Profile: Axtim France specializes in stimulation and biofeedback probes. Our stimulation probes are designed for facial, auricular or body treatments. These probes are suitable accessories for the electro-therapy devices.
FDA Registration Number: 9615768
US Agent: David Lennarz / Registrar Corp
Phone: +1-(757)-224-0177 Fax: +1-(757)-224-0179 E-Mail:
2 Products/Services (Click for related suppliers)
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• 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. |