Apparatuses for priming a drip chamber of an infusion tube seta are described. A priming apparatus may be incorporated into a cavity of a body, such as a drip chamber cap, that is attached to or integrally formed with the inlet side of drip chamber. The priming apparatus includes a closure mechanism at least a portion of which is accommodated in a cavity in the body. The cavity is part of an outflow or vent passage through the body (e.g., the drip chamber cap) and the closure mechanism is operable, e.g., responsive to user force, to selectively open the outflow passage, thereby unsealing the vent cavity to ambient air and allowing air to be purged from the fluid system during priming of the drip chamber. When the closure mechanism is an closed position, the outflow passage and vent cavity as sealed from ambient air, preventing any air from passing into the fluid system through the cap.

Oxygen concentrator apparatus provides variation in therapy gas during a breathing cycle such as by varying flow rate and/or oxygen purity of enriched air. The apparatus may include a compressor and a valve set that operates sieve bed(s) for the enriching air and to vent exhaust gas from the bed(s). The therapy gas may include released enriched air and exhaust gas. The apparatus has a supply valve to selectively release enriched air from an accumulator via a primary path to a delivery conduit. The apparatus may include a secondary path, such as with a valve, to release a portion of exhaust gas to the delivery conduit. A controller actuates the valve set to produce the enriched air, and the supply valve to release enriched air to the delivery conduit. The controller may actuate the secondary valve in anti-sync with the supply valve to release exhaust gas to the delivery conduit.

IV filters are described herein. An IV filter includes a filter housing, a filter media, a filter channel, a priming channel, and a disk valve. The filter housing defines an inlet and an outlet. The filter media is disposed within the filter housing. The filter channel is disposed within the filter housing. The filter channel is in fluid communication with the inlet and the filter media, and the filter media permits flow from the filter channel to the outlet and captures particulate from the flow. The priming channel is disposed within the filter housing. The priming channel is in fluid communication with the inlet and the outlet. The disk valve is coupled to the filter housing. The disk valve is moveable to direct flow from the inlet to the priming channel in a first position and to direct flow from the inlet to the filter channel in a second position.

A biocontainment assembly for use with a patient suspected of having or diagnosed with a transmissible disease(s) capable of respiratory, airborne, contact, or droplet transmission includes a housing configured to be positioned over and at least partially enclose a head, neck, and/or torso of the patient. A sidewall of the housing includes an open portion contiguous with an at least partially pen bottom portion of the housing, sized to fit over at least a portion of the head, neck, and/or a torso of the patient. The housing also includes an airflow opening for evacuating fluid from an interior defined by the housing. The assembly also includes a drape configured to extend across the open portion of the sidewall having a first portion removably connected to the housing and an opposing second portion configured to be draped over the torso, abdomen, waist, and/or legs of the patient.

Disclosed herein are embodiments of a wound treatment apparatus with electronic components integrated within a wound dressing. In some embodiments, a wound dressing apparatus can comprise a wound contact layer, an absorbent layer over the wound contact layer, the absorbent layer comprising one or more apertures, a cover layer configured to cover and form a seal over the wound contact layer and the absorbent layer, and an electronics assembly comprising a negative pressure source. A portion of the cover layer overlying the one or more apertures in the absorbent layer can be configured to be compressed within the aperture in the absorbent layer when negative pressure is applied to the wound dressing apparatus. The compressed cover layer can indicate a level of negative pressure below the cover layer. In some embodiments, the wound dressing apparatus can comprise an indicator material layer and a cover layer configured to cover and form a seal over the wound contact layer and the indicator material layer. The indicator material layer can be configured to protrude relative to a surrounding surface of an upper surface of the wound dressing apparatus when negative pressure is applied to the wound dressing apparatus and the protruding indicator material layer indicates a level of negative pressure below the cover layer.

A method and a system (10a) comprising an integrated water purifying apparatus (110) with a pre-filter circuit (402) including a particle filter and an activated carbon filter arranged to produce pre-treated water; a fluid circuit (404) arranged to receive pre-treated water from the pre-filter circuit (402), the fluid circuit (404) includes an RO-pump (450) and a Reverse Osmosis, RO, device, (301) arranged to produce purified water; a heating device (302) arranged to heat purified water from the RO device (301) to a temperature above 65°; the water purifying apparatus (110) is further arranged to heat disinfect the fluid circuit (404) using the heated purified water. The system (1) further comprises a line set (40) connected to the purified water outlet connector (128) at a water line connector (68) of the line set (40), wherein the line set (40) includes at least one sterile sterilizing grade filter (70a, 70b) arranged to filter the purified water into sterile purified water.

Methods and apparatus may implement controlled generation of oxygen enriched air in an oxygen concentrator while implementing control that reduces pneumatic imbalance between the concentrator's canisters, such as dynamic pressure imbalance or other pneumatic characteristic. One or more controllers may regulate operation of a compressor that feeds a pressurised air stream to the concentrator's canisters. This may regulate speed of the compressor to a speed set point for generating the pressurised stream. The regulating may involve generating a compressor control signal having a characteristic parameter such as a power parameter. The controller(s) may operate valve(s) in a cyclic pattern so as to produce oxygen enriched air in an accumulator. A cycle of the cyclic pattern may include a plurality of phases, where each of the plurality of phases has a duration. The controller(s) may then generate a dynamic adjustment to the duration(s) based on an evaluation of the characteristic parameter.

Systems and methods for collecting breathing gas properties via a medical ventilatory filter and wirelessly transmitting the data to another device. For example, the filter includes a first housing enclosing filtration media for filtering breathing gases flowing through the filter, the first housing defining a first port and a second port exposed to the breathing gases; and a sensor assembly. The sensor assembly includes a first sensor coupled to the first port, the first sensor configured to capture measurement data for a first gas property of breathing gases flowing through the filter; a second sensor coupled to the second port, the second sensor configured to capture measurement data for a first gas property of the breathing gases flowing through the filter; and a second housing. The second housing includes a processor and communication circuitry operative to wirelessly communicate the sensor data to a computing device located remotely from the filter.

Disclosed herein are several embodiments of a negative pressure appliance and methods of using the same in the treatment of wounds. Some embodiments are directed to improved fluidic connectors or suction adapters for connecting to a wound site, for example using softer, kink-free conformable suction adapters.

A hemodialysis system includes a dialyzer; a dialysis fluid circuit including a fresh dialysis fluid pump, and a used dialysis fluid pump; a blood circuit including a blood pump operable with an arterial line upstream of the dialyzer, a medical fluid source in fluid communication with the arterial line between a patient end of the arterial line and the blood pump, a drip chamber located along a venous line; a blood rinseback sequence wherein blood is transferred to the patient by the medical fluid, wherein the medical fluid is introduced from its source into the arterial line between an arterial line patient end and the blood pump, and flowed through the dialyzer, through the venous drip chamber along the venous line; and a blood circuit priming sequence initiated in the blood circuit via the arterial line.