BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ACE BL RP IMPLANT 4.8X10MM

    MDR report key: 11736611 · Received April 28, 2021

    Report

    Report Number
    8010516-2021-00013
    Event Type
    Injury
    Date Received
    April 28, 2021
    Date of Event
    August 10, 2020
    Report Date
    April 26, 2021
    Manufacturer
    HAGER & MEISINGER GMBH
    Product Code
    DZE
    UDI-DI
    E0HM220061
    PMA / PMN Number
    K170287
    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

    EXPLANTATION OF IMPLANT DUE TO MISSING OSSEOINTEGRATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    638083 ACE BL RP IMPLANT 4.8X10MM DENTAL IMPLANT DZE HAGER & MEISINGER GMBH 3622006DU0ACE B59092 E0HM220061

    Patients

    Seq Age Sex Outcome Treatment
    1 82 YR Other