EMC Tables
Vividimage
®
4K Surgical Display
OPM3000, Rev. C
Operation Manual
23
EMC Tables
The following tables are referenced from IEC 60601-1-2:2014; Medical Electrical Equipment - Part 1-2: General
requirements for basic safety and essential performance - Collateral standard: Electromagnetic compatibility -
Requirements and test.
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 normally 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-orienting the equipment
Table 1
(Page 20, Table 1 from IEC 60601-1-2:2014)
Vividimage
®
4K Surgical Display guidance and manufacturer's declaration - electromagnetic emissions
The Vividimage
®
4K Surgical Display is intended for use in the electromagnetic environment specified below.
The customer or the user of the Vividimage
®
4K Surgical Display should assure that it is used in such an environ-
ment.
Emissions test
Compliance
Electromagnectic environment - guidance
RF emissions
CISPR 11
Group 1
The Vividimage
®
4K Surgical Display 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 Vividimage
®
4K Surgical Display 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 domes-
tic purposes.
Harmonic emissions
IEC 61000-3-2
Class A
Voltage fluctuations/
flicker emissions
IEC 61000-3-3
Complies