FujiFilm PB-30 Operation Manual page 75

<Medical Device Directive>
This product complies with the requirements of
European Directive 93/42/EEC.
Classification : Class IIa
<Electromagnetic Compatibility (EMC) Information>
This product is intended for use in the electromagnetic environments specified below.
The customer or the user of this product should assure that it is used in such an
environment.
Electromagnetic emission compliance information and guidance
RF emissions
EN 55011
Radiated emissions
EN 55011
Harmonic emissions
EN 61000-3-2
Voltage fluctuations/
flicker emissions
EN 61000-3-3
Emission standard Compliance
This product uses RF (Radio Frequency) energy
only for its internal function. Therefore, its
Group I RF emissions are very low and are not likely
to cause any interference in nearby electric
equipment.
This product is intended for use in medical
Class B
facilities and commercial facilities.
I f t h i s p r o d u c t i s u s e d i n d o m e s t i c
establishments, electromagnetic interference
Class B
may occur on any equipments.
In this case, it is recommended to use this
product according to Chapter 1 "Safety."
Applicable
Main Specifications
Guidance
75