BEUDAMED
    FDA Adverse Event Other Summary report: N

    8043404-2006-00001

    MDR report key: 709937 · Received May 8, 2006

    Report

    Report Number
    8043404-2006-00001
    Event Type
    Other
    Date Received
    May 8, 2006
    Product Code
    HDC
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1