BEUDAMED
    16 results · 29ms · Sources: EU EUDAMED, US FDA

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    ORL Video NasoPharyngo-Larngoscope

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    Vilex Guidewire

    FDA UDI
    VILEX IN TENNESSEE, INC.·00841731120588·Guidewire 2.4x150mm Sgl Trocar

    AngioSystems Tray

    FDA UDI
    ANGIOSYSTEMS, INCORPORATED·00816611026557·

    S-LIFT®

    FDA UDI
    SPINEFRONTIER, INC.·00190361038603·TRIAL RASP, STRAIGHT, 22MM WIDE, 14MM

    S-LIFT®

    FDA UDI
    SPINEFRONTIER, INC.·00190361038580·TRIAL RASP, STRAIGHT, 22MM WIDE, 6MM

    S-LIFT®

    FDA UDI
    SPINEFRONTIER, INC.·00190361038016·TRIAL RASP, STRAIGHT, 22MM WIDE, 12MM

    S-LIFT®

    FDA UDI
    SPINEFRONTIER, INC.·00190361037996·TRIAL RASP, STRAIGHT, 22MM WIDE, 10MM

    S-LIFT®

    FDA UDI
    SPINEFRONTIER, INC.·00190361037972·TRIAL RASP, STRAIGHT, 22MM WIDE, 8MM

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·July 30, 2021

    DRFP PROSMART ROOT CANAL OBTURATION SYSTEM, PROPOINTS 4% 6%, PT, S

    FDA 510(k)
    FDA Class 2 ·Dental

    ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·April 22, 2020

    CRE? WIREGUIDED

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - CORK·Product code KNQ·June 6, 2013

    3002 SECURE II

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·June 10, 2011

    SYNERGY

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO·Product code LGW·September 3, 2008

    MEDTRONIC DUAL CHAMBER TEMPORARY EXTERNAL PACEMAKER 510(K) K150246

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code DTE·February 10, 2021