Declaration Of Conformity - Integra VIAFLO II Manual De Instrucciones

Declaration of conformity

INTEGRA Biosciences AG – 7205 Zizers, Switzerland
declares on its own responsibility that the devices
Description
VIAFLO II Pipettes
VOYAGER II Pipettes
comply with:
EU Directives (DoW: Date of Withdrawal)
Low Voltage Equipment
Electromagnetic Compatibility
Restriction of Hazardous Substances
Waste Electrical and Electronic Equipment
Battery Directive
EU Regulations
Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) 1907/2006
Capacity Labelling of Portable Secondary Batteries
Standards for EU
Safety requirements for electrical equipment for measurement,
control and laboratory use - General requirements.
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.
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.
International Standards
Piston-operated volumetric apparatus - Part 2: Piston pipettes
Zizers, November 4, 2016
Models
4011, 4012, 4013, 4014, 4015, 4016, 4621, 4622, 4623, 4624,
4626, 4631, 4632, 4633, 4634, 4636, 4641, 4642, 4646
4721, 4722, 4723, 4724, 4726, 4731, 4732, 4736, 4743, 4744,
4763, 4764
Elmar Morscher
CEO
Before DoW DoW
2006/95/EC 20.04.2016
2004/108/EC 20.04.2016
2011/65/EU
2012/19/EU
2006/66/EC
Thomas Neher
Quality Manager
After DoW
2014/35/EU
2014/30/EU
1103/2010
EN 61010-1: 2010
EN 61326-1: 2013
CAN/CSA-C22.2
No. 61010-1
UL 61010-1
Part 15 of the
FCC Rules
Class A
ISO 8655-2