Acutus Medical, Inc.
12 devices · 32 adverse event reports · 1 deaths reported · 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.
- FlexCath Cross Transseptal Solution 900310Introducer, Catheter1 death8 reports
- AcQMap 900003Catheter,Intracardiac Mapping,High-Density Array5 reports
- AcQCross Qx 900305Introducer, Catheter4 reports
- AcQCross Qx 900304Introducer, Catheter3 reports
- FlexCath Cross Transseptal Solution 900304-003Introducer, Catheter3 reports
- FlexCath Cross Transseptal Solution 900308-003Dilator, Vessel, For Percutaneous Catheterization2 reports
- AcQGuide 900002Catheter, Steerable2 reports
- AcQGuide MAX 900200Catheter, Steerable1 report
- AcQCross Qx Integrated Transseptal Dilator/Needle 900308Introducer, Catheter1 report
- FlexCath Cross Transseptal Solution 900301-003Dilator, Vessel, For Percutaneous Catheterization1 report
- FlexCath Cross Transseptal Solution 900311Introducer, Catheter1 report
- AcQMap 800500Computer, Diagnostic, Programmable1 report