A control body is coupled or coupleable with a cartridge to form an aerosol delivery device, with the cartridge being equipped with a heating element. The control body includes a power source and a microprocessor. The power source is connected to an electrical load that includes the heater when the control body is coupled with the cartridge, and includes a supercapacitor configured to provide power to the electrical load. The microprocessor is configured to operate in an active mode in which the control body is coupled with the cartridge. In the active mode, the microprocessor is configured to direct power from the supercapacitor to the heating element to activate and vaporize components of the aerosol precursor composition.

The present disclosure provides a coupling system for coupling a medical accessory to an accessory support is provided. The present disclosure also provides a system for powering a medical accessory with an accessory support.

A driving mechanism of a drug infusion device, includes at least one driving unit and at least one driving wheel, the driving unit, moving in the driving direction, driving the driving wheel to rotate; a linear actuator, electrically connected with the driving unit, pulling the driving unit to move in the driving direction after being powered; a switch unit group, including a first switch unit and a second switch unit, the first switch unit electrically connected with the linear actuator; a power supply, the power supply, the switch unit group and the linear actuator electrically connected to form a power supply circuit that supplies power to the linear actuator; when the linear actuator being powered, the driving unit implementing driving, and the driving unit triggering a first signal, indicating the end point of the driving direction.

A pharmaceutical product including a housing that defines a cavity, wherein the cavity stores a pharmaceutical material, and wherein the housing comprises a material configured to dissolve based on contact with a fluid, an ingestible device to encode information in a current signature, wherein the ingestible device is positioned within the housing, and a protective material that encompasses the ingestible device. The ingestible device may be attached to a flexible component, wherein the flexible component is configured to releasably secure the ingestible device within the housing.

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 method of treating a patient by implanting a system comprising an infusion device for injecting a substance, at least one reservoir comprising at least one compartment which accommodates and preserves the substance to be injected, and an active cooling device adapted to cool the reservoir and thereby keep the substance within said at least one compartment of the reservoir at a temperature below 37 C. The method comprises the steps of: cutting the skin, dissecting free at least one area within the patient's body, placing the infusion device and the at least one reservoir inside the patient's body along with the cooling device, such that the at least one reservoir is in fluid connection with the infusion device to supply to the infusion device the substance to be injected into the patient's body, and closing at least the skin after implantation of at least parts of the system.

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.

A control body is coupled or coupleable with a cartridge to form an aerosol delivery device, with the cartridge being equipped with a heating element. The control body includes a power source and a microprocessor. The power source is connected to an electrical load that includes the heater when the control body is coupled with the cartridge, and includes a supercapacitor configured to provide power to the electrical load. The microprocessor is configured to operate in an active mode in which the control body is coupled with the cartridge. In the active mode, the microprocessor is configured to direct power from the supercapacitor to the heating element to activate and vaporize components of the aerosol precursor composition.

A method for determining system resistance of at least one power supply of a handheld medical device, the method including: a) generating at least one excitation voltage signal, wherein the excitation voltage signal comprises at least one direct current (DC) voltage signal, wherein the excitation voltage signal has a fast transition DC flank of 20 ns or less; b) applying the excitation voltage signal to at least one reference resistor having a predetermined or pre-defined resistance value, wherein the reference resistor is arranged in series with the power supply; c) measuring a response signal of the power supply; d) determining a signal flank from the response signal and determining an ohmic signal portion from one or both of shape and height of the signal flank; and e) determining the system resistance of the power supply from the ohmic signal portion.

Systems and devices for improving wireless power transmission are disclosed herein. The system can include an implantable medical device that can include an energy storage component and a secondary coil electrically coupled to the energy storage component. The system can include a charging device. The charging device can include a flexible housing defining an internal volume, a resonant circuit, a plurality of sensors coupled to the primary coil, and processor. The resonant circuit can include a deformable primary coil located within the internal volume of the housing. The processor can determine a deformation of the primary coil based on at least one signal received from at least one of the plurality of sensors.