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

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    RESTORE BUNION CORRECTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Symmetry Meyerding

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482000199·Symmetry® Blade, Meyerding, 2 in Blade Depth, 1...

    NEXGEN POROUS, UNCEMENTED FEMORAL AND TIBIAL BASEPLATE COMPONENTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    REVERSE SHOULDER MONOBLOCK PROSTHESIS (RSP)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ANGIOCATH 22GA X 1,00IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·October 8, 2021

    QUANTA SYSTEM S.P.A.

    FDA Adverse Event
    Malfunction ·QUANTA SYSTEM, S.P.A.·Product code GEX·July 10, 2015

    OT PING ENHANCED METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 1, 2014

    PARIETEX UGYTEX PP 15X10CM X1

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code FTL·May 21, 2013

    PACEART SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DPS·June 16, 2011

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·July 16, 2020