EEA-Lex

With EEA-Lex you can find information about proposed EU legal acts with possible EEA relevance, adopted EU acts under consideration for incorporation into the EEA Agreement, and acts that have already been incorporated into the Agreement.

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Commission Decision 2002/364/EC of 7 May 2002 on common technical specifications for in vitro-diagnostic medical devices notified under document C (2002) 1344
Entscheidung der Kommission vom 7. Mai 2002 über Gemeinsame Technische Spezifikationen für In-Vitro-Diagnostika (2002/364/EG)
Ákvörðun framkvæmdastjórnarinnar 2002/364/EB frá 7. maí 2002 um sameiginlegar tækniforskriftir fyrir lækningabúnað til sjúkdómsgreiningar í glasi
Kommisjonsvedtak 2002/364/EF av 7. mai 2002 om felles tekniske spesifikasjoner for medisinsk utstyr til in vitro-diagnostikk
Commission Decision 2002/65/EC of 25 January 2002 on the national provisions concerning HIV testing kits notified under Article 95(4) of the EC Treaty by the UK as regards Directive 98/79/EC on in vitro diagnostic medical devices
Entscheidung der Kommission vom 25. Januar 2002 über die einzelstaatlichen Rechtsvorschriften zu HIV-Test-Sets, die gemäß Artikel 95 Absatz 4 EG-Vertrag vom Vereinigten Königreich in Bezug auf die Richtlinie 98/79/EG über In-vitro-Diagnostika notifiziert wurden (2002/65/EG)
Directive 2001/104/EC of the European Parliament and of the Council of the 7 December 2001 amending Council Directive 93/42/EEC concerning medical devices
Richtlinie 2001/104/EG des Europäischen Parlaments und des Rates vom 7. Dezember 2001 zur Änderung der Richtlinie 93/42/EWG des Rates über Medizinprodukte
Tilskipun Evrópuþingsins og ráðsins 2001/104/EB frá 7. desember 2001 um breytingu á tilskipun ráðsins 93/42/EBE um lækningatæki
Europaparlaments- og rådsdirektiv 2001/104/EF av 7. desember 2001 om endring av rådsdirektiv 93/42/EØF om medisinsk utstyr
Directive 2000/70/EC of the European Parliament and of the Council of 16 November 2000 amending Council Directive 93/42/EEC as regards medical devices incorporating stable derivates of human blood or human plasma
Richtlinie 2000/70/EG des Europäischen Parlaments und des Rates vom 16. November 2000 zur Änderung der Richtlinie 93/42/EWG des Rates hinsichtlich Medizinprodukten, die stabile Derivate aus menschlichem Blut oder Blutplasma enthalten
Tilskipun Evrópuþingsins og ráðsins 2000/70/EB frá 16. nóvember 2000 um breytingu á tilskipun ráðsins 93/42/EBE að því er varðar lækningabúnað sem í eru stöðugar afleiður úr blóði eða blóðvökva manna
Europaparlaments- og rådsdirektiv 2000/70/EF av 16. november 2000 om endring av rådsdirektiv 93/42/EØF med hensyn til medisinsk utstyr som inneholder stabile produkter av blod eller plasma fra mennesker
COM(1995) 130
Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices
Richtlinie 98/79/EG des Europäischen Parlaments und des Rates vom 27. Oktober 1998 über In-vitro-Diagnostika
Tilskipun Evrópuþingsins og ráðsins 98/79/EB frá 27. október 1998 um lækningabúnað til sjúkdómsgreiningar í glasi
Europaparlaments- og rådsdirektiv 98/79/EF av 27. oktober 1998 om medisinsk utstyr til in vitro-diagnostikk
Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
Richtlinie 93/42/EWG des Rates vom 14. Juni 1993 über Medizinprodukte
Council Directive 90/385/EEC of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices
Richtlinie 90/385/EWG des Rates vom 20. Juni 1990 zur Angleichung der Rechtsvorschriften der Mitgliedstaaten über aktive implantierbare medizinische Geräte
Commission Implementing Regulation (EU) …/... laying down rules for the application of Regulation (EU) 2017/745 of the European Parliament and of the Council as regards common specifications for the reprocessing of single-use medical devices

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