Alaris

  • Model / Serial
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide in the United States, Canada, Mexico, and the European Union
  • Product Description
    Alaris PC unit Model 8000 only when used with Alaris Pump module or Alaris Syringe module
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    CareFusion Corporation, 10020 Pacific Mesa Blvd, San Diego CA 92121
  • Manufacturer Parent Company (2017)
  • Source
    USFDA

284 devices with a similar name

Learn more about the data here

  • Model / Serial
    Model: Models: 80063UN01, 80263UN01, 80263UN01-G, 9002MED01, 9002MED01-G, Affected: All pumps
  • Manufacturer
  • Model / Serial
    Model: Models: 80263UN01, 80263UN01-G, 9002MED01, 9002MED01-G, Affected: Pumps manufactured between Dec 2009 and Jan 2012
  • Manufacturer
  • Model / Serial
    Model: Model: 2000e, Affected: Lots: 13086446, 13095944, 13095778, 13106753, 13106848, 13096013, 13095675, 13106018
  • Manufacturer
279 more