A wearable, conductive textile patch is provided that may include any of a number of features for monitoring body analytes and/or delivering fluids to a body. In one embodiment of the invention, a single, patch-mounted system monitors glucose levels of a diabetic person and provides appropriate doses of insulin in response to the glucose measurements. A hand-held user interface can be provided for wirelessly controlling the system and/or receiving information from it. Conductive pathways can be formed in the fabric of the patch. Components that can be integrated into the flexible patch include a power source, controller, transmitter, antenna, temperature and other sensors, fluid pump, infusion set, electrical pathways, switches, controls, electrodes, connectors, resistors and other circuit elements. Such components can be embedded, interwoven or coated on to the flexible patch instead of or in addition to surface mounting. Methods associated with use of the flexible patch system are also covered.

Cartridges are configurable between a closed state and an open state. The cartridges include a cartridge body and a reservoir disposed in the cartridge body. The cartridge body has an outer locking element, and the reservoir has a rotational locking element. In the closed state, the outer locking element engages the rotational locking element such that the reservoir cannot be rotated out of a first rotational position relative to the cartridge body in which a fluid outlet of the reservoir is not in fluid communication with a fluid outlet of the cartridge body. In the open state, the outer locking element of the cartridge body does not engage the rotational locking element of the reservoir, and the reservoir is in a second rotational position relative to the cartridge body such that the fluid outlet of the reservoir is in fluid communication with the fluid outlet of the cartridge body.

Method and apparatus for providing an integrated analyte sensor and data processing unit assembly is provided.

The present invention provides an injection device (1, 101, 201) comprising a housing (2, 102, 202), a cartridge (30, 130, 230) holding a medical substance and comprising an outlet and a piston (31, 131, 231), a dose expelling mechanism comprising a piston rod system (10, 50, 110, 150, 210, 250) adapted to be moved relative to the housing (2, 102, 202) during a dose expelling action to thereby advance the piston (31, 131, 231) in the cartridge (30, 130, 230), and a ratchet arm (12) operatively coupled with the piston rod system (10, 50, 110, 150, 210, 250) and configured to undergo a deflecting motion relative to the housing (2, 102, 202) during a particular movement of the piston rod system (10, 50, 110, 150, 210, 250) which corresponds to a predetermined volume of the medical substance being expelled from the cartridge (30, 130, 230), the deflecting motion comprising a first part motion which decelerates the piston rod system (10, 50, 110, 150, 210, 250) followed by a second part motion which accelerates the piston rod system (10, 50, 110, 150, 210, 250), an integrated sensor (76, 176, 276) arranged to detect occurrences of acceleration of the piston rod system (10, 50, 110, 150, 210, 250), and a processor (75, 175, 275) configured to register the occurrences detected by the integrated sensor (76, 176, 276) during the dose expelling action.

Described herein is a respiratory therapy system comprising: a primary power supply, a secondary power supply, and a breathing apparatus configured to provide respiratory therapy. The breathing apparatus comprises a controller. There is a connection between the primary power supply and the breathing apparatus configured to facilitate transmission of power and data between the primary power supply and the breathing apparatus. The controller is configured to monitor a parameter of the primary power supply, and disengage the primary power supply if the parameter differs from a parameter threshold. The controller is configured to engage the secondary power supply on disconnection of the primary power supply such that the breathing apparatus can continue operation without interruption.

A breast pump relating to the technical filed of breast pumps is provided, comprising a base, a breast pump assembly and a ventilation tube. The base includes a housing and a pneumatic pump, and the pneumatic pump is arranged in the housing. The breast pump assembly is used for pumping the milk of the mammary gland, and is detachably connected to the housing. When the breast pump assembly is separated from the housing, the ventilation tube is connected to the pneumatic pump and the breast pump assembly, so that the pneumatic pump forms a negative pressure on the breast pump assembly. The breast pump assembly is connected to the housing when the ventilation tube is disconnected from the pneumatic pump and the breast pump assembly. The base included in the above breast pump assembly is detachably connected to the breast pump assembly. When it needs to be used separately, the base and the breast pump assembly is disassembled and separated first, and then the ventilation tube is connected to the pneumatic pump and the breast pump assembly. When it is not required to be used separately, the ventilation tube is disassembled and the breast pump assembly can be connected to the base. The breast pump has strong compatibility, can meet the various needs of users, and has a good user experience.

An atomizer for an inhaler includes a housing, a gasket, a liquid absorbing sheet, a wick, and an atomizing element. The housing includes a first housing and a second housing, the first housing and the second housing form a liquid reservoir therebetween for storing liquid. The gasket is sleeved on the first housing, the gasket defines a liquid conducting hole in communication with the liquid reservoir. The liquid absorbing sheet is sleeved on the first housing in contact with the gasket, the liquid absorbing, sheet is configured to absorb the liquid in the liquid reservoir via the liquid conducting hole. The wick is in contact with the liquid absorbing sheet and configured to draw the liquid from the liquid absorbing sheet. The atomizing element is fixed to the wick and configured to atomize the liquid in the wick.

A respiratory apparatus includes components to protect operations of the apparatus. For example, in some versions, the apparatus may include a power supply, a motor powered by the power supply, and a transient absorption diode circuit between the motor and the power supply. The transient absorption diode circuit may be configured to absorb energy generated by the motor from rotational kinetic energy. Such absorption may serve to protect the components of the apparatus. In some examples, the apparatus may include a fault mitigation integrated circuit (IC). The IC circuit may be included in the respiratory apparatus to detect one or more faults based on physical and system parameters of the apparatus. The fault mitigation integrated circuit may generate a signal to stop the motor based on the detected fault, and may digitally communicate with a processor information about the detected fault.

A liquid medicine injection device includes: a liquid medicine storage unit including a cylinder including a space configured to store liquid medicine therein and a discharge hole connected to the space, and a piston arranged inside the cylinder and moving toward the discharge hole depending on discharge of the liquid medicine; a first electrode on an outer surface of the cylinder; a second electrode on the outer surface of the cylinder, the second electrode facing the first electrode with the piston therebetween; and a circuit unit including a substrate electrically connected to the first electrode and the second electrode.

A monitoring device may include a housing, which may include a distal end, a proximal end, and a fluid pathway extending through the proximal end and distal end. The distal end may include a connector configured to couple to a catheter assembly. The monitoring device may include one or more sensors disposed within the fluid pathway. The sensors may facilitate identification of an occlusion within the catheter assembly.