GE TONOPORT VI, Руководство оператора

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Electromagnetic Compatibility (EMC)
2001589-312 Revision B TONOPORT VI 31
11 Appendix–Electromagnetic Com-
patibility (EMC)
Changes or modifications to this system not expressly
approved by GE Healthcare could cause EMC issues with
this or other equipment. This system is designed to
comply with applicable regulations regarding EMC. Its
compliance with these requirements has been verified. It
needs to be installed and put into service according to the
EMC information stated as follows.
Warning
Use of portable telephones 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.
Guidance and Manufacturer’s Declaration—Electromagnetic Emissions
TONOPORT VI is intended for use in the electromagnetic environment specified below. It is the responsibility of the
customer or user to ensure that TONOPORT VI is used in such an environment.
Emissions Test Compliance Electromagnetic Environment—Guidance
RF emissions to EN 55011/
CISPR 11 Group 1 TONOPORT VI 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.
RF emissions to EN 55011/
CISPR 11 Class B TONOPORT VI 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.
Harmonic emissions to
EN 61000-3-2/IEC 61000-3-2 not applicable
Voltage fluctuations/flicker
emissions to EN 61000-3-3/
IEC 61000-3-3 not applicable