Ventana Medical Systems Inc

9 dispositifs dans la base de données

  • Modèle / numéro de série
    5277965001 | Y10759, Y17402, Y21312, Y13938, Y17403
  • Classification du dispositif
  • Description du dispositif
    IVD: Haematoxylin solution IVD
  • Modèle / numéro de série
    760-500 (05269806001)
  • Description du dispositif
    IVD: DNA in situ hybridization kit
  • Modèle / numéro de série
    760-091 (05266157001)
  • Description du dispositif
    IVD: DNA in situ hybridization kit
  • Modèle / numéro de série
    760-500 (05269806001) | A05885, B00988
  • Description du dispositif
    IVD: DNA in situ hybridization kit
  • Modèle / numéro de série
  • Description du dispositif
    IVD: Automated histological analysis instrument
4 en plus

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
  • Adresse du fabricant
    Ventana Medical Systems Inc, 1910 E Innovation Park Dr, Tucson AZ 85737
  • 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
8 en plus