ISO/TC 150/SC 2

Registration number (WIID)Project No.TitleStatus
85497ISO/TR 18965:2025Medical devices — Examples of the application of the risk management process to cardiac valve replacement and repair systemsStandarts spēkā
84372ISO 23500-5:2024Preparation and quality management of fluids for haemodialysis and related therapies — Part 5: Quality of dialysis fluid for haemodialysis and related therapiesStandarts spēkā
84371ISO 23500-4:2024Preparation and quality management of fluids for haemodialysis and related therapies — Part 4: Concentrates for haemodialysis and related therapiesStandarts spēkā
84370ISO 23500-3:2024Preparation and quality management of fluids for haemodialysis and related therapies — Part 3: Water for haemodialysis and related therapiesStandarts spēkā
84369ISO 23500-2:2024Preparation and quality management of fluids for haemodialysis and related therapies — Part 2: Water treatment equipment for haemodialysis applications and related therapiesStandarts spēkā
84368ISO 23500-1:2024Preparation and quality management of fluids for haemodialysis and related therapies — Part 1: General requirementsStandarts spēkā
83184ISO 7199:2024Cardiovascular implants and artificial organs — Blood-gas exchangers (oxygenators)Standarts spēkā
80895ISO/TR 12417-2:2022Cardiovascular implants and extracorporeal systems — Vascular device-drug combination products — Part 2: Local regulatory informationStandarts spēkā
77991ISO 25539-4:2021Cardiovascular implants — Endovascular devices — Part 4: Application of ISO 17327-1 for coated endovascular devicesStandarts spēkā
77083ISO 18242:2016/Amd 1:2023Cardiovascular implants and extracorporeal systems — Centrifugal blood pumps — Amendment 1: Worst-case conditions for testingStandarts spēkā
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