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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
EN 1060-4:2004 Standard
Medical devices Directive (93/42/EEC)
Medical electrical equipment - Part 2-24: Particular requirements for the safety of infusion pumps and controllersIEC 60601-2-24:1...
Medical devices Directive (93/42/EEC)
Symbol for use in the labelling of medical devices - Requirements for labelling of medical devices containing phthalates
Medical devices Directive (93/42/EEC)
Pressure vessels for human occupancy (PVHO) - Multi-place pressure chamber systems for hyperbaric therapy - Performance, safety re...
Medical devices Directive (93/42/EEC)
Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01)
Medical devices Directive (93/42/EEC)
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.
CLICK HERE TO GET TESTS AND INFO ON THE EN 1060-4:2004 STANDARD
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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