{
  "url": "https://openlegislation.uk/eu-directive-2012-41/annex",
  "json_url": "https://openlegislation.uk/eu-directive-2012-41/annex.json",
  "legislation": "eudr/2012/41",
  "legislation_title": "Commission Directive 2012/41/EU of 26 November 2012 amending Directive 98/8/EC of the European Parliament and of the Council to extend the inclusion in Annex I thereto of the active substance nonanoic acid to product type 2 (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-directive-2012-41",
  "path": "annex",
  "kind": "annex",
  "number": null,
  "heading": null,
  "text": "The following is added to entry ‘No 41’ in Annex I to Directive 98/8/EC:\nFor the implementation of the common principles of Annex VI, the content and conclusions of assessment reports are available on the Commission website: http://ec.europa.eu/comm/environment/biocides/index.htm\nNo\nCommon Name\nIUPAC NameIdentification Numbers\nMinimum purity of the active substance in the biocidal product as placed on the market\nDate of inclusion\nDeadline for compliance with Article 16(3) (except for products containing more than one active substance, for which the deadline to comply with Article 16(3) shall be the one set out in the last of the inclusion decisions relating to its active substances)\nExpiry date of inclusion\nProduct type\nSpecific provisions\n‘1 October 2014\n30 September 2016\n30 September 2024\n2\nWhen assessing the application for authorisation of a product in accordance with Article 5 and Annex VI, Member States shall assess, where relevant for the particular product, those uses or exposure scenarios and those risks to human populations and to environmental compartments that have not been representatively addressed in the Union level risk assessment.\nMember States shall ensure that authorisations of products for non-professional use are subject to the packaging being designed to minimise user exposure, unless it can be demonstrated in the application for product authorisation that risks for human health can be reduced to acceptable levels by other means.’",
  "extent": "E+W+S+N.I.",
  "status": null,
  "version": "current",
  "annotations": [
    {
      "type": "footnote",
      "label": "f1",
      "text": "For the implementation of the common principles of Annex VI, the content and conclusions of assessment reports are available on the Commission website: http://ec.europa.eu/comm/environment/biocides/index.htm"
    }
  ],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/eudr/2012/41/annex",
    "retrieved_at": "2026-11-01T15:21:55.791777+00:00"
  },
  "licence": "Open Government Licence v3.0",
  "licence_url": "https://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/",
  "attribution": "Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives."
}