| MEDRAD, INC. Patent applications |
| Patent application number | Title | Published |
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| 20120074330 | Device and Method for Determining Activity of Radiopharmaceutical Material - A detector system measures radioactive material. A fluid path receives at least one aliquot of radiopharmaceutical. The fluid path locates the aliquot within a positioner formed with a concave configuration. A detector is located at an axial distance from the concave surface and determines the level of radioactivity of the aliquot. Alternatively, the fluid path may be less concave and a variable attenuator may be placed between the fluid path and detector. The variable attenuator may have a concavity that is based on the concavity of the fluid path so that the detector's ability to read the radioactivity is optimized. A method for forming an aliquot of radiopharmaceutical in a concave fluid passage. Positioning a detector located a distance from the concave surface to optimize reading spectral energy of the aliquot and activity is determining activity regardless of the position of the aliquot in the passage. | 03-29-2012 |
| 20110152908 | Catheter Including Composite Guide and Methods for use and manufacturing of the Same - A catheter assembly includes a catheter body having a catheter lumen. A manifold assembly is coupled with a proximal catheter portion. A manifold lumen extends through the manifold assembly, and the manifold lumen includes an assembly cavity extending around the proximal catheter portion. A fluid jet loop is coupled with a high pressure tube at a distal catheter portion. The catheter assembly further includes a composite guide having first and second guide portions. The first guide portion includes a proximal guide insert near the proximal catheter portion, the proximal guide insert is positioned within the assembly cavity, and includes a guide insert surface flush with a catheter body interior wall. The second guide portion includes a distal guide near the distal catheter portion including a tapered loop guide surface and an intermediate guide surface of the catheter lumen flushly engaged with a leading edge of the tapered loop guide surface. | 06-23-2011 |
| 20110106015 | SYRINGE ASSEMBLIES, METHODS OF FORMING SYRINGE ASSEMBLIES AND ADAPTERS FOR FORMING SYRINGE ASSEMBLIES - A syringe assembly connectible to an injector including a syringe interface and a drive member includes a syringe portion including a barrel section to contain fluid to be pressurized and an outlet in fluid connection with the barrel section. The syringe assembly also includes an adapter formed separately from the syringe portion and including a plurality of sections. At least two sections of the plurality of sections are engageable to nonremovably connect the adapter to the syringe portion. In a number of embodiment, the adapter includes only two section the engage to nonremovably connect the adapter to the syringe portion. The adapter further includes a mounting mechanism adapted to be connected to the injector syringe interface. The adapter can also include a passage in operative connection with the barrel section after connection of the adapter to the syringe portion so that upon connection of the adapter with the syringe portion, the drive member can pass through the passage to impart motion to a plunger slidably positionable within the barrel section. | 05-05-2011 |
| 20110049866 | FLUID PATH CONNECTORS AND CONTAINER SPIKES FOR FLUID DELIVERY - A fluid connector includes an extending section including a spiked end to pierce the container port. The extending section includes at least one air conduit and at least one fluid conduit therethrough. The extending section further includes a first abutment member and second abutment member. The first abutment member is adapted to abut a first or air side of the container port upon piercing of the container port. The second abutment member is spaced from the first abutment member and is adapted to abut a second or fluid sided of the container port. The fluid connector can further include grasping members extending from the extending section to facilitate rotation of the extending section relative to the container port during piercing thereof. The fluid connector can also include a check valve in fluid connection with the air line. In several embodiments, the check valve is positioned within the extending section. | 03-03-2011 |
| 20110028908 | SYSTEM FOR PROCESSING CELLS AND CONTAINER FOR USE THEREWITH - A system for processing cells (and/or other injectate components) includes a container and a plunger adapted to be slidably positioned within the container. The system includes at least one inlet port through which a fluid can enter the system and at least one effluent port through which an effluent can exit the system. The plunger section forms a sealing engagement with the inner wall of the container such that rearward motion of the plunger is adapted to draw fluid into the system via the inlet and forward motion of the plunger is adapted to force effluent out of the system via the effluent port. | 02-03-2011 |
| 20110002802 | CONTINUOUS FLUID DELIVERY SYSTEM - The continuous fluid delivery systems includes a fluid pumping device comprising a pump housing comprising a base member with a plurality of inlet ports and at least one outlet port and at least two pairs of opposing pistons movably associated with the housing. Each pair of opposing pistons at least in part defines a respective pumping chamber of the fluid pumping device. The pistons in each pair of opposing pistons may be independently controlled such that any one of the plurality of inlet ports or the at least one outlet port is independently selectable to be in fluid communication with one of the respective pumping chambers. A drive system may be interfaced with the respective pistons to at least reciprocally operate the pistons relative to the base member. The pump housing and the at least two pairs of opposing pistons may comprise a disposable unit. | 01-06-2011 |
| 20100312223 | RAPID EXCHANGE FLUID JET CATHETER AND METHOD - Catheters including guidewire tubes having a limited length and methods of using the catheters are described. The catheters may be delivered over guidewires in procedures that are commonly referred to as rapid-exchange delivery. In some embodiments, the catheters may be miniature flexible thrombectomy catheters that may be used to remove thrombus or other unwanted material from a body blood vessel or other small regions of body cavities in which the distal portion of the catheter has smaller external dimensions than the larger proximal portion | 12-09-2010 |
| 20100298699 | System and Method for Proportional Mixing and Continuous Delivery of Fluids - A system and method for mixing and delivering fluids such as contrast media and saline is disclosed including at least two fluid sources, a pump, a joining fluid path connecting the at least two fluid sources to an inlet to the pump, and a valve device in the fluid path upstream of the pump. The valve device includes an actuator adapted to restrict flow in at least one of respective fluid lines connecting the at least two fluid sources to the pump inlet. A patient interface device may be associated with an outlet of the pump. The valve device actuator is generally adapted to restrict the flow in at least one of the respective fluid lines such that a positional change in valve device actuator position provides a change in fluid mixture ratio of the fluids from the at least two fluid sources to the pump inlet. | 11-25-2010 |
| 20100268264 | INTRAVASCULAR GUIDEWIRE FILTER SYSTEM FOR PULMONARY EMBOLISM PROTECTION AND EMBOLISM REMOVAL OR MACERATION - An intravascular emboli capture and retrieval system for intravascular embolism protection and embolism removal or maceration. Guidewire mounted proximally and distally located multiple opening filters are deployed within the vasculature and used to part, divide and macerate embolic debris and to capture such embolic debris within the confines thereof. A deployable flexible preformed memory shaped capture sleeve is alternatively used to collapse one or more filters and embolic debris therein for subsequent proximal withdrawal from the vasculature. | 10-21-2010 |
| 20100241085 | BLOW-MOLDED SYRINGE FOR USE WITH INJECTORS - A syringe for use in a pressurized injection of a fluid includes a syringe barrel including a polymeric material having undergone expansion via blow molding. An inner diameter of the syringe barrel can, for example, be sufficiently constant (over at least a portion of the axial length of the syringe) that a plunger slidably positioned within the syringe barrel and in generally sealing contact with an inner wall of the syringe barrel can be used within the syringe barrel to generate a pressure of at least 1 psi within the syringe barrel. In several embodiment, the inner diameter of the syringe barrel is sufficiently constant to generate a pressure of at least 100 psi, at least 300 psi, or even at least 500 psi within the syringe barrel. A method of forming a syringe includes the steps of: injection molding at least one polymeric material to form a preform; placing the preform into an blow mold die; and expanding at least a portion of the preform while heating the preform within the die to form a barrel of the syringe. The syringes can be formed to withstand relatively high pressures as described above. The at least one polymeric material can, for example, be polyethyleneterephthalate, cyclic olefin polymer, polypropylene, polystyrene, polyvinylidene chloride, polyethylene napthalate and/or nylon. | 09-23-2010 |
| 20100237545 | METHOD OF MANUFACTURING SYRINGES AND OTHER DEVICES - A syringe for use in a pressurized injection of a fluid includes a syringe barrel including a polymeric material having undergone expansion via blow molding. An inner diameter of the syringe barrel can, for example, be sufficiently constant (over at least a portion of the axial length of the syringe) that a plunger slidably positioned within the syringe barrel and in generally sealing contact with an inner wall of the syringe barrel can be used within the syringe barrel to generate a pressure of at least 1 psi within the syringe barrel. In several embodiment, the inner diameter of the syringe barrel is sufficiently constant to generate a pressure of at least 100 psi, at least 300 psi, or even at least 500 psi within the syringe barrel. A method of forming a syringe includes the steps of: injection molding at least one polymeric material to form a preform; placing the preform into an blow mold die; and expanding at least a portion of the preform while heating the preform within the die to form a barrel of the syringe. The syringes can be formed to withstand relatively high pressures as described above. The at least one polymeric material can, for example, be polyethyleneterephthalate, cyclic olefin polymer, polypropylene, polystyrene, polyvinylidene chloride, polyethylene napthalate and/or nylon. | 09-23-2010 |
| 20100222768 | METHODS FOR CAPACITANCE VOLUME CORRECTION IN FLUID DELIVERY SYSTEMS - A method of capacitance volume correction in fluid-containing expandable bodies and associated fluid pathways is disclosed for application in fluid delivery systems used to supply fluids to patients during radiographic imaging procedures including angiography. One embodiment is directed to a method of controlling delivery of fluid to a downstream process, including providing a fluid-containing expandable body, including a pressurizing element and in fluid communication with the downstream process, pressurizing the expandable body by moving the pressurizing element forward in the expandable body to reduce volume therein, and ceasing movement of the pressurizing element after allowing the pressurizing element to over-travel a sufficient distance to compensate for expansion of the expandable body under pressure. The expandable body may be a syringe and the pressurizing element may be a plunger disposed within the syringe. Movement of the pressurizing element is controlled by an algorithm associated with a computer. | 09-02-2010 |
| 20100222674 | MEDICAL INJECTOR SYSTEM - A syringe includes a body and a plunger movably disposed within the body. The syringe may be used with an injector including a drive member. The drive member preferably includes at least one pin adapted to form a retractable abutting connection with an interior of a plunger to enable the drive member to retract the plunger with the body of the syringe. | 09-02-2010 |
| 20100204573 | FLUID PATH SET PROVIDING GRAVITY FLOW PREVENTION - A fluid path set for delivery of an injection fluid includes a flexible tube. The flexible tube has a first end and a second end and a length defined between the first and second ends when the flexible tube is straightened. The flexible tube has a longitudinal axis extending along the length of the flexible tube. The flexible tube defines a transverse formation extending generally perpendicular to the longitudinal axis of the flexible tube. The fluid path set further includes a clip mechanism for maintaining the transverse formation in the flexible tube such fluid contained within the flexible tube at one end portion cannot flow through the length of the flexible tube to displace a less dense fluid contained within the flexible tube at the other end portion thereof by means of gravitational flow. | 08-12-2010 |
| 20100204572 | Devices, Systems and Methods for Determination of Parameters for a Procedure, for Estimation of Cardiopulmonary Function and for Fluid Delivery - A method of determining at least one parameter for an imaging procedure including the injection of a contrast enhancement fluid which includes a contrast enhancing agent, includes: substituting into a model discrete point data determined from at least one contrast time enhancement curve measured using an imaging system for a first region of interest resulting from injection of a bolus of the contrast enhancement fluid. In several embodiments, a sufficient number of data points can be substituted into the model to determine values for physiological variables in the model. The variables can, for example, be related to cardiopulmonary function. At least one data point from at least a second contrast time enhancement curve for a second region of interest measured using the imaging system can also substituted into the model. | 08-12-2010 |
| 20100185040 | FLUID DELIVERY SYSTEMS, DEVICES AND METHODS FOR DELIVERY OF HAZARDOUS FLUIDS - A system for injecting a patient, includes a container enclosing a hazardous pharmaceutical; a first pump to deliver a hazardous pharmaceutical to a patient and a fluid path operably connected to the first pump, the container, and the patient. The system further includes a hazardous material containment suitable to confine the hazardous pharmaceutical during connection of the hazardous pharmaceutical container to the fluid path. | 07-22-2010 |
| 20100174183 | MULTIPLE LUMEN DIFFUSION CATHETER - A method and device for the simultaneous or sequential introduction of multiple fluids into the bloodstream including a multiple lumen catheter with corresponding multiple hole sets. By introducing a second fluid such as saline, the concentration and bolus of a first fluid, such as a contrast agent, can be controlled and optimized. | 07-08-2010 |
| 20100114064 | MITIGATION OF CONTRAST-INDUCED NEPHROPATHY - A system, includes a pressurizing mechanism to pressurize a fluid including a contrast enhancement agent for delivery to a patient; and a control system in operative connection with the pressurizing mechanism. The control system includes a system to adjust control of fluid injection based upon a measurement of renal function of the patient. | 05-06-2010 |
| 20100114040 | FLUID MIXING CONTROL DEVICE FOR A MULTI-FLUID DELIVERY SYSTEM - The control device is used to control delivery of fluids from a multi-fluid delivery system during a medical injection procedure. The fluid delivery system includes an injector used to deliver injection fluids to a patient. The control device is operatively associated with the injector for controlling discrete flow rates of injection fluids delivered to the patient. The control device includes a housing, first and second actuators associated with the housing, and an electronic substrate disposed within the housing and having a conductive pattern. The first actuator is operatively associated with the conductive pattern. The conductive pattern includes a plurality of predetermined digital values corresponding to discrete flow rates of injection fluids to be delivered by the injector. The second actuator is operatively associated with the electronic substrate and initiates output signals to the injector corresponding to desired mixture ratios of the injection fluids to be delivered by the injector. | 05-06-2010 |
| 20100113887 | PATIENT-BASED PARAMETER GENERATION SYSTEMS FOR MEDICAL INJECTION PROCEDURES - A system includes a parameter generation system to determine parameters of at least one phase of an injection procedure based at least in part upon a type of the injection procedure. The parameter generator system determines the amount of a pharmaceutical that is to be delivered to a patient at least in part on the basis of the concentration of an agent in the pharmaceutical and at least on part on the basis of a function that depends upon and varies with a patient parameter. The patient parameter can, for example, be weight, body mass index, body surface area or cardiac output. The pharmaceutical can, for example, include a contrast enhancing agent for use in an imaging procedure. | 05-06-2010 |
| 20100076307 | FLOW BASED PRESSURE ISOLATION MECHANISM FOR A FLUID DELIVERY SYSTEM - The fluid delivery system includes a pressurizing device for delivering a pressurized injection fluid, a low pressure fluid delivery system, and a pressure isolation mechanism adapted for fluid communication with the pressurizing device and low pressure fluid delivery system. The pressure isolation mechanism includes a housing defining an inlet port, an isolation port, and an internal cavity. The housing defines a seal seat in the internal cavity between the inlet port and isolation port. A valve member is disposed in the internal cavity. The valve member is free floating in the internal cavity and is adapted to engage the seal seat. The valve member has an open position permitting fluid communication between the inlet port and isolation port, and is fluid flow responsive to fluid flow in the inlet port to engage the seal seat and attain a closed position preventing fluid flow between the inlet port and isolation port. | 03-25-2010 |
| 20100063481 | CONNECTOR SYSTEM HAVING A COMPRESSIBLE SEALING ELEMENT AND A FLARED FLUID PATH ELEMENT TO REDUCE FLUID FLOW RESTRICTIONS - A system for connecting a conduit to a fluid path element, includes a length of conduit, a compressible sealing element positioned on a distal end of the length of conduit to be attached to the fluid path element, a first cooperating connector positioned around the length of conduit proximal to the sealing element and a second cooperating connector. The first cooperating connector includes a first cooperating connection mechanism and the second cooperating connector includes a second cooperating connection mechanism. The first cooperating connection mechanism and the second cooperating connection mechanism are adapted to form a connection between the first cooperating connector and the second cooperating connector. The connection causes the compression of the sealing element. The second cooperating connector further includes a passage therein in fluid connection with a connection for the fluid path element. Another system for connecting to a fluid path section includes a connector including a connection mechanism to connect the connector to the fluid path section and a passage therethrough. The passage is in fluid connection with a first fluid path element downstream of the connector. The first fluid path element includes a lumen therethrough. The diameter of the lumen is flared outward to a larger diameter at a proximal end of the fluid path element. The proximal end of the first fluid path element can abut a surface of the connector in which the distal end of the fluid path is formed. The inner diameter of the proximal end is greater than the diameter of the passage of the second cooperating connector. The outer diameter of the proximal end of the first fluid path element can also be flared outward | 03-11-2010 |
| 20100058603 | DEPTH STOP DEVICES AND SYSTEMS - A depth stop device for use in connection with another device or apparatus (for example, a medical device) includes a stop member slidably positionable on the device, at least one abutment member in operative connection with the stop member to adjustably contact the device to lock the stop member in a desired position relative to the device or to free the stop member to slide relative to the device, and an adjustment member connected to the abutment member to control a position of the abutment member relative to the device. The force applicable by the abutment member to the device is limited to be less than a certain force. | 03-11-2010 |
| 20100030073 | MODELING OF PHARMACEUTICAL PROPAGATION - A method of delivering a contrast enhancing fluid to a patient using an injector system, including: determining at least one patient transfer function for the patient based upon data specific to the patient and, the at least one patient transfer function providing a time enhancement output for a given input; determining a desired time enhancement output; using the at least one patient transfer function to determine an injection procedure input; and controlling the injector system at least in part on the basis of the determined injection procedure input. The injection procedure input can determined considering at least one operational limitation or constraint of the injector system. A method of modeling propagation of a pharmaceutical fluid in a patient, includes: collecting data corresponding to a time response curve resulting from injection of the fluid; and determining at least one mathematical model describing the data. The mathematical model can, for example, be a model which is not determined by a continuous or a discrete-time Fourier deconvolution of the data. A method of controlling injection of a pharmaceutical fluid into a patient using an injector in a medical procedure, includes: collecting data corresponding to a patient response curve resulting from injection of the fluid; determining at least one mathematical model describing the data; and controlling the injector during the medical procedure to control injection of the fluid into the patient to create patient response at least in part on the basis of the mathematical model. A method of controlling injection of a contrast medium into a patient using an injector in a medical imaging procedure using an imaging scanner, includes: determining at least one mathematical model to predict a time enhancement response resulting from injection of the contrast medium; determining an injection protocol to approximate a predetermined time enhancement response in the patient by determining a constrained input solution to the mathematical model; and using the injection protocol to control the injector during the medical imaging procedure to control injection of the contrast medium into the patient to create an image of a region of interest. Patient transfer functions for the patient of the present invention can also be based at least in part on a measurement of cardiac output of the patient. Likewise, mathematical models of the present invention can be based at least in part on a measurement of cardiac output of the patient. | 02-04-2010 |
| 20090326370 | INTERFACE UNIT FOR USE WITH INJECTORS AND IMAGING SYSTEMS AND RELATED DEVICES - A system for producing a contrast-enhanced medical image of a patient includes a source of a contrast or enhancement medium, a pressurizing unit in fluid connection with the source of contrast or enhancement medium, an energy source operable to apply energy to a region of the patient, an imaging unit providing a visual display of an internal view of the patient based upon a signal resulting from the energy applied to the region of the patient, and a control unit. In an embodiment, the signal is affected by a condition of the contrast or enhancement medium in the patient. To control the procedures, the control unit adjusts the condition of the contrast or enhancement medium in the patient based upon the signal. A communication interface preferably enables information between an injector subsystem and an imaging subsystem. | 12-31-2009 |
| 20090316970 | IDENTIFICATION OF REGIONS OF INTEREST AND EXTRACTION OF TIME VALUE CURVES IN IMAGING PROCEDURES - A method of extracting at least one time-value curve to determine a protocol in an imaging procedure using an imaging system, includes: determining a first N-dimensional data set of pixel values of a portion of a body of the patient at a first time using the imaging system, wherein N is an integer; determining at least a second N-dimensional data set of pixel values of the portion at a second time using the imaging system; computing a predetermined number of correlated segments of the imaged portion corresponding to a predetermined number of regions of interest of the patient by computing a similarity metric of a time series of pixel values; computing the at least one time-value curve for at least one of the regions of interest; and determining a protocol for a diagnostic scan using the image system based at least in part upon data from the time value curve. | 12-24-2009 |
| 20090312632 | SYRINGE PLUNGER SENSING MECHANISM FOR A MEDICAL INJECTOR - Embodiments of an injector, syringe, syringe interface, syringe adapter, and piston/plunger assembly for an injector (of contrast medium, for example) are described. Preferably, the syringe is adapted to engage a syringe interface mechanism such that the syringe may be connected to an injector without regard to any particular orientation of the syringe to the injector or to the piston/plunger assembly. The injector piston or drive member includes a sensing pin positioned at a forward end thereof to sense contact with the syringe plunger during advancement of the piston or drive member to contact the plunger. The piston can be advanced automatically upon connection of, for example, the syringe to the injector, or piston advance can be automated to occur after operator initiation. The injector may include or be adapted to accommodate two syringes, which for example provide for simultaneous injection of fluid into separate injection sites on a patient. | 12-17-2009 |
| 20090247867 | INJECTOR SYSTEM FOR ENCODING AND SENSING OF SYRINGE INFORMATION - A syringe for use with a powered injector to inject a fluid into a patient includes at least a first indicator positioned on the syringe at a predetermined axial position. The distance between a rearward surface of the first indicator and a predetermined position on the powered injector provides information about the syringe configuration. The first indicator can, for example, be a rear surface of the attachment flange. An injector system includes a powered injector having a drive member and at least one sensor for detecting energy. The injector system also includes a syringe having at least a first indicator positioned on the syringe at a predetermined axial position. The energy detected by the sensor is determined by the axial position of the indicator when the syringe is attached to the powered injector. The axial position of the indicator thereby provides information about the syringe configuration. | 10-01-2009 |
| 20090247866 | DATA COMMUNICATION AND CONTROL FOR MEDICAL IMAGING SYSTEMS - A method of coordinating an imaging procedure and an injection procedure, the method comprising the steps of providing an injector system having first and second pressurizing units for pressurizing a contrast medium and a diluent for injection into a patient; providing an imaging system for producing an image of an internal region of the patient from a signal resulting from energy applied to the patient; and providing a data interface interconnecting the injector and imaging systems for enabling exchange of digital information therebetween such that the digital information transmitted between the systems is usable to enable closed loop control of at least one of the injection and the imaging procedures during which the contrast medium and the diluent injected into the patient is adjustable so as to achieve a desired level of enhancement within the internal region of the patient of which the images are acquired during the imaging procedure. | 10-01-2009 |
| 20090247865 | DRIP CHAMBER AND FLUID LEVEL SENSING MECHANISM FOR A FLUID DELIVERY SYSTEM - The fluid injector system includes a source of injection fluid, a pump device, a fluid control device operably associated with the pump device, and a fluid path set in fluid connection with the source of injection fluid and the pump device. The fluid path set includes a drip chamber including an elongated body having a top end, a bottom end and a raised projection, the raised projection being substantially rectangular in shape and extending longitudinally from the top end along the drip chamber body and terminating adjacent to the bottom end. A fluid level sensing mechanism is operably associated with the fluid control device, and includes a drip chamber support for supporting the drip chamber body and a fluid level sensor associated with the drip chamber support. The drip chamber support is adapted to support the drip chamber body such that the raised projection is in operational contact with the fluid level sensor and the fluid level sensing mechanism is operable to transmit ultrasonic or light energy through the raised projection to be sensed by the fluid level sensor for sensing the injection fluid level in the drip chamber. | 10-01-2009 |
| 20090240197 | CENTRAL VENOUS CATHETERS AND RELATED EQUIPMENT - Systems, devices, and methods towards improved diagnosis and therapy in connection with central venous catheters (including PICC lines). Included among the many improvements broadly contemplated herein are: arrangements via which a venous catheter can move passively into position in central venous circulation; arrangements via which a catheter can be actively guided without the use of a needle or guide wire; arrangements via which a catheter can be packaged to facilitate easy, rapid, and positionally accurate deployment by medical personnel while maintaining device sterility; and arrangements via which a catheter tip can be imaged during and after insertion. | 09-24-2009 |
| 20090216193 | FLUID INJECTION APPARATUS HAVING A SYRINGE PRESENCE SENSOR - The fluid injection apparatus is adapted for use with a syringe and includes an injector and a pressure jacket associated with the injector. The injector includes a housing defining an opening for a drive piston extendable from the housing. The pressure jacket secures the syringe during an injection procedure. The pressure jacket has a distal end defining a syringe receiving opening for receiving the syringe, and a proximal end associated with the housing and generally aligned with the opening. The apparatus includes a syringe sensor adapted for engagement by the syringe when loaded into the pressure jacket. The housing may have an engagement tab adapted to engage an engagement recess in the pressure jacket to removably engage the pressure jacket with the housing. The apparatus may have one or more light sources associated with the housing for illuminating the syringe received in the pressure jacket. | 08-27-2009 |
| 20090216192 | FLUID INJECTION APPARATUS HAVING ANTI-ROTATION ELEMENTS TO LIMIT SYRINGE PLUNGER ROTATION - The fluid injection apparatus is adapted for use with a syringe and includes an injector and a pressure jacket associated with the injector. The injector includes a drive piston having a plunger engaging end. The syringe includes a body and a plunger movably disposed within the body, the plunger having a proximal end adapted for engagement by the plunger engaging end of the drive piston. An anti-rotation connection is formed by complementary anti-rotation elements associated with the proximal end of the plunger and the plunger engaging end of the drive piston to limit rotation of the plunger within the syringe body. | 08-27-2009 |
| 20090216190 | SYRINGE HAVING A PROXIMAL END WITH AN OUTWARD EXTENDING LIP - A syringe includes a body having a distal end, a proximal end and a center section therebetween, a plunger movably disposed in the body, and a lip extending outward from the proximal end of the body. The outward extending lip has an outer diameter no greater than the outer diameter of the center section. The outward extending lip may extend around the circumference of the proximal end. | 08-27-2009 |
| 20090182274 | SYRINGE WITH ALIGNMENT FLANGE AND EXPANSION SECTION WITH REDUCED WALL THICKNESS - A syringe includes a cylindrical body having a distal end and a proximal end, an injection section at the distal end and an expansion section at the proximal end, the injection section and the expansion section being connected by a cylindrical center section of relatively uniform outer diameter. The injection section includes a conical portion and an injection neck, the conical portion including an alignment flange extending outward from at least a portion of the conical portion. The syringe further includes a plunger movably received in the body and having a coupling end with a pair of flexible coupling members defining a slot therebetween for engaging a drive piston of an injector, the slot being substantially aligned with the alignment flange such that the alignment flange provides an indication of the orientation of the slot, the plunger seated for storage in the expansion section. A syringe has a reduced wall thickness at the expansion section such that an inner diameter of the expansion section is larger than the inner diameter of the center section for allowing the expansion section to expand under radial outward force exerted by the plunger. | 07-16-2009 |
| 20090177155 | FLUID INJECTION SYSTEM AND PRESSURE JACKET ASSEMBLY WITH SYRINGE ILLUMINATION - The fluid injection apparatus for use with a syringe includes an injector and a pressure jacket assembly associated with the injector. The injector includes a housing defining a central opening and a drive piston extendable through the central opening for imparting motive forces to a syringe plunger disposed within the syringe. The pressure jacket assembly includes a pressure jacket and at least one support arm associated with and extending outward from the housing. A syringe retaining member is attached to the at least one support arm. The syringe-retaining member defines a syringe receiving slot for receiving at least a portion of the syringe. A light source is located on the support arm and faces the pressure jacket for illuminating the syringe. | 07-09-2009 |
| 20090177050 | INTEGRATED MEDICAL IMAGING SYSTEMS - An image acquisition system operable to obtain an image of at least a portion of a body, includes an imaging system including at least one energy sensor to measure energy from the body, an image creating system adapted to create an image based at least in part from a signal from the at least one energy sensor, an image display in operative connection with the image creating system and a user interface in operative connection with the image creating system. The image acquisition system further includes a fluid injector system including at least one source of a first fluid, a pressurizing system in operative connection with the source of the first fluid, and a user interface in operative connection with the pressurizing system. The imaging system and the injector system are operatively integrated in at least two of the following and/or other aspects: physical connection, data input via at least one common user interface, displaying of information via at least one common display, electrical connection to at least one common power conditioning system, receipt of common data from at least one patient physiological sensor, at least one common communication port to at least one information system, and a common control system (including any common portion of a control system). | 07-09-2009 |
| 20090171267 | RHEOLYTIC THROMBECTOMY CATHETER WITH SELF-INFLATING PROXIMAL BALLOON WITH DRUG INFUSION CAPABILITIES - The present disclosure involves a rheolytic thrombectomy catheter with a self-inflating proximal balloon having drug infusion capabilities. A self-inflating balloon having a plurality of outflow orifices located about the peripheral circumference thereof is located proximal to an inflow gap or orifices and a fluid jet emanator and which balloon is inflated and expanded by internal operating pressures to uniformly space and position the outflow orifices of the self-inflating balloon in close proximity to or in intimate contact with the thrombus or walls of the blood vessel. Devices of the present disclosure can be used for the purposes of thrombectomies, embolectomies, thrombus or vessel dilation and for the delivery of drugs to a thrombus or vessel site. | 07-02-2009 |
| 20090156983 | RHEOLYTIC THROMBECTOMY CATHETER WITH SELF-INFLATING DISTAL BALLOON - The devices of the present disclosure are rheolytic thrombectomy catheters with a self-inflating distal balloon. A self-inflating balloon is located distal to an inflow gap or orifice and distal to a fluid jet emanator, which self-inflating balloon is inflated and expanded by the utilization of internal operating forces consisting of forwardly directed high velocity fluid jet streams and/or entrained thrombus particulate therein. The self-inflating balloon, when inflated, impinges on the wall of the blood vessel to isolate sections of the blood vessel distal and proximal to the inflated balloon in order to prevent flow of thrombus particulate, fluids and the like distal to the self-inflating balloon and to provide a stagnant nonflow region proximal to the self-inflating balloon. The devices of the present disclosure also provide for a uniform spacing of the catheter tube with respect to the thrombus and/or wall of the blood vessel. | 06-18-2009 |
| 20090143729 | TORQUEABLE KINK-RESISTANT GUIDEWIRE - An occlusive guidewire system having an ergonomic handheld control mechanism and torqueable kink-resistant guidewire having a distally located inflatable balloon. The present invention provides convenient structure and overall mechanism for operation of a torqueable kink-resistant guidewire, including evacuation and inflation control of an occlusive balloon, and sealing and severing of a crimpable inflation tube which is in communication with an occlusive balloon. The torqueable kink-resistant guidewire includes a centrally located shaft which imparts robustness to the torqueable kink-resistant guidewire. An inflation lumen aligns within the torqueable kink-resistant guidewire for inflation of the balloon. | 06-04-2009 |
| 20090112164 | SYSTEM AND METHOD FOR PROPORTIONAL MIXING AND CONTINUOUS DELIVERY OF FLUIDS - A system and method for mixing and delivering fluids such as contrast media and saline is disclosed including at least two fluid sources, a pump, a joining fluid path connecting the at least two fluid sources to an inlet to the pump, and a valve device in the fluid path upstream of the pump. The valve device includes an actuator adapted to restrict flow in at least one of respective fluid lines connecting the at least two fluid sources to the pump inlet. A patient interface device may be associated with an outlet of the pump. The valve device actuator is generally adapted to restrict the flow in at least one of the respective fluid lines such that an incremental positional change in valve device actuator position provides a substantially linear change in fluid mixture ratio of the fluids from the at least two fluid sources to the pump inlet. | 04-30-2009 |
| 20090076378 | INTRACAVITY PROBES AND INTERFACES THEREFOR FOR USE IN OBTAINING IMAGES AND SPECTRA OF INTRACAVITY STRUCTURES USING HIGH FIELD MAGNETIC RESONANCE SYSTEMS - An intracavity probe for use with an MR system allows images or spectra of a region of interest within a cavity of a patient to be obtained. The probe includes a shaft, a balloon at one end thereof, and a coil loop within the balloon. The coil loop preferably includes two drive capacitors and a tuning capacitor, all of which in series. A junction node between the drive capacitors serves as a ground for electrically balancing the coil loop. Diametrically opposite the junction node, the tuning capacitor enables the coil loop to resonate at the operating frequency of the MR system. Across each drive capacitor is connected an output cable having an electrical length of S | 03-19-2009 |
| 20090070342 | SYSTEM AND METHOD FOR AUTOMATED BENCHMARKING FOR THE RECOGNITION OF BEST MEDICAL PRACTICES AND PRODUCTS AND FOR ESTABLISHING STANDARDS FOR MEDICAL PROCEDURES - A system for the collection, management, and dissemination of information relating at least to a medical procedure is disclosed. The system includes a user interface adapted to provide raw data information at least about one of a patient, the medical procedure, and a result of the medical procedure. A medical device communicates with the user interface, receives the raw data information from the user interface, and generates operational information during use. A central database communicates at least with the medical device and receives data from the medical device. The central database is used to create related entries based on the raw data information and the operational information and optionally transmits the related entry to the medical device or the medical device user. The related entry includes information that provides guidance based on previously tabulated, related medical procedures. A system for the iterative analysis of medical standards is also disclosed along with methods for the evaluation of medical procedures and standards. | 03-12-2009 |
| 20090050216 | VALVE SYSTEMS FOR USE WITH A FLUID INJECTOR SYSTEM - A valve system for use in a system including a first source of a first pressurized fluid and a second source of a second pressurized fluid includes a valve housing including a first inlet port adapted to be placed in fluid connection with the first source, a second inlet port adapted to be placed in fluid connection with the second source and an outlet port. The valve system further includes a backflow prevention system to prevent flow of the first pressurized fluid through the second inlet and to prevent flow of the second pressurized fluid through the first inlet port. The valve system is adapted to provide a fluid path between at least the first inlet port and the outlet port to enable fluid to be drawn from the outlet port to the first inlet port. Several of the valve systems of the present invention provide for flow from the first inlet port to the outlet port and concurrent flow from the second inlet port to the outlet port. | 02-26-2009 |
| 20090012497 | SYSTEMS AND METHODS OF DELIVERING A DILATED SLURRY TO A PATIENT - A system for delivering a slurry to a patient includes a fluid, a material that is non-dissolvable or immiscible in the fluid, thereby forming a slurry, a container adapted to contain the slurry and a supernate of the slurry, the container defining an outlet through which the slurry is delivered to the patient, a fluidizing system associated with the container, a pressurizing mechanism adapted to create a pressure to cause the slurry contained within the container to flow for delivery to the patient and a control unit in communication with and adapted to control the fluidizing system and the pressurizing mechanism. The fluidizing system is adapted to effect dilation of the slurry while maintaining at least a portion of the supernate. | 01-08-2009 |
| 20080294096 | Delivery of Agents Such as Cells to Tissue - A system for delivering a fluid comprising cells to tissue of a patient, includes: a least a first container for holding an injection fluid in which the agent is carried; a first powered drive in operative connection with the container, the first powered drive being operable to pressurize contents of the container; a control system in operative connection with the first powered drive and operative to control the first powered drive; a fluid path in fluid connection with the container, the fluid path including a patient interface adapted to deposit the cells within tissue of the patient; a sensor system; and a communication system in connection with at least the control system and the sensor system. The communication system is adapted to provide information to the control system. The control system in adapted to transmit a control signal to at least the first powered drive based at least in part on information provided to the control system. The cells can for example be pregenitor cells or stem cells. | 11-27-2008 |
| 20080290870 | TRANSMIT-MODE PHASED ARRAY COILS FOR REDUCED SAR AND ARTIFACT ISSUES - Systems and methods for the selection of and application of RF power to a plurality of transmit and/or transmit/receive coil elements to decrease patient SAR and to limit the potential for artifact problems. Without any change to the hardware or software of an MR scanner, the present local coil system provides system logic and coil design flexibility such that only transmit coil elements that are required for a particular portion of an MR scan will be utilized at that time. The local coil system may include any combination of transmit-only, receive-only and transmit/receive coil elements as part of the coil system (array of coil elements). The logic controller of the local coil system gathers input data from the MR scanner, from the attached coil elements and optionally from one or more sensors attached to the coil system itself. | 11-27-2008 |
| 20080275332 | Head Coil and Neurovascular Array for Parallel Imaging Capable Magnetic Resonance Systems - A head coil for use with a parallel-imaging compatible MR system is disclosed, as is a method of making, and a neurovascular array (NVA) equipped with, same. The head coil includes conductive rings and rods configured to produce a plurality of electrically-adjacent primary resonant substructures about a birdcage-like structure, with each such primary resonant substructure including two rods neighboring each other and the short segment of each of the first and second rings interconnecting them. The primary resonant substructures are isolated from each other via a preamplifier decoupling scheme and an offset tuning scheme thereby enabling each primary resonant substructure (i) to receive an MR signal from tissue within its field of view and (ii) to be operatively couplable to one processing channel of the MR system for conveyance of the MR signal received thereby (iii) while being simultaneously decoupled from the other primary resonant substructures. | 11-06-2008 |
| 20080262328 | Pulse Oximetry Grip Sensor and Method of Making Same - A probe for use with a pulse oximeter apparatus is disclosed, as are a fixture for and a method of making the probe. The probe includes a housing and two fiber optic bundles. The first bundle has an emitter portion at one end, and is used for conducting light from a source thereof to the emitter portion from which the light is transmitted for transillumination through a body part. The second bundle is for conducting the transilluminated light incident upon a detector portion thereof to the pulse oximeter apparatus. The housing is overmolded onto the bundles so that the emitter and detector portions are securely positioned diametrically opposite each other across an opening defined by the housing. The overmolding makes the alignment of the emitter and detector portions largely impervious to movement of the body part when placed within the opening and thus between the emitter and detector portions. | 10-23-2008 |
