Catheter, hemodialysis, triple lumen, non-implanted
FDA product code NIE · Class 2 · 108 devices · 379 reports · 8 deaths reported · 71 devices named in recalls
- MAHURKAR Elite 8888231330Mozarc Medical US LLC · CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED1 death1 report
- MAHURKAR Elite 8888231416Mozarc Medical US LLC · CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED1 report
- MAHURKAR Elite 8888233213Mozarc Medical US LLC · CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED1 report
- MAHURKAR Elite 8888233224Mozarc Medical US LLC · CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED1 report
- MAHURKAR Elite 8888233313Mozarc Medical US LLC · CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED1 report
- MAHURKAR Elite 8888233316Mozarc Medical US LLC · CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED1 report
- MAHURKAR 8888102003HPMozarc Medical US LLC · CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED1 report
- ARROW IPN036958Teleflex Incorporated · Catheter, hemodialysis, triple lumen, non-implanted1 report