BEUDAMED
    FDA Adverse Event Other Summary report: N

    REDSENSE ALARM

    MDR report key: 1908974 · Received November 22, 2010

    Report

    Report Number
    MW5018309
    Event Type
    Other
    Date Received
    November 22, 2010
    Date of Event
    November 19, 2010
    Report Date
    November 22, 2010
    Manufacturer
    REDSENSE MED INC
    Product Code
    ODX
    Report Source
    Voluntary report
    Reporter Location
    DE, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    REDSENSE ALARM FAILED TO ALARM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 REDSENSE ALARM NONE ODX REDSENSE MED INC M0100308AA

    Patients

    Seq Age Sex Outcome Treatment
    1