BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TRIMLINE

    MDR report key: 3033437 · Received February 22, 2013

    Report

    Report Number
    3033437
    Event Type
    Injury
    Date Received
    February 22, 2013
    Date of Event
    February 14, 2013
    Report Date
    February 22, 2013
    Manufacturer
    WELCH ALLYN
    Product Code
    DXQ
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    CA, US
    Reporter Occupation
    RISK MANAGER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    78535 TRIMLINE BLOOD PRESSURE CUFF DXQ WELCH ALLYN 39048 *

    Patients

    Seq Age Sex Outcome Treatment
    1 51 YR Hospitalization| R