BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 490111 · Received October 15, 2003

    Report

    Report Number
    9611894-2003-00003
    Event Type
    Other
    Date Received
    October 15, 2003
    Date of Event
    September 8, 2003
    Manufacturer
    NUCLETRON B.V.
    Product Code
    JAQ
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * JAQ NUCLETRON B.V. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *