Commission Implementing Decision (EU) 2023/1155 of 9 June 2023 on the unresolved objections regarding the terms and conditions of the authorisation of the biocidal product Rapid Pro referred by France in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (notified under document C(2023) 3666) (Text with EEA relevance)

The biocidal product identified by the asset numbers AT-0016213-0000, BE-0011978-0000, CH-0016234-0000, DE-0015430-0000, DK-0012634-0000, ES-0014035-0000, FR-0012648-0000, IE-0014481-0000, IT-0014977-0000, LU-0012652-0000, LT-0018189-0000, NL-0016288-0000, NO-0015333-0000, PT-0020295-0000 in the Register for Biocidal Products (‘the biocidal product’) does not fully meet the conditions laid down in Article 19(1), point (b)(iii), of Regulation (EU) No 528/2012. The biocidal product may only be authorised in accordance with Article 19(5) of Regulation (EU) No 528/2012 in Member States who consider that not authorising it would result in disproportionate negative impacts for society when compared to the risks to human health, animal health or the environment arising from the use of the biocidal product under the conditions laid down in the authorisation. The use of the biocidal product shall be subject to appropriate risk mitigation measures, as referred to in Article 19(5) of Regulation (EU) No 528/2012, which shall be adopted in each Member State based on the particular circumstances and available evidence of the occurrence of primary and secondary poisoning incidents in that Member State.

This Decision is addressed to the Member States.