BEUDAMED
    6 results · 17ms · Sources: EU EUDAMED, US FDA

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    OHMEDA BIOX 3700 PULSE OXIMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Proteus Digital Health Feedback Device

    FDA 510(k)
    FDA Class 2 ·General Hospital

    The OsteoCentric Bone Plate and Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NATURALYTE

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE·Product code KPO·May 20, 2014

    SPRINT FIDELIS

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 1, 2010

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 27, 2012