BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 980787 · Received December 30, 2005

    Report

    Report Number
    2523209-2004-00007
    Event Type
    Other
    Date Received
    December 30, 2005
    Manufacturer
    CUSTOM ULTRASONICS
    Product Code
    FLG
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * FLG CUSTOM ULTRASONICS * *

    Patients

    Seq Age Sex Outcome Treatment
    1