Biotek Cytation 5 Instructions For Use Manual page 8

viii | Preface
CE Mark
Based on the testing described below and information
contained herein, this instrument bears the CE mark
Refer to the Declaration of Conformity for specific details.
Directive 2014/30/EU: Electromagnetic Compatibility
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: 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 EM Fields
EN 61000-4-4, Electrical Fast Transient/Burst
EN 61000-4-5, Surge Immunity
EN 61000-4-6, Conducted Disturbances from RFI
EN 61000-4-8, Power Frequency Magnetic Field Immunity Test
EN 61000-4-11, Voltage Dips, Short Interruptions and 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 61010-2-081. "Particular requirements for automatic and semi-automatic
laboratory equipment for analysis and other purposes."
EN 61010-2-010. "Particular requirements for laboratory equipment for the heating of
materials."
BioTek Instruments, Inc.