BEUDAMED
    FDA Adverse Event Other Summary report: N

    CODEMASTER XL

    MDR report key: 299837 · Received October 6, 2000

    Report

    Report Number
    1218950-2000-00095
    Event Type
    Other
    Date Received
    October 6, 2000
    Report Date
    August 17, 2000
    Manufacturer
    AGILENT TECHNOLOGIES, INC.
    Product Code
    LDD
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TW
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE DEFIBRILLATOR SHOWED A LOW BATTERY WHEN IT WAS POWERED ON. THE BATTERY WAS FULL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CODEMASTER XL DEFIB/MON/REC LDD AGILENT TECHNOLOGIES, INC. M1722A NA

    Patients

    Seq Age Sex Outcome Treatment
    1 *