Devices

Device Recall AFX Endovascular AAA System, Endoleak Type IIIA

  • Modèle / numéro de série
    The correction is not lot specific. It applies to AFX procedures conducted after June 2013
  • Classification du dispositif
    Cardiovascular Devices
  • Classe de dispositif
    3
  • Dispositif implanté ?
    Yes
  • Distribution
    Worldwide Distribution - US Distribution and to the countries of : Austria, Belgium, Czech Republic, France, Germany, Greece, Ireland, Israel, Italy, Latvia, Luxembourg, Monaco, Netherlands, Poland, Portugal, Spain, Sweden, Switzerland, Turkey and United Kingdom.
  • Description du dispositif
    AFX Endovascular AAA System, Endoleak Type IIIA
  • Manufacturer
    Endologix
  • 1 Event

Fabricant

Endologix
  • Adresse du fabricant
    Endologix, 35 Hammond, Irvine CA 92618-1607
  • Société-mère du fabricant (2017)
    Endologix Inc.
  • Source
    USFDA