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2011/48/EU: Commission Decision of 24 January 2011… Article 2

2011/48/EU: Commission Decision of 24 January 2011… Article 2

Article 2

1.   When allowing the placing on the market of biocidal products containing temephos in accordance with Article 1, France shall ensure that the following conditions are complied with: (a) continued use is only possible under the conditions that biocidal products containing temephos are approved for the intended essential use; (b) the continued use is only accepted so far as it has no unacceptable effect on human or animal health or on the environment; (c) all appropriate risk reduction measures are imposed when granting approval; (d) such biocidal products remaining on the market after 1 September 2006 are relabelled in order to match the restricted use conditions; (e) where appropriate, alternatives for such uses are being sought by the holders of the approvals or by France. 2.   France shall inform the Commission annually on the application of paragraph 1 and in particular on the actions taken pursuant to point (e) of that paragraph.

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Other provisions in 2011/48/EU: Commission Decision of 24 January 2011…

Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗ · Data as of 2026-07-04

CitationArticle 2 of 2011/48/EU: Commission Decision of 24 January 2011… (LawPlayer, data as of 2026-07-04)

© European Union, https://eur-lex.europa.eu, 1998-2026. Reuse authorised under Commission Decision 2011/833/EU, provided the source is acknowledged.

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