Part A of the Annex to Implementing Regulation (EU) No 540/2011 is amended in accordance with the Annex to this Regulation.
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Commission Implementing Regulation (EU) 2017/1511 of 30 August 2017 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances 1-methylcyclopropene, beta-cyfluthrin, chlorothalonil, chlorotoluron, cypermethrin, daminozide, deltamethrin, dimethenamid-p, flufenacet, flurtamone, forchlorfenuron, fosthiazate, indoxacarb, iprodione, MCPA, MCPB, silthiofam, thiophanate-methyl and tribenuron (Text with EEA relevance. )
This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union .
Schedules & Appendices
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 40, Deltamethrin, the date is replaced by ‘31 October 2018’;
(2)
in the sixth column, expiration of approval, of row 48, Beta-cyfluthrin, the date is replaced by ‘31 October 2018’;
(3)
in the sixth column, expiration of approval, of row 50, Iprodione, the date is replaced by ‘31 October 2018’;
(4)
in the sixth column, expiration of approval, of row 64, Flurtamone, the date is replaced by ‘31 October 2018’;
(5)
in the sixth column, expiration of approval, of row 65, Flufenacet, the date is replaced by ‘31 October 2018’;
(6)
in the sixth column, expiration of approval, of row 67, Dimethenamid-P, the date is replaced by ‘31 October 2018’;
(7)
in the sixth column, expiration of approval, of row 69, Fosthiazate, the date is replaced by ‘31 October 2018’;
(8)
in the sixth column, expiration of approval, of row 70, Silthiofam, the date is replaced by ‘31 October 2018’;
(9)
in the sixth column, expiration of approval, of row 101, Chlorothalonil, the date is replaced by ‘31 October 2018’;
(10)
in the sixth column, expiration of approval, of row 102, Chlorotoluron, the date is replaced by ‘31 October 2018’;
(11)
in the sixth column, expiration of approval, of row 103, Cypermethrin, the date is replaced by ‘31 October 2018’;
(12)
in the sixth column, expiration of approval, of row 104, Daminozide, the date is replaced by ‘31 October 2018’;
(13)
in the sixth column, expiration of approval, of row 105, Thiophanate-methyl, the date is replaced by ‘31 October 2018’;
(14)
in the sixth column, expiration of approval, of row 106, Tribenuron, the date is replaced by ‘31 October 2018’;
(15)
in the sixth column, expiration of approval, of row 107, MCPA, the date is replaced by ‘31 October 2018’;
(16)
in the sixth column, expiration of approval, of row 108, MCPB, the date is replaced by ‘31 October 2018’;
(17)
in the sixth column, expiration of approval, of row 117, 1-methylcyclopropene, the date is replaced by ‘31 October 2018’;
(18)
in the sixth column, expiration of approval, of row 118, Forchlorfenuron, the date is replaced by ‘31 October 2018’;
(19)
in the sixth column, expiration of approval, of row 119, Indoxacarb, the date is replaced by ‘31 October 2018’.
Cite this act
Commission Implementing Regulation (EU) 2017/1511 of 30 August 2017 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances 1-methylcyclopropene, beta-cyfluthrin, chlorothalonil, chlorotoluron, cypermethrin, daminozide, deltamethrin, dimethenamid-p, flufenacet, flurtamone, forchlorfenuron, fosthiazate, indoxacarb, iprodione, MCPA, MCPB, silthiofam, thiophanate-methyl and tribenuron (Text with EEA relevance. ) (EUR-Lex). Retrieved via LawPlayer, https://lawplayer.com/eu/act/32017R1511
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