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dc.contributor.authorIrish Medicines Board (IMB)
dc.date.accessioned2011-02-14T09:09:26Z
dc.date.available2011-02-14T09:09:26Z
dc.date.issued2010-08
dc.identifier.urihttp://hdl.handle.net/10147/121769
dc.language.isoenen
dc.publisherIrish Medicines Board (IMB)en
dc.relation.ispartofseriesSUR-G0006-2en
dc.subjectMEDICAL DEVICESen
dc.subjectREGULATIONen
dc.titleGuide for class I manufacturers on compliance with European Communities (medical devices) regulations, 1994en
dc.typeGuidelineen
refterms.dateFOA2018-08-22T11:01:57Z


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