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

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    IMPLANTOLOGY MODULE, MODEL 2175

    FDA 510(k)
    FDA Class 2 ·Dental

    ANKLE ARTHRODESIS NAIL, LEFT 10X150MM

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·July 8, 2010

    BLOOD PRESSURE MONITOR, MODEL KP-7000

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LIAISON 25 TOTAL-D

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    UNKNOWN NEXGEN CR KNEE IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·January 24, 2013

    PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-CLONMEL·Product code NIQ·December 18, 2010

    PRECISE SDS SELF EXPANDING

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code FGE·July 14, 2014