BEUDAMED
    12 results · 17ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    SMOOTH BECKER EXPANDER/MAMMARY PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR·Product code FTR·November 24, 1998

    NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM FOR CHILDREN

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code MCM·December 17, 1996

    M/H MODULAR CALCAR STEM

    FDA Adverse Event
    Injury ·BIOMET, INC.·Product code JDI·June 19, 1998

    CRYOVALVE

    FDA Adverse Event
    Injury ·CRYOLIFE, INC.·Product code MIE·June 8, 1998

    SYNTHES

    FDA Adverse Event
    Injury ·SYNTHES·Product code KWQ·July 9, 1998

    14MM UNIVERSAL FEMORAL

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code JDS·February 15, 2002

    AUTO SUTURE SURGINEEDLE 150MM

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL CORP.·Product code GCJ·February 3, 1999

    STAR

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code LZS·May 14, 2019

    ROTALINK CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code MCX·December 4, 2008

    ELECTRIC DERMATOME HANDPIECE

    FDA Adverse Event
    Injury ·ZIMMERBIOMET SURGICAL·Product code GFD·September 22, 2015

    STAR S4 IR

    FDA Adverse Event
    Injury ·AMO MANUFACTURING USA, LLC·Product code LZS·February 11, 2021

    STAR S4 IR

    FDA Adverse Event
    Injury ·AMO MANUFACTURING USA, LLC·Product code LZS·February 11, 2021