Fluke Biomedical 601PRO XL - Manual (Page 9)

N O T I C E S , W A R N I N G S A N D C O N T E N T
i x
Based on the testing described below, this instrument bears the CE mark.
EC Directive 89/336/EEC Electromagnetic Compatibility
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Emissions - CLASS A
The system has been type tested by an independent, accredited testing laboratory and
found to meet the requirements of EN 61326-1:1998 for Radiated Emissions and Line
Conducted Emissions. Verification of compliance was conducted to the limits and
methods of the following:
CISPR 16-1:1993 and CISPR 16-2:1996
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Immunity
The system has been type tested by an independent, accredited testing laboratory and
found to meet the requirements of EN 61326-1:1998 for Immunity. Verification of
compliance was conducted to the limits and methods of the following:
EN 61000-4-2 (1991) Electrostatic Discharge
EN 61000-4-3 (1995) Radiated EM Fields
EN 61000-4-4 (1995) Electrical Fast Transient/Burst
EN 61000-4-5 (1995) Surge Immunity
EN 61000-4-6 (1996) Conducted Disturbances
EN 61000-4-11 (1994) Voltage Dips, Short Interruptions and Variations
EC Directive 73/23/EEC Low Voltage (Safety)
The system has been type tested by an independent testing laboratory and found to meet
the requirements of EC Directive 73/23/EEC for Low Voltage. Verification of compliance
was conducted to the limits and methods of the following:
EN 61010-1 (1993) & IEC 1010-1
“Safety Requirements for Electrical Equipment for Measurement, Control and
Laboratory Use, Part 1: General requirements” (including amendments 1 & 2).