BEUDAMED
    FDA Adverse Event Death Summary report: N

    *

    MDR report key: 172926 · Received May 26, 1998

    Report

    Report Number
    8031563-1998-00001
    Event Type
    Death
    Date Received
    May 26, 1998
    Report Date
    May 26, 1998
    Manufacturer
    JMS CO., LTD.
    Product Code
    GKT
    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 * * GKT JMS CO., LTD. * *

    Patients

    Seq Age Sex Outcome Treatment
    1