BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TOSHIBA MEDICAL SYSTEMS

    MDR report key: 160621 · Received March 31, 1998

    Report

    Report Number
    2020563-1998-00001
    Event Type
    Injury
    Date Received
    March 31, 1998
    Date of Event
    February 9, 1998
    Product Code
    JAK
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOSHIBA MEDICAL SYSTEMS JAK

    Patients

    Seq Age Sex Outcome Treatment
    1