BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Injury ·RICE CREEK MFG·Product code DXY·February 9, 2013

    REGENEREX TIBIAL COMPONENTS

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MBH·June 29, 2017

    VANGUARD COMPLETE KNEE SYSTEM - CR POR FEM-RT 60

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·June 29, 2017

    REGENEREX TIBIAL COMPONENTS

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MBH·June 29, 2017

    EXPEDIUM PRE-CUT HEX END ROD, 5.5X480MM, TI

    FDA Adverse Event
    Injury ·DEPUY SYNTHES SPINE·Product code NKB·January 11, 2013

    TYPE 7B

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·November 24, 2010

    CURRENT DR RF

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·July 2, 2014

    REGENEREX PATELLA COMPONENTS

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code MBH·May 10, 2017