Hach BioTector B7000 - EC Declaration of Conformity; Compliance with EU Directives and Harmonized Standards

EC Declaration of Conformity
Manufacturer: BioTector Analytical Systems Ltd., Raffeen House, Ringaskiddy, Co.Cork, Ireland
Tel: (+353) 21 437 42 37, Fax: (+353) 21 437 42 36, e-mail: info@biotector.com.
Declares that all models of following product:
BioTector B7000, all models:
comply with the essential requirements of the following Directive(s):
2014/30/EU
EMC Directive
2014/68/EU
Pressure Equipment Directive
2006/42/EC
Machinery Directive
The following harmonized standards were used to meet the requirements of the stated Directive(s):
EN 61000-6-2:2005 &
AC:2005
Electromagnetic compatibility (EMC) -- Part 6-2: Generic standards - Immunity for
industrial environments
EN 61000-6-4:2007 &
A1:2011
Electromagnetic compatibility (EMC) -- Part 6-4: Generic standards - Emission standard
for industrial environments
EN 61326-1:2013
Electrical equipment for measurement, control and laboratory use - EMC requirements --
Part 1: General requirements
EN 61000-3-2:2006 &
A1:2009 & A2:2009
Electromagnetic compatibility (EMC) -- Part 3-2: Limits - Limits for harmonic current
emissions (equipment input current <= 16 A per phase)
EN 61010-1:2010
Safety requirements for electrical equipment - General requirements
Authorised Person to compile the technical file:
Seamus O’ Mahony – Research and Development Director
BioTector Analytical Systems Ltd., Raffeen House, Ringaskiddy, Co.Cork, Ireland.
CE Co-ordinator:
Seamus O’ Mahony – Research and Development Director
BioTector Analytical Systems Ltd., Raffeen House, Ringaskiddy, Co.Cork, Ireland.
Year of primary CE marking of the products: CE 2003
………………………………………………………………………………..
Seamus O’ Mahony – Research and Development Director
BioTector Analytical Systems Ltd., Raffeen House, Ringaskiddy, Co.Cork, Ireland.
07 July 2016