BEUDAMED
    3 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    COREVALVE 29MM AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·May 20, 2014

    ASR XL TAP SLV ADAP 11/13+0

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·November 6, 2012

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·August 25, 2010