Declaration Of Conformity - Integra VIAFLO 96 Mode D'emploi

Declaration of conformity

INTEGRA Biosciences AG – 7205 Zizers, Switzerland
declares on its own responsibility that the devices
Description
VIAFLO 96
VIAFLO 384
comply with:
EU Directives (DoW: Date of Withdrawal)
Low Voltage Equipment
Electromagnetic Compatibility
Restriction of Hazardous Substances
Waste Electrical and Electronic Equipment 2012/19/EU
EU Regulations
Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) 1907/2006
Standards for EU
Safety requirements for electrical equipment for measurement,
control and laboratory use - General requirements.
Particular requirements for automatic and semi-automatic
laboratory equipment for analysis and other purposes.
Electrical equipment for measurement, control and laboratory use
- EMC requirements.
Standards for Canada and USA
Safety requirements for electrical equipment for measurement,
control and laboratory use - General requirements
Safety requirements for electrical equipment for measurement,
control and laboratory use - General requirements
Particular requirements for automatic and semi-automatic laboratory
equipment for analysis and other purposes
Operation is subject to the following two conditions: (1) this device may not
cause harmful interference, and (2) this device must accept any interfer-
ence received, including interference that may cause undesired operation.
a
NRTL certificate number (TÜV Süd): U8 17 05 42035 007
Zizers, June 19, 2017
Models
6000, 6001
6030, 6031
a
.
Elmar Morscher
CEO
Before DoW DoW
2006/95/EC 20.04.2016
2004/108/EC 20.04.2016
2011/65/EU
a
.
a
.
Thomas Neher
Quality Manager
After DoW
2014/35/EU
2014/30/EU
EN 61010-1: 2010
EN 61010-2-81: 2015
EN 61326-1: 2013
CAN/CSA-C22.2
No. 61010-1
UL 61010-1
UL 61010-2-81
Part 15 of the
FCC Rules
Class A