Hartmann Veroval Compact+ - Technical Data; Device Specifications

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Clinical measuring
accuracy
Complies with the requirements of ENISO81060-2
and IEC 80601-2-30; Korotko 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
electric shock
Internally powered ME device Application part:
Type BF
Protection against
harmful ingress of water
or solid materials
IP22
Ination pressure About 190 mmHg for rst measurement
Automatic switch-o 2 minutes after measurement/otherwise 30 sec.
Cu 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
conditions
Ambient temperature:
–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)
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
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 conrm 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
Subject to error and changes
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IFU_9252050_020323.indd 32-33IFU_9252050_020323.indd 32-33 02.03.23 10:4202.03.23 10:42