VENTANA MEDICAL SYSTEMS INC

6 devices in the database

  • Model / Serial
    Model Catalog: P/N 860-019 (Lot serial: 812498)
  • Product Description
    Jones Staining Kit
  • Model / Serial
    Model Catalog: N750-DISXT-FS (Lot serial: 710000-711288); Model Catalog: N750-BMKLT-FS (Lot serial: 610000-610266); Model Catalog: N750-BMK-FS (Lot serial: ALL); Model Catalog: N750-XT-FS (Lot serial: 710000-711289)
  • Product Description
    Discovery XT
  • Model / Serial
    Model Catalog: 790-2991 (Lot serial: Lot#680957)
  • Product Description
    MONOCLONAL PRIMARY ANTIBODY
  • Model / Serial
    Model Catalog: (Lot serial: s/n 390051-390060)
  • Product Description
    Symphony Automated Staining System
  • Model / Serial
    Model Catalog: N750-BMK-FS (Lot serial: )
  • Product Description
    Benchmark Automated Slide Stainer
One more

13 manufacturers with a similar name

Learn more about the data here

  • Manufacturer Address
    Ventana Medical Systems Inc, 1910 E Innovation Park Dr, Oro Valley AZ 85755-1962
  • Manufacturer Parent Company (2017)
  • Source
    USFDA
  • Manufacturer Address
    Ventana Medical Systems Inc, 1910 E Innovation Park Dr, Tucson AZ 85737
  • Source
    USFDA
  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    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
  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    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 more