BEUDAMED
    7 results · 23ms · Sources: EU EUDAMED, US FDA

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    MAINSTER WIDE FIELD LASER LENS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756663601·DR. PRESS'S SINUSOTOMY PACK

    PARAMED MODEL 9350 BLOOD PRESSURE MONITOR (9350)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ZAROLAN, DUALAN, TITAN AND SUPERON

    FDA 510(k)
    FDA Class 2 ·Dental

    POWERGLIDE MIDLINE CATHETER 20G, 10CM

    FDA Adverse Event
    Injury ·BARD·Product code FOZ·June 20, 2014

    EON

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 10, 2012

    IDENTITY ADX XL DR

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·November 10, 2010