BEUDAMED
    3 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    MITEK RIGIDFIX FEMORAL ROD 8MM ST

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code FZX·June 10, 2014

    HEARTSTART SLA BATTERY

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code DQA·November 2, 2012

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·June 23, 2015