BEUDAMED
    6 results · 28ms · Sources: EU EUDAMED, US FDA

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    PROFIX POSTERIOR-STABILIZED KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    I/A VITROPHAGE MODEL YPR 2001

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    PEDIATRIC PERCUTANEOUS NEPHROSTOMY SETS

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    CARDIA VR

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code LWS·February 11, 2013

    DURATA STS OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011

    NEXGEN LOCK ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·July 16, 2014