BEUDAMED
    10,000 results · 84ms · Sources: EU EUDAMED, US FDA

    GEM Premier 7000 with iQM3 PAK (BG/ISE/COOX 75 Tests)

    FDA UDI
    INSTRUMENTATION LABORATORY COMPANY·00195226000764·GEM Premier 7000 with iQM3 PAK pH, pCO2, pO2, N...

    GEM Premier 5000 PAK BG/ISE/GL/COOX 300 TEST

    FDA UDI
    INSTRUMENTATION LABORATORY COMPANY·08426950807759·GEM Premier 5000 PAK pH, pCO2, pO2, Na+, K+, Cl...

    GEM Premier 7000 with iQM3 PAK (BG/ISE/COOX 450 Tests)

    FDA UDI
    INSTRUMENTATION LABORATORY COMPANY·00195226000733·GEM Premier 7000 with iQM3 PAK pH, pCO2, pO2, N...

    GEM Premier 5000 PAK BG/ISE/GL/COOX 600 TEST

    FDA UDI
    INSTRUMENTATION LABORATORY COMPANY·08426950807599·GEM Premier 5000 PAK pH, pCO2, pO2, Na+, K+, Cl...

    GEM Premier 5000 PAK BG/ISE/GL/COOX 150 TEST

    FDA UDI
    INSTRUMENTATION LABORATORY COMPANY·08426950807698·GEM Premier 5000 PAK pH, pCO2, pO2, Na+, K+, Cl...

    EmbryoScope time-lapse incubator

    FDA UDI
    Vitrolife A/S·05712714603013·The EmbryoScope time-lapse incubator (Version D...

    gammaCore-2

    FDA UDI
    ELECTROCORE, LLC·00815203020126·gammaCore-2 is a multi-use, hand-held, recharge...

    gammaCore-2

    FDA UDI
    ELECTROCORE, LLC·00815203020119·gammaCore-2 is a multi-use, hand-held, recharge...

    gammaCore-2

    FDA UDI
    ELECTROCORE, LLC·00815203020102·gammaCore-2 is a multi-use, hand-held, recharge...

    Might Patch Surface,10ct

    FDA registration
    CHURCH & DWIGHT CO., INC.·1 product·🇺🇸 United States

    Mighty Patch Face 5ct

    FDA registration
    CHURCH & DWIGHT CO., INC.·1 product·🇺🇸 United States

    Daily Wear Soft Contact Lens To Reduce The Progression Of Myopia

    FDA Pre-Market Approval
    FDA Class 3 ·MiSight 1 Day (omafilcon A) Soft (Hydrophilic) Contact Lenses for Daily Wear

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·CAPSURE/CAPSURESP/NOVUS

    Stimulator, Autonomic Nerve, Implanted For Epilepsy

    FDA Pre-Market Approval
    FDA Class 3 ·NEUROCYBERNETIC PROSTHESIS (NCP) SYSTEM

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·CAPSUREFIX/SUREFIX

    Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented

    FDA Pre-Market Approval
    FDA Class 3 ·Trident(R), ABC(R)

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·EPIC AND ATLAS FAMILIES OF DEVICES

    Permanent Pacemaker Electrode

    FDA Pre-Market Approval
    FDA Class 3 ·CAPSUREZ NOVUS

    Catheter, Coronary, Atherectomy

    FDA Pre-Market Approval
    FDA Class 3 ·ATHEROCATH-BANTAM(TM) DIRECTIONAL CORONARY ATHERECTOMY SYSTEM

    Daily Wear Soft Contact Lens To Reduce The Progression Of Myopia

    FDA Pre-Market Approval
    FDA Class 3 ·MiSight 1 Day (omafilcon A) Soft (Hydrophilic) Contact Lenses for Daily Wear