Commission Implementing Regulation (EU) No 1186/2012 of 11 December 2012 amending the Annex to Regulation (EU) No 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance phoxim Text with EEA relevance

• CELEX: Implementing Regulation (EU) No 1186/2012
• 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 third day following that of its publication in the Official Journal of the European Union .

It shall apply from 13 February 2013.

Schedules & Appendices

ANNEX

ANNEX

The entry corresponding to phoxim in Table 1 of the Annex to Regulation (EU) No 37/2010 is replaced by the following:

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

‘Phoxim

Phoxim

All food-producing species except fin fish.

25  μg/kg

Muscle

For porcine and poultry species the fat MRL relates to “skin and fat in natural proportions”.

Not for use in animals from which milk is produced for human consumption.

Antiparasitic agents/Agents against ectoparasites.’

550  μg/kg

Fat

50  μg/kg

Liver

30  μg/kg

Kidney

60  μg/kg

Eggs