Abstract: A tubular set is provided for use with extracorporeal treatment of blood. The set comprises: a flow reversing valve having a patient arterial line and a patient venous line each separately connected to one side of the valve. A unit arterial line and a unit venous line are each separately connected to the other side of the valve. The patient arterial line connects with the unit arterial line in a first position of a valve, and the patient venous line connects with the unit venous line in the same first valve position. The patient arterial line connects with the patient venous line in a second position of a valve, while the patient venous line connects with the unit arterial line in the same second valve position. The flow reversing valve is movable between the first and second positions by relative rotation of part of the valve and adjacent portions of the respective lines.

Abstract: A needle point protection sheath comprises a protector tube having a bore for receiving a hollow needle plus a needle hub within the bore. The protector tube has closure cap at one end thereof and has a retention member at the other end to engage an end of the hub, to prevent the hub from passing out of the other tube end. The cap may carry a sleeve having a needle-pierceable wall at its inner end, or a mass of resilient material which is capable of being penetrated by the needle as the cap is closed, to seal the needle tip and thus prevent the spilling of blood residue when a blood collection needle is being enclosed for protection.

Abstract: A cannula for providing an external connection with an implanted artificial port for communicating with the body lumen of a patient. The artificial port has an entrance conduit with an inwardly tapering section. The tapered cannula is sized and proportioned to substantially match and seal with the inwardly tapering section of the entrance conduit. Thus the cannula can form a readily removable seal with the inwardly tapering section. A typical angle of taper is one to two degrees.

Abstract: A combined arterial-venous blood flow set comprises connected lengths of flexible tubing for receiving blood from a patient, for conveying the blood to a blood processing device such as a dialyzer or an LDL filter, and for returning the blood to the patient. An optional first bubble trap chamber is connected in series flow between two of the lengths of tubing at a flow position downstream from the patient and upstream from the blood processing device. A second bubble trap chamber is connected in series flow between two of the lengths of tubing at a flow position downstream from the blood processing device and upstream from the patient. A first portion of the tubing which is in a flow position upstream from the blood processing device extends by the second bubble trap chamber, and is physically, laterally connected to it without direct flow connection. This helps to stabilize the positioning of components of the flow set and to reduce confusion in set-up and priming.

Abstract: A needle point protection sheath comprises a protector tube having a bore for receiving a hollow needle plus a needle hub within the bore. The protector tube has closure cap at one end thereof and has a retention member at the other end to engage an end of the hub, to prevent the hub from passing out of the other tube end. The cap may carry a sleeve having a needle-pierceable wall at its inner end, or a mass of resilient material which is capable of being penetrated by the needle as the cap is closed, to seal the needle tip and thus prevent the spilling of blood residue when a blood collection needle is being enclosed for protection.

Abstract: A tubular set is provided for the extracorporeal treatment of blood, for example hemodialysis. The set comprises a patient arterial line and a patient venous line, each line having a patient connector at one end thereof. Each patient line connects at its other end to a reversing flow valve. The valve also connects to respective first ends of a blood processing unit arterial line and a blood processing unit venous line. Each of the unit lines carry a connector at ends opposed to the first ends for connection respectively to arterial and venous ports of a blood processing device, typically a dialyzer. The reversing flow valve has a first position that respectively connects the patient and unit arterial lines with the patient and unit venous lines. The reversing flow valve has a second position that connects the patient arterial line with the unit venous line, and the unit arterial line with the patient venous line.

Abstract: A flow through bubble trap for fluid flow lines comprises a chamber-defining wall and a flow inlet/outlet tube at least substantially extending through the chamber and open at opposed tube ends to respectively define an inlet and an outlet of the bubble trap. The tube defines a flow inlet port and a flow outlet port within the chamber interior. A flow blocking partition closes the bore of the tube between the flow inlet and outlet ports. Additionally, the chamber defining wall carries a retaining-sealing member for removable, sealing connection with a tube connector of a fluid flow line. The retaining-sealing member is free of fluid flow connection with the interior of the chamber defined by the wall, and thus serves as a seal for connectors on tube ends of a set carrying the bubble trap. Also, the chamber defining wall has a bottom wall that defines a third port.

Abstract: An extracorporeal, flow-through bubble trap for blood lines having improved capabilities at high flow rates and with smaller bubbles. The bubble trap comprises a chamber-defining wall, plus a blood inlet and a blood outlet, each extending through the wall to communicate with the interior of the chamber. The blood outlet connects with the chamber interior adjacent the bottom thereof. The chamber interior has a height that is less than 1.6 times the longest horizontal dimension of the chamber interior. As a result of this, blood flow in the bubble trap chamber is substantially horizontal.

Abstract: A squeeze clamp for flexible tubing comprises a strip of plastic which is bent back on itself so that the ends are adjacent to each other. The strip defines a pair of spaced apertures to permit a flexible tube to extend through and be carried by the clamp. First and second latches at the respective ends can hold the clamp in a closed position, or it can spring outwardly into an open position. The apertures extend laterally through a first side edge of the strip, with the apertures thus being each located next to a narrow strip portion connected to wider strip portions on either side of the narrow strip portion. At least one of the narrow strip portions extends laterally outwardly beyond the side edge of the rest of the plastic strip for strengthening of the narrow strip portion, to reduce problems of involuntary twisting or torsion as the clamp is closed.

Abstract: An injection site for passing a needle into an enclosed space surrounded by a wall, typically defined by a tubular section incorporated in a tubular set. An aperture in the wall communicates between the enclosed space and the exterior, having an elastic, needle-pierceable member such as a plug occluding the aperture. The plug is exposed to the exterior on one side and defines a route of needle access through the plug and aperture to the enclosed space. A first flange is positioned adjacent to the plug and extends transversely outwardly from the plug. The first flange carries a second flange, which extends longitudinally relative to the plug, and is spaced transversely outwardly from the plug to define a catch area for needles, which catch area surrounds the plug.

Abstract: A combined arterial-venous blood flow set comprises connected lengths of flexible tubing for receiving blood from a patient, for conveying the blood to a blood processing device such as a dialyzer or an LDL filter, and for returning the blood to the patient. An optional first bubble trap chamber is connected in series flow between two of the lengths of tubing at a flow position downstream from the patient and upstream from the blood processing device. A second bubble trap chamber is connected in series flow between two of the lengths of tubing at a flow position downstream from the blood processing device and upstream from the patient. A first portion of the tubing which is in a flow position upstream from the blood processing device extends by the second bubble trap chamber, and is physically, laterally connected to it without direct flow connection. This helps to stabilize the positioning of components of the flow set and to reduce confusion in set-up and priming.

Abstract: A flow through bubble trap comprises a chamber-defining wall having a flow inlet/outlet tube extending through the chamber and open at opposed tube ends. The tube has its bore closed with a partition, with ports in the side wall communicating with the chamber interior on opposite sides of the partition and adjacent to the bottom wall of the chamber.

Abstract: A needle point protection sheath comprises a protector tube having a bore for receiving a hollow needle plus a needle hub within the bore. The protector tube has a closure cap at one end thereof and has a retention member at the other end to engage an end of the hub, to prevent the hub from passing out of the other tube end. The cap may carry a sleeve having a needle-pierceable wall at its inner end, or a mass of resilient material which is capable of being penetrated by the needle as the cap is closed, to seal the needle tip and thus prevent the spilling of blood residue when a blood collection needle is being enclosed for protection.

Abstract: A tubular set for the conveyance of blood includes flexible set tubing and a bubble trap chamber connected to the tubing for any desired extracorporeal blood transport process. The bubble trap chamber includes a housing defining an outer wall, a flow inlet to the interior of the housing, and a flow outlet at or near the bottom of the housing. The housing also includes an inner wall adjacent to its top. The inner wall is radially inwardly spaced from the outer wall within the chamber, extending circumferentially and generally parallel to the outer wall for at least about 90.degree. of the circumference of the outer wall and preferably at least 180.degree., to define a circumferential passageway between the inner and outer walls. The flow inlet communicates with the circumferential passageway, so that blood can be directed to flow from the inlet horizontally and circumferentially through the passageway to a pair of passageway outlets.

Abstract: A flow through bubble trap for fluid flow lines comprises a chamber having a substantially flat, lateral side, a first port tube, and a second, opposed port tube. A flow directing baffle system is positioned in the chamber to direct incoming fluid from one of the port tubes into a first, lateral flow direction to allow substantially horizontal fluid flow circulation in the chamber. Fluid flow from the circulating fluid in the chamber enters into the other of the port tubes in a lateral flow direction that is generally the same as the first lateral flow direction, while the baffle system prevents direct flow between the first and second port tubes. The chamber is adaptable to fit with a large variety of conventional dialysis machines and the like, having multi-purpose supplemental access ports, for a simplification of the number of codes necessary for product distribution.

Abstract: A flow through bubble trap for fluid flow lines comprises a chamber having a substantially flat, lateral side, a first port tube, and a second, opposed port tube. A flow directing baffle system is positioned in the chamber to direct incoming fluid from one of the port tubes into a first, lateral flow direction to allow substantially horizontal fluid flow circulation in the chamber. Fluid flow from the circulating fluid in the chamber enters into the other of the port tubes in a lateral flow direction that is generally the same as the first lateral flow direction, while the baffle system prevents direct flow between the first and second port tubes. The chamber is adaptable to fit with a large variety of conventional dialysis machines and the like, having multi-purpose supplemental access ports, for a simplification of the number of codes necessary for product distribution.

Abstract: A medical needle protector sheath having slotted sidewalls to receive a winged needle. The sidewalls define at least one catch projection and preferably one in each sidewall, spaced from closed ends of the slots in the sidewalls, to prevent needle wings occupying the sheath adjacent the closed ends from easily sliding away. The catch projection defines an elongated member having a first end that defines a wing catching tip extending into one of the slots. The elongated member is attached to the sidewall only at an elongated member end that is opposed to the first end. This permits the elongated member to flex in the sidewall plane, providing improved receipt and retention of the needle wings.

Abstract: A medical needle protector sheath which comprises a body having a top wall, side walls, an open first end, and slot formed in each side wall to receive a needle wing extending through each of the slots. The slots extend from the first end toward a second sheath end opposed to the first end, with the slots terminating in the side walls at end points which are spaced from the second end. Typically, first portions of the slots adjacent to the end points slope away from the top wall as the slots extend toward the second end. Other portions of the slots slope toward the top wall as the slots extend to the second end. Various improvements are described which result in safer-and easier use of the needle protector sheath.

Abstract: A surgical instrument has a hollow elongated shaft for insertion into the body, the shaft having a longitudinal axis and supporting a pair of interacting pivotable jaws on its distal end and being connected at its proximal end to a first movable component of an operating handle, with a reciprocable rod located within the shaft. The rod is connected to a second movable component of the handle for reciprocation within the shaft when the first and second components are moved relative to each other. The jaws are pivotally connected by a pivot pin supported on the shaft transversely to the axis. Each of the jaws has a proximal end extending proximally from the pivot pin. Each of the proximal ends is provided with an elongated opening therethrough, each the openings forming an elongated slot oriented at an oblique angle relative to the longitudinal axis of the shaft. The reciprocable rod has a distal end extending into each slot whereby reciprocation of the rod causes the jaws to open and close.

Abstract: A port and closure assembly for a container is provided. The port and closure assembly includes a port having a tubular portion that extends from a base and terminates at an end including an opening. The tubular portion is divided into an upper and lower section by a pierceable membrane. The upper section including an end that terminates at the opening and including a resealing injection site. A closure member for removably surrounding at least a portion of the end of the port including the opening is provided. The closure includes a sleeve that circumscribes at least a portion of an outer surface of the upper section of the tubular portion. The sleeve is so constructed and arranged as to cause portions of the upper section to contact the resealing member during a sterilization step that softens the portions and further causes the portions of the upper section to retain the resealing injection site within the tubular portion after the portions have hardened.