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Biotek PowerWave - Page 12

Biotek PowerWave
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viii
Based on the testing below, PowerWave bears the CE mark.
EC DIRECTIVE 89/336/EEC
EN 50081-1, CLASS A-Emissions
The system has been type tested by an independent testing laboratory and
found to meet the requirements of EC Directive 89/336/EEC for Radiated
Emissions and Line Conducted Emissions. Verification was to the limits
and methods of EN 55022. The device is classified as EN 55022, Class A.
EN 50082-1 Immunity
The system was also tested and found to meet requirements for
Electrostatic Discharge Susceptibility, Radiated Susceptibility, and
Electrical Fast Transient/Burst Susceptibility. Verification of compliance
was conducted to the limits and methods of EN 50082-1:1992; IEC 1000-4-
2:1995; IEC 1000-4-3:1995; and IEC 1000-4-4:1995.
Safety
This device has been type tested by an independent laboratory and found
to meet the requirements of:
North America
Canadian Standards Association CAN/CSA C22.2 No. 1010.1-1992
Safety Requirements for Electrical Equipment for Measurement,
Control and Laboratory Use, Part 1: General Requirements
International
IEC 1010-1 (1990) "Safety requirement for electrical equipment for
measurement, control and laboratory use. Part 1, General
requirements."
EC Directive 73/23/EEC Low Voltage Directive
EN 61010-1 (1990) "Safety requirement for electrical equipment for
measurement, control and laboratory use. Part 1, General
requirements."

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