BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CODEMASTER XE

    MDR report key: 3810138 · Received February 4, 2014

    Report

    Report Number
    1218950-2014-00517
    Event Type
    Malfunction
    Date Received
    February 4, 2014
    Report Date
    January 10, 2014
    Manufacturer
    AGILENTTECHNOLOGIES, INC.
    Product Code
    LDD
    PMA / PMN Number
    K954957
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FR
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). A FOLLOW UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE BATTERY TEST FAILED. THERE WAS NO PATIENT INVOLVEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    73481 CODEMASTER XE LDD, MKJ, DQA LDD AGILENTTECHNOLOGIES, INC. M1724A

    Patients

    Seq Age Sex Outcome Treatment
    1