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Acteon C50 - Electromagnetic Compatibility

Acteon C50
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011807-EN--B (2022-12_S617 S717F S900 S950 C50_IFU)
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8 ELECTROMAGNETIC COMPATIBILITY
All the information below is based on the requirements of standards to which the manufacturers of electrical medical devices
must adhere, as stated in standard IEC 60601-1-2.
The medical device complies with the electromagnetic compatibility standards in force.
However, the user must make sure that any electromagnetic interference does not create an additional risk, such as radio-
frequency transmitters or other electronic devices.
This chapter contains the information required for you to install and use your medical device in optimum conditions in terms
of electromagnetic compatibility.
Different medical device leads must be kept separate from each other.
Sometimes mobile telecommunication devices such as mobile phones can interfere with the medical device. The
recommended separation distances in this chapter must therefore be strictly observed.
WARNING: The use of accessories, transducers and cables other than those specified or sold by SOPRO as replacement parts,
may have as a consequence an increase of emission or decreased immunity of the medical device and result in inadequate
operation.
8.1 CABLES LENGTH
Cables and accessories
Maximum length
USB connection cable
< 3 m
8.2 APPLICABLE TESTS
Test type
In compliance with
Applicable (A)/
Non-applicable (N/A)
Conducted disturbances (conducted emissions)
CISPR 11
A
Electromagnetic radiation disturbance (radiated emissions)
CISPR 11
A
Harmonic current emissions
IEC 61000-3-2
A
N/A for C50
Voltage changes, voltage fluctuations and flickers emissions
IEC 61000-3-3
A
N/A for C50
Electrostatic discharge immunity
IEC 61000-4-2
A
Radiated RF electromagnetic field immunity
IEC 61000-4-3
A
Immunity to proximity fields from RF wireless communications
equipment
IEC 61000-4-3
A
Electrical fast transient/burst immunity A.C Mains
IEC 61000-4-4
A
Electrical fast transient/burst immunity I/O SIP/SOP PORTS
IEC 61000-4-4
A
N/A for C50
Surge immunity
IEC 61000-4-5
NA
Immunity to conducted disturbances, induced by RF fields
(Immunity to conducted RF disturbances) A.C Mains
IEC 61000-4-6
A
Immunity to conducted disturbances, induced by RF fields
(Immunity to conducted RF disturbances) SIP/SOP PORTS
IEC 61000-4-6
A
Power frequency magnetic field immunity
IEC 61000-4-8
A
Voltage dips immunity
IEC 61000-4-11
NA
Voltage short interruptions and voltage variations immunity
IEC 61000-4-11
NA
Proximity magnetic fields (ROUMAIN ONLY FOR THE MOMENT)
IEC 61000-4-39
Applicable only for C50
N/A for other cameras
8.3 RECOMMENDED SEPARATION DISTANCES
The medical device is designed to be used in an electromagnetic environment in which interferences due to RF radiation are
controlled.
The user or installer of the medical device can help prevent any electromagnetic interference by applying a minimum distance,
according to the maximum power of the radio-frequency transmission equipment.

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