Nihon Kohden America, Inc.

Address: 90 Icon Street, Foothill Ranch, California 92610, USA
Phone: +1-(949)-580-1555 | Fax: +1-(949)-580-1550 | Map/Directions >>

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: Steve Geerdes / Nihon Kohden America, Inc.
Phone: +1-(949)-580-1555  Fax: +1-(949)-580-1550  E-Mail:

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• Acute Care Physiological Monitor
• Airflow Cannula Sensors
• Ambulatory Sleep Study Systems
• Amplitude-Integrated Electroencephalograph (FDA Code: OMA / 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.
• Anesthetic Infusion Pump (FDA Code: FRN / 880.5725)
An infusion pump is a device used in a health care facility to pump fluids into a patient in a controlled manner. The device may use a piston pump, a roller pump, or a peristaltic pump and may be powered electrically or mechanically. The device may also operate using a constant force to propel the fluid through a narrow tube which determines the flow rate. The device may include means to detect a fault condition, such as air in, or blockage of, the infusion line and to activate an alarm.
• Arm Supports (FDA Code: IOY / 890.3475)
A limb orthosis (brace) is a device intended for medical purposes that is worn on the upper or lower extremities to support, to correct, or to prevent deformities or to align body structures for functional improvement. Examples of limb orthoses include the following: A whole limb and joint brace, a hand splint, an elastic stocking, a knee cage, and a corrective shoe.
• Arrhythmia Detector and Alarm (FDA Code: DSI / 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.
• Audio Sensors
• Automated Hematology Analyzers
• Automatic Blood Pressure Monitors
• Batteries & Battery Assemblies for Pulse Oximeters
• Battery-Operated Operating Headlamp (FDA Code: HPP / 886.4335)
An operating headlamp is an AC-powered or battery-powered device intended to be worn on the user's head to provide a light source to aid visualization during surgical, diagnostic, or therapeutic procedures.
• Battery-Powered Defibrillator/Monitor
• Bed Patient Monitor (FDA Code: KMI / 880.2400)
A bed-patient monitor is a battery-powered device placed under a mattress and used to indicate by an alarm or other signal when a patient attempts to leave the bed.
• Bedside Monitor
• Blood Pressure kits
• Blood Pressure Measuring Equipment
• Blood Pressure Monitors
• Blood Pressure Monitors
• Body Position Sensors
• Breathing Frequency Monitor (FDA Code: BZQ / 868.2375)
A breathing (ventilatory) frequency monitor is a device intended to measure or monitor a patient's respiratory rate. The device may provide an audible or visible alarm when the respiratory rate, averaged over time, is outside operator settable alarm limits. This device does not include the apnea monitor classified in 868.2377.
• Capnometer
• Cardiac Analysis
• Cardiac Catheterization Equipment & Systems
• 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.
• Cardiac Pacemakers
• Carts
• Clinical Lab Equipment
• Collecting Vessel Gas (FDA Code: KGK / 868.1575)
A gas collection vessel is a container-like device intended to collect a patient's exhaled gases for subsequent analysis. It does not include a sampling pump.
• Computer Softwares
• Cystometric Gas on Hydraulic Device (FDA Code: FAP / 876.1620)
A urodynamics measurement system is a device used to measure volume and pressure in the urinary bladder when it is filled through a catheter with carbon dioxide or water. The device controls the supply of carbon dioxide or water and may also record the electrical activity of the muscles associated with urination. The device system may include transducers, electronic signal conditioning and display equipment, a catheter withdrawal device to enable a urethral pressure profile to be obtained, and special catheters for urethral profilometry and electrodes for electromyography. This generic type of device includes the cystometric gas (carbon dioxide) device, the cystometric hydrualic device, and the electrical recording cystometer, but excludes any device that uses air to fill the bladder.
• 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.
• Diagnostic Electromyograph Needle Electrode (FDA Code: IKT / 890.1385)
A diagnostic electromyograph needle electrode is a monopolar or bipolar needle intended to be inserted into muscle or nerve tissue to sense bioelectrical signals. The device is intended for medical purposes for use in connection with electromyography (recording the intrinsic electrical properties of skeletal muscle).
• Differential Gas Pressure Transducer (FDA Code: BYR / 868.2875)
A differential pressure transducer is a two-chambered device intended for medical purposes that is often used during pulmonary function testing. It generates an electrical signal for subsequent display or processing that is proportional to the difference in gas pressures in the two chambers.
• Digital Polysomnography Devices
• Digital Pulse Oximeter
• Disposbale Pulse Oximeter Sensors
• Ecg Analysis System (FDA Code: LOS)
• ECG Electrodes
• ECG Leads
• ECG Machine
• ECG Management Software
• ECG Monitor
• ECG Monitoring Electrodes
• ECG Monitors Service
• ECG Physiological Telemetry Unit
• ECG Polysomnography Kits
• EEG Electrodes
• EEG Monitor
• EEG Physiological Telemetry Unit

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