Getting To Know Your Instrument - Beurer medical BM 49 Mode D'emploi

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.
You are also warned of possible existing cardiac arrhythmia.
The recorded values are classified and evaluated graphically.
Store these instructions for use for future reference and make them accessible to other users.
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
Note
Note on important information
Follow instructions for use
Type BF applied part
Direct current
Disposal in accordance with EC
Directive WEEE (Waste Electrical
and Electronic Equipment).
ENGLISH
Storage
50°C
-20°C
RH ≤85%
Operating
+40°C
+10°C
RH ≤85%
46
Manufacturer
Permissible storage temperature
and humidity
Permissible operating tempera-
ture and humidity
Keep dry
Serial number
The CE labelling certifies that the
product complies with the essen-
tial requirements of Directive
93/42/EEC on medical products.