Commission Implementing Regulation (EU) 2025/1138

Contents

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1. THE EUROPEAN COMMISSION, Having regard to the Treaty on the Functioning of the European Union, Having regard to Regulation (EU) No 528/2012 of the European Parl
   1. (1) On 29 September 2017, Tevan B.V submitted an application to the European Chemicals Agency (‘the Agency’) in accordance with Article 43(1) of Regulation (EU)
   2. (2) ‘Tevan Panox Family’ contains peracetic acid as the active substance, included in the Union list of approved active substances referred to in Article 9(2) o
   3. (3) On 15 November 2023, the evaluating competent authority submitted, in accordance with Article 44(1) of Regulation (EU) No 528/2012, an assessment report and
   4. (4) On 26 June 2024, the Agency submitted to the Commission its opinion, the draft summary of the biocidal product characteristics (‘SPC’) of ‘Tevan Panox Famil
   5. (5) The opinion concludes that ‘Tevan Panox Family’ is a biocidal product family within the meaning of Article 3(1), point (s), of Regulation (EU) No 528/2012,
   6. (6) On 19 July 2024, the Agency transmitted to the Commission the draft SPC in all the official languages of the Union in accordance with Article 44(4) of Regul
   7. (7) The Commission concurs with the opinion of the Agency and considers it therefore appropriate to grant a Union authorisation for the biocidal product family
   8. (8) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on Biocidal Products,
2. 1
3. 2
4. Summary of product characteristics for a biocidal product family
   1. Tevan Panox family
   2. Product type(s)
   3. PT02: Disinfectants and algaecides not intended for direct application to humans or animals
   4. PT03: Veterinary hygiene
   5. PT04: Food and feed area
   6. Authorisation number: EU-0032875-0000
   7. R4BP asset number: EU-0032875-0000
   8. Part I — first information level
   9. Part II — second information level – meta spc(s)