Vaporizer and/or electronic cigarette chargers useful for the recharging of rechargeable vaporizer or electronic cigarette power supplies such as batteries, compatible vaporizers and/or electronic cigarettes, their components, charging contacts, methods of their use and kits containing such chargers are disclosed.

Packaging (4) for an injection device (6, 92), the packaging comprising: a compartment (32) forming a recess configured to house the injection device therein, the compartment extending in a longitudinal direction, a depth direction, and having a variable lateral width to accommodate the injection device; a first sidewall (54) extending in the depth direction and longitudinal direction contiguous a portion of the compartment; and a lip (56) adjoining the sidewall and said portion of the compartment, wherein the first sidewall is arranged within a field of width of the compartment, the lip arranged at a height (h) from a base of said portion of the compartment, such that the lip and first sidewall prevent user gripping of a housed injection device at said portion of the compartment.

The present invention is directed to an improved cannula systems for use with tracheostomies and endotracheal tubes. The presently disclosed cannula system permits efficient delivery of an external substance or compound into the respiratory system of a patient. A method of use of the cannula system is also disclosed herein.

Disclosed herein is a nebulizer comprising of a medicine cup reservoir containing an aqueous pirfenidone solution a medicine cup reservoir cap, an aerosol generator, an aerosol mixing chamber to which freshly generated aerosol resides until inhaled, a one-way inhalation valve, a mouthpiece and a one-way exhalation valve. The invention allows atmospheric pressure to be maintained inside the medicine cup reservoir during nebulization and optimizes the volume of the aerosol mixing chamber to minimize freshly generated aerosol inter-droplet collision, impaction of aerosol to the aerosol mixing chamber wall, droplet growth and/or condensation during exhalation, prior to inhalation, or during inhalation. The larger aerosol mixing chamber volume also allows the aerosol to accumulate during the exhalation phase. Despite venting producing a larger generated aerosol droplet population mean compared to the non-vented aerosol generator, The combined effect of the invention increases device output rate of respirable aerosol droplets, increases pirfenidone Cmax and AUC to improve treatment or prevention of various diseases, including disease associated with the lung, heart and kidney, including fibrosis, inflammatory conditions and transplant rejection.

The present invention concerns an apparatus (1) for measuring and recording the remaining quantity of medicament in a medicament dosing device (2). The apparatus (1) has a location where the medicament dosing device (2) can be inserted. Combined with that location the apparatus (1) has equipment for measuring and analysing. The apparatus is characterised in that this equipment for measuring and analysing comprises a contact image sensor (3) combined with that location for the medicament dosing device, and a software in connection with the contact image sensor. In addition the object of this invention is the corresponding method for measuring and recording the remaining quantity of medicament in a medicament dosing device (2).

A system to generate a vapor from a liquid includes an electric heater and an elongate wick. The electric heater defines an interior void having an inner surface and a plurality of apertures, and it is formed of an electrically resistive material contained within a heat diffusing material. The elongate wick is formed of a durable elongate structure having a plurality of liquid-conducting features on the outer surface. At least a portion of the liquid-conducting features of the elongate wick proximate the first end engage at least a portion of the one inner surface of the electric heater and are capable of conducting a the liquid from a source proximate the second end of the wick along the outer surface of the elongate wick to the electric heater.

The current pandemic due to Covid-19 stresses the importance of effectively treating highly contagious and deadly infections. The described medical device is meant to help the medical community by enabling them to treat patients more effectively. The delivery mechanism focuses on the mucous membrane. It is noninvasive and easy to use by patients directly. The device is hand-held, with incorporated germicidal UVC lights. It has two chambers connected by an internal application tip. The tip connects to a removable container which can be used with the prescribed treatment/therapy, vaccine, or viral testing fluid/reagent, as needed. Due to its versatility, non-invasive nature and germicidal properties, this device supports rapid response to infectious diseases, such as COVID-19. It may also further promote the development and use of different inoculation and drug techniques and delivery systems by enabling easy administration, via the mucous membrane.

A facial skin indentation preventer has a central base core surrounded by an entrapment flap and a securing flap. The core and flaps have at least a single layer of soft moleskin, felt, or similar material forming an outer skin-contact layer that is non-adhesive. A rigid component is attached to the outer skin-contact layer in a center of the preventer, thereby defining a central base core. The central base core can have a cannula or similar item placed thereon. The flaps are then folded inwards, over the rigid component, creating a cannula pocket above the rigid component and entrapping and holding the cannula therein. An entrapment hinge and securing hinge ensure the folds remain rounded and soft. A flap attachment is used to lock the securing flap to the entrapment flap and ensure the cannula stays within the cannula pocket.

Disclosed is a packaging for a number of pre-filled drug cartridges comprising a body to which an infusion set with tubing and needle can be fitted, the body having an open rear end, wherein a stopper is slidably disposed within the body, wherein a peg is arranged on the packaging, the peg having a height which is such that when a cartridge is being put on the peg with the rear end and pushed against it until the rear end abuts a surface of the packaging, the stopper is moved within the body by such a distance that a predetermined volume of a medicament is displaced from the cartridge for priming the cartridge and infusion set.

An applicator comprises a first structural element which has a shape determined according to a digital geometric representation of a target structure, the applicator further comprises an active agent located according to a diagnostic scan of the target structure.