BEUDAMED
    FDA Adverse Event Death Summary report: N

    MULTI-LINK MINI VISION RX CORONARY STENT SYSTEM

    MDR report key: 696785 · Received April 5, 2006

    Report

    Report Number
    2024168-2006-00243
    Event Type
    Death
    Date Received
    April 5, 2006
    Date of Event
    April 20, 2005
    Report Date
    February 24, 2006
    Manufacturer
    GUIDANT VASCULAR INTERVENTION
    Product Code
    MAF
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    A PT DEATH IN 2005, DUE TO A MYOCARDIAL INFARCTION (MI). REPORTEDLY, HTE DEATH WAS PROBABLY DEVICE RELATED; HOWEVER, THIS IS BEING CONSERVATIVELY FILED. NO ADDITIONAL INFO WAS AVAILABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MULTI-LINK MINI VISION RX CORONARY STENT SYSTEM CORONARY STENT SYSTEM MAF GUIDANT VASCULAR INTERVENTION NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 47 YR Death