Devices

Device Recall TriActiv System Procedure Kit 190 cm

  • Modelo / Serial
    Lot number 47303 exp 9/30/06
  • Clasificación del producto
    Cardiovascular Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide. The products are shipped to hospitals in AL, DE, Fl, IL, IN, MI, PA, SC, TN and TX.
  • Descripción del producto
    TriActiv System Procedure Kit. Balloon Protected Flush Extraction System 190 cm (for embolism protection). The kit includes AutoStream Flow Control, Flush Kit, ShieldWire (temporary occlusion balloon guidewire), and Balloon Inflation Syringe). The system is used with a standard 7F guide catheter using the standard femoral approach.
  • Manufacturer
    Kensey Nash Corp
  • 1 Event

Fabricante

Kensey Nash Corp
  • Dirección del fabricante
    Kensey Nash Corp, 735 Pennsylvania Dr, Exton PA 19341-1130
  • Source
    USFDA