CANNULA, CATHETER
FDA product code DQR · Class 2 · 6 devices · 14 reports · 2 devices named in recalls
- OptiSite Arterial Perfusion Cannula OPTI16Edwards Lifesciences LLC · CANNULA, CATHETER1 recall3 reports
- OptiSite Arterial Perfusion Cannula OPTI18Edwards Lifesciences LLC · CANNULA, CATHETER1 recall2 reports
- AngioDynamics 06597004Angiodynamics, Inc. · CANNULA, CATHETER4 reports
- AngioDynamics 06597015Angiodynamics, Inc. · CANNULA, CATHETER2 reports
- AngioDynamics 06597053Angiodynamics, Inc. · CANNULA, CATHETER2 reports
- Arterial Cannula A212-65CSorin Group Italia Srl · CANNULA, CATHETER1 report