BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

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    OXFORD PH3 CEMENTLESS FEM SZ L

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·December 15, 2017

    OXF UNI CMNTLS TIB SZ F RM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·December 15, 2017

    OXF ANAT BRG RT LG SIZE 5 PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·December 15, 2017

    DXTEND SCREW LOCK D4.5X30MM

    FDA Adverse Event
    Injury ·DEPUY FRANCE S.A.S.-SAINT PRIEST 3003895575·Product code KWS·May 30, 2014

    PROSTAR XL SUTURE-MEDIATED CLOSURE

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·November 20, 2012

    TERUMO CDI 540 CALIBRATOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·September 17, 2010

    VERSYS FEMORAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER, TURPEAUX INDUSTRIAL PARK·Product code JDI·March 31, 2016