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

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    Filters FDA Adverse Event ×

    REGEN/RNGLC+ MULTI 56MM SZ 24

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWZ·March 20, 2018

    ARCOS CON SZ E HI 80MM HA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 20, 2018

    ARCOS 20X190MM SPL TPR DIST HA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·March 20, 2018

    36MM COCR BIOMET FEM HD +6 NK

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·September 7, 2018

    SYMBIQ 3.13 DUAL CHA

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·November 5, 2014

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·September 16, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2013

    BD¿ SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON DE MEXICO·Product code FMF·May 26, 2023