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Eudamed and In-vitro Diagnostic Medical Devices
Current: Eudamed and in-vitro diagnostic medical devices

Eudamed and in-vitro diagnostic medical devices - Timeline

Timeline
Interinstitutional Timeline

Elfogadott vélemények on 20/03/2024 - Bureau decision date: 13/02/2024

Hivatkozás

INT/1060-EESC-2024-00746-00-00-AC-TRA

Opinion Type

Mandatory

Commission References

COM(2024) 43 final 2024/0021 COD

Official Journal

OJ , 31.5.2024, p.

Plenary session number

586

Mar 20, 2024 - Mar 21, 2024
Download — EGSZB-vélemény: Eudamed and in-vitro diagnostic medical devices

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15Feb2024

Type:
Committee opinion (AC)

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15Feb2024

Type:
Committee opinion (PAC)

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Procedure 2024/0021/COD
COM (2024) 43: Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL amending Regulations (EU) 2017/745 and (EU) 2017/746 as regards a gradual roll-out of Eudamed, information obligation in case of interruption of supply and the transitional provisions for certain in vitro diagnostic medical devices

Completed (Adopted act: 32024R1860)

Type: Ordinary legislative procedure (COD)

What is an Ordinary legislative procedure

Legal basis:

Commission: 12016E114 ; 12016E168-P4 ; 12016E294

EuroVoc thesaurus:

single market; medical device; public health
security of supply; information system; medical diagnosis; market approval; EC conformity marking; exchange of information

Directory code:

15.20.30.00 Environment, consumers and health protection / Consumers / Protection of health and safety

Type of the competence conferred on the EU:

Shared competence

More details on European Parliament - Legislative observatory website

For a detailed overview of the procedure, please visit the EU Law Tracker.
EU Law Tracker

Steps of procedure 2024/0021/COD

Reverse Order

/

Publication in the Official Journal

Date of publication

09/07/2024

CELEX number of the main document:

32024R1860

Signature

Signature by the President of the EP and by the President of the Council

13/06/2024

First reading

52024AP0368

25/04/2024

CELEX number of the main document:

52024AP0368

30/05/2024

Procedure:

Ordinary legislative procedure (COD)

Documents:

PE 54 2024 COR 1
PE 54 2024 INIT
ST 10225 2024 INIT
ST 10234 2024 INIT

28/05/2024

Procedure:

Ordinary legislative procedure (COD)

Documents:

ST 10225 2024 INIT

24/05/2024

Procedure:

Ordinary legislative procedure (COD)

Documents:

PE 54 2024 INIT

29/04/2024

Procedure:

Ordinary legislative procedure (COD)

Documents:

ST 9237 2024 INIT

12/04/2024

Procedure:

Ordinary legislative procedure (COD)

Documents:

ST 8879 2024 INIT

11/04/2024

Procedure:

Ordinary legislative procedure (COD)

Documents:

ST 8816 2024 INIT

21/03/2024

Procedure:

Ordinary legislative procedure (COD)

Documents:

ST 8102 2024 INIT

22/02/2024

Procedure:

Ordinary legislative procedure (COD)

Documents:

ST 6746 2024 INIT

08/02/2024

Procedure:

Ordinary legislative procedure (COD)

Documents:

ST 6067 2024 INIT

23/01/2024

Procedure:

Ordinary legislative procedure (COD)

Documents:

ST 5712 2024 INIT

Opinions

52024AE0746
EESC internal procedure

20/03/2024

Responsible body:

Section for the Single Market, Production and Consumption

Rapporteur:

Danko RELIĆ

Procedure:

Ordinary legislative procedure (COD)

Plenary session:

586

Plenary date:

20/03/2024 - 21/03/2024

Documents:

EESC 2024-00746

CELEX number of the main document:

52024AE0746

Proposal

52024PC0043
Commission internal procedure

23/01/2024

Leading person:

Stella KYRIAKIDES

Leading service:

Directorate-General for Health and Food Safety

Decision mode:

Written procedure

Addressee for formal act:

European Parliament ; Council of the European Union ; National parliaments

Addressee for mandatory consultation:

European Economic and Social Committee ; European Committee of the Regions

Legal basis:

12016E114 ; 12016E168-P4 ; 12016E294

Procedure:

Ordinary legislative procedure (COD)

Documents:

COM/2024/43/FINAL

CELEX number of the main document:

52024PC0043

Commission internal procedure

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