english
english
EN-48
EN-49
Technical information
Technical information
E
E
3. Technical data
Model:
visomat handy
Size:
approx. W = 70 mm x H = 70 mm x D = 80 mm
with cuff
Weight:
121 g with cuff, not including batteries
Display:
LCD display (liquid crystal display) for measured
values and check displays
Memory:
60 measured values (stored automatically) and
average value (A)
Measurement procedure:
Oscillometric determination of systole, diastole
and pulse
Reference procedure of clini-
cal testing:
Auscultatory measurement
Inflating pressure:
Automatically controlled
Pressure display range:
0-300 mmHg
Measurement range:
Systolic: 50-250 mmHg
Diastolic: 40-180 mmHg
Pulse measurement: 40-160 pulses/min
Measurement precision:
Blood pressure measurement (cuff pressure): ±
3 mmHg
Pulse rate: ± 5%
Power supply:
Battery type: 2 x 1.5 V, AAA, LR 03, durability:
over 700 measurements in 2 years
Power consumption:
2 W
Cuff:
Cuff type visomat H5, wrist circumference 12.5
cm - 21.5 cm
Operating conditions:
Ambient temperature 10°C to 40°C, relative hu-
midity 15% to 85% non-condensing, air pressure
700 to 1060 hPa
Storage and transportation
conditions:
Ambient temperature -20 °C to 60 °C, relative
humidity 15 to 95%, non-condensing
Time to adjust from minimum/
maximum storage tempera-
ture to operating temperature:
2 hours
Inflation and deflation:
Regulated automatically
Protection class IP:
IP 20: Protected against solid foreign particles
with a diameter of more than 12.5 mm, no
protection against water.
Protection against electric
shock:
Internal power supply, applied part type BF (cuff)
Expected service life:
5 years
Operating mode:
Continuous operation
Classification:
Internally powerd ME Equipment
4. Original spare parts and accessories
The following original spare parts and accessories are available from spe-
cialist dealers:
Subject to technical modifications.
• Cuff type H5 (for wrist circumference 12.5-21.5 cm)
Part no. 2105001, PZN-06414493
5. Metrological inspection
Generally, it is recommended that a metrological inspection is performed
every two years. However, professional users in Germany are obligated
to do so in accordance with the “Medical Products Operator Ordinance”
(Medizinprodukte-Betreiberverordnung). This can be performed either by
UEBE Medical GmbH, an authority responsible for metrology or an author-
ised maintenance service. Please refer to your national regulations.
Upon request, responsible authorities or authorised maintenance services
receive a “Test instruction for metrological inspection” from the manu-
facturer.
Please only submit the device for metrological inspection together with
the cuff and the instructions for use.
Important: No modifications, e.g. opening the device (except to replace
the batteries), may be made to this device without the manufacturer’s
permission.
Summary of Contents for handy
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