Device Recall LuMend OUTBACK LTD

  • Modelo / Serial
    All lots
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Worldwide
  • Descripción del producto
    Outback LTD Re-Entry Catheter, Sterile, Single Use. The Cordis LuMend OUTBACK LTD Re-Entry Catheter is indicated for placement and positioning of guidewires within the peripheral vasculature. The cannula is a nitinol needle that is used to re-enter the true lumen of the vessel.
  • Manufacturer
  • 1 Event

Fabricante

  • Dirección del fabricante
    Cordis Corporation, 14201 NW 60th Avenue, Miami Lakes FL 33014
  • Empresa matriz del fabricante (2017)
  • Source
    USFDA