BEUDAMED
    20 results · 43ms · Sources: EU EUDAMED, US FDA

    DePuy Synthes Porous Polyethylene Implants And Titanium Wires Portfolio – MR Conditional

    FDA registration
    Synthes (USA) Products LLC·2 products·🇺🇸 United States

    DePuy Synthes Porous Polyethylene Implants and Titanium Wires Portfolio – MR Conditional

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

    k083472

    FDA registration
    BD SWITZERLAND SARL·1 product·🇨🇭 Switzerland

    Mesh, Surgical

    FDA classification
    FDA Class 2 ·Mesh, Surgical

    set, administration, intravascular

    FDA registration
    CAREFUSION·1 product·🇺🇸 United States

    SISTEMAS MEDICOS ALARIS, S.A. DE C.V,

    FDA registration
    SISTEMAS MEDICOS ALARIS, S.A. DE C.V,·1 product·🇲🇽 Mexico

    Trinity Plus Facial Toning Device

    FDA registration
    Carol Cole Company·1 product·🇺🇸 United States

    CAREFUSION (SDB) - MaxPlus pressure rated extension set with needleless connector

    FDA registration
    Synergy Health AST, LLC·1 product·🇺🇸 United States

    Carefusion5709 (NT) - MaxPlus pressure rated extension set with removable needleless connector

    FDA registration
    Isomedix Operations, Inc·1 product·🇺🇸 United States

    set, administration, intravascular

    FDA registration
    CAREFUSION 2200, INC.·1 product·🇺🇸 United States

    SISTEMAS MEDICOS ALARIS, S.A De C.V.

    FDA registration
    SISTEMAS MEDICOS ALARIS, S.A De C.V.·1 product·🇲🇽 Mexico

    Micro Dermal Tone

    FDA registration
    The Beauty Tech Group Ltd·1 product·🇬🇧 United Kingdom

    Synergy Sterilisation Kulim (m) Sdn. Bhd.

    FDA registration
    Synergy Sterilisation Kulim (m) Sdn. Bhd.·1 product·🇲🇾 Malaysia

    Quiver Extendable A100604

    FDA registration
    ITL ASIA PACIFIC SDN BHD·1 product·🇲🇾 Malaysia

    Sterigenics US LLC

    FDA registration
    Sterigenics US LLC·1 product·🇺🇸 United States

    MySpine Pedicle Screw Placement Guides – MC and Drill Pilot Instruments

    FDA registration
    BBF STERILISATIONSSERVICE GMBH·1 product·🇩🇪 Germany

    NUFACE PLUS

    FDA 510(k)
    FDA Class 2 ·Neurology

    MEDEGEN PRESSURE RATED EXTENSION SETS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Stimulator, Transcutaneous Electrical, Aesthetic Purposes

    FDA classification
    FDA Class 2 ·Stimulator, Transcutaneous Electrical, Aesthetic Purposes

    Set, Administration, Intravascular

    FDA classification
    FDA Class 2 ·Set, Administration, Intravascular