BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SGW STAB XS .014 300CM J SS

    MDR report key: 223286 · Received May 15, 1999

    Report

    Report Number
    1016427-1999-00065
    Event Type
    Injury
    Date Received
    May 15, 1999
    Date of Event
    March 30, 1999
    Report Date
    May 14, 1999
    Manufacturer
    CORDIS CORP.
    Product Code
    DQX
    Report Source
    Manufacturer report
    Reporter Location
    WI, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE GUIDEWIRE WAS CAUGHT BETWEEN THE TWO IMPLANTED STENTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SGW STAB XS .014 300CM J SS CARDIOLOGY WIRES & METALS DQX CORDIS CORP. NA A0998382

    Patients

    Seq Age Sex Outcome Treatment
    1