A gas trap apparatus (100) is for medical fluids, such as in infusion systems. The apparatus has a chamber (101), an inlet (103) to the bubble entrapment chamber with multiple of inlet ports (104, 105), and an outlet with at least one outlet port (110). The ports and the chamber are arranged to allow mixing of gases from the different fluids and which are trapped in the chamber. The inlet ports merge at a confluence space and the chamber comprises a diffuser with apertures (107) around an inflow tube for inflow of fluids into the chamber with a lateral dimensional component. Where the inlet ports (104, 105) have a diameter in the range of 1.5 mm to 8.0 mm, and the distance between an upper end of a confluence space between the ports (104, 105) and the diffuser apertures (107) is no more than 20 mm. This promotes turbulence as the fluids mix, and this turbulence continues through the diffuser, thereby enhancing bubble formation and hence migration of the gas as bubbles away from the outlet, towards an upper end of the chamber in use.

An intravenous delivery system may have a liquid source containing a liquid, tubing, and an anti-run-dry membrane positioned such that the liquid, flowing form the liquid source to the tubing, passes through the anti-run-dry membrane. The anti-run-dry membrane may be positioned within an exterior wall of a drip unit, and may be secured to a seat of the exterior wall by an attachment component. The attachment component may have various forms, such as a secondary exterior wall that cooperates with the exterior wall to define a drip chamber, a washer positioned such that the anti-run-dry membrane is between the washer and the seat, and an adhesive ring formed of a pressure sensitive adhesive and secured to the anti-run-dry membrane and the seat via compression. Interference features may protrude inward from the exterior wall or outward from the anti-run-dry membrane to help keep the anti-run-dry membrane in place.

A device for delivering an ionic material includes a storage module including a reservoir configured to store the ionic material, a bipolar membrane configured to pass the ionic material in a single direction based on an ionic current, electrodes, disposed on a lower end of the reservoir and an upper end of the bipolar membrane, respectively, configured to form an electric field generating the ionic current, and a control module configured to control either one or both of a release amount and a release period of the ionic material passing through the bipolar membrane by adjusting a direction and an intensity of the electric field.

An intravenous delivery system may have a liquid source containing a liquid, tubing, and an anti-run-dry membrane positioned such that the liquid, flowing form the liquid source to the tubing, passes through the anti-run-dry membrane. The anti-run-dry membrane may be positioned within an exterior wall of a drip unit, and may be secured to a seat of the exterior wall by an attachment component. The attachment component may have various forms, such as a secondary exterior wall that cooperates with the exterior wall to define a drip chamber, a washer positioned such that the anti-run-dry membrane is between the washer and the seat, and an adhesive ring formed of a pressure sensitive adhesive and secured to the anti-run-dry membrane and the seat via compression. Interference features may protrude inward from the exterior wall or outward from the anti-run-dry membrane to help keep the anti-run-dry membrane in place.

Presented herein are methods, systems, and apparatus for administering an antibody treatment via an infusion device, e.g., a rapid infusion device, e.g., for the treatment of a disease or condition that requires one or more infusions of monoclonal and/or polyclonal antibodies.

Provided herein are systems and methods for monitoring one or more health or physiological parameters in a subject. The systems and methods may comprise a patch coupled to an injector. Data may be transmitted to a mobile device or remote server, where the data may be processed. Processed data may be used to inform a subject on a health or physiological condition.

An apparatus for filtering amniotic fluid containing particulate matter and amniotic cells is disclosed, comprising a filter for filtering the particulate matter from the amniotic fluid, a chamber enclosing the filter, wherein the chamber comprises a fluid inlet and a fluid outlet, and an inlet connector arranged to form a sealing connection between the fluid inlet and an amniotic fluid sample source, wherein, in use, the amniotic fluid pass the filter when flowing from the fluid inlet to the fluid outlet, whereby particulate matter is deposited on the filter and the amniotic fluid flows through the fluid outlet containing amniotic cells.

IV filters are described herein. An IV filter includes a body, a filter media, and a bulb. The body defines a body volume. The filter media is disposed within the body volume. The filter media defines an inlet portion of the body volume and an outlet portion of the body volume. The filter media permits inlet flow from the inlet portion of the body volume to the outlet portion of the body volume and captures particulate from the inlet flow. The bulb defines a bulb volume in fluid communication with the outlet portion of the body volume. The bulb is deformable to compress the bulb volume and direct back flow from the outlet portion of the body volume through the filter media and into the inlet portion of the body volume, displacing particulate captured in the filter media into the inlet portion of the body volume.

In-line filter devices are described herein. An in-line filter device includes an inlet portion, an outlet portion, a first filter housing, a first flow path, and a first filter media. The first filter housing defining a first filter volume. The first flow path is defined between the inlet portion and the first filter volume to provide fluid communication between the inlet portion and the first filter volume. The second flow path is defined between the first filter volume and the outlet portion to provide fluid communication between the first filter volume and the outlet portion. The first filter media is disposed within the first filter volume, wherein the first filter media permits flow from the first flow path to the second flow path and captures particulate from the flow.

A system for intravascular oxygenation may include a catheter shaft, a vibratory member, and an oxygen source. The catheter shaft may have a wall that extends from a proximal end to a distal end along a longitudinal axis to form a lumen. The distal end may terminate in an atraumatic tip that seals off an interior space of the lumen from an adjacent exterior space. The distal end may include a coiled spring whose coils are tightly disposed against adjacent coils. The vibratory member may be configured to produce and transmit via the wall, to the coiled spring, mechanical vibration or high-frequency acoustic energy. The oxygen source may be configured to be coupled to the proximal end and to deliver a flow of oxygen to an interior space for communication to the exterior space, through gaps that exist or are created between adjacent coils of the coiled spring.