CATHETER, NEPHROSTOMY
FDA product code LJE · Class U · 109 devices · 1,562 reports · 3 deaths reported · 7 devices named in recalls
- Ultraxx G30364Cook Incorporated · CATHETER, NEPHROSTOMY1 report
- Ultrathane G30404Cook Incorporated · CATHETER, NEPHROSTOMY1 report
- Ultraxx G46023Cook Incorporated · CATHETER, NEPHROSTOMY1 report
- Ultraxx G46038Cook Incorporated · CATHETER, NEPHROSTOMY1 report
- Universa G55801Cook Incorporated · CATHETER, NEPHROSTOMY1 report
- Universa G55802Cook Incorporated · CATHETER, NEPHROSTOMY1 report
- Universa G55804Cook Incorporated · CATHETER, NEPHROSTOMY1 report
- NA M0062601500Boston Scientific Corporation · CATHETER, NEPHROSTOMY1 report
- Amplatz Type Renal Sheath M0069001230Boston Scientific Corporation · CATHETER, NEPHROSTOMY1 report