Preliminary Remarks - AND UA-779 Manual De Instrucciones

Preliminary remarks

The device conforms to the following requirements: European Directive 93/42 EEC
for Medical Products Act; Medical Products Act; European Standards for Electrical
Medical Equipment EN 60601-1 (General Safety Provisions), EN 60601-1-2 and
EN 55011 (Electromagnetic Compatibility).
The above is evidenced by the CE mark of conformity accompanied by the
reference number of a designated authority.
This device is designed for adults only.
Environment for use
The device is for use in a hospital and / or patient's home.
1. Precision components were used in the
construction of this device. Extremes in
temperature, humidity, direct sunlight, shock
or dust should be avoided.
2. Clean the device with a dry, soft cloth. Never
use thinner, alcohol, benzene, or wet
dusters.
3. Avoid tightly folding the cuff or storing the
hose tightly twisted for long periods, as such
treatment may shorten the life of the
components.
4. The device, cuff and tubing are not water
resistant. Prevent rain, sweat and water from
wetting the device, cuff and tubing.
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Precaution
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