Shunt, Portosystemic, Endoprosthesis
FDA product code MIR · Class 3 · 7 devices · 28 reports · 0 devices named in recalls
- GORE VIATORR TIPS Endoprosthesis PTB8108275W. L. Gore & Associates, Inc. · Shunt, Portosystemic, Endoprosthesis15 reports
- GORE VIATORR TIPS Endoprosthesis PTB8106275W. L. Gore & Associates, Inc. · Shunt, Portosystemic, Endoprosthesis5 reports
- GORE VIATORR TIPS Endoprosthesis PTB8107275W. L. Gore & Associates, Inc. · Shunt, Portosystemic, Endoprosthesis3 reports
- WALLSTENT® Endoprosthesis H965402110Boston Scientific Corporation · SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS2 reports
- GORE VIATORR TIPS Endoprosthesis PTB8104275W. L. Gore & Associates, Inc. · Shunt, Portosystemic, Endoprosthesis1 report
- GORE VIATORR TIPS Endoprosthesis PTB8105275W. L. Gore & Associates, Inc. · Shunt, Portosystemic, Endoprosthesis1 report
- WALLSTENT™ RP Endoprosthesis M001711360Boston Scientific Corporation · SHUNT, PORTOSYSTEMIC, ENDOPROSTHESIS1 report