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

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    KOWA nonmyd 8

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Oticon

    FDA UDI
    Oticon A/S·05707131340429·SIYA 2, KIT 10 85 PB C001

    Sklar

    FDA UDI
    SKLAR CORPORATION·10649111457715·LERICHE TISSUE FORCEPS 5x6 6 IN

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 22, 2025

    IMPAX NEXT GENERATION

    FDA 510(k)
    FDA Class 2 ·Radiology

    NEODENT IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    CAEMPRISE DR+

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CARDIAC RHYTHM MANAGEMENT DIVISI·Product code DXY·January 13, 2014

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 27, 2013

    ALIMAXX-E

    FDA Adverse Event
    Other ·ALVEOLUS INC·Product code JCT·June 25, 2008