Article 1
Open ↗The Annex to Implementing Regulation (EU) No 540/2011 is amended in accordance with the Annex to this Regulation.
Source
Commission Implementing Regulation (EU) 2025/1092 of 2 June 2025 amending Implementing Regulation (EU) No 540/2011 to update the list of active substances approved or deemed to have been approved under Regulation (EC) No 1107/2009 of the European Parliament and of the Council
Commission Implementing Regulation (EU) 2025/1092 of 2 June 2025 amending Implementing Regulation (EU) No 540/2011 to update the list of active substances approved or deemed to have been approved under Regulation (EC) No 1107/2009 of the European Parliament and of the Council
Data as of 2026-07-04 · Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗
Article 2
Open ↗This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union .
Supplementary provisions
ANNEXSupplementary provisions
Open ↗ANNEX The Annex to Implementing Regulation (EU) No 540/2011 is amended as follows: 1. Part A is amended as follows: (1) entry 240, plant oils/citronella oil and entry 264, dodemorph are deleted; (2) (a) entry 204, Trichoderma atroviride (formerly T. harzianum ) is replaced by the following entry: Number Common Name, Identification Numbers IUPAC Name Purity ( 1 ) Date of approval Expiration of approval Specific provisions ‘204 Trichoderma atroviride (formerly T. harzianum) STRAIN: T-11 Culture collection: No Spanish type culture collection CECT 20498, identical with IMI 352941 Not applicable No relevant impurities 1 May 2009 30 November 2026 PART A Only uses as fungicide may be authorised. PART B For the implementation of the uniform principles as referred to in Article 29(6) of Regulation (EC) No 1107/2009, the conclusions of the review report on Trichoderma atroviride (formerly T. harzianum ) T-11 (SANCO/1841/2008), and in particular Appendices I and II thereof, as finalised in the Standing Committee on the Food Chain and Animal Health, shall be taken into account. Conditions of use shall include, where appropriate, risk mitigation measures.’ (b) entry 230, fatty acids C7 to C20 is replaced by the following entry: Number Common Name, Identification Numbers IUPAC Name Purity ( 2 ) Date of approval Expiration of approval Specific provisions ‘230 Fatty acids C7 to C20 CAS No 112-05-0 (Pelargonic Acid) CAS No 67701-09-1 (Fatty acids C7-C18 and C18 unsaturated potassium salts) 124-07-2 (Caprylic Acid) 334-48-5 (Capric Acid) CIPAC No not allocated Nonanoic acid Caprylic Acid, Capric Acid (ISO in each case) Octanoic Acid, Decanoic Acid (IUPAC in each case) ≥ 889 g/kg (Pelargonic Acid) ≥ 838 g/kg fatty acids 1 September 2009 1 December 2026 PART A Only uses as insecticide, acaricide, and herbicide and plant growth regulator may be authorised. PART B For the implementation of the uniform principles as referred to in Article 29(6) of Regulation (EC) No 1107/2009, the conclusions of the review report on fatty acids (SANCO/2610/2008) and in particular Appendices I and II thereof, as finalised in the Standing Committee on the Food Chain and Animal Health shall be taken into account. Conditions of use shall include, where appropriate, risk mitigation measures.’ 2. In Part B, the following entries are deleted: (1) entry 1, bispyribac; (2) entry 25, fenpyrazamine; (3) entry 26, Adoxophyes orana granulovirus; (4) entry 30, Zucchini Yellow Mosaic Virus – weak strain; (5) entry 36, Bacillus firmus I-1582; (6) entry 41, spiromesifen; (7) entry 55, penflufen; (8) entry 60, spirotetramat; (9) entry 64, pyridalyl; (10) entry 66, L-ascorbic acid; (11) entry 67, spinetoram; (12) entry 74, flubendiamide; (13) entry 75, Bacillus pumilus QST 2808; (14) entry 78, metaflumizone; (15) entry 80, meptyldinocap; (16) entry 81, chromafenozide; (17) entry 82, gamma-cyhalothrin. 3. In Part E, entry 1, flumetralin is deleted. ( 1 ) Further details on the identity and the specification of the active substance are provided in the renewal report. ( 2 ) Further details on the identity and the specification of the active substance are provided in the renewal report.
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Source: EUR-Lex (Publications Office of the EU), © European Union, reuse permitted under Commission Decision 2011/833/EU.
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