BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 1262364 · Received November 12, 2008

    Report

    Report Number
    1221261-2008-00037
    Event Type
    Malfunction
    Date Received
    November 12, 2008
    Manufacturer
    MRI MEDICAL INC.
    Product Code
    KOD
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Narratives

    Additional Manufacturer Narrative · 1

    EVAL - OTHER: SMITHS MEDICAL IS ANTICIPATING THE RECEIPT OF THE SUPPLIER INVESTIGATION OF THE EVENT SAMPLE. UPON RECEIPT OF THE REPORT, A F/U REPORT WILL BE SUBMITTED. A REVIEW OF OUR COMPLAINTS DATABASE REVEALS NO OTHER REPORTS ON THIS DEVICE LOT NUMBER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * KOD MRI MEDICAL INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1