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Query: ((DN = "32012R0207" AND DD <= 21/03/2023) OR (RESOURCE_LEGAL_CORRECTS_RESOURCE_LEGAL = "32012R0207" AND DD >= 09/03/2012 AND DD < 21/03/2023 AND (EMBEDDED_ACT_CONSOLIDATED_DATE > 09/03/2012 OR EMBEDDED_ACT_CONSOLIDATED_DATE = NULL)) OR ((RESOURCE_LEGAL_REPEALS_RESOURCE_LEGAL = "32012R0207" OR RESOURCE_LEGAL_IMPLICITLY_REPEALS_RESOURCE_LEGAL = "32012R0207" OR RESOURCE_LEGAL_RENDERS_OBSOLETE_RESOURCE_LEGAL = "32012R0207" OR RESOURCE_LEGAL_REPLACES_RESOURCE_LEGAL = "32012R0207" OR RESOURCE_LEGAL_SUSPENDS_RESOURCE_LEGAL = "32012R0207" OR RESOURCE_LEGAL_PARTIALLY_SUSPENDS_RESOURCE_LEGAL = "32012R0207" OR RESOURCE_LEGAL_AMENDS_RESOURCE_LEGAL = "32012R0207") AND DD > 09/03/2012 AND DD <= 21/03/2023)) AND (EMBEDDED_WHE_EXPRESSION_LG=ENG), Search language: English

Commission Implementing Regulation (EU) 2021/2226 of 14 December 2021 laying down rules for the application of Regulation (EU) 2017/745 of the European Parliament and of the Council as regards electronic instructions for use of medical devices

C/2021/8984

In force

CELEX number:
32021R2226
Form:
Implementing regulation
Responsible body:
SANTE
Author:
European Commission, Directorate-General for Health and Food Safety
Date of document:
14/12/2021; Date of adoption

Commission Regulation (EU) No 207/2012 of 9 March 2012 on electronic instructions for use of medical devices Text with EEA relevance

In force

CELEX number:
32012R0207
Form:
Regulation
Author:
European Commission
Date of document:
09/03/2012