(fra kommisjonsbeslutningen)

(1) K-HDO was included in Annex I to Directive 98/8/EC of the European Parliament and of the Council (2) as an active substance for use in biocidal products of product-type 8. Pursuant to Article 86 of Regulation (EU) No 528/2012, it was therefore considered approved until 30 June 2020 under that Regulation subject to the requirements set out in Annex I to Directive 98/8/EC.

(2) On 14 December 2018, an application was submitted in accordance with Article 13(1) of Regulation (EU) No 528/2012 for the renewal of the approval of K-HDO for use in biocidal products of product-type 8 (‘the application’).

(3) On 6 May 2019, the evaluating competent authority of Austria informed the Commission that it had decided, pursuant to Article 14(1) of Regulation (EU) No 528/2012, that a full evaluation of the application was necessary. Pursuant to Article 8(1) of that Regulation, the evaluating competent authority is to perform a full evaluation of the application within 365 days of its validation.

(4) It is possible for the evaluating competent authority to require the applicant to provide sufficient data to carry out the evaluation, in accordance with Article 8(2) of Regulation (EU) No 528/2012. In that event, the 365-day period is suspended for a period that may not exceed 180 days in total unless a longer suspension is justified by the nature of the data requested or by exceptional circumstances.

(5) Within 270 days of receipt of a recommendation from the evaluating competent authority, the European Chemicals Agency (‘the Agency’) is to prepare and submit to the Commission an opinion on renewal of the approval of the active substance in accordance with Article 14(3) of Regulation (EU) No 528/2012.

(6) Commission Implementing Decision (EU) 2019/1950 (3) postponed the expiry date of the approval of K-HDO for use in biocidal products of product-type 8 to 31 December 2022, in order to allow sufficient time for the examination of the application.

(7) Commission Implementing Decision (EU) 2022/1488 (4) postponed again the expiry date of the approval to 31 December 2026 because studies were needed to assess the criteria for the determination of endocrine-disrupting properties of K-HDO.

(8) On 29 January 2026, the evaluating competent authority informed the Commission that the evaluation is delayed linked with the assessment of data related to the efficacy and the examination of the endocrine-disrupting properties of the substance. The Commission understood from the information provided by the evaluating competent authority that, for reasons beyond the control of the applicant, it is unlikely that that authority will submit a renewal assessment report to the Agency before the fourth quarter of 2027.

(9) Consequently, for reasons beyond the control of the applicant, the approval is likely to expire before a decision has been taken on its renewal. It is therefore appropriate to further postpone the expiry date of the approval for a period of time sufficient to enable the examination of the application. Taking into account the time-limits for evaluation by the evaluating competent authority, for preparation and submission by the Agency of its opinion and the time needed for the Commission to decide whether to renew the approval of K-HDO for use in biocidal products of product-type 8, the expiry date of that approval should be postponed to 30 June 2029.

(10) After the further postponement of the expiry date of the approval, K-HDO remains approved for use in biocidal products of product-type 8 subject to the requirements set out in Annex I to Directive 98/8/EC,