Commission Implementing Decision (EU) 2022/874 of 1 June 2022 on the terms and conditions of the authorisation of a biocidal product containing N-(trichloromethylthio)phthalimide (Folpet) referred by the Netherlands in accordance with Article 36(1) of Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2022) 3465) (Text with EEA relevance)

• CELEX: Implementing Decision (EU) 2022/874
• Articles: 3

Article 1

This Decision applies to the biocidal product identified by the case number BC-FS027255-29 in the Register for Biocidal Products.

Article 2

Without the submission of the relevant information in point 4 of Title 1 of Annex III to Regulation (EU) No 528/2012, subject to the general possibilities for the adaptation of data requirements set out in Annex IV to that Regulation, it has not been demonstrated that the biocidal product meets the conditions laid down in Article 19(1), point (d), of Regulation (EU) No 528/2012.

Article 3

This Decision is addressed to the Member States.