BEUDAMED
    11 results · 32ms · Sources: EU EUDAMED, US FDA

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    IS4000 da Vinci EndoWrist Instruments

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

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·April 22, 2020

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517566225·CoRoent Ant TLIF PEEK, 15x10x28mm 4°

    Oticon

    FDA UDI
    Oticon A/S·05707131287137·RIA2 PRO, DESIGNRITE 10 WL CBE

    Slap Hammer

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215041410·

    LIQUIBAND ULTIMA, LUT 003

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

    NOVEL III SPINAL FIXATION AND ADJUSTABLE BRIDGE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OT VERIO FLEX METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 1, 2015

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 7, 2014

    U BY KOTEX CLICK

    FDA Adverse Event
    Malfunction ·AVENT S. DE R.L. DE C.V.·Product code HEB·June 6, 2013

    PROLIEVE THERMODILATATION KIT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MEQ·August 21, 2008