Device Recall Vitrectomy Kit

  • Modèle / numéro de série
    Lot numbers:   75908 78658 79157 79577 81959 83285 84916 85168 86500 87319 88343 88984 89749 96802 99415 102487
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution including CA, CO, FL, GA, IA, KY, MA, MN, MO, ND, NJ, NV, OH, SD, TX, UT, WI, and WY.
  • Description du dispositif
    Vitrectomy Kit, part number CMP1016(A. || Product packaged in a convenient manner for use in a general clinical procedure
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Windstone Medical Packaging, Inc., 1602 4th Ave N, Billings MT 59101-1521
  • Société-mère du fabricant (2017)
  • Source
    USFDA