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Regulation (EU) 2017/745 : 2017

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

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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.)

Available format(s)

Hardcopy

Language(s)

English

Published date

05-04-2017

Superseded date

21-12-2022

Free
Summarise this standard

Describes rules concerning the placing on the market, making available on the market or putting into service of medical devices for human use and accessories for such devices in the Union. Pertains to clinical investigations concerning such medical devices and accessories conducted in the Union.

DevelopmentNote
Supersedes 93/42/EEC. (08/2017) Supersedes 90/385/EEC, 2001/104/EC & 2007/47/EC which remain valid until 25/05/2020. (09/2017)
DocumentType
Standard
Pages
228
PublisherName
European Union
Status
Superseded
SupersededBy
Supersedes

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A newer version of this standard is available.

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