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Biotek Epoch 2 User Manual

Biotek Epoch 2
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Preface Page 8 of 42
Epoch 2 Instructions for Use 1771011 Revision A BioTek Instruments, Inc.
CE Mark
Directive 2014/30/EU: Electromagnetic Compatibility
EmissionsClass A
The system has been type-tested by an independent, accredited testing laboratory and
found to meet the requirements of EN 61326-1: Class A for Radiated Emissions and
Line Conducted Emissions.
Verification of compliance was conducted to the limits and methods of EN 55011
(CISPR 11) Class A. In a domestic environment it may cause radio interference, in which
case you may need to mitigate the interference.
Immunity
The system has been type-tested by an independent, accredited testing laboratory and
found to meet the requirements of EN 61326-1 and EN 61326-2-6 for Immunity.
Verification of compliance was conducted to the limits and methods of the following:
EN 61000-4-2, Electrostatic Discharge
EN 61000-4-3, Radiated Radio Frequency (RF) Immunity
EN 61000-4-4, Electrical Fast Transient/Burst Immunity
EN 61000-4-5, Surge Immunity
EN 61000-4-6, Conducted RF Disturbance Immunity
EN 61000-4-11, Voltage Dips, Interruptions and Short Variations
Directive 2014/35/EU Low Voltage (Safety)
The system has been type-tested by an independent testing laboratory and was found
to meet the requirements of this Directive. Verification of compliance was conducted
to the limits and methods of the following:
EN 61010-1. "Safety requirement for electrical equipment for measurement, control
and laboratory use. Part 1, General requirements."
EN 61010-2-010. "Particular requirements for laboratory equipment for the heating of
materials."
Directive 2012/19/EU: Waste Electrical and Electronic Equipment
Disposal Notice: Dispose of the instrument according to Directive 2012/19/EU, “on
waste electrical and electronic equipment (WEEE)” or local ordinances.

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Biotek Epoch 2 Specifications

General IconGeneral
BrandBiotek
ModelEpoch 2
CategoryLaboratory Equipment
LanguageEnglish

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