Mega Electronics Ltd.

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Contact: Arto Remes
Web: http://www.megaemg.com
E-Mail:
Address: Microkatu 1, Kuopio 70210, Finland
Phone: +358-(17)-581-7700 | Fax: +358-(17)-580-0978 | Map/Directions >>

Profile: Mega Electronics Ltd. specializes in the production of bio signal monitoring systems for neurology, rehabilitation, occupational health, sports medicine and gynecology. Our product line comprises of ME 6000, WBA, eMotion, FemiScan, NeurOne, Neurone Matrix, Nemo, Cleo, Foot scan, Magstim and In body bio signal monitoring systems. Our biomonitor is a portable telemetry and data logger designed to meet the most demanding needs in measurement and monitoring of electromyography and other physiological signals up to 16 channels, simultaneously. We supply eMotion that introduces a reliable and convenient way to measure heart rate variability. Our Femi scan is an interactive biofeedback device designed in collaboration with gynecologists and physical therapists. Our Cleo gives an audible interpretation of muscle activity, which is sensed by needle electrodes that are placed into the relevant muscles controlled by those nerves to be monitored.

FDA Registration Number: 1000425315
US Agent: Rene Van De Zande / Emergo Global Representation Llc
Phone: +1-(512)-327-9997 Fax: +1-(512)-327-9998 E-Mail:

6 Products/Services (Click for related suppliers)

• Biofeedback Device (FDA Code: HCC / 882.5050)

A biofeedback device is an instrument that provides a visual or auditory signal corresponding to the status of one or more of a patient's physiological parameters (e.g., brain alpha wave activity, muscle activity, skin temperature, etc.) so that the patient can control voluntarily these physiological parameters.

• Non-Implantable Electrical Stimulator (FDA Code: KPI / 876.5320)

A nonimplanted electrical continence device is a device that consists of a pair of electrodes on a plug or a pessary that are connected by an electrical cable to a battery-powered pulse source. The plug or pessary is inserted into the rectum or into the vagina and used to stimulate the muscles of the pelvic floor to maintain urinary or fecal continence. When necessary, the plug or pessary may be removed by the user. This device excludes an AC-powered nonimplanted electrical continence device and the powered vaginal muscle stimulator for therapeutic use (884.5940).

• Pain Management Devices

• Pain Management System

• Perineometer (FDA Code: HIR / 884.1425)

A perineometer is a device consisting of a fluid-filled sack for intravaginal use that is attached to an external manometer. The devices measure the strength of the perineal muscles by offering resistence to a patient's voluntary contractions of these muscles and is used to diagnose and to correct, through exercise, uninary incontinence or sexual dysfunction.

• Telemetry Systems