BEUDAMED
    7 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    GMK-SPHERE TIBIAL INSERT FIXED FLEX SIZE 4/10 MM LEFT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·December 9, 2016

    GMK-SPHERE TIBIAL INSERT FIXED FLEX #4/10 MM L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·December 15, 2017

    GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 4/10 MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·May 22, 2019

    MAXISKY 600

    FDA Adverse Event
    Injury ·ARJOHUNTLEIGH MAGOG INC·Product code FSA·May 10, 2013

    PINN MAR +4 NEUT 40IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·July 7, 2011

    SWAN-GANZ CONTINUOUS CARDIAC OUTPUT CATHETER

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCINECES·Product code DYG·September 5, 2008

    ADVIA CENTAUR XP VB12 ASSAY

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code CDD·May 11, 2018