BEUDAMED
    FDA Adverse Event Other Summary report: N

    2250051-2003-00074

    MDR report key: 450338 · Received March 21, 2003

    Report

    Report Number
    2250051-2003-00074
    Event Type
    Other
    Date Received
    March 21, 2003
    Date of Event
    November 6, 2002
    Product Code
    JTL
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1