Devices

Device Recall AFX Endovascular AAA System, Endoleak Type IIIA

  • Modelo / Serial
    The correction is not lot specific. It applies to AFX procedures conducted after June 2013
  • Clasificación del producto
    Cardiovascular Devices
  • Clase de dispositivo
    3
  • ¿Implante?
    Yes
  • Distribución
    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.
  • Descripción del producto
    AFX Endovascular AAA System, Endoleak Type IIIA
  • Manufacturer
    Endologix
  • 1 Event

Fabricante

Endologix
  • Dirección del fabricante
    Endologix, 35 Hammond, Irvine CA 92618-1607
  • Empresa matriz del fabricante (2017)
    Endologix Inc.
  • Source
    USFDA