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

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    OPTISOL-GS CORNEAL STORAGE MEDIA

    FDA 510(k)
    FDA Unclassified ·Unknown

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981191467·Interbody, 9mm x 24mm x 16mm, 15 Deg

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981205607·Trial, 9mm x 24mm x 16mm, 15 Deg

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471121928·K-WIRE - DOUBLE TROCAR 1.6mm DIA x 125mm

    WaveForm TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981286514·Interbody, 9mm x 24mm x 16mm, 15 Deg, 3D

    WaveForm™ TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981234928·Interbody, 9mm x 24mm x 16mm, 15 Deg, 3D

    DUAL-LUMEN CATHETER

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    SENSORY NERVE CONDUCTION VELOCITY TESTING UNIT

    FDA 510(k)
    FDA Class 2 ·Neurology

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 22, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 14, 2010

    TENDRIL SDX

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014