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

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    BARRICADE EMBOLIZATION COIL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    Biogel

    FDA UDI
    Bosma Enterprises·10818634023763·Biogel Skinsense Surgical 7.5 - 50 Pair/Box

    VuMesh™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981036706·End Cap (10mm Cage) 14mm, 7.5 Deg

    COMPRESS ANTI-ROTATION SPINDLES

    FDA 510(k)
    FDA Class 3 ·Orthopedic

    OSSEOTITE NT CERTAIN IMPLANTS

    FDA 510(k)
    FDA Class 2 ·Dental

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·August 5, 2019

    CART 9733856 S7 STAFF ASSEMBLED 110V

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·June 4, 2019

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·September 6, 2019

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·February 5, 2019

    STEALTHSTATION® S7´

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·June 20, 2019

    CART 9733856 S7 STAFF ASSEMBLED 110V

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·June 17, 2019

    ALTRUA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 1, 2014

    CLINITEK 50

    FDA Adverse Event
    Other ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code KQO·May 10, 2013

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·June 16, 2011

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·July 7, 2025

    CPS TIB SPINDLE LT 12X37X42MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·September 16, 2019