Technical Information - HoMedics theraP Gebrauchsanleitung

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TECHNICAL INFORMATION

theraP treatment emits a pulsating magnetic field using a modified saw tooth
waveform, which pulses approximately every 1 sec.
theraP is CE marked according to EU Medical Devices Directive 2007/47/EC. It is
classified as an active therapeutic device in Class IIa. The Applied Part (the entire
device) is type BF (fully encapsulated).
theraP is approved for Electrical Safety according to the standard EN60601-1:2006
and for EMC compatibility according to standard EN60601-1-2:2007.
WarnInG: no modification of this equipment is allowed.
The theraP should not be used to or stacked with other equipment and that if
adjacent or stacked use is necessary, the equipment should be observed
to verify normal operation in the configuration in which it will be used
Technical data:
The magnetic field level is approximately 100 Gauss
Operating temperature range: +10ºC to +35ºC
Storage & transportation temperature range: -25ºC to +70ºC
Equipment type: Ordinary
Mode of operation: Continuous
Fully isolated patient circuit type BF
Further technical data are available from the manufacturer
Manufacturer:
HoMedics Group Ltd, HoMedics House, Somerhill Business Park,
Five Oak Green Road, Tonbridge, Kent, TN11 0GP.
Guidance and manufacturer's declaration – electromagnetic emissions
The theraP is intended for use in the electromagnetic environment specified below. The
customer or the user of the theraP should assure that it is used in such an environment.
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