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

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    Filters Regulation: Us FDA ×

    KINESTHETIC ABILITY TRAINER (K.A.T., MODEL 1000)

    FDA 510(k)
    FDA Unclassified ·Unknown

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909117952·REVELATION DIAMOND 379-023M - 5 PACK

    AOCup Lens Case with AODisc

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    WORLAND UNICONDYLAR TIBIAL BEARING

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INGENIO

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·January 11, 2013

    RESOLUTION HEMOSTASIS CLIPPING DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code MND·December 1, 2010

    HOMECHOICE PRO

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·July 3, 2014

    ELECSYS TSH V2

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JLW·January 26, 2026

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021