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

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    OSBON PERSONAL LUBRICANT

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867055278·ELEVATOR, KEY, 3/8" X 7.5" LONG

    DETECTABUSE DRUG CONTROLS

    FDA 510(k)
    FDA Class 1 ·Clinical Toxicology

    BALLOON (NEPHROSTOMY TRACT) DILATION CATHETER SET

    FDA 510(k)
    FDA Unclassified ·Unknown

    3.5MM LOCKING SCREW SLF-TPNG W/STARDRIVE(TM) RECESS 18MM

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·June 25, 2014

    8F ANGIO-SEAL EVOLUTION

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code MGB·November 4, 2010

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·January 3, 2013