The present disclosure provides compositions and methods for using topical, isotonic compositions comprising a prebiotic oligosaccharide, a metal co-factor, and an essential oil comprising bornyl acetate. The compositions support the genital microbiota and are useful for, for example, hydrating, lubricating, cleaning, and/or decreasing irritation or inflammation of the urogenital and/or anogenital region of a subject, and/or enhancing the beneficial genital microbiota of a subject. Such compositions are useful before, during, and/or after sexual and/or reproductive activity. Kits for gel compositions including these compositions are also provided which may be used to aid delivery to and administration in low-resource settings.

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.

A multi-purpose balloon intra-cavity catheter includes a catheter having a proximal end portion, a central portion and a non-branching distal end portion, a plurality of lumens associated with the catheter extending from the proximal end portion, and a plurality of inflatable balloons positioned in the central portion and/or the non-branching distal end portion. Each of the plurality of inflatable balloons is communicatively associated with a corresponding one of the plurality of lumens, the plurality of inflatable balloons being selectively inflated or deflated to position and stabilize the catheter in a cavity for delivery of a medical treatment. The catheter can include an extraction opening associated with a lumen to remove fluids and materials from the cavity, and a connector associated with a corresponding lumen adapted to selectively receive one or more of a fluid medium or a radioactive isotope provided to a corresponding lumen for delivery of the medical treatment.

An applicator 270 includes a stem 174 having an axially-formed slot delivery passage 200. A slot 350 is formed transaxially through the stem 174 and is in communication with the slot delivery passage 200. An extended side wall 350b is formed on one side of the slot 350. A flat surface 354, which is formed in the stem 174, is spaced and extends angularly away from an opposite side of the slot 176 and from the extended side wall 350b to provide for direct and lateral dispensing of a cream 280 onto a tissue 242 of a patient.

A urinary catheter insertion alignment device for use by a female patient is disclosed. The urinary catheter insertion alignment device is molded to the patient's vaginal anatomy using impression material while an intermittent urinary catheter is inserted into the urethral orifice. Once the urinary catheter insertion alignment device has hardened, the intermittent urinary catheter is removed therefrom. Thereafter, the urinary catheter insertion alignment device may be fitted to the vaginal anatomy by the patient, which positions the passageway therethrough (formerly occupied by the urinary catheter in place during the molding operation) directly over the urethral orifice. The patient may then easily insert an intermittent urinary catheter (of a size smaller than that used during the molding operation) through the passageway, into the urethral orifice, and into the bladder for drainage of the bladder.

A medical device includes: a hollow body part formed in a predetermined between shape; a head part provided at a tip portion thereof with a discharge port for discharging cleaning water and detachably coupled to a front end of the body part; a connection part connected to a shower hose and a rear end of the body part and provided with a control valve for controlling water supply, a water flow rate and a water pressure; a water purification tube built in the body part and provided with leakage preventing grilles at both ends thereof; and a purified water discharge part provided inside the head part and configured to remove foreign substances in the water by using a filter.

A biocompatible intravaginal device adapted for the delivery of therapeutic active ingredients (agents) is provided. The device is constructed to be insertable and remain in the vagina for up to a month (28 to 31 days) or more. The device is loaded with the active agents prior to insertion and constructed to continuously release a therapeutically effective amount of the agents during the duration of up to a one month insertion. Preferred agents include contraceptive and anti-infection agents. It is preferred that the agents are non-hormonal.

A system for automatically removing by suction urine voided by a female. The system includes an external catheter, a canister and a suction regulator. The external catheter is applied at the urethra opening to receive urine voided by the female. The canister collects the urine and is coupled to a source of suction having a first value. The suction regulator is interposed between the external catheter and the canister to regulate the amount of suction to a regulated value which is applied the external catheter, whereupon urine from the external catheter is carried through the suction regulator and into the canister. The system may also include an adapter or an adapter/splitter for to connection between the source of suction and the canister.

A method for automatically removing by suction urine voided by a female by use of a system that includes an external catheter, a suction canister and a suction regulator. The external catheter is applied at the urethra opening to receive urine voided by the female. The suction canister collects the urine and is coupled to a source of suction providing suction having a first value. The suction regulator is interposed between the external catheter and the canister to regulate the amount of suction to a regulated value which is applied the external catheter, whereupon urine from the external catheter is carried through the suction regulator and into the canister.

A multi-purpose balloon intra-cavity catheter includes a catheter having a proximal end portion, a central portion and a non-branching distal end portion, a plurality of lumens associated with the catheter extending from the proximal end portion, and a plurality of inflatable balloons positioned in the central portion and/or the non-branching distal end portion. Each of the plurality of inflatable balloons is communicatively associated with a corresponding one of the plurality of lumens, the plurality of inflatable balloons being selectively inflated or deflated to position and stabilize the catheter in a cavity for delivery of a medical treatment. The catheter can include an extraction opening associated with a lumen to remove fluids and materials from the cavity, and a connector associated with a corresponding lumen adapted to selectively receive one or more of a fluid medium or a radioactive isotope provided to a corresponding lumen for delivery of the medical treatment.