BEUDAMED
    3 results · 23ms · 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 ×

    VIPER MIS SINGLE INNER SETSCW

    FDA Adverse Event
    Injury ·DEPUY SYNTHES SPINE·Product code NKB·June 3, 2014

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·November 26, 2012

    NATURAL KNEE II STEMMED TIBIAL BASEPLATE

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JWH·September 23, 2010