DIALYZER, CAPILLARY, HOLLOW FIBER
FDA product code FJI · Class 2 · 11 devices · 2,357 reports · 7 deaths reported · 1 devices named in recalls
- Optiflux® 0500316EFresenius Medical Care Holdings, Inc. · DIALYZER, CAPILLARY, HOLLOW FIBER2 recalls7 deaths2,282 reports
- Polyflux 170HGambro Dialysatoren GmbH · DIALYZER, CAPILLARY, HOLLOW FIBER23 reports
- Polyflux 140HGambro Dialysatoren GmbH · DIALYZER, CAPILLARY, HOLLOW FIBER14 reports
- Hemoflow™ 0520165AFresenius Medical Care Holdings, Inc. · DIALYZER, CAPILLARY, HOLLOW FIBER11 reports
- Hemoflow™ 0520161AFresenius Medical Care Holdings, Inc. · DIALYZER, CAPILLARY, HOLLOW FIBER10 reports
- Hemoflow™ 0500164AFresenius Medical Care Holdings, Inc. · DIALYZER, CAPILLARY, HOLLOW FIBER7 reports
- Polyflux 21LGambro Dialysatoren GmbH · DIALYZER, CAPILLARY, HOLLOW FIBER5 reports
- Polyflux 14LGambro Dialysatoren GmbH · DIALYZER, CAPILLARY, HOLLOW FIBER2 reports
- Hemoflow™ 0500145AFresenius Medical Care Holdings, Inc. · DIALYZER, CAPILLARY, HOLLOW FIBER1 report
- Polyflux 17LGambro Dialysatoren GmbH · DIALYZER, CAPILLARY, HOLLOW FIBER1 report
- Polyflux 210HGambro Dialysatoren GmbH · DIALYZER, CAPILLARY, HOLLOW FIBER1 report