The present invention provides means and methods for delivering a predetermined volume of a substance, within at least one body cavity of a subject, comprising a predefined volume for containing the predetermined volume of the at least one substance; a delivery end for placement in proximity to the body cavity; the delivery end comprises at least one orifice of diameter D [mm]; a valve mechanically connectable to the container, characterized by at least two configurations: (i) an ACTIVE CONFIGURATION in which the valve enables delivery of predetermined volume V.sub.sub [ml] of the substance; and, (ii) an INACTIVE CONFIGURATION, in which the valve prevents delivery of the predetermined volume V.sub.sub [ml] of the substance from the container to the body cavity; and a fluid tight chamber configured to contain predetermined volume V.sub.gas [ml] of pressurized gas at a predetermined pressure, P.sub.gas [barg].

Among other things, a system and a method are provided for generating space-filling foam for treating vulvodynia with medication compounded of multiple reactants; the system comprises an aerosol surmounted on a vulva-enclosing container configured to seal the vulva; the actuator on the aerosol operates a one-way valve to dispense said space-filling foam; and the method includes the following steps: selecting the vulvar cap delivery dispenser, affixing the dispenser over the vulva, depressing the pressure-sensitive switch operating the valve to deliver the appropriate quantity of medication in a space-filling foam, removing the delivery dispenser, and cleansing the dispenser; repeating the procedure according to a treatment regimen.

The present invention provides means and methods for delivering a predetermined volume of a substance, within at least one body cavity of a subject, comprising a predefined volume for containing the predetermined volume of the at least one substance; a delivery end for placement in proximity to the body cavity; the delivery end comprises at least one orifice of diameter D [mm]; a valve mechanically connectable to the container, characterized by at least two configurations: (i) an ACTIVE CONFIGURATION in which the valve enables delivery of predetermined volume V.sub.sub [ml] of the substance; and, (ii) an INACTIVE CONFIGURATION, in which the valve prevents delivery of the predetermined volume V.sub.sub [ml] of the substance from the container to the body cavity; and a fluid tight chamber configured to contain predetermined volume V.sub.gas [ml] of pressurized gas at a predetermined pressure, P.sub.gas [barg].

Methods and devices to affect types, proportion, quantity, distribution, or proliferation of microorganisms within a female reproductive system.

A system and method are provided for performing predictive permeation on the skin of a patient, particularly where the skin has no corneum. For this purpose, a device is provided which has an elongated probe, with an electrode array that extends along an active segment of the probe. Also, a voltage source is connected to the electrode array to generate an electric field. Operationally, an electro-conductive emulsion is applied onto the skin of the patient where the predictive permeation procedure is to be performed and the probe is positioned to contact the skin to be treated. The emulsion then interacts with the electric field that is generated by the electrode array to increase the permeability of the skin. Particles from a blood sample of the patient are included in the emulsion, and are introduced into the skin during the predictive permeation procedure to increase skin density.

A multi-purpose balloon catheter includes a catheter having a proximal end portion, a central portion and a 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 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 and deflated to position and stabilize the catheter in a cavity for delivery of a treatment. The catheter can include an extraction point associated with a lumen to remove fluids and material from the cavity, and a connector associated with a corresponding lumen adapted to selectively receive one or more of a liquid saline solution, a fluid medium, or a radioactive isotope provided to a corresponding lumen for delivery of the treatment.

A device and method for preparing a female patient to receive a catheter includes a female catheter starter cone that is shaped and constructed for insertion into the urethral fold of a women's body that holds the labia majora and labia minora out of the way so that a nurse can visually identify the urethral opening and to facilitate single handed insertion of the catheter tube.

A medicant dispenser enabling the effective administration of tableted pharmaceutical products within a body cavity has a plunger, a barrel, and a deformable tip. The deformable tip provides a suitable leading element to allow the barrel to enter a body cavity, wherein the plunger may be pushed to eject said tableted pharmaceutical products into said body cavity through the deformable tip. More specifically, the deformable tip will comprise a plurality of cuspids fixed to a support ring, wherein the support ring is fitted to a terminal end of the barrel. The plurality of cuspids will collapse concentrically to form a tapered leading element of the medicant applicator while retaining the capacity to separate to allow passage of said tableted pharmaceutical products and the head of the plunger therethrough.

A vaginal insertion portion is disclosed, the vaginal insertion portion including a base portion, a proximal holding portion located on a proximal side of the base portion, and a suction portion located on distal side of the proximal holding portion.

The present invention provides a device for delivering a predetermined volume of a substance, within at least one body cavity of a subject, comprising a predefined volume for containing the predetermined volume of the at least one substance; a delivery end for placement in proximity to the body cavity; the delivery end comprises at least one orifice of diameter D [mm]; a valve mechanically connectable to the container, characterized by at least two configurations: (i) an active configuration in which the valve enables delivery of predetermined amount M.sub.sub of the substance; and, (ii) an inactive configuration, in which the valve prevents delivery of the predetermined amount M.sub.sub of the substance from the container to the body cavity; and a fluid tight chamber configured to contain predetermined volume V.sub.gas of pressurized gas at a predetermined pressure, P.sub.gas.