BEUDAMED
    6 results · 36ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    MIRA-I CS RETRACTOR SYSTEM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·April 15, 2014

    ULTIMATE-C HIP 120MM SIZE 2

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·October 15, 2010

    EDWARDS SAPIEN TRANSCATHETER HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·December 13, 2012

    THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP TYPE S

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code GEI·January 28, 2020

    M2A-MAGNUM PF CUP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·May 5, 2020

    M2A-MAGNUM MODULAR HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·May 4, 2020