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现行 32021D2165
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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)
发布日期: 2021-12-03
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)
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)
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