BEUDAMED
    FDA Adverse Event Death Summary report: N

    AVI 3M IV INFUSION PUMP

    MDR report key: 237686 · Received August 24, 1999

    Report

    Report Number
    2183502-1999-00026
    Event Type
    Death
    Date Received
    August 24, 1999
    Date of Event
    July 7, 1999
    Manufacturer
    SIMS DELTEC, INC.
    Product Code
    FRN
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 AVI 3M IV INFUSION PUMP IV INFUSION PUMP FRN SIMS DELTEC, INC. NA

    Patients

    Seq Age Sex Outcome Treatment
    1