Device Recall Multifunctional electrode/defibrillation electrode

  • Modèle / numéro de série
    DF20 SKINTACT  Lot #'s 80506-0771, 80527-0776, 80628-0776, 80826-0773, 80911-0773,
  • Classification du dispositif
  • Classe de dispositif
    3
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution - US - FL Foreign: Austria, Germany, Romania, France, Dubai, Greece, Italy, South Korea, United Kingdom, Hungary, Latvia, Saudi Arabia and Lebanon
  • Description du dispositif
    SKINTACT Electrodes for Defibrillation, 10X REF DF20, Rx only, Manufactured by Leonhard Lang GmbH, Archenweg 56, 6020 Innsbruck, Austria. || The device is non-sterile and single use. || For use on adults and children over eight years old for external defibrillation, pacing, monitoring, and cardioversion.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Leonhard Lang Gmbh, Archenweg 56, Innsbruck Austria
  • Société-mère du fabricant (2017)
  • Source
    USFDA

Un dispositif médical avec un nom similaire

En savoir plus sur les données ici

  • Modèle / numéro de série
    DF-20 S&W;  Lot #'s 80505-0778, 80814-0773, 80930-0775, 81017-0777, 90226-0776, 90403-0779, 90420-0775
  • Classification du dispositif
  • Classe de dispositif
    3
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution - US - FL Foreign: Austria, Germany, Romania, France, Dubai, Greece, Italy, South Korea, United Kingdom, Hungary, Latvia, Saudi Arabia and Lebanon
  • Description du dispositif
    S&W; Electrodes for Defibrillation, 10 Defibrillation Electrodes, Reorder #90101, S & W Healthcare Corp, 1525 Flight Path Drive Brooksville, Florida 34604 || The device is non-sterile and single use. || For use on adults and children over eight years old for external defibrillation, pacing, monitoring, and cardioversion.
  • Manufacturer