Beurer BM 49 Bedienungsanleitung PDF herunterladen (Seite 43)

Dear Customer,

thank you for choosing one of our products. Our name stands for high-quality, thoroughly tested products

for the applications in the areas of heat, weight, blood pressure, body temperature, pulse, gentle therapy,

massage and air. Please read these instructions for use carefully and keep them for later use, be sure to

make them accessible to other users and observe the information they contain.

Best regards,

Your Beurer Team

1. Getting to know your instrument

Check that the packaging of the Beurer BM 49 blood pressure monitor has not been tampered with and

make sure that all the required contents are present. Before use, ensure that there is no visible damage to

the device or accessories and that all packaging material has been removed. If you have any doubts, do

not use the device and contact your retailer or the specified Customer Services address.

The upper arm blood pressure monitor is used for non-invasive measurement and monitoring of adults’

arterial blood pressure.

You can use it to measure your blood pressure quickly and easily, storing the results and displaying the

progression of readings together with the average.

A warning is issued for anyone suffering from cardiac arrhythmia.

The values determined are classified and graphically evaluated according to WHO guidelines.

Keep these instructions carefully for further use and also let other users have access to them.

2. Important information

Signs and symbols

The following symbols are used in these instructions for use, on the packaging and on the type plate for

the device and accessories:

Caution Manufacturer

Note

Note on important information

Storage

RH ≤85%

-20°C

50°C

Permissible storage temperature

and humidity

Follow instructions for use

Operating

RH ≤85%

+10°C

+40°C

Permissible operating tempera-

ture and humidity

Type BF applied part Keep dry

Direct current SN Serial number

Disposal in accordance with EC

Directive WEEE (Waste Electrical

and Electronic Equipment).

The CE labelling certifies that the

product complies with the essen-

tial requirements of Directive

93/42/EEC on medical products.

ENGLISH

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