BEUDAMED
    5 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    M2A 38MMX50MM CUP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 13, 2018

    M2A 38MM MOD HD+9MM NK NO SKRT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 13, 2018

    UNICEL DXC 600 PRO SYNCHRON SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code JJE·June 19, 2014

    UNKNOWN DEPUY ASR HIP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code JDI·October 22, 2010

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·December 26, 2012