Commission Directive 2003/32/EC of 23 April 2003 introducing detailed specificiations as regards the requirements laid down in Council Directive 93/42/EEC with respect to medical devices manufactured utilising tissues of animal origin
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Incorporated into the EEA Agreement but no longer in force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EU legal act incorporated into the EEA Agreement, but no longer in force in the Agreement
Area (EEA Agreement)
II Technical Regulations, Standards, Testing and Certification
II.XXX Medical Devices
Joint committee decision (JCD)
072/2004
In force in the EEA
No
Legal Documents
Commission Directive 2003/32/EC of 23 April 2003 introducing detailed specificiations as regards the requirements laid down in Council Directive 93/42/EEC with respect to medical devices manufactured utilising tissues of animal origin
Tilskipun framkvæmdastjórnarinnar 2003/32/EB frá 23. apríl 2003 um nákvæmar forskriftir varðandi kröfurnar sem mælt er fyrir um í tilskipun ráðsins 93/42/EBE að því er tekur til lækningatækja sem eru framleidd með eða úr vefjum, upprunnum úr dýraríkinu
Richtlinie 2003/32/EG der Kommission vom 23. April 2003 mit genauen Spezifikationen bezüglich der in der Richtlinie 93/42/EWG des Rates festgelegten Anforderungen an unter Verwendung von Gewebe tierischen Ursprungs hergestellte Medizinprodukte
Kommisjonsdirektiv 2003/32/EF av 23. april 2003 om detaljerte spesifikasjoner med hensyn til de krav som er fastsatt i rådsdirektiv 93/42/EØF for medisinsk utstyr framstilt av vev av animalsk opprinnelse
History
Disclaimer: EEA-Lex is provided for information purposes only. The information is not guaranteed or promised to be current or complete and is not intended to replace any applicable legal sources.