Commission Implementing Decision (EU) 2022/137 of 28 January 2022 concerning the extension of the action taken by the Health and Safety Executive of the United Kingdom permitting the making available on the market and use of the biocidal product Mydis in accordance with Article 55(1) of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2022) 408) (Only the English text is authentic)
根据欧洲议会和理事会第528/2012号法规（EU）第55（1）条（根据C（2022）号文件通知） 委员会执行2022年1月28日第2022/137号决定（EU）关于延长英国健康与安全执行局采取的行动 允许在市场上提供和使用杀生物产品Mydis408）（只有英文文本是真实的）

2022-01-28

Commission Implementing Decision (EU) 2022/2054 of 21 October 2022 on the unresolved objections regarding the conditions for granting an authorisation for the biocidal product Preventol A 12 TK 50 in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2022) 7408) (Text with EEA relevance)
根据欧洲议会和理事会第528/2012号法规（EU）（根据文件C（2022）7408通知） 委员会执行2022年10月21日第2022/2054号决定 该决定针对授予生物杀灭剂产品Preventol A 12 TK 50授权条件的未解决异议（与欧洲经济区相关的文本）

2022-10-21

Commission Implementing Decision (EU) 2016/1174 of 15 July 2016 on the terms and conditions of the authorisation of a biocidal product containing difenacoum referred by Spain in accordance with Article 36 of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2016) 4380) (Text with EEA relevance)
根据欧洲议会和理事会第528/2012号法规（EU）第36条（根据C（2016）4380号文件通知） 委员会于2016年7月15日就西班牙提及的含有杀生物剂的杀生物产品的授权条款和条件作出的第2016/1174号实施决定（EU）（与EEA相关的文本）

2016-07-15

Commission Implementing Decision (EU) 2021/2174 of 3 December 2021 on unresolved objections regarding the terms and conditions of the authorisation of the biocidal product Konservan P40 in accordance with Article 36(1) of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2021) 8686) (Text with EEA relevance)
根据欧洲议会和理事会第528/2012号法规（EU）第36（1）条（根据C（2021）8686号文件通知） 委员会于2021 12月3日就关于杀生物产品Konservan P40的授权条款和条件的未解决异议作出的2021第2174号实施决定（EU）（与EEA相关的文本）

2021-12-03

Commission Implementing Decision (EU) 2015/1751 of 29 September 2015 on the terms and conditions of the authorisation of a biocidal product containing bromadiolone referred by the United Kingdom in accordance with Article 36 of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2015) 6516) (Text with EEA relevance)
根据欧洲议会和理事会第528/2012号法规（EU）第36条（根据C（2015）6516号文件通知） 委员会于2015年9月29日就联合王国提及的含有溴敌隆的杀生物产品的授权条款和条件作出了第2015/1751号实施决定（EU）（与EEA相关的文本）

2015-09-29

Commission Implementing Decision (EU) 2022/146 of 1 February 2022 determining whether a product containing Alkyl (C12-16) dimethylbenzyl ammonium chloride is a biocidal product, pursuant to Article 3(3) of Regulation (EU) No 528/2012 of the European Parliament and of the Council (Text with EEA relevance)
根据欧洲议会和理事会第528/2012号法规（EU）第3（3）条（与EEA相关的文本） 委员会2022年2月1日第2022/146号实施决定（EU）确定含有烷基（C12-16）二甲基苄基氯化铵的产品是否为杀生物产品

2022-02-01

Commission Implementing Decision (EU) 2017/722 of 20 April 2017 concerning the extension of the action taken by the Netherlands on the making available on the market and use of the biocidal product VectoMaxFG in accordance with Article 55(1) of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2017) 2436)
2017年4月20日委员会执行决定（EU）2017/722 关于延长荷兰根据欧洲议会和理事会第528/2012号法规（EU）第55（1）条（根据C（2017）2436号文件通知）在市场上提供和使用杀生物产品VectoMaxFG所采取的行动

2017-04-20

Commission Implementing Decision (EU) 2018/1297 of 25 September 2018 on a derogation from mutual recognition of the authorisation of biocidal products containing creosote by France in accordance with Article 37 of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2018) 5412)
根据欧洲议会和理事会第528/2012号法规（EU）第37条（根据C（2018）5412号文件通知） 委员会于2018年9月25日通过了第2018/1297号执行决定（EU） 该决定涉及法国对含有杂酚油的杀生物产品的授权相互承认的减损

2018-09-25

Commission Implementing Decision (EU) 2016/1175 of 15 July 2016 on the terms and conditions of the authorisation of a biocidal product containing spinosad referred by the United Kingdom in accordance with Article 36 of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2016) 4385) (Text with EEA relevance)
根据欧洲议会和理事会第528/2012号法规（EU）第36条（根据C（2016）4385号文件通知） 委员会于2016年7月15日通过了关于英国提及的含有多杀菌素的杀生物产品的授权条款和条件的第2016/1175号实施决定（EU）（与EEA相关的文本）

2016-07-15

Commission Implementing Decision (EU) 2022/155 of 31 January 2022 concerning the extension of the action taken by the Health and Safety Executive of the United Kingdom permitting the making available on the market and use of the biocidal product Clinisept + Skin Disinfectant in accordance with Article 55(1) of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2022)457) (Only the English text is a
根据欧洲议会和理事会第528/2012号法规（EU）第55（1）条 委员会执行2022年1月31日第2022/155号决定 该决定涉及延长英国健康与安全执行局采取的行动 允许在市场上提供和使用杀生物产品克林司特+皮肤消毒剂（根据文件C（2022）457通知）（只有英文文本是

2022-01-31

Commission Implementing Decision (EU) 2018/232 of 15 February 2018 concerning the extension of the action taken by Belgium on the making available on the market and use of the biocidal products VectoMax G and Aqua-K-Othrine in accordance with Article 55(1) of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2018) 759)
根据欧洲议会和理事会第528/2012号法规（EU）第55（1）条（根据C（2018）759号文件通知） 委员会2018年2月15日第2018/232号执行决定（EU）关于延长比利时在市场上提供和使用杀生物产品VectoMax G和Aqua-K-Othrine方面采取的行动

2018-02-15

Commission Decision (EU) 2022/258 of 21 February 2022 granting the Hellenic Republic a derogation from certain provisions of Regulation (EU) 2019/943 of the European Parliament and of the Council and Directive (EU) 2019/944 of the European Parliament and of the Council as regards Crete (notified under document C(2022) 1140) (Only the Greek text is authentic) (Text with EEA relevance)
2022年2月21日委员会第2022/258号决定（EU）授予希腊共和国克减欧洲议会和理事会第2019/943号条例（EU）以及欧洲议会和理事会关于克里特岛的第2019/944号指令（EU）的某些规定（根据C（2022）1140号文件通知）（只有希腊文本是真实的）（与欧洲经济区相关的文本）

2022-02-21

Commission Implementing Decision (EU) 2021/2166 of 3 December 2021 on the unresolved objections regarding the conditions for granting an authorisation for the biocidal product Teknol Aqua 1411-01 in accordance with Article 36 of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2021) 8694) (Text with EEA relevance)
根据欧洲议会和理事会第528/2012号法规（EU）第36条（根据C（2021）8694号文件通知） 委员会于2021 12月3日就关于授权生物杀灭产品Teknol Aqua 1411-01的条件的未解决异议作出了2021第2021/2166号实施决定（EU）（与EEA相关的文本）

2021-12-03

Commission Implementing Decision (EU) 2018/696 of 4 May 2018 concerning the extension of the action taken by the French Ministry of Environment, Energy and Sea, in charge of international negotiations on climate permitting the making available on the market and use of the biocidal product Phéro-Ball Pin in accordance with Article 55(1) of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2018) 26
委员会2018年5月4日关于延长法国环境、能源和海洋部所采取行动的第2018/696号执行决定（欧盟） 负责根据欧洲议会和理事会第528/2012号法规（EU）第55（1）条（根据C（2018）26号文件通知） 就允许市场上提供和使用杀生物产品Phero球销的气候问题进行国际谈判

2018-05-04

Commission Implementing Decision (EU) 2018/1477 of 2 October 2018 on the terms and conditions of the authorisations of biocidal products containing ethyl butylacetylaminopropionate referred by Belgium in accordance with Article 36 of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2018) 6291) (Text with EEA relevance.)
委员会2018年10月2日第2018/1477号执行决定（欧盟） 关于比利时根据欧洲议会和理事会第528/2012号法规（欧盟）第36条（根据C（2018）6291号文件通知）提交的含有丁乙酰氨基丙酸乙酯的杀生物产品的授权条款和条件（与欧洲经济区相关的文本）

2018-10-02

Commission Implementing Decision (EU) 2021/2165 of 3 December 2021 concerning the extension of the action taken by the Ministry of Health of the Czech Republic permitting the making available on the market and use of the biocidal product Biobor JF in accordance with Article 55(1) of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2021) 8684) (Only the Czech text is authentic)
根据欧洲议会和理事会第528/2012号法规（EU）第55（1）条（根据C（2021）8684号文件通知） 委员会于2021 12月3日通过的关于延长捷克共和国卫生部采取的允许在市场上提供和使用杀生物产品Biobor JF的行动的委员会执行决定（EU）2021/2165（只有捷克语文本是真实的）

2021-12-03

Commission Implementing Decision (EU) 2021/2185 of 6 December 2021 concerning the extension of the action taken by the Health and Safety Executive of the United Kingdom permitting the making available on the market and use of the biocidal product Micronclean Hand Sanitiser in accordance with Article 55(1) of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2021) 8736) (Only the English text is a
根据欧洲议会和理事会第528/2012号法规（EU）第55（1）条的规定 委员会于2021 12月6日通过了第2021/2185号实施决定（EU） 该决定涉及延长英国健康与安全执行局采取的行动 允许在市场上提供和使用杀生物产品Micronclean洗手液（根据文件C（2021）8736通知）（只有英文文本是

2021-12-06