BEUDAMED
    9 results · 33ms · Sources: EU EUDAMED, US FDA

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    MERIDIAN AG

    FDA registration
    MERIDIAN AG·1 product·🇨🇭 Switzerland

    UNKNOWN_COCR FEMORAL HEAD

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·July 20, 2020

    UNKNOWN_STRYKER STEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·July 20, 2020

    LENSX LASER SYSTEM

    FDA Adverse Event
    Injury ·ALCON - LENSX LASERS, INC.·Product code OOE·November 29, 2012

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DTK·November 3, 2014

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DTK·November 3, 2014

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Malfunction ·CORDIS CORPORATION·Product code DTK·November 3, 2014

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DTK·November 3, 2014

    MERIDIAN STRESS ASSESSMENT MACHINE

    FDA Adverse Event
    NA·Product code LLZ·December 6, 2013