Device Recall Cordis Avanti Sheath Introducer

  • Modèle / numéro de série
    Catalog 402656X Lot # 15076369.  Catalog 504606X Lot # 15075717.  Catalog 504656X Lot # 15076362, 15076363, and 15076364.
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide.
  • Description du dispositif
    Cordis, AVANTI+ Introducer, STERILE EO, For one use only. || Catalog 402656X Lot # 15076369. || Catalog 504606X Lot # 15075717. || Catalog 504656X Lot # 15076362, 15076363, 15076364.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Cordis Corporation, 14201 Nw 60th Ave, Miami Lakes FL 33014-2802
  • Société-mère du fabricant (2017)
  • Source
    USFDA