BEUDAMED
    FDA Adverse Event Death Summary report: N

    2530088-1996-00004

    MDR report key: 44786 · Received October 23, 1996

    Report

    Report Number
    2530088-1996-00004
    Event Type
    Death
    Date Received
    October 23, 1996
    Date of Event
    July 19, 1996
    Product Code
    MCV
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 Implant MCV NA NI

    Patients

    Seq Age Sex Outcome Treatment
    1 *