20
Measurement
range
Cuff pressure 0 – 299 mmHg,
systolic 40 – 250 mmHg,
diastolic 40 – 250 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 accord-
ing to clinical testing: systolic 8 mmHg /
diastolic 8 mmHg
Memory 2 x 50 memory spaces
Dimensions L 156 mm x W 105 mm x H 74,5 mm
Weight Approx. 315 g (without batteries)
Cuff size 24 to 36 cm
Permissible oper-
ating conditions
+10 °C to + 40 °C, 40 – 85 % relative air
humidity (non-condensing)
Permissible stor-
age conditions
-10 °C to + 60 °C, 10 – 90 % relative air humid-
ity, 800 –1050 hPa ambient pressure
Power supply
4 x 1,5 V
AA batteries
Battery life For approx. 300 measurements, depend-
ing on the blood pressure level and/or pump
pressure
Accessories Instruction for use, 4 x 1.5 V AA batteries,
storage pouch
Classification Internal supply, IPX0, no AP or APG, continu-
ous operation, type BF applied part
Technical information is subject to change without notification
to allow for updates.
•
This unit is in line with European Standard EN 60601-1-2
and is subject to particular precautions with regard to elec-
tromagnetic compatibility (EMC). Please note that portable
and mobile HF communication systems may interfere with
this unit. More details can be requested from the stated Cus-
tomer 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/EC, the “Medizinproduktegesetz” (German Medi-
cal Devices Act) and the standards EN1060-1 (non-inva-
sive sphygmomanometers, Part 1: General requirements),
EN1060-3 (non-invasive sphygmomanometers, Part 3: Sup-
plementary requirements for electro-mechanical blood pres-
sure measuring systems) and IEC80601-2-30 (Medical elec-
trical 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 must
be regularly tested for accuracy by appropriate means. Pre-
cise instructions for checking accuracy may be requested
from the service address.
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