83 results about "Fluid aspiration" patented technology

A fluid aspiration device is provided having a syringe, a disposal reservoir and a disposal fluid passageway. The syringe has a variable-volume fluid chamber and an aspiration fluid passageway between the fluid chamber and a region of the body containing a fluid for aspiration. An aspiration valve is positioned in the aspiration fluid passageway. The disposal fluid passageway is between the fluid chamber and disposal reservoir and has a disposal valve positioned therein. The fluid is aspirated by expanding the variable volume of the fluid chamber to draw the fluid through the open aspiration valve into the fluid chamber. The aspiration valve is closed and the variable volume of the fluid chamber is contracted to open the disposal valve and displace the fluid into the disposal reservoir. When aspiration is terminated, the fluid aspiration device is maintained intact and the intact device including the fluid is disposed.

A method for operating a surgical system including a control unit having a vacuum sensor and/or a flow rate sensor, the method including placing a handpiece in an operative relationship with an eye for a surgical procedure and thereafter supplying irrigation fluid to the handpiece while applying a vacuum to the handpiece to aspirate the irrigation fluid from the eye through the handpiece. During fluid aspiration, a vacuum level and/or flow rate is sensed which corresponds to an occlusion of the handpiece and from the sensed vacuum level and/or flow rate, a duration of the occlusion is determined. In response to the determined duration of occlusion, at least one of the handpiece parameters is varied.

A distraction pin for aspiration of a bone fluid and marrow. The pin includes an elongate metallic shaft of generally uniform diameter having a proximate end. The proximate end of the shaft includes an adaptor (attachment means) and a longitudinal bore extending from the distal end to the proximate end. The distal end of the shaft includes threading adapted for screwing the shaft into bone. The distal end also includes at least two fenestrations transverse to the longitudinal bore.

A fluid aspirating/dispensing member includes a sample cavity for sample acquisition and a sealable cavity that, once sealed, permits the separation of particles from the remainder of a fluid sample within the sample cavity after centrifugation or other separation means. The fluid aspirating/dispensing members, either individually or as part of an array, increase the efficiency of sample processing before analysis by a clinical analyzer.

A method for differentiating between a liquid sample having clogs therein and a liquid sample having an abnormally elevated viscosity during a liquid aspiration process by relating the ratio between the maximum negative pressure during aspiration and an equilibrium pressure prior to dispensation to viscosity.

A device is employed that can be retrofit onto existing feed pumps to remediate the problem of fluid aspiration in patients being fed through a feeding tube from the pump. In one embodiment the feeding pump is plugged into the device which is plugged into a power outlet. A patient angle sensor triggers power cutoff to the pump and stoppage of fluid flow. The angle sensor and operating program may be part of a smart phone. Power to the pump may be shut off due to a Bluetooth signal from the smart phone to a Bluetooth controlled power strip into which the pump is plugged to receive power.

A method detects proper connection of fixtures to a channel in an endoscope and proper flow through the channel during a cleaning or disinfection procedure. The endoscope has a first opening into one of its channels to which is connected a fixture and a second opening which is placed into a liquid. Negative pressure at the first opening draws an amount of liquid through the channel which is measured. If the channel is blocked insufficient liquid will flow an be measured. If the fixture is not connected properly air will leak in and insufficient liquid will flow an be measured.

Medical device assemblies capable of aspirating liquid into a syringe barrel or other medical devices while evacuating any air from the syringe are described. An exemplary medical device includes a syringe barrel, plunger rod and stopper assembly having an air permeable and liquid impermeable porous portion and structure for forming a vacuum within either the stopper or the plunger rod. Described is a medical device including a syringe barrel, plunger rod and stopper assembly having an air permeable and liquid impermeable porous portion and structure for forming a vacuum within chamber between the stopper and plunger rod wherein the plunger rod includes a sealing edge and is moveable relative to the stopper. Exemplary medical devices may include a vent for allowing air that permeates through the porous portion to escape to atmosphere. Methods for aspirating a syringe barrel with a liquid are also provided.

An electrosurgical instrument having active and return electrodes with a movable suction sheath for variable fluid and debris removal during surgical procedures is disclosed. The suction apparatus has an outer sheath that is external to a shaft to provide a lumen. The sheath assembly is axially movable relative to the fluid aspiration element between first and second positions for treating the target site and fluid and debris removal, respectively. The first position positions the distal end of the shaft axially distal to a leading edge of the sheath assembly. The second position positions the distal leading edge of the sheath assembly axially adjacent to the end of the shaft. The fluid aspiration element comprises an inner lumen extending through the shaft, and at least one port extending radially through the shaft. The port is in communication with the inner lumen. A vacuum provides suction through the port and inner lumen.

Method and system for controllably administering and/or withdrawing fluid from a patient. In one embodiment, the system may include a needle assembly, an ultrasound imager, a fluid supply storage unit, a waste storage unit, a fluid pump, and a foot pedal assembly. A syringe may serve as the fluid supply storage unit and the waste storage unit. The pump may include a bi-directional motor and a gear coupled to the motor. The gear may be engageable with a rack on the syringe plunger to drive the plunger either for fluid aspiration or infusion. Depression of one portion of the foot pedal assembly causes the motor to drive the gear in one direction, and depression of another portion of the foot pedal assembly causes the motor to drive the gear the other direction. The system may include a control device to keep pressure in the fluid path from exceeding a limit.

Apparatus and method for aspirating liquid from a container, e.g., a test tube or other vessel, includes apparatus for sensing that an aspiration probe tip is contacting the inside bottom wall of the container, whereby a maximum volume of liquid can be aspirated from the container. According to the invention, an encoder is mounted on the driven member of a motor (e.g., on a rotatably-driven drive shaft or a nut of a stepper or D.C. motor, or on a linearly-driven shaft of a linear actuator) used to rectilinearly advance the probe tip into the container. Such encoder produces a series of pulses indicating the speed and/or linear position of the probe tip. A motor controller responds to a predetermined change in pattern of pulses from the encoder indicating that movement of the probe tip has been resisted by the vessel bottom, whereby further movement of the driven member and of the probe connected thereto is arrested, and the probe tip remains in contact with the vessel bottom.

Disclosed is a disposable needle filter apparatus with a universal truncated syringe-receiving neck to enable the filtration of fluids/solutions aspirated into a needle-bearing syringe. The apparatus includes a needle seal stopper and needle stop to create a substantially airtight chamber to facilitate fluid aspiration through an enclosed filter and into the syringe. In an alternative embodiment, the filter apparatus includes an extended syringe-receiving neck configured to receive a specifically sized syringe/needle combination. In a further embodiment, the receiving neck is constructed as a modular unit to allow for interchangeable necks to accommodate different needle and syringe sizes with different cross-sectional diameters. In a yet further embodiment, the neck is constructed with stepped tapered segments of serially larger cross-sectional diameters to accommodate differently sized syringes. In a still further embodiment, the apparatus includes an accessory needle secured to the apparatus inlet.

There are provided a method of detecting dispensed quantity in which without the need of detecting a surface of liquid accommodated in a container, a liquid quantity can be detected only by measuring pressure change; and a relevant liquid suction monitoring dispensing apparatus. There is provided a method of detecting dispensed quantity for detection of the quantity of liquid suctioned and discharged by a dispensing apparatus including a pipette tip, a liquid suctioning/discharging mechanism for the pipette tip, a pressure sensor capable of detecting the pressure within the pipette tip, and a lifting and lowering mechanism for the pipette tip, which method comprises: an insertion step for inserting a distal end of the pipette tip down to the deepest zone of a container accommodating liquid to be measured; a suction pressure measuring step for without moving of the pipette tip, while suctioning the liquid into the pipette tip at a predetermined suctioning rate, measuring any pressure change during the suctioning; and a suction detecting step for on the basis of pressure change measured, determining the state of suction. Further, there is provided a liquid suction monitoring dispensing apparatus capable of practicing this method.

A method is provided for treating a neuromuscular defect in a subject. One step of the method includes locating a target nerve. After locating the target nerve, a treatment probe is provided. The treatment probe includes an elongated body member having a proximal end portion and a distal end portion. The distal end portion includes an energy delivery mechanism for stimulating or ablating the target nerve, a monitoring mechanism, and a fluid aspiration/delivery mechanism. Next, the target nerve is verified as an appropriate target for ablation by stimulating and then monitoring the target nerve via the energy delivery mechanism and the monitoring mechanism, respectively. After verifying the target nerve, a tumescent fluid is injected into the tissue surrounding the target nerve. An electric current is then delivered to the energy delivery mechanism to substantially ablate the target nerve.

A method for improving the accuracy or precision of a metered fluid includes: estimating a fluidic property of the fluid being metered; and adjusting one or more control parameters based on the estimated property to improve the accuracy or precision of a metered fluid. Preferably, the estimating the property of the fluid being metered includes: monitoring a physical event during the metering operation to collect sensed data; extracting features from the sensed data; and using the features to estimate fluid properties. In another preferred embodiment, the estimated fluidic property is viscosity and the sensed data is a pressure profile during a fluid aspiration. In another preferred embodiment, the method includes a diagnostic analyzer which includes a metering probe having a hard probe or a probe having a disposable tip and wherein the fluid is a body fluid sample. Another method includes: estimating a fluidic property of the fluid being metered; and adjusting one or more control parameters or thresholds that determine when an error is flagged based on the estimated property to improve the detection of the failure.

Disclosed is a disposable patient interface for an intraductal fluid aspiration system. The interface has a flexible tubular distal member for contacting the patient, and a proximal support portion forming a vacuum chamber therein. The support portion has a vacuum aperture for communication with a source of vacuum, and a retention structure for releasably mounting within a hand piece of an intraductal fluid aspiration system. The flexible member preferably has a low modulus of elasticity and a high tear strength, such that it can be stretched to fit over a rigid support without rupture.

The invention discloses a novel balloon expandable stent conveying system which comprises a balloon, an inner tube, a far-end outer tube, a corrugated tube, a soft head and a stent pushing tube. The inner tube runs through an inner cavity of the far-end outer tube and an inner cavity of the balloon; a combination body of the soft head and the inner tube is placed and connected into the neck part of the far end of the balloon; the farthest end of the far-end outer tube is placed into the neck part of the near end of the balloon and is connected with the neck part of the near end of the balloon; the balloon is of a one-layer or multilayer structure; and at least one layer of the balloon is made of a material with a micropore structure. The stent conveying system disclosed by the invention has a simple structure, also has the functions of pre-expanding a narrow tube cavity and conveying a stent, has good operation and control performance and strong passing performance, is rapid and convenient to operate and is cost-saving. When adopting the ePTFE (expanded polytetrafluoroethylene) material with the micropore structure, the balloon does not need to be folded and is simple to process; and time of sucking liquid in the balloon is short, the blood supply of far-end blood vessels is high in recovery speed, the balloon is changed into a cylinder shape with a small diameter after the liquid is pumped out, and the blood vessels cannot be damaged or the stent shifting cannot be caused in the retracting process. The balloon with the double-layer structure has higher pressure resistance capacity.

A microfluidic chip interface for providing fluid communication with external fluid sources and external fluid waste containers, and for providing electrical contact with voltage sources and voltage and current measuring devices, is described. The microchip is first placed into electrical communication with at least one electrical source and at least one electronic measurement device, and reversibly secured in place. Chosen fluids are provided into the microchip and directed through the chip using a fluid manifold having dispensing tubes and fluid aspiration tubes, which is brought into the vicinity of the secured microchip. The distance between the fluid manifold and the microchip is chosen such that the injection tubes are located within wells in the microchip connected to microfluidic channels, and the aspiration tubes are located near the surface of the microchip in the vicinity of the wells such that fluid spillage onto the surface of the microchip during fluid transfer is avoided. The fluid manifold is removed from fluid communication with the microchip during electrical measurements.