Commission Implementing Regulation (EU) 2018/1076 of 30 July 2018 amending Regulation (EU) No 37/2010 to classify the substance isoflurane as regards its maximum residue limit (Text with EEA relevance.)

• CELEX: Implementing Regulation (EU) 2018/1076
• 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 29 September 2018.

Schedules & Appendices

ANNEX

ANNEX

In Table 1 of the Annex to Regulation (EU) No 37/2010, the entry for the substance ‘isoflurane’ 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

‘Isoflurane

NOT APPLICABLE

Equidae

No MRL required

NOT APPLICABLE

For use by inhalation

General anaesthetics’

Porcine

No MRL required

NOT APPLICABLE

For use by inhalation in piglets up to 7 days of age