BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BATTERY 14.8V, 6.3 AH LI-ION BATTERY

    MDR report key: 4915803 · Received July 15, 2015

    Report

    Report Number
    1218950-2015-03799
    Event Type
    Malfunction
    Date Received
    July 15, 2015
    Report Date
    June 22, 2015
    Manufacturer
    PHILIPS MEDICAL SYSTEMS
    Product Code
    MKJ
    PMA / PMN Number
    K031187
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    BR
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ORIGINAL SERIAL NUMBER INITIALLY REPORTED WAS FOR THE DEVICE.

    Additional Manufacturer Narrative · 1

    A FOLLOW UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THE DEVICE IS NOT CONNECTING TO THE ELECTRICAL NETWORK. THERE WAS NO REPORT OF PATIENT INVOLVEMENT.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THE DEVICE IS NOT CONNECTING TO THE ELECTRICAL NETWORK. THERE WAS NO REPORT OF PATIENT INVOLVEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    460133 BATTERY 14.8V, 6.3 AH LI-ION BATTERY DEFIBRILLATOR MKJ PHILIPS MEDICAL SYSTEMS M3538A

    Patients

    Seq Age Sex Outcome Treatment
    1