BEUDAMED
    4 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    FORTIFY DR, DF4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·February 28, 2013

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVZ·February 1, 2011

    REOCOR D

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code OVJ·August 6, 2014

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·April 14, 2015