Article 1
The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.
Commission Implementing Regulation (EU) 2020/1712 of 16 November 2020 amending Regulation (EU) No 37/2010 to classify the substance lidocaine as regards its maximum residue limit (Text with EEA relevance)
Commission Implementing Regulation (EU) 2020/1712 of 16 November 2020 amending Regulation (EU) No 37/2010 to classify the substance lidocaine as regards its maximum residue limit (Text with EEA relevance)
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 2
This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union .
Supplementary provisions
ANNEXSupplementary provisions
ANNEX In Table 1 of the Annex to Regulation (EU) No 37/2010, the entry for the substance ‘lidocaine’ 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 ‘Lidocaine NOT APPLICABLE Equidae No MRL required NOT APPLICABLE For local/regional anaesthesia only. Local anaesthetic’ Porcine For use in piglets up to 7 days of age only. For cutaneous and epilesional use only. Lidocaine Bovine 150 μg/kg 200 μg/kg 1 μg/kg 200 μg/kg 30 μg/kg Muscle Fat Liver Kidney Milk NOT APPLICABLE
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