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Commission Delegated Regulation (EU) 2023/502 of 1 December 2022 amending Regulation (EU) 2017/745 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:
32023R0502
Official Journal:
JOL_2023_070_R_0001
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) 2017/745 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. )
Affected by case
Legal basis
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. )
EuroVoc Vocabulary
Market supervision
Safety standard
Medical devices
Marketing standard
Market approval
Quality standard
Harmonisation of standards
EC conformity marking
Health legislation
Testing
Protection of health and safety
Internal market - Principles
Public health
Medical device