BEUDAMED
    12 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    LOTUS EDGE VALVE SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NPT·January 4, 2021

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 26, 2013

    RESTYLANE INJECTABLE GEL

    FDA Adverse Event
    Other ·Q-MED AB·Product code LMH·March 10, 2011

    LIFEPAK 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Death ·PHYSIO-CONTROL, INC.·Product code MKJ·March 27, 2008

    ACIST

    FDA Adverse Event
    Injury ·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·February 10, 2012

    ACIST

    FDA Adverse Event
    Malfunction ·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·April 20, 2007

    ACIST

    FDA Adverse Event
    Injury ·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·February 10, 2012

    UNK - NAIL HEAD ELEMENTS: PFNA BLADE

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HSB·July 14, 2021

    UNK - CONSTRUCTS: PFNA SHORT

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HSB·July 14, 2021

    UNK - CONSTRUCTS: PFNA SHORT

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HSB·July 14, 2021

    UNK - NAIL HEAD ELEMENTS: PFNA BLADE

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HSB·July 14, 2021

    PRECISION SPECTRA ?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·August 25, 2025