BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    INTROCAN SAFETY®

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code FOZ·December 13, 2018

    INTROCAN SAFETY®

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code FOZ·August 14, 2018

    INTROCAN SAFETY

    FDA Adverse Event
    Injury ·B. BRAUN MELSUNGEN AG·Product code FOZ·July 23, 2013

    INTROCAN SAFETY

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code FOZ·February 20, 2013

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR - CARDIAC THERAPIES·Product code NIQ·December 2, 2008

    ALARIS SYRINGE MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP.·Product code FRN·August 31, 2011

    LYNX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·July 29, 2013

    INTROCAN SAFETY®

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code FOZ·December 23, 2025