Ec Declaration Of Conformity - Leica ASP300 S Manual De Instrucciones

We herewith declare, in exclusive responsibility, that the
Leica ASP300 S – Vacuum Tissue Processor
was developed, designed and manufactured to conform with the
• Directive 2006/95/EC of the European Parliament and of the Council (Low Voltage),
• Directive 2004/108/EC of the European Parliament and of the Council (electromagnetic compatibility) and
• Direktive 98/79/EC of the European Parliament and of the Council (in-vitro diagnostic medical devices).
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 61010-2-010: 2003
Safety requirements for electrical equipment for measurement, control and laboratory use -
Part 2: Particular requirements for laboratory equipment for the heating of materials.
• EN 61326-1: 2006
Electrical equipment for measurement, control and laboratory use - EMC requirements -
Part 1: General requirements
• DIN EN 61010-2-101: 2002
Safety requirements for electrical equipment for measurement, control and laboratory use -
Part 2: Particular requirements for laboratory equipment for the heating of materials.
• EN 14971: 2007
Medical devices - Application of risk management to medical devices
• EN 591: 2001
Instruction for use for in vitro diagnostic instruments for professional use
In addition, the following in-house standards were applied:
• DIN EN ISO 9001: 2000
Leica Biosystems Nussloch GmbH
Postfach 1120
D-69222 Nussloch
March 10, 2008
Leica ASP300 S

EC Declaration of Conformity

9. EC Declaration of Conformity
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Anne De Greef-Safft
President Biosystems Devision
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