Devices

Device Recall Powerlink (R) System with IntuiTrak Delivery System

  • Modèle / numéro de série
    MODEL NUMBER 34-34-80LE, LOTS W09-2967 AND W09-3000.
  • Classification du dispositif
    Cardiovascular Devices
  • Classe de dispositif
    3
  • Dispositif implanté ?
    No
  • Distribution
    Recalled devices were distributed to medical centers and hospitals in OR, PA, FL, TX, MI and LA.
  • Description du dispositif
    Powerlink System with IntuiTrak Delivery System (Endovascular Graft): Model Number 34-34-80LE, LOTS W09-2967 AND W09-3000.
  • Manufacturer
    Endologix Inc
  • 1 Event

Fabricant

Endologix Inc
  • Adresse du fabricant
    Endologix Inc, 11 Studebaker, Irvine CA 92618-2013
  • Source
    USFDA

Un dispositif médical avec un nom similaire

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Device Recall Powerlink (R) System with IntuiTrak Delivery System
  • Modèle / numéro de série
    MODEL NUMBER 34-34-80L, LOTS W09-2966 AND W09-2998.
  • Classification du dispositif
    Cardiovascular Devices
  • Classe de dispositif
    3
  • Dispositif implanté ?
    No
  • Distribution
    Recalled devices were distributed to medical centers and hospitals in OR, PA, FL, TX, MI and LA.
  • Description du dispositif
    Powerlink System with IntuiTrak Delivery System (Endovascular Graft): Model Number 34-34-80L, LOTS W09-2966 AND W09-2998.
  • Manufacturer
    Endologix Inc