BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2242445-2008-00038

    MDR report key: 1226083 · Received October 31, 2008

    Report

    Report Number
    2242445-2008-00038
    Event Type
    Injury
    Date Received
    October 31, 2008
    Product Code
    GBZ
    PMA / PMN Number
    K905229
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    FOLLOW-UP REPORT WILL BE FILED IF ADDITIONAL INFO BECOMES AVAILABLE.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1