Hartmann Veroval Compact+ Instructions For Use Manual page 17

EN English
Clinical measuring Complies with the requirements of EN ISO 81060-2
accuracy and IEC 80601-2-30; Korotkoff validation method:
Phase I (SYS), Phase V (DIA)
Operating mode Continuous mode
Nominal voltage DC 3V
Expected service life 10,000 measurements
Power supply 2 x 1.5 V alkaline manganese (AAA/LR03) batteries
Battery capacity Approx. 800 measurements
Protection against Internally powered ME device Application part:
electric shock Type BF
Protection against IP22
harmful ingress of water
or solid materials
Inflation pressure About 190 mmHg for first measurement
Automatic switch-off 2 minutes after measurement/otherwise 30 sec.
IFU_9252050_020323.indd 32-33 IFU_9252050_020323.indd 32-33
Cuff For wrist diameters of 12.5 - 21 cm
Memory capacity 2 x 100 measurements with average value of all
measurements and morning/evening average value
of the last 7 days
Operating conditions Ambient temperature: +10 °C to +40 °C
Relative humidity:
≤85 %, non-condensing
Air pressure: 700-1060 hPa
Storage / transport Ambient temperature:
conditions –20 °C to +50 °C
Relative humidity: ≤85 %, non-condensing
Air pressure: 700-1060 hPa
Serial number On the rating label
Reference to standards IEC 60601-1; IEC 60601-1-2
(In accordance with CISPR 11, IEC 61000-4-2,
IEC 61000-4-3, IEC 61000-4-8)
Weight Approx. 115 g (without batteries)
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Dimensions Approx. 70(L) x 85(W) x 24(H) mm
Data transfer 2402 MHz – 2480 MHz frequency band
Transmission power max. +3 dBm
The blood pressure monitor uses Bluetooth® low
energy technology
Compatible with Bluetooth® ≥ 4.0 smartphones/
tablets
English
Legal requirements and guidelines
• The Veroval® BPW 26 conforms with the Regulation (EU) 2017/745 of the European
Parliament and of the Council on medical devices, as well as the respective national
provisions, and bears the CE mark.
• The device complies, for example, with the European standard EN IEC 80601-2-30.
• This product is subject to special precautionary measures with regard to
electromagnetic compatibility.
• Clinical testing of measuring accuracy was performed in accordance with the
European Standard EN 81060-2.
• Beyond the statutory requirements, the device has been clinically validated by the
ESH-IP2 Protocol of the European Society of Hypertension (ESH).
• We hereby confirm that this product complies with the European RED Directive
2014/53/EU. The CE Declaration of Conformity for this product can be found under:
www.veroval.info
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EN
02.03.23 10:42 02.03.23 10:42