BEUDAMED
    3 results · 26ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    NEXGEN MIS STEMMED TIBIAL COMPONENT

    FDA Adverse Event
    Malfunction ·ZIMMER·Product code JWH·May 19, 2014

    TENDRIL ST

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·November 10, 2010

    6F ANGIO-SEAL VASCULAR CLOSURE DEVICE VIP

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, PUERTO RICO, B.V.·Product code MGB·December 28, 2012