Commission Implementing Regulation (EU) 2024/780 of 5 March 2024 concerning the renewal of the authorisation of a preparation of endo–1,4-beta-xylanase produced by Trichoderma citrinoviride DSM 34663 as a feed additive for all poultry species for fattening, all poultry species for laying and reared for laying, weaned piglets, pigs for fattening and carp, the authorisation of that preparation as a feed additive for all poultry species for breeding, turkeys reared for breeding, minor poultry species reared for breeding, ornamental birds, suckling piglets and minor porcine species for fattening (holder of authorisation: Huvepharma NV) and repealing Implementing Regulations (EU) 2015/1043, (EU) 2017/1906 and (EU) 2018/327
Proposed act with possible EEA relevance
Act under scrutiny by EEA EFTA
Draft Joint Committee Decision (JCD) under consideration
Entry into force of Joint Committee Decision (JCD) pending
Incorporated into the EEA Agreement and in force
Incorporated into the EEA Agreement but no longer in force
Legal status
EU legal act incorporated into the EEA Agreement by a Joint Committee Decision (JCD)
Area (EEA Agreement)
I Veterinary and Phytosanitary Matters
I.II Feedingstuffs
Joint committee decision (JCD)
187/2024
In force in the EEA
Yes
Legal Documents
Commission Implementing Regulation (EU) 2024/780 of 5 March 2024 concerning the renewal of the authorisation of a preparation of endo–1,4-beta-xylanase produced by Trichoderma citrinoviride DSM 34663 as a feed additive for all poultry species for fattening, all poultry species for laying and reared for laying, weaned piglets, pigs for fattening and carp, the authorisation of that preparation as a feed additive for all poultry species for breeding, turkeys reared for breeding, minor poultry species reared for breeding, ornamental birds, suckling piglets and minor porcine species for fattening (holder of authorisation: Huvepharma NV) and repealing Implementing Regulations (EU) 2015/1043, (EU) 2017/1906 and (EU) 2018/327
Framkvæmdarreglugerð framkvæmdastjórnarinnar (ESB) 2024/780 frá 5. mars 2024 um endurnýjun á leyfi fyrir blöndu með endó–1,4-betaxýlanasa, sem er framleiddur með Trichoderma citrinoviride DSM 34663, sem fóðuraukefni fyrir allar tegundir alifugla til eldis, allar tegundir alifugla til varps og sem eru aldar til varps, fráfærugrísi, eldissvín og vatnakarpa, um leyfi fyrir þeirri blöndu sem fóðuraukefni fyrir allar tegundir alifugla til eldis, kalkúna sem eru aldir til undaneldis, aukategundir alifugla sem eru aldar til undaneldis, skrautfugla, mjólkurgrísi og aukategundir svína til eldis (leyfishafi er Huvepharma NV) og um niðurfellingu á framkvæmdarreglugerðum (ESB) 2015/1043, (ESB) 2017/1906 og (ESB) 2018/327
Durchführungsverordnung (EU) 2024/780 der Kommission vom 5. März 2024 zur Verlängerung der Zulassung einer Zubereitung aus Endo–1,4-beta-Xylanase, gewonnen aus Trichoderma citrinoviride DSM 34663, als Futtermittelzusatzstoff für alle Mast- und Legegeflügelarten, Jungtiere aller Legegeflügelarten, Absetzferkel, Mastschweine und Karpfen, zur Zulassung dieser Zubereitung als Futtermittelzusatzstoff für alle Zuchtgeflügelarten, Jungtruthühner für die Zucht, Jungtiere aller Zuchtgeflügelarten von geringerer wirtschaftlicher Bedeutung, Ziervögel, Saugferkel und Zuchtschweinearten von geringerer wirtschaftlicher Bedeutung (Zulassungsinhaber: Huvepharma NV) und zur Aufhebung der Durchführungsverordnungen (EU) 2015/1043, (EU) 2017/1906 und (EU) 2018/327
Kommisjonens gjennomføringsforordning (EU) 2024/780 av 5. mars 2024 om fornya godkjenninga av eit preparat av endo-1,4-betaxylanase framstilt av Trichoderma citrinoviride DSM 34663 som tilsetjingsstoff i fôr til alle fjørfeartar meinte for slakt, alle fjørfeartar meinte for eggproduksjon og som vert fôra opp for eggproduksjon, avvande smågrisar, slaktesvin og karpe, om godkjenning av dette preparatet som tilsetjingsstoff i fôr til alle fjørfeartar meinte for avl, kalkunar som vert fôra opp for avl, mindre utbreidde fjørfeartar som vert fôra opp for avl, prydfuglar, spedgrisar og mindre utbreidde svineartar meinte for slakt (innehavar av godkjenninga: Huvepharma NV) og om oppheving av gjennomføringsforordning (EU) 2015/1043, (EU) 2017/1906 og (EU) 2018/327
History
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