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Commission Implementing Regulation (EU) 2018/523 of 28 March 2018 amending Regulation (EU) No 37/2010 to classify the substance fluazuron as regards its maximum residue limit (Text with EEA relevance. )

Commission Implementing Regulation (EU) 2018/523 of 28 March 2018 amending Regulation (EU) No 37/2010 to classify the substance fluazuron as regards its maximum residue limit (Text with EEA relevance. )

Implementing Regulation (EU) 2018/523 · Regulation · 3 articles

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 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 3 June 2018.

Supplementary provisions

ANNEXSupplementary provisions

ANNEX In Table 1 of the Annex to Regulation (EU) No 37/2010, the entry for the substance ‘fluazuron’ is replaced by the following: Pharmacologically active Substance Marker residue Animal Species MRLs Target Tissues Other Provisions (according to Article 14(7) of Regulation (EC) No 470/2009) Therapeutic Classification ‘Fluazuron Fluazuron All ruminants except bovine and ovine 200 μg/kg Muscle Not for use in animals from which milk is produced for human consumption Antiparasitic agents/Agents (acting) against ectoparasites’ 7 000 μg/kg Fat 500 μg/kg Liver 500 μg/kg Kidney Bovine 200 μg/kg Muscle NO ENTRY 7 000 μg/kg Fat 500 μg/kg Liver 500 μg/kg Kidney 200 μg/kg Milk Fin fish 200 μg/kg Muscle and skin in natural proportions NO ENTRY

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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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