BEUDAMED
    15 results · 29ms · Sources: EU EUDAMED, US FDA

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    Latitude EV Total Elbow Arthroplasty

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LATITUDE ELBOW ANATOMIC HUMERAL SPOOL SZ PETIT+ SIDE DROIT

    FDA Adverse Event
    Injury ·TORNIER INC·Product code JDB·September 20, 2024

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·14026704722379·

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704292282·K-WIRE STEINMAN PIN CASE

    MEGA SPINE SYSTEM

    FDA UDI
    BK MEDITECH CO.,LTD.·08809763500534·French Rod Bender

    Solstice Occipito-Cervico-Thoracic System

    FDA UDI
    Life Spine, Inc.·00190837038953·Angulating Cervical T15 Screwdriver

    Facebow

    FDA UDI
    ORMCO CORPORATION·00889989079821·Facebow ,S/SH OB,STD M/S IB,045

    PERSONA®

    FDA UDI
    Zimmer, Inc.·00889024238671·

    TIZIAN CERAMIC, FLOW, PLATE, FIX & ZR BLANKS

    FDA 510(k)
    FDA Class 2 ·Dental

    FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR MODEL: KD-5963NU, KD-5008

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BELLAFILL DERMAL FILLER

    FDA Adverse Event
    Injury ·SUNEVA MEDICAL, INC.·Product code LMH·December 20, 2017

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 14, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 30, 2011

    2250051-2008-00313

    FDA Adverse Event
    Malfunction ·Product code JTC·June 7, 2008

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·November 6, 2017