Profile: Comepa Industries focuses on non-implantable electrical stimulator and perineometer.
FDA Registration Number: 3007582665
US Agent: Barbara Mornet / Laborie Medical Technologies
Phone: +1-(802)-857-1300 Fax: +1-(802)-878-1122 E-Mail:
2 Products/Services (Click for related suppliers)
|
• 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. |