BEUDAMED
    FDA Adverse Event Other Summary report: N

    OHMEDA MEDICAL GIRAFFE OMNIBED

    MDR report key: 470608 · Received July 2, 2003

    Report

    Report Number
    1121732-2003-00003
    Event Type
    Other
    Date Received
    July 2, 2003
    Date of Event
    June 3, 2003
    Report Date
    June 5, 2003
    Manufacturer
    OHMEDA MEDICAL
    Product Code
    FMZ
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Location
    MS, US
    Reporter Occupation
    BIOMEDICAL ENGINEER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT IN 2003 A PT FELL FROM THE PORTHOLE OF THE OMNIBED. THERE WAS A PULSE OXIMETER PROBE ATTACHED TO THE PT'S FOOT THAT PREVENTED THE PT FROM FALLING TO THE FLOOR. NO INJURY WAS SUSTAINED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OHMEDA MEDICAL GIRAFFE OMNIBED INFANT INCUBATOR FMZ OHMEDA MEDICAL NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 6 DAY Other PULSE OXIMETER (BRAND UNKNOWN.)