A delivery head for a fluid dispenser for coupling to a fluid store. The delivery head has a nozzle unit with a plurality of fine nozzle openings with a maximum clear cross-section of 0.02 mm.sup.2. The protective cap is configured to encourage the fluid to remain in the nozzle openings for a long time, or to remove the fluid from the nozzle openings in a targeted fashion.

In one embodiment, a filter assembly for use in an insufflation system is described. The filter assembly comprises: a filter medium operative to filter medical gases; a housing comprising an inlet, an outlet and the filter medium, the housing defining a gases flow path through the filter medium between the inlet and the outlet; and at least one heating element being positioned in the housing and being configured to heat the filter medium; and wherein, the at least one heating element is spaced apart from the filter medium and from an inner surface of the housing.

Systems and methods are provided for portable and compact nitric oxide (NO) generation that can be embedded into other therapeutic devices or used alone. In some embodiments, an ambulatory NO generation system can be comprised of a controller and disposable cartridge. The cartridge can contain filters and scavengers for preparing the gas used for NO generation and for scrubbing output gases prior to patient inhalation. The system can utilize an oxygen concentrator to increase nitric oxide production and compliment oxygen generator activity as an independent device. The system can also include a high voltage electrode assembly that is easily assembled and installed. Various nitric oxide delivery methods are provided, including the use of a nasal cannula.

Provided herein are systems and methods for monitoring one or more health or physiological parameters in a subject. The systems and methods may comprise a patch coupled to an injector. Data may be transmitted to a mobile device or remote server, where the data may be processed. Processed data may be used to inform a subject on a health or physiological condition.

A wound dressing for use in negative pressure wound therapy includes: a wound contacting layer; a spacer layer; a hydrophilic absorbent layer positioned above the wound contacting layer; a cover layer comprising a cover layer aperture; a sealing layer adhered to the cover layer, the sealing layer comprising a sealing layer aperture, the sealing layer aperture being in fluidic communication with the cover layer aperture; and a filter element arranged to cover the sealing layer aperture.

A fluid check-valve for venting gas from a fluidic system comprises a retention body defining a fluid aperture having an upstream side and a downstream side, a hydrophilic porous material held by the retention body and disposed to cover the fluid aperture, and a hydrophobic porous material held by the retention body and disposed to cover the fluid aperture and adjacent the hydrophilic porous material. One face of the hydrophilic porous material is in fluid communication with the upstream side of the aperture, and one face of the hydrophobic porous material is in fluid communication with the downstream side of the aperture. The hydrophilic porous material is configured to retain liquid from the upstream side to hinder passage of gas from the downstream side to the upstream side, and the hydrophobic porous material is configured to hinder passage of liquid from the upstream side to the downstream side.

A mask 100 configured to substantially surround an opening of a patient's airway. The mask has a mask body 101 comprising a filter 103 configured to filter a fluid from a patient facing side of the mask to a non-patient facing side 105 of the mask, wherein the non-patient facing side faces an ambient environment AE. The mask has an interfacing feature 121 configured to, in use, interface with a patient interface 10100, 10100 provided on the patient 10020.

A drug delivery device includes a housing defining a shell and an inner volume, a container, a drive mechanism, a needle assembly, a fluid flow connection, and a backflow prevention mechanism. The container has an inner volume to contain a medicament to be administered to a user. The drive mechanism is at least partially disposed within the housing and exerts a force to urge the medicament out the container. The fluid flow connection is coupled to the container and the needle assembly and allows the medicament to flow from the container to the needle assembly to be administered. The backflow prevention mechanism is associated with at least one of the container, the fluid flow connection, or the needle assembly and includes at least one flow restrictor to restrict a fluid from flowing from the needle assembly to the container.

The present disclosure provides an aerosol delivery device that may comprise a housing defining an outer wall. The device may further include a power source and a control component, an exit aerosol path defined through an opening, a tank portion that includes a reservoir configured to contain a liquid composition, and an atomization assembly configured to vaporize the liquid composition to generate an aerosol. The atomization assembly may comprise two or more vibrating assemblies each of which includes a mesh plate. In some implementations, the mesh plates may be substantially coplanar and substantially perpendicular to the exit aerosol path. In other implementations, the mesh plates may be non-coplanar.

Embodiments of the present invention are directed to a liquid delivery apparatus. A non-limiting example of the apparatus includes a substrate including a cavity formed in a surface of the substrate. The apparatus can also include a membrane disposed on the surface of the substrate covering an opening of the cavity. The apparatus can also include a hydrophobic layer disposed on the membrane. The apparatus can also include a seal disposed between the membrane and the substrate, wherein the seal surrounds the opening of the cavity. The apparatus can also include an electrode layer coupled to the membrane.