BEUDAMED
    21 results · 28ms · Sources: EU EUDAMED, US FDA

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    NUVASCULAR INC.

    FDA registration
    NUVASCULAR INC.·1 product·🇺🇸 United States

    HARBOR

    FDA UDI
    Nuvascular, Inc.·00850072397535·HARBOR Occlusion Device

    HARBOR

    FDA UDI
    Nuvascular, Inc.·00850072397504·HARBOR Occlusion Device

    HARBOR

    FDA UDI
    Nuvascular, Inc.·00850072397597·HARBOR Occlusion Device

    HARBOR

    FDA UDI
    Nuvascular, Inc.·00850072397481·HARBOR Occlusion Device

    HARBOR

    FDA UDI
    Nuvascular, Inc.·00850072397627·HARBOR Occlusion Device

    HARBOR

    FDA UDI
    Nuvascular, Inc.·00850072397573·HARBOR Occlusion Device

    HARBOR

    FDA UDI
    Nuvascular, Inc.·00850072397559·HARBOR Occlusion Device

    HARBOR

    FDA UDI
    Nuvascular, Inc.·00850072397498·HARBOR Occlusion Device

    HARBOR

    FDA UDI
    Nuvascular, Inc.·00850072397566·HARBOR Occlusion Device

    HARBOR

    FDA UDI
    Nuvascular, Inc.·00850072397610·HARBOR Occlusion Device

    HARBOR

    FDA UDI
    Nuvascular, Inc.·00850072397634·HARBOR Occlusion Device

    HARBOR

    FDA UDI
    Nuvascular, Inc.·00850072397528·HARBOR Occlusion Device

    HARBOR

    FDA UDI
    Nuvascular, Inc.·00850072397603·HARBOR Occlusion Device

    HARBOR

    FDA UDI
    Nuvascular, Inc.·00850072397511·HARBOR Occlusion Device

    HARBOR

    FDA UDI
    Nuvascular, Inc.·00850072397542·HARBOR Occlusion Device

    HARBOR

    FDA UDI
    Nuvascular, Inc.·00850072397580·HARBOR Occlusion Device

    DIAGNOSTIC CARDIOLOGY CATHETER- 6F

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code DQO·March 21, 2014

    INTRODUCER, CATHETER (SHEATH)

    FDA Adverse Event
    Injury ·ABIOMED, INC. - 1220648·Product code DYB·April 30, 2026

    DAVINCI X

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·May 13, 2022