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ISO 10993-18:2020/Amd1:2022- Amendment 1: Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process - Amendment 1: Determination of the uncertainty factorAmendment by International Organization for Standardization, 05/01/2022
ISO 10993-18:2005Biological evaluation of medical devices - Part 18: Chemical characterization of materialsstandard by International Organization for Standardization, 07/01/2005
ISO 10993-17:2002Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substancesstandard by International Organization for Standardization, 12/01/2002
ISO 10993-16:2017Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachablesstandard by International Organization for Standardization, 05/01/2017
ISO 10993-16:2010Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachablesstandard by International Organization for Standardization, 02/01/2010
ISO 10993-16:1997Biological evaluation of medical devices -- Part 16: Toxicokinetic study design for degradation products and leachablesstandard by International Organization for Standardization, 09/01/1997
ISO 10993-15:2000Biological evaluation of medical devices -- Part 15: Identification and quantification of degradation products from metals and alloysstandard by International Organization for Standardization, 12/01/2000
ISO 10993-14:2001Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramicsstandard by International Organization for Standardization, 11/15/2001
ISO 10993-13:2010Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devicesstandard by International Organization for Standardization, 06/15/2010
ISO 10993-13:1998Biological evaluation of medical devices -- Part 13: Identification and quantification of degradation products from polymeric medical devicesstandard by International Organization for Standardization, 11/01/1998
ISO 10993-12:2012Biological evaluation of medical devices - Part 12: Sample preparation and reference materialsstandard by International Organization for Standardization, 07/01/2012
ISO 10993-12:2007Biological evaluation of medical devices - Part 12: Sample preparation and reference materialsstandard by International Organization for Standardization, 11/01/2007