Commission Implementing Decision (EU) 2016/135 of 29 January 2016 postponing the expiry date of approval of flocoumafen, brodifacoum and warfarin for use in biocidal products for product-type 14
Proposed act with possible EEA relevance
Act under scrutiny by EEA EFTA
Draft Joint Committee Decision (JCD) under consideration
Entry into force of Joint Committee Decision (JCD) pending
Incorporated into the EEA Agreement and in force
Incorporated into the EEA Agreement but no longer in force
Legal status
EU legal act incorporated into the EEA Agreement by a Joint Committee Decision (JCD) Area (EEA Agreement)
II Technical Regulations, Standards, Testing and Certification
II.XV Dangerous Substances
Joint committee decision (JCD)
084/2016 In force in the EEA
Yes Legal documents
Commission Implementing Decision (EU) 2016/135 of 29 January 2016 postponing the expiry date of approval of flocoumafen, brodifacoum and warfarin for use in biocidal products for product-type 14
Framkvæmdarákvörðun framkvæmdastjórnarinnar (ESB) 2016/135 frá 29. janúar 2016 um frestun að því er varðar lokadag samþykkis fyrir flókúmafeni bródífakúmi og varfaríni til notkunar í sæfivörur í vöruflokki 14
Durchführungsbeschluss (EU) 2016/135 der Kommission vom 29. Januar 2016 zur Verschiebung des Ablaufdatums der Genehmigung von Flocoumafen, Brodifacoum und Warfarin zur Verwendung in Biozidprodukten der Produktart 14
Kommisjonens gjennomføringsbeslutning (EU) 2016/135 av 29. januar 2016 om utsettelse av utløpsdatoen for godkjenningen av flokumafen, brodifakum og warfarin til bruk i biocidprodukter av type 14
History
30.04.2016
Adopted JCD confirmed entry into force date
30.04.2016
Compliance date in the EEA
29.04.2016
Adoption of Joint Commitee Decision (JCD) incorporating the act into the EEA Agreement
16.03.2016
Draft Joint Commitee Decision (JCD) incorporating the act into the EEA Agreement sent to Commission
29.01.2016
Adoption date in the EU
22.02.2016
Compliance date in the EU
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