BEUDAMED
    11 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    DANEK PLATE AND SCREW

    FDA Adverse Event
    Injury ·SOFAMOR DANEK MANUFACTURING·Product code HRS·May 19, 1999

    95 DEGREE DCS PLATE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·October 7, 1999

    INFLATABLE PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS·Product code FAE·July 22, 1993

    DUAL CHAMBER PACEMAKER

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS, INC. CPI·Product code LWP·February 4, 1994

    UNKNOWN

    FDA Adverse Event
    Injury ·UNKNOWN·Product code FAG·August 31, 1993

    BROVIAK 2.7 FRENCH SINGLE LUMEN CATHETER

    FDA Adverse Event
    Malfunction ·BARD ACCESS·Product code FEF·August 11, 1993

    GENERATOR

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·December 4, 2008

    1020279-2011-00367

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC·Product code JDH·September 16, 2011

    APEX HOLE ELIM POSITIVE STOP

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 29, 2013

    RED BLOOD CELL UNITS

    FDA Adverse Event
    Death ·SAN DIEGO BLOOD BANK·July 29, 1994

    NA

    FDA Adverse Event
    Injury ·BIRD CORPORATION - 3M·Product code BZE·March 15, 1993