Abstract: The disclosure relates to plate-fin and manifold assemblies for heat exchangers. In some examples, an assembly includes a first plate and a second plate. The assembly also includes a plurality of fins disposed between the first plate and the second plate. In addition, the plurality of fins are spaced apart by a width large enough adapted for counter-flow of a plurality of fluids between adjacent fins of the plurality of fins. Further, the plurality of fins are configured to direct fluid flow across a length of the first plate and the second plate.

Abstract: A system for delivering a medicinal fluid to a patient includes a variable volume pressure delivery chamber, a variable volume medication chamber, an optional medication reservoir, a movable delivery element, a fixed reference volume chamber, a pressure source, and a control sub-system. The variable volume pressure delivery chamber is configured to store pressure controllably. The variable volume medication chamber is fluidically isolated from the pressure delivery chamber and is configured to store medicinal fluid. The movable delivery element is disposed between the medication chamber and the pressure delivery chamber. The pressure source is coupled to the pressure delivery chamber.

Abstract: The disclosure relates to fin inserts for heat and mass exchangers and corresponding methods. For instance, in some examples, a fin insert to a heat and mass exchanger includes a generally rigid, longitudinally-extending member that includes a top portion and side portions. The side portions may be disposed on opposite sides of the top portion, and may include a concave shape facing away from one another. The side portions may further are each be positioned around a portion of a respective heat transfer tube.

Abstract: A system for delivering a medicinal fluid to a patient includes a variable volume pressure delivery chamber, a variable volume medication chamber, an optional medication reservoir, a movable delivery element, a fixed reference volume chamber, a pressure source, and a control sub-system. The variable volume pressure delivery chamber is configured to store pressure controllably. The variable volume medication chamber is fluidically isolated from the pressure delivery chamber and is configured to store medicinal fluid. The movable delivery element is disposed between the medication chamber and the pressure delivery chamber. The pressure source is coupled to the pressure delivery chamber.

Abstract: A device, system and method are provided for controlling the rate of infusion of fluids during infusion therapy using non-electric infusion devices. Rotation of a flow regulator dial causes an orifice connected to the inlet to modify its position relative to a particular one or more orifices or groove portions, the characteristics of which provide a certain flow rate characteristic. The flow regulator allows for the infusion pump to infuse at a rate that may be varied during use by the user. Additionally, the flow regulator is made from a material selected to operate under a wide range of pressures, from 5-40 PSI, making the flow regulator compatible with pressurized devices, such as, a non-electric pump.

Abstract: A device, system and method are provided for controlling the rate of infusion of fluids during infusion therapy using non-electric infusion devices. Rotation of a flow regulator dial causes an orifice connected to the inlet to modify its position relative to a particular one or more orifices or groove portions, the characteristics of which provide a certain flow rate characteristic. The flow regulator allows for the infusion pump to infuse at a rate that may be varied during use by the user. Additionally, the flow regulator is made from a material selected to operate under a wide range of pressures, from 5-40 PSI, making the flow regulator compatible with pressurized devices, such as, a non-electric pump.

Abstract: A device, system and method are provided for controlling the rate of infusion of fluids during infusion therapy using non-electric infusion devices. Rotation of a flow regulator dial causes an orifice connected to the inlet to modify its position relative to a particular one or more orifices or groove portions, the characteristics of which provide a certain flow rate characteristic. The flow regulator allows for the infusion pump to infuse at a rate that may be varied during use by the user. Additionally, the flow regulator is made from a material selected to operate under a wide range of pressures, from 5-40 PSI, making the flow regulator compatible with pressurized devices, such as, a non-electric pump.

Abstract: A device, system and method are provided for controlling the rate of infusion of fluids during infusion therapy using non-electric infusion devices. Rotation of a flow regulator dial causes an orifice connected to the inlet to modify its position relative to a particular one or more orifices or groove portions, the characteristics of which provide a certain flow rate characteristic. The flow regulator allows for the infusion pump to infuse at a rate that may be varied during use by the user. Additionally, the flow regulator is made from a material selected to operate under a wide range of pressures, from 5-40 PSI, making the flow regulator compatible with pressurized devices, such as, a non-electric pump.

Abstract: Methods and circuits for distributing power to suspended-particle-device (SPD) film products including SPD windows, SPD shades, and other SPD products, which are referred to generally as SPD loads. A driving voltage derived from a primary power source is provided to an SPD load by backbone wiring which carries a low AC or DC voltage derived from the primary power source, and a conversion stage which converts the low voltage to an AC driving voltage which is then supplied to the SPD load.

Abstract: Method and apparatus for associating the color of an object with an event preferably provides linked information for the object in any one of a plurality of succeeding video frames based only on the color value of the object. Preferably, at least one computer is coupled to a GUI and to a pointing structure, and is configured to: (i) identify coordinates of the object in a first video frame where the pointing structure has pointed; (ii) determine the color values of the identified object; (iii) store the color values of the identified object; (iv) detect an action of the object being selected in any one of the plurality of succeeding video frames; (v) determine the color values of the selected object; (vi) determine whether the selected object color values correspond to the stored color values; and (vii) automatically provide the linked information to the GUI only when the color values correspond.

Abstract: An atrial ablation catheter with an electrode array particularly adapted to locate and ablate foci of arrhythmia which are required for sustained atrial fibrillation is provided. The array is easily deployed and retracted from the catheter, and presents a proximally oriented electrode array that can be pulled against the septal wall of the left atrium to engage the septal wall.

Abstract: An inverting transfer mechanism of a blow molding apparatus for receiving preforms or blow-molded products that are upright or inverted and are transported along a first circular transportation passage, inverting a posture of the preforms or blow-molded products while transporting the preforms or blow-molded products along a second circular transportation passage, and transferring the preforms or blow-molded products to a third circular transportation passage.

Abstract: A radio frequency tissue ablation system with a radio frequency generator, the generator comprising a radio frequency source, at least four independently controllable radio frequency outputs, a user interface and a controller configured to delivery radio frequency energy from the radio frequency source to the radio frequency outputs in one of at least two different output configurations in response to a configuration selection made through the user.

Abstract: An ablation therapy system and systematic method is provided for treating continuous atrial fibrillation. The therapy system includes a Multi-Channel RF Ablation Generator, an ECG interface, an assembly of at least three ablation catheters, and an ECG interface operably coupling and interfacing the catheters to both an ECG unit and the RF Ablation Generator. The systematic method includes transseptally accessing the Left Atrium (LA) through the septum of the patient's heart, and performing an endocardial pulmonary vein ablation procedure on the pulmonary vein ostial tissue surrounding one or more pulmonary veins in a manner treating aberrant conductive pathways therethrough. After performing the pulmonary vein ablation, the method further includes performing an endocardial atrial septum ablation procedure on the septal tissue in a manner treating aberrant conductive pathways therethrough.

Abstract: A blow molding apparatus that includes a preform supplying station for supplying preforms in an upright state, a heating station for heating the preforms to a suitable temperature condition for blow-molding while transporting the preforms, a blow station for blowing the heated preforms to form blow-molded products, and a collection station for collecting the blow-molded products.

Abstract: An atrial ablation catheter and methods for its use. The endocardial catheter includes an electrode array particularly adapted to locate and ablate foci of arrhythmia which are required for sustained atrial fibrillation is provided. The array is easily deployed and retracted from the catheter, and presents a distally oriented electrode array that can be pressed against the wall of the atrium.

Abstract: A preparation combining a complex of a cancer antigen and a hydrophobized polysaccharide with an agent, e.g., an extract from hemolytic streptococcus, which binds to a Toll-like receptor to stimulate the antigen presenting cells activates all of the antigen presenting cells, the killer T cells and the helper T cells which are major immune cells when antigen specific immunity against cancer cells is induced and activated, and exerts a potent vaccinal effect. A vaccine preparation of the present invention induces immune responses to the cancer antigen, in particular, has effects of activation and induction of cytotoxic T cells and helper T cells, and thus, can be used as a therapeutic or preventive vaccine for cancer therapy.

Abstract: A mold opening/closing mechanism of a blow molding apparatus in which a plurality of blow-molding molds are transported along a circular transportation passage with a fixed feed pitch, and each blow-molding mold has a pair of molding dies capable of opening and closing in a lateral direction, including a turntable on which a plurality of blow-molding molds are mounted at intervals of a fixed angle; a vertical moving shaft that rises and falls as the turntable rotates; a slider that slides in a direction perpendicular to an opening/closing direction of the blow-molding molds as the vertical moving shaft rises and falls; and a pair of operation arms that convert sliding movement of the slider to opening/closing movement of the blow-molding molds.

Abstract: A first transfer mechanism of a biaxial stretch blow-forming apparatus has sliders that are transported along a circular transportation passage. The sliders slide along a circular guide rail installed on a turntable. Each of the sliders is swung to left and right by a swing arm as the turntable rotates, and a feed pitch of a preform holding groove formed in a holding plate installed at an end of each of the sliders is changed. The feed pitch can be changed by a simple mechanism. Because the holding groove always faces a radial direction, receiving and handing over actions of a preform sent along the circular transportation passage can be reliably performed.

Abstract: An inverting transfer mechanism of a blow molding apparatus for receiving preforms or blow-molded products that are upright or inverted and are transported along a first circular transportation passage, inverting a posture of the preforms or blow-molded products while transporting the preforms or blow-molded products along a second circular transportation passage, and transferring the preforms or blow-molded products to a third circular transportation passage.