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
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
77991ISO 25539-4:2021Cardiovascular implants — Endovascular devices — Part 4: Application of ISO 17327-1 for coated endovascular devicesStandarts 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
84370ISO 23500-3:2024Preparation and quality management of fluids for haemodialysis and related therapies — Part 3: Water for haemodialysis and related therapiesStandarts spēkā
84368ISO 23500-1:2024Preparation and quality management of fluids for haemodialysis and related therapies — Part 1: General requirementsStandarts 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
88491ISO 5840-2:2021/Amd 1:2025Cardiovascular implants — Cardiac valve prostheses — Part 2: Surgically implanted heart valve substitutes — Amendment 1Standarts spēkā
74733ISO 15674:2016/Amd 1:2020Cardiovascular implants and artificial organs — Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags — Amendment 1: ConnectorsStandarts spēkā
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