《is.en.iso.10993.12.2016》.pdf

Republic of Ireland ≠ EDICT OF GOVERNMENT ± In order to promote public education and public safety, equal justice for all, a better informed citizenry, the rule of law, world trade and world peace, this legal document is hereby made available on a noncommercial basis, as it is the right of all humans to know and speak the laws that govern them. I.S. EN ISO 10993-12 (2012) (English): Biological evaluation of medical devices - Part 12: Sample preparation and reference materials [Authority: The European Union Per Directive 90/385/EEC] · . ··. @ NSAI . Irish Standard I.S. EN ISO 10993-12:2012 Standards Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012) © NSAI 2012 No copying without NSAI permission except as pe rmitted by copyright law . 1.5. EN ISO 10993-12:2012 Incorporating amendments/corrigenda/NationalAnnexes issued since publication: The National Standards Authority of Ireland (NSAI) produces the following categories of formal documents: 1.5. xxx: Irish Standard national specification based 011 the consensus of an expert panel and subject to public consultation. S.R. xxx: Standard Recommendation - recommendation based on the consensus of an expert panel and subject to public consultation. SWiFT xxx: A rapidly developed recommendatory document based on the consensus of the participants of an NSAI workshop. This document replaces: EN ISO 10993-12:2009 This document is based on: Published: EN ISO 10993-12:2012 9 July, 2012 ICS number: This document was published under the authority of the NSAI 11.1