BEUDAMED
    FDA Adverse Event Other Summary report: N

    IMPLANTIUM

    MDR report key: 1002905 · Received February 22, 2008

    Report

    Report Number
    3004578807-2008-00030
    Event Type
    Other
    Date Received
    February 22, 2008
    Date of Event
    September 22, 2006
    Report Date
    October 12, 2007
    Manufacturer
    DENTIUM CO., LTD.
    Product Code
    DZE
    PMA / PMN Number
    K041368
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

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

    Description of Event or Problem · 1

    THE IMPLANT FAILED DUE TO PATIENT HEALTH HABIT AND POOR ORAL HYGIENE. FIXTURE WAS PLACED AT #27 AND REMOVED AFTER 2 MONTHS. BONE GRAFT MATERIAL WAS USED. PROSTHETICS ATTACHMENT (BRIDGE). POOR ORAL HYGIENE. POOR BONE CONDITION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 IMPLANTIUM ENDOSSEOUS DENTAL IMPLANT DZE DENTIUM CO., LTD. MF4808W 05J24-L

    Patients

    Seq Age Sex Outcome Treatment
    1 65 YR Required Intervention