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Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
Annex II
Division 5

Division 5.1

United Kingdom

Original text. Later amendments are not shown.

The aim of surveillance is to ensure that the manufacturer duly fulfils the obligations imposed by the approved quality system.

Division 5.1

Division 5.2 →

Legislation: Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
Citation: EU Directive 1993/42, division 5.1
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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