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EN 1060-4:2004 Standard
Keywords:
Directive
Last Official Journal reference
Description:
Purpose
Publication
Medical devices Directive (93/42/EEC)
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Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01)
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Anaesthetic and respiratory equipment - Compatibility with oxygen (ISO 15001:2010)
Medical devices Directive (93/42/EEC)
Ophthalmic instruments - Fundamental requirements and test methods - Part 1: General requirements applicable to all ophthalmic ins...
CELAB is Notified Body No.2037 for the EMC Directive and Italian office of a Notified Body for the RED Directive.
CELAB performs voluntary inspection activities on technical construction files to check their contents.
CELAB can accomplish all the required tests in order to affix the CE-marking related to EMC, LVD, RED, MDD, machines and many others.
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This Free of Charge application was designed to help manufacturers, consultants, notified bodies to keep under control the EU declaration of conformity
This software allows you to compose in few minutes declaration of conformity compliant with applicable directives taking under control list of products, declarations of conformity, amended declarations
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