Devices

Device Recall Deltec PortACath II

  • Modelo / Serial
    Lots M26975 and M27127
  • Clasificación del producto
    General Hospital and Personal Use Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    Yes
  • Distribución
    The recalled products were shipped nationwide in the United States and worldwide.
  • Descripción del producto
    Port-A-Cath II Dual-lumen Low Profile Polysulfone/Titanium Venous Access System, with Dual-lumen PolyFlow Polyurethane Catheter, 2.2mm O.D. x 1.0mm I.D., 7 French Introducer Set, REF 21-8066-24
  • Manufacturer
    Deltec, Inc
  • 1 Event

Fabricante

Deltec, Inc
  • Dirección del fabricante
    Deltec, Inc, 1265 Grey Fox Rd, Saint Paul MN 55112-6929
  • Source
    USFDA

2 dispositivos con un nombre similar

Más información acerca de la data acá

Device Recall Deltec PortACath II FluoroFree
  • Modelo / Serial
    Lot M27047
  • Clasificación del producto
    General Hospital and Personal Use Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    Yes
  • Distribución
    The recalled products were shipped nationwide in the United States and worldwide.
  • Descripción del producto
    Port-A-Cath II Fluoro-Free Low Profile Venous Access System, with PolyFlow Polyurethane Catheter, 2.6mm O.D. x 1.6mm I.D., and with CATH-FINDER Sensor Wire, REF 21-4685-24
  • Manufacturer
    Deltec, Inc
Device Recall Deltec PortACath II
  • Modelo / Serial
    Lot M26983
  • Clasificación del producto
    General Hospital and Personal Use Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    Yes
  • Distribución
    The recalled products were shipped nationwide in the United States and worldwide.
  • Descripción del producto
    Port-A-Cath II Dual-lumen Low Profile Polysulfone/Titanium Venous Access System, with Dual-lumen PolyFlow Polyurethane Catheter, 3.2mm O.D. x 1.4mm I.D., 10 French Introducer Set, REF 21-8068-24
  • Manufacturer
    Deltec, Inc