BEUDAMED
    FDA Adverse Event Other Summary report: N

    VESICA

    MDR report key: 350311 · Received August 30, 2001

    Report

    Report Number
    350311
    Event Type
    Other
    Date Received
    August 30, 2001
    Date of Event
    August 23, 2001
    Report Date
    August 30, 2001
    Manufacturer
    VESICA MICROVASIVE
    Product Code
    FHK
    Report Source
    User Facility report
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    REMOVAL OF EXPOSED AND INFECTED VESICA VAGINAL SLING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    39453 VESICA VAGINAL SLING FHK VESICA MICROVASIVE * *

    Patients

    Seq Age Sex Outcome Treatment
    1 3 YR Other