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Classification Internal supply, IPX0, no AP or
APG, continuous operation, type BF
applied part
Technical information is subject to change without notifica-
tion to allow for updates.
This unit is in line with European Standard EN 60601-
1-2 and is subject to particular precautions with regard
to electromagnetic compatibility (EMC). Please note that
portable and mobile HF communication systems may
interfere with this unit. More details can be requested
from the stated Customer Service address or found at the
end of the instructions for use.
This device is in line with the EU Medical Devices Direc-
tive 93/42/EEC, the „Medizinproduktegesetz“ (German
Medical Devices Act) and the standards EN1060-1 (non-
invasive sphygmomanometers, Part 1: General require-
ments), EN1060-3 (non-invasive sphygmomanometers,
Part 3: Supplementary requirements for electro-mechani-
cal blood pressure measuring systems) and IEC80601-2-
30 (Medical electrical equipment – Part 2 30: Particular
requirements for the safety and essential performance of
automated non-invasive blood pressure monitors).
The accuracy of this blood pressure monitor has been
carefully checked and developed with regard to a long
useful life. If using the device for commercial medical pur-
poses, it must be regularly tested for accuracy by appro-
priate means. Precise instructions for checking accuracy
may be requested from the service address.
Subject to errors and changes
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