BEUDAMED
    21 results · 48ms · Sources: EU EUDAMED, US FDA

    Nihon Kohden JE-120A Multi Electrode Junction Box

    FDA registration
    NIHON KOHDEN AMERICA, INC.·1 product·🇺🇸 United States

    Nihon Kohden JE-120A Multi Electrode Junction Box

    FDA registration
    NIHON KOHDEN CORP.·1 product·🇯🇵 Japan

    Nihon Kohden JE-120A Multi Electrode Junction Box

    FDA registration
    Nihon Kohden Corporation - Eastern Japan Logistics Center·1 product·🇯🇵 Japan

    Nihon Kohden JE-120A Multi Electrode Junction Box

    FDA registration
    NIHON KOHDEN TOMIOKA PRODUCTION CENTER·1 product·🇯🇵 Japan

    NIHON KOHDEN EEG-1200A WITH JE-120A MULTI CHANNEL ELECTRODE JUNCTION BOX

    FDA 510(k)
    FDA Class 2 ·Neurology

    ADPT-NKSS-DRS-BCD Adapter Cable

    FDA UDI
    NEURALYNX, INC.·00867718000223·The ADPT-NKSS-DRS-BCD is an adapter that allows...

    ADPT-NKSS-DRS-A AdapterCable

    FDA UDI
    NEURALYNX, INC.·00867718000216·The ADPT-NKSS-DRS-A is an adapter cable that al...

    JOBST forMen Casual

    FDA UDI
    BSN MEDICAL, INC.·00035664131173·FOR MEN CASUAL 20-30 MM HG KNEE HIGH CLOSED TOE...

    Full-Montage Standard Electroencephalograph

    FDA classification
    FDA Class 2 ·Full-Montage Standard Electroencephalograph

    n/a

    FDA UDI
    Ortho Development Corporation·00822409076499·Trial Head 28mm - 3.5

    ITOTAL CRUCIATE RETAINING IJIGS

    FDA registration
    ConforMIS, Inc.·1 product·🇺🇸 United States

    PPD MEDITECH, DIV. OF INDUSTRIES PPD INC.

    FDA registration
    PPD MEDITECH, DIV. OF INDUSTRIES PPD INC.·1 product·🇨🇦 Canada

    Resect Ablator Trident

    FDA registration
    Linvatec Corporation d/b/a ConMed Linvatec·1 product·🇺🇸 United States

    JARVIS SURGICAL INC.

    FDA registration
    JARVIS SURGICAL INC.·1 product·🇺🇸 United States

    Trident Omega 4.2mm Mako Resection Ablator Trident

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

    General Instrument

    FDA UDI
    Life Spine, Inc.·00190837079536·

    RESECTION ABLATOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ITOTAL CRUCIATE RETAINING (CR) KNEE REPLACEMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Arthroscope

    FDA classification
    FDA Class 2 ·Arthroscope