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. )

• CELEX: Implementing Regulation (EU) 2018/523
• Articles: 3

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.

Schedules & Appendices

ANNEX

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