A disposable single-piston dual-action reciprocating pump part includes a single piston, an output port, and a balloon damper. The output port is configured for outputting fluid pumped by the single piston. The balloon damper is fitted in the output port, and the balloon damper is configured to suppress a pulsation in a flow rate of the outputted fluid.

The present technology is directed to a respiratory pressure therapy system, that includes a plenum chamber pressurisable to a therapeutic pressure above ambient air pressure, a seal-forming structure to form a seal with an entrance to the patient's airways to maintain said therapeutic pressure in the plenum chamber throughout the patient's respiratory cycle in use, a positioning and stabilising structure constructed and arranged to provide an elastic force to hold the seal-forming structure in a therapeutically effective position on the patient's head, a blower configured to generate the flow of air and pressurise the plenum chamber to the therapeutic pressure, the blower having a motor, the blower being connected to the plenum chamber such that the blower is suspended from the patient's head and the axis of rotation of the motor is perpendicular to the patient's sagittal plane, and a power supply configured to provide electrical power to the blower.

This disclosure describes devices, systems, and methods related to a connector for a dressing, such as a dressing of a hyperbaric oxygen therapy system. An example of a connector includes a connector body configured to define at least a portion of a first channel. The connector also includes a viewing member coupled to the connector body. The connector further includes a deformable member positioned within the first channel. The deformable member is configured to deform based on a pressure associated with the deformable member and to provide a visual indication, via the viewing member, of the pressure.

In one example embodiment, a system for stimulating healing of tissue at a wound site is disclosed. The system comprises a dressing including a porous pad and a drape covering the pad at a wound site for maintaining negative pressure at a wound site, a negative-pressure source including a pump and an electric motor to generate a pump pressure (PP) for applying to the wound site, and a first pressure sensor for sensing the pump pressure (PP). The system further comprises a controller coupled to the first pressure sensor and electric motor and including a PID controller that compares the pump pressure (PP) to a target pump pressure (TPP) and a bang-bang controller that controls wound pressure (WP) proximate the wound site, and wherein the controller is configured to alternatively select the bang-bang controller when the system is in a low-leakage condition or the PID controller when the system is in a high-leakage condition.

Provided is an oxygen concentration device, a control method, and a control program with which a start-up interval until a desired high-concentration oxygen gas can be supplied can be reduced. The oxygen concentration device includes a pressurized air supply unit for supplying pressurized air, an adsorption tube which concentrates oxygen in the pressurized air by adsorbing nitrogen in the supplied pressurized air to generate oxygen gas, an oxygen gas tank for storing oxygen gas, a flow rate adjustment unit which adjusts an oxygen gas flow rate to be output to the exterior from the oxygen gas tank, and a control unit which controls the flow rate adjustment unit so that the oxygen gas flow rate becomes a set flow rate and controls the pressurized air supply unit so that the pressurized air achieves a supply amount corresponding to the set flow rate.

A suction discharge unit of a suction discharge device includes a first unit and a second unit. The second unit controls the pressure inside the first unit. The first unit includes a storage chamber and a water sealing chamber. The water sealing chamber includes a first chamber communicating with the storage chamber, and a second chamber is sealed from the first chamber by sealing water. A negative pressure control unit is disposed in the second chamber. The negative pressure control unit includes a liquid retaining part retaining a liquid, a control member including control holes, and a support tube supporting the control member. The negative pressure control unit controls the pressure of the first chamber by causing gas to flow from the second chamber into the first chamber via the control holes and the liquid based on the pressure of the second chamber and the pressure of the first chamber.

The present technology is directed to a respiratory pressure therapy system, that includes a plenum chamber pressurisable to a therapeutic pressure above ambient air pressure, a seal-forming structure to form a seal with an entrance to the patients airways to maintain said therapeutic pressure in the plenum chamber throughout the patients respiratory cycle in use, a positioning and stabilising structure constructed and arranged to provide an elastic force to hold the seal-forming structure in a therapeutically effective position on the patients head, a blower configured to generate the flow of air and pressurise the plenum chamber to the therapeutic pressure. the blower having a motor, the blower being connected to the plenum chamber such that the blower is suspended from the patients head and the axis of rotation of the motor is perpendicular to the patients sagittal plane, and a power supply configured to provide electrical power to the blower.

A method for safe radioisotope preparation and injection of H.sub.2.sup.15O for use in Positron Emission Tomography (PET). The disclosure also relates to a safety valve for controlling a flow of H215O for use in PET, to a use of said safety valve and to a method for preparing and injecting H.sub.2.sup.15O.

A cuff pressure stabilizer (100, 200, 300, 500, 600, 800) is provided that includes an inflation lumen proximal port connector (134), which is shaped to form an air-tight seal with an inflation lumen proximal port (15) of a catheter (10) additionally having an inflatable cuff (11) and an inflation lumen (13); a fluid reservoir (120, 524, 624); a liquid column container (118, 518, 618), which is (a) open to the atmosphere (99) at at least one site along the liquid column container, (b) in fluid communication with the fluid reservoir (120, 524, 624), and (c) in communication with the inflation lumen proximal port connector (134) via the fluid reservoir (120, 524, 624); and a liquid (121), which is contained (a) in the fluid reservoir (120, 524, 624), (b) in the liquid column container (118, 518, 618), or (c) partially in the fluid reservoir (120, 524, 624) and partially in the liquid column container (118, 518, 618), and which has a density of between 1.5 and 5 g/cm3 at 4 degrees Celsius at 1 atm.

Pressure conditioning systems for supplying insufflation gas to an open-ended body conduit such as a rectal cavity during a transanal minimally invasive surgery (TAMIS) procedure can reduce billowing of walls of the body conduit. A pressure conditioning system can include a pressure storage component, an accumulator, and a flow restrictor. The pressure storage component can include a variable volume reservoir that is biased to a relatively low volume state. The flow restrictor can include insufflation tubing with a restrictor plate having a relatively low diameter orifice. The pressure storage component, accumulator, and flow restrictor can be fluidly connected in various orders in series or as side branches from a gas flow conduit. Despite a pulsed or otherwise discontinuous insufflation gas flow and leakage and absorption from the body conduit, the pressure conditioning system can maintain a constant pressure within the body conduit.