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) 2019/707 of 7 May 2019 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances alpha-cypermethrin, beflubutamid, benalaxyl, benthiavalicarb, bifenazate, boscalid, bromoxynil, captan, cyazofamid, desmedipham, dimethoate, dimethomorph, diuron, ethephon, etoxazole, famoxadone, fenamiphos, flumioxazine, fluoxastrobin, folpet, foramsulfuron, formetanate, metalaxyl-m, methiocarb, metribuzin, milbemectin, Paecilomyces lilacinus strain 251, phenmedipham, phosmet, pirimiphos-methyl, propamocarb, prothioconazole, s-metolachlor and tebuconazole (Text with EEA relevance.)
This Regulation shall enter into force on the twentieth 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 35, Famoxadone, the date is replaced by ‘30 June 2020’;
(2)
in the sixth column, expiration of approval, of row 37, Metalaxyl-M, the date is replaced by ‘30 June 2020’;
(3)
in the sixth column, expiration of approval, of row 39, Flumioxazine, the date is replaced by ‘30 June 2020’;
(4)
in the sixth column, expiration of approval, of row 44, Foramsulfuron, the date is replaced by ‘31 July 2020’;
(5)
in the sixth column, expiration of approval, of row 46, Cyazofamid, the date is replaced by ‘31 July 2020’;
(6)
in the sixth column, expiration of approval, of row 83, Alpha-cypermethrin, the date is replaced by ‘31 July 2020’;
(7)
in the sixth column, expiration of approval, of row 84, Benalaxyl, the date is replaced by ‘31 July 2020’;
(8)
in the sixth column, expiration of approval, of row 85, Bromoxynil, the date is replaced by ‘31 July 2020’;
(9)
in the sixth column, expiration of approval, of row 86, Desmedipham, the date is replaced by ‘31 July 2020’;
(10)
in the sixth column, expiration of approval, of row 88, Phenmedipham, the date is replaced by ‘31 July 2020’;
(11)
in the sixth column, expiration of approval, of row 97, S-metolachlor, the date is replaced by ‘31 July 2020’;
(12)
in the sixth column, expiration of approval, of row 99, Etoxazole, the date is replaced by ‘31 July 2020’;
(13)
in the sixth column, expiration of approval, of row 109, Bifenazate, the date is replaced by ‘31 July 2020’;
(14)
in the sixth column, expiration of approval, of row 110, Milbemectin, the date is replaced by ‘31 July 2020’;
(15)
in the sixth column, expiration of approval, of row 141, Fenamiphos, the date is replaced by ‘31 July 2020’;
(16)
in the sixth column, expiration of approval, of row 142, Ethephon, the date is replaced by ‘31 July 2020’;
(17)
in the sixth column, expiration of approval, of row 145, Captan, the date is replaced by ‘31 July 2020’;
(18)
in the sixth column, expiration of approval, of row 146, Folpet, the date is replaced by ‘31 July 2020’;
(19)
in the sixth column, expiration of approval, of row 147, Formetanate, the date is replaced by ‘31 July 2020’;
(20)
in the sixth column, expiration of approval, of row 148, Methiocarb, the date is replaced by ‘31 July 2020’;
(21)
in the sixth column, expiration of approval, of row 149, Dimethoate, the date is replaced by ‘31 July 2020’;
(22)
in the sixth column, expiration of approval, of row 150, Dimethomorph, the date is replaced by ‘31 July 2020’;
(23)
in the sixth column, expiration of approval, of row 152, Metribuzin, the date is replaced by ‘31 July 2020’;
(24)
in the sixth column, expiration of approval, of row 153, Phosmet, the date is replaced by ‘31 July 2020’;
(25)
in the sixth column, expiration of approval, of row 154, Propamocarb, the date is replaced by ‘31 July 2020’;
(26)
in the sixth column, expiration of approval, of row 156, Pirimiphos-methyl, the date is replaced by ‘31 July 2020’;
(27)
in the sixth column, expiration of approval, of row 158, Beflubutamid, the date is replaced by ‘31 July 2020’;
(28)
in the sixth column, expiration of approval, of row 163, Benthiavalicarb, the date is replaced by ‘31 July 2020’;
(29)
in the sixth column, expiration of approval, of row 164, Boscalid, the date is replaced by ‘31 July 2020’;
(30)
in the sixth column, expiration of approval, of row 166, Fluoxastrobin, the date is replaced by ‘31 July 2020’;
(31)
in the sixth column, expiration of approval, of row 167, Paecilomyces lilacinus strain 251, the date is replaced by ‘31 July 2020’;
(32)
in the sixth column, expiration of approval, of row 168, Prothioconazole, the date is replaced by ‘31 July 2020’;
(33)
in the sixth column, expiration of approval, of row 192, Diuron, the date is replaced by ‘30 September 2020’;
(34)
in the sixth column, expiration of approval, of row 268, Tebuconazole, the date is replaced by ‘31 August 2020’.
Cite this act
Commission Implementing Regulation (EU) 2019/707 of 7 May 2019 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances alpha-cypermethrin, beflubutamid, benalaxyl, benthiavalicarb, bifenazate, boscalid, bromoxynil, captan, cyazofamid, desmedipham, dimethoate, dimethomorph, diuron, ethephon, etoxazole, famoxadone, fenamiphos, flumioxazine, fluoxastrobin, folpet, foramsulfuron, formetanate, metalaxyl-m, methiocarb, metribuzin, milbemectin, Paecilomyces lilacinus strain 251, phenmedipham, phosmet, pirimiphos-methyl, propamocarb, prothioconazole, s-metolachlor and tebuconazole (Text with EEA relevance.) (EUR-Lex). Retrieved via LawPlayer, https://lawplayer.com/eu/act/32019R0707
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