BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9617604-2009-00054

    MDR report key: 1345440 · Received March 3, 2009

    Report

    Report Number
    9617604-2009-00054
    Event Type
    Malfunction
    Date Received
    March 3, 2009
    Product Code
    LGZ
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1