BEUDAMED
    69 results · 36ms · Sources: EU EUDAMED, US FDA

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    M.U.S.T. MINI Posterior Cervical Screws System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Positioner (Standard Set-Up)

    FDA UDI
    FIVE STAR ORTHODONTIC LABORATORY & SUPPLY INC·D82852001300·

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776420277·Jarcho Cannula, Self-Retaining, 25cm (10") with...

    GERALD TISSUE FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896060135·GERALD TISSUE FORCEPS STRAIGHT SERRATED TIP

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180107922·JARCHO CANNULA 25CM (10") SELF RETAINING

    Golden Isles Pedicle Screw System

    FDA UDI
    Intelivation, LLC·G079C2522001300·Straight Titanium Rod

    CorticaLINK MI

    FDA UDI
    LINKSPINE, INC.·00817329023159·5.0mm Cobalt Chrome Rod: 130mm Curved

    INSTRUMENT

    FDA UDI
    Howmedica Osteonics Corp.·07613327245714·ACCOLADE TMZF STARTER RASP

    Preference 2

    FDA UDI
    SINTX Technologies, Inc.·M555102200130·Straight Rod 6.0mm, 130mm

    Taurus Pedicle Screw System

    FDA UDI
    SINTX Technologies, Inc.·M555252200130·Taurus Pedicle Screw System- Straight Rod 5.5x1...

    HARDYDISK, NALIDIXIC ACID, 30MCG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ROLOR POWERED MUSCLE STIMULATOR, MODEL GP-8016M

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·May 4, 2005

    NEW CORONA VIRUS NUCLEIC ACID DETECTION KIT

    FDA Adverse Event
    Malfunction ·PERKINELMER, INC.·Product code QJR·March 5, 2021

    ENDOPATH THORACIC ENDOSCOPIC LINEAR CUTTER RELOAD UNIT

    FDA Adverse Event
    *·Product code KOG·December 12, 2001

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 23, 2015

    STABLE BASE

    FDA Adverse Event
    Injury ·LEONHARD LANG GMBH·Product code DRX·November 17, 2020

    PDS PLATE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code NHB·October 22, 2019

    LEAD, UNKNOWN

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·September 18, 2013

    ACCU-CHEK COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·October 15, 2008