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

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    CYTO-STAT TRICHROME CD45-FITC/CD56-RD1/CD3-PC5 MONOCLONAL ANTIBODY REAGENT WITH CYTO-STAT TRICHROME CD45-FITC/MSIGG1-RD1

    FDA 510(k)
    FDA Class 2 ·Hematology

    Modulus

    FDA UDI
    Nuvasive, Inc.·00195377049766·Modulus ALIF Trial, 8x38x30mm 15°Med

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091982166·posteriors; shade A2 light; size S; upper jaw

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471122802·K-WIRE - DOUBLE TROCAR 1.6mm DIA x 150mm

    MASTERGRAFT STRIP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Wrist Blood Pressure Monitor Model BP4350

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SONICISION

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY VALLEYLAB, A DIVISION OF TYCO HEALTHCARE·Product code LFL·February 25, 2013

    SONARA

    FDA Adverse Event
    CAREFUSION·Product code IYN·February 3, 2011

    RUBY COIL

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code HCG·August 5, 2014

    FILLER, RECOMBINANT HUMAN BONE MORPHOGENETIC PROTEIN, COLLAGEN SCAFFOLD WITH MET

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·August 11, 2020

    FILLER, RECOMBINANT HUMAN BONE MORPHOGENETIC P

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·April 2, 2020

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·September 17, 2018

    FILLER, RECOMBINANT HUMAN BONE MORPHOGENETIC P

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·January 22, 2020