Gambro Dialysatoren GmbH

13 devices · 92 adverse event reports · 1 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.

All Gambro Dialysatoren GmbH devices

• REVACLEAR Revaclear 400

  Dialyzer, high permeability with or without sealed dialysate system
  1 recall1 report
• Revaclear 400

  Dialyzer, high permeability with or without sealed dialysate system
  24 reports
• Polyflux 170H

  DIALYZER, CAPILLARY, HOLLOW FIBER
  23 reports
• Polyflux 140H

  DIALYZER, CAPILLARY, HOLLOW FIBER
  14 reports
• Revaclear 300

  Dialyzer, high permeability with or without sealed dialysate system
  10 reports
• Ultrafilter U 9000 112062

  Subsystem, water purification
  6 reports
• Polyflux 21L

  DIALYZER, CAPILLARY, HOLLOW FIBER
  5 reports
• REVACLEAR Revaclear 300

  Dialyzer, high permeability with or without sealed dialysate system
  3 reports
• Polyflux 14L

  DIALYZER, CAPILLARY, HOLLOW FIBER
  2 reports
• Polyflux 6H

  Dialyzer, high permeability with or without sealed dialysate system
  1 report
• Polyflux 17L

  DIALYZER, CAPILLARY, HOLLOW FIBER
  1 report
• Polyflux 210H

  DIALYZER, CAPILLARY, HOLLOW FIBER
  1 report
• THERANOVA 500

  Hemodialyzer with expanded solute removal profile
  1 report