Hartmann Veroval Instructions For Use Manual page 95

Table 2
For all medical-electrical (ME) DEVICES and ME SYSTEMS
Guidance and Manufacturer's Declaration – Electromagnetic immunity
The Veroval upper arm blood pressure monitor is intended for use in the electromagnetic
®
environment specified below. The customer or the user of the Veroval
pressure monitor should assure that it is used in such an environment.
Immunity tests
Electrostatic dis-
charge (ESD) IEC
61000-4-2
Magnetic field at
supply frequency
(50 Hz) as per IEC
61000-4-8
IEC 60601 test level
± 6 kV contact
± 8 kV air
3 A/m
Compliance level
± 6 kV contact
± 8 kV air
3 A/m
95
English
upper arm blood
®
Electromagnetic
Environment –
Guidance
Floors should be wood,
concrete or ceramic tile.
If floors are covered with
synthetic material, the
relative humidity should
be at least 30%.
Power frequency mag-
netic fields should be
at levels characteristic
of a typical location in
a typical commercial or
hospital environment.
GB