Article 1
Open ↗Part A of the Annex to Implementing Regulation (EU) No 540/2011 is amended in accordance with the Annex to this Regulation.
Source
Commission Implementing Regulation (EU) 2016/549 of 8 April 2016 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances bentazone, cyhalofop butyl, diquat, famoxadone, flumioxazine, DPX KE 459 (flupyrsulfuron-methyl), metalaxyl-M, picolinafen, prosulfuron, pymetrozine, thiabendazole and thifensulfuron-methyl (Text with EEA relevance)
Commission Implementing Regulation (EU) 2016/549 of 8 April 2016 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances bentazone, cyhalofop butyl, diquat, famoxadone, flumioxazine, DPX KE 459 (flupyrsulfuron-methyl), metalaxyl-M, picolinafen, prosulfuron, pymetrozine, thiabendazole and thifensulfuron-methyl (Text with EEA relevance)
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 Part A of the Annex to Implementing Regulation (EU) No 540/2011 is amended as follows: (1) in the sixth column, expiration of approval, of row 11, Bentazone, the date of ‘30 June 2016’ is replaced by ‘30 June 2017’; (2) in the sixth column, expiration of approval, of row 15, Diquat, the date of ‘30 June 2016’ is replaced by ‘30 June 2017’; (3) in the sixth column, expiration of approval, of row 17, Thiabendazole, the date of ‘30 June 2016’ is replaced by ‘30 June 2017’; (4) in the sixth column, expiration of approval, of row 19, DPX KE 459 (flupyrsulfuron-methyl), the date of ‘30 June 2016’ is replaced by ‘30 June 2017’; (5) in the sixth column, expiration of approval, of row 23, Pymetrozine, the date of ‘30 June 2016’ is replaced by ‘30 June 2017’; (6) in the sixth column, expiration of approval, of row 26, Thifensulfuron-methyl, the date of ‘30 June 2016’ is replaced by ‘30 June 2017’; (7) in the sixth column, expiration of approval, of row 31, Prosulfuron, the date of ‘30 June 2016’ is replaced by ‘30 June 2017’; (8) the sixth column, expiration of approval, of row 34, Cyhalofop butyl, the date of ‘30 June 2016’ is replaced by ‘30 June 2017’; (9) in the sixth column, expiration of approval, of row 35, Famoxadone, the date of ‘30 June 2016’ is replaced by ‘30 June 2017’; (10) in the sixth column, expiration of approval, of row 37, Metalaxyl-M, the date of ‘30 June 2016’ is replaced by ‘30 June 2017’; (11) in the sixth column, expiration of approval, of row 38, Picolinafen, the date of ‘30 June 2016’ is replaced by ‘30 June 2017’; (12) in the sixth column, expiration of approval, of row 39, Flumioxazine, the date of ‘30 June 2016’ is replaced by ‘30 June 2017’.
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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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