Devices

Device Recall Deltec PortACath

Fabricante

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

18 dispositivos con un nombre similar

Más información acerca de la data acá

Device Recall Deltec PortACath
  • Modelo / Serial
    Lot M27134
  • 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 Titanium Venous Access System, with Silicone Catheter, 2.8mm O.D. x 1.0mm I.D., 9 Fr Introducer Set, REF 21-4009-24
  • Manufacturer
    Deltec, Inc
Device Recall Deltec PortACath
  • Modelo / Serial
    Lot M27051
  • 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 Low Profile Titanium Venous Access System, with Silicone Catheter, 2.8mm O.D. x 1.0mm I.D., 9 Fr Introducer Set, REF 21-4035-24
  • Manufacturer
    Deltec, Inc
Device Recall Deltec PortACath
  • Modelo / Serial
    Lots M27118 and M27262
  • 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 Low Profile Titanium Venous Access System, with PolyFlow Polyurethane Catheter, 1.9mm O.D. x 1.0mm I.D., 6 Fr Introducer Set, REF 21-4037-24
  • Manufacturer
    Deltec, Inc
Device Recall Deltec PortACath
  • Modelo / Serial
    Lot M27037
  • Distribución
    The recalled products were shipped nationwide in the United States and worldwide.
  • Descripción del producto
    Port-A-Cath II Epidural Low Profile Polysulfone/Titanium Access System, with PolyFlow Polyurethane Catheter, 1.2mm O.D. x 5mm I.D., REF 21-1501-22
  • Manufacturer
    Deltec, Inc
Device Recall Deltec PortACath
  • Modelo / Serial
    Lot M26890
  • Clasificación del producto
    Cardiovascular Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    The recalled products were shipped nationwide in the United States and worldwide.
  • Descripción del producto
    6 Fr Introducer Set, REF 21-2320-24
  • Manufacturer
    Deltec, Inc
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