Vaginal rehabilitative device
First Claim
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1. A vaginal rehabilitative device comprising:
- a liquid-sealed vaginal electrical stimulation applicator, comprising;
a) two stimulation electrodes configured to apply a voltage for executing an electrical stimuli, andb) a detection electrode that is configured to detect insertion of the applicator into a bodily cavity; and
a control module connectable by a wire to said applicator and comprising (a) a user interface for controlling the electrical stimuli applied by said applicator and (b) a display module configured to display data received from said applicator,wherein, responsive to a signal from the detection electrode indicating that the applicator is inserted within the bodily cavity, the control module is configured to allow selection of a treatment program in accordance with a physiological sensitivity threshold determined via a sensitivity test, andwherein, responsive to a signal from the detection electrode indicating that the applicator is not inserted within the bodily cavity, the control module is configured to prevent the application of the electrical stimuli.
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Abstract
A vaginal rehabilitative device comprising: a vaginal electrical stimulation applicator; and a control module connectable by a wire to said applicator and comprising a user interface for controlling electrical stimuli by said applicator and a display module configured to display data received from said applicator.
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Citations
15 Claims
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1. A vaginal rehabilitative device comprising:
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a liquid-sealed vaginal electrical stimulation applicator, comprising; a) two stimulation electrodes configured to apply a voltage for executing an electrical stimuli, and b) a detection electrode that is configured to detect insertion of the applicator into a bodily cavity; and a control module connectable by a wire to said applicator and comprising (a) a user interface for controlling the electrical stimuli applied by said applicator and (b) a display module configured to display data received from said applicator, wherein, responsive to a signal from the detection electrode indicating that the applicator is inserted within the bodily cavity, the control module is configured to allow selection of a treatment program in accordance with a physiological sensitivity threshold determined via a sensitivity test, and wherein, responsive to a signal from the detection electrode indicating that the applicator is not inserted within the bodily cavity, the control module is configured to prevent the application of the electrical stimuli. - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15)
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Specification