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European Union
Commission Implementing Regulation (EU) 2017/1383
preamble
Recital (15)

Commission Implementing Regulation (EU) 2017/1383

law://eu/reg/2017/1383/rct_15@2026-11-12

Version in force onWhereEuropean Union

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Key facts

Type: Implementing regulation · Commission Implementing Regulation (EU) 2017/1383 · EEA relevant
Adopted: 25 Jul 2017
In force: 15 Aug 2017
Made by: Directorate-General for Health and Food Safety, European Commission
Official: EUR-Lex 32017R1383 · ELI

Topics

chemical product health risk market approval marketing standard rodent toxic substance Pesticides, biocides Plant health legislation

Connections

Cited by 1: Commission Implementing Decision (EU) 2024/7342 provisions
Cites 1: Commission Implementing Regulation (EU) 2017/1376

History · 1 version

25 Jul 2017Reading

This text since 25 Jul 2017

In force

(15)As the examination of the applications for the renewal of the approval of flocoumafen, brodifacoum and warfarin for use in biocidal products of product-type 14 is now finalised, Commission Implementing Decision (EU) 2016/135^note is repealed by Commission Implementing Regulation (EU) 2017/1376^note.

Source: EUR-Lex, © European Union, 1998-2026. Reuse authorised under Decision 2011/833/EU.