BEUDAMED
    4 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    QUALICHECK, LEVEL 1

    FDA Adverse Event
    Malfunction ·RADIOMETER MEDICAL APS·Product code GIO·April 5, 2013

    S-ROM*SLEEVE PRX ZTT, 18D-LRG

    FDA Adverse Event
    Injury ·DEPUY IRELAND·Product code MRA·January 17, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010

    VERITY DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWP·July 8, 2014