Specifications - Beurer BM 26 Manual De Instrucciones

In the above cases, you must repeat the measurement. Make sure
that the cuff tube is properly inserted and that you do not move or
talk. Re­insert the batteries if necessary, or else replace them.

9. Specifications

Model no. BM 26
Measurement method Oscillometric, non­invasive blood pressure
measurement on the upper arm
Measurement range Cuff pressure 0 – 300 mmHg,
systolic 0 – 280 mmHg,
diastolic 0 – 280 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 +5 °C to +40 °C, 15 – 90 % relative air hu­
conditions midity (non­condensing)
Permissible storage ­ 20 °C to + 55 °C, 15 – 90 % relative air hu­
conditions midity, 800 –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
AA alkaline batteries.
21
Accessories Instruction for use, 4 x 1.5 V AA alkaline
batteries., storage pouch
Classification Internal supply, IPX0, no AP or APG, con­
tinuous operation, type BF applied part
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 and
is subject to particular precautions with regard to electromag­
netic compatibility (EMC). Please note that portable and mobile
HF communication systems may interfere with this unit. More
details can be requested from the stated Customer Service ad­
dress 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 1060­1 (non­invasive
sphygmomanometers, Part 1: General requirements),
EN 1060­3 (non­invasive sphygmomanometers, Part 3:
Supplementary requirements for electro­mechanical blood
pressure measuring systems) and IEC 80601­2­30 (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
carefully checked and developed with regard to a long
useful life. If using the device for commercial medical pur­
poses, it must be regularly tested for accuracy by appropri­
ate means. Precise instructions for checking accuracy may
be requested from the service address.