BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FR3, REFURB ECG AED - UK ENGLISH

    MDR report key: 2980131 · Received February 21, 2013

    Report

    Report Number
    3030677-2013-00290
    Event Type
    Malfunction
    Date Received
    February 21, 2013
    Report Date
    January 29, 2013
    Manufacturer
    PHILIPS MEDICAL SYSTEMS
    Product Code
    MKJ
    PMA / PMN Number
    K111693
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AS
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). PRODUCT EVAL PENDING. ISSUE IS BEING REPORTED AS ALERT COULD NOT BE CLEARED BY OPERATOR.

    Description of Event or Problem · 1

    IT HAS BEEN REPORTED THAT THE AED DID NOT PASS SELF DIAGNOSTIC CHECK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    76967 FR3, REFURB ECG AED - UK ENGLISH MKJ PHILIPS MEDICAL SYSTEMS 861389

    Patients

    Seq Age Sex Outcome Treatment
    1