BEUDAMED
    FDA Adverse Event Death Summary report: N

    ATLAS + HF CRT-D

    MDR report key: 1010582 · Received March 10, 2008

    Report

    Report Number
    2017865-2008-01223
    Event Type
    Death
    Date Received
    March 10, 2008
    Date of Event
    March 2, 2006
    Report Date
    June 21, 2006
    Manufacturer
    ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION
    Product Code
    NIK
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ATLAS + HF CRT-D IMPLANTABLE CARDIOVERTER DEFIBRILLATOR NIK ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION V-343 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 * Death