A vaporizer device includes a resistive heating element; circuitry configured to control delivery of electrical power to the resistive heating element from a power source; and a controller configured to perform operations including: receiving inputs representative of a power delivery to the resistive heating element, a temperature of the resistive heating element, and/or a flow rate of air past the resistive heating element; predicting, using the received inputs, an amount of evaporation of the vaporizable material at the resistive heating element; and controlling the power delivery to the resistive heating element in response to the predicted amount of evaporation of the vaporizable material, the controlling including increasing or decreasing an instantaneous power delivery to the heating element such that a target aerosol yield is produced. Related devices, systems, methods, and articles are also described.

A resuscitation management system for a manual resuscitator may include a radio frequency identification (RFID) tag that may be configured to be mounted on a first side of a bag of the manual resuscitator. The RFID tag may be configured to transmit information indicative of the presence of the RFID tag. The system may further include an RFID reader that may be configured to be mounted on an opposite second side of the bag. The RFID reader may be configured to generate an output signal corresponding to the presence of the RFID tag responsive to receiving the information transmitted by the RFID tag. The RFID reader may be configured to receive the information transmitted by the RFID tag responsive to the RFID tag being at a distance from the RFID reader smaller than a predetermined threshold.

Magnetic-based electronic valve readers for determining a location and orientation of magnets coupled to implantable medical devices to determine a setting of the device (e.g., setting of a fluid flow control valve of the medical device). The electronic valve readers include an orientation sensing mechanism that is provided and configured to enable the electronic valve reader to: 1) allow for internal offset calculation of an orientation change of the electronic valve reader during a reading process; and/or 2) during the reading process, provide an indication or warning to the clinician that the orientation of the electronic valve reader has changed to an extent at or exceeding a predetermined angular acceptance threshold or window. Systems including the disclosed electronic valve readers and methods of reading a setting of the device are also disclosed.

Devices, systems, and methods are provided herein for delivering medication (e.g., insulin) via a wearable pump having a patch-style form factor for adhesion to a user's body. The reusable pump may be coupled to a disposable cap housing a microdosing system for delivering precise, repeatable doses of medication to a cannula configured to deliver medication to a target infusion area beneath the user's outer skin layer. The system further may include an applicator for inserting the cannula into the user's skin and/or applying an adhesive pad to the skin.

An autoinjector includes a housing, a product container, a torsion spring, a drive element, and a propulsion element. In order to discharge liquid out of the product container, the torsion spring rotates the drive element, and the rotating drive element produces a propulsive movement of the propulsion element and of a piston in the product container. A rotation sensor is configured for an alternating continuous detection of at least two rotational positions per revolution of the drive element during the discharge process, and a processor unit is configured for determining the axial position of the piston in the product container from the detected rotational positions.

The invention relates to device (1) for measuring volumes of a liquid in a container (B) by means of measuring emitted high-frequency radiation, comprising control unit (C), a transmitter (TX), at least one first transmitting antenna (ANT_TX1) and at least one second transmitting antenna (ANT_TX2), at least one receiving antenna (ANT_RX1) and a receiver (RX), wherein the transmitter (TX) is configured to emit high-frequency radiation when in operation, wherein the first transmitting antenna (ANT_TX1) and the second transmitting antenna (ANT_TX2) are configured to emit high-frequency radiation during operation so that radiation can reach the container (B), wherein first receiving antenna (ANT_RX1) is configured to record high-frequency radiation reflected from the container (B), wherein the receiver (RX) is configured to take up the high-frequency radiation received by the receiving antenna (ANT_RX1), wherein the control unit (C) is configured to control the transmitters so that the transmitter (TX) emits high-frequency radiation, and wherein the control unit (C) is also configured to evaluate high-frequency radiation taken up by the receiver (RX) so that a measurement of the volume of the liquid in the container (B) is determined, wherein the measurement of the volume of liquid in the container (B) is determined from channel state information. The invention also relates to device (1) for measuring volumes of a liquid in a container (B) by means of measuring emitted high-frequency radiation, comprising a control unit (C), a transmitter (TX), at least one first transmitting antenna (ANT_TX1) and at least one second transmitting antenna (ANT_TX2), a least one first receiving antenna (ANT_RX1) and a second receiving antenna (ANT_RX2) and a receiver (RX), wherein the transmitter (TX) is configured to emit high-frequency radiation when in operation, wherein the first transmitting antenna (ANT_TX1) and the second transmitting antenna (ANT_TX2) are configured to emit high-frequency radiation during operation so that radiation can reach the container (B), wherein the first receiving antenna (ANT_RX1) is configured to record high-frequency radiation reflected from the container (B), wherein the second receiving antenna (ANT_RX2) is configured to record high-frequency radiation transmitted from the container (B), wherein the control unit (C) is configured to control the transmitters so that the transmitter (TX) emits high-frequency radiation, and wherein the control unit (C) is also configured up to evaluate high-frequency radiation taken up by the r

A security tag can prohibit unauthorized usage of a device or product. The device may include an electronic nicotine delivery systems (“ENDS”) device, which may include aerosol delivery devices such as smoking articles that produce aerosol. The security tag can prevent usage until authorized. Attempts at usage without authorization can result in the device being unusable. The authorization may include identity confirmation or age verification.

Aspects of the instant disclosure relate to an elongated medical device. In particular, the instant disclosure relates to apparatuses for sensing contact force. In various embodiments, a force sensing element including a tip and a catheter shaft, wherein the tip is configured to move relative to the shaft when an external force is applied to the tip comprising a transmitter configured to transmit a transmitter signal when external force is applied to the tip, a first plurality of sensors and a second plurality of sensors positioned proximate the transmitter, wherein each of the sensors is configured to receive the transmitter signal and the first plurality of sensors is longitudinally offset from the second plurality of sensors.

An injection system can have a Syringe Dose and Position Apparatus (SDPA) mounted to a syringe. The SDPA can have one or more circuit boards. The SDPA can include one or more sensors for determining information about an injection procedure, such as the dose measurement, injection location, and the like. The SDPA can also include a power management board, which can be a separate board than a board mounted with the sensors. The syringe can also include a light source in the needle. Light emitted from the light source can be detected by light detectors inside a training apparatus configured to receive the injection. The syringe can have a power source for powering the sensors and the light source. The SDPA and the power source can be mounted to the syringe flange.

An extracorporeal blood treatment apparatus is provided comprising a filtration unit (2) connected to a blood circuit (17) and to a dialysate circuit (32), a preparation device (9) for preparing and regulating the composition of the dialysis fluid; a control unit (12) is configured for receiving a conductivity or sodium concentration set point for the dialysis fluid and for calculating a mass transport of a substance at an instant t of a treatment session based on said set value of the parameter for the dialysis fluid in the dialysis supply line (8).