BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    PROSPORE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PEEK Corpectomy

    FDA UDI
    Nuvasive, Inc.·00887517623874·PEEK Corp Core, Ø14x32mm

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704293395·

    SILVERHAWK-R PERIPHERAL PLAQUE EXCISION SYSTEM FOR SURGICAL USE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HICALIQ IVH BAG

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SJM MASTERS SERIES VALVE EXPANDED CUFF W/SILZONE

    FDA Adverse Event
    Death ·ST. JUDE MEDICAL, PUERTO RICO, INC. (CS)·Product code LWQ·January 21, 2011

    TSH, THYROTROPIN

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JLW·July 31, 2014

    FLUOROSCOPIC X-RAY

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC·Product code JAA·October 4, 2007