Nexstim Oy
Profile: Nexstim Oy develops, manufacturers and markets navigated brain stimulation devices for clinical use in hospitals & scientific research centers. We also offer transcranial magnetic stimulators.
FDA Registration Number: 3007147067
US Agent: Paul Skelton / Nexstim Inc.
Phone: +1-(770)-664-1000 Fax: +1-(770)-664-1217 E-Mail:
5 Products/Services (Click for related suppliers)
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| • Deep Brain Stimulation (DBS) |
| • Deep Brain Stimulators |
| • 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. |
| • 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. |
| • Neurological Stereotaxic Instrument (FDA Code: HAW / 882.4560) A stereotaxic instrument is a device consisting of a rigid frame with a calibrated guide mechanism for precisely positioning probes or other devices within a patient's brain, spinal cord, or other part of the nervous system. |
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