BEUDAMED
    FDA Adverse Event Other Summary report: N

    1310 EDITRCE 2/PK 20/CA

    MDR report key: 602928 · Received May 12, 2005

    Report

    Report Number
    9681860-2005-00006
    Event Type
    Other
    Date Received
    May 12, 2005
    Report Date
    May 9, 2005
    Manufacturer
    TYCO HEALTHCARE
    Product Code
    LDD
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    EMERGENCY MEDICAL TECHNICIAN

    Narratives

    Description of Event or Problem · 1

    A CUSTOMER HAD A PROBLEM WITH A DEFIBRILLATION PAD. ACCORDING TO THE CUSTOMER EMTS APPLIED THE ELECTRODES AND WHEN THE POWER WAS APPLIED, THE MONITOR READ "APPLY ELECTRODES". THE EMTS PUT ON ANOTHER SET WITH GOOD RESULTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 1310 EDITRCE 2/PK 20/CA DEFIBRILLATION ROAD LDD TYCO HEALTHCARE UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN