BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SEG

    MDR report key: 22394330 · Received July 3, 2025

    Report

    Report Number
    3004082462-2024-72001
    Event Type
    Malfunction
    Date Received
    July 3, 2025
    Manufacturer
    ZIMMER
    Product Code
    DZE
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 0

    ESG NEXTGEN, TO SEE IF THE XML FROM ESUBMITTER CONTAINS KG EVEN THOUGH I DIDN'T SELECT IT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1530221 SEG MPLANT, ENDOSSEOUS, ROOT-FORM DZE ZIMMER

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Female