Beurer medical BM 75 Gebrauchsanweisung Seite 30

11. Specifications
Model no.
Measurement
method
Measurement range
Display accuracy
Measurement
inaccuracy
Memory
Dimensions
Weight
Cuff size
Permissible operating
conditions
Permissible storage
and transport condi-
tions
Power supply
Battery life
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BM 75
Oscillometric, non-invasive blood pres-
sure measurement on the upper arm
Cuff pressure 0 – 300 mmHg,
systolic 30 – 260 mmHg,
diastolic 30 – 260 mmHg,
Pulse 40 –199 beats/minute
Systolic ± 3 mmHg, diastolic ± 3 mmHg,
pulse ± 5 % of the value shown
Max. permissible standard deviation
according to clinical testing:
systolic 8 mmHg /diastolic 8 mmHg
2 x 60 memory spaces
L 175 mm x W 117 mm x H 50 mm
Approx. 478 g (without batteries)
24 to 36 cm
+10 °C to + 40 °C, 15 % – 85 % relative
air humidity (non-condensing)
- 10 °C to + 60 °C, 10 % – 90 % relative
air humidity, 700 –1060 hPa ambient
pressure
4 x 1,5 V AAA batteries
For approx. 120 measurements, de-
pending on the blood pressure level
and/or pump pressure
manuals search engine
Accessories Cuff, cuff holder, instructions for use,
4 x 1.5 V AAA batteries, USB cable,
storage pouch
Classification Internal supply, IP21, no AP or APG,
continuous operation, application part
type BF
Technical information is subject to change without notification
to allow for updates.
• This device is compatible with the NFC model in accordance
with ISO 15693 and ISO 18000-3.
• This unit is in line with European Standard EN 60601-1-2 and
is subject to particular precautions with regard to electro-
magnetic compatibility (EEC). 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 Directive
93/42/EEC, the "Medizinproduktegesetz" (German Medical
Devices Act) and the standards EN 1060-1 (non-invasive
sphygmomanometers, Part 1: General requirements),
EN 1060-3 (non-invasive sphygmomanometers, Part 3:
Supplementary requirements for electro-mechanical 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 care-
fully checked and developed with regard to a long useful
life. If using the device for commercial medical purposes, it
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