Abstract: An extension for a catheter assembly may include a distal end and a proximal end. The distal end may include one or more cantilever arms and an insertion feature spaced apart from the cantilever arms. The insertion feature may be configured to insert into a lumen of a catheter adapter to provide a fluid connection between the catheter adapter and the extension. The one or more cantilever arms may be configured to engage in a snap-fit with the catheter adapter. The proximal end of the extension may include a female luer fitting.

Abstract: Pinch clamps are provided which generate positive displacement while also preventing rebound. To prevent rebound while providing positive displacement, the upper and lower clamping surfaces may be configured to form a pinch profile along which the tubing is compressed with the pinch point being formed at the distal end of the pinch profile. To further prevent rebound, the lower arm of the pinch clamp can include blocking ribs that interface with the upper clamping surface to prevent distal travelling of the pinch point even if the upper arm is forced into an over-engaged position.

Abstract: 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 have a plurality of pores through which the liquid flows, and may be formed of a hydrophilic material that resists passage of air through the pores. The intravenous delivery system may further have a bubble point raising component that raises the bubble point of the anti-run-dry membrane. The bubble point raising component may, in some embodiments, be a high surface energy coating or additive.

Abstract: Pinch clamps are provided which generate positive displacement while also preventing rebound. To prevent rebound while providing positive displacement, the upper and lower clamping surfaces may be configured to form a pinch profile along which the tubing is compressed with the pinch point being formed at the distal end of the pinch profile. To further prevent rebound, the lower arm of the pinch clamp can include blocking ribs that interface with the upper clamping surface to prevent distal travelling of the pinch point even if the upper arm is forced into an over-engaged position.

Abstract: 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.

Abstract: 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 have a plurality of pores through which the liquid flows, and may be formed of a hydrophilic material that resists passage of air through the pores. The intravenous delivery system may further have a bubble point raising component that raises the bubble point of the anti-run-dry membrane. The bubble point raising component may, in some embodiments, be a high surface energy coating or additive.

Abstract: 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.

Abstract: A catheter system may include a catheter adapter and a wing extending outwardly from the catheter adapter. The wing may include a groove or slot. The catheter system may include a needle hub and a paddle extending outwardly from the needle hub. The paddle may include an extension disposed within the groove or the slot to reduce axial movement between the catheter adapter and the needle hub, which may be advantageous during insertion of the catheter system into a patient. The extension may be removable from the groove or the slot to allow axial movement between the catheter adapter and the needle hub during removal of the needle hub from the catheter adapter, for example. The paddle and/or the wing may include a shape to reduce axial movement between the catheter adapter and the needle hub, which may also be advantageous during insertion of the catheter system.

Abstract: A device to couple a vascular access device to a medical device may include a body, a spring, and a housing. The body may include a distal end, a proximal end, and a lumen extending through the distal end and the proximal end. The proximal end of the body may include a connector. The housing may be coupled to a proximal end of the spring and may enclose the connector. A distal end of the spring may be coupled to the body. The housing may include a flap, which may include an antimicrobial compound. When the housing is disposed in a proximal position, the flap may cover the connector, the antimicrobial compound may contact the connector, and the spring may be uncompressed. In response to movement of the housing from the proximal position to a distal position, the spring may be compressed and the flap may open.

Abstract: An intravenous delivery system may have a liquid source containing a liquid, tubing, and a vent cap. The tubing may be connected to the liquid source and the vent cap to convey liquid from the liquid source to the vent cap. The vent cap may have a vent that is substantially impermeable to the liquid and permeable to air, and therefore releases air from the liquid from the vent cap. The vent cap may also have a chamber in communication with the vent. The chamber may have a volume selected to enable the chamber to receive a quantity of liquid from the tubing in which the air, if entrained in the liquid, is likely to reside after the tubing has been primed with the liquid.

Abstract: Pinch clamps are provided which generate positive displacement while also preventing rebound. To prevent rebound while providing positive displacement, the upper and lower clamping surfaces may be configured to form a pinch profile along which the tubing is compressed with the pinch point being formed at the distal end of the pinch profile.

Abstract: A catheter assembly (10) comprises a catheter (20), a needle (22) having a sharp distal tip and disposed within the catheter (20), a catheter hub (30) connected to the catheter (20) having the needle (22) passing therethrough, and a housing (70) that encloses the sharp distal tip of the needle (22). An external surface of the catheter hub (30) and an internal surface of the housing (70) each include at least one of a channel member (34) and a raised portion (72) that interfit to restrict motion between the catheter hub (30) and the housing (70).