Specifications - Beurer BM 26 Manual De Instrucciones

10. Specifications

Model no. BM 26
Measurement method Oscillometric, non­invasive blood pressure
measurement on the upper arm
Measurement range Cuff pressure 0 – 300 mmHg,
systolic 60 – 280 mmHg,
diastolic 30 – 200 mmHg,
Pulse 30 – 180 beats/minute
Display accuracy Systolic ± 3 mmHg, diastolic ± 3 mmHg,
pulse ± 5 % of the value shown
Measurement Max. permissible standard deviation ac­
inaccuracy cording to clinical testing:
systolic 8 mmHg /diastolic 8 mmHg
Memory 4 x 30 memory spaces
Dimensions L 155 mm x W 110 mm x H 70 mm
Weight Approx. 395 g (without batteries, with cuff)
Cuff size 22 to 35 cm
Permissible operating
+10 °C to +40 °C,
conditions midity (non­condensing)
Permissible storage
­ 25 °C to + 70 °C,
conditions ity, 700 –1060 hPa ambient pressure
Power supply
4 x 1,5 V
Battery life For approx. 180 measurements,
depending on the blood pressure level
and/or pump pressure
Classification Internal supply, IPX0, no AP or APG, con­
tinuous operation, type BF applied part
All manuals and user guides at all-guides.com
15­9
0% relative air hu­
≤ 93
% relative air humid­
AA alkaline batteries.
The serial number is located on the device or in the battery
compartment.
Technical information is subject to change without notification
to allow for updates.
• This unit is in line with European Standard EN 60601­1­2 (In
accordance with CISPR 11, IEC61000­3­2, IEC61000­3­3,
IEC61000­4­2, IEC61000­4­3, IEC61000­4­4, IEC61000­4­5,
IEC61000­4­6, IEC61000­4­8, IEC61000­4­11) and is subject
to particular precautions with regard to electromagnetic com­
patibility (EMC). Please note that portable and mobile HF com­
munication systems may interfere with this unit.
• This device is in line with the EU Medical Devices Directive
93/42/EEC, the "Medizinproduktegesetz" (German Medical
Devices Act) and the standards EN 1060­1 (non­invasive
sphygmomanometers, Part 1: General requirements),
EN 1060­3 (non­invasive sphygmomanometers, Part 3: Sup­
plementary requirements for electro­mechanical blood pres­
sure measuring systems) and IEC 80601­2­30 (Medical elec­
trical equipment – Part 2 – 30: Particular requirements for the
safety and essential performance of automated non­invasive
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
must be regularly tested for accuracy by appropriate means.
Precise instructions for checking accuracy may be requested
from the service address.
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