BEUDAMED
    4 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    VERSYS FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER INC·Product code LPH·February 25, 2016

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWP·February 9, 2013

    FOLFUSOR SV 4ML/H

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·January 7, 2011

    CORAIL2 LAT COXA VARA SIZE 9

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS 3003895575·Product code KWA·July 23, 2014