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EMC
June 12, 2003
EN60601-1-1: Medical electrical equipment - Part 1: General
requirements for safety - Section 1: Collateral standard: Safety
requirements for medical electrical systems.
EN60825-1: Safety of laser products - Part 1: Equipment classification,
requirements and user's guide.
Rest of World
IEC 60950: Safety of information technology equipment.
IEC 60601-1-1: Medical electrical equipment - Part 1: General
requirements for safety - Section 1: Collateral standard: Safety
requirements for medical electrical systems.
IEC 60825-1: Safety of laser products - Part 1: Equipment classification,
requirements and user's guide.
United States
FCC Rules and Regulations, Title 47, Part 15, Subpart B, Class A: Radio
Frequency Devices: Unintentional Radiators.
This equipment has been tested and been found to comply with the limits
for a Class A digital device pursuant to part 15 of the FCC rules. Those limits
are designed to provide reasonable protection against harmful
interference in a residential installation.
FCC Rules and Regulations, Title 47, Part 15, Subpart C, Radio Frequency
Devices: Intentional Radiators. This Device Contains "FCC ID: PA 48E1587"
Canada
CAN/CSA-C108.6-M91, Class A: Limits and Methods of Measurement of
Electromagnetic Disturbance Characteristics of Industrial, Scientific and
Medical (ISM) Radio-Frequency Equipment.
Intentional Radiation. This Device contains "IC: 1016B-8E1587"
This Class A digital apparatus complies with Canadian ICES-003.
CET APPAREIL NUM ENRIQUE DE CLASSE A EST CONFORME A LA NORME
NMB–003 DU CANADA.
5E6155
Safety and Related Information
1-11
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