Commission Implementing Decision (EU) 2019/641 of 17 April 2019 on the terms and conditions of the authorisation of a biocidal product family containing 1R-trans phenothrin referred by Ireland in accordance with Article 36 of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2019) 2837) (Text with EEA relevance.)

• CELEX: Implementing Decision (EU) 2019/641
• Articles: 3

Article 1

This Decision applies to the biocidal product family identified by the case number BC-LR019221-36 in the Register for Biocidal Products.

Article 2

The biocidal product family referred to in Article 1 meets the condition laid down in Article 19(1)(b)(i) of Regulation (EU) No 528/2012.

Article 3

This Decision is addressed to the Member States.