BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NA

    MDR report key: 1052227 · Received May 16, 2008

    Report

    Report Number
    2523676-2008-00039
    Event Type
    Injury
    Date Received
    May 16, 2008
    Date of Event
    January 15, 2008
    Report Date
    May 6, 2008
    Manufacturer
    B. BRAUN MEDICAL INC.
    Product Code
    NGT
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    NURSE

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 * Hospitalization| O