An infusion device (1) for acting onto a tube set (2) to transport a medical fluid through the tube set (2) comprises a first housing element (10) constituted to receive a tube section (200, 201) of the tube set (2) and a second housing element (11) being movable with respect to the first housing element (10) such that, in a closed position of the second housing element (11), the first housing element (10) and the second housing element (11) are constituted to receive the tube section (200, 201) in between each other. A sensor device (3) is arranged on the first housing element (10) and having a sensor element (30) for measuring a force on the tube section (200, 201) of the tube set (2). Herein it is provided that the sensor device (3) is arranged on the first housing element (10) in an elastically displaceable manner, wherein the sensor device (3) is supported on the first housing element (10) via at least one spring element (33). In this way an infusion device is obtained which may be less prone to variations in the squeezing of a tube section in between the sensor element and a movable housing element, potentially reducing the effort for calibrating infusion devices and increasing the reliability of pressure measurements on a tube section.

Systems and methods are disclosed for monitoring for an occlusion in an aspiration line during an ophthalmic surgical procedure. An ophthalmic surgical system may comprise a first aspiration pump located in a handpiece, a second aspiration pump located away from the handpiece such as in a console, and a pressure sensor located between the first aspiration pump and the second aspiration pump. The pressure sensor is adapted to monitor for an occlusion in the aspiration line upstream of the first aspiration pump. The second aspiration pump may be operated at the same flow rate as the first aspiration pump and/or to maintain a constant pressure between the second aspiration pump and the first aspiration pump. Systems and methods as disclosed allow for a handpiece pump located close to the working tip while providing reliable occlusion detection with a pressure sensor located away from the handpiece.

Methods and systems are provided for delivering anesthetic agent to a patient. In one embodiment, a system includes an anesthetic agent reservoir, a pump fluidically coupled to the agent reservoir, an injector configured to receive pressurized anesthetic agent from the pump, a vaporizer comprising a heated chamber configured to receive and vaporize the anesthetic agent injected by the injector and supply a mix of the vaporized anesthetic agent and medical gas to a subject via a supply line, and a controller. The controller stores instructions executable to determine a concentration of the vaporized anesthetic agent in the mix and adjust one or more injector parameters based on a difference between the concentration of the vaporized anesthetic agent and a commanded concentration.

A device and method of generating an enriched gas within a nasal vestibule of a patient includes a housing, a chamber, a chamber inlet, a pump, a molecular sieve bed, a release outlet, and a breath duct. The chamber is configured to be received within the nasal vestibule. The pump is configured to direct an ambient air from an ambient environment into the chamber. The molecular sieve bed is positioned within the chamber and configured to collect a predetermined molecule from the ambient air thereby generating the enriched gas. The release outlet is configured to discharge the enriched gas from the chamber into the nasal vestibule. The breath duct longitudinally extends through the housing such that the breath duct is configured to fluidly communicate a fluid flow through the housing for nasal breathing by the patient while the chamber is positioned within the nasal vestibule.

A system for extracorporeal blood temperature control includes a heat exchanger configured to cool a circulated fluid, a thermal exchange module including a first volume fluidly isolated from a second volume, a fluid pump, a blood pump, and a controller. The fluid pump can pump the circulated fluid through the heat exchanger and the first volume of the thermal exchange module. The fluid pump can establish a negative pressure within the first volume of the thermal exchange module The blood pump can pump blood through a first blood flow line, the second volume of the thermal exchange module, and a second blood flow line. The controller can cool the blood by controlling thermal exchange between the circulated fluid pumped through the first volume of the thermal exchange module and the blood pumped through the second volume of the thermal exchange module.

The disclosed subject matter relates to extracorporeal blood processing or other processing of fluids. Volumetric fluid balance, a required element of many such processes, may be achieved with multiple pumps or other proportioning or balancing devices which are to some extent independent of each other. This need may arise in treatments that involve multiple fluids. Safe and secure mechanisms to ensure fluid balance in such systems are described.

A fan unit includes a fan case and a fan. The fan case has an intake port and a discharge port. The fan is provided inside the fan case and has a holding plate having a first surface and being rotatably supported; and a plurality of blade members provided upright on the first surface. The fan unit includes a first passage that is connected to the intake port and is defined by an inner surface of the fan case, the first surface of the holding plate, and two adjacent blades; and a second passage that is on a second surface side of the holding plate and is connected to the discharge port. An outer circumferential end section of the holding plate is positioned progressively lower towards the outside in the radial direction and has a skirt shape having a sharp gradient.

The disclosed subject matter relates to extracorporeal blood processing or other processing of fluids. Volumetric fluid balance, a required element of many such processes, may be achieved with multiple pumps or other proportioning or balancing devices which are to some extent independent of each other. This need may arise in treatments that involve multiple fluids. Safe and secure mechanisms to ensure fluid balance in such systems are described.

A system allows for collection and re-use of a fluid medium derived from diverting at least some of the fluid medium of an injection. The system comprises a sterile container, an injector, a delivery catheter, a flow diverter assembly and a diversion reservoir assembly. The delivery catheter is in communication with a selected site within a patient's body. The flow diverter assembly is disposed in a flow path between the injector and the delivery catheter and is configured to divert at least a portion of a medium of the injection from the flow path. The diversion reservoir assembly has a reservoir chamber fluidly coupled to the flow diverter assembly. The reservoir chamber is configured to receive the diverted portion of the fluid medium to allow re-use by the medium injector of the diverted portion.

An automated peritoneal dialysis system provides both cycler-assisted peritoneal dialysis treatment. The system includes a fluid preparation and treatment device with concentrate dilution components connected to a source of purified water and medicament concentrate. The treatment device has at least one mixing container connected via a pump and valves to the sources, the valves and the pump mixing and diluting the concentrate to form a medicament. Conductivity sensors are provided for fluid quality measurement, calibration, error trapping, and fluid characterization.