Stent, metallic, expandable, duodenal
FDA product code MUM · Class 2 · 12 devices · 219 reports · 5 deaths reported · 0 devices named in recalls
- Evolution G48026Cook Ireland Ltd · STENT,METALLIC,EXPANDABLE,DUODENAL1 death57 reports
- WallFlex™ Duodenal M00565020Boston Scientific Corporation · STENT,METALLIC,EXPANDABLE,DUODENAL42 reports
- WallFlex™ Duodenal M00565030Boston Scientific Corporation · STENT,METALLIC,EXPANDABLE,DUODENAL2 deaths38 reports
- WallFlex™ Duodenal M00565010Boston Scientific Corporation · STENT,METALLIC,EXPANDABLE,DUODENAL1 death30 reports
- Evolution G48027Cook Ireland Ltd · STENT,METALLIC,EXPANDABLE,DUODENAL30 reports
- Evolution G48025Cook Ireland Ltd · STENT,METALLIC,EXPANDABLE,DUODENAL14 reports
- WallFlex™ Duodenal M00555860Boston Scientific Corporation · Stent, metallic, expandable, duodenal2 reports
- WallFlex™ Duodenal M00555870Boston Scientific Corporation · Stent, metallic, expandable, duodenal1 death2 reports
- WALLSTENT™ Enteral Endoprosthesis M00565570Boston Scientific Corporation · STENT,METALLIC,EXPANDABLE,DUODENAL1 report
- WallFlex™ Duodenal M00555880Boston Scientific Corporation · Stent, metallic, expandable, duodenal1 report
- HANAROSTENT LowAxTM Duodenum/Pylorus(NNN) DNJF-22-120-230M.I.Tech Co., Ltd. · Stent, Metallic, Expandable, Duodenal1 report
- HANAROSTENT® LowAxTM Duodenum/Pylorus(NNN) DNJF-22-120-230M.I.Tech Co., Ltd. · Stent, Metallic, Expandable, Duodenal1 report