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Commission Delegated Regulation (EU) 2023/503 of 1 December 2022 amending Regulation (EU) 2017/746 of the European Parliament and of the Council as regards the frequency of complete re-assessments of notified bodies (Text with EEA relevance)
Text
Chronology
Context
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Basic information
In force
CELEX number:
32023R0503
Official Journal:
JOL_2023_070_R_0002
Form:
Regulation
Procedure number:
--
Languages:
bg
cs
da
de
el
en
et
fi
fr
ga
hr
hu
it
lv
lt
mt
nl
pl
pt
ro
sk
sl
es
sv
Dates
Date of document:
December 1, 2022
Date of publication:
March 8, 2023
Date of effect:
March 11, 2023
Entry into force - Date pub. +3 See Art 2
Modified by
Modifies
Modifies:
Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU (Text with EEA relevance. )
Affected by case
Legal basis
Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU (Text with EEA relevance. )
EuroVoc Vocabulary
Single market
Public health
Medical devices
Marketing standard
Safety standard
Quality standard
Medical diagnosis
Technical barriers
Patient's rights
Medical device
Public health
Protection of health and safety
Internal market - Principles
Genetics