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

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    Filters FDA Adverse Event ×

    K-WIRE, RECON 3.2X400 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·June 29, 2011

    SYNERGY

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·October 22, 2010

    FORFIFY DR, DF-4 CONNECTOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL INC., CRMD·Product code LWS·January 13, 2014

    PROTECTA CRT-D

    FDA Adverse Event
    Death ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·December 29, 2012