BEUDAMED
    FDA Adverse Event Other Summary report: N

    2250051-2002-00027

    MDR report key: 386018 · Received March 27, 2002

    Report

    Report Number
    2250051-2002-00027
    Event Type
    Other
    Date Received
    March 27, 2002
    Date of Event
    February 27, 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