Registration number (WIID)Project No.TitleStatus
53468ISO 10993-12:2012Biological evaluation of medical devices — Part 12: Sample preparation and reference materialsAtcelts
18971ISO 10993-10:1995Biological evaluation of medical devices — Part 10: Tests for irritation and sensitizationAtcelts
56669ISO 10993-1:2009/Cor 1:2010Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process — Technical Corrigendum 1Atcelts
35977ISO 10993-11:2006Biological evaluation of medical devices — Part 11: Tests for systemic toxicityAtcelts
18969ISO 10993-8:2000Biological evaluation of medical devices — Part 8: Selection and qualification of reference materials for biological testsAtcelts
26212ISO 10993-9:1999Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation productsAtcelts
18961ISO 10993-2:1992Biological evaluation of medical devices — Part 2: Animal welfare requirementsAtcelts
55441ISO/TR 15499:2012Biological evaluation of medical devices — Guidance on the conduct of biological evaluation within a risk management processAtcelts
21225ISO 10993-1:1992/Cor 1:1992Biological evaluation of medical devices — Part 1: Guidance on selection of tests — Technical Corrigendum 1Atcelts
69217ISO/TR 15499:2016Biological evaluation of medical devices — Guidance on the conduct of biological evaluation within a risk management processAtcelts
Displaying 101-110 of 146 results.