A respiratory filter and condensate management apparatus is provided for use in a breathing circuit during patient respiration. The apparatus includes a housing having an air inlet port for receiving a flow of respiratory air, and an air outlet port for outputting the flow of respiratory air to a ventilator. A filter compartment is provided within the housing and includes a filter member located in a flow path of the respiratory air from the air inlet port to the air outlet port. A condensate collection compartment is provided within the housing and includes at least one reservoir and at least one self-sealing drainage port. The reservoir collects liquid formed by condensation of the respiratory air within the filter compartment, and the drainage port allows removal of the collected liquid from the reservoir while the housing remains connected to the breathing circuit.

A display device of an anesthesia machine which is communicable with at least one syringe pump that is an external apparatus displays an anesthesia information display screen. When a call switch is operated, a syringe pump information display screen indicating operation information of the syringe pump is displayed on the display device, in addition to the anesthesia information display screen.

An HME device, used in a closed breathing circuit of a ventilation system, has a housing with an inlet opening and with an outlet opening, an HME chamber (50a; 50b; 50c; 50d; 50e; 50f; 50g; 50h; 50i) arranged between the inlet opening and the outlet opening for receiving an HME medium and a switching mechanism (70a; 70b; 70c; 70d; 70e; 70f; 70g; 70h; 70i). The HME device can be switched over between an HME mode (M1), in which an HME fluid passage is provided from the inlet opening through the HME chamber to the outlet opening, and a bypass mode (M2), in which a fluid bypass passage is provided from the inlet opening past the HME chamber through a bypass channel (80a; 80b; 80d; 80e; 80f; 80h) in the housing to the outlet opening. The bypass channel is blocked with respect to the HME chamber in the bypass mode (M2).

Disclosed is a respirator which comprises an electronic control device and a pneumatic main line in which the following are connected pneumatically: a respiratory gas source, a valve, a mixing chamber, a gas-dosing unit, and a supply line. The gas-dosing unit is configured to convey external air and/or oxygen and/or anesthetic gas into the mixing chamber, the respiratory gas source is configured to deliver respiratory gas to the supply line, the mixing chamber is configured to make available respiratory gas, the supply line is configured to supply the patient with respiratory gas, and the valve is configured to at least temporarily reduce a stream of respiratory gas to a patient.

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 preflushing unit (10) preflushes a breathing gas circuit (210) of a closed-circuit respirator (200). A basic body (20) has an inlet port (22), feeding breathing gas from a breathing gas supply (220), an outlet port (24) discharging breathing gas into the breathing circuit, and a flow section (32) fluid connecting a valve chamber (30). A valve body (40) with a sealing surface (42) is arranged in the valve chamber (30). An elastomer body (50) with a counter-sealing surface (52) in the valve chamber, fluid tight separates the flow section from a control section (34). The counter-sealing surface acts with a sealing force against the valve body for sealing the flow section. A control port (26) of the basic body provides a controlled feed of breathing gas from the breathing gas supply into the control section for pressure equalization between the flow section and the control section.

Apparatus for the respiration of patients with means for the circulation in one direction of respiratory gas, with a connection for the patient and with further connections for the supply and discharge of the various components of the gas, whereby the device is provided with means by which the pressure in the line system can be varied according to a certain respiratory pattern, with a primary part that is connected to means for the generating of a work fluidum, the varying pressure of which can establish the varying of the pressure in the line system, and with a secondary part that is part of or is connected to the line system, whereby a cylinder is provided which is divided in a part that connects to the primary part and a part that connects to the secondary part by a disc that is movable relative to the inner wall thereof.

Systems and methods are provided for portable and compact nitric oxide (NO) generation that can be embedded into other therapeutic devices or used alone. In some embodiments, an ambulatory NO generation system can be comprised of a controller and disposable cartridge. The cartridge can contain filters and scavengers for preparing the gas used for NO generation and for scrubbing output gases prior to patient inhalation. The system can utilize an oxygen concentrator to increase nitric oxide production and compliment oxygen generator activity as an independent device. The system can also include a high voltage electrode assembly that is easily assembled and installed. Various nitric oxide delivery methods are provided, including the use of a nasal cannula.

A control system controls fresh gas dispensing for an anesthesia device, with a patient gas-measuring unit, an anesthetic-dispensing unit, a user interface, and a fresh gas regulation unit. With a transition from deactivated assistance mode to activated assistance mode, a processing unit receives a measured signal, a fresh gas signal and an assistance signal and calculates an end tidal anesthetic concentration over time based on a current volume flow, a predefined volume flow and on a current end tidal anesthetic concentration and stores this as a preset curve. A fresh gas correction signal is output upon the determined current end tidal anesthetic concentration leaving a surrounding range of the preset curve. A predefined volume flow curve is changed as a function of the correction signal. The volume flow of fed fresh gas is increased when the surrounding range is undershot and is reduced when the surrounding range is exceeded.

Nasal tracheal devices include a tube with visual indicia of insertion depth corresponding to patient height and an inflatable cuff. The tube comprises or provides a plurality of lumens that are in fluid isolation including an airpath lumen and a pressurized fluid source for inflating the cuff. The devices may also be configured to suction patient fluid from a location adjacent and/or above the cuff.