Preliminary Remarks - AND UB-401 Manual De Instrucciones

Preliminary Remarks

The device conforms to European Directive 93/42 EEC for Medical Products.
This is evidenced by the CE mark of conformity accompanied by the reference
number of a designated authority.
The device is designed for all except neonates and infants.
Environment for use
The device is for use in a 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, benzine, 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 and cuff are not water resistant.
Prevent rain, sweat and water from wetting
the device and cuff.
5. Measurements may be impaired if the device
is used close to televisions, microwave
ovens, cellular telephones, X-ray or other
devices with strong electrical fields.
6. Used equipment, parts and batteries are not
treated as ordinary household waste, and
must be disposed of according to the
applicable regulations.
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Precautions
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