BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 1151283 · Received July 1, 2008

    Report

    Report Number
    2250051-2008-00340
    Event Type
    Malfunction
    Date Received
    July 1, 2008
    Manufacturer
    ORTHO-CLINICAL DIAGNOSTICS, INC.
    Product Code
    JTC
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    THE INSTRUMENT HAS BEEN INVESTIGATED. THE FIELD SERVICE ENGINEER (FSE) EVALUATED THE INSTRUMENT AND COULD NOT REPRODUCE THE PROBLEM. THE SCANNER WAS CLEANED AND LUBRICATED. THE INSTRUMENT WAS TESTED WITHOUT FURTHER PROBLEM AND IT WAS RETURNED TO EXPECTED OPERATION.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1