A vaginal cleansing device is composed of an outer film, an inner support cylinder and a plug. The outer film has conical tapered rings formed on an outer wall of the outer film and tapered upward. The inner support cylinder has microvias formed on a wall of the inner support cylinder and corresponsive to the conical tapered rings of the outer film respectively; the inner support cylinder is plugged into the outer film, so that the microvias of the inner support cylinder are corresponsive to the conical tapered rings of the same height; and the microvias are attached onto the interior of the conical tapered rings. The plug is plugged into the opening of the inner support cylinder tightly and has a gas passing tube passing through the center of the opening of the inner support cylinder and a connector connected to the bottom end of the gas passing tube.

Certain embodiments of a medicinal applicator can comprise a base, a medicinal cream receiving port in the base, and a shaft extending along a conceptual shaft axis from the base and terminating at an applicator tip. There is at least one exit aperture located along a portion of the shaft. An unobstructed pathway is in communication with the receiving port and the exit aperture. A stop plate that extends essentially radially from the base delineating the base from the shaft. The shaft possesses a shaft outer shape defined by essentially a flat trailing edge and a shaped leading edge. The shaped leading edge comprises a narrow diameter proximal zone that extends along the shaft from the stop plate to a gradually increasing diameter transition zone that extends to a large diameter paddle zone, which terminates into a shaft distal end.

An intravaginal device (1600) includes arms (1602) and struts (1604). Each strut has a first end (1610) coupled to a shaft (1606) arranged to slide in a tube (1608) and a second end (1612) coupled to one of the arms (1602). A string (1616) is coupled to the shaft (1606). The arms (1602) have a stowed orientation in which the struts (1604) are folded inwards and a deployed orientation in which the struts (1604) point radially outwards and tautly hold the arms (1602) in an expanded position.

Nocilytic devices and methods for treatment of dyspareunia are provided. In particular, a device is provided, which inserts intravaginally with inflatable balloons to map the location of pain during application of force exerted against/on the luminal side of the vaginal wall and/or vulva of a human patient, or sensors to detect locations for application of nocilytic therapy.

Systems for the treatment and prevention of pelvic dysfunction are provided. In one embodiment, a vaginal dilation device includes a handle portion and a shaft portion. The shaft portion is configured to expand from a collapsed configuration to an expanded configuration. The shaft portion can include a distal tip region, a spine region, and a distal arm region connecting the distal tip region to the spine region. The spine region can extend distally from the handle portion to the distal arm region, and can be generally tubular in shape. The distal arm region can be generally conical in shape and be configured to provide a gradual increase in diameter from the distal tip region to the spine region. Methods of use are also provided.

Devices, system and methods for heating pelvic floor tissues are provided. The devices of the present invention can be used to apply heat to pelvic floor tissues such as rectal, vaginal, urethral and/or bladder tissues in order to treat disorders associated with such tissues.

The present invention is related to a vaginal drug delivery device and to a vaginal diagnostic device that comprises a first and second rigid member, wherein the first and/or second rigid member comprises a reservoir holding a medicament to be delivered, an opening, and a pump for pumping said medicament out of said opening, and/or wherein the first rigid member and/or second rigid member comprises a diagnostic device for performing an intravaginal diagnosis or measurement therefor. The device further comprises a first flexible member and flexible part, wherein at least one of the first flexible member and the flexible part is at least partially elastic having an elasticity such that the device can be squeezed from an extended shape to a collapsed shape. The device is pre-biased to assume the extended shape when little to no external force is being applied thereto. Furthermore, the device assumes a shape substantially corresponding to the extended shape when the device is inserted with the squeezed rigid member first, so that these naturally unfold in the formix posterior vaginae.

An illustrated view of an exemplary endocervical labor induction medicine injection apparatus for administering medication prior to or in the early stages of childbirth. The endocervical labor induction medicine injection apparatus is a medication apparatus that provides for controlled insertion of tablet style medication in an endocervical or lower uterine body area. The endocervical labor induction medicine injection apparatus provides increased functionality over the current manual placement methods ensuring maximum benefit and reduction of unwanted side effects. The endocervical labor induction medicine injection apparatus has a guide tube and an ejector tube. The ejector tube has an ejector head with a receiving cavity at a distal end of the ejector tube for receiving and dispensing the medication. A wire couples the receiving cavity at the distal end to a handle at a proximal end of the ejector tube. The guide tube is inserted into the cervical cavity of a patient. After determining proper positioning and loading of the medication into the receiving cavity, the distal end of the ejector tube is slid through the guide tube. The handle is then manipulated to release the medication at the desired location.

A personal hygiene device includes a bottle body configured to hold a fluid, and an extension tube, connected to the bottle body through a connector. In some embodiments, the extension tube includes a brush and an orifice configured to release the fluid. In other embodiments, the extension tube is designed to be inserted into a body cavity and does not include a brush.

A medical device is disclosed including a needle guide. The needle guide includes abase, a guide member, and a handle arrangement. The base defines a base channel and the guide member includes a guide member channel in communication with one another and configured for receiving a flexible needle. The guide member includes a non-linear portion and is generally flexible to accommodate passage of a flexible needle through a corresponding portion of the guide member channel. The handle arrangement is configured to accommodate stabilization of the needle guide during deployment.