BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 1173964 · Received July 14, 2008

    Report

    Report Number
    2250051-2008-00318
    Event Type
    Malfunction
    Date Received
    July 14, 2008
    Manufacturer
    ORTHO-CLINICAL DIAGNOSTICS, INC.
    Product Code
    JTC
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    CUSTOMER DID NOT REQUEST ANY SVC. NO FURTHER INVESTIGATION REQUIRED AT THIS TIME. NO SVC ACTIVITY PERFORMED. EVENT COULD NOT BE INVESTIGATED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1