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LBL000097A
LightForce FX User Manual, DCN: O
FX
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Electromagnetic Compatibility (EMC) Tables
All medical electronic devices must conform to the requirements of IEC 60601-
1-2. Precautions, adherences to the EMC guideline information provided in this
manual and verification of all medical devices in simultaneous operation are
required to ensure the electromagnetic compatibility and coexistence of all
other medical devices prior to a laser therapy treatment.
Table 16.1 - Guidance and Manufacturer’s Declaration - Emissions
(All ME Equipment and ME Systems)
The LightForce® FX is intended for use in the electromagnetic environment specified below. The
customer or user of the LightForce FX should ensure that it is used in such an environment.
Emissions Test
Compliance
Electromagnetic Environment – Guidance
RF Emissions
CISPR 11
Group 1
The LightForce FX 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 or B
Failed Class A
Harmonics
IEC 61000-3-2
Class A,B,C,D or N/A
Class A
Flicker
IEC 61000-3-3
Complies or N/A
Complies
The LightForce FX is suitable for use in all establishments,
other than domestic, and those directly connected to the
public low-voltage power supply network that supplies
buildings used for domestic purposes.
RF Emissions
CISPR 14-1
Complies
The LightForce FX is not suitable for interconnection with
other equipment.
RF Emissions
CISPR 15
Complies
The LightForce FX is not suitable for interconnection with
other equipment.
