The invention discloses a closed-loop artificial pancreas device with integrated detection and infusion, comprising: infusion unit configured to deliver drugs; program unit comprising input end and output end, and the input end comprises a plurality of electrically connective regions for receiving signals of analyte data in the body fluid, after the output end is electrically connected to the infusion unit, according to the received signals of analyte data in the body fluid, the program unit controls whether the infusion unit delivers drugs; an infusion cannula with conductive area, the infusion cannula is the drug infusion channel; and a plurality of electrodes for detecting analyte data in body fluid, the electrode comprising conductive-area electrode and cannula-wall electrode, the conductive area of the infusion cannula being at least as a conductive-area electrode, and one or more cannula-wall electrodes being located on/in the wall of the infusion cannula.

A needle end and a safety syringe are provided, belonging to technical field of medical instruments. The safety syringe includes an injection end, a liquid storage device, and a base. The injection end includes a needle base, an injection needle, and a needle guard assembly. The injection needle is fixed to the needle base. The needle guard assembly is connected to the needle base. The needle guard assembly includes a protective casing and a spring, wherein a first terminal of the spring is connected to the needle base and a second terminal of the spring is connected to the protective casing. The liquid storage device includes a liquid storage container and a liquid storage sleeve. The liquid storage is sleeved on an outer surface the liquid storage container, wherein the liquid storage container is detachably connected to the injection end. The base is detachably connected to the liquid storage device.

This invention provides for a component forming a part of a breathing tube, or forming the breathing tube, for example as a part of a breathing circuit for respiratory therapy. The component comprising a tubular body having a foamed wall. The foamed wall can be formed from extrusion of a single extrudate. The foamed wall is of a sufficient minimum optical transparency such that, in use, there is enabled the visual detection of a liquid (or condensate that may have formed) within the tubular body.

Multiple approaches to incorporating multiple conductors on a guidewire by building the multiple conductor traces of variable sizes and material compositions on separate insulating layers are described. The approaches described in the invention facilitate ease of assembly of sensors to the guidewire or catheter element. This approach is particularly useful in scenarios where electrical or mechanical properties of the device need to be altered in specific sections to either enhance device performance and reliability (e.g. selective abrasion resistance), or facilitate ease of assembly (e.g. soldering or connection ease), or in some instances achieve desired electrical characteristics (e.g. impedance). The desired properties are incorporated into the same device requiring an innovative approach to forming signal wires in an otherwise tight space without impacting the primary mechanical performance of the devices.

A unilaterally driven drug infusion device with multiple infusion modes includes a reservoir, a piston, a screw, a driving unit, at least one driving wheel provided with teeth, a linear actuator, a reset unit, and a control unit. The piston is arranged in the reservoir. The driving unit includes a rotating shaft and a driving member, and the driving member includes a driving end. The linear actuator and the reset unit are respectively connected to the driving member. The control unit controls the linear actuator or the reset unit to apply different driving powers on the driving member to make the driving member have a variety of different operating modes.

A personal vapor inhaling unit is disclosed. An electronic flameless vapor inhaler unit that may simulate a cigarette has a cavity that receives a cartridge in the distal end of the inhaler unit. The cartridge brings a substance to be vaporized in contact with a wick. When the unit is activated, and the user provides suction, the substance to be vaporized is drawn out of the cartridge, through the wick, and is atomized by the wick into a cavity containing a heating element. The heating element vaporizes the atomized substance. The vapors then continue to be pulled by the user through a mouthpiece and mouthpiece cover where they may be inhaled.

A system for cooling the brain of a human subject, includes a cooling subsystem which inputs a flow of air or breathable gas, cool the air or breathable gas, and outputs cooled air or breathable gas which is delivered to a human subject. A flow control device controls a flow rate of the flow of the air or breathable gas input to the cooling subsystem and a flow rate of the cooled air or breathable gas delivered to the human subject. One or more flow rate sensors measure at least a flow rate of flow of cooled air or breathable gas. One or more temperature sensors measure at least a temperature of a brain and the temperature of the flow of cooled air or breathable gas. A controller adjusts a cooling rate, the temperature, and the flow rate of flow of cooled air or breathable gas delivered to the human subject to cool the brain of the human subject.

The invention relates to a microneedle array having a heat-generating element and its use for the intradermal application of active ingredients, particularly active pharmaceutical ingredients (API) and drugs, wherein this microneedle array is suitable for skin penetration on humans or animals and the microneedles consist of a water-soluble formulation, which contains at least one active ingredient.

A wall of a catheter (a) includes a braided portion having an outer surface, an inner surface, and a braided interior between the outer and inner surfaces, and (b) is shaped to define first and second longitudinally-running channels therethrough. A distal portion of the catheter is shaped to define first and second lateral openings. An angle between (a) a first line running between the first and second lateral openings, and (b) a second line that is parallel to a central longitudinal axis of the catheter when the catheter is straight, is between 30 and 150 degrees. A flexible longitudinal member passes from a proximal portion of the catheter to the distal portion via the first channel, out of the first channel via the first lateral opening, into the second channel via the second lateral opening, and from the distal portion to the proximal portion via the second channel.

An injection device comprises a housing with a receptacle for a product, a dosing mechanism for setting a product dosage to be administered and for displaying the product dosage that has been set, and a dispensing mechanism for dispensing the product. The dosing mechanism comprises a dosing sleeve which is rotatable relative to the housing in a first direction for setting a product dosage and which is rotatable relative to the housing in a second, opposite direction for correcting or dispensing a product dosage. The dispensing mechanism comprises a piston rod, at least one sleeve, and a clutch. The device further comprises a first detector for detecting movement of the clutch relative to the dosing sleeve and/or the housing and/or the at least one sleeve and a data processing unit connected to the first detector for reading, storing, processing, transmitting, and/or displaying signals received from the first detector.