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Expected
500hours
Service life
Classification
Internal supply, IP21, no AP or APG,
continous operation, application part
type BF
Technical information is subject to change without
notification to allow for updates. The serial number is
located on the device or in the battery compartment.
• This device complies with European Standard EN 60601-
1-2 (in accordance with CISPR 11, IEC 61000-4-2, IEC
61000-4-3, IEC 61000-4-4, IEC 61000-4-5, IEC 61000-
4-6, IEC 61000-4-8, IEC 61000-4-11) and is subject to
particular precautions with regard to electromagnetic
compatibility. The device is suitable for use in all
environments listed in these instructions for use, including
domestic environments. Please note that portable and
mobile HF communication systems may interfere with this
device.
• The device complies with the EU Medical Devices
Directive 93/42/EEC, the German Medical Devices
Act (Medizinproduktgesetz) and the standards EN
1060-3 (Non-invasive sphygmomanometers – Part 3:
Supplementary requirements for electro-mechanical
blood pressure measuring systems) and IEC 80601-
2-30 (Medical electrical equipment – Part 2 – 30:
Particular requirements for the basic safety and
essential performance of automated non-invasive
sphygmomanometers).
• The accuracy of this blood pressure monitor has been
carefully checked and developed with regard to a long
useful life. If the device is used for commercial medical
purposes, it must be regularly tested for accuracy by
appropriate means. Precise instructions for checking
accuracy may be requested from the service address.

12. Power Supply Unit

Input
100 – 240 V, 50 – 60 Hz, 0.5 A max.
Output
6 V DC, 600 mA, only in connection with
Beurer blood pressure monitor.
Protection
This device is double insulated and
protected against short circuit and overload
by a primary thermal fuse
Make sure to take the batteries out of
the compartment before using the mains
adapter.
Polarity of the the DC voltage connection
Double insulated / equipment class 2
16

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