A device for carrying out a lavage-like, repetitive supply and draining of a flushing, cleaning or other therapeutically active substance in the context of a return-flow enema, the device comprising: a catheter unit (SK) for receiving and draining feces, which can be permanently placed atraumatically and anorectally; a flushing and collecting bag unit (5, SB) with a combined flushing and collecting function; and a hose unit (4) connecting the catheter unit (SK) to the flushing and collecting bag unit (5, SB), comprising a single-lumen or multi-lumen, film-like, flatly collapsible, hose, and enabling a bidirectional flow communication between the catheter unit (SK) and the flushing and collecting bag unit (5; SB); characterized by at least one throughflow element with a flow-direction-dependent throttle function, providing a large lumen for draining of the patient's intestinal contents into the flushing and collecting bag unit (5; SB), so that shaped stool fractions can be drained, and which facilitates a supply of liquid from the flushing and collecting bag unit (5; SB) towards the patient, but wherein the supply of liquid towards the patient is throttled, so as to be reduced in flow amount or flow speed in relation to the draining of the patient's intestinal contents and thereby reduces the supply of liquid to the patient to a non-irritating amount that is compatible with the patient avoiding painful sensations and/or vegetative responses by an immediate dilation of the patient's colon and/or a triggering of a premature or only partially coordinated defecation reflex.

A wound irrigation device including a container with an opening along the outer surface of the container and a nozzle assembly coupled to the container and configured to selectively allow the liquid to exit the container when pressure is applied to the container.

Systems and methods for nasal irrigation are provided in which a nasal irrigation device includes a source of saline solution, an effluent receptacle, a nasal interface, a vacuum source, a fluid passageway to communicate the source of saline solution with the effluent receptacle through the nasal interface and a nasal cavity of the user, and a switch and valve assembly for selectively controlling the vacuum source and flow of the saline solution through the fluid passageway. The saline solution source bottle is disposed relative to the device to provide gravitational inducement of saline solution to the nasal interface in engagement to the device user's nostrils. A combination of the gravitational inducement and the relative vacuum from an effluent receptacle generates a fluid flow for irrigating, cleansing and massaging the nasal cavity and ostia of a user. The entire device is assembled as a hand-held device for convenient lifting and disposal against the user's nostrils.

A nozzle (10) for a container for the intranasal administration of a liquid formulation comprises a nozzle body (12) with an upper end (18) and a lower end (16), a channel (40) traversing the nozzle body (12) and ending with an orifice (17) in the upper end (18), and a nozzle cover (14) covering an area of the outer surface of the nozzle body (12) which is designed to be introduced into a user's nostril, wherein the nozzle body (12) is made out of a first material and the nozzle cover (14) is made out of a second material, said first material being a rigid plastic material, and said second material being an elastic plastic material, and wherein the nozzle cover (14) is not in contact with the orifice (17). A packaging for a liquid formulation for intranasal administration comprises a container and such nozzle (10). A product comprises such a packaging and a liquid formulation in said packaging.

The scope of the invention encompasses novel, multifunctional tools for maintaining the neovagina. The tools comprise novel dilator shapes that conform the anatomical pathway of the neovagina. The tools may further include a douching function for the effective and thorough washing of the neovagina, which is not achieved with standard douching devices. The tools may also comprise a measurement function for medical evaluation of the neovagina and to aid in proper dilation. Also presented herein are novel devices for delivery of agents to the natal vagina, including insemination devices.

The oral irrigation/liquid delivery device provides flow controlled fluid to body areas specifically the mouth, or parts of body or other non-body areas via pump device or connection to water source through a wand handle with bulbous smooth head with multiple openings/orifices for the fluid to flow to ensure that no high-pressure jets result (unless within the design) and can be used in confined area; idea for irrigating or rinsing the mouth after jaw surgery or other situation where it is not possible or recommended to use a high-pressure “water pick” type of device; allows user who may have a problem sucking in water to rinse to have fluids safely delivered to mouth to clear and clean it; allows for the delivery of medicated and or other liquid delivery of water or any other liquid to rinse or even imbibe; said device could also deliver feeding fluids; optional connection via any pump or faucet diverter system to delivery fluids, including option to have a siphon mix of one solution along with another with the secondary solution being introduced to the flow as a result of the pump mechanism or a siphon mechanism based upon the flow of a fluid that is the primary solution. Optionally, a rubber or other suitable tube or hose may be connected between the wand and the tip/connecting point to the pump or fluid delivery device. The same device or its components could be incorporated into other devices such as water bottles or syringe ends.

A method of treatment for mixed carbon dioxide, carbonic acid, saline and optional active additives for treating lower body cavity ailments includes delivery of dosage of the treatment at specified flow rates, using a) main housing having a hollow central area containing the dosage; b) a dosage dispenser head located at the distal end of the main housing, and having at least one flow channel for movement of the dosage from the main housing through the dosage dispenser head and to external of the dosage dispenser head; c) a dosage release control component located between the main housing and the dosage dispenser head to permit flow of the dosage through the dosage dispenser head in response to increased pressure against the dosage; and d) a pressure-changing moveable component on the main housing.

An irrigation system including a reservoir with an inlet adapted to guide liquid into the reservoir, the inlet defining a closure for closing the inlet, an insertion member defining an insertion end sized for insertion into a body cavity of a human being, the insertion member defining at least one opening, and a liquid tube fluidly connecting the reservoir with the insertion member, at least one of the reservoir and the insertion member being permanently fastened to the liquid tube and further including an electrical pump adapted to pump liquid from the reservoir and out through the at least one opening of the insertion member, the electrical pump adapted to be separable from the system.

A temporary tube placement system includes a tube having a proximal end and a distal end, a camera supported by the tube at the distal end, a plurality of fiber optic filaments through which light from a light source travels from the proximal end to the distal end, a screen for displaying images from the camera, and a power source electrically attached to the camera and the light source. The enteral tube includes a tube having a distal end portion for placement within a patient and a proximal end portion and a lumen increasing in cross section from the proximal end portion toward the distal end portion along at least a portion of the tube.

A method of treatment for mixed carbon dioxide, carbonic acid, saline and optional active additives for treating non-nasal ailments includes delivery of dosage of the treatment at specified flow rates, using a) main housing having a hollow central area containing the dosage; b) a dosage dispenser head located at the distal end of the main housing, and having at least one flow channel for movement of the dosage from the main housing through the dosage dispenser head and to external of the dosage dispenser head; c) a dosage release control component located between the main housing and the dosage dispenser head to permit flow of the dosage through the dosage dispenser head in response to increased pressure against the dosage; and d) a pressure-changing moveable component on the main housing.