77210163GB Issue 3
58
Issued by:
K Waldron
Quality Manager
Thermo Fisher Scientific
Clinical Diagnostics, Anatomical Pathology
This product conforms with the essential requirements of the following directives:
In Vitro Diagnostics Directive 98/79/EC
Low Voltage Directive
73/23/EEC
(as amended by 93/68/EEC)
This product complies with the following International Standards:
EMC:
EN61326-2-6
EN61000-3-2
EN61000-3-3
Safety:
IEC 1010-1
CAN / CSA - C22.2 No 1010.1-92
UL Std No. 3101
Declaration of Conformity
This Declaration of Conformity is only valid when the instrument is used in accordance with this Operator Manual
Manufacturer’s Name:
Thermo Shandon Limited (Trading as
Thermo Fisher Scientific)
Manufacturer’s Address:
Tudor Road, Manor Park, Runcorn,
Cheshire, WA7 1TA
ENGLAND
Product Description:
Electronic Cryostat
Product Designation: Cryotome
®
E
(0620E, 0620E/G, 0620E/F, 0620E/110)
including accessories supplied as standard, and
the following accessories:
Orientation Heads: 0620-006, 0620-008
Cryocassettes: 603, 605, 77210080, 0620-001, 0620-007,
0620-026, 0620-036, 0620-039, 0620-041,
0620-405, 0620-820, A77210155
Knife Holders: 0620-021H, 0620-021L, 0620-022H, 0620-022L,
0620-023
Year of Marking (CE):
1996
Date: 8 January 2010
Optional accessories considered subject to the In Vitro Diagnostic 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
Содержание Cryotome
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