BEUDAMED
    6 results · 29ms · Sources: EU EUDAMED, US FDA

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    aprevo® anterior lumbar interbody fusion device with interfixation

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Patient Monitoring Cables

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    KINETIS Total Knee System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·November 11, 2014

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·July 27, 2011

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 23, 2013