BEUDAMED
    6 results · 32ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ARTICULEZE M HEAD 36MM +5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD 8010379·Product code JDI·January 5, 2015

    PINNACLE MTL INS NEUT36IDX54OD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD 8010379·Product code JDI·January 5, 2015

    UNKNOWN DEPUY STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·February 19, 2015

    THUNDERBEAT 5MM 10CM INLINE GRIP

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code GEI·January 20, 2014

    STRATUS® CS STAT FLUOROMETRIC ANALYZER

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC - BROOKFIELD·Product code JHX·November 7, 2012

    PRESEP - CENTRAL VENOUS OXIMETRY CATHETER KIT

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES, PR·Product code DQE·September 1, 2010