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

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    Filters FDA Adverse Event ×

    VIASYS

    FDA Adverse Event
    Malfunction ·CAREFUSION 207, INC·Product code CBK·October 26, 2009

    VIASYS

    FDA Adverse Event
    Other ·CAREFUSION 207, INC·Product code CBK·October 27, 2009

    VIASYS

    FDA Adverse Event
    Other ·CAREFUSION 207, INC.·Product code CBK·October 27, 2009

    SOLETRA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MRU·April 16, 2013

    WECK VISISTAT SKIN STAPLER, DISPOSABLE, 35R

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GDW·March 16, 2011

    MICRO DRIVER RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code MAF·June 18, 2008

    PRISMAFLEX

    FDA Adverse Event
    Injury ·GAMBRO LUNDIA AB·Product code KDI·October 7, 2010