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

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    ULTRA-LINE RONGEUR

    FDA 510(k)
    FDA Class 2 ·Neurology

    aprevo® anterior lumbar interbody fusion device with interfixation

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    KINETIS Total Knee System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ENDOVIVE TWO-PORT TTP JEJUNAL FEEDING TUBE CAP

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code KNT·February 5, 2013

    SYNCHROMED

    FDA Adverse Event
    Other ·MEDTRONIC NEUROMODULATION·Product code LKK·December 14, 2010

    OSSEOTITE® CERTAIN® 2 IMPLANT 5 X 11.5MM

    FDA Adverse Event
    Injury ·BIOMET 3I·Product code DZE·July 18, 2014