BEUDAMED
    9 results · 41ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·July 6, 2017

    GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·COOK INC·Product code DTK·July 6, 2017

    SERVO-I

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·May 13, 2014

    REPLACEMENT HEART VALVE

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES·Product code DYE·December 1, 2010

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    LAND AMERICA HEALTH & FITNESS·Product code FSA·January 11, 2013

    UNKNOWN

    FDA Adverse Event
    Malfunction ·WILLIAM COOK EUROPE·Product code DTK·October 23, 2017

    UNKNOWN

    FDA Adverse Event
    Malfunction ·WILLIAM COOK EUROPE·Product code DTK·October 23, 2017

    INJECTOR N35-O

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FPA·January 7, 2021

    GUNTHER TULIP NAVALIGN FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code DTK·October 20, 2017