Abstract: A needle-free connector for accessing a patient’s intravenous line includes a hollow body having a first end with a first opening, a second end with a second opening, and an inner wall defining a chamber. A hollow piston disposed in the chamber is axially collapsible to allow fluid to flow between the inner wall of the hollow body and the outer surface of the hollow piston. An inner surface of the hollow piston includes a fluted section having a radial array of axial slots. The fluted section has a first radial thickness configured to buckle in response to axial force applied to the hollow piston. The hollow piston further includes a retrograde-reducing stiffener. The retrograde-reducing stiffener has a second radial thickness that is greater than the first radial thickness.

Abstract: An exemplary compounding system and device for mixing materials can include a housing, a first material source and a second material source. A first fluid line can be operationally connected to the housing and configured to transport a first volume of fluid per unit time from the first material source to a final container. A second fluid line can be operationally connected to the housing and configured to transport a second volume of fluid per unit time from the second material source to the final container.

Abstract: A connector is configured to connect a drug container with a solution container and permit contents of the drug container to be combined with the solution container. The connector has a connector body with a first coupling for fluid connection with the drug container. The first coupling defines a first fluid passage. The connector body also has a second coupling for fluid connection with the solution container. The second coupling defines a second fluid passage. A control valve has a movable valve body that defines a third fluid passage. The valve body is positionable relative to the connector body in a first position, in which the first fluid passage is sealed from the second fluid passage. The valve body is also positionable in a second position, in which the first fluid passage is connected in fluid communication with the second fluid passage by the third fluid passage.

Abstract: An exemplary compounding system and method can include a transfer set that includes a manifold for assisting in transferring a plurality of ingredients from supply container(s) to a final container. The manifold can include a first channel in fluid communication with at least one primary ingredient, and a second channel in fluid communication with a plurality of secondary ingredients. The first channel and second channel can be in fluid isolation from each other such that the at least one primary ingredient does not mix with the plurality of secondary ingredients within the manifold. The transfer set can include a plurality of inlet lines in fluid communication with the manifold and two outlet lines configured for connection to two separate pumps and eventually being in fluid communication with the final container.

Abstract: A connector is configured to connect a drug container with a solution container and permit contents of the drug container to be combined with the solution container. The connector has a connector body with a first coupling for fluid connection with the drug container. The first coupling defines a first fluid passage. The connector body also has a second coupling for fluid connection with the solution container. The second coupling defines a second fluid passage. A control valve has a movable valve body that defines a third fluid passage. The valve body is positionable relative to the connector body in a first position, in which the first fluid passage is sealed from the second fluid passage. The valve body is also positionable in a second position, in which the first fluid passage is connected in fluid communication with the second fluid passage by the third fluid passage.

Abstract: An exemplary compounding system and method can include two pump heads for simultaneously drawing two different fluids from at least two separate input containers such that the at least two different fluids are mixed and distributed to an output container. The system can include a manifold that maintains separation of certain of the different fluids until after passing by a first pump and a second pump and/or additional pumps. A junction can be placed in the fluid line downstream of the first and second pumps and/or additional pumps such that all or some of the fluids are mixed prior to output to the output container. The method of using the system can include incorporating software that selects various fluids at certain times and sequences to ensure optimum efficiency and safety for the system, and can continue compounding actions even when an input supply container runs out or otherwise fails to supply a particular fluid/material.

Abstract: A peristaltic infusion pump with improved low flow performance. The pump includes a cam shaft having cams offset in an axial direction, pump fingers that engage a tube, each finger coupled to a respective cam, the fingers creating a pumping region and an occlusion region within the tube, a motor coupled to the cam shaft, a memory, and a controller. The controller implements cam rotation instructions received from the memory to cause the pump to position the fingers in the occlusion region prior to beginning an infusion therapy to deliver fluid to patient through the tube at a patient fluid delivery rate, rotate the cam shaft to transition the fingers from the occlusion region to the pumping region at a startup rate that is faster than a patient fluid delivery rate, and rotate the cam shaft at the patient fluid delivery rate in the pumping region.

Abstract: A connector is configured to connect a drug container with a solution container and permit contents of the drug container to be combined with the solution container. The connector has a connector body with a first coupling for fluid connection with the drug container. The first coupling defines a first fluid passage. The connector body also has a second coupling for fluid connection with the solution container. The second coupling defines a second fluid passage. A control valve has a movable valve body that defines a third fluid passage. The valve body is positionable relative to the connector body in a first position, in which the first fluid passage is sealed from the second fluid passage. The valve body is also positionable in a second position, in which the first fluid passage is connected in fluid communication with the second fluid passage by the third fluid passage.

Abstract: Ostomy appliance components providing filtered release of gasses from a surgical stoma. Filter shape, positioning, and positioning structure relate to potential advantages in manufacturing and operation of components.

Abstract: Infusion systems and related methods involving a catheter hub and an extension or IV administration set having a male Luer connector for fluid communication with the catheter hub. A support adaptor is provided with the extension or IV administration set and has a body with a length between first and second ends, and a body wall having a continuous wall surface in a radial direction relative to the length and which defines an exterior of the body. An internal wall of the support adaptor defines a bore with the body wall, wherein the bore has first and second openings. A tubing length is located in the bore and extends out of the second opening. The bore includes first and second bore sections. Optionally, the second bore section is angled relative to the first bore section. A support surface is located beneath the bore, elevation wise.

Abstract: A cassette with free flow prevention for use with an ambulatory pump. The cassette includes a free flow prevention clamp and a housing. The free flow prevention clamp includes a clamping section having a first side and a second side, a first elongate section extending from the first side, and a second elongate section extending from the second side. The housing supports the free flow prevention clamp and defines a channel for receiving a tube. The elongate sections extend parallel to the channel and the clamping section extends across the channel. The free flow prevention clamp is configurable within the housing in an open condition that allows fluid flow through the tube when force is applied to one of the elongate sections and in a closed condition that prevents fluid flow through the tube when the force is removed from the elongate sections.

Abstract: The purpose of the invention is to create a urine bag that can be easily folded in order to occupy less space prior to use and that can be easily manipulated by a patient, in particular a paraplegic patient. This is achieved using a urine collection bag (1) formed by two sheets of plastic material that are stacked and welded along the periphery (2) thereof. The collection bag (1) comprises a collection compartment (3), said inlet being in communication with the intake port (4) and delimiting the upper portion of the collection compartment (3). The intake port (4) is provided with a vertical extension (8) closed along their periphery (22) thereof and comprising a urinary catheter (9). The bag (1) of the invention is characterised in that the intake port (4) and the inlet (6) are offset vertically, and in that the vertical height (ho) of the bag (1) corresponds to a multiple of the height (hp) of the extension (8).

Abstract: An ambulatory pump and a battery compartment for use in an ambulatory pump. The ambulatory pump includes a pump, a controller coupled to the pump for controlling the pump to deliver fluid to a patient, and a battery compartment electrically coupled to the pump and the controller. The battery compartment defines a cavity for alternately receiving a battery pack and a plurality of household batteries. A flex guide is positioned within the cavity. The flex guide has a compressed state and a non-compressed state where a profile of the flex guide has a height that is greater than half the insertion depth of the household batteries in the non-compressed state and that is less than half the insertion depth in the compressed state.

Abstract: A peristaltic infusion pump with improved low flow performance. The pump includes a cam shaft having cams offset in an axial direction, pump fingers that engage a tube, each finger coupled to a respective cam, the fingers creating a pumping region and an occlusion region within the tube, a motor coupled to the cam shaft, a memory, and a controller. The controller implements cam rotation instructions received from the memory to cause the pump to position the fingers in the occlusion region prior to beginning an infusion therapy to deliver fluid to patient through the tube at a patient fluid delivery rate, rotate the cam shaft to transition the fingers from the occlusion region to the pumping region at a startup rate that is faster than a patient fluid delivery rate, and rotate the cam shaft at the patient fluid delivery rate in the pumping region.

Abstract: An ambulatory pump and a battery compartment for use in an ambulatory pump. The ambulatory pump includes a pump, a controller coupled to the pump for controlling the pump to deliver fluid to a patient, and a battery compartment electrically coupled to the pump and the controller. The battery compartment defines a cavity for alternately receiving a battery pack and a plurality of household batteries. A flex guide is positioned within the cavity. The flex guide has a compressed state and a non-compressed state where a profile of the flex guide has a height that is greater than half the insertion depth of the household batteries in the non-compressed state and that is less than half the insertion depth in the compressed state.

Abstract: A cassette with free flow prevention for use with an ambulatory pump. The cassette includes a free flow prevention clamp and a housing. The free flow prevention clamp includes a clamping section having a first side and a second side, a first elongate section extending from the first side, and a second elongate section extending from the second side. The housing supports the free flow prevention clamp and defines a channel for receiving a tube. The elongate sections extend parallel to the channel and the clamping section extends across the channel. The free flow prevention clamp is configurable within the housing in an open condition that allows fluid flow through the tube when force is applied to one of the elongate sections and in a closed condition that prevents fluid flow through the tube when the force is removed from the elongate sections.

Abstract: An adhesive composition is intended to provide the attaching to human skin, comprising a continuous phase and a discontinuous phase of hydrocolloids, with the continuous phase comprising by weight, based on the total weight of the adhesive composition: (i) 1 to 12% by weight of a sequenced polymer of the styrene-isoprene-styrene or styrene-butadiene-styrene type, (ii) (a) 1 to 15% of a polymer of the elastomer butyl type, possibly as a mixture with up to 25% by weight of a polymer of the polyisobutylene type, or (b) more than 10% to 30% of a polymer of the polyisobutylene type, free of polymer of the elastomer butyl type, (iii) 1 to less than 10% of a polymer of the ethylene vinyl acetate type, with the sum of these three types of polymers representing from 10 to 40%.

Abstract: An exemplary pharmaceutical compounding system and device for mixing materials from at least two distinct material sources can include a valve including a valve housing and a valve structure located within the valve housing. The valve structure can be configured to permit fluid to flow through the valve when in an open position, and can include a gravity wall wherein, when the valve structure is in the open position, fluid moving through the valve structure moves upward against a force of gravity when travelling through the valve and traversing the gravity wall.