BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 523748 · Received October 17, 2003

    Report

    Report Number
    523748
    Event Type
    Other
    Date Received
    October 17, 2003
    Date of Event
    October 1, 2003
    Report Date
    October 1, 2003
    Manufacturer
    *
    Product Code
    BSZ
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    KY, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * BSZ * * *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other