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

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    Filters FDA Adverse Event ×

    MITEK EXPRESSEW II NEEDLE

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code LXH·June 6, 2014

    HS III PROXIMAL SEAL SYSTEM 3.8MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·November 29, 2012

    TUBE, GASTROINTESTINAL (AND ACCESS)

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD)·Product code KNT·September 7, 2010