BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    Loss of Pulse Detection

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AxTiHA Stand-Alone ALIF System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    A&D MEDICAL LIFESOURCE DIGITAL BLOOD PRESSURE MONITORS, MODELS UB-511 & UB-512

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·January 27, 2020

    SYNCHROMED EL

    FDA Adverse Event
    Injury ·RICE CREEK MANUFACTURING·Product code LKK·November 21, 2008

    ATLAS PLUS DR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 11, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 23, 2013