Thermo Scientific Shandon TissueWave 2, Operator'S Manual

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56 TissueWave 2 Operator Guide
Declaration of Conformity
This Declaration of Conformity is only valid when the instrument is used in accordance with the Operator Guide
Manufacturer’s Name:
Manufacturer’s Address:
Product Description:
Product Designation:
Part numbers:
Year of Marking (CE):
Thermo Shandon Limited
(Trading as Thermo Fisher Scientific)
Chadwick Road, Astmoor, Runcorn,
Cheshire, WA7 1PR
ENGLAND
including accessories supplied as standard
This product conforms with the essential requirements of the following directives:
In Vitro Diagnostics Directive
Low Voltage Directive
98/79/EC
2006/95/EC
This product complies with the following International Standards:
EMC:
Safety:
Issued by:
K. Waldron
Quality Manager
Thermo Fisher Scientific
Anatomical Pathology, Diagnostics Division
Date:
Optional accessories considered subject to the In Vitro Diagnostics Directive (IVDD) are specifically identified on this Declaration of Conformity.
Further supplies of standard accessories are treated as spares. Convenience aids offered as accessories are not subject to the IVDD.
L aboratory M icrowave T issue P rocessor
Shandon TissueWave® 2
B35600001, B35600002
2005
EN /IEC 61326:1997
I
nc A 1:1998+ A 2:2001 + A 3:2003
EN 61010-1:2001
CAN /CSA C22.2N
o . 61010-1-04
UL 61010-1, 1 stedition
27 th F ebruary , 2007