BEUDAMED
    FDA Adverse Event Other Summary report: N

    2250051-2002-00001

    MDR report key: 372691 · Received January 4, 2002

    Report

    Report Number
    2250051-2002-00001
    Event Type
    Other
    Date Received
    January 4, 2002
    Date of Event
    December 5, 2001
    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