BEUDAMED
    FDA Adverse Event Injury Summary report: N

    *

    MDR report key: 1080769 · Received July 11, 2008

    Report

    Report Number
    2523676-2008-00063
    Event Type
    Injury
    Date Received
    July 11, 2008
    Manufacturer
    B. BRAUN MEDICAL, INC.
    Product Code
    NGT
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * NORMAL SALINE IV FLUSH, 10 ML NGT B. BRAUN MEDICAL, INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 Other