BEUDAMED
    FDA Adverse Event Injury Summary report: N

    IMTEC

    MDR report key: 1152089 · Received September 8, 2008

    Report

    Report Number
    MW5008235
    Event Type
    Injury
    Date Received
    September 8, 2008
    Date of Event
    June 16, 2007
    Report Date
    August 29, 2008
    Manufacturer
    IMTEC
    Product Code
    DZE
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    DENTIST

    Narratives

    Description of Event or Problem · 1

    ILL-FITTING PROSTHESIS OVER MINI-IMPLANTS AND NEED TO REMOVE ALL 9 IMTEC MINI-IMPLANTS. ALL 9 MINI-IMPLANTS REMOVED IN '08.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 IMTEC MINI-IMPLANT DZE IMTEC

    Patients

    Seq Age Sex Outcome Treatment
    1