A gas distributor for a rebreather, the gas distributor being configured for connection with an inhale hose and with an exhale hose with a mouthpiece in between, wherein the gas distributor comprises a gas distributor housing, an inhale chamber at the gas distributor housing and comprising a first inhale port for connection with an inhale counterlung or with a scrubber, a second inhale port for connection with the inhale hose, and a gas supply valve for supplying gas on demand, an exhale chamber at the gas distributor housing and comprising a first exhale port for connection with an exhale counterlung or with a scrubber, a second exhale port for connection with the exhale hose, and an overpressure valve for opening in an event of overpressure, and a switch arranged at the gas distributor housing and configured for being switchable between an open circuit mode and a closed circuit mode.

A patient interface assembly includes a frame with a central aperture by which a flow of pressurized breathable gas is introduced in use. The frame includes a wall on a central portion of the frame that surrounds the central aperture. A cushion is removably secured to the frame at the wall surrounding the central aperture and is made of a material that is relatively softer than the frame. A headgear assembly includes a pair of strap portions constructed of a flexible fabric material. A pair of yoke portions is positioned between the strap portions and the frame. Each yoke portion has a proximal end adjacent the frame and a distal end having a connector slot that connects to the respective strap portion of the headgear assembly. The yoke portions have a multilayer construction with one layer being a fabric layer. The yoke portions have a degree of flexibility in one direction and are more resistant to bending in another direction generally orthogonal to the one direction to resist vertical rotation of the patient interface assembly.

An anesthetic vaporizer system includes a reservoir containing anesthetic agent, an agent level sensor measuring an agent level of the anesthetic agent in the reservoir, a display, and a controller. The controller is configured to receive agent level measurements from the agent level sensor over a time period, and determine the anesthetic agent is being added to the reservoir from an agent source based on the agent level measurements over the time period. A filling status is determined based on the agent level measurements and a filling status indicator is displayed based on the determined filling status.

A gas washout vent, and a patient interface with the gas washout vent, configured to allow patient-exhaled CO.sub.2 to flow to an exterior of the plenum chamber to minimise rebreathing of exhaled CO.sub.2 by the patient, the gas washout vent including at least one outlet orifice; a diffusing member at least partly covering the outlet orifice; and a blocking member having an air-impermeable material, the blocking member preventing gas exiting from the outlet orifice from flowing straight through the diffusing member.

A gas washout vent, and a patient interface with the gas washout vent, configured to allow patient-exhaled CO.sub.2 to flow to an exterior of the plenum chamber to minimise rebreathing of exhaled CO.sub.2 by the patient, the gas washout vent including at least one outlet orifice; a diffusing member at least partly covering the outlet orifice; and a blocking member having an air-impermeable material, the blocking member preventing gas exiting from the outlet orifice from flowing straight through the diffusing member.

A relay administration device 50 for use in connection to a nitric oxide administration device 20 which supplies NO generated from air, includes an NO densitometer 506, a flowmeter 507 or pressure gauge 504, a control unit 600 which calculates a dosage of NO to be administered to a patient based on an NO concentration measured by the NO densitometer 506 and a value of the flowmeter 507 or the pressure gauge 504, and a two-way valve 505 which is configured to increase a flow rate when the calculated dosage is less than a predetermined value and to decrease the flow rate when the calculated dosage is greater than a predetermined value.

Systems and methods for generating nitric oxide are disclosed. A nitic oxide (NO) generation system includes at least one pair of electrodes configured to generate a product gas containing NO from a flow of a reactant gas; and a controller configured to regulate the amount of nitric oxide in the product gas produced by the at least one pair of electrodes by utilizing duty cycle values of plasma pulses selected from a plurality of discrete duty cycles to produce a target rate of NO production based on an average of discrete production rates associated with each of the plurality of discrete duty cycles.

A ventilator for respiration gas supply, comprising a respiration gas source, a control unit, a memory, a pressure sensor and/or a flow sensor, an exchangeable respiration gas tube, at least one connection stub for the respiration gas tube, a patient interface and a valve. The control unit is set up to use signals from the pressure sensor and/or flow sensor to ascertain the patient's respiration phase and to ascertain the patient's current tidal volume during successive inhalations and exhalations and to compare a first set volume threshold for the tidal volume with the current tidal volume and to determine whether the latter is below the former and if so, to react by driving the respiration gas source to set a second pressure for the respiration gas for inhalation and driving the respiration gas source to set the CPAP pressure for the respiration gas for exhalation.

A ventilator for respiration gas supply, comprising a respiration gas source, a control unit, a memory, a pressure sensor and/or a flow sensor, an exchangeable respiration gas tube, at least one connection stub for the respiration gas tube, a patient interface and a valve. The control unit is set up to use signals from the pressure sensor and/or flow sensor to ascertain the patient's respiration phase and to ascertain the patient's current tidal volume during successive inhalations and exhalations and to compare a first set volume threshold for the tidal volume with the current tidal volume and to determine whether the latter is below the former and if so, to react by driving the respiration gas source to set a second pressure for the respiration gas for inhalation and driving the respiration gas source to set the CPAP pressure for the respiration gas for exhalation.

Techniques described herein can identify usage information for sensors. In one example, an anesthesia device can include a processor to obtain usage information from a first flow sensor coupled to the anesthesia device. The processor can also determine the usage information exceeds a predetermined limit and generate an alert indicating the first flow sensor is to be replaced.