Device Recall PRECISE RX

  • Modelo / Serial
  • Clasificación del producto
  • Clase de dispositivo
  • ¿Implante?
  • Distribución
    Product was distributed to 415 domestic hospital accounts nationwide and to two related international distributores in Isreal and the Netherlands.
  • Descripción del producto
    This medical device is packaged in an inner Tyvek pouch and then in an outer carton. The outer carton is labeled as Cordis PRECISE RX Nitinol Stent Transhepatic Biliary System Cordis a Johnson n Johnson Company ENDOVASCULAR Cat. No. Lot No. Use By. The inner pouch is similarly labled.
  • Manufacturer
  • 1 Event


  • Dirección del fabricante
    Cordis Corporation, 14201 NW 60th Ave, Miami Lakes FL 33014-2802
  • Empresa matriz del fabricante (2017)
  • Source