Registration number (WIID)Project No.TitleStatus
93384ISO/PWI TR 26398Biological evaluation of medical devices - Information on the use of clinical data in the application of ISO 10993-1Izstrādē
93385ISO/PWI TS 26399Biological evaluation of medical devices – Guidance on the application of ISO 10993-1 throughout the medical device life cycleIzstrādē
93386ISO/PWI 10993-5Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicityIzstrādē
93387ISO/PWI 10993-10Biological evaluation of medical devices — Part 10: Tests for skin sensitizationIzstrādē
64780ISO/WD TS 29741Biological evaluation of medical devices — Development of tolerable intake values for Di(2-ethylhexyl)phthalate (DEHP)Izstrādē
64763ISO/WD 10993-7Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residualsIzstrādē
90931ISO/CD TS 25364-2Analytical chemistry matters associated with ISO 10993-18 — Part 2: Quantification of medical device extractables and leachables using Non-Targeted Analysis (NTA)Izstrādē
90743ISO/AWI 10993-14Biological evaluation of medical devices — Part 14: Identification and quantification of degradation products from ceramicsIzstrādē
71146ISO/NP TR 37137-1Cardiovascular biological evaluation of medical devices — Guidance for absorbable implants — Part 1: Title missingIzstrādē
22696ISO 10993-4:1992/DAmd 1Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood — Amendment 1Izstrādē
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