A rotor for medical flow-regulating devices is described. The rotor comprises a central body and a margin extending from the central body. The margin comprises at least one actionable section that is movable from a rest position to a stretched position with respect to the central body upon application of a force and is configured to resiliently return to the rest position upon removal of the force. A medical flow-regulating device comprising the rotor is also described. A system comprising the medical flow-regulating device and a hand-held activation device is also described. A method of manufacturing a rotor is also described.

A device has a hollow guide shell including an injection end and a longitudinal axis. An actuator magnet is disposed in the hollow guide shell. An injection pin is coupled to the actuator magnet. A driver magnet is positioned on the device radially outward from the actuator magnet. A fluid cartridge is disposed in the injection end of the hollow guide shell, the fluid cartridge including a needle and a plunger. The driver magnet selectively exerts an injection force on the actuator magnet in a direction oriented towards the injection end of the hollow guide shell to engage the injection pin with the fluid cartridge. A liquid, gas or other agent can selectively be ejected from the cartridge by the device to inject the fluid, gas or other agent into another object.

A wireless power transmission method and apparatus are provided. The wireless power transmission method receives a signal associated with a relative position of the wireless power transmission based on a frequency in a high frequency band, and determines whether to wirelessly transmit a power based on an intensity of the received signal.

The present invention relate to a method and corresponding apparatus for just in time mixing of a solid or powdered formulation and its subsequent delivery to a biological body. In some embodiments, a powdered formulation is maintained in a first chamber of a plurality of chambers. A plurality of electromagnetic actuators are in communication with the plurality of chambers. The actuators, when activated, generate a pressure within at least the first chamber. The pressure results in mixing of the powdered formulation and a diluent in time for delivering into the biological body.

A wristwatch wirelessly connected to an implanted medical device such as a VAD is a component of a coplanar energy transfer system. The wristwatch monitors the operation and performance of the VAD or its battery and provides alerts to potentially dangerous situations. The watch can receive signals related to, for example, the current status of the implant (e.g., operating metrics, energy demand, etc.) and current status of the internal battery (e.g., remaining useful life of battery, battery faults, etc.). The wristwatch serves as a redundant external controller of the implanted VAD. The user can interface with the wristwatch to send commands to the VAD and control its performance, power, or charging characteristics with the push of a button. The wristwatch also includes alarm features, which indicate to the user when a fault has occurred or whether there is some situation that requires medical attention.

An infusion system for infusing a medication in a patient, comprising a medication dose dispensing device and a control device for controlling the dispensing device. The infusion system can be configured in a non-operating configuration, in which the dispensing device and the control device are spaced apart from each other, and in an operating configuration, in which the dispensing device and the control device are temporarily proximity-coupled. The actuating rotor of the control device and the actuated rotor of the dispensing device have a common rotation axes, and the system can compensate or block the rotation of the control device with respect to the dispensing device.

The present invention refers to a system for medical treatment comprising a medical device and a separate hand-held device. The medical device comprises an energy-receiving unit and the separate hand-held device comprises a housing and an energy-transfer unit to transfer energy to be used at least in part for performing medical treatment to the energy-receiving unit of the medical device when the energy-receiving unit and the energy-receiving unit are in an energy-transfer position. The system further comprises at least one position sensor adapted to detect at least when the energy-transfer unit and the energy-receiving unit are in the energy-transfer position. The system further comprises a controller for controlling the energy-transfer unit such that the transfer of energy needed for medical treatment from the energy-transfer unit to the energy-receiving unit is enabled only when the energy-transfer unit and the energy-receiving unit are in the energy-transfer position.

An implantable fluid management device, designed to drain excess fluid from a variety of locations in a living host into a second location within the host, such as the bladder of that host. The device may be used to treat ascites, chronic pericardial effusions, normopressure hydrocephalus, hydrocephalus, pulmonary edema, or any fluid collection within the body of a human, or a non-human mammal.

A dry powder delivery device may be configured to provide micronized dry powder particles to airways of a user. The device may include a cylindrical container delimiting a chamber containing at least one magnetically-responsive object, a motor external to said chamber, a magnet external to the chamber and rotatably coupled with the motor, and an outflow member configured to direct airflow to a user. The magnetically-responsive object may be coated with micronized dry powder particles, and the motor may be operable to rotate the magnet about an axis. Rotation of the magnet creates a magnetic field that causes the magnetically-responsive object to move in response to the magnetic field and collide with a side wall of the container to deaggregate the dry powder particles and aerosolize the dry powder in the chamber.

A dry powder delivery device may be configured to provide micronized dry powder particles to airways of a user. The device may include a cylindrical container delimiting a chamber containing at least one magnetically-responsive object, a motor external to said chamber, a magnet external to the chamber and rotatably coupled with the motor, and an outflow member configured to direct airflow to a user. The magnetically-responsive object may be coated with micronized dry powder particles, and the motor may be operable to rotate the magnet about an axis. Rotation of the magnet creates a magnetic field that causes the magnetically-responsive object to move in response to the magnetic field and collide with a side wall of the container to deaggregate the dry powder particles and aerosolize the dry powder in the chamber.