BEUDAMED
    12 results · 20ms · Sources: EU EUDAMED, US FDA

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    CYTOLOGY BRUSH

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981191214·Interbody, 9mm x 24mm x 10mm, 5 Deg

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150713·K-WIRE - SINGLE TROCAR 1.0mm DIA x 100mm

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123069·K-WIRE - DOUBLE TROCAR 1.0mm DIA x 100mm

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981205355·Trial, 9mm x 24mm x 10mm, 5 Deg

    WaveForm TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981286323·Interbody, 9mm x 24mm x 10mm, 5 Deg, 3D

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867377141·GLENOID INSERTER/IMPACTOR, X-LARGE

    ENDOPATH UNSHIELDED DISPOSABLE SURGICAL TROCAR

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ENDOSTAT

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SCREW-IN

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 14, 2010

    DIMENSION VISTA 1500

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code JJE·January 22, 2013

    TENDRIL ST

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