BEUDAMED
    7 results · 25ms · Sources: EU EUDAMED, US FDA

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    MODELS DM-360 & DM-350-L SINGLE PATIENT

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ROSA ONE Spine application

    FDA 510(k)
    FDA Class 2 ·Neurology

    STETHOSCOPE, ELECTRONIC

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 8, 2014

    HT70 VENTILATOR

    FDA Adverse Event
    Injury ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·October 11, 2012

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code MDS·August 10, 2010

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·August 15, 2023