Devices

Device Recall Guidant ENDOTAK SQ Array

  • Modèle / numéro de série
    model 0048, serial numbers 200652 and 200655.  model 0049, serial numbers 202864 thru 202900. model 0085, serial numbers 102087 thru 103287.
  • Classification du dispositif
    Cardiovascular Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    nationwide and worldwide.
  • Description du dispositif
    Guidant ENDOTAK SQ Array models 0048, 0049, 0085. Subcutaneous Lead Array. Cardioversion/Defibrillation Lead. Guidant Corporation Cardiac Rhythm Management 4100 Hamline Avenue North, St. Paul, MN 55112-5798. Sterilized with gaseous ethylene oxide.
  • Manufacturer
    Guidant Corporation
  • 1 Event

Fabricant

Guidant Corporation
  • Adresse du fabricant
    Guidant Corporation, 4100 Hamline Ave N, Saint Paul MN 55112-5700
  • Source
    USFDA