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

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    Filters FDA Adverse Event ×

    PHILOS II DR

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO.·Product code DXY·September 1, 2006

    SELOX SR 45

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO.·Product code DTB·September 1, 2006

    LIFESTENT FLEXSTAR XL BILIARY STENT

    FDA Adverse Event
    Injury ·ANGIOMED GMBH & CO.·Product code FGE·November 21, 2008

    LIFESTENT FLEXSTAR XL BILIARY STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO.·Product code FGE·November 5, 2008

    LIFESTENT FLEXSTAR XL BILIARY STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK·Product code FGE·February 20, 2009

    LIFESTENT FLEXSTAR XL BILIARY STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO.·Product code FGE·November 4, 2008

    LIFESTENT FLEXSTAR XL BILIARY STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO, MEDIZINTECHNIK·Product code FGE·February 13, 2009

    JUVEDERM ULTRA PLUS XC TSK ROW

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LMH·April 11, 2013

    OSCILLATING SAW BLADE

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS·Product code DWH·May 19, 2008

    GYNECARE MORCELLEX* TISSUE MORCELLATOR

    FDA Adverse Event
    Malfunction ·ETHICON·Product code HET·April 15, 2011

    EVOLUT FX VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code NPT·July 9, 2025