Ventana Medical Systems Inc

3 dispositifs dans la base de données

  • Modèle / numéro de série
    Lot 400566
  • Classification du dispositif
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide.
  • Description du dispositif
    iVIEW DAB Detecion Kit. || Catalog Number 760-091
  • Modèle / numéro de série
    Lot Numbers; 23095A, 23340A, and 30116A.
  • Classification du dispositif
  • Classe de dispositif
    3
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide and to Japan, France and Puerto Rico.
  • Description du dispositif
    CONFIRM c-KIT, Antibody (rabbit polyclonal), Catalog number 790-2939
  • Modèle / numéro de série
    Lot numbers: R20061A, R20429A, R21002A, and R21002B.
  • Distribution
    Nationwide to pathology laboratories and hospitals.
  • Description du dispositif
    ChemMate (brand) Keratin Primary Antibody, Clones AE1, AE3, CAM 5.2 and 35betaH11. Catalog number PAB111.

13 fabricants avec un nom similaire

En savoir plus sur les données ici

  • Adresse du fabricant
    Ventana Medical Systems Inc, 1910 E Innovation Park Dr, Oro Valley AZ 85755-1962
  • Société-mère du fabricant (2017)
  • Source
    USFDA
  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.
  • Source
    IGJ
  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.
  • Source
    IGJ
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