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

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    REGENCY PLUS BRACKET

    FDA 510(k)
    FDA Class 1 ·Dental

    Ventura NanoMetalene System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981152116·Ventura NM Trial, 11mm x 28mm x 08mm, Lordotic

    HYDROPHILIC GUIDEWIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CENTERVUE MACULAR INTEGRITY ASSESSMENT

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    GYNECARE TVT OBTURATOR

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code OTN·September 24, 2019

    ENCOR BREAST BIOPSY PROBE

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·April 3, 2014

    UNKNOWN_RECONSTRUCTIVE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·January 29, 2013

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·December 16, 2010