BEUDAMED
    FDA Adverse Event Death Summary report: N

    8031563-1997-00001

    MDR report key: 136350 · Received December 2, 1997

    Report

    Report Number
    8031563-1997-00001
    Event Type
    Death
    Date Received
    December 2, 1997
    Date of Event
    November 18, 1997
    Product Code
    FIE
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1