BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 950184 · Received November 29, 2006

    Report

    Report Number
    2250051-2006-00514
    Event Type
    Malfunction
    Date Received
    November 29, 2006
    Manufacturer
    ORTHO-CLINICAL DIAGNOSTICS, INC.
    Product Code
    JTQ
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * JTQ ORTHO-CLINICAL DIAGNOSTICS, INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1