intestinal Stimulator
FDA product code LNQ · Class f · 9 devices · 1,430 reports · 18 deaths reported · 0 devices named in recalls
- ENTERRA® II 37800Medtronic, Inc. · intestinal Stimulator1 death544 reports
- Enterra® II 37800Medtronic, Inc. · intestinal Stimulator16 deaths359 reports
- Enterra® II 37800Medtronic, Inc. · intestinal Stimulator1 death248 reports
- ENTERRA® 3116Medtronic, Inc. · intestinal Stimulator179 reports
- ENTERRA® II 37800Medtronic, Inc. · intestinal Stimulator73 reports
- ENTERRA® 4351-35Medtronic, Inc. · intestinal Stimulator17 reports
- ENTERRA ™ 4351-35Medtronic, Inc. · intestinal Stimulator5 reports
- ENTERRA ™ 4351-35Medtronic, Inc. · intestinal Stimulator4 reports
- Enterra ReliaStim Unipolar Lead 30101Enterra Medical, Inc. · Intestinal Stimulator1 report