Beurer BM 28 Instructions For Use Manual page 22

Upper arm blood pressure monitor
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Disposal in accordance with the Waste Elec-
trical and Electronic Equipment EC Directive
– WEEE
Do not dispose of batteries containing harmful
substances with household waste
Manufacturer
CE labelling
This product satisfies the requirements of the
applicable European and national directives.
Dispose of packaging in an environmentally
friendly manner
Marking to identify the packaging material.
A = material abbreviation,
B
B = material number:
1–7 = plastics,
A
20–22 = paper and cardboard
Separate the product and packaging elements
and dispose of them in accordance with local
regulations.
Protected against solid foreign objects 12.5
IP21
mm in diameter and larger, and against verti-
cally falling drops of water
Direct current
The device is suitable for use with direct
current only
Unique device identifier (UDI)
UDI
Identifier for unique product identification
Batch designation
Item number
Serial number
SN
Medical device
Type BF applied part
Galvanically isolated applied part (F stands
for "floating"); meets the requirements for
leakage currents for type B
22

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