Abstract: Improved cassette-based medical fluid therapy systems, apparatuses and methods are provided. In one aspect, various peristaltic pump tubing materials are provided. Cassette and membrane materials, configurations and manufacturing improvements are provided. Various aspects of the invention include: a head height sensing and compensating method and apparatus; an admixing method and apparatus; a pH measuring method and apparatus; an air detecting and removal methods and apparatuses; an active priming apparatus and method; and a volumetric accuracy improvement apparatus and method.

Abstract: Methods and systems for preparing blood products that are ready for treatment in established pathogen inactivation procedures are disclosed. The methods include providing a source of a blood component and combining the blood component with a synthetic medium in a selected ratio of the blood component to the synthetic media, whereby the resulting blood product is treatment-ready.

Abstract: Devices for controlling the flow of fluid through plastic tubes, such as tubes which are part of a disposable blood donation tubing set are disclosed. The device has a clamp adapted for attachment with one or more other clamps to allow for easy flow control through two or more tubing segments.

Abstract: Systems and methods manually process blood and blood components in sterile, closed environments, which further condition the blood components for subsequent pathogen inactivation processes. The systems and methods mate the manual collection of random donor platelet units with the creation of larger therapeutic doses of platelets targeted to undergo pathogen inactivation prior to long term storage and/or transfusion.

Abstract: Devices for controlling the flow of fluid through plastic tubes, such as tubes which are part of a disposable blood donation tubing set are disclosed. The device comprises a clamp adapted for attachment with one or more other clamps to allow for easy flow control through two or more tubing segments.

Abstract: A biological suspension processing system is disclosed that may include a suspension treatment device for treating one or more components of a biological suspension, a first fluid flow path for introducing a suspension into the treatment device and a second fluid flow path for withdrawing a constituent of the suspension from the device. At least on microelectromechanical (MEM) sensor communicates with one of the fluid flow paths for sensing a selected characteristic of the fluid therewith. The MEM sensor may be located elsewhere, such as on a container or bag and communicate with the interior for sensing a characteristic of the fluid contained therein. A wide variety of characteristics may be sensed, such as flow rate, pH, cell type, cell antigenicity, DNA, viral or bacterial presence, cholesterol, hematocrit, cell concentration, cell count, partial pressure, pathogen presence, or viscosity.

Abstract: A bearing supports a rotating element. The bearing comprises an inner annular body and an outer annular body about the inner annular body. A bearing surface, which is located between the inner annular body and the outer annular body, supports the outer annular body for rotation about the inner annular body. A cage supports the bearing surface during rotation of the outer annular body about the inner annular body. The cage includes a material that imparts increased flexural modulus that resists deformation during rotation.

Abstract: A steam sterilizable monolayer medical tubing comprising a blend of a melt strength enhancing agent of a homopolymer or copolymer of polypropylene having free-end long chain branches of propylene units, a melt flow index of greater than 10 and in an amount of 1-10% by weight and a second component selected from the group of (i) a selectively hydrogenated block copolymer of a vinyl aromatic hydrocarbon and a conjugated diene and (ii) a selectively hydrogenated block copolymer of a vinyl aromatic hydrocarbon and a conjugated diene to which has been grafted, an alpha, beta-olenfically unsaturated monocarboxylic or dicarboxylic acid reagent.

Abstract: An antimicrobial material incorporated with a molecular halogen is provided. The antimicrobial material includes a plastic material and a molecular halogen entrapped within the plastic material. A directional release material is also provided in the present application. The directional release material allows for the control of the rate and site of halogen release. Still further, method of impregnating a plastic material are also provided.

Abstract: A system and a method for administering a solution (12) from a container (10) to a patient (35) are provided. The container (10) is divided into a solution side (16) and a drain side (18) separated by a tear line (20). The solution side (16) and the drain side (18) are in fluid communication with one another and with a port (28) that connects to the patient (35). The container (10) is separable at the tear line (20) such that contents of a peritoneum cavity of the patient (35) may be drained into the drain side (18) of the container (10). Then, the solution (12) from the solution side (16) of the container (10) may be drained from the container (10) into the patient (35).

Abstract: A system and a method for administering a solution (12) from a container (10) to a patient (35) are provided. The container (10) is divided into a solution side (16) and a drain side (18) separated by a tear line (20). The solution side (16) and the drain side (18) are in fluid communication with one another and with a port (28) that connects to the patient (35). The container (10) is separable at the tear line (20) such that contents of a peritoneum cavity of the patient (35) may be drained into the drain side (18) of the container (10). Then, the solution (12) from the solution side (16) of the container (10) may be drained from the container (10) into the patient (35).

Abstract: A parenteral fluid delivery bag having a line set formed integral with the bag, the line set being peelably releasable from the remainder of the bag so as to assume a deployed position adapted to enter into fluid communication with a patient. In an alternate embodiment, a plurality of bags connected by an integrally formed wye-junction are adapted for delivery to a patient and retrieval of fluid from a patient.

Abstract: A flexible fluid junction that links three or more fluid ducts is provided. The junction includes a pair of flexible webs with at least three tubes or fluid ducts disposed between the flexible webs. The outer periphery of the webs is sealed together and around the tubes to define a chamber. An end of each tube terminates inside the chamber so that fluid may flow from each tube through the chamber. Still further, a method of manufacturing a flexible fluid junction and a method of using a flexible fluid junction are also provided.

Abstract: A connector assembly and disinfectant system is provided for any system requiring a connection, such as during a peritoneal dialysis procedure. The connector assembly includes a transfer set connector and a disposable connector. The transfer set connector and disposable connector each include a member that join to create a fluid path. The disposable connector contains a housing that includes a ring partially saturated with disinfectant for bathing the transfer set member near the opening of the fluid path when a connection is made. The ring forms an opening through which the transfer set member passes. At disconnection, the transfer set member passes through a section of the ring having wiping properties to wipe the member dry.

Abstract: An improved system and method for providing sterile connections. To this end, a device is provided comprising a body, a chamber defined, at least in part, by a portion of the body, the chamber including an interior having a solid sterilizing agent that can sublimate at ambient conditions, and a member that defines., in part, the chamber and is so constructed and arranged to allow the solid sterilizing agent to release in a rate controlled manner through the member.

Abstract: A tubing has members located on the inside surface of a tubing. The flow through the tubing is completely occluded when the tubing is clamped due to the members filling channels around the clamped site. Reduced clamping pressure is required to fully occlude the flow through the tubing. The tubing undergoes less deformation upon clamping and returns to its pre-clamped form upon recovery.

Abstract: A method is provided for creating a plastic component constructed, at least in part, from polychlorotrifluoroethylene, having improved properties. The method creates a component from a composition that has polychlorotrifluoroethylene, heats the component to a temperature that is greater than the melting point of the composition, and rapidly quenches the component in a cold medium.

Abstract: A connector assembly is provided having a male component (12) and a female component (10) to provide fluid communication between a fluid source and a destination such as a patient. The female component (10) includes a door (28) rotatable about a hinge (30). The door (28) is forced open by a longitudinal member (34) within the male component (12). The door (28) is converted into a position parallel to the length of the female component (10) providing fluid communication between a tubing (36) extending into the female component (10). A sleeve (44) is further provided to permit and to prevent fluid flow through a tubing by rotation of the sleeve (44) resulting in compression and expansion of longitudinal members (46) within the sleeve (44) and thereby the tubing.

Abstract: A non-cross-linked extrudable flame retardant composition and fabricated sheets extruded therefrom are described wherein the composition comprises a blend of polypropylene, a flame retardant and a non-vulcanized copolymer of ethylene and propylene wherein the ratio of polypropylene to copolymer is within the range of from approximately 0.5 to approximately 0.8.

Abstract: The present invention provides an improved coextruded medical port tubing. The medical port tubing provides characteristics that are desirable in the medical industry and therefore can be used as a medical port tubing in, for example, renal therapy or blood donor tubes. To this end, the present invention provides a coextruded medical grade port tubing comprising: an outer layer comprising a blend of polypropylene copolymer and styrene-ethylene-butylene-styrene copolymer; a tie layer; and a core layer comprising polyvinyl chloride.