# Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC (Text with EEA relevance) (revoked), Annex III: TECHNICAL DOCUMENTATION ON POST-MARKET SURVEILLANCE

Extent: E+W+S+N.I.
Status: repealed

The technical documentation on post-market surveillance to be drawn up by the manufacturer in accordance with Articles 83 to 86 shall be presented in a clear, organised, readily searchable and unambiguous manner and shall include in particular the elements described in this Annex.

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Source: https://www.legislation.gov.uk/eur/2017/745/annex/III (the official version)
Page: https://openlegislation.uk/eu-regulation-2017-745/annex-III
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.