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Query: ((DN = "32010L0005" AND DD <= 29/09/2022) OR (RESOURCE_LEGAL_CORRECTS_RESOURCE_LEGAL = "32010L0005" AND DD >= 08/02/2010 AND DD < 29/09/2022 AND (EMBEDDED_ACT_CONSOLIDATED_DATE > 08/02/2010 OR EMBEDDED_ACT_CONSOLIDATED_DATE = NULL)) OR ((RESOURCE_LEGAL_REPEALS_RESOURCE_LEGAL = "32010L0005" OR RESOURCE_LEGAL_IMPLICITLY_REPEALS_RESOURCE_LEGAL = "32010L0005" OR RESOURCE_LEGAL_RENDERS_OBSOLETE_RESOURCE_LEGAL = "32010L0005" OR RESOURCE_LEGAL_REPLACES_RESOURCE_LEGAL = "32010L0005" OR RESOURCE_LEGAL_SUSPENDS_RESOURCE_LEGAL = "32010L0005" OR RESOURCE_LEGAL_PARTIALLY_SUSPENDS_RESOURCE_LEGAL = "32010L0005" OR RESOURCE_LEGAL_AMENDS_RESOURCE_LEGAL = "32010L0005") AND DD > 08/02/2010 AND DD <= 29/09/2022)) AND (EMBEDDED_WHE_EXPRESSION_LG=ENG), Search language: English

Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products Text with EEA relevance

In force

CELEX number:
32012R0528
Form:
Regulation
Author:
European Parliament, Council of the European Union
Date of document:
22/05/2012

Commission Directive 2010/5/EU of 8 February 2010 amending Directive 98/8/EC of the European Parliament and of the Council to include acrolein as an active substance in Annex I thereto (Text with EEA relevance)

No longer in force

CELEX number:
32010L0005
Form:
Directive
Author:
European Commission
Date of document:
08/02/2010