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

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    DYNAREX GAUZE SPONGE

    FDA 510(k)
    FDA Unclassified ·Unknown

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123168·K-WIRE - SINGLE TROCAR THREADED 1.6mm DIA x 150mm

    MultiFIX S Knotless Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DENTRONIX DDS 7000 RAPID DRY HEAT STERILIZER STERILIZATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    VANGUARD PS TIBIAL BEARING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HRY·December 28, 2017

    VANGUARD SERIES-STANDARD PATELLA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HRY·December 28, 2017

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·RICE CREEK MFG·Product code DXY·February 9, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·January 6, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2014

    BIOMET MODULAR FINNED STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·December 28, 2017