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

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    Filters FDA Adverse Event ×

    ANGIO-SEAL DEVICE UNKNOWN

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code MGB·November 20, 2008

    ATLAS PLUS HF CRT-D

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·September 11, 2011

    PRECISION®

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 23, 2013