Beurer BM 28 Manual De Instrucciones página 20

Do not dispose of batteries containing harmful sub-
stances with household waste
Manufacturer
CE labelling
This product satisfies the requirements of the applica-
ble European and national directives.
Dispose of packaging in an environmentally friendly
manner
Marking to identify the packaging material.
B
A = material abbreviation, B = material number:
A 1–7 = plastics, 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 mm in
IP21
diameter and larger, and against vertically 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 "float-
ing"); meets the requirements for leakage currents for
type B
Temperature range
Humidity range
Atmospheric pressure limitation
Type
Date of manufacture
Importer
2. INTENDED USE
Purpose
The blood pressure monitor (hereinafter, device) is intended for
the fully automatic, non-invasive measurement of arterial blood
pressure and pulse values on the upper arm.
It is designed for self-measurement by adults in a domestic en-
vironment.
Target group
The blood pressure measurement is suitable for adult users
whose upper arm circumference is within the range printed on
the cuff.
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