BEUDAMED
    FDA Adverse Event Other Summary report: N

    MICROLOK

    MDR report key: 509203 · Received January 14, 2004

    Report

    Report Number
    1045056-2001-00013
    Event Type
    Other
    Date Received
    January 14, 2004
    Date of Event
    January 22, 2000
    Report Date
    November 19, 2003
    Manufacturer
    BIO-LOK INTL., INC.
    Product Code
    DZE
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SP
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    IMPLANT "LOSS OSSEOINTEGRATION."

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MICROLOK ENDOSSEOUS DZE BIO-LOK INTL., INC. IHPSS310D 2875A

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other