BEUDAMED
    12 results · 22ms · Sources: EU EUDAMED, US FDA

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    ALLY Adaptive Cataract Treatment System

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Symmetry Ribbon

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482059135·Symmetry® Retractor, Ribbon, Malleable, 5 in Wi...

    TISSUE FORCEPS MICRO SUTURE SURGICAL, 6" CURVED ROUND HANDLE SMOOTH

    FDA UDI
    W.H. Holden, Inc.·D9282202590·

    Headless Compression Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Parcus GFS II and GFS Mini, GFS Naked, GFS Ultimate, GFS BTB, ATLAS, Synd-EZ Ti, Actiflip Naked, Actiflip Cinch, Actiflip Whip, and GFS Ultimate Hip

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DO NOT USE - FULL OSSEOTITE XP¿ IMPLANT 4/5 X 13MM

    FDA Adverse Event
    Injury ·BIOMET 3I·Product code DZE·November 22, 2022

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code ITI·November 3, 2014

    PENTA LEAD

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·August 16, 2011

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·July 11, 2013

    FULL OSSEOTITE XP¿ IMPLANT 4/5 X 10MM

    FDA Adverse Event
    Injury ·BIOMET 3I·Product code DZE·November 22, 2022

    PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code LPH·October 17, 2025

    BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code QJR·September 8, 2020