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Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices
Annex III

Division 6

United Kingdom

Original text. Later amendments are not shown.

For devices for self-testing the manufacturer shall lodge an application for examination of the design with a notified body.

6.1Division 6.1
6.2Division 6.2
6.3Division 6.3

Division 6

Division 6.1 →

Legislation: Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices
Citation: EU Directive 1998/79, division 6
Official version: legislation.gov.uk

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Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives. legislation.gov.uk is the official version.

Not legal advice.

👋 Jason Cartwright
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