Implanted Tibial Electrical Urinary Continence Device

FDA product code QXM · Class 2 · 3 devices · 26 reports · 0 devices named in recalls

• Revi™ Implant MA-1007-0600_US_CM

  Bluewind Medical Ltd · Implanted Tibial Electrical Urinary Continence Device
  16 reports
• Revi™ System Patient Kit KA-9000-0001_US_CM

  Bluewind Medical Ltd · Implanted Tibial Electrical Urinary Continence Device
  9 reports
• Revi™ Wearable Device MA-1004-0500

  Bluewind Medical Ltd · Implanted Tibial Electrical Urinary Continence Device
  1 report