Registration number (WIID)Project No.TitleStatus
81493prEN ISO 8637-2Extracorporeal systems for blood purification - Part 2: Extracorporeal blood and fluid circuits for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO/DIS 8637‑2:2025)Aptauja slēgta
81518prEN ISO 23500-3 revPreparation and quality management of fluids for haemodialysis and related therapies — Part 3: Water for haemodialysis and related therapiesIzstrādē
81519prEN ISO 23500-1 revPreparation and quality management of fluids for haemodialysis and related therapies — Part 1: General requirementsIzstrādē
81520prEN ISO 23500-4 revPreparation and quality management of fluids for haemodialysis and related therapies — Part 4: Concentrates for haemodialysis and related therapiesIzstrādē
81521prEN ISO 23500-2 revPreparation and quality management of fluids for haemodialysis and related therapies — Part 2: Water treatment equipment for haemodialysis applications and related therapiesIzstrādē
81522prEN ISO 23500-5 revPreparation and quality management of fluids for haemodialysis and related therapies — Part 5: Quality of dialysis fluid for haemodialysis and related therapiesIzstrādē
82045prEN ISO 8871-3 revElastomeric parts for parenterals and for devices for pharmaceutical use — Part 3: Determination of released-particle countIzstrādē
82046prEN ISO 8871-1 revElastomeric parts for parenterals and for devices for pharmaceutical use — Part 1: Extractables in aqueous autoclavatesIzstrādē
82142EN ISO 11608-3:2022/prA1:2025Needle-based injection systems for medical use - Requirements and test methods - Part 3: Containers and integrated fluid paths - Amendment 1 (ISO 11608-3:2022/DAmd1:2025)Aptauja
82384prEN 455-4 revMedical gloves for single use - Part 4: Requirements and testing for shelf life determinationIzstrādē
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