BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ACE BL RP IMPLANT 4.8X12MM

    MDR report key: 11736636 · Received April 28, 2021

    Report

    Report Number
    8010516-2021-00017
    Event Type
    Injury
    Date Received
    April 28, 2021
    Date of Event
    October 14, 2020
    Report Date
    April 27, 2021
    Manufacturer
    HAGER & MEISINGER GMBH
    Product Code
    DZE
    UDI-DI
    E0HM220071
    PMA / PMN Number
    K143539
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    DENTIST

    Narratives

    Additional Manufacturer Narrative · 1

    THE INVESTIGATION OF THE COMPLAINT WAS CARRIED OUT CONSIDERING THE ANALYSIS OF THE INFORMATION GIVEN BY THE DENTIST IN THE GUARANTEE FORM, VISUAL CONFERENCE OF THE PRODUCT RETURNED BY THE DENTIST AND THE EVALUATION OF RELEVANT PRODUCTION RECORDS.

    Description of Event or Problem · 1

    SURGEON NEEDED A LONGER IMPLANT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    633176 ACE BL RP IMPLANT 4.8X12MM DENTAL IMPLANT DZE HAGER & MEISINGER GMBH 3622007DU0ACE B44820 E0HM220071

    Patients

    Seq Age Sex Outcome Treatment
    1 62 YR Other