BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MEDFUSION 3500 SYRINGE INFUSION PUMP

    MDR report key: 1000231 · Received January 24, 2008

    Report

    Report Number
    2183502-2007-00397
    Event Type
    Malfunction
    Date Received
    January 24, 2008
    Manufacturer
    SMITHS MEDICAL MD, INC.
    Product Code
    FRN
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MEDFUSION 3500 SYRINGE INFUSION PUMP SYRINGE INFUSION PUMP FRN SMITHS MEDICAL MD, INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1