE or its representatives.
MODIFICATIONS — Do not make any modifications to
the device.
AFTER DEVICE USE — Clean the device after each use
to ensure trouble-free operation for the next use.
Use a piece of damp cloth with alcohol to clean the
device and the patient cable.
The device cannot be sterilized.
Do not use xylene and petrol related liquid for
cleaning the device.
To ensure proper operation of the device, it is
necessary to periodically have the device checked by
authorized service personnel.
Check the patient cable and connectors every month
by connecting them to an ECG simulator.
INSTALLATION — Adhere to the following
recommendations during installation:
Install and keep device away from splashing water.
Do not install the device where it may be affected by
humidity, ventilation, direct sunlight, air
conditioning, dust, salt, sulfur, etc.
Prevent the device from tilting, and protect it from
the possibility of vibration or shock.
Do not install the device in a chemical storage area or
where gas is generated.
Serial Number
Every GE Medical Systems Information Technologies device has a
unique serial number for identification. The serial number appears on
the device label similar to the one shown below
.
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