A male connector (100) includes a first fitting structure (127) on an inner circumferential surface of a hood (120) surrounding a male member (110). A female connector (200) includes a rotating cylinder (250) rotatably provided on a female connector main body (210) that includes a partition member (220) made of an elastic material. A second fitting structure (257) is provided on an outer circumferential surface of the rotating cylinder. When the male connector is connected to the female connector, the male member passes through a slit (223) of the partition member, the female connector is inserted into the hood, and the first fitting structure fits to the second fitting structure.

A biopharmaceutical flow port, a biopharmaceutical liquid container assembly, and a method for manufacturing the biopharmaceutical flow port and the biopharmaceutical liquid container assembly are described. The biopharmaceutical flow port includes a hose barb coupled to an elliptic body. The hose barb includes a bore. The elliptic body includes a flow passage, a first edge, and a second edge. The flow passage is fluidly coupled to the bore. The first edge extends from the elliptic body away from the flow passage in a first direction and the second edge extends from the elliptic body away from the flow passage in a second direction opposite the first direction. The biopharmaceutical liquid container assembly includes a biopharmaceutical liquid container with an opening and the biopharmaceutical flow port coupled to the biopharmaceutical liquid container within the opening and in fluid communication with a volume of the biopharmaceutical liquid container.

An adapter set that is attached to artery-side and vein-side shunt connectors-that are provided on a blood circuit. The adapter set includes: an artery-side adapter that has one end thereof connected to the artery-side shunt connector, has the other end thereof connected to a drainage port that is provided on the outside of the blood circuit, and thereby connects the artery-side shunt connector and the drainage port fluid tight; and a vein-side adapter that has one end thereof connected to the vein-side shunt connector, has the other end thereof connected to a supply port that is provided on the outside of the blood circuit, and thereby connects the vein-side shunt connector and the supply port fluid tight. The structure of the other end of the artery-side adapter and the structure of the other end of the vein-side adapter are different.

An adapter for making a fluid connection between first and second medical fluid flow components, where the first component includes a first male or female Luer connector of a first configuration, and the component includes a second male female Luer connector of a second configuration, that is not compatible with the first configuration, includes a fluid flow conduit with a first adapter connector at a first end of the conduit and a second adapter connector at a second end of the conduit. The conduit includes a fluid flow lumen extending between the first and second ends. The first adapter connector is a male or female Luer having a first configuration that is compatible with the first medical fluid flow component connector. The second adapter connector is a male or female Luer having a second configuration that is compatible with the second medical fluid flow component connector.

A syringe having barrel defining an outer circumferential surface, and a distal end including a non-luer tip that is not connectable to an intravenous device. The syringe barrel defines a snap-in, syringe engagement feature, adjacent to its distal end, oriented on its outer circumferential surface, which is selectively insertable within a bore of a complementary enteral collar. A proximal end of the enteral collar has a snap-in, enteral collar engagement feature, in the bore of the collar. In some embodiments, the snap-in, enteral collar engagement feature includes one or more cantilever snap joints, which engage a recess in the syringe engagement feature, upon axial insertion of the syringe tip into the bore of the collar. In some embodiments, the enteral collar engagement feature includes a discontinuous-annular snap joint. The enteral collar is sized to permit connection to an enteral device and prevent connection to a device having a luer connector.

The present invention relates to a fitting for an enteral feeding line, comprising: attachment means configured to connect the fitting to a complementary fitting, a tapered tip coaxial with an axis and a flange extending around the tip and coaxial with the tip, the flange extending away from the tip and delimiting with the tip an annular space configured to receive the complementary fitting, the attachment means being disposed at the annular space, the annular space comprising a first portion comprising the attachment means and a second portion not provided with attachment means, the second portion having an axial length along the axis and the tip having a predetermined diameter at an interface I between the first portion and the second portion, a ratio of the predetermined diameter to the axial length being greater than or equal to 1.0 and less than or equal to 2.0.

A fluid injector system includes a powered fluid injector, a connection port configured to receive a single-use disposable set having tubing connected to a fluid inlet port at a first end and connected to a waste outlet port at a second end, and a detector associated with the connection port and configured to generate a signal in response to a sonic, infrasonic, or ultrasonic wave emitted from the single-use disposable set during a priming operation of the single-use disposable set. In some examples, the detector is configured to generate a signal if the frequency of the wave emitted from the single-use disposable set is outside a predetermined range of frequencies corresponding to a predetermined range of frequencies of air expelled from the tubing. A method for detecting the multiple uses of a single-use disposable set connected to a fluid injector system is also provided.

The present invention provides a novel device and method of generating and bagging dialysate for continuous veno-venous hemodialysis (CVVHD). The procedure involves the use of standard hemodialysis (HD) equipment and the device of the present invention. The device of the present invention is an adapter configured to be used with standard hemodialysis equipment.

A one-piece fluid line connector for connecting a fluid feed line to a fluid container includes a main body having a male luer lock fitting, and a cap coupled to the main body by a living hinge. The living hinge is configured such that the cap is moveable to an aligned position in which the cap is aligned with a central axis of the male luer lock fitting of the main body. The cap includes a through-hole configured such that, in the aligned position, the shape of the through-hole permits a correspondingly-shaped female luer lock fitting to pass therethrough and engage the male luer lock fitting.

A connector system for medical fluid administration has a female connection member, which can act as an access port for a container of medical fluid, and a male connection member, for accessing the container of medical fluid. The female connection member defines a sheath for receiving a portion of the male connection member and this sheath is spanned at one end by a septum, which acts to close the container of medical fluid. A lumen is defined through the male connection member to allow passage of fluid therethrough. The septum has a central region and a peripheral region, the central region being of substantially greater thickness than the peripheral region. The male connection member comprises means for rupturing the peripheral region of the septum when it is received in the female connection member to form a connection.