BEUDAMED
    FDA Adverse Event Death Summary report: N

    ANCURE

    MDR report key: 831773 · Received February 21, 2007

    Report

    Report Number
    2954310-2007-81456
    Event Type
    Death
    Date Received
    February 21, 2007
    Date of Event
    March 12, 2003
    Report Date
    February 20, 2007
    Manufacturer
    GUIDANT ENDOVASCULAR SOLUTIONS
    Product Code
    MIH
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    THIS REPORT SERVES AS SUMMARY REPORTING OF EIGHT (8) DEATH EVENTS. THE NOTIFICATION OF THESE EVENTS WAS PROVIDED BETWEEN 1/22/2007 AND 2/2/2007 BY THE LAW FIRM AS A RESULT OF CLAIMS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ANCURE ENDOGRAFT MIH GUIDANT ENDOVASCULAR SOLUTIONS 13290 *

    Patients

    Seq Age Sex Outcome Treatment
    1 *