BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    MG II POROUS TOTAL KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756298032·EYE PACK

    LONG NAIL KIT R2.0, TI, LEFT GAMMA3 ?11X400MM X 13

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·December 4, 2012

    ANTI-WRINKLE (AGING) LIGHT, MODEL AAL

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Streamline TL Spinal Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·June 24, 2014

    PS

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·January 2, 2013

    UNKNOWN PRODUCT - RIGHT HIP

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS CORK·Product code JDO·November 3, 2010