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

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    Filters FDA Adverse Event ×

    PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code NIQ·October 17, 2008

    BOOMERANG PEEK FUSION DEVICE

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code MQP·January 14, 2011

    LIFEVEST WCD 3100 SYSTEM

    FDA Adverse Event
    Injury ·ZOLL LIFECOR CORPORATION·Product code MVK·March 26, 2013

    TRILOGY ACETABULAR SHELL WITH OUT HOLES

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code LPH·March 18, 2011

    CLEARSTAR PUMP

    FDA Adverse Event
    Malfunction ·ROSS PRODUCTS DIVISION·Product code LZH·April 15, 2008

    MOSAIC AORTIC BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·HEART VALVES SANTA ANA·Product code LWR·December 17, 2013