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)

CELEX: 32022D2054
Document type: DEC_IMPL
Sector: Legislation
Date of document: 2022-10-21
In force since: 2022-10-21
Status: In force
ELI: http://data.europa.eu/eli/dec_impl/2022/2054/oj

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Article 1

Given that the safe use of the biocidal product in treated articles cannot be ensured only by imposing conditions on the use of the biocidal products in the treated articles, the biocidal product identified by the case number BC-HH028132-58 in the Register for Biocidal Products does not meet the conditions laid down in Article 19(1), points (b)(iii) and (b)(iv), of Regulation (EU) No 528/2012.

Article 2

This Decision is addressed to the Member States.

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