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EU MDR Regulation

Regulation (EU) 2017/745

Medical Device Regulation
European UnionEuropean CommissionRegistrationEffective May 26, 2021
What this code is

Regulation (EU) 2017/745 is the official EC identifier for “Medical Device Regulation”. Regulation (EU) 2017/745 is the official identifier EC uses for this instrument.

Instrument
Regulation
Full name
Regulation (EU) 2017/745
Category
Registration
Source links
Authority source
English
Issuing-authority publication; confirm whether a later amendment or consolidated version applies.
Readable HTML
123 articles · 1 language version
Direct citations can link to a specific article or section by appending its fragment identifier.
Dates
Published
May 5, 2017
Effective
May 26, 2021
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Each version has stable article anchors for direct citations and highlighting. The readable text is generated from an authority source and does not replace the legally controlling publication.

About this regulation

Medical Device Regulation

Authentic Official Journal expression of the EU Medical Device Regulation. Ingested from EUR-Lex CONVEX HTML for CELEX 32017R0745. Date of the act is 5 April 2017; OJ L 117 publication is 5 May 2017. Date of application 26 May 2021 is from Article 123.

Regulation (EU) 2017/745 is the official identifier EC uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.