Appendix - Electromagnetic Compatibility (Emc) - GE TONOPORT V Operator's Manual

Ambulatory blood pressure system
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11 Appendix - Electromagnetic
Compatibility (EMC)
Changes or modification to this system not expressly
approved by GE Healthcare could cause EMC issues with
this or other equipment This system is designed and
tested to comply with applicable regulation regarding
EMC. It needs to be installed and put into service
according to the EMC information stated as follows.
Guidance and Manufacturer's Declaration – Electromagnetic Emissions
TONOPORT V is intended for use in the electromagnetic environment specified below. It is the responsibility of the
customer or user to ensure that TONOPORT V is used in such an environment.
Emissions Test
RF emissions to EN 55011/
CISPR 11
RF emissions to EN 55011/
CISPR 11
Harmonic emissions to EN
61000-3-2/IEC 61000-3-2
Voltage fluctuations/flicker
emissions to EN 61000-3-3/IEC
61000-3-3
2001589-085 Revision G
Electromagnetic Compatibility (EMC)
Compliance
Group 1
Class B
not applicable
not applicable
TONOPORT V
Warning
Use of portable phones or other radio frequency
(RF) emitting equipment near the system may cause
unexpected or adverse operation.
Warning
The equipment or system should not be used
adjacent to, or stacked with, other equipment. If
adjacent or stacked use is necessary, the equipment
or system should be tested to verify normal
operation in the configuration in which it is being
used.
Electromagnetic Environment - Guidance
TONOPORT V uses RF energy only for its internal
function. Therefore, its RF emissions are very low and
are not likely to cause any interference in nearby
electronic equipment.
TONOPORT V is suitable for use in all
establishments, including domestic and those directly
connected to the public low-voltage power supply
network that supplies buildings used for domestic
purposes.
30

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