(1)On 30 July 2024, Evonik Operations GmbH submitted an application to the European Chemicals Agency (‘the Agency’) in accordance with Article 43(1) of Regulation (EU) No 528/2012 and Article 4 of Commission Implementing Regulation (EU) No 414/2013note for Union authorisation of the same single biocidal, as referred to in Article 1 of Implementing Regulation (EU) No 414/2013, named ‘CLARMARIN® 350 LD’, of product-type 2, as described in Annex V to Regulation (EU) No 528/2012. The application was recorded under case number BC-KL099229-17 in the Register for Biocidal Products. The application referred to the single biocidal product ‘CLARMARIN® 350’ (authorisation number EU-0028964-0005), which is a part of the related reference biocidal product family ‘Evonik’s Hydrogen Peroxide Product Family’. The application also indicated the authorisation number of the related reference biocidal product family ‘Evonik’s Hydrogen Peroxide Product Family’ authorised by Commission Implementing Regulation (EU) 2023/2183note, with authorisation number EU-0028964-0000.
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