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Commission Implementing Regulation (EU) 2017/201 of 6 February 2017 amending Regulation (EU) No 37/2010 to classify the substance fluralaner as regards its maximum residue limit (Text with EEA relevance. )

Commission Implementing Regulation (EU) 2017/201 of 6 February 2017 amending Regulation (EU) No 37/2010 to classify the substance fluralaner as regards its maximum residue limit (Text with EEA relevance. )

Implementing Regulation (EU) 2017/201 Β· Regulation Β· 3 articles

Data as of 2026-07-04 Β· Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. Β· Read the official text β†—

Article 1

The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.

Article 2

This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union . It shall apply from 8 April 2017.

Supplementary provisions

ANNEXSupplementary provisions

ANNEX In Table 1 of the Annex to Regulation (EU) No 37/2010, an entry for the following substance is inserted in alphabetical order: Pharmacologically active Substance Marker residue Animal Species MRL Target Tissues Other Provisions (according to Article 14(7) of Regulation (EC) No 470/2009) Therapeutic Classification β€˜Fluralaner Fluralaner Poultry 65 ΞΌg/kg Muscle NO ENTRY Antiparasitic agents/Agents against ectoparasites’ 650 ΞΌg/kg Skin and fat in natural proportions 650 ΞΌg/kg Liver 420 ΞΌg/kg Kidney 1Β 300 ΞΌg/kg Eggs

Source: EUR-Lex (Publications Office of the EU), Β© European Union, reuse permitted under Commission Decision 2011/833/EU.

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