14.EC Declaration of Conformity
EC Declaration of Conformity
We herewith declare, in exclusive responsibility, that the
Leica CM1950 Cryostat
was developed, designed and manufactured to conform with the
•Council Directive 2006/95/EC (Low Voltage),
•Council Directive 89/336/EEC, Appendix I (Electromagnetic Compatibility) and
•European council Directive 98/79/EC (IVD)
including their amendments up to the date mentioned below. The following harmonized standards were applied:
•EN
Safety requirements for electrical equipment for measurement, control and laboratory use - Part 1: General requirements
•EN
Safety requirements for electrical equipment for measurement, control and laboratory use - Part
•EN 591: 2001
Instruction for use for in vitro diagnostic instruments for professional use
•EN
Electrical equipment for measurement, control and laboratory use - EMC requirements - Part 1: General requirements
•EN
Electrical equipment for measurement, control and laboratory use - EMC requirements
•EN
Electromagnetic compatibility (EMC)
Part
•EN
Part 3: Limits -
Section 3: Limitation of voltage changes, voltage fluctuations and flicker in public
Electromagnetic compatibility (EMC)
• EN 418: 1992 | • EN 1037: 1995 |
Emergency stop equipment. | Safety of machinery. |
Principles for design. | Prevention of unexpected |
In addition, the following
•DIN EN ISO 9001: 2000
Quality management system - requirements.
Leica Biosystems Nussloch GmbH
Postfach 1120
October 11, 2007
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