Devices

Device Recall KLSBP001 Battery Pack

  • Modèle / numéro de série
    Lots 509567, K055R
  • Classification du dispositif
    General and Plastic Surgery Devices
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    Distributed in FL.
  • Description du dispositif
    Battery Pack || KLS-SD-1000 || Single || Models: KLS-BP-001 Used to power the KLS Martin Max Driver (battery powdered surgical screwdriver).
  • Manufacturer
    Pro-Dex Inc
  • 1 Event

Fabricant

Pro-Dex Inc
  • Adresse du fabricant
    Pro-Dex Inc, 2361 McGaw Ave, Irvine CA 92614-5831
  • Société-mère du fabricant (2017)
    Pro-Dex Inc
  • Source
    USFDA