Appendix 1. Electromagnetic Compatibility
Like other electrical medical equipment, the system requires special precautions to ensure electromagnetic compatibility
with other electrical medical devices. To ensure electromagnetic compatibility (EMC) the system must be installed and
operated according to the EMC information provided in this manual. The system has been designed and tested to comply
with IEC 60601-1-2 requirements for EMC with other devices.
Guidance and manufacturer’s declaration – electromagnetic emission
The system is intended for use in the electromagnetic environment specified below. The customer or the user of the
system should assure that it is used in such an environment.
Emissions Test
Compliance
Electromagnetic Environment Guidance
RF emission CISPR 11
Group 1
The system 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 emission CISPR 11
Class A
The system is suitable for use in all establishments other than
domestic, and may be used in domestic establishments and those
directly connected to the public low-voltage power supply
network that supplies buildings used for domestic purposes, ,
provided the following NOTE 1 is heeded.
Harmonic emission IEC/
EN 61000-3-2
Not applicable
Voltage fluctuations /
flicker emissions IEC/EN
61000-3-3
Complies
NOTE 1:
The emissions Characteristics of this equipment makes it suitable for use in industrial areas and hospitals (CISPR
11 class A). If it is used in a residential environment (for which CISPR 11 class B is normally required) this equipment might
not offer adequate protection to the radio-frequency communication service. The user might need to take mitigation
measures, such as relocating or re-orienting the equipment.
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