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1.16 EMC
Special
Instructions & Notes regarding the RhythmPad
compatibility (EMC) testing to EN60601-1-2:2007.
The RhythmPad
containing other electrical/electronic equipment (including other medical devices).
The purpose of this testing is to ensure the RhythmPad
affect the normal operation of other electrical/electronic equipment and that other
electrical/electronic equipment is not likely to adversely affect the normal operation
of the RhythmPad
Despite the testing of the RhythmPad
of the RhythmPad
portable and mobile RF communications equipment. As the RhythmPad
equipment,
special
compatibility).
It is important that the RhythmPad
accordance with the instructions/guidance provided herein and is used only in the
configuration as supplied.
The RhythmPad
supplied. If the RhythmPad
result in increased emissions or decreased immunity of the RhythmPad
to EMC performance. It should also be noted that the USB cable provided with the
GP
RhythmPad
should not be used with other equipment. To do so may result in
increased emissions or decreased immunity of the other equipment in relation to EMC
performance.
The RhythmPad
If adjacent or stacked use with other equipment is necessary, the RhythmPad
the other equipment should be observed/monitored, to verify normal operation in the
stacked/adjacent configuration in which it will be used.
For the purposes of EN60601-1-2, the RhythmPad
performance.
electrical/electromagnetic interference in the form of conducted and radiated RF
fields (EMC phenomena detailed in the specifications EN61000-4-6 and EN61000-4-
3/EN61000-4-8 respectively), incorrect operation of the RhythmPad
the form of noise being present on measured waveforms or the RhythmPad
cease to respond (3
solid green). To correct this condition, the RhythmPad
any suspected sources of interference (with the USB cable disconnected and re-
connected, should the RhythmPad
The user should also be aware that if the RhythmPad
interference in the form of Electrostatic Discharges (EMC phenomenon detailed in the
specification EN61000-4-2), incorrect operation of the RhythmPad
form of noise being present on measured waveforms or the RhythmPad
rd
to respond (3
green). To correct this condition, the RhythmPad
suspected sources of interference (with the USB cable disconnected and re-
connected, should the RhythmPad
sensors be directly subject to Electrostatic Discharges in excess of 2kV, this may
result in permanent damage to the sensors (which would require service/repair).
RhythmPadGP Manual.doc 20/05/16
GP
has been tested regarding its ability to operate in an environment
GP
.
GP
can be affected by other electrical/electronic equipment and
precautions
are
GP
GP
has been tested (and should be used only with) the USB cable
GP
is used with USB cables other than supplied, this may
GP
should not be used adjacent to, or stacked with, other equipment.
The user should be aware that if the RhythmPad
rd
party software stops responding and the RhythmPad
GP
have ceased responding).
party software stops responding and the RhythmPad
GP
cease responding). In addition, should the hand
Cardiocity Limited – RhythmPad
GP
GP
that has been undertaken, normal operation
needed
regarding
is configured and installed/put into service, in
GP
does not have an essential
GP
should be moved away from
GP
is subject to electromagnetic
GP
should be moved away from any
GP
– User Guide- Page 11
GP
& Electromagnetic
is not likely to adversely
GP
is medical
EMC
(electromagnetic
GP
in relation
GP
GP
is subject to
GP
may occur in
GP
may
GP
LED is lit
GP
may occur in the
GP
may cease
GP
LED is lit solid
and
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