BEUDAMED
    21 results · 51ms · Sources: EU EUDAMED, US FDA

    Cardioblate™ Gemini™

    FDA registration
    Medtronic Grand Rapids·1 product·🇺🇸 United States

    Cardioblate® Gemini® -s Surgical Ablation Device

    FDA registration
    MIDWEST STERILIZATION CORP.·1 product·🇺🇸 United States

    Cardioblate® Gemini® -s Surgical Ablation Device

    FDA registration
    MIDWEST STERILIZATION CORP.·1 product·🇺🇸 United States

    CEA Medical Manufacturing, Inc. d.b.a Nissha Medical Technologies

    FDA registration
    CEA Medical Manufacturing, Inc. d.b.a Nissha Medical Technologies·1 product·🇺🇸 United States

    Cardioblate™ Gemini™

    FDA registration
    MEDTRONIC PERFUSION SYSTEMS·1 product·🇺🇸 United States

    Cardioblate Gemini-s Surgical Ablation Device

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue

    FDA classification
    FDA Class 2 ·Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377047533·RELINE-O Trial,10mm H Offset Right L-pop

    METZENBAUM SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896055216·METZENBAUM SCISSORS CURVED TUNGSTEN CARBIDE SER...

    BIOFILM, INC.

    FDA registration
    BIOFILM, INC.·1 product·🇺🇸 United States

    COMBE INCORPORATED

    FDA registration
    COMBE INCORPORATED·1 product·🇺🇸 United States

    MHH800/MHH800SQ DVT Pump

    FDA registration
    MedHealth Medical Limited·1 product·🇨🇳 China

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613252095965·LOW PROFILE BURR HOLE COVER, W/TAB, 14mm

    24M - Duke Energy FA/BBP

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588015149·24M - Duke Energy FA/BBP

    A-CIFT® SoloFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361021414·A-CIFT SoloFuse 4.2 Screw, Lag, 14mm

    Standard Trocar

    FDA registration
    SHENZHEN JPY ION-TECH. CO., LTD. GUANGMING BRANCH·1 product·🇨🇳 China

    Aria

    FDA registration
    RESMED CORP·1 product·🇺🇸 United States

    PULPDENT GLAZE II

    FDA 510(k)
    FDA Class 2 ·Dental

    RUMBAR DRAINAGE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    Shunt, Central Nervous System And Components

    FDA classification
    FDA Class 2 ·Shunt, Central Nervous System And Components