BEUDAMED
    FDA Adverse Event Injury Summary report: N

    OCKAGON DENTEL IMPLANT

    MDR report key: 17011215 · Received May 26, 2023

    Report

    Report Number
    1287163-2023-54089
    Event Type
    Injury
    Date Received
    May 26, 2023
    Date of Event
    December 28, 2022
    Report Date
    May 26, 2023
    Manufacturer
    HAGER & MEISINGER GMBH
    Product Code
    DZE
    UDI-DI
    EDRS311511
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    SP
    Reporter Occupation
    DENTIST
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    NO INTEGRATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1437031 OCKAGON DENTEL IMPLANT DENTAL IMPLANT DZE HAGER & MEISINGER GMBH 31151 B62068 EDRS311511

    Patients

    Seq Age Sex Outcome Treatment
    1 29 YR Female Required Intervention