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Prometheus Group

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Web: http://www.theprogrp.com
E-Mail:
Address: 1 Washington St, Suite 303, Dover, New Hampshire 03820, USA
Phone: +1-(603)-749-0733 | Fax: +1-(603)-749-0511 | Map/Directions >>
 
 

Profile: Prometheus Group concentrates on physical therapists, occupational therapists and speech pathologists. We also deal with urologists, urogynecologists, colon and rectal physicians. Our products are used for the evaluation and treatment of urinary incontinence, fecal incontinence & bladder dysfunction.

FDA Registration Number: 1224842

27 Products/Services (Click for related suppliers)  
• Adapter for Disposable Lead Wire Electrodes
• Biofeedback & Electrotherapy
• 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.
• Biofeedback Electrodes
• Biofeedback Machines
• Biofeedback Systems
• Disposable Lead Wire Electrodes
• Dual Channel EMG System
• Dual Channel EMG Trainer
• EasytrodeT Pregelled Electrodes
• Electromedical Biofeedback Devices
• Electromedical Kits, Electrodes
• Electromedical Muscle Stimulators
• External Pelvic Muscle EMG Lead Wires
• Muscle Stimulators, Combo UltraSound
• 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).
• Pathway PathwayT Electrodes
• Patient Electrode Kit
• 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.
• Rectal EMG / Stimulation Sensor
• Rectal Silicon Pressure Sensor
• Single Channel EMG System
• Single Channel EMG Trainer
• Uroflowmeter (FDA Code: EXY / 876.1800)
A urine flow or volume measuring system is a device that measures directly or indirectly the volume or flow of urine from a patient, either during the course of normal urination or while the patient is catheterized. The device may include a drip chamber to reduce the risk of retrograde bacterial contamination of the bladder and a transducer and electrical signal conditioning and display equipment. This generic type of device includes the electrical urinometer, mechanical urinometer, nonelectric urinometer, disposable nonelectric urine flow rate measuring device, and uroflowmeter.
• Vaginal and Rectal Intracavity Stimulator
• Vaginal EMG / Stimulation Sensor
• Vaginal Silicon Pressure Sensor

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