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.

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.

Systems and methods for modulating delivery of a fluid medium to a selected site within a patient's body are described. A system includes a syringe for injecting the fluid medium, a delivery catheter including a conduit for delivering the fluid medium from outside of the body to the selected site within the body, a diversion reservoir configured to receive a portion of the fluid medium, and a flow diverter assembly disposed in a fluid medium flow path between the syringe and the delivery catheter. The flow diverter assembly is configured to divert the portion of the fluid medium from the chamber of the syringe away from the delivery of the medium through the delivery catheter conduit during injecting with the syringe. The flow diverter assembly simultaneously increases fluid medium flow resistance with increasing pressure level of the fluid medium passing into the flow diverter assembly.

A ventilator is configured to supply a gas mixture to the lungs of a subject. The gas mixture comprises a first gas (e.g. oxygen) and a second gas (e.g. ambient air). The ventilator comprise a first gas inlet, a second gas inlet, flow modulator of the first gas, a flow modulator of the second gas, a junction configured to mix the first gas and the second gas, a patient interface configured to deliver the gas mixture to a subject, a pressure sensor, a plurality of flow sensors comprising at least a first flow sensor and a second flow sensor, and at least one controller configured for obtaining data from the pressure sensor and flow sensors and controlling the flow modulators to provide a gas mixture having a target pressure and a target oxygen content.

A system for modulating delivery of a fluid medium includes an injector for injecting the fluid medium during an injection cycle, a delivery catheter including a conduit for delivering the fluid medium, a manifold disposed in a fluid medium flow path between the injector and the delivery catheter, and a pulsatile generator. The pulsatile generator is configured to apply a pulsatile force to the fluid medium defined by a plurality of duty cycles during the injection cycle, each of the duty cycles including a first pressure level and a second pressure level that is lower than the first pressure level.

An electronically controllable pillow is thermally regulated. At least one temperature sensor is configured to communicate temperature measurements. Temperature measurements comprise the internal temperature of a pillow. Temperature measurements are communicated to a processing unit. At least one presence sensor is configured to communicate presence measurements. Presence measurements are configured to indicate the presence of a user employing a pillow. Presence measurements are communicated to a processing unit. At least one transceiver is connected to a processing unit. A transceiver is configured to communicate with at least one remote device. At least one thermal element is activated, based at least in part on, temperature measurements and presence measurements over at least one period of time.

A portable device for oxygen generation comprising at least one reservoir for holding a hydrogen peroxide solution, a reactor, for reacting hydrogen solution with a catalyst, a feeding system for supplying said hydrogen peroxide solution to said reactor from said reservoir, a system for cooling, interconnected to an outlet of said reactor, a hydrophobic filter membrane, for removing water at an oxygen outlet of said cooling system and an oxygen flow regulator, for regulating oxygen flow at said oxygen outlet.

A drug delivery device may include a pressure sensor, a microprocessor, a fluid pathway including a reservoir, a pump downstream of the reservoir, and/or a fluid line downstream of the pump. The reservoir may be configured to receive a fluid, and the pump may be configured to deliver the fluid from the reservoir to the fluid line. The pressure sensor may be configured to measure a pressure in the fluid pathway downstream of the pump. The microcontroller may be programmed and/or configured to: receive, from the pressure sensor, the pressure measured in the fluid pathway downstream of the pump as the fluid is delivered to the fluid line; determine, based on the pressure measured in the fluid pathway, whether the fluid delivered to the fluid line includes a gas bubble; and control an output device to provide an indication associated with the determination a gas bubble.

A cuff pressure controller device (100) is connected to a foregoing cuff (10) via an air supply tube (125). The cuff pressure controller device (100) includes a controller unit (111), a cuff pressure detector unit (113), a driver circuit (119), a piezoelectric pump (101), a check valve (121), and a release valve (122). The cuff pressure detector unit (113) detects the cuff pressure of the cuff (10). The driver circuit (119) drives the piezoelectric pump (101) at a drive frequency of 20 kHz or higher. The controller unit (111) controls the cuff pressure detector unit (113), the driver circuit (119), and the release valve (122) in such a way that the cuff pressure stays within a predetermined range based on detection results of the cuff pressure detector unit (113) and the like.

The present invention relates to a dosing mechanism including: a body (2); and a disposable portion (3) that is removably attached to the body (2), in which the disposable portion (3) includes: a pump that sucks a medicine from a medicine vessel and discharges the medicine to a patient; a suction-side tube (33) that extends from the pump toward the medicine vessel; a discharge-side tube (34) that extends from the pump toward the patient; and a connector (331, 341) that is located at a front end of at least one of the suction-side tube (33) and the discharge-side tube (34), and the body (2) includes a sensor (24) in a position corresponding to the suction-side tube (33) or the discharge-side tube (34) attached to the body (2).