BEUDAMED
    6 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    DEVILBISS

    FDA Adverse Event
    Injury ·SUNRISE MEDICAL HHG, INC.·Product code CAF·November 8, 2001

    TITANIUM NEXGEN LCCL FEMORAL SZ C-LT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 21, 2018

    PINNACLE MTL INS NEUT36IDX54OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·February 20, 2013

    COOL PATH DUO 7F, 1304-CP2-7-1.5 (5)- L1-TE4BE1AB

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, IRVINE·Product code OAD·January 14, 2011

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·July 31, 2014

    NEXGEN LEGACY POSTERIOR STABILIZED ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·June 16, 2016