Operation Manual

EN
23
INTRODUCTION
• Please ensure that the operation
of the device does not interrupt
blood circulation for a longer
period.
• Avoid squeezing or constriction
of the connecting tube.
• The Blood Pressure Monitor
has been clinically tested pursu-
ant to the requirements of
EN 1060-4:2004.
Metrological maintenance and
care information
• Do not perform any metrolog-
ical maintenance if the device
is in use.
• For reliable operation, we
recommend that the device is
subject to metrological control
once every two years pursuant
to Sec. 14 of the Medical Prod-
uct Operating Directive (MPBe-
triebV). We recommend testing
the device’s performance
once every two years and after
metrological control and repair,
at a minimum by testing the
tolerance requirements of the
pressure display and tightness
of the cuff (testing at least at 50
mmHg and 200 mmHg).
• The metrological control must
be performed by a licensed
tester or testing institute.
• We recommend cleaning the
device and cuff only with a soft
cloth.
Storage information
• If the device is not being used,
store it and the adapter in a dry
location away from heat, dust,
fibres, lint, and out of direct
sunlight. Do not place heavy
objects on the storage box.
Information about handling
batteries
• Do not mix new and used
batteries.
• Do not use different types of
batteries at the same time.
• Do not throw batteries into a fire.
Batteries may explode or leak.
Remove the batteries if the de
-
vice is not used for a long time.
Disposal information
Battery disposal
EC Directive 2008/12/EC
Batteries are not a part of
your regular household waste. You
must return batteries or recharge-
able batteries to your municipali-
ty’s public collection or wherever
batteries of the respective type
are being sold.