Bioventus EXOGEN Guia Del Usuario página 31

EXOGEN Classifications
EXOGEN has the following classifications:
• Internally Powered Equipment
• Type BF Applied Part
• EXOGEN device: IP-22
• Transducer: IP-67
• Equipment not suitable for use in the presence of a
flammable anaesthetic mixture with air or with
oxygen or with nitrous oxide.
• Mode of operation – Intermittent
Guidance and Manufacturer's
Declaration – Electromagnetic
Emissions and Immunity Testing
Electromagnetic
Compatibility Testing
Summary: Testing Report for:
Bioventus LLC.
Equipment Under Test: EXOGEN
Used for Life Support: No
Use in shielded enclosure: No
Guidance and manufacturer's declaration – electromagnetic emissions
EXOGEN is intended for use in the electromagnetic environment specified below. The customer or the user
of EXOGEN should assure that it is used in such an environment.
Emissions Test
RF emissions
CISPR 11
RF emissions
CISPR 11
Harmonic emissions
IEC 61000-3-2
Voltage fluctuations /
flicker emissions
IEC 61000-3-3
®
Compliance Electromagnetic environment – guidance
Group 1 EXOGEN 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 equip-
ment.
Class B EXOGEN is suitable for use in all establishments including domestic and those
directly connected to the public low-voltage power supply network that supplies
buildings used for domestic purposes.
Class A
Complies
28