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

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    Genesys Spine 3DP AIS-C II Cervical Interbody System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OPTIMUM GP (OXYGEN PERMEABLE) DAILY WEAR CONTACT LENSES

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    EyeCTester

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·September 12, 2024

    4.5MM TI CORTEX SCREW SELF-TAPPING 44MM

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code KTT·August 27, 2021

    ADAPTER SLEEVE 11/13+9

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD·Product code KWA·November 14, 2008

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 2, 2011

    GYNECARE TVT ABBREVO CONTINENCE SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·July 18, 2013