Registration number (WIID)Project No.TitleStatus
61089ISO 10993-6:2016Biological evaluation of medical devices — Part 6: Tests for local effects after implantationStandarts spēkā
63448ISO 10993-4:2017Biological evaluation of medical devices — Part 4: Selection of tests for interactions with bloodStandarts spēkā
63449ISO/CD 10993-5Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicityIzstrādē
64238ISO/DTR 17137-2Cardiovascular implants and extracorporeal systems — Cardiovascular absorbable implants — Part 2: Guidance on biological evaluation of absorbable implantsIzstrādē
64580ISO 10993-9:2019Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation productsStandarts spēkā
64581ISO/PWI 10993-13Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devicesIzstrādē
64582ISO 10993-16:2017Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachablesStandarts spēkā
64744ISO/PWI 10993-17Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substancesIzstrādē
64750ISO 10993-18:2020Biological evaluation of medical devices — Part 18: Chemical characterization of medical device materials within a risk management processStandarts spēkā
64751ISO/NP TS 10993-19Biological evaluation of medical devices — Part 19: Physico-chemical, morphological and topographical characterization of materialsIzstrādē
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