BEUDAMED
    FDA Adverse Event Death Summary report: N

    2023988-1996-90001

    MDR report key: 58959 · Received November 19, 1996

    Report

    Report Number
    2023988-1996-90001
    Event Type
    Death
    Date Received
    November 19, 1996
    Date of Event
    October 22, 1996
    Product Code
    HCA
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 Implant HCA

    Patients

    Seq Age Sex Outcome Treatment
    1