Steris HarmonyAIR G Series, Operator'S Manual

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Appendix - EMC Compliance Technical Data Operator Manual 10043124
Guidance and Manufacturer’s Declaration – Electromagnetic Emissions for all ME Equipment and
ME Systems
NOTE: The emissions characteristics of this equipment make 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 required), this
equipment might not offer adequate protection to radio frequency communication services. The user might need to
take mitigation measures, such as relocating or re-orientating the equipment.
Table 9-1. Guidance and Manufacturer’s Declaration – Electromagnetic Emissions – for all ME
Equipment and ME Systems (per IEC 60601-1-2 clause 5.2.2.1 c) Table 1)
The HarmonyAIR™ Surgical Lighting System G Series is intended for use in the electromagnetic
environment specified below. The Customer or the user of the HarmonyAIR Surgical Lighting
System G Series should assure that it is used in such an environment.
Emissions test Compliance
Electromagnetic environment – guidance
RF emissions
CISPR 11
Group 1 The HarmonyAIR Surgical Lighting System G Series 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
CISPR 11
Class A
The HarmonyAIR Surgical Lighting System G Series is
suitable for use in all establishments other than domestic
establishments and those directly connected to the
public low-voltage power supply network that supplies
buildings used for domestic purposes.
Harmonic emissions
IEC 61000-3-2
Class A
Voltage fluctuations/
flicker emissions IEC
61000-3-3
Complies
APPENDIX– EMC Compliance Technical Data
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