BEUDAMED
    FDA Adverse Event Other Summary report: N

    KENDALL VISTEC REF# 7317

    MDR report key: 528398 · Received August 5, 2003

    Report

    Report Number
    528398
    Event Type
    Other
    Date Received
    August 5, 2003
    Date of Event
    June 16, 2003
    Report Date
    August 5, 2003
    Manufacturer
    KENDALL, TYCO HEALTHCARE GROUP
    Product Code
    GDY
    Report Source
    User Facility report
    Reporter Location
    IA, US
    Reporter Occupation
    RISK MANAGER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KENDALL VISTEC REF# 7317 X-RAY DETECTABLE SPONGE GDY KENDALL, TYCO HEALTHCARE GROUP 7317 30718852

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other