ISO/TC 150/SC 2
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 90340 | ISO/PWI 5840-1 | Cardiovascular implants — Cardiac valve prostheses — Part 1: General requirements | Izstrādē |
| 63851 | ISO/TR 12417-2:2017 | Cardiovascular implants and extracorporeal systems — Vascular device-drug combination products — Part 2: Local regulatory information | Atcelts |
| 80895 | ISO/TR 12417-2:2022 | Cardiovascular implants and extracorporeal systems — Vascular device-drug combination products — Part 2: Local regulatory information | Standarts spēkā |
| 85497 | ISO/TR 18965:2025 | Medical devices — Examples of the application of the risk management process to cardiac valve replacement and repair systems | Standarts spēkā |
| 63757 | ISO/TR 19024:2016 | Evaluation of CPB devices relative to their capabilities of reducing the transmission of gaseous microemboli (GME) to a patient during cardiopulmonary bypass | Standarts spēkā |
| 51419 | ISO/TS 12417:2011 | Cardiovascular implants and extracorporeal systems — Vascular device-drug combination products | Atcelts |
| 28154 | ISO/TS 15539:2000 | Cardiovascular implants — Endovascular prostheses | Atcelts |
| 59194 | ISO/TS 17137:2014 | Cardiovascular implants and extracorporeal systems — Cardiovascular absorbable implants | Atcelts |
| 74669 | ISO/TS 17137:2019 | Cardiovascular implants and extracorporeal systems — Cardiovascular absorbable implants | Atcelts |
| 41865 | ISO/TS 23810:2006 | Cardiovascular implants and artificial organs — Checklist for preoperative extracorporeal circulation equipment setup | Atcelts |
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