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Cimetra Llc

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Contact: Cindy Bruneau
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Address: 20 Gateway Drive, Plattsburgh, New York 12901, USA
Phone: +1-(518)-5625334 | Map/Directions >>
 
 

Profile: Cimetra Llc provides biofeedback device, perineometer and non implantable electrical simulators.

FDA Registration Number: 1317927

4 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.
• Electrical-Powered Muscle Stimulator (FDA Code: IPF / 890.5850)
A powered muscle stimulator is an electrically powered device intended for medical purposes that repeatedly contracts muscles by passing electrical currents through electrodes contacting the affected body area.
• 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).
• 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.

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