Nihon Kohden Tomioka Corp.

Contact: Fumio Suzuki - President
Web: http://www.nihonkohden.co.jp
Address: 1-31-4 Nishiochiai, Shinjuku-ku, Tokyo 161-8560, Japan
Phone: +81-(3)-5996-8036 | Fax: +81-(3)-5996-8100 | Map/Directions >>

Profile: Nihon Kohden Tomioka Corp. is a manufacturer, developer and distributor of medical electronic equipment. Our major products include patient monitors, electroencephalographs, evoked potential & electromyograph systems, electrocardiographs, defibrillators, and hematology analyzers.

FDA Registration Number: 8030229
US Agent: Thomas Bento / Nihon Kohden America, Inc.
Phone: +1-(949)-680-9048 Fax: +1-(913)-273-0732 E-Mail:

10 Products/Services (Click for related suppliers)

• Cardiac Monitor (Cardiotachometer and Rate Alarm) (FDA Code: DRT / 870.2300)

A cardiac monitor (including cardiotachometer and rate alarm) is a device used to measure the heart rate from an analog signal produced by an electrocardiograph, vectorcardiograph, or blood pressure monitor. This device may sound an alarm when the heart rate falls outside preset upper and lower limits.

• Diagnostic Electromyograph (FDA Code: IKN / 890.1375)

A diagnostic electromyograph is a device intended for medical purposes, such as to monitor and display the bioelectric signals produced by muscles, to stimulate peripheral nerves, and to monitor and display the electrical activity produced by nerves, for the diagnosis and prognosis of neuromuscular disease.

• ECG Analyzer

• 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.

• 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.

• 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.

• Patient Physiological Monitor (FDA Code: MHX / 870.1025)

The arrhythmia detector and alarm device monitors an electrocardiogram and is designed to produce a visible or audible signal or alarm when atrial or ventricular arrhythmia, such as premature contraction or ventricular fibrillation, occurs.

• Radiofrequency Physiological Transmitter/Receiver System (FDA Code: DRG / 870.2910)

A radiofrequency physiological signal transmitter and receiver is a device used to condition a physiological signal so that it can be transmitted via radiofrequency from one location to another, e.g., a central monitoring station. The received signal is reconditioned by the device into its original format so that it can be displayed.