BEUDAMED
    FDA Adverse Event Other Summary report: N

    2250051-2002-00015

    MDR report key: 378444 · Received February 19, 2002

    Report

    Report Number
    2250051-2002-00015
    Event Type
    Other
    Date Received
    February 19, 2002
    Date of Event
    January 15, 2002
    Product Code
    JTC
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1