BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CODEMASTER XL+

    MDR report key: 3170349 · Received May 28, 2013

    Report

    Report Number
    1218950-2013-02037
    Event Type
    Malfunction
    Date Received
    May 28, 2013
    Report Date
    May 6, 2013
    Manufacturer
    PHILIPS MEDICAL SYSTEMS
    Product Code
    LDD
    PMA / PMN Number
    K954957
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SP
    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

    CUSTOMER STATES THAT THE BATTERY WILL NOT CHARGE. THERE WAS NO PATIENT INVOLVEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    233085 CODEMASTER XL+ LDD, MKJ, DQA LDD PHILIPS MEDICAL SYSTEMS M1722B

    Patients

    Seq Age Sex Outcome Treatment
    1