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Leica CM3050 S User Manual

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Dag Graupner
Managing Director
We herewith declare, in exclusive responsibility, that the
Leica CM3050 S – Cryostat
was developed, designed and manufactured to conform with the
•
Council Directive 73/23/EEC (Low Voltage),
•
Council Directive 89/336/EEC, Appendix I (Electromagnetic Compatibility) and
•
European council Directive 98/79/EG (IVDD).
The following harmonized standards were applied:
•
EN 61010-1: 2001
Safety requirements for electrical equipment for measurement, control and laboratory use -
Part 1: General requirements
•
EN 61010-2-101: 2002
Safety requirements for electrical equipment for measurement, control and laboratory use -
Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
•
EN 61326-1: 1997 + A1: 1998 + A2: 2001 + A3: 2003
Electrical equipment for measurement, control and laboratory use - EMC requirements -
Part 1: General requirements
•
EN 61000-3-2: 2000
Electromagnetic compatibility (EMC)
Part 3-2: Limits - Limits for harmonic current emissions
•
EN 61000-3-3: 1995 + A1: 2001
Part 3: Limits -
Section 3: Limitation of voltage fluctuations and flicker in low-voltage
supply systems for equipment with rated current £ 16 A
Electromagnetic compatibility (EMC)
•
EN 418: 1992
•
EN 1037: 1995
Emergency stop equipment.
Safety of machinery.
Principles for design.
      Prevention of unexpected start-up.
In addition, the following in-house standards were applied:
•
DIN EN ISO 9001: 2000.
EC Declaration of Conformity
Leica Microsystems Nussloch GmbH
Postfach 1120
D-69222 Nussloch
January 12, 2004
10.
EC Declaration of Conformity