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dc.contributor.authorIrish Medicines Board (IMB)
dc.date.accessioned2010-04-16T14:40:45Z
dc.date.available2010-04-16T14:40:45Z
dc.date.issued2004-10-21
dc.identifier.urihttp://hdl.handle.net/10147/96650
dc.language.isoenen
dc.publisherIrish Medicines Board (IMB)en
dc.relation.ispartofseriesGuidance noteen
dc.relation.ispartofseries3en
dc.subjectMEDICAL DEVICESen
dc.subjectREGULATIONen
dc.titleGuidance note for the registration of persons responsible for placing in-vitro diagnostic medical devices on the market in accordance with Directive 98/79/EC and S.I. No. 304 of 2001.en
dc.typeOtheren
refterms.dateFOA2018-09-03T10:53:51Z


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