2018年9月26日，歐盟委員會發布法規（EU）2018/1292，根據歐洲議會和理事會法規（EU）No 528/2012，批準苯醚氰菊酯（cyphenothrin）作為活性物質用于18類產品的生物農藥產品，活性物質的最低純度為92%w/w（總異構體），批準日期為2020年2月1日，到期日為2030年1月31日。
本法規在歐盟官方公報公布后20天生效。
部分原文報道如下：
This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European unio.
Cyphenothrin is considered a candidate for substitution in accordance with point （d） of Article 10（1） of Regulation （EU） No 528/2012.
The authorisations of biocidal products are subject to the following conditions:
1）The product assessment shall pay particular attention to the exposures, the risks and the efficacy linked to any uses covered by an application for authorisation, but not addressed in the unio level risk assessment of the active substance.
2）In view of the risks identified for the uses assessed, the product assessment shall pay particular attention to:a）professional users;b）toddlers;c）surface water, sediment, soil and groundwater, following indoor surface treatment;d）earthworm-eating mammals and fish-eating mammals due to secondary poisoning, following indoor surface treatment.
3）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 （2） or Regulation （EC） No 396/2005 of the European Parliament and of the Council （3） shall be verified, and any appropriate risk mitigation measures shall be taken to ensure that the applicable MRLs are not exceeded.
本文由食品伙伴網食品資訊中心編輯，供網友參考，歡迎轉載，轉載請注明出處！有任何疑問，請聯系news@foodmate.net。
日期：2018-09-27
本法規在歐盟官方公報公布后20天生效。
部分原文報道如下：
This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European unio.
Cyphenothrin is considered a candidate for substitution in accordance with point （d） of Article 10（1） of Regulation （EU） No 528/2012.
The authorisations of biocidal products are subject to the following conditions:
1）The product assessment shall pay particular attention to the exposures, the risks and the efficacy linked to any uses covered by an application for authorisation, but not addressed in the unio level risk assessment of the active substance.
2）In view of the risks identified for the uses assessed, the product assessment shall pay particular attention to:a）professional users;b）toddlers;c）surface water, sediment, soil and groundwater, following indoor surface treatment;d）earthworm-eating mammals and fish-eating mammals due to secondary poisoning, following indoor surface treatment.
3）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 （2） or Regulation （EC） No 396/2005 of the European Parliament and of the Council （3） shall be verified, and any appropriate risk mitigation measures shall be taken to ensure that the applicable MRLs are not exceeded.
本文由食品伙伴網食品資訊中心編輯，供網友參考，歡迎轉載，轉載請注明出處！有任何疑問，請聯系news@foodmate.net。
日期：2018-09-27
