The Medical Devices (Amendment) Regulations 2003

Information

Type

Regulation

Regulated products

Medical Devices

Published

July 4, 2003

Last updated

September 1, 2003

Description

These Regulations amend the Medical Devices Regulations 2002 (“the principal Regulations”), which contain the legislative measures necessary for the implementation of the European Community scheme for regulating the placing on the market and putting into service of medical devices. The amendments include amendments that are necessary for the implementation of Commission Directive 2003/12 of 3rd February 2003 on the reclassification of breast implants within the framework of Directive 93/42/EEC on medical devices (“Directive 2003/12”) and Commission Directive 2003/32 of 23rd April 2003 on medical devices utilising tissues of animal origin (“Directive 2003/32”).

Organization

Country / Region

United Kingdom

License

Open Government Licence 3.0 (United Kingdom)

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