BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NA

    MDR report key: 1850143 · Received September 21, 2010

    Report

    Report Number
    1218950-2010-01655
    Event Type
    Malfunction
    Date Received
    September 21, 2010
    Report Date
    August 23, 2010
    Manufacturer
    AGILENT TECHNOLOGIES, INC.
    Product Code
    MKJ
    PMA / PMN Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SP
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). THE CUSTOMER REPORTED THAT THE UNIT UNEXPECTEDLY SHUTDOWN ON BATTERY POWER. THE UNIT WAS REPAIRED LOCALLY BY REPLACING THE BATTERY. THE UNIT PASSED ALL POST-SERVICING TESTING AND IS BACK AT THE CUSTOMER SITE.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE UNIT UNEXPECTEDLY SHUTDOWN ON BATTERY POWER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NA NA MKJ AGILENT TECHNOLOGIES, INC. M3516A

    Patients

    Seq Age Sex Outcome Treatment
    1