BEUDAMED
    12 results · 21ms · Sources: EU EUDAMED, US FDA

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    CLARITY II Laser System

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

    Vanguard® Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304271647·

    Vanguard Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304473218·

    Sontec Calvian Case

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896115699·Sontec Calvian Case

    FORMATK MAGMA PLATFORM LASER

    FDA Adverse Event
    Injury ·FORMATK SYSTEMS LTD.·Product code GEX·December 19, 2019

    OPTMIZER CTS T-CELL EXPANSION SERUM FREE MEDIUM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    R3 CONSTRAINED LINER, CONSTRAINED LINER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TOTAL KNEE REPLACEMENT CEMENT KLASSIC TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·TOTAL JOINT ORTHOPEDICS, INC.·Product code JWH·August 18, 2020

    FORMATK MAGMA PLATFORM

    FDA Adverse Event
    Malfunction ·FOMATK SYSTEMS, LTD·Product code GEX·January 8, 2020

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 18, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 22, 2013

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·July 29, 2011