BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNKNOWN DURASEAL PRODUCT

    MDR report key: 2945764 · Received February 1, 2013

    Report

    Report Number
    1219930-2013-00047
    Event Type
    Injury
    Date Received
    February 1, 2013
    Report Date
    January 9, 2013
    Manufacturer
    COVIDIEN, FORMERLY US SURGICAL
    Product Code
    NQR
    PMA / PMN Number
    P040034
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    PATIENT

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4).

    Description of Event or Problem · 1

    PROCEDURE: ACCORDING TO THE REPORTER: PT COMPLAINED OF URINATING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    44623 UNKNOWN DURASEAL PRODUCT DURASEAL NQR COVIDIEN, FORMERLY US SURGICAL

    Patients

    Seq Age Sex Outcome Treatment
    1 Other