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EN-60
EN-61
Technical information
Technical information
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5. Metrological inspection
Generally, it is recommended that a metrological inspection is per-
formed every two years. However, professional users in Germany are
obligated to do so in accordance with the “Medical Products Operator
Ordinance” (Medizinprodukte-Betreiberverordnung).
This can be performed either by UEBE Medical GmbH, an authority re-
sponsible for metrology or an authorised maintenance service. Please
refer to your national regulations.
Important: No modifications, e.g. opening the device (except to re-
place the batteries), may be made to this device without the manufac-
turer’s permission.
Please only submit the device for metrological inspection together
with the cuff and the instructions for use.
Upon request, responsible authorities or authorised maintenance ser-
vices receive a “Test instruction for metrological inspection“ from the
manufacturer.
Device serial number
Reference number = item number
Manufacturer
Mains adapter information
When using the optionally available mains adapter:
Protected against solid foreign bodies with a diameter from
12.5 mm, no protection against water.
Technical equipment and batteries do not belong in house-
hold waste. They must be disposed of at appropriate collec-
tion and disposal points.
Protection class II (double insulation)
Direct current
For indoor use only
Polarity inside plus
IP20
7. Disposal
Degree of protection against electric shock TYPE BF
Consult the instructions for use
Keep dry
6. Explanation of symbols
This product complies with Council Directive 93/42/EEC of 5
September 2007 concerning medical devices and bears the
mark CE 0123 (TÜV SÜD Product Service GmbH).
0123
