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					<dc:identifier>http://www.legislation.gov.uk/eur/2016/1937/annex</dc:identifier><dc:title>Commission Implementing Regulation (EU) 2016/1937 of 4 November 2016 approving cyfluthrin as an existing active substance for use in biocidal products of product-type 18 (Text with EEA relevance)</dc:title><dct:alternative>Commission Implementing Regulation (EU) 2016/1937</dct:alternative><dc:description>Commission Implementing Regulation (EU) 2016/1937 of 4 November 2016 approving cyfluthrin as an existing active substance for use in biocidal products of product-type 18 (Text with EEA relevance)</dc:description><dc:modified>2020-12-09</dc:modified><dc:publisher>King's Printer of Acts of Parliament</dc:publisher><dc:source>https://webarchive.nationalarchives.gov.uk/eu-exit/https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:32016R1937</dc:source><dc:type>text</dc:type><dc:format>text/xml</dc:format><dc:language>en</dc:language><dct:valid>2016-11-04</dct:valid>
					
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                              <Footnote xmlns="http://www.legislation.gov.uk/namespaces/legislation" id="f00004">
                                 <FootnoteText>
                                    <Para>
                                       <Text>The purity indicated in this column was the minimum degree of purity of the active substance evaluated in accordance with Article 89(1) of Regulation (EU) No 528/2012. The active substance in the product placed on the market can be of equal or different purity if it has been proven technically equivalent with the evaluated active substance.</Text>
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                           </td></tr><tr><td colspan="7">
                              <Footnote xmlns="http://www.legislation.gov.uk/namespaces/legislation" id="f00005">
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                                    <Para>
                                       <Text>Regulation (EC) No 470/2009 of the European Parliament and of the Council of 6 May 2009 laying down Community procedures for the establishment of residue limits of pharmacologically active substances in foodstuffs of animal origin, repealing Council Regulation (EEC) No 2377/90 and amending Directive 2001/82/EC of the European Parliament and of the Council and Regulation (EC) No 726/2004 of the European Parliament and of the Council (<Citation id="c00004" Class="EuropeanUnionOfficialJournal" Year="2009" URI="https://webarchive.nationalarchives.gov.uk/eu-exit/https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=uriserv:OJ.L_.2009.152.01.0011.01.ENG" Date="2009-06-16">OJ L 152, 16.6.2009, p. 11</Citation>).</Text>
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                           </td></tr><tr><td colspan="7">
                              <Footnote xmlns="http://www.legislation.gov.uk/namespaces/legislation" id="f00006">
                                 <FootnoteText>
                                    <Para>
                                       <Text>Regulation (EC) No 396/2005 of the European Parliament and of the Council of 23 February 2005 on maximum residue levels of pesticides in or on food and feed of plant and animal origin and amending Council Directive 91/414/EEC (<Citation id="c00005" Class="EuropeanUnionOfficialJournal" Year="2005" URI="https://webarchive.nationalarchives.gov.uk/eu-exit/https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=uriserv:OJ.L_.2005.070.01.0001.01.ENG" Date="2005-03-16">OJ L 70, 16.3.2005, p. 1</Citation>).</Text>
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                     <tbody><tr><th>Common Name</th><th>IUPAC NameIdentification Numbers</th><th>Minimum degree of purity of the active substance<FootnoteRef xmlns="http://www.legislation.gov.uk/namespaces/legislation" Ref="f00004"/>
                           </th><th>Date of approval</th><th>Expiry date of approval</th><th>Product type</th><th>Specific conditions</th></tr><tr><td>Cyfluthrin</td><td>
                              <Para xmlns="http://www.legislation.gov.uk/namespaces/legislation">
                                 <Text>IUPAC Name:</Text>
                              </Para>
                              <Para xmlns="http://www.legislation.gov.uk/namespaces/legislation">
                                 <Text>(RS)-α-Cyano-4-fluoro-3-phenoxybenzyl (1RS,3RS;1RS,3SR)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate</Text>
                              </Para>
                              <Para xmlns="http://www.legislation.gov.uk/namespaces/legislation">
                                 <Text>EC No: 269-855-7</Text>
                              </Para>
                              <Para xmlns="http://www.legislation.gov.uk/namespaces/legislation">
                                 <Text>CAS No: 68359-37-5</Text>
                              </Para>
                           </td><td>955 g/kg (95,5 % w/w)</td><td>1 March 2018</td><td>28 February 2028</td><td>18</td><td>
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                                 <Text>The authorisations of biocidal products are subject to the following conditions:</Text>
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                                       <Text>The product assessment shall pay particular attention to the exposures, the risks and the efficacy linked to any use covered by an application for authorisation, but not addressed in the Union-level risk assessment of the active substance.</Text>
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                                       <Text>In view of the risks identified for the uses assessed, the product assessment shall pay particular attention to:</Text>
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                                                <Text>surface water and sediment for products used in domestic premises and animal housing with release to a sewage treatment plant;</Text>
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                                          <ListItem NumberOverride="(b)">
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                                                <Text>surface water and sediment for products used in animal housing with direct release to surface water;</Text>
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                                                <Text>surface water and sediment after manure application on agricultural soil for products used in animal housings.</Text>
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                                       <Text>For products that may lead to residues in food or feed, the need to set new or to amend existing maximum residue levels (MRLs) in accordance with Regulation (EC) No 470/2009 of the European Parliament and of the Council<FootnoteRef Ref="f00005"/> or Regulation (EC) No 396/2005 of the European Parliament and of the Council<FootnoteRef Ref="f00006"/> shall be verified, and any appropriate risk mitigation measures shall be taken to ensure that the applicable MRLs are not exceeded.</Text>
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