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

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    Active-X Total Knee System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    N/A

    FDA UDI
    GEORGE TIEMANN & CO.·B5821601590·SCISSORS, SURGICAL TISSUE, DENTAL

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221044488·Unitek(TM) Molar Band General Purpose Narrow Re...

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172973646·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172973561·

    SMITH AND NEPHEW TWINFIX ULTRA TI SUTURE ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACTIVECARE SFT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TRUEMETRIX

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·February 20, 2019

    PROGRASP (TM) FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·June 10, 2013

    PROMUS ELEMENT EVEROLIMUS-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·July 13, 2011

    PARADIGM REAL -TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 19, 2014