Registration number (WIID)Project No.TitleStatus
63757ISO/TR 19024:2016Evaluation of CPB devices relative to their capabilities of reducing the transmission of gaseous microemboli (GME) to a patient during cardiopulmonary bypassStandarts spēkā
86614ISO 8637-3:2024Extracorporeal systems for blood purification — Part 3: PlasmafiltersStandarts spēkā
84371ISO 23500-4:2024Preparation and quality management of fluids for haemodialysis and related therapies — Part 4: Concentrates for haemodialysis and related therapiesStandarts spēkā
77083ISO 18242:2016/Amd 1:2023Cardiovascular implants and extracorporeal systems — Centrifugal blood pumps — Amendment 1: Worst-case conditions for testingStandarts spēkā
61854ISO 18241:2016Cardiovascular implants and extracorporeal systems — Cardiopulmonary bypass systems — Venous bubble trapsStandarts spēkā
66925ISO 25539-1:2017Cardiovascular implants — Endovascular devices — Part 1: Endovascular prosthesesStandarts spēkā
77033ISO 5840-1:2021Cardiovascular implants — Cardiac valve prostheses — Part 1: General requirementsStandarts spēkā
77034ISO 5840-2:2021Cardiovascular implants — Cardiac valve prostheses — Part 2: Surgically implanted heart valve substitutesStandarts spēkā
88490ISO 5840-1:2021/Amd 1:2025Cardiovascular implants — Cardiac valve prostheses — Part 1: General requirements — Amendment 1Standarts spēkā
69838ISO/TS 23810:2018Cardiovascular implants and artificial organs — Checklists for use of extracorporeal circulation equipmentStandarts spēkā
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