BEUDAMED
    FDA Adverse Event Death Summary report: N

    LASER-STAR CATHETER

    MDR report key: 254084 · Received December 10, 1999

    Report

    Report Number
    2020638-1999-00028
    Event Type
    Death
    Date Received
    December 10, 1999
    Date of Event
    November 6, 1999
    Report Date
    November 9, 1999
    Manufacturer
    CORDIS WEBSTER, INC.
    Product Code
    DYG
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    PT DIED FROM POST OPERATION COMPLICATIONS FOLLOWING LEFT VENTRICLE PSEUDOANEURYSM REPAIR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LASER-STAR CATHETER THERAPEUTIC CATHETER DYG CORDIS WEBSTER, INC. UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 * Death