Registration number (WIID)Project No.TitleStatus
90742ISO/AWI 10993-13Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devicesIzstrādē
93386ISO/PWI 10993-5Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicityIzstrādē
93385ISO/PWI TS 26399Biological evaluation of medical devices – Guidance on the application of ISO 10993-1 throughout the medical device life cycleIzstrādē
93384ISO/PWI TR 26398Biological evaluation of medical devices - Information on the use of clinical data in the application of ISO 10993-1Izstrādē
35976ISO/DIS 10993-6Biological evaluation of medical devices — Part 6: Tests for local effects after implantationIzstrādē
63449ISO/CD 10993-5Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicityIzstrādē
86248ISO/PWI TS 10993-22Biological evaluation of medical devices — Part 22: Guidance on nanomaterialsIzstrādē
45651ISO/AWI TS 29741Biological evaluation of medical devices — Development of tolerable intake values for Di(2-ethylhexyl)phthalate (DEHP)Izstrādē
42997ISO/CD 10993-1Biological evaluation of medical devices — Part 1: Evaluation and testingIzstrādē
90932ISO/CD TS 25364-3Analytical chemistry matters associated with ISO 10993-18 — Part 3: Instrumental and human requirements for evaluating organic medical device extractables and leachables via Non-Targeted Analysis (NTA)Izstrādē
Displaying 91-100 of 159 results.