BEUDAMED
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    HANDI PORCH ELEVATOR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707036333·WEB I MOL BANDS G8421-17+G2820-00 LL 19

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756732000·ANGIOGRAPHY PACK

    RESOUND DEMO. BEHIND-THE-EAR HRNG., MODEL DEMO BTE

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

    LATEX SURGICAL GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SMARTSITE EXTENSION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP·Product code FPA·May 16, 2014

    PROXIMATE** HCS PROCEDURE FOR PROLAPSE AND HEMORRHOIDS (PPH)

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·January 4, 2013

    UROLOGICAL BALLOON DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code EZN·November 11, 2010

    ANGIOGRAPHY PACK

    FDA Adverse Event
    Malfunction ·DEROYAL INDUSTRIES, INC.·Product code OEQ·May 4, 2017