The aerosol-generating device includes a device housing, and a receiving chamber defined within the device housing. The receiving chamber is configured to receive at least a first-type consumable and a second-type consumable, the receiving chamber including a first structure for receiving the first-type consumable and a second structure for receiving the second-type consumable. A structure selector selects between the first structure and the second structure, the first and second structures differing in at least one of a shape, a size and a position within the receiving chamber. An aerosolization system is included with at least a portion of the receiving chamber, where the receiving chamber is configured to prevent an insertion of more than one consumable into the receiving chamber.

A patient care system is configured for infusing fluid to a patient. The system includes a plurality of modular fluid infusion pumps that each has a connector for connecting to a modular programming unit or to one another. Systems and methods are configured for verifying that the connectors are reliably performing their functions or communicatively connecting the pumps to one another or to the programming unit.

An auto-injector includes a base housing, an ampule, a needle arrangement, at least one drive assembly and a securing assembly which secures the drive assembly in its position with respect to the base housing until activated for the injection procedure. The securing assembly includes a securing cap with a cap jacket, a cap wall and a securing pin arranged inside the cap jacket. Arranged between the securing cap and the base housing is a guide arrangement with a first and a second guide element which define an adjustment path delimited in the axial direction on the side directed away from the distal end. In its release position, the securing cap is still arranged and held on the base housing.

Methods and systems are described herein for fluid handling and dispensing liquid substances using vaporization or nebulization in a controlled, safe manner. A dispensing device may be configured to receive one or more cartridges storing different types of vaporizable or nebulizable substances. A controller may be provided to regulate the amount of a given substance dispensed over a defined time period. Optionally, in response to detecting tampering of the dispensing device and/or a liquid cartridge the dispensing device may be disabled and/or a liquid stored in a substance cartridge may be rendered inert.

A Positive Airway Pressure (PAP) device includes a flow generator that generates a supply of pressurized air. The flow generator includes a programmable controller. The programmable controller is adapted to allow continuous access to at least one active operating mode and selective access to at least one dormant operating mode. The programmable controller includes a mode control system adapted to receive a data signal to control the selective access to the at least one dormant operating mode.

The present invention is generally related to a device and method for sanitizing a medical instrument with ozone, in particular the invention relates to a system, method and a device for sanitizing a continuous positive airway pressure (CPAP) device. The device has an ozone compartment, an ozone operating system and one or more ozone distribution lines that distribute ozone to a continuous positive airway pressure device. The device may further include a heater adapter unit to connect heating systems in CPAP devices while distributing ozone to sanitize the CPAP device in accordance with the present invention.

The present invention provides a single-dose powder-medication inhaler (10) for nasal application, comprising a flat inhaler housing consisting of two flat housing parts (1, 2) connected to one another along a connecting plane (E). Formed in the two flat housing parts are: a medication chamber (11) having at least one powder receiving hollow (11); an air inlet opening (14); and an air channel delimited by walls (7), the air channel extending from the air inlet opening (14), via the medication chamber (11) to a discharge opening (12). According to the invention the air inlet opening (14) does not lie on a side facing away from the discharge opening (12), whereby the air channel provides a direction change of an air flow through the air inlet opening (14) relative to the discharge opening (12). The outlet section (13) of the air channel between the medication chamber (11) and the discharge opening (12) has more than one bend (6). Furthermore a nose piece (4), designed for inserting in only one nostril or in both nostrils, is formed on the discharge opening (12).

Systems and methods for automatically delivering medication to a user. A sensor coupled to a user can collect information regarding the user. A controller can use the collected information to determine an amount of medication to provide the user. The controller can instruct a drug delivery device to dispense the medication to the user. The drug delivery device can be a wearable insulin pump that is directly coupled to the user. The controller can be part of or implemented in a cellphone. A user can be required to provide a confirmation input to allow a determined amount of insulin to be provided to the user based on detected glucose levels of the user. The sensor, controller, and drug delivery device can communicate wirelessly.

Methods and devices for locking and tagging a medical tube are disclosed. The locking device connects to a medical tube and restricts full manipulation of the medical tube. The locking and tagging devices can communicate instructions or notices relevant to the medical tube, including its placement, purpose, function, operation, care, maintenance, removal, replacement, indication of manipulation or tampering, as well as the patient's healthcare information and health care provider information. In some configurations, the tagging device may be configured to communicate instructions and notices as a primary function, with or without a locking function.

The invention relates to a method of loading a medical device, in particular to a dialysis device, and preferably a peritoneal dialysis device, which comprises a device control and a user interface, wherein at least one fluid-filled container is connected to a corresponding interface of the device, wherein at least one property of the container is checked by the device before or during its connection and the measured value is compared with least one desired value stored in the device control.