Profile: Nihon Kohden America, Inc. manufactures, develops and distributes medical electronic equipment. We are an ISO-9001, EN 46001, ISO 13485, ISO 17025 & EC certified company. Our product line includes patient monitors, electroencephalographs, evoked potential & electromyography systems, electrocardiographs, defibrillators, cardiac catheterization equipment and veterinary hematology analyzers. We supply compact, lightweight patient transmitters for wireless bedside monitors & wireless networks. We significantly contribute to the advancement of modern medical treatment with many innovative products and technologies. We design and manufacture medical equipment in conformity with the standards of IEC601-1. Our wide range of imported equipment includes cardiology, urology, respiratory care, anesthesiology, emergency care, sports medicine and rehabilitation. We supply high quality medical equipment all over the world.

The company was founded in 1951, has revenues of USD 500 Million to 1 Billion, has ~3370 employees and is ISO 9001, CE certified. TYO:6849 (SEC Filings)

FDA Registration Number: 9611252
US Agent: Thomas Bento / Nihon Kohden America, Inc.
Phone: +1-(949)-680-9048  Fax: +1-(913)-273-0732  E-Mail:

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• EEG Polysomnography Kits

• EKG Supplies

• Electro Diagnostic Equipment

• Electrocardiograph (FDA Code: DPS / 870.2340) An electrocardiograph is a device used to process the electrical signal transmitted through two or more electrocardiograph electrodes and to produce a visual display of the electrical signal produced by the heart.

• Electrocardiograph Transmitter/Receiver System (FDA Code: DXH / 870.2920) A telephone electrocardiograph transmitter and receiver is a device used to condition an electrocardiograph signal so that it can be transmitted via a telephone line to another location. This device also includes a receiver that reconditions the received signal into its original format so that it can be displayed. The device includes devices used to transmit and receive pacemaker signals.

• Electrocardiography

• Electroconductive Media (FDA Code: GYB / 882.1275) Electroconductive media are the conductive creams or gels used with external electrodes to reduce the impedance (resistance to alternating current) of the contact between the electrode surface and the skin.

• Electrode Conductive Gels

• Electrode Gel

• Electrodes Adhesives

• Electrodiagnostic Polysomnography Kits

• Electrodiagnostic Testing Kits

• Electroencephalogram Signal Spectrum Analyzer (FDA Code: GWS / 882.1420) An electroencephalogram (EEG) signal spectrum analyzer is a device used to display the frequency content or power spectral density of the electroencephalogram (EEG) signal.

• Electroencephalograph Digital EEG Monitor

• Electroencephalograph Electrode/Lead Tester (FDA Code: GYA / 882.1410) An electroencephalograph electrode/lead tester is a device used for testing the impedance (resistance to alternating current) of the electrode and lead system of an electroencephalograph to assure that an adequate contact is made between the electrode and the skin.

• Electroencephalographs (FDA Code: GWQ / 882.1400) An electroencephalograph is a device used to measure and record the electrical activity of the patient's brain obtained by placing two or more electrodes on the head.

• Electroencephalography, Routine EEG Systems

• Electromyograph

• Electromyography (EMG)

• Electromyography Machines

• Electronystagmograph

• Electroretinograph

• EMG Electrodes

• EMG Electrodes

• EMG Monitor

• EMG Monitoring System

• EMG Polysomnography Kits

• End-tidal Carbon Dioxide Monitors

• ENT Probe (FDA Code: KAK / 874.4420)

• ETCO2 Monitors

• Event ECG Monitors

• Evoked Potential EMG Measuring System

• Evoked Potential Systems

• Evoked Response Auditory Stimulator (FDA Code: GWJ / 882.1900) An evoked response auditory stimulator is a device that produces a sound stimulus for use in evoked response measurements or electroencephalogram activation.

• Evoked Response Electrical Stimulator (FDA Code: GWF / 882.1870) An evoked response electrical stimulator is a device used to apply an electrical stimulus to a patient by means of skin electrodes for the purpose of measuring the evoked response.

• Evoked Response Photic Stimulator (FDA Code: GWE / 882.1890) An evoked response photic stimulator is a device used to generate and display a shifting pattern or to apply a brief light stimulus to a patient's eye for use in evoked response measurements or for electroencephalogram (EEG) activation.

• Evoked Response Unit

• Exercise Stress Test Electrocardiograph

• Extravascular Blood Pressure Transducer (FDA Code: DRS / 870.2850) An extravascular blood pressure transducer is a device used to measure blood pressure by changes in the mechanical or electrical properties of the device. The proximal end of the transducer is connected to a pressure monitor that produces an analog or digital electrical signal related to the electrical or mechanical changes produced in the transducer.

• Fetal Pulse Oximeter (FDA Code: MMA)

• Fingertip Pulse Oximeter

• Flow Sensors

• Fluoroscopic Imaging Systems

• Galvanic Skin Response Measurement Device (FDA Code: GZO / 882.1540) A galvanic skin response measurement device is a device used to determine autonomic responses as psychological indicators by measuring the electrical resistance of the skin and the tissue path between two electrodes applied to the skin.

• Gas Pressure Transducer (FDA Code: BXO / 868.2900) A gas pressure transducer is a device intended for medical purposes that is used to convert gas pressure into an electrical signal for subsequent display or processing.

• Gaseous Phase Carbon-Dioxide Gas Analyzer (FDA Code: CCK / 868.1400) A carbon dioxide gas analyzer is a device intended to measure the concentration of carbon dioxide in a gas mixture to aid in determining the patient's ventilatory, circulatory, and metabolic status. The device may use techniques such as chemical titration, absorption of infrared radiation, gas chromatography, or mass spectrometry.

• Gaseous Phase Enflurane Gas Analyzer (FDA Code: CBQ / 868.1500) An enflurane gas analyzer is a device intended to measure the concentration of enflurane anesthetic in a gas mixture.

• Gaseous Phase Halothane Gas Analyzer (FDA Code: CBS / 868.1620) A halothane gas analyzer is a device intended to measure the concentration of halothane anesthetic in a gas mixture. The device may use techniques such as mass spectrometry or absorption of infrared or ultraviolet radiation.

• Gaseous Phase Nitrous-Oxide Gas Analyzer (FDA Code: CBR / 868.1700) A nitrous oxide gas analyzer is a device intended to measure the concentration of nitrous oxide anesthetic in a gas mixture. The device may use techniques such as infrared absorption or mass spectrometry.

• Gaseous Phase Oxygen Gas Analyzer (FDA Code: CCL / 868.1720) An oxygen gas analyzer is a device intended to measure the concentration of oxygen in respiratory gases by techniques such as mass spectrometry, polarography, thermal conductivity, or gas chromatography. This generic type of device also includes paramagnetic analyzers.