Profile: Cadwell Laboratories, Inc. develops and markets diagnostic & monitoring products for the world of neurophysiology including electroneurodiagnostic & intraoperative-neuromonitoring devices. We offer products such as EEG, LTM, ICU, EMG, NCV, EP, PSG & IONM equipment plus all the accessories to operate them. Our product easy III amplifier can be configured with 46, 54, 86, or 150 channels. The amplifier has an integrated impedance measurement panel to allow a technician to quickly verify impedance levels. The amplifier includes 8 DC inputs, ambient light detection, and our easy net input connectors. These connectors provide on the body network of plug and play modules for oximetry, airflow, body position, and limb movement. A patient event button can be connected to the amplifier through a DC input. The amplifier can be placed on a bedside table or mounted on the wall with a bracket. Connection from the amplifier hardware to the computer is achieved through an ethernet connection in the Easy III computer. We offer several input box configurations that are color coded to simplify patient setup. Patient input boxes have a detachable 10 or 20-foot cable.
The company was founded in 1979, has revenues of USD 10-25 Million, has ~40 employees and is CE certified.
FDA Registration Number: 3020018
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• (FDA Code: BXM / 868.2775) An electrical peripheral nerve stimulator (neuromuscular blockade monitor) is a device used to apply an electrical current to a patient to test the level of pharmacological effect of anesthetic drugs and gases. |
• (FDA Code: HLX / 886.1630) An AC-powered photostimulator is an AC-powered device intended to provide light stimulus which allows measurement of retinal or visual function by perceptual or electrical methods (e.g., stroboscope). |
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• (FDA Code: HLZ / 886.1220) A corneal electrode is an AC-powered device, usually part of a special contact lens, intended to be applied directly to the cornea to provide data showing the changes in electrical potential in the retina after electroretinography (stimulation by light). |
• (FDA Code: GXY / 882.1320) A cutaneous electrode is an electrode that is applied directly to a patient's skin either to record physiological signals (e.g., the electroencephalogram) or to apply electrical stimulation. |
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• (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. |
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