88135 results about "Building construction" patented technology

A valve prosthesis device is disclosed suitable for implantation in body ducts. The device comprises support stent, comprised of a deployable construction adapted to be initially crimped in a narrow configuration suitable for catheterization through the body duct to a target location and adapted to be deployed by exerting substantially radial forces from within by means of a deployment device to a deployed state in the target location, the support stent provided with a plurality of longitudinally rigid support beams of fixed length; valve assembly comprising a flexible conduit having an inlet end and an outlet, made of pliant material attached to the support beams providing collapsible slack portions of the conduit at the outlet. When flow is allowed to pass through the valve prosthesis device from the inlet to the outlet the valve assembly is kept in an open position, whereas a reverse flow is prevented as the collapsible slack portions of the valve assembly collapse inwardly providing blockage to the reverse flow.

The present invention is a more durable expanded material that enables thinner wall thicknesses and a more flexible reinforcement suitable for stenting. The present invention is especially useful in the construction of grafts, stents, and stent-grafts which are used, for example, in repairing or replacing blood vessels that are narrowed or occluded by disease, aneurismal blood vessels, or other medical treatments. The inventive material and configurations allow expansion or contraction in size or adjustment in size in an incremental manner so that the optimum size, shape, and fit with other objects can be obtained. The present invention is also optionally capable of more accurately delivering one or more active ingredients such as drugs over longer periods of time. The present invention optionally includes surface modifications and additives that increase the surface adhesion of active ingredients, coatings, or combinations thereof. Finally, the present invention optionally includes growing cells on the inventive material so that the expanded material, reinforcement, or combinations thereof are useful, for example, in producing lab-grown blood vessels or organs.

This invention relates to improvements in prosthetic cardiac and venous valves and implantable medical devices having moveable septa. The inventive prosthetic cardiac and venous valves have metallic or pseudometallic valves coupled to metallic or pseudometallic stents that permit percutaneous delivery of the devices.

The present invention relates to an apparatus for conducting a variety of assays for the determination of analytes in liquid samples, and relates to the methods for such assays. In particular, the invention relates to a single-use cartridge designed to be adaptable to a variety of real-time assay protocols, preferably assays for the determination of analytes in biological samples using immunosensors or other ligand/ligand receptor-based biosensor embodiments. The cartridge provides novel features for processing a metered portion of a sample, for precise and flexible control of the movement of a sample or second fluid within the cartridge, for the amending of solutions with additional compounds during an assay, and for the construction of immunosensors capable of adaptation to diverse analyte measurements. The disclosed device and methods of use enjoy substantial benefits over the prior art, including simplicity of use by an operator, rapid in situ determinations of one or more analytes, and single-use methodology that minimizes the risk of contamination of both operator and patient. The disclosed invention is adaptable to the point-of-care clinical diagnostic field, including use in accident sites, emergency rooms, surgery, nursing homes, intensive care units, and non-medical environments.

The present invention is an artificial cornea designed to restore vision in patients who are not candidates to receive a natural cornea transplant (allograft). The present device construction involves the use of a biocompatible, non-porous optic disk intimately bonded to one or more anchoring layers of porous polymeric material, and a unique sealing region which enhances sealing of the artificial cornea in the recipient's eye.

This invention relates generally to footwear and methods for making the same, more particularly to a seamless upper for footwear and methods for making a seamless upper. In one aspect of the invention, the upper is seamless and/or is of unitary construction that defines an interior void for comfortably receiving a foot.

An article of footwear and a method of manufacturing the article of footwear are disclosed. The footwear may include an upper and a sole structure. The upper incorporates a textile element with edges that are joined together to define at least a portion of a void for receiving a foot. The textile element may also have a first area and a second area with a unitary construction. The first area is formed of a first stitch configuration, and the second area is formed of a second stitch configuration that is different from the first stitch configuration to impart varying textures to a surface of the textile element. Various warp knitting or weft knitting processes may be utilized to form the textile element.

A sensor system for use in a vehicle that integrates sensor data from more than one sensor in an effort to facilitate collision avoidance and other types of sensor-related processing. The system include external sensors for capturing sensor data external to the vehicle. External sensors can include sensors of a wide variety of different sensor types, including radar, image processing, ultrasonic, infrared, and other sensor types. Each external sensor can be configured to focus on a particular sensor zone external to the vehicle. Each external sensor can also be configured to focus primarily on particular types of potential obstacles and obstructions based on the particular characteristics of the sensor zone and sensor type. All sensor data can be integrated in a comprehensive manner by a threat assessment subsystem within the sensor system. The system is not limited to sensor data from external sensors. Internal sensors can be used to capture internal sensor data, such a vehicle characteristics, user attributes, and other types of interior information. Moreover, the sensor system can also include an information sharing subsystem of exchanging information with other vehicle sensor systems or for exchanging information with non-vehicle systems such as a non-movable highway sensor system configured to transmit and receive information relating to traffic, weather, construction, and other conditions. The sensor system can potentially integrate data from all different sources in a comprehensive and integrated manner. The system can integrate information by assigning particular weights to particular determinations by particular sensors.

A Flogrid Simulation Gridding Program includes a Flogrid structured gridder. The structured gridder includes a structured areal gridder and a block gridder. The structured areal gridder will build an areal grid on an uppermost horizon of an earth formation by performing the following steps: (1) building a boundary enclosing one or more fault intersection lines on the horizon, and building a triangulation that absorbs the boundary and the faults; (2) building a vector field on the triangulation; (3) building a web of control lines and additional lines inside the boundary which have a direction that corresponds to the direction of the vector field on the triangulation, thereby producing an areal grid; and (4) post-processing the areal grid so that the control lines and additional lines are equi-spaced or smoothly distributed. The block gridder of the structured gridder will drop coordinate lines down from the nodes of the areal grid to complete the construction of a three dimensional structured grid. A reservoir simulator will receive the structured grid and generate a set of simulation results which are displayed on a 3D Viewer for observation by a workstation operator.

A valve prosthesis device is disclosed suitable for implantation in body ducts. The device comprises a support stent, comprised of a deployable construction adapted to be initially crimped in a narrow configuration suitable for catheterization through the body duct to a target location and adapted to be deployed by exerting substantially radial forces from within by means of a deployment device to a deployed state in the target location, and a valve assembly comprising a flexible conduit having an inlet end and an outlet, made of pliant material attached to the support beams providing collapsible slack portions of the conduit at the outlet. The support stent is provided with a plurality of longitudinally rigid support beams of fixed length. When flow is allowed to pass through the valve prosthesis device from the inlet to the outlet, the valve assembly is kept in an open position, whereas a reverse flow is prevented as the collapsible slack portions of the valve assembly collapse inwardly providing blockage to the reverse flow. The device is configured so that retrograde flow will be altered from laminar flow and directed towards the leaflets to effect closing.

First, second and third lighting devices each comprise a thermal conduction element, solid state light emitters and a reflective element. In the second device, the conduction element defines an opening; and the emitters and reflective element are mounted on a first side of the conduction element. In the third device, the conduction element defines an opening; a first portion of a first side of the conduction element is in contact with a contact region of a construction surface; and the emitters and reflective element are mounted on the first side. A fourth device comprises a conduction element and emitters; a first portion of a first side of the conduction element is in contact with a contact region of a construction surface; the emitters are mounted on a second portion of the first side of the conduction element; and a second side of the conduction element is exposed to ambient air.

A combined-rib cavity member for space-structure flooring includes cavity form and structure bottom plate, which are connected into one integral whole. It is characterized by that there are at least two cavity forms arranged alternate with each other on the structure bottom plate, its side forms with the structure bottle plate at least one subrit form cavity of casti-in-situ structure, and other other sides of the cavity form forms the side fromboard of main rib or beam or wall for cast-in-situ structure. By this, the subrib of cast-in-situ structure can be formed in the sub-rib form cavity on the structure battom plate, the sub-rib participates in load bearing of structural bottom slat, cast-in-situ main rib, cast-in-sita upper slab so to a load-bearing space structure, improved mechanical property, raise integrity and anti-shock property, decrease structural wt. lower cost and make construction be convenient.

The invention relates to a medical or dental-medical treatment instrument (1) having a grip sleeve (11), an oscillatory rod (13) which extends longitudinally in the grip sleeve (11) and is mounted therein in a radially or also axially elastically yielding manner, and an oscillation generator (31) for transmitting oscillations to the oscillatory rod (13). In order to attain a compact construction, the oscillatory rod (13) is of a base part and an attachment part which is fixed on the base part.

A computer-implemented automated building design and modeling and construction project cost estimating and scheduling system (“DMES system”) is described. The DMES system provides a central source for all of the design and construction information for a construction project in a coordinated two-dimensional and three-dimensional spatial database that is freely accessible by all of the members of an interdisciplinary construction project team as a means to produce automatically coordinated design development and construction document information. The DMES system acquires and stores all of the appropriate design, engineering, and construction expertise and information available for any building type for use in automatically assembling and coordinating the design, cost-estimating, and scheduling for a construction project. In one embodiment, the DMES system consists of a plurality of objects, comprising elements and massing elements arranged in an assembly hierarchy. Each of the objects includes programming code that defines an interface and discrete internal functions that define its behavior. When instantiated in the database, the objects automatically create further instances of other objects in the hierarchy, which in turn do the same, thus assembling a complete building model automatically from the initial manually-placed instance. The building model enables automatic generation of drawings and cost and scheduling information. By running automatic iterations of the building model, multiple designs may be evaluated to determine the optimum design.

A method for generating an interactive profile of a structure, such as a building, employing an interactive profile system that preferably utilizes an Internet web browser to interface with a user. The interactive profile system includes an application engine embodied in a computer program that is preferably based within a server. A plan set, usually in a CAD format, is received into the interactive profile system, typically submitted by the user or client. The building can be any structure, such as a home, office or warehouse, and can also include the property that the structure occupies. The plan set is converted to a profile data set by the profiling engine. In compliance with an enhanced data protocol, which is a specific format for organizing the profile data set in a standardized array. The profiling engine parses, or extracts, the profile data set to develop and link a plurality of potentially interrelated building. The profiling engine performs a systematic enhancement of the plan set, building upon the elemental physical descriptions of the plan set. Each element of the physical description is functionally analyzed for relational attributes and then expanded and tagged. The user directs a profile query to the application engine of the interactive profile system. The profile query is relatable to the enhanced profile and more specifically relatable to at least one of the plurality of interrelated elements of the building. Typical profile requests can include proposed or actual changes to the building, requests for material listings, and project assessments.

A medical balloon catheter assembly includes a balloon having a permeable region and a non-permeable region. The balloon is constructed at least in part from a fluid permeable tube such that the permeable region is formed from a porous material which allows a volume of pressurized fluid to pass from within a chamber formed by the balloon and into the permeable region sufficiently such that the fluid may be ablatively coupled to tissue engaged by the permeable region. The non-permeable region is adapted to substantially block the pressurized fluid from passing from within the chamber and outwardly from the balloon. The porous material may be a porous fluoropolymer, such as porous polytetrafluoroethylene, and the pores may be created by voids that are inherently formed between an interlocking node-fibril network that makes up the fluoropolymer. Such voids may be created according to one mode by expanding the fluoropolymer. The balloon may be formed such that the porous material extends along both the permeable and non-permeable regions. In one mode of this construction, the porous material is porous along the permeable region but is non-porous along the non-permeable region, such as for example by expanding only the permeable region in order to render sufficient voids in the node-fibril network to provide permeable pores in that section. The voids or pores in the porous material may also be provided along both permeable and non-permeable sections but are substantially blocked with an insulator material along the non-permeable section in order to prevent fluid from passing therethrough. The insulator material may be dip coated, deposited, or extruded with the porous material in order to fill the voids. The insulator material may in one mode be provided along the entire working length of the balloon and then selectively removed along the permeable section, or may be selectively exposed to only the non-permeable sections in order to fill the voids or pores there.

For electronic commerce, selected items are tracked in a database and are made available for purchase by interactions with a customer. The construction and maintenance of the database may be summarized by three general steps. The first general step in the construction of the electronic commerce site is the establishment of a link between a particular product and a particular program or program episode that features the product. The second general step is creating a database of the records or links that are established from the first general step. The third general step is establishing an interface with the customer, which may be accomplished through the internet. A preferable technique for generating product tracking information uses radio frequency identification (RFID) tags to dynamically track products located in the video frame.

A catheter system for localized or semi-localized administration of agents through the wall of a blood vessel is provided. Various catheter system constructions which use at least one expandable occluding device to create an isolated region are provided. Constructions using one catheter and one occlusion device are provided, along with constructions using two catheters and multiple occlusion devices. The catheter system may include a catheter with a variable stiffness along its length. The catheter system may also include a guide wire integrated with an inner catheter. The catheter can infuse the agent into the blood vessel in a pressure regulated manner. Methods for delivery and infusion of the agent within a blood vessel are also provided.

Construction systems for erecting building structures comprise a plurality of prefabricated interconnectable modular building units, each unit not meeting at least one of the ISO certification criteria for transport of cargo but each unit comprising a frame shaped as a rectangular parallelopiped and comprised of framing members and a plurality of nodes, each node situated at a corner of said frame for selective interconnection with other units, the nodes and the exterior dimensions of the frame conforming to ISO shipping standards such that each unit is transportable using the ISO intermodal transportation system, and such that when the units are aggregated horizontally and vertically and adjacent units are interconnected, a building structure comprising at least one habitable space is formed. The modular units are assembled in a factory remote from the job site, and are there constructed to a semi-finished state, including installation of one or more of interior fit-out systems and finishes, exterior envelope systems, plumbing systems, electrical systems, environmental systems, and fire protection systems, following which the semi-finished modular units are transported from the factory to the job site, where they are craned into place and secured to form the structure being erected, a plurality of adjacent pairs of semi-finished modular units also being “stitched” together, and the semi-finished modular units are thereafter constructed to a finished state.

A system and methods are provided for interactive construction of data queries. One method comprises: generating a query based upon a plurality of user-identified data items, wherein the user-identified data items are data items representing desired results from a query, and wherein information related to the user-identified data items is included in a “given” clause of the query, assigning received input data to a hierarchical set of categories, presenting to a user a plurality of new query results, wherein the plurality of new query results are determined by scanning the received input data to find data elements in the same hierarchical categories as those in the “given” query clause and not in the same hierarchical categories as those of an “unlike” clause of the query, receiving from the user an indication as to whether each query result of the presented plurality of new query results is a desirable query result, adding query results indicated by the user as desirable to the “given” clause of the query, adding query results indicated by the user as undesirable to the “unlike” clause of the query, evaluating a metric indicative of the accuracy of the query, and responsive to a determination that the query achieves a predetermined threshold level of accuracy, storing the query.

The present invention relates to identity construction and verification on the Internet, and provides a block chain identity construction and verification method. The method comprises the following steps: a certificate authority constructs a user identity block chain according to an identity verification request submitted by a user; and the certificate authority performs user identity verification processing by means of the identity block chain. According to the method provided by the present invention, user identity information is written into the block chain, and multiple certificate authorities jointly complete confirmation and storage of the identity information by means of an agreement mechanism, and then the user can conveniently perform identity verification by using the block chain. The method is not only capable of improving efficiency of user identity verification, but also will not affect accuracy of the user identity information due to the problem of an individual certificate authority, thereby greatly improving security of an identity verification process.

Bioprosthetic devices for soft tissue attachment, reinforcement, or construction are provided. The devices comprise a sheet of naturally occurring extracellular matrix and a sheet of synthetic mesh coupled to the naturally occurring extracellular matrix portion.

A system and method for constructing a graphical user interface for an application being accessed by a user are provided. The method includes measuring the user's current work rate, deriving a threshold from the user's current work rate, determining the user's current activity within the application, assigning a value to the user's current activity, accessing a model for the application, the model defining links between activities within the application, assigning values to activities linked within the accessed model to the user's current activity, and displaying a control element in a graphical user interface for each activity with a value above the derived threshold.

Methods for easy, atraumatic access to areas of the vasculature that are otherwise difficult to access, using steerable guide catheters constructed with components that are selected to provide optimal navigability, torque transfer, and push ability for a variety of typical percutaneous access routes. The catheter wall thickness in the deflecting segment of the guide catheter is about 1 French (⅓ mm) or less, and includes a slotted deflection tube, and this construction allows a very tight turning radius which in turn enables guide catheter access to regions of the vasculature that are otherwise inaccessible.

A system and method for spinal fusion comprising a spinal fusion implant of non-bone construction releasably coupled to an insertion instrument dimensioned to introduce the spinal fusion implant into any of a variety of spinal target sites.

Provided are a device and a method for stabilizing two or more vertebrae by joining the vertebrae with a flexible device. The flexible device is of unitary construction and includes anchor posts constructed and arranged for insertion into holes drilled into the vertebrae, preferably after removing all or a portion of the pedicles from the target vertebrae. Removal of the pedicles provides an acceptable fastening site, prevents interference with the device by the pedicles, and provides native donor bone tissue, thereby obviating the need for a second surgery to harvest bone tissue from a different site, such as the hip.

The present invention relates to a spoken dialog system and method based on dual dialog management using a hierarchical dialog task library that may increase reutilization of dialog knowledge by constructing and packaging the dialog knowledge based on a task unit having a hierarchical structure, and may construct and process the dialog knowledge using a dialog plan scheme about relationship therebetween by classifying the dialog knowledge based on a task unit to make design of a dialog service convenient, which is different from an existing spoken dialog system in which it is difficult to reuse dialog knowledge since a large amount of construction costs and time is required.

Coding within noisy communications channels is essential but a theoretical maximum rate defines the rate at which information can be reliably transmitted on this noisy channel. Capacity-achieving codes with an explicit construction eluded researchers until polar codes were proposed. However, whilst asymptotically reaching channel capacity these require increasing code lengths, and hence increasingly complex hardware implementations. It would be beneficial to address architectures and decoding processes to reduce polar code decoder complexity both in terms of the number of processing elements required, but also the number of memory elements and the number of steps required to decode a codeword. Beneficially architectures and design methodologies established by the inventors address such issues whilst reducing overall complexity as well as providing methodologies for adjusting decoder design based upon requirements including, but not limited to, cost (e.g. through die area) and speed (e.g. through latency, number of cycles, number of elements etc).

The inventive subject matter relates to the methods for the induction of immunity and prevention of diarrhea resulting from Escherichia coli. The inventive subject matter also relates to the use Escherichia coli adhesins as immunogens and to the construction of conformationally stability and protease resistant Escherichia coli adhesin constructs useful for inducing immunity to Escherichia coli pathogenic bacteria. The methods provide for the induction of B-cell mediated immunity and for the induction of antibody capable of inhibiting the adherence and colonization of Escherichia coli including enterotoxigenic Escherichia coli, to human cells.

The focal length estimation method and apparatus claimed in this application aligns plural overlapping images with one another for constructing an image mosaic. This is accomplished by computing a planar perspective transformation between each overlapping pair of the images, computing from the planar perspective transformation a focal length of each image of the pair, computing from the focal length of each image a focal length transformation, computing a rotational transformation for each of the pair of images whereby a combination of the rotational transformation and the focal length transformation relates the respective image to a three-dimensional coordinate system. Registration errors between the pair of images are reduced by incrementally deforming the rotational transformation of one of the pair of images. The planar perspective transform is a matrix of warp elements, and the focal length is computed as a function of the warp elements, the function being derivable by constraining a first two rows or the first two columns of the matrix to have the same norm and to be orthogonal. The focal length of one image of a pair of images is found by applying the constraint on the matrix columns, while the focal length of the other image of the pair is found by applying the constraint on the matrix rows