A device for controlling the functioning of a cardiac prosthesis, the device for controlling includes a control path, the control path having a control system designed and arranged to monitor and regulate the electrical supply of a cardiac prosthesis; a first insulating system designed and arranged to electrically insulate the cardiac prosthesis from the electrical supply; and a controller designed and arranged to monitor and regulate the electrical supply.

Over-enthalpy conditions when using a respiratory and/or surgical humidifier system can be prevented. A heating element power in an inspiratory conduit can be limited based at least in part on one or more parameters of the gases flow, and/or on an ambient temperature. The limit on the heating element power in the inspiratory conduit can be achieved using a processor and/or protection circuit(s) located outside the processor. For example, the system can use the processor to determine and/or apply the limit as a level of protection and use the protection circuit(s) as another level of protection.

Embodiments of negative pressure wound therapy systems and methods are disclosed. In one embodiment, a system includes a wound dressing, negative pressure source, switch, and control circuitry. The switch can include an actuator that toggles states of first and second pairs of contacts in response to a user input. The control circuitry can supply negative pressure with the negative pressure source when the state of the first pair of contacts is a first state and the state of the second pair of contacts is a second state, and the control circuitry can disable supply of negative pressure with the negative pressure source when the state of the first pair of contacts is not the first state or the state of the second pair of contacts is not the second state.

A connector unit for a control unit is configured to control an implantable blood pump. The connector unit includes a supply interface designed for connecting the connector unit to a power supply, a data interface designed for connecting the connector unit to a data processing unit, and a control interface designed for connecting the connector unit to an integrated interface of the control unit. A supply connection of the control unit to the power supply and a data connection of the control unit to the data processing unit can be established at the same time by means of the connector unit. The application furthermore relates to a control unit for controlling an implantable blood pump and to a control system for an implantable blood pump.

Therapy gas delivery systems that provide run-time-to-empty information to a user of the system and methods for administering therapeutic gas to a patient. The therapeutic gas delivery system may include a gas pressure sensor attachable to a therapeutic gas source that communicates therapeutic gas pressure data to a therapeutic gas delivery system controller, a gas temperature sensor positioned to measure gas temperature in the therapeutic gas source that communicates therapeutic gas temperature data to the therapeutic gas delivery system controller, at least one flow controller that communicates therapeutic gas flow rate data to the therapeutic gas delivery system controller, at least one flow sensor that communicates flow rate data to the therapeutic gas delivery system controller, and at least one display that communicates run-time-to-empty to a user of the therapeutic gas delivery system. The therapeutic gas delivery system controller of the system includes a processor that executes an algorithm to calculate the run-time-to-empty from the data received from the gas pressure sensor, temperature sensor, flow controller and flow sensor, and directs the result to the display.

The present invention relates to a system (1; 1A) for use in connection with mechanical ventilation of a patient (3), provided by a ventilator (5). The system comprises a sensor arrangement (7; 7A; 7B) configured to register at least one signal (S.sub.LP; S.sub.LP(TA), S.sub.LP(CT); S.sub.e1-5; S.sub.e11-12), herein referred to as LP signal, related to muscular activity of at least one muscle (17, 19) in the laryngopharyngeal region (9) of said patient (3). Furthermore, the system comprises at least one control unit (11; 11A, 11B) configured to control the operation of said ventilator (5) based on said at least one LP signal, and/or to cause display of information related to said at least one LP signal on a display unit (13A, 13B) for monitoring said patient (3) and/or the operation of the ventilator (5).

An aerosol delivery system that includes an aerosol generator that aerosolizes a fluid for delivery to a patient. The aerosol generator includes a housing with a fluid chamber that fluidly communicates with a housing inlet and a housing outlet. Within the housing, the aerosol generator includes a support plate with an aperture that fluidly communicates with the housing outlet. A vibratable member couples to the support plate across the aperture. A piezoelectric actuator also couples to the support plate, and in operation expands and contracts to vibrate the vibratable member, which aerosolizes a fluid. The aerosol generator receives fluid through a fluid conduit that couples to the housing.

An infusion pump device comprises a pump unit having an inlet and an outlet, a connector being in fluid communication with the inlet of said pump unit, a medication reservoir accommodation portion for accommodating a medication reservoir having a label or tag so that an outlet of the medication reservoir is to be coupled to said connector, and a reader which is provided at said medication reservoir accommodation portion so that the reader is adapted to read a label or tag of the medication reservoir when arranged at said medication reservoir accommodation portion.

A peristaltic infusion pump tube segment comprises a first tube portion having a surrounding wall adapted for an upstream occlusion detection, a second tube portion downstream of said first tube portion and adapted to be temporally engaged by an engagement structure, wherein said second tube portion comprises a surrounding wall being at least partly thicker than the wall of said first tube portion and made of an elastic material which allows said second tube portion to be essentially reformed at those portions which are currently not subject to the engagement by the engagement structure, a third tube portion downstream of said second tube portion and having a surrounding wall adapted for an air in line detection, and a fourth tube portion adapted for a downstream pressure detection. The peristaltic infusion pump tube segment is provided in an infusion pump device which comprises a pump mechanism configured as a peristaltic mechanism.

Embodiments relate to systems and methods for gas delivery for personal medical consumption having safety features. A hydrogen or oxygen gas delivery system herein can include electrolytic cores performing electrolysis-based reactions, and obtain free hydrogen (H2) gas for collection and delivery to a user. In aspects, the electrolytic core(s) can be scaled to produce a sufficient amount of hydrogen (H2) or oxygen (O2) gas so that the user can ingest that gas directly, without a need for storage. The system can be portable, and configured with a delivery tube for transmitting hydrogen or oxygen gas to a user. While safety risks are generally minimal, the system can be configured with sensors to detect fault conditions or hazards such as combustion or overpressure, which can only be caused by deliberate user action to expose gaseous products to flame or spark, and even then would not be likely to trigger violent combustion.