30
11. Specifications
Model no. BM 75
Measurement
method
Oscillometric, non-invasive blood pres-
sure measurement on the upper arm
Measurement range Cuff pressure 0 – 300 mmHg,
systolic 30 – 260 mmHg,
diastolic 30 – 260 mmHg,
Pulse 40 –199 beats/minute
Display accuracy Systolic ± 3 mmHg, diastolic ± 3 mmHg,
pulse ± 5 % of the value shown
Measurement
inaccuracy
Max. permissible standard deviation
according to clinical testing:
systolic 8 mmHg /diastolic 8 mmHg
Memory 2 x 60 memory spaces
Dimensions L 175 mm x W 117 mm x H 50 mm
Weight Approx. 478 g (without batteries)
Cuff size 24 to 36 cm
Permissible operating
conditions
+10 °C to + 40 °C, 15 % – 85 % relative
air humidity (non-condensing)
Permissible storage
and transport condi-
tions
- 10 °C to + 60 °C, 10 % – 90 % relative
air humidity, 700 –1060 hPa ambient
pressure
Power supply
4 x 1,5 V
AAA batteries
Battery life For approx. 120 measurements, de-
pending on the blood pressure level
and/or pump pressure
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 EN1060-1 (non-invasive
sphygmomanometers, Part 1: General requirements),
EN1060-3 (non-invasive sphygmomanometers, Part 3:
Supplementary requirements for electro-mechanical blood
pressure measuring systems) and IEC80601-2-30 (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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