Abstract: A U-shaped vehicle with flexible beams equipped with an adjustable toe-angle, variable height suspension. Containers are attached between the beams of the vehicle. The rear suspension has a variable toe angle to control the spread of the beams so the vehicle can back around a container. Rear wheel axles are mounted on arms connected to pivot joints. An axle and its pivot points are non-co-planer. The pivot points are angled so that an outer pivot point is higher than an inner pivot point. When the vehicle is lowered close to the ground, the rear wheels develop slight toe out. When the vehicle is raised above Its normal ride height, the rear wheels develop slight toe in, and the beams of the vehicle spread apart when the vehicle is driven in reverse.

Abstract: A water supply sub-system for connection to a main water supply system includes a storage tank having an inlet with a flow control valve for connection to the main water supply system. The sub-system may be disconnected from the main system and configured as a closed system for disinfecting the sub-system. An outlet line connects the storage tank to a pump that pumps water from the tank to a sub-system supply line. One or more branch connections may connect the sub-system supply line to high-demand water using devices, such as dialysis machines. The supply line may be a feedback loop. A shunt feedback loop parallel to the feedback loop of the supply line has a pressure control valve that regulates pressure in the supply line feedback loop. A filtration device may also be included to ensure the purity of the water circulating through the sub-system.

Abstract: An extracorporeal blood processing system is disclosed which includes a variety of novel components and which may be operated in accordance with a variety of novel methodologies. For instance, the system includes a graphical operator interface which directs the operator through various aspects of the apheresis procedure. Moreover, the system also includes a variety of features relating to loading a blood processing vessel into a blood processing channel and removing the same after completion of the procedure. Furthermore, the system also includes a variety of features relating to utilizing a blood priming of at least portions of the apheresis sytem in preparation for the procedure. In addition, the system includes a variety of features enhancing the performance of the apheresis system, including the interrelationship between the blood processing vessel and the blood processing channel and the utilization of high packing factors for the procedure.

Abstract: An extracorporeal blood processing method includes a set-up phase establishing certain conditions in blood being processed prior to separation of the blood into components. Also, a blood processing method contemporaneously extracts selected multiple blood components from a blood processing vessel. Blood is separated into components in the blood processing vessel in a centrifugal field. Further, an extracorporeal blood processing method establishes a packing factor in the blood processing vessel prior to collecting red blood cells.

Abstract: A centrifugal fluid separation system separates a composite fluid into components. The system includes a rotor that has a composite fluid containment area, an inlet channel, a peripheral separation channel, outlet channels and separated component collection areas, which together form a processing area. The separation channel may be semi-spiraled. The inlet channel may connect to the center of the separation channel and an outlet channel may connect to each end of the separation channel. The outlet channels have different heights. The ends of the separation channels may have different heights. The separation channels may have extensions. The rotor may have multiple processing areas. The collection areas may be pockets slanted radially outwardly and downwardly. A motor may produce a rotating magnetic field, which co-acts with a magnetically reactive material in the rotor. A disposable bag and tubing system may be used in a processing area of the rotor.

Abstract: An arrow hold down for use with a compound bow having bow string cables and an arrow rest and a cable guard bar mounted above the arrow rest, the cable guard bar extending rearward from the bow and having a cable block on the cable guard bar. The arrow hold down comprises a pivot block secured to the cable guard bar and a holding apparatus in the pivot block. The holding apparatus comprises a forwardly extending arm with a tip to press against an arrow on the arrow rest and a rearwardly extending trigger. The trigger has a transverse portion that is struck by the cables of the bow as an arrow is shot. The arrow is held on the arrow rest by the tip of the forwardly extending arm. The tip is disengaged from the arrow by the motion of the cables or bowstring as the arrow is shot from the bow.

Abstract: The claimed invention relates to a method and a device for processing blood concentrate products before they are exposed to a continued process for extracting those remaining medicinally interesting sub-components. The appropriate pre-processing, in relation to the invention, primarily entails a mechanically powered resolution of the viscous flowing concentrate products in a diluting solution for the adaptation of the total products for a renewed centrifuging. The device includes a centrifuge machine containing one or more suspended product bags that can be oscillated forwards and backwards in an incomplete pendulum swing by operation of a motor mounted in a lid of the machine. The product bag(s) are connected to a ring bag for subsequent processing and to a bag containing diluting solution by a multi-way connector.

Abstract: A centrifugal separation device separates a composite fluid, such as blood, into the components thereof. The fluid is delivered to a fluid receiving area in a rotor from which area the fluid travels through a radial inlet channel having an inlet channel height to a proximal end of a circumferential fluid separation channel. Near a distal end of the separation channel, fluid components travel into distinct first and second outlet channels. The height of the first channel is greater than the height of the more distal second channel. The inlet channel height is greater than the height of the first channel. The rotor may be balanced by axially symmetrical sets of inlet channels, separation channels and outlet channels or by a balance channel connected to the separation channel but displaced from the outlet channels.

Abstract: Methods and apparatus particularly involving the separation of blood into blood components and the collection of such components are disclosed. In one aspect, an extracorporeal method for the collection of plasma and red blood cells is provided, wherein the collection of plasma and red blood cells may occur simultaneously or subsequently utilizing the same dual stage blood processing vessel. The flow of blood to the blood processing vessel and return of uncollected blood components may be provided via a single needle, wherein blood is removed from and returned to a donor/patient during alternating blood removal and blood return submodes. Platelet separation and collection options are also described. In either case, prior to red blood cell collection, a set-up phase may be carried out to set a predetermined hematocrit and AC ratio. Replacement fluid delivery may optionally also be provided either substantially continuously during any collection phase(s) and/or in a bolus mode.

Abstract: A spider-less and suspension-less speaker system, having a diaphragm constrained to move in a linear direction and supported by a frictionless or low friction support. A voice coil coupled to an audio input drives the speaker diaphragm. A position sensor determines the physical position of the diaphragm. A control circuit uses the sensed position information to modify the audio signal in such a way that the interaction of the voice coil and the magnetic field both drives the diaphragm to produce an audible output and restores the diaphragm to a neutral position in the absence of a further audio signal.

Abstract: A schema-isolated system is disclosed for developing, modifying, or maintaining client applications that accesses target databases. The system includes a middleware-table inserter that inserts middleware tables into the target database. The middleware tables include a set of compatibility data relating one or more client-application data requests with one or more corresponding target-database data capabilities. The middleware tables also include a data communication component. This component receives a client-application data request from the client application, and, based on at least a first datum of the set of compatibility data, provides to the client application the one or more target-database data capabilities corresponding to the client-application data request. The first compatibility datum relates the one or more client-application data requests with the one or more corresponding target-database data capabilities based, at least in part, on an application-usage-independent criterion.

Abstract: An apparatus and method for treatment of congestive heart failure from the right side of the heart. An implantable cardiac stimulation system with a multi-electrode lead having three or more selectable electrodes, together with apparatus for identifying an optimal subset of electrodes, apparatus for shaping a propagating wave front, and apparatus for modifying the intrinsic ventricular cardiac activation sequence, or generating simultaneous or near simultaneous pacing pulses to the septum or right ventricular outflow tract during ventricular systole in order to improve left ventricular cardiac efficiency and reduce mitral regurgitation in patients with dilated cardiomyopathy. A three dimensional map of electrode placement may be calculated. A sub set of the available electrodes in the right side of the heart is selected for stimulation such that septal motion during systole is reduced or the mitral valve area is stiffened to reduce mitral regurgitation.

Abstract: An arrow support for supporting an arrow in an archery bow. The arrow support provides a simple, compact, lightweight and non-bulky apparatus that corrects distortion induced in the arrow upon its release by the archer. Single screws provide secure, non-rotating connections where adjustments are to be made. A planar ring has locking apparatus extending through the ring to lock support members in place using a single adjustment. The planar ring has a scalloped inner surface, accommodating a range of fletches, with a minimal outside diameter of the ring. Silencers are provided on at least some of the support members to suppress sounds as an arrow is drawn into a shooting position.

Abstract: An athletic track having a post-tensioned concrete slab supporting a resilient surface. The athletic track has opposed, parallel rectangular side areas and opposed semi-circular end areas connecting the side areas. The concrete slab is cast in place without requiring expansion joints between segments. Cables are cast into the slab for providing a tension load in the concrete slab. A first set of cables is tilted away from the perpendicular in a first direction while a second set of cables is parallel to the edges of the rectangular areas such that members of the second set of cables cross members of the first set of cables. A third set of circumferential cables is provided in the semi-circular end areas. A fourth set of cables intersecting the circumferential cables is non-radially disposed. The slab has a relatively flat lower surface. Pour strips situated along a line of symmetry are provided between adjacent quadrants of the end areas.

Abstract: An implantable esophageal sphincter apparatus with an adjustable band to be placed at the lower part of the esophagus. The inflation of the band, or sphincter body, can be increased or decreased to adjust the tightness of the device. The inflatable sphincter body may be wrapped around the esophagus and may be connected to an inflation device with a fluid reservoir. The inflation device may have a pump mechanism that will respond to external control to increase or decrease the inflation of the sphincter body. The sphincter apparatus will be held in place at the area of implantation by sutures and by fenestration mechanisms, which will allow ingrowths of tissue or fibrous elements of the body around the sphincter apparatus or into porous materials on the sphincter apparatus. The apparatus may also include a circumferential shield on a distal side of the sphincter apparatus.

Abstract: A bite block for upper gastrointestinal endoscopy having a tubular body with a proximal end and a distal end and defining a channel open at the proximal and distal ends, a shield connected to the tubular body at the proximal end, and a tongue depressor connected to the tubular body at the distal end. The tongue depressor comprises a plate connected to a bottom side of the distal end of the tubular body and is curved downwardly. The bite block has a chamber open to the channel in the bite block. A viscous bio-compatible lubricant in said chamber can contact and coat the end of an endoscope or other instrument when the instrument is inserted through the bite block. A removable tab can be pulled away from an opening into the chamber to expose the lubricant after the bite block has been placed in a patient's mouth. A lumen extends from the proximal end to the distal end of the tubular body, through the wall of the tubular body.

Abstract: A lead assembly adapted for endocardial fixation to a human heart is provided. The lead assembly includes a lead body that has a proximal end provided with a connector for electrical connection to a cardiac stimulator. The cardiac stimulator may be a pacemaker, a cardioverter/defibrillator, or a sensing instrument. The distal end of the lead body is connected to a tubular electrode housing. The lead body consists of a noncoiled conductor cable surrounded by a coextensive insulating sleeve. In contrast to conventional leads, the lead body of the present invention does not require coiled conductor wires or an internal lumen. Manipulation of the lead body is via an external guide tube. Lead body diameters of 0.25 mm or smaller are possible.

Abstract: A method and apparatus for classifying and treating tachyarrhythmias. A cardiac stimulator includes an algorithm that uses dual chamber sensing to determine the type of tachyarrhythmia detected. If the tachyarrhythmia is of a type that responds well to ventricular therapy, such as a tachyarrhythmia originating in the ventricle rather than the atrium, the tachyarrhythmia is grouped into a treatable category. Accordingly, the cardiac stimulator applies therapy, or therapies, to the ventricle to remedy the ventricular tachyarrhythmia.

Abstract: A lead assembly for fixation to a human heart via thoracoscopy is provided. The lead assembly includes a lead that has a connector for connection to a cardiac stimulator, such as a pacemaker, a cardioverter/defibrillator, or a sensing instrument. A fixation mechanism is coupled to the lead that includes a tubular housing and a proximally projecting hook that is adapted to engage heart tissue. The hook is pivotable between a retracted position and an extended position. The lead and the hook are manipulated by a stylet. The lead assembly also includes a tubular introducer that is passed through the chest wall of a patient and used to place the lead proximate the epicardium.

Abstract: A lead assembly adapted for endocardial fixation to a human heart is provided. The lead assembly includes a lead body that has a proximal end provided with a connector for electrical connection to a cardiac stimulator. The cardiac stimulator may be a pacemaker, a cardioverter/defibrillator, or a sensing instrument. The distal end of the lead body is connected to a tubular electrode housing. The lead body consists of a noncoiled conductor cable surrounded by a coextensive insulating sleeve. In contrast to conventional leads, the lead body of the present invention does not require coiled conductor wires or an internal lumen. Manipulation of the lead body is via an external guide tube. Lead body diameters of 0.25 mm or smaller are possible.