BEUDAMED
    FDA Adverse Event Summary report: N

    3003135857-2007-00030

    MDR report key: 881414 · Received June 27, 2007

    Report

    Report Number
    3003135857-2007-00030
    Date Received
    June 27, 2007
    Product Code
    CBK
    Report Source
    Manufacturer report

    Narratives

    Additional Manufacturer Narrative · 1

    DEVICE EVALUATED BY MFR? THE FAILED UNIT HAS NOT BEEN RECEIVED BY NEWPORT MEDICAL INSTRUMENTS INC. YET, AS SOON AS THE UNIT IS RETURNED, IT WILL BE FORWARDED TO MFR/FLIGHT MEDICAL LTD. FOR FURTHER INVESTIGATION, A FAILURE ANALYSIS REPORT AND ACTION TAKEN IN RESOLVING THIS ISSUE WILL BE SUBMITTED TO MEDWATCH PROGRAM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CBK

    Patients

    Seq Age Sex Outcome Treatment
    1