BEUDAMED
    11 results · 18ms · Sources: EU EUDAMED, US FDA

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    X6000D SILENT SUN LIGHT SOURCE

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

    VERTEX® Reconstruction System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074239262·BONE SCREW 6955510 4.5 X 10MM CORTICAL

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704286953·CURETTE ENDOSCOPIC SCOVILLE 9 X 15 MILLIMETER C...

    Zuma

    FDA UDI
    Seaspine Orthopedics Corporation·10889981097103·Ratchet Handle

    Duo Ti Expandable Interbody Fusion System

    FDA UDI
    SPINEOLOGY INC.·M7402955510·Duo Ti, 55 x 10mm, 0°

    LIFEPAK 9 DEFIBRILLATOR & CARDIAC MONITOR/MODIFIED

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODEL 90478 & 90479 TELEMETRY REC. MODULE&HOUSING

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SECURI-T

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code KNT·April 13, 2007

    SPRINT QUATTRO

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·February 11, 2013

    TENDRIL ST

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·January 10, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE REHABILITATION EQUIP·Product code CAW·July 24, 2014