CEN/TC 205
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 81493 | prEN ISO 8637-2 | Extracorporeal systems for blood purification - Part 2: Extracorporeal blood and fluid circuits for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO/DIS 8637‑2:2025) | Aptauja slēgta |
| 81518 | prEN ISO 23500-3 rev | Preparation and quality management of fluids for haemodialysis and related therapies — Part 3: Water for haemodialysis and related therapies | Izstrādē |
| 81519 | prEN ISO 23500-1 rev | Preparation and quality management of fluids for haemodialysis and related therapies — Part 1: General requirements | Izstrādē |
| 81520 | prEN ISO 23500-4 rev | Preparation and quality management of fluids for haemodialysis and related therapies — Part 4: Concentrates for haemodialysis and related therapies | Izstrādē |
| 81521 | prEN ISO 23500-2 rev | Preparation and quality management of fluids for haemodialysis and related therapies — Part 2: Water treatment equipment for haemodialysis applications and related therapies | Izstrādē |
| 81522 | prEN ISO 23500-5 rev | Preparation and quality management of fluids for haemodialysis and related therapies — Part 5: Quality of dialysis fluid for haemodialysis and related therapies | Izstrādē |
| 82045 | prEN ISO 8871-3 rev | Elastomeric parts for parenterals and for devices for pharmaceutical use — Part 3: Determination of released-particle count | Izstrādē |
| 82046 | prEN ISO 8871-1 rev | Elastomeric parts for parenterals and for devices for pharmaceutical use — Part 1: Extractables in aqueous autoclavates | Izstrādē |
| 82142 | EN ISO 11608-3:2022/prA1:2025 | Needle-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 slēgta |
| 82384 | prEN 455-4 rev | Medical gloves for single use - Part 4: Requirements and testing for shelf life determination | Izstrādē |
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