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ISO 10993-11:2017PublishedBiological evaluation of medical devices — Part 11: Tests for systemic toxicityISO 10993-4:2017PublishedBiological evaluation of medical devices — Part 4: Selection of tests for interactions with bloodISO 10993-16:2017PublishedBiological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachablesISO/TR 10993-22:2017PublishedBiological evaluation of medical devices — Part 22: Guidance on nanomaterialsISO 10993-13:2010PublishedBiological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devicesISO 10993-5:2009PublishedBiological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicityISO/TS 10993-20:2006PublishedBiological evaluation of medical devices — Part 20: Principles and methods for immunotoxicology testing of medical devicesISO 10993-14:2001PublishedBiological evaluation of medical devices — Part 14: Identification and quantification of degradation products from ceramicsISO/TS 11796:2023PublishedBiological evaluation of medical devices — Requirements for interlaboratory studies to demonstrate the applicability of validated in vitro methods to assess the skin sensitization of medical devicesISO 12771:1997PublishedPlastics laboratory ware — Disposable serological pipettesISO 12772:1997PublishedLaboratory glassware — Disposable microhaematocrit capillary tubesISO 13022:2012PublishedMedical products containing viable human cells — Application of risk management and requirements for processing practicesISO 13079:2011PublishedLaboratory glass and plastics ware — Tubes for the measurement of the erythrocyte sedimentation rate by the Westergren methodISO 13130:2011PublishedLaboratory glassware — DesiccatorsISO 13132:2023PublishedLaboratory glassware — Petri dishesISO 14155:2026PublishedClinical investigation of medical devices for human subjects — Good clinical practiceISO 15189:2022PublishedMedical laboratories — Requirements for quality and competenceISO 15190:2020PublishedMedical laboratories — Requirements for safetyISO 15193:2026PublishedIn vitro diagnostic medical devices — Requirements for reference measurement proceduresISO 15194:2026PublishedIn vitro diagnostic medical devices — Requirements for certified reference materials and the content of supporting documentationISO 15195:2018PublishedLaboratory medicine — Requirements for the competence of calibration laboratories using reference measurement proceduresISO 15197:2013PublishedIn vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitusISO 16256:2021PublishedClinical laboratory testing and in vitro diagnostic test systems — Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseasesISO/TS 16766:2024PublishedManufacturers’ considerations for in vitro diagnostic medical devices in a public health emergencyISO/TS 16782:2016PublishedClinical laboratory testing — Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testing