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ISO/TR 10993-9:1994WithdrawnBiological evaluation of medical devices — Part 9: Degradation of materials related to biological testingISO 10993-6:1994WithdrawnBiological evaluation of medical devices — Part 6: Tests for local effects after implantationISO 10993-11:1993WithdrawnBiological evaluation of medical devices — Part 11: Tests for systemic toxicityISO 10993-1:1992WithdrawnBiological evaluation of medical devices — Part 1: Guidance on selection of testsISO 10993-3:1992WithdrawnBiological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicityISO 10993-4:1992WithdrawnBiological evaluation of medical devices — Part 4: Selection of tests for interactions with bloodISO 10993-5:1992WithdrawnBiological evaluation of medical devices — Part 5: Tests for cytotoxicity: in vitro methodsISO 10993-2:1992WithdrawnBiological evaluation of medical devices — Part 2: Animal welfare requirementsISO 13132:2011WithdrawnLaboratory glassware — Petri dishesISO 14155:2020WithdrawnClinical investigation of medical devices for human subjects — Good clinical practiceISO 14155:2011WithdrawnClinical investigation of medical devices for human subjects — Good clinical practiceISO 14155-1:2003WithdrawnClinical investigation of medical devices for human subjects — Part 1: General requirementsISO 14155-2:2003WithdrawnClinical investigation of medical devices for human subjects — Part 2: Clinical investigation plansISO 14155:1996WithdrawnClinical investigation of medical devicesISO 15189:2012WithdrawnMedical laboratories — Requirements for quality and competenceISO 15189:2007WithdrawnMedical laboratories — Particular requirements for quality and competenceISO 15189:2003WithdrawnMedical laboratories — Particular requirements for quality and competenceISO 15190:2003WithdrawnMedical laboratories — Requirements for safetyISO 15193:2009WithdrawnIn vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for content and presentation of reference measurement proceduresISO 15193:2002WithdrawnIn vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Presentation of reference measurement proceduresISO 15194:2009WithdrawnIn vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for certified reference materials and the content of supporting documentationISO 15194:2002WithdrawnIn vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Description of reference materialsISO 15195:2003WithdrawnLaboratory medicine — Requirements for reference measurement laboratoriesISO 15197:2003WithdrawnIn vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitusISO 15198:2004WithdrawnClinical laboratory medicine — In vitro diagnostic medical devices — Validation of user quality control procedures by the manufacturer