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ISO 10993-9:2009WithdrawnBiological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation productsISO 10993-1:2009WithdrawnBiological evaluation of medical devices — Part 1: Evaluation and testing within a risk management processISO 10993-7:2008WithdrawnBiological evaluation of medical devices — Part 7: Ethylene oxide sterilization residualsISO 10993-12:2007WithdrawnBiological evaluation of medical devices — Part 12: Sample preparation and reference materialsISO 10993-6:2007WithdrawnBiological evaluation of medical devices — Part 6: Tests for local effects after implantationISO 10993-11:2006WithdrawnBiological evaluation of medical devices — Part 11: Tests for systemic toxicityISO/TS 10993-19:2006WithdrawnBiological evaluation of medical devices — Part 19: Physico-chemical, morphological and topographical characterization of materialsISO 10993-2:2006WithdrawnBiological evaluation of medical devices — Part 2: Animal welfare requirementsISO 10993-18:2005WithdrawnBiological evaluation of medical devices — Part 18: Chemical characterization of materialsISO 10993-3:2003WithdrawnBiological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicityISO 10993-1:2003WithdrawnBiological evaluation of medical devices — Part 1: Evaluation and testingISO 10993-17:2002WithdrawnBiological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substancesISO 10993-4:2002WithdrawnBiological evaluation of medical devices — Part 4: Selection of tests for interactions with bloodISO 10993-10:2002WithdrawnBiological evaluation of medical devices — Part 10: Tests for irritation and delayed-type hypersensitivityISO 10993-12:2002WithdrawnBiological evaluation of medical devices — Part 12: Sample preparation and reference materialsISO 10993-8:2000WithdrawnBiological evaluation of medical devices — Part 8: Selection and qualification of reference materials for biological testsISO 10993-15:2000WithdrawnBiological evaluation of medical devices — Part 15: Identification and quantification of degradation products from metals and alloysISO 10993-5:1999WithdrawnBiological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicityISO 10993-9:1999WithdrawnBiological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation productsISO 10993-13:1998WithdrawnBiological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devicesISO 10993-1:1997WithdrawnBiological evaluation of medical devices — Part 1: Evaluation and testingISO 10993-16:1997WithdrawnBiological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachablesISO 10993-12:1996WithdrawnBiological evaluation of medical devices — Part 12: Sample preparation and reference materialsISO 10993-10:1995WithdrawnBiological evaluation of medical devices — Part 10: Tests for irritation and sensitizationISO 10993-7:1995WithdrawnBiological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals