BEUDAMED
    7 results · 24ms · Sources: EU EUDAMED, US FDA

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    DIRECT BONDED BRACKET REMOVER

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

    Define RF Microneedling System

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

    NEOGEN ONE, CLOSED WOUND DRAIN SYSTEM, PART NUMBER: NG9900

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

    FREESTYLE FLASH

    FDA Adverse Event
    Injury ·Product code NBW·February 23, 2010

    2954354-2014-00001

    FDA Adverse Event
    CUTERA, INC.·Product code GEX·January 14, 2014

    PINNACLE MTL INS NEUT36IDX50OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·November 14, 2012

    SUNDT EXTERNAL SHUNT 3MM X 4MM

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCIENCES PR, INC.·Product code JXG·September 3, 2010