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Commission Implementing Regulation (EU) 2021/843 ANNEX II

Commission Implementing Regulation (EU) 2021/843 ANNEX II

ANNEX IISupplementary provisions

ANNEX II The Annex to Commission Implementing Regulation (EU) No 540/2011 is amended as follows: (1) in Part A, entry 46 on cyazofamid is deleted; (2) in Part B, the following entry is added: No Common Name, Identification Numbers IUPAC Name Purity    ( 1 ) Date of approval Expiration of approval Specific provisions ‘146 Cyazofamid CAS No: 120116-88-3 CIPAC No: 653 4-chloro-2-cyano-N,N-dimethyl-5-p-tolylimidazole-1-sulfonamide ≥ 935 g/kg 01/08/2021 31/07/2036 For the implementation of the uniform principles, as referred to in Article 29(6) of Regulation (EC) No 1107/2009, the conclusions of the renewal report on cyazofamid, and in particular Appendices I and II thereto, shall be taken into account. In this overall assessment Member States shall pay particular attention to: (a) the specification of the technical material as commercially manufactured; (b) the impact of processing on the consumer risk assessment; (c) the protection of non-target arthropods and earthworms. The applicant shall submit to the Commission, the Member States and the Authority confirmatory information as regards: 1. the effect of water treatment processes on the nature of residues present in surface water and groundwater, when surface water or groundwater is abstracted for drinking water; 2. points 3.6.5 and 3.8.2 of Annex II of Regulation (EC) No 1107/2009, as amended by Commission Regulation (EU) 2018/605. The applicant shall submit the requested information referred to in point 1 within two years from the date of publication by the Commission, of a guidance document on evaluation of the effect of water treatment processes on the nature of residues present in surface and groundwater. As regards point 2 the applicant shall provide an updated assessment of the information already submitted and, where relevant, further information to confirm the absence of endocrine activity by 16 June 2023’ ( 1 )   Further details on the identity and the specification of the active substance are provided in the renewal report.

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Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗ · Data as of 2026-07-04

CitationANNEX II of Commission Implementing Regulation (EU) 2021/843 (LawPlayer, data as of 2026-07-04)

© European Union, https://eur-lex.europa.eu, 1998-2026. Reuse authorised under Commission Decision 2011/833/EU, provided the source is acknowledged.

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