BEUDAMED
    3 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    MOSAIC AORTIC BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES, INC.·Product code LWR·July 8, 2011

    PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·June 14, 2013

    3M ELECTROSURGICAL PATIENT PLATE, STANDARD, NON CORDED

    FDA Adverse Event
    Injury ·3M HEALTHCARE, 3M CO.·Product code ODR·September 18, 2008