IceCure Medical Ltd.
DSR3210000 rev. D
ProSense™
Confidential
User Manual
129
Return to first page
15
Manufacturer’s Declaration of the EUT
Guidance and
manufacturer’s declaration
-electromagnetic emission- for all
EQUIPMENT AND SYSTEMS
1 Guida
nce and manufacturer’s declaration
-electromagnetic emission
2 The model
ProSense™
Cryotherapy product is intended for use in the electromagnetic
environment specified below. The customer or the user of the model
ProSense™
Cryotherapy
product should ensure that it is used in such an environment.
3
Emissions test
Compliance
Electromagnetic environment - guidance
4 RF emissions
CISPR 11
Group 1
The model
ProSense™
Cryotherapy product
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.
5 RF emissions
CISPR 11
Class B
6 Harmonic emissions
EN 61000-3-2
Class A
7 Voltage fluctuations /
flicker emissions
EN 61000-3-3
Complies