The Medical Devices Regulations 2002

Information

Type

Regulation

Regulated products

IVDMD, Medical Devices

Published

May 20, 2002

Last updated

June 13, 2002

Description

These Regulations contain the legislative measures necessary for the implementation of three European Community Directives: Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, as amended; Council Directive 93/42/EEC concerning medical devices, as amended; and Directive 98/79/EC of the European Parliament and of the Council onin vitro diagnostic medical devices (“the Medical Devices Directives”). They also contain the legislative measures necessary for the implementation, in relation to medical devices, of the agreements on mutual recognition between the European Community and Australia, New Zealand, Canada and the United States of America—and of the Association Agreement between the European Communities, and their Member States, and Hungary.

Organization

Country / Region

United Kingdom

License

Open Government Licence 3.0 (United Kingdom)

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