1447 results about "Fluid injection" patented technology

A jet injector system for injecting fluid into a body. The jet injection system includes capsules for holding the material to be injected, apparatus for applying force to the capsule(s) to eject the injection material(s) and a perforator for directing the jet stream for the respective materials into the body. A flyweight system is described for developing jet injection pressures, and latching devices control the flyweight system. An injector system for injecting more than one fluid is described.

An active needle device (10) for fluid injection or extraction includes at least one hollow elongated shaft (11) defining at least one channel (12). The channel (12) provides communication between at least one input port (15) and at least one output port (16) of the needle device (10). At least one active component (17) such as a sensor or actuator is placed or integrated into the elongated shaft (1 1). The needle device (10) can include a macroneedle, a microneedle (21), or an array of macroneedles or microneedles (25a). The microneedles (21) can be fabricated on a substrate (26) which can remain attached to the microneedles (21) or be subsequently removed. The active component can facilitate biochemical, optical, electrical, or physical measurements of a fluid injected or extracted by the needle device (10).

One embodiment provides a method of using contextual lighting to assist a user of a medical fluid injection system. In this embodiment, the method includes providing a lighted display in proximity to a component of the injection system during setup of the medical fluid injection system. If the user has properly performed a setup function that is associated with the component of the injection system, the method further comprises providing a first visual indication on the lighted display. If the user has not properly performed the setup function that is associated with the component of the injection system, the method further comprises providing a second visual indication on the lighted display.

A method and apparatus for injecting fluid into areas having high density tissue that creates a high backpressure resistance on the injection device is disclosed. The high backpressure resistance is overcome through a mechanical advantage achieved by using a secondary reservoir having a cross-sectional area smaller than the cross-sectional area of a primary reservoir. Exemplary injection device reservoir housings may comprise a primary reservoir, a secondary reservoir, a check valve, a septum penetrating cannula, travel limits, a pen needle connecting portion, sliding seal guide ribs, a sliding seal, a pen needle assembly, a needle stop, and a patient needle.

A fluid-type multiple electrochemical system. The system includes a substrate for an electric circuit having a plurality of electrode parts formed at regular intervals. The electrode parts each include a reference electrode and an auxiliary electrode. Also provided is a fluid-type substrate having a fluid injection part, a fluid ejection part and a plurality of fluid storages. The fluid storages are formed at the same regular intervals as the electrode parts of the substrate and are connected with each other through fluid passages. The system also includes a sensor substrate having a plurality of unit sensors formed at the same regular intervals as the electrode parts of the substrate. Each unit sensor has an electrode part, an electrode pad for supplying power voltage simultaneously, and an electrode wiring.

Devices, systems and methods are disclosed for determining the composition of a plaque at a plaque site, which could be inside a blood vessel. Through a combination of fluid injection with different conductivities and measurement of the resultant conductances, a parallel tissue conductance measure is obtained that assists in determining the composition of the site plaque. Lower parallel conductance levels are determinative of a higher lipid and / or fatty plaque, which is a type that may break out of its position and cause organ injury or death.

A multi-fluid injector system and methods of operation thereof are presented. One embodiment of such a fluid injector system includes an automatic refill procedure for a fluid injector system comprising a fluid injector and an operably engaged syringe. The procedure includes the step of determining, using an electronic control device operably controlling the fluid injector system, whether a fluid injection procedure involving the syringe is impending. If the electronic control device determines that the fluid injection procedure is not impending, such that the automatic refill will not interfere with the fluid injection procedure, an automatic refill of the syringe is initiated.

A combined fluid injection and inflation system is disclosed and includes a fluid delivery system including at least one pressurizing device, a fluid path, and a control unit. The fluid path is adapted to connect the pressurizing device to a patient via a catheter including a balloon and inserted in the patient. The control unit is operable to control the fluid delivery system. In operation, the control unit selectively actuates the fluid delivery system to operate in a fluid injection mode or in a balloon inflation mode. In the fluid injection mode the pressurizing device delivers fluid to the fluid path for a fluid injection procedure. In the balloon inflation mode, the pressurizing device delivers fluid to the fluid path for inflating the balloon associated with the catheter. An operator control may be connected to the control unit for controlling the fluid delivery system and may be a handheld device.

A system comprising: a plasma production chamber configured to produce a plasma; a reaction chamber vaporize a precursor material with the plasma to form a reactive mixture; a quench chamber having a frusto-conical surface and a quench region formed within the quench chamber between an ejection port of the reaction chamber and a cooled mixture outlet, wherein the quench region configured to receive the reactive mixture from the ejection port, to cool the reactive mixture to form a cooled mixture, and to supply the cooled mixture to the cooled mixture outlet; and a conditioning fluid injection ring disposed at the ejection port and configured to flow a conditioning fluid directly into the reactive mixture as the reactive mixture flows through the ejection port, thereby disturbing the flow of the reactive mixture, creating turbulence within the quench region and cooling the reactive mixture to form a cooled mixture comprising condensed nanoparticles.

A medical instrument for fluid injection includes a tubular member and a plurality of hollow needle elements connected to one end of the tubular member. Generally, the tubular member has a lumen and all the needle elements communicate with the lumen to enable a distribution of a diagnostic or therapeutic fluid to various points in a predetermined region. The tubular member is provided with a fluid introduction port at an end of the tubular member opposite the needle elements, the fluid introduction port communicating with the lumen. The needle elements are disposed in a predetermined configuration adapted to carry out a desired function. The needle elements are at least partially made of resilient material with a memory so that the needle elements are biased by their internal stresses towards a predetermined rest configuration and are alternately disposable in the rest configuration and at least one stressed or loaded configuration.

A formation treatment tool assembly is conveyed within a well casing by a tubing string and has a housing defining treatment fluid supply and discharge passages and a fluid injection port through which treatment fluid is directed from the supply passage into a packer isolated casing interval and a fluid inlet port permitting flow from the isolated casing interval to the fluid discharge passage. Spaced straddle packer elements of the tool are energized to establish sealing engagement with the well casing and define an isolated casing interval and are de-energized to retract from sealing engagement with the well casing and permit tubing conveyance. A dump valve connected with the tool housing is opened to permit flow of treatment fluid from the isolated casing interval through the treatment fluid discharge passage and is closed to confine treatment fluid to the isolated casing interval. A hydraulic or mechanically actuated tubing isolation valve is selectively closed to isolate the tubing string from casing or formation pressure and permit tool conveyance while maximizing the service life of the tubing string and to accommodate overpressured and underbalanced reservoir conditions.

A thermal in-situ method and apparatus are provided for recovering hydrocarbons from subterranean hydrocarbon-containing formations such as oil sands, oil shale and other heavy oil systems. Recovery of viscous hydrocarbon by hot fluid injection into subterranean formations is assisted by using a specially designed wellbore with an active hydraulic seal, with a axial communication zone with multiple injection perforations separated from the production perforations by a moveable packer. In addition, a novel downhole thermal sensing apparatus is used to monitor and control oil production. A producing mechanism including pumping equipment lifts the produced oil from the central cavity to the surface.

Methods and apparatus for delivering precise amounts of fluid under pressure into cardiac tissue for the purpose of facilitating ablation of the tissue along a desired lesion line. One method injects fluid under pressure through a discharge orifice in a needle-less injection device. The injected fluid can be a cytotoxic fluid and / or a highly conductive fluid injected in conjunction with radio frequency ablation to create an ablative virtual electrode. The injected fluid can provide deeper and narrower conduction paths and resulting lesions. Radio frequency ablation can be performed at the same time as the fluid injection, using the injection device as an electrode, or subsequent to the fluid injection, using a separate device. In some methods, the injected fluid is a protective fluid, injected to protect tissue adjacent to the desired lesion line. Fluid delivery can be endocardial, epicardial, and epicardial on a beating heart. The present methods find one use in performing maze procedures to treat atrial fibrillation.

A wafer-scale apparatus and method is described for the automation of forming, aligning and attaching two-dimensional arrays of microoptic elements on semiconductor and other image display devices, backplanes, optoelectronic boards, and integrated optical systems. In an ordered fabrication sequence, a mold plate comprised of optically designed cavities is formed by reactive ion etching or alternative processes, optionally coated with a release material layer and filled with optically specified materials by an automated fluid-injection and defect-inspection subsystem. Optical alignment fiducials guide the disclosed transfer and attachment processes to achieve specified tolerances between the microoptic elements and corresponding optoelectronic devices and circuits. The present invention applies to spectral filters, waveguides, fiber-optic mode-transformers, diffraction gratings, refractive lenses, diffractive lens / Fresnel zone plates, reflectors, and to combinations of elements and devices, including microelectromechanical systems (MEMS) and liquid crystal device (LCD) matrices for adaptive, tunable elements. Preparation of interfacial layer properties and attachment process embodiments are taught.

This wet compression invention with a vaporizable fluid mist demonstrates major performance improvements over the relevant art in achieving a high degree of saturation, providing sensible cooling, strongly reducing the temperature increase due to compression work, reducing excess diluent air flow for downstream combustion, reducing compression noise, and increasing the achievable compressor pressure ratio. These improvements are obtained by one or more of: high mist or overspray from a) progressive axial injection of vaporizable fluid along the streamwise compression flow path, and b) transverse vaporizable fluid delivery from stators, rotors, perforated tubes, and / or duct walls, matching the gaseous fluid flow distribution across the compressor stream; c) reducing the compressor cross-sectional flow area of downstream compressor stages relative to up-stream stages, and d) increasing the rate of downstream vaporizable fluid injection relative to the rate of upstream injection, as a function of each compressor stage pressure ratio.

A device for injecting additive fluids into a stream of a primary fluid as it passes through a common central bore is characterized by a series of specially formed layers each having a particular fluid flow pattern formed therein. The layers are registered one above the other and sandwiched together to form an integral unit in which there are separate fluid flow channels for each of a desired number of additive fluids. Each channel has an inlet for receiving fluid from an associated pressurized source and a plurality of outlets terminating in angularly spaced relationship around an interior perimeter surface of the common bore. A selection mechanism provides for choosing a desired additive fluid for injection into the primary fluid in a manner coordinated with the flow of the primary fluid through the common bore.