Devices

Device Recall PremierEdge MICROSURGICAL KNIFE 3.0mm Slit Knife

  • Modèle / numéro de série
    Lot No: DK1106J, DK0207M, DK0207AH, DK0307H, DK0407L, and DK0507E
  • Classification du dispositif
    Ophthalmic Devices
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide: USA, Kuwait, Lebanon, Lithuania, Mexico, Netherlands, Norway, South Africa, Saudi Arabia, Slovakia, Spain, Sweden, Switzwerland, Turkey, United Kingdom, Ecuador, Finland, France, Germany, Greece, Italy, Denmark, Columbia, Chile, Brazil, Belgium, and Australia
  • Description du dispositif
    PremierEdge MICROSURGICAL KNIFE, 3.0mm Slit Knife, Item Code/REF: PE 3830; OASIS Glendora, CA 91741
  • Manufacturer
    Oasis Medical Inc
  • 1 Event

Fabricant

Oasis Medical Inc
  • Adresse du fabricant
    Oasis Medical Inc, 514 S Vermont Ave Bldg 510-528, Glendora CA 91741-6205
  • Société-mère du fabricant (2017)
    Oasis Medical Inc.
  • Source
    USFDA

Un dispositif médical avec un nom similaire

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Device Recall PremierEdge MICROSURGICAL KNIFE 3.0mm Slit Knife Straight
  • Modèle / numéro de série
    Lot Code: DK0107AD and DK0207N
  • Classification du dispositif
    Ophthalmic Devices
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide: USA, Kuwait, Lebanon, Lithuania, Mexico, Netherlands, Norway, South Africa, Saudi Arabia, Slovakia, Spain, Sweden, Switzwerland, Turkey, United Kingdom, Ecuador, Finland, France, Germany, Greece, Italy, Denmark, Columbia, Chile, Brazil, Belgium, and Australia
  • Description du dispositif
    PremierEdge MICROSURGICAL KNIFE, 3.0mm Slit Knife - Straight Item Code/REF: PE 3830S; OASIS Glendora, CA 91741
  • Manufacturer
    Oasis Medical Inc