The present invention relates to an inhalation chamber including a body having an inlet orifice suitable for being connected to the outlet end piece of a metered dose inhaler and an outlet orifice suitable for being connected to a mouthpiece or a mask to apply on the face of a patient, and a support suitable for receiving the outlet end piece of the metered dose inhaler, the support opening into the inlet orifice, characterised in that the axis (X) of the inlet orifice is non-colinear with the axis (Y) of the outlet orifice and in that the support is pivotally mounted on the body around the axis (X) of the inlet orifice.

This aerosol supply device is provided with: an accommodating section (cartridge) that accommodates a liquid; an atomizing unit that atomizes the liquid to generate an aerosol; and an atomizing amount adjusting unit (gyro sensor and control unit) that adjusts the atomizing amount of the atomizing unit. The aerosol supply device is characterized in that the atomizing amount adjusting unit (gyro sensor and control unit) stabilizes the atomizing amount regardless of the inclination of the aerosol supply device within at least a certain range.

An aerosol-generating system is provided, including: a cartridge including a storage compartment configured to contain a liquid composition including an aerosol-forming substrate; an aerosol-generating device configured to receive the cartridge and including a power supply and control electronics operably coupled to the power supply; a light source operably coupled to the control electronics and positioned and oriented to emit light into the storage compartment, light emitted from the source is absorbed by the liquid composition; and a detector operably coupled to the control electronics and positioned and oriented to detect light emitted from the source, the source and the detector are both located adjacent to a same side of the storage compartment, and a surface of the storage compartment opposite the source is configured to absorb light emitted into the storage compartment from the source.

The present invention relates to a medicament delivery device, comprising an outer body, a receptacle for a medicament, a needle for the administration of the medicament, an injection mechanism with an actuating mechanism for injecting the medicament into the patients body, and a needle guard for the needle. The medicament delivery device further comprising a detecting element for the detection of the orientation of the medicament delivery device, and a locking mechanism releasing the actuating mechanism, if the detecting element is in the at least first position, and locking the actuating mechanism, if the detecting element is in the at least second position, wherein the locking mechanism is controlled and/or actuated by the detecting element.

An injection device includes a container receiving receptacle configured for receiving a container for containing a medicinal product to be administered; a dispensing mechanism for causing the product in the container to be injected; and a RFID system associated with the container receiving receptacle capable of communicating bidirectionally with a RFID tag attached to the container and enabling the administration of the product only under given conditions. The RFID tag can be therefore read and written by the RFID system. The RFID system further includes an antenna arranged at least partially covering the RFID tag. The dispensing mechanism is triggered by a contact sensor when the device is pressed onto the animal's skin. The needle-free injection device is capable of communicating with external devices (PC, laptops, tablets, smartphones and the like).

A method of oral delivery of a medication to a user's lungs with an inhaler that includes the steps of (a) receiving an actuation signal in response to release of the medication from the inhaler, (b) receiving a first accelerometer measurement indicating an orientation of the inhaler, (c) storing the actuation signal and the first accelerometer measurement in a memory, (d) determining whether the orientation of the inhaler exceeds a predetermined proper orientation threshold, and (d) determining a quality of use of the inhaler based on the actuation signal and the first accelerometer measurement.

A cuff pressure stabilizer (100, 200, 300, 500, 600, 800) is provided that includes an inflation lumen proximal port connector (134), which is shaped to form an air-tight seal with an inflation lumen proximal port (15) of a catheter (10) additionally having an inflatable cuff (11) and an inflation lumen (13); a fluid reservoir (120, 524, 624); a liquid column container (118, 518, 618), which is (a) open to the atmosphere (99) at at least one site along the liquid column container, (b) in fluid communication with the fluid reservoir (120, 524, 624), and (c) in communication with the inflation lumen proximal port connector (134) via the fluid reservoir (120, 524, 624); and a liquid (121), which is contained (a) in the fluid reservoir (120, 524, 624), (b) in the liquid column container (118, 518, 618), or (c) partially in the fluid reservoir (120, 524, 624) and partially in the liquid column container (118, 518, 618), and which has a density of between 1.5 and 5 g/cm3 at 4 degrees Celsius at 1 atm.

An intelligent vaporizing system includes a vaporizing device having a cartridge detachably coupled with a main body, the cartridge includes: a container configured to receive a liquid; a sensor for detecting a user’s action of inhalation; and a memory chip embedded inside the cartridge and communicated with the sensor, the memory chip configured to: record collected data from the sensor; receive associated data from an application; and transfer the collected data to the application; wherein the main body includes a heating element configured to heat the liquid to form a vaporized form; and a controller configured to receive the collected data and activate the heating element for heating the liquid.

Disclosed is an auto injector for administering a medicament. The auto injector comprising: a housing; a cartridge receiver configured to receive a cartridge assembly comprising a cartridge and a cartridge code feature, the cartridge containing the medicament; a code sensor configured to read the cartridge code feature; a drive module coupled to move a plunger rod; and a processing unit coupled to the code sensor and the drive module. The processing unit being configured to: receive from the code sensor a code signal indicative of the cartridge code feature; control the drive module to move the plunger rod to a first plunger rod position, the first plunger rod position being based on the code signal; receive a trigger event; control the drive module to move the plunger rod to a second plunger rod position following reception of the trigger event.

An apparatus for treating a respiratory disorder in a patient, includes a respiratory pressure therapy device that generates a flow of air at positive pressure for treating the respiratory disorder. An air circuit transports the flow of air generated by the respiratory pressure therapy device to a patient interface. A nebuliser module is located at or adjacent to a proximal end of the air circuit to nebulise a liquid to form a nebula of the liquid. The nebula is admitted into the flow of air generated by the respiratory pressure therapy device. A vaporiser is located at the distal end of the air circuit to receive and vaporise the nebula to form a humidified flow of air.