Profile: Medoc Ltd. Advanced Medical Systems developer and manufacturer of neuro-diagnostic medical systems used to assess & monitor acute and chronic pain. Our products are pathway and TSA-II, which are applicable in pain research, clinical use and pharmaceutical trials. The pathway pain & sensory evaluation system introduces new technology and capabilities in the area of objective evoked pain potential and advanced stimulator products. These systems are available in two versions, are pathway model contact heat-evoked potential stimulator and advanced thermal stimulator. Our TSA-II neurosensory analyzer is a precise, computer-controlled device capable of generating and documenting response to highly repeatable thermal and vibratory stimuli, such as warmth, cold, heat-induced pain, cold-induced pain or vibration. This delivers quantitative assessment of small-caliber sensory nerve function, as well as for large caliber A-beta fibers. It is also used for identifying thermal pain thresholds in various clinical and research applications.
FDA Registration Number: 8044062
US Agent: George Hattub / Medicsense, Usa
Phone: +1-(508)-479-6116 Fax: +1-(509)-277-1418 E-Mail:
6 Products/Services (Click for related suppliers)
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• Non-Powered Dynamometer (FDA Code: HRW / 888.1250) A nonpowered dynamometer is a mechanical device intended for medical purposes to measure the pinch and grip muscle strength of a patient's hand. |
• Temperature Discrimination Test (FDA Code: LQW / 882.1200) |
• Therapeutic Vibrator (FDA Code: IRO / 890.5975) A therapeutic vibrator is an electrically powered device intended for medical purposes that incorporates various kinds of pads and that is held in the hand or attached to the hand or to a table. It is intended for various uses, such as relaxing muscles and relieving minor aches and pains. |
• Thermal Diffusion Cerebral Blood Flow Monitor (FDA Code: LME) |
• Thermal Evoked Potential Stimulator (FDA Code: NTU / 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. |
• Vibration Threshold Measurement Device (FDA Code: LLN / 882.1200) |