Bluewind Medical Ltd
3 devices · 26 adverse event reports · 0 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
- Revi™ Implant MA-1007-0600_US_CMImplanted Tibial Electrical Urinary Continence Device16 reports
- Revi™ System Patient Kit KA-9000-0001_US_CMImplanted Tibial Electrical Urinary Continence Device9 reports
- Revi™ Wearable Device MA-1004-0500Implanted Tibial Electrical Urinary Continence Device1 report