BEUDAMED
    FDA Adverse Event Death Summary report: N

    1121732-1997-00012

    MDR report key: 97413 · Received June 13, 1997

    Report

    Report Number
    1121732-1997-00012
    Event Type
    Death
    Date Received
    June 13, 1997
    Date of Event
    May 14, 1997
    Product Code
    FMT
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1