Devices

Device Recall Deltec PortACath P.A.S. Port

  • Modèle / numéro de série
    Lot M27049
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    The recalled products were shipped nationwide in the United States and worldwide.
  • Description du dispositif
    Port-A-Cath P.A.S. Port T2 Titanium Venous Access System, with PolyFlow Polyurethane Catheter, 1.9mm O.D. x 1.0mm I.D., 6 French Introducer Set, REF 21-4573-24
  • Manufacturer
    Deltec, Inc
  • 1 Event

Fabricant

Deltec, Inc
  • Adresse du fabricant
    Deltec, Inc, 1265 Grey Fox Rd, Saint Paul MN 55112-6929
  • Source
    USFDA