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European Union
Regulation (EU) 2023/607
Article 1
(3)

Regulation (EU) 2023/607

In forceThis text since 20 Mar 2023law://eu/reg/2023/607/art_1__pnt_3@2026-11-12

Version in force onWhereEuropean Union

(1) Article 120 is amended as follows:
(2) Article 122 is amended as follows:
(3) in Article 123(3), point (d), the 24th indent is replaced…

Contents

(1) Article 120 is amended as follows:
(2) Article 122 is amended as follows:
(3) in Article 123(3), point (d), the 24th indent is replaced…

(3)in Article 123(3), point (d), the 24th indent is replaced by the following:

—Article 120(3d).’.

Key facts

Type: Regulation · (EU) 2023/607 · EEA relevant
Adopted: 15 Mar 2023
In force: 20 Mar 2023
Made by: Council of the European Union, European Parliament
Official: EUR-Lex 32023R0607 · ELI

Topics

EC conformity marking market approval marketing standard medical device medical diagnosis public health quality standard safety standard security of supply single market Internal market - Principles Medical devices

History · 1 version

20 Mar 2023Reading

Connections

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Amends 1: Regulation (EU) 2017/745
Cited by 3: Council Decision (EU) 2026/15352 provisions; Commission Regulation (EU) 2023/2482; Commission Implementing Regulation (EU) 2023/11943 provisions