8578: Suturless Pump Connector Revision Kit

  • Modèle / numéro de série
    All lots numbers included
  • Classification du dispositif
  • Classe de dispositif
    3
  • Dispositif implanté ?
    Yes
  • Distribution
    International Distribution --- country of Belgium.
  • Description du dispositif
    Medtronic 8578 Sutureless Pump Connector Revision Kit || Medtronic Inc., Minneapolis, MN 55432 || A part of the SynchroMed II Infusion system, which is designed to restore and provide intrathecal administration of drug therapy.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Medtronic Neuromodulation, 800 53rd Ave NE, PO Box 1250, Minneapolis MN 55440-1250
  • Source
    USFDA