BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    SeptAlign

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

    FLOWMEDICA BIFURCATED INFUSION SYSTEM, INFUSION CATHETER AND INTRODUCER SHEATH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TRUE DILATATION BALLOON VALVULOPLASTY CATHETER, 20MM X 4.5 CM, 22MM X 4.5CM, 24 MM X 4.5CM, 26MM X 4.5CM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·September 2, 2011

    SENSOR ENLITE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OZO·November 6, 2014

    GYNECARE PROSIMA PELVIC FLOOR REPAIR SYSTEM

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

    M2A-MAGNUM MOD HD SZ 48MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·August 17, 2018

    M2A-MAGNUM 42-50 TPR INSRT STD

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·August 17, 2018

    M2A-MAGNUM RECAP CUP 54ODX48ID

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·August 17, 2018