A medical device operable to deliver a fluid to a patient, including a base having a base body and a hollow cannula for insertion into a patient, the hollow cannula being one of fixed to the base and movable relative to the base to a patient insertion position. The base body includes a fluid pathway that is one of fluidly connected with the hollow cannula and fluidly connectable with the hollow cannula. The fluid pathway includes a pathway portion sealed with a sealer, and the pathway portion includes an adsorbent operable to modify a fluid traversing the pathway portion by removing one or more compounds or substances from the fluid prior to delivery of the fluid to the patient through the hollow cannula.

Provided herein are devices, systems, and methods for the removal of preservatives/excipients/stabilizers from pharmaceutical preparations/medicaments. The devices and systems include a resin for the filtering of preservatives from pharmaceutical preparations. The methods allow for a period of time of incubation of the pharmaceutical preparation in the resin that effectively removes preservatives, while at the same time maintaining the required amount or concentration of active compound in the preparation. Also provided herein are devices, systems, and methods for the controlled release of anti-inflammatory agents in an insulin infusion set.

A delivery device (10, 40, 100) for delivering a substance, such as an insulin formulation, to a patient includes a storage container (12, 112) containing the insulin formulation, a delivery member (20, 42) connected to the storage container by a fluid pathway for injecting the insulin formulation into the patient for delivering the insulin formulation to the patient at a controlled basal flow rate or bolus flow. The delivery device can have a pump mechanism for delivering the substance to the patient. An activated charcoal adsorbent (51 57, 87) or activated carbon is positioned in the fluid pathway between the storage container and the delivery member for removing at least a portion of a phenolic stabilizing agent from the insulin formulation before delivering to the patient. A method of delivering an insulin formulation to a patient includes the step of contacting the insulin formulation with an activated charcoal or activated carbon adsorbent to remove at least a portion of a phenolic stabilizing agent from the insulin formulation before introducing the treated insulin formulation to the patient.

An inhalation device is described, which inhalation device comprises an inlet for vapors and/or for aerosol, at least one terpene holding element configured to hold a selected terpene composition, and an outlet for vapors and/or for aerosol and wherein the device is configured to receive vapors and/or aerosol through the inlet, move the received vapors and/or aerosol through the device, infuse terpene composition into the moved vapors and/or aerosol and generate and emit terpene-enriched vapors and/or aerosol through the outlet, wherein at least one of the inlet, the holding element and the outlet is configured to limit the concentration of terpenes in the emitted terpenes-enriched vapors and/or aerosol to less than one percentage (by weight), when the moved vapors and/or aerosol is at 10 degrees Celsius and at atmospheric pressure.

A blood purification device includes a porous molded body containing an inorganic ion-adsorbing material and is characterized by the following: the concentrations of Mg, Al, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Ga, Rb, Sr, Y, Zr, Mo, Ru, Ag, Cd, Sn, Cs, La, Pr, Sm, Gd, Tb, Ta, Au, Tl, Co, In, and Bi are each 0.1 ppb or less and the concentrations of Ba, Nd, Pb, And Ce are each 1 ppb or less in a physiological saline solution for injection both three months and six months after said physiological saline solution for injection is sealed in the blood purification device; and the number of fine particles having a size of 10 m or more is 25 or less and the number of fine particles having a size of 25 m or more is 3 or less in 1 mL of the physiological saline solution for injection.

Provided herein are devices, systems, and methods for the removal of preservatives/excipients/stabilizers from pharmaceutical preparations/medicaments. The devices and systems include a resin for the filtering of preservatives from pharmaceutical preparations. The methods allow for a period of time of incubation of the pharmaceutical preparation in the resin that effectively removes preservatives, while at the same time maintaining the required amount or concentration of active compound in the preparation. Also provided herein are devices, systems, and methods for the controlled release of anti-inflammatory agents in an insulin infusion set.

A blood purification device includes a porous molded body containing an inorganic ion-adsorbing material and is characterized by the following: the concentrations of Mg, Al, Ti, V, Cr, Mn, Fe, Ni, Cu, Zn, Ga, Rb, Sr, Y, Zr, Mo, Ru, Ag, Cd, Sn, Cs, La, Pr, Sm, Gd, Tb, Ta, Au, Tl, Co, In, and Bi are each 0.1 ppb or less and the concentrations of Ba, Nd, Pb, And Ce are each 1 ppb or less in a physiological saline solution for injection both three months and six months after said physiological saline solution for injection is sealed in the blood purification device; and the number of fine particles having a size of 10 m or more is 25 or less and the number of fine particles having a size of 25 m or more is 3 or less in 1 mL of the physiological saline solution for injection.

The present system introduces a showerhead and sinks faucet kit in personal hygiene technology, offering a comprehensive solution for enema and vaginal wash hygiene practices. A crafted from medical-grade, BPA-free materials, this innovative showerhead and sink faucet attachment kit comprises a range of components designed to ensure convenience, hygiene, and user-friendliness. From different nozzle tip attachments catering to individual preferences to a flexible silicone tube-hose facilitating water transport, each part is meticulously engineered to provide optimal performance and comfort. The water flow pressure regulator switch valve and secure threaded coupling connector fittings, users can customize their hygiene experience while maintaining safety and reliability. The water filtration mesh washers and lock-in washers further enhances hygiene standards, ensuring clean and continuous water flow during procedures. Versatile and adaptable, the kit's stretchable universal water inlet rubber silicone attachment ensures compatibility with various water sources, offering convenience for users across different settings.