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Biotek EL800 - Directive 2002;96;EC: Waste Electrical and Electronic Equipment; Directive 73;23;EEC Low Voltage; Directive 89;336;Eec:electromagnetic Compatibility; Directive 98;79;EC: in Vitro Diagnostics

Biotek EL800
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Hazards and Precautions | xix
ELx800 Operator's Manual
Directive 89/336/EEC:Electromagnetic Compatibility
Emissions - CLASS A
EN 61326-1:2002
EN 55022:2000 Class A, CISPR 16-1:1993, CISPR 16-2:1999
Immunity
EN 61326-1:2002
EN 61000-4-2: Electrostatic Discharge
EN 61000-4-3: Radiated EM Fields
EN 61000-4-4: Electrical Fast Transient/Burst
EN 61000-4-5: Surge Immunity
EN 61000-4-6: Conducted Disturbances
EN 61000-4-11: Voltage Dips, Short Interruptions and Variations
Directive 73/23/EEC Low Voltage
IEC 1010: “Safety requirement for electrical equipment for measurement, control
and laboratory use. Part 1, General requirements”.
Directive 2002/96/EC: Waste Electrical and Electronic Equipment
Disposal Notice
This instrument contains printed circuit boards and wiring with lead solder. Dispose
of the instrument according to Directive 2002/96/EC, “on waste electrical and
electronic equipment (WEEE).”
Directive 98/79/EC: In Vitro Diagnostics
Product registration with competent authorities
Traceability to the U.S. National Institute of Standards and Technology
(NIST):
Optical density measurements, and if equipped, incubator
temperature readings, are traceable to NIST.
Specific data for a particular serial number is available on request from BioTek
Instruments. See page x for contact information.
Based on the testing described below and information contained
herein, this instrument bears the CE mark.

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