Device Recall PADPRO DULT Radiotranslucent Pad w/Zoll connector

  • Modèle / numéro de série
    Lots Y040605-1, Y040605-2, Y052605-4, Y120805-2, Y111605-3, Y092805-6, Y010506-10, Y010506-9.
  • 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/Zoll¿ connector. Defibrillation/Pacing/Cardioversion/Monitoring Electrodes, REF/Catalog # 2516Z. RX ONLY. 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