Device Recall PADPRO ADULT Radiotranslucent Pad w/Medtronic connector

  • Modèle / numéro de série
    Lot Y101105-4
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide, including USA, Canada, Romania, Chile, and Belgium
  • Description du dispositif
    PADPRO ADULT Radiotranslucent Pad w/Medtronic¿ connector, REF/Catalog #2516M. RX ONLY. Defibrillation/Pacing/Cardioversion/Monitoring Electrodes. Made in USA for: CONMED CORPORATION Utica, New York, 13502.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Conmed Corporation, 525 French Road, Utica NY 13502-5945
  • Source
    USFDA