BEUDAMED
    FDA Adverse Event Other Summary report: N

    MICROLOK IMPLANT

    MDR report key: 509170 · Received January 14, 2004

    Report

    Report Number
    1045056-2002-00017
    Event Type
    Other
    Date Received
    January 14, 2004
    Date of Event
    September 20, 2002
    Report Date
    November 19, 2003
    Manufacturer
    BIO-LOK INTL., INC.
    Product Code
    DZE
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    "LOST BONE MOBILE."

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MICROLOK IMPLANT ENDOSSEOUS DZE BIO-LOK INTL., INC. IHTSS410D 3265A-RS

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other