BEUDAMED
    FDA Adverse Event Other Summary report: N

    IMPLANTIUM

    MDR report key: 1003102 · Received February 22, 2008

    Report

    Report Number
    3004578807-2008-00061
    Event Type
    Other
    Date Received
    February 22, 2008
    Date of Event
    September 21, 2007
    Report Date
    December 6, 2007
    Manufacturer
    DENTIUM CO., LTD.
    Product Code
    DZE
    PMA / PMN Number
    K041368
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    DENTIST

    Narratives

    Additional Manufacturer Narrative · 1

    ACCORDING TO OUR INVESTIGATION, THERE WAS NO DISCREPANCY ON OUR PRODUCT.

    Description of Event or Problem · 1

    THE IMPLANT FAILED DUE TO BONE CONDITION. THE IMPLANT WAS PLACED AT #36 AND REMOVED AFTER 1 MONTH. TRADITIONAL 2 STAGE SURGERY, BONE GRAFT MATERIAL WAS USED, MODERATE ORAL HYGIENE, MODERATE BONE CONDITION, PT HAVE A BRUXISM HABIT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 IMPLANTIUM ENDOSSEOUS DENTAL IMPLANT DZE DENTIUM CO., LTD. MF4808W 05K03-O

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention BONE GRAFT MATERIALS