BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 2772366 · Received August 27, 2012

    Report

    Report Number
    2772366
    Event Type
    Malfunction
    Date Received
    August 27, 2012
    Date of Event
    April 3, 2012
    Report Date
    August 27, 2012
    Manufacturer
    B.BRAUN MEDICAL
    Product Code
    BXN
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MI, US

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * CONTINUOUS NERVE BLOCK SET BXN B.BRAUN MEDICAL * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *