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

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    Filters FDA Adverse Event ×

    M2A-MAGNUM 42-50M TPR INSRT +3

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·November 13, 2012

    M2A-MAGNUM MOD HD SZ 50MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·November 13, 2012

    MAGNUM TRISPIKE CUP 56ODX50ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·November 13, 2012

    PROMUS ELEMENT¿ PLUS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·March 13, 2013

    5F DBL LMN VASC-PICC/FULL NURSING

    FDA Adverse Event
    Malfunction ·MEDCOMP·Product code LJS·January 28, 2011

    TERUMO ADVANCED PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·July 9, 2014

    M2A 38MM MOD HD +3MM NK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·November 13, 2012

    M2A 38MM MOD HD STD NK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·November 13, 2012