Beurer BM 26 Manual De Instrucciones página 18

Measurement Max. permissible standard devia-
inaccuracy tion according to clinical testing:
systolic 8 mmHg /diastolic 8 mmHg
Memory 4 x 30 memory spaces
Dimensions L 6.1 in x W 4.3 in x H 2.75 in
(L 155 mm x W 110 mm x H 70 mm)
Weight Approx. 13.9 oz (395 g) without
batteries
Cuff size 8.6 – 16.5 in (22 – 42 cm)
Permissible oper- 50°F to 104°F (+10 °C to +40 °C),
ating conditions 15-93% relative air humidity
(non-condensing)
Permissible stor- -13°F to 158°F (- 25 °C to + 70 °C),
age conditions ≤93% relative air humidity,
800 –1060 hPa ambient pressure
Power supply 4 x 1,5 V
teries.
Battery life For approx. 180 measurements,
depending on the blood pressure
level and/or pump pressure
Accessories Instruction for use, 4 x 1.5 V AA
alkaline batteries, Quick Start
Guide, storage pouch
Classification Internal supply, IPX0, no AP or
APG, continuous operation, type
BF applied part
These specifications are subject to change without notice
for purpose of improvement.
• This unit is in line with European Standard EN 60601-
• This device is in line with the EU Medical Devices
AA alkaline bat-
• The accuracy of this blood pressure monitor has been
18
Type BF applied part
1-2 (In accordance with CISPR 11, IEC 61000-4-2, IEC
61000-4-3, IEC 61000-4-8) and is subject to particular
precautions with regard to electromagnetic compatibility
(EMC). Please note that portable and mobile HF
communication systems may interfere with this unit.
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).
carefully 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