Commission Implementing Decision (EU) 2024/888of 22 March 2024on the non-approval of certain active substances for use in biocidal products in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council(Text with EEA relevance)
European Union
Commission Implementing Decision (EU) 2024/888 of 22 March 2024 on the non-approval of certain active substances for use in biocidal products in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (Text with EEA relevance) 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 Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products OJ L 167, 27.6.2012, p. 1, ELI: http://data.europa.eu/eli/reg/2012/528/oj. , and in particular Article 89(1), third subparagraph, thereof, Whereas: (1) Commission Delegated Regulation (EU) No 1062/2014 Commission Delegated Regulation (EU) No 1062/2014 of 4 August 2014 on the work programme for the systematic examination of all existing active substances contained in biocidal products referred to in Regulation (EU) No 528/2012 of the European Parliament and of the Council (OJ L 294, 10.10.2014, p. 1, ELI: http://data.europa.eu/eli/reg_del/2014/1062/oj). establishes in its Annex II a list of active substance/product-type combinations included in the review programme of existing active substances in biocidal products. (2) For a number of active substance/product-type combinations included in that list, all the participants have withdrawn or are considered to have withdrawn their support in a timely manner. (3) In accordance with Article 14(1) of Delegated Regulation (EU) No 1062/2014, the European Chemicals Agency (the Agency) published an open invitation to take over the role of participant for those active substance/product-type combinations for which the role of participant had not previously been taken over. For those combinations no notification has been submitted to the Agency within the time limit provided for by Article 14(2) of Delegated Regulation (EU) No 1062/2014. Therefore, those active substance/product-type combinations, in accordance with Article 20, first paragraph, point (b), of that Delegated Regulation, should not be approved for use in biocidal products. Those active substance/product-type combinations are the following: (a) biphenyl-2-ol (product-type 7); (b) potassium dimethyldithiocarbamate (product-types 9, 11, 12); (c) silver-polyethylenimine-chloride (product-types 1, 2, 9); (d) reaction products of glutamic acid and N-(C12-C14-alkyl)propylenediamine (Glucoprotamin) (product-types 2, 4); (e) poly(oxy-1,2-ethanediyl),.alpha.-[2-(dide-cylmethylammonio)ethyl]-.omega.-hydroxy, propanoate (salt) (Bardap 26) (product-types 2, 4, 10). (4) In addition, in accordance with Article 12(3) of Delegated Regulation (EU) No 1062/2014, the Agency informed the Commission of those active substance/product-type combinations for which all participants have withdrawn or are considered to have withdrawn their support in a timely manner, and for which the role of participant had previously been taken over. Those active substance/product-type combinations which, in accordance with Article 20, first paragraph, point (a), of that Delegated Regulation, should not be approved for use in biocidal products are the following:
(a) 2,2-Dibromo-2-cyanoacetamide (DBNPA)(product-type 2); (b) active chlorine generated from magnesium chloride hexahydrate and potassium chloride by electrolysis (product-type 2); (c) garlic, ext. - Extractives and their physically modified derivatives such as tinctures, concretes, absolutes, essential oils, oleoresins, terpenes, terpene-free fractions, distillates, residues, etc., obtained from Allium sativum, Liliaceae (product-type 19); (d) brandy (product-type 19). (5) The measures provided for in this Decision are in accordance with the opinion of the Standing Committee on Biocidal Products, HAS ADOPTED THIS DECISION:
Article 1
The active substances listed in the Annex are not approved for the product-types indicated therein.
Article 2
This Decision shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union. Done at Brussels, 22 March 2024. For the Commission The President Ursula von der Leyen
Annex
ANNEX Active substance/product-type combinations not approved: Entry Number in Annex II to Regulation (EU) No 1062/2014Substance nameRapporteur Member StateEC numberCAS numberProduct-type(s)92Biphenyl-2-olES201-993-590-43-77187Potassium dimethyldithiocarbamateSE204-875-1128-03-09, 11, 121076Silver-polyethylenimine-chlorideSENot availableNot available1, 2, 94942,2-Dibromo-2-cyanoacetamide (DBNPA)DK233-539-710222-01-221051Active chlorine generated from magnesium chloride hexahydrate and potassium chloride by electrolysisFRNot availableNot available2779Reactions products of glutamic acid and N-(C12-C14-alkyl)propylenediamine (Glucoprotamin)DE403-950-8164907-72-62, 4869Poly(oxy-1,2-ethanediyl),.alpha.-[2-(dide-cylmethylammonio)ethyl]-.omega.-hydroxy-, propanoate (salt) (Bardap 26)ITPolymer94667-33-12, 4, 101071Garlic, ext.Extractives and their physically modified derivatives such as tinctures, concretes, absolutes, essential oils, oleoresins, terpenes, terpene-free fractions, distillates, residues, etc., obtained from Allium sativum, Liliaceae.AT232-371-18008-99-9191072BrandytbdNot availableNot available19
Metadata
- Type
- Afgørelse
- År
- 2024
- Ikrafttrædelsesdato
- 1. januar 1970