Ventana Medical Systems Inc

9 dispositivos en la base de datos

  • Modelo / Serial
    5277965001 | Y10759, Y17402, Y21312, Y13938, Y17403
  • Clasificación del producto
  • Descripción del producto
    IVD: Haematoxylin solution IVD
  • Modelo / Serial
    760-500 (05269806001)
  • Descripción del producto
    IVD: DNA in situ hybridization kit
  • Modelo / Serial
    760-091 (05266157001)
  • Descripción del producto
    IVD: DNA in situ hybridization kit
  • Modelo / Serial
    760-500 (05269806001) | A05885, B00988
  • Descripción del producto
    IVD: DNA in situ hybridization kit
  • Modelo / Serial
  • Descripción del producto
    IVD: Automated histological analysis instrument
4 más

13 fabricantes con un nombre similar

Más información acerca de la data acá

  • Dirección del fabricante
    Ventana Medical Systems Inc, 1910 E Innovation Park Dr, Oro Valley AZ 85755-1962
  • Empresa matriz del fabricante (2017)
  • Source
    USFDA
  • Dirección del fabricante
    Ventana Medical Systems Inc, 1910 E Innovation Park Dr, Tucson AZ 85737
  • Source
    USFDA
  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    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
  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    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 más