BEUDAMED
    6 results · 18ms · Sources: EU EUDAMED, US FDA

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    NATURAL-KNEE ALL-POLY TIBIA

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PRECISE SHP DIODE LASER

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MEDS-3 NEUROMUSCULAR STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    UNICEL® DXH 800 COULTER® CELLULAR ANALYSIS SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code GKZ·December 13, 2010

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·January 22, 2013

    QUICKFLEX MICRO LV LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code OJX·July 9, 2014