BEUDAMED
    12 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Klassic BiPolar System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526550179·GENUMEDI PT KNEE SUP SILVER R EW III

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221038180·Unitek(TM) Bicuspid Band General Purpose Narrow...

    TEMPFIX EXTERNAL FIXATION SYSTEM, MR SAFE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VASCULAIRE COMPRESSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PELVICOL 4 X 12 CM

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY TISSUE·Product code FTL·May 24, 2013

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL ¿ NEUROMODULATION·Product code GZB·September 23, 2014

    WALLFLEX¿ BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code FGE·June 28, 2011

    MICROVASCULAR PLUG

    FDA Adverse Event
    Injury ·REVERSE MEDICAL·Product code KRD·September 8, 2021

    MICROVASCULAR PLUG

    FDA Adverse Event
    Injury ·REVERSE MEDICAL·Product code KRD·September 8, 2021

    ESOPHYX Z

    FDA Adverse Event
    Injury ·ENDOGASTRIC SOLUTIONS, INC.·Product code ODE·June 22, 2017

    CABLE CUTTER

    FDA Adverse Event
    Malfunction ·OBERDORF : SYNTHES PRODUKTIONS GMBH·Product code HXZ·January 31, 2018