Commission Regulation (EC) No 2007/2006 of 22 December 2006 implementing Regulation (EC) No 1774/2002 of the European Parliament and of the Council as regards the importation and transit of certain intermediate products derived from Category 3 material intended for technical uses in medical devices, in vitro diagnostics and laboratory reagents and amending that Regulation
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Incorporated into the EEA Agreement but no longer in force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)
I Veterinary and Phytosanitary Matters
I.I Veterinary Issues
Joint committee decision (JCD)
135/2007 In force in the EEA
Yes Legal documents
Commission Regulation (EC) No 2007/2006 of 22 December 2006 implementing Regulation (EC) No 1774/2002 of the European Parliament and of the Council as regards the importation and transit of certain intermediate products derived from Category 3 material intended for technical uses in medical devices, in vitro diagnostics and laboratory reagents and amending that Regulation
Reglugerð framkvæmdastjórnarinnar (EB) nr. 2007/2006 frá 22. desember 2006 um framkvæmd reglugerðar Evrópuþingsins og ráðsins (EB) nr. 1774/2002 að því er varðar innflutning og umflutning tiltekinna milliafurða, sem fást úr efni í 3. flokki og ætlaðar eru til tæknilegra nota í lækningatækjum, búnað til greininga í glasi og í prófefni á rannsóknarstofum, og um breytingu á þeirri reglugerð
Verordnung (EG) Nr. 2007/2006 der Kommission vom 22. Dezember 2006 zur Durchführung der Verordnung (EG) Nr. 1774/2002 des Europäischen Parlaments und des Rates hinsichtlich der Einfuhr und Durchfuhr bestimmter aus Material der Kategorie 3 gewonnener Zwischenerzeugnisse für technische Verwendungszwecke in Medizinprodukten, In-vitro-Diagnostika und Laborreagenzien sowie zur Änderung der genannten Verordnung
Kommisjonsforordning (EF) nr. 2007/2006 av 22. desember 2006 om gjennomføring av europaparlaments- og rådsforordning (EF) nr. 1774/2002 med hensyn til import og transitt av visse halvfabrikater framstilt av kategori 3-materiale beregnet på tekniske formål i medisinsk utstyr, in vitro-diagnostikk og laboratoriereagenser samt om endring av nevnte forordning
History
01.05.2010
Adopted JCD confirmed entry into force date
01.05.2010
Compliance date in the EEA
17.03.2010
Constitutional requirements under Art. 103 fulfillment date (IS)
Iceland
26.10.2007
Adoption of Joint Commitee Decision (JCD) incorporating the act into the EEA Agreement
30.03.2007
Draft Joint Commitee Decision (JCD) incorporating the act into the EEA Agreement sent to Commission
22.12.2006
Adoption date in the EU
01.01.2007
Compliance date in the EU
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