BEUDAMED
    FDA Adverse Event Other Summary report: N

    CODEMASTER XL

    MDR report key: 319077 · Received March 2, 2001

    Report

    Report Number
    1218950-2001-00079
    Event Type
    Other
    Date Received
    March 2, 2001
    Report Date
    January 31, 2001
    Manufacturer
    AGILENT TECHNOLOGIES, INC.
    Product Code
    LDD
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT A NEW DEFIBRILLATOR FAILED. IT INTERMITTENTLY FAILED THE 100J TEST.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    9018 CODEMASTER XL DEFIB/MON/REC LDD AGILENT TECHNOLOGIES, INC. M1722A NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA