BEUDAMED
    FDA Adverse Event Other Summary report: N

    RESUSCITAIRE

    MDR report key: 1356390 · Received April 2, 2009

    Report

    Report Number
    2510954-2009-00002
    Event Type
    Other
    Date Received
    April 2, 2009
    Date of Event
    March 2, 2009
    Report Date
    March 2, 2009
    Manufacturer
    DRAEGER MEDICAL SYSTEMS, INC. (PNC)
    Product Code
    FMT
    PMA / PMN Number
    K003335
    Report Source
    Manufacturer report
    Reporter Location
    MU

    Narratives

    Additional Manufacturer Narrative · 1

    WE ARE STILL INVESTIGATING THIS REPORT. A FOLLOW UP REPORT WILL BE SUBMITTED WHEN THE INVESTIGATION IS COMPLETED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT A STAFF NURSE WAS MOVING A DEVICE FROM THE LABOR ROOM TO THE NEONATAL WARD AND INJURED HER LEG WHILE TRANSPORTING THE DEVICE. THERE WAS NO PATIENT INJURY REPORTED. (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RESUSCITAIRE INFANT RADIANT WARMTH FMT DRAEGER MEDICAL SYSTEMS, INC. (PNC) RW82 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA