BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODES

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867241619·REVERS HUMERAL CUP SCREW GUIDE, 42MM

    Frontier Medical Devices In-Line Orthopedic Cable Cerclage System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PITT-EASY DENTAL IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    SPRINT QUATTRO

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·February 9, 2013

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·January 7, 2011

    DURATA STS OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Death ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·July 23, 2014

    EVOLUT FX DCS

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NPT·August 8, 2025

    THERMA CARE

    FDA Adverse Event
    Injury ·PROCTER & GAMBLE PAPER PRODUCT CO·Product code IMD·March 6, 2002