Irrigation and/or aspiration devices and methods may be configured to aspirate and irrigate alone, sequentially, or concurrently. The devices and methods may provide a base with a removable head, and adapted for partial or complete separation of the irrigation and aspiration functions. The devices and methods can be configured to aspirate and/or irrigate the nasal and sinus cavities. The devices and methods may be manually and/or automatically controlled. The devices and methods may include removable, and/or replaceable, and/or refillable, and easily cleanable reservoirs for aspirant and irrigant. The device head and/or aspirant reservoir may comprise a diagnostic device, i.e., test device and/or container after use of the devices and methods.

A injection site information cap includes a housing, a cover portion, an engagement portion configured to couple to and cover an injection port of an injection site, and at least one information element on the cover portion that is positioned to be automatically sensed by at least one sensor of the injection site when the engagement portion is coupled to or is being coupled to the medication injection port. Related apparatus, systems, and techniques are also described.

An aerosol delivery device is provided that includes a reservoir configured to retain an aerosol precursor composition, a heating element, and a power source connected to an electrical load that includes the heating element. The power source includes a rechargeable lithium-ion battery and a linear regulator between the power source and load, the linear regulator being configured to maintain a constant voltage level at the electrical load. The aerosol delivery device also includes a microprocessor configured to operate in an active mode in which the microprocessor is configured to direct power from the power source to the heating element and thereby control the heating element to activate and vaporize components of the aerosol precursor composition.

A system and method to match an interface to the face of a user for respiratory therapy. A facial image of the user is stored. Facial features based on the facial image are determined. A database stores facial profiles based on facial features and a corresponding plurality of interfaces. A database stores operational data of respiratory therapy devices with the plurality of corresponding interfaces. A selection engine is coupled to the databases. The selection engine is operative to select an interface for the user from the plurality of corresponding interfaces based on a desired outcome based on the stored operational data and the facial features. The collected data may also be employed to determine whether the selected interface is correctly fitted to the face of the user.

Provided is a navigation device for guiding a coil location, a brain stimulating device comprising same, and a bio-navigation robot system. The navigation device for guiding a coil location comprises: a 3D camera unit for capturing an image of a user to obtain a 3D camera image; and a location data calculating unit for mapping the camera image to a 3D medical image including brain region information or mapping the 3D medical image to the camera image to obtain a mapped image and calculating location data of a brain region to be stimulated from the mapped image.

Devices, and methods for generating variable inhalable products (e.g., variable density, phase, and size products) are provided. Methods for treating or preventing a disorder in a subject using variable products generated by the devices are also provided herein. Additionally, inhalers and breathing systems comprising the devices are provided.

The invention concerns a rack module for forming a support column, such as a rack, by stacking at least two rack modules, the rack module having at least one site for receiving a device for administering a medical product, this site comprising at least one plug for electric current supply to the administering device and for data transfer. It is also provided with an inlet connector and an outlet connector for connecting two successive modules to each other, power lines and data transfer lines connecting the inlet connector with the plug of the sites on the one hand side and with the outlet connector on the other hand side. In order to improve the connection between the rack modules in order to make its use easier, it is suggested according to the invention that the inlet connector or the outlet connector is movable between a stocking position and a connected position, the movable connector being called mobile connector and the other connector being called second connector, wherein, when a second module is placed over or under the module, the mobile connector in the connected position is in connection with the second connector of a second module placed over or under the module. This allows to stock in a safe position one of the connectors so that during the stocking and the handling of the module there is no risk for it to be damaged.

Disclosed are hemodialysis and similar dialysis systems including fluid flow circuits. Hemodialysis systems may include a blood flow path, and a dialysate flow path including balancing, mixing, and/or a directing circuits. Preparation of dialysate may be decoupled from patient dialysis. Circuits may be defined within one or more cassettes. The fluid circuit and/or the various fluid flow paths may be isolated from electrical components. A gas supply may be provided that, when activated, is able to urge dialysate through the dialyzer and blood back to the patient. Such a system may be useful during a power failure. The hemodialysis system may also include fluid handling devices, such as pumps, valves, mixers, etc., actuated using a control fluid. The control fluid may be delivered to the fluid handling devices using a detachable external pump. The fluid handling devices may have a spheroid shape with a diaphragm dividing it into two compartments.

In some embodiments, a humidification system includes a heater base having a heater plate, a humidification chamber, and circuit. The circuit can include various conduits, including an inspiratory conduit, expiratory conduit, Y-piece, patient conduit, and/or dry conduit. In use, the chamber contains a quantity of liquid. The heater base heats the heater plate, which in turn heats the liquid to a temperature that causes at least some of the liquid to become vapor, thereby humidifying the gases within the chamber. The gas is delivered to the patient via the inspiratory conduit. Various features can help control the system and ensure the patient receives gases having the desired conditions. These features can be used individually or in various combinations and subcombinations both in existing humidification systems and improved systems for respiratory humidification, laparoscopy, and other purposes.

An aerosol delivery device includes at least one housing; and contained within the at least one housing, a control component and motion sensor. The control component may control operation of the aerosol delivery device based on a detected flow of air through at least a portion of the at least one housing. The motion sensor may detect a defined motion of the aerosol delivery device that indicates a vulnerability of the aerosol delivery device or a user thereof, with the motion sensor being configured to convert the defined motion to an electrical signal. The control component or motion sensor may recognize the vulnerability and an operation associated with the vulnerability based on the electrical signal, and the control component may control at least one functional element of the aerosol delivery device to perform the operation, which may thereby be performed in response to detection of the vulnerability.