C. R. Bard, Inc. Patent applications |
Patent application number | Title | Published |
20160136389 | ACCESS PORT AND CATHETER ASSEMBLY INCLUDING CATHETER DISTAL PORTION STABILITY FEATURES - A stabilized catheter tube for insertion into a body of a patient. The catheter tube includes a distal portion that remains stable during fluid infusion into the patient, thus reducing or eliminating whipping of the catheter distal tip. In one embodiment, the catheter tube defines at least one lumen and is formed from a tube material that defines a proximal portion and a distal portion of the catheter tube. The catheter tube is configured such that the arithmetic product of an elastic modulus and an area moment of inertia for the distal portion of the catheter tube is greater relative the arithmetic product of an elastic modulus and an area moment of inertia for the proximal portion of the tube. In one embodiment, the catheter tube is operably attached to an implantable access port and includes an enlarged distal portion relative a proximal portion of the catheter tube. | 05-19-2016 |
20150375011 | Brachytherapy Seed Insertion and Fixation System - Brachytherapy seed insertion and fixation devices and systems to decrease implanted brachytherapy seed migration within tissue and minimize trauma. Component(s) with cavity or opening features are attached to a brachytherapy seed or series of seeds. The cavity or opening features interact with the patient's tissue to fix the seed and component assembly in place and inhibit movement/migration of the seed(s). The cavity or opening features may optionally be filled with an adhesive or other beneficial material. The seed(s) or seed and component assembly may be inserted using a delivery device having a needle through which the seed(s) or assembly are implanted and a stylet extending through the needle to cut tissue and facilitate insertion of the needle. The stylet has a reduced diameter cutting tip to cut a narrow hole in tissue, and a tapered region that stretches the narrow hole to accommodate insertion of the larger diameter needle. | 12-31-2015 |
20150367102 | Securement Device Having An Integral Strap And Dressing - A medical article, such as a catheter hub or extension set, is stabilized on a patient with a retainer and a dressing integrally attached to an anchor pad supporting the retainer. The catheter hub or extension set may be integrally formed with the retainer. The retainer may comprise a channel and an integral strap. The channel may include an abutment. One or more of the anchor pad, dressing, and catheter may comprise an antibacterial or antimicrobial agent. | 12-24-2015 |
20150238175 | BIOPSY APPARATUS INCLUDING A BIOPSY DEVICE HAVING A SAMPLE RECEIVING NOTCH WITH A TISSUE ANCHOR - A biopsy device includes a vacuum source, and an elongate member having a lumen and a sample receiving notch. The sample receiving notch has a proximal hole, a distal end wall, and a floor. The proximal hole is separated from the distal end wall along the longitudinal axis. The proximal hole is in fluid communication with the lumen. A tissue anchor has a cantilever portion with a free end. The cantilever portion is configured to extend in a direction from the distal end wall toward the proximal hole. The free end has a tip portion configured to extend toward the floor. The tissue anchor and the proximal hole are collectively configured to place tissue received in the sample receiving notch in a state of tension between the tip portion and the proximal hole when a vacuum is applied by the vacuum source to the proximal hole via the lumen. | 08-27-2015 |
20150133814 | SELF-CONTAINED HANDHELD BIOPSY NEEDLE - A method of operating a biopsy device includes inserting a sampling probe having a first component and a second component into a biological tissue mass, the first component having a sample chamber and a side port that opens to the sample chamber, and the second component having a side opening; generating a vacuum in the sample chamber during a first drive interval; rotating at least one of the first component and the second component of the sampling probe during a second drive interval until the side port of the first component and the side opening of the second component are in radial alignment; and rotating at least one of the first component and the second component of the sampling probe during a third drive interval to sever tissue drawn by vacuum into the sample chamber to deposit a tissue sample in the sample chamber. | 05-14-2015 |
20150025478 | Reinforced Septum for an Implantable Medical Device - A septum for sealably covering a fluid cavity defined in an implantable device, which may be an access port, and methods for assembling the implantable device. The septum may include a resilient septum body, an annular flange extending radially outward from the septum body, and a reinforcement component disposed in the annular flange for reinforcing engagement with a corresponding annular groove defined in a body of the implantable device. The reinforcement component may inhibit unintended detachment of the septum from the implantable device. | 01-22-2015 |
20140330118 | Assemblies for Identifying a Power Injectable Access Port - An assembly for identifying a power injectable vascular access port, including a vascular access port and an identification feature. The port is structured for power injection and includes a housing and a septum together defining a reservoir. A radiographic feature incorporated into the port is perceivable via x-ray following subcutaneous implantation, the radiographic feature identifying the port as suitable for flowing fluid at a fluid flow rate of at least 1 mL/sec therethrough. A structural feature of the port is perceivable via palpation following subcutaneous implantation, the structural feature identifying the port as suitable for accommodating a pressure within the reservoir of at least 35 psi. The identification feature is separated from the port and confirms that the port is both suitable for flowing fluid at a rate of at least 1 mL/sec therethrough and suitable for accommodating a pressure within the reservoir of at least 35 psi. | 11-06-2014 |
20140309737 | IMPLANTABLE PROSTHESIS FOR RECONSTRUCTION OF AN ANATOMICAL FEATURE - An implantable prosthesis is provided for reconstructing an anatomical feature, such as a breast nipple. The prosthesis may be formed from a biologic and/or synthetic material. The prosthesis may include a body with a shape that is suitable for reconstructing the anatomical feature. A base may be located at an end of the body to facilitate anchoring the prosthesis in position. The prosthesis may be provided with openings that allow fluid flow therethrough, tissue ingrowth, revascularization, neovascularization and/or fat or stem cell deposition. The prosthesis may include a plurality of layers of biocompatible material arranged in a stacked configuration. The layers may be in spaced relation relative to each other and secured or fixed in position to maintain the spacing therebetween. Each layer may have one or more openings extending therethrough. The spaced layer arrangement may provide a desired tactile response and/or natural movement for the prosthesis. | 10-16-2014 |
20140303429 | SELF-ANCHORING SLING AND INTRODUCER SYSTEM - A system for supporting the urethra using an introducer needle, the ends of which are flattened and which have openings therethrough, a handle having a latch mechanism which engages the opening in the flattened portion of the first end of the introducer needle, an implant, and a connector joining the end of the implant to the flattened portion of one of the ends of the introducer needle. These components are used to draw the implant into position, either through vaginal or abdominal incisions, to form a U-shaped loop beneath the urethra. The ends of the implant are adjusted to provide proper support for the urethra. The implant can have slits that open under applied tensile force. | 10-09-2014 |
20140276472 | Short-Bevel Non-Coring Needle - A non-coring needle for use in accessing an implanted medical device is disclosed. The non-coring needle is configured so as to include a compact bevel face relative to standard non-coring needles. In one embodiment, the non-coring needle comprises a hollow cannula that defines a lumen and terminates at a sharpened distal tip. The cannula includes a proximal portion and a bent distal portion. The distal portion defines a bevel face extending proximally from the distal tip, and the bevel face includes the lumen distal opening. The bevel face defines an open angle of at least about one degree with respect to a longitudinal axis of the proximal portion of the cannula. The bevel face is also laterally offset from the proximal portion of the cannula by an offset distance of no more than about 0.010 inch. A portion of the bevel face is dulled to prevent access port septum coring. | 09-18-2014 |
20140275922 | Sacrificial Catheter - A sacrificial catheter assembly and method of use for placing a functional catheter within the body of a patient, such as into the patient's vasculature, is disclosed. In one embodiment, the sacrificial catheter assembly comprises a sacrificial catheter including an elongate body that defines a longitudinally extending lumen. A stylet is removably received within the lumen of the sacrificial catheter such that the catheter and stylet can be advanced together to a target destination within the body of the patient. The sacrificial catheter is configured so as to then be proximally slid over the stylet to remove the sacrificial catheter from the body while the stylet remains in place at the target destination. A functional catheter can then be distally slid over the stylet to place the functional catheter at the target destination. The stylet can then be removed from the body of the patient. | 09-18-2014 |
20140275918 | Closed Catheter Tip Including Electrically Conductive Pathway - A closed-ended catheter assembly that includes an electrically conductive pathway is disclosed. The conductive pathway enables electrical signals, such as ECG signals produced by a patient's heart, to pass through the closed-ended tip of the indwelling catheter while still preventing unintended fluid flow. In one embodiment, therefore, a catheter assembly is disclosed and comprises an elongate catheter tube including a closed distal end. The catheter tube defines at least one lumen and includes a valve defined in the catheter tube that is configured to selectively enable fluids to pass therethrough. The catheter tube includes a conductive element that provides an electrically conductive pathway between the at least one lumen and an exterior portion of the catheter. The conductive element includes a porous material extending between the at least one lumen and the exterior portion of the catheter, the porous material being transmissive to electrical signals and non-permeable to blood. | 09-18-2014 |
20140262859 | Enhanced Pre-Wetted Intermittent Catheter with Lubricious Coating - The present disclosure relates to a packaged urinary catheter. The catheter includes a conduit having a proximal end and a distal end. The distal end includes at least one aperture for receiving urine from the bladder. The catheter is contained within a sleeve having a length, a width, and a size configured to receive the catheter. According to one embodiment, the catheter and the sleeve may be arranged in a helical coil. The outer surface of the catheter may have a lubricious and/or an antimicrobial coating. | 09-18-2014 |
20140243785 | Extensible Internal Bolster for a Medical Device - An internal bolster for use securing a medical device, such as a feeding tube, within a body of a patient is disclosed. In one embodiment, a feeding tube includes an internal bolster, comprising one or more bolster arms that each include a first end hingedly connected to a distal end of the medical device and a free second end. The bolster arms are selectively deployable between a first position wherein the bolster arms are substantially in-line with an axis of feeding tube, and a second position wherein the bolster arms are substantially deflected from the axis of the feeding tube to enable securement of the feeding tube within a stoma or other opening defined in the body. Various means for selectively moving the bolster arms between the first and second positions are disclosed. Related methods of use are also disclosed. | 08-28-2014 |
20140239050 | Self-Expansible Stent with Radiopaque Markers and Method of Making Such a Stent - Pushing a self-expanding stent from one of its ends, during release of the stent at a stenting site in a bodily lumen, by proximal withdrawal of a surrounding sheath, can impose unacceptably high stresses on parts of the strut network of the stent. For location of stents in a bodily lumen, it is customary to equip the end annulus of a stent with radiopaque markers. The present invention involves arranging the markers so that they share with non-marker portions of the end annulus the stresses imposed in the stent by the end pushing, whereby the high stresses are shared more equally by all the struts of the stent in the end annulus. | 08-28-2014 |
20140208913 | Flanged Graft with Trim Lines - A vascular graft with trim lines is described, the trim lines providing a guide for precision shaping of the cuff. The trim lines may be printed or otherwise disposed on a surface of the cuff or included on a template designed for disposition over the cuff. The trim lines may also be disposed on a side of a pocket into which the cuff is positioned for trimming. Also described is an apparatus and method for precise trimming of a vascular graft. | 07-31-2014 |
20140194892 | MARKER DELIVERY DEVICE FOR TISSUE MARKER PLACEMENT - A marker delivery device is configured for deploying a tissue marker. The marker delivery device includes a handle having a chamber, and a cannula. According to one aspect, the cannula has a flexible portion formed by a slot arrangement having of a plurality of spaced-apart substantially parallel peripheral slots extending through the side wall of the cannula to the lumen. A marker introducer rod is movably disposed in the lumen of the cannula for deploying the mark, and has a flexible region that corresponds to the flexible portion of the cannula. According to another aspect, a retraction mechanism is mounted to the handle and is configured to facilitate a complete retraction of both the cannula and the marker introducer rod into the chamber of the housing of the handle upon an actuation of the retraction mechanism. | 07-10-2014 |
20140188133 | Iconic Representations for Guidance of an Indwelling Medical Device - An integrated catheter placement system for accurately placing a catheter within a patient's vasculature is disclosed. In one embodiment, the integrated system comprises a system console, a tip location sensor for temporary placement on the patient's chest, and an ultrasound probe. The tip location sensor senses a magnetic field of a stylet disposed in a lumen of the catheter when the catheter is disposed in the vasculature. The ultrasound probe ultrasonically images a portion of the vasculature prior to introduction of the catheter. ECG signal-based catheter tip guidance is included in the integrated system to enable guidance of the catheter tip to a desired position with respect to a node of the patient's heart. Iconic representations for depiction on the display of the system and relating to positional and other characteristics of the catheter or medical device are also disclosed. | 07-03-2014 |
20140182623 | Insert for a Microbial Scrubbing Device - The microbial scrub brush in one embodiment employs an insert that is impregnated with an anti-bacterial disinfectant and that is housed within a housing of alcohol-compatible material and sealed over by a removable lid. The insert is maintained in sterile condition until ready for use. After removal of the lid, the insert is moved over the end of a female luer or other portion of a medical device and rotated in order to clean the exterior surface as well as the interior luminal surface of the device. In one embodiment, the insert includes a base from which extends an outer wall that defines a chamber. A plurality of complaint fingers extend from the base into the chamber. A plurality of wipers extend radially inward from the outer wall into the chamber to enable the cleansing of both the exterior surface and an interior surface of the medical device. | 07-03-2014 |
20140172073 | Helical High Fatigue Stent-Graft - An implantable prosthesis, including a generally tubular substrate and a continuous shape memory member disposed over the outer surface of the substrate. The shape memory member may include a series of zig-zag struts alternating between a first strut with a first length and a second strut with a second length different from the first length. A graft member may be positioned over the substrate and shape memory member. | 06-19-2014 |
20140163356 | Insertion Guidance System for Needles and Medical Components - A guidance system for assisting with the insertion of a needle or other medical component into the body of a patient is disclosed. The guidance system utilizes ultrasound imaging or other suitable imaging technology. In one embodiment, the guidance system comprises an imaging device including a probe for producing an image of an internal body portion target, such as a vessel. One or more sensors are included with the probe. The sensors sense a detectable characteristic related to the needle, such as a magnetic field of a magnet included with the needle. The system includes a processor that uses data relating to the detectable characteristic sensed by the sensors to determine a position and/or orientation of the needle in three spatial dimensions. The system includes a display for depicting the position and/or orientation of the needle together with the image of the target. | 06-12-2014 |
20140148896 | Stent with a Bio-Resorbable Connector - A stent including a plurality of curved sections and a connector. The curved sections surround a longitudinal axis to define a tube portion and are distributed along the longitudinal axis to form a helix. The connector includes a bioresorbable material and is positioned between two adjacent curved sections. The stent has a spring constant that changes to a different spring constant after exposure to biological material. | 05-29-2014 |
20140148894 | Stent Delivery Device - A delivery device and method for use, the delivery device including a stent device, a restraining sheath, and a pull member. The restraining sheath is mounted coaxially over the stent device for maintaining the stent device in a delivery configuration, and may include a line of weakness extending axially. The pull member is to be pulled so as to split the restraining sheath at the line of weakness and withdraw the restraining sheath from over the stent device. The pull member and the line of weakness may be located on opposing sides of the restraining sheath. The pull member may have an inner part extending inside of the restraining sheath, an outer part extending outside of the restraining sheath, and a wrap around portion therebetween for wrapping around an axial end of the restraining sheath to radially capture the restraining sheath between the inner and outer parts. | 05-29-2014 |
20140142510 | Catheter Assembly, Catheter Systems Including Same, and Method of Manufacture - A catheter assembly, includes a catheter body, a tubular structure and a stabilizing cuff around a longitudinal length of the tubular structure. The tubular structure may be affixed to an exterior surface of the catheter body, and may include a tapered outer surface at a first terminal end of the tubular structure. The tapered outer surface may have a first outer diameter at the first terminal end of the tubular structure and a second outer diameter greater than the first outer diameter at a terminal end of the tapered outer surface opposite the first terminal end. The tubular structure may have a third outer diameter greater than the first outer diameter at a second terminal end of the tubular structure opposite the first terminal end. | 05-22-2014 |
20140135619 | Grafts and Stent Grafts Having a Radiopaque Marker - A graft device comprising a layer of synthetic non-metallic material having a first surface and a second surface spaced apart from the first surface. The device further includes a radiopaque marker at least partially embedded in the layer. | 05-15-2014 |
20140121753 | Catheter Delivery System to Release a Self-Expanding Implant - A percutaneous trans-luminal catheter delivery system for an implant. The system includes a catheter shaft with a distal end to carry the implant and an elongate housing at a proximal end that an operator can grasp when deploying the implant. The shaft has an inner push component which can push on the implant in a distal direction and an outer sheath component which radially surrounds the implant until deployment of the implant into the bodily lumen. The outer sheath component is capable of being pulled proximally, from the housing, to deploy the implant, the housing being mounted on a proximal end portion of the push component and defining a channel. The housing may contain a sheath slitter that is fixedly mounted relative to the length of the channel that can slit the outer sheath as the outer sheath is caused to move proximally in the channel relative to the slitter. | 05-01-2014 |
20140114344 | Non-Entangling Vena Cava Filter - A method of treating a patient includes providing an implantable vessel filter including a plurality of legs and a center-post, inserting the filter into a delivery assembly, and deploying the filter at a desired location in a patient's body. One or more of the legs may have a hook at a distal end thereof and the center-post includes a grooved distal section to receive the hooks. The filter legs transition from a compressed configuration to an expanded configuration during deployment. | 04-24-2014 |
20140107757 | Hand Unit to Release a Self-Expanding Implant - An elongate hand unit for deploying an elongate implant from the distal end of a delivery catheter. The hand unit has a distal end and a proximal end separated by a hand unit length. The hand unit may include a pull component and a push component. The pull component may include a pull grip sliding on the push component to deploy the implant. The push component may be operatively connected to the push element and include at its proximal end a push surface to receive during deployment of the implant a force that pushes on the push element shaft to resist proximal movement of the implant during deployment. The push component may provide a guide rail that defines a guide path for the pull grip, whereby proximal movement of the pull grip along the guide path deploys the implant. | 04-17-2014 |
20140107695 | Tubular Filter - A method of preparing a filter for delivery into a body vessel. The filter includes a hub disposed along a longitudinal axis and a plurality of anchor members extending from the hub. Each anchor member includes either a cranial extension or a caudal extension at a distal end thereof. At least one anchor member distal end may be spaced from the hub at each of a first, second, and third distance along the longitudinal axis. The filter also includes a plurality of locator members extending from the hub, the locator members alternatingly interposed between the anchor members. | 04-17-2014 |
20140107619 | Infusion Apparatuses and Methods of Use - A method of providing a fluid communication path to an implanted device. The method includes positioning at least a portion of a slender pointed element within a catheter, penetrating a septum of an implanted device with the slender pointed element positioned within the catheter, positioning at least a portion of the catheter within the implanted device, removing the slender pointed element from the catheter, and retaining at least a portion of the catheter within the implanted device. | 04-17-2014 |
20140107614 | Connection System for Multi-Lumen Catheter - A catheter connection system and a method of connecting the catheter connection system to a catheter. The catheter connection system includes a hub assembly and a collar. The hub assembly includes a cannula extending from a distal end thereof, and a collet defining an inner surface spaced apart from the cannula to permit passage of a catheter wall between the body and the cannula. | 04-17-2014 |
20140107591 | Tip Configurations for Multi-Lumen Catheter - Multi-lumen catheters with improved tip configurations, including a triple-lumen catheter which may be useful for apheresis. In one variation, the catheter has three lumens with distal openings angularly spaced apart and staggered axially with respect to one another. In another variation, the catheter has two lumens exiting distally and one centrally positioned lumen exiting proximally. A third variation is a catheter with a single distal opening and two proximal openings. The staggered lumen openings along the axial length of the catheter may decrease recirculation while maximizing flow rates. | 04-17-2014 |
20140107475 | Apparatus for Use with Needle Insertion Guidance System - A guidance system utilizes ultrasound imaging or other suitable imaging technology. In one embodiment, the guidance system includes an imaging device including a probe for producing an image of an internal body portion target, such as a vessel. One or more sensors may be associated with the probe. The system may include a medical device, such as a needle, separate from the probe, the medical device having a magnetic field associated therewith. The system may include a processor that uses data relating to the magnetic field sensed by the one or more sensors to determine a position and/or orientation of the medical device. The system may also include a display that shows an image of the internal body portion target taken by the ultrasound imaging probe and a depiction of the medical device positioned and/or oriented with respect to the image. | 04-17-2014 |
20140100534 | Septum Feature for Identification of an Access Port - A power-injectable access port, and a method of identifying a subcutaneously implanted power-injectable access port. The power-injectable access port includes a body capturing a septum that covers a cavity defined by the body, and a pattern of protrusions extending from an outer surface of the septum away from the cavity, the pattern of protrusions detectable through palpation to identify the access port as a power-injectable access port. | 04-10-2014 |
20140094778 | Shape Memory Medical Device and Methods of Use - A method of treating a patient includes providing a guidewire having an elongate body defining a proximal end and a distal end, the elongate body including a shapeable portion disposed proximate the proximal end, the shapeable portion being malleable so as to be shaped into a shape and remain in the shape until reshaped. The distal end of the elongate body is advanced into a vasculature of the patient. The shapeable portion of the elongate body is shaped into a first shape that prevents advancement of the guidewire further into the vasculature of the patient. | 04-03-2014 |
20140094774 | Guidewire Extension System for a Catheter Placement Device - An insertion tool for inserting a catheter into a patient's body is disclosed. The insertion tool unifies needle insertion, guidewire advancement, and catheter insertion in a single device. In one embodiment, the insertion tool comprises a housing in which at least a portion of the catheter is initially disposed, a hollow needle distally extending from the housing with at least a portion of the catheter pre-disposed over the needle, and a guidewire pre-disposed within the needle. A guidewire advancement assembly is also included for selectively advancing the guidewire distally past a distal end of the needle in preparation for distal advancement of the catheter. In one embodiment a catheter advancement assembly is also included for selectively advancing the catheter into the patient. Each advancement assembly can include a slide or other actuator that enables a user to selectively advance the desired component. Guidewire and catheter advancement assemblies are also disclosed. | 04-03-2014 |
20140094760 | Waste Management System - A waste management system includes a waste transport device and a waste collection device. The waste transport device includes a collection member, a retention cuff disposed about an outer surface of the collection member, a first connector, and a proximal end opening biased in a sealed position. The waste collection device includes a second connector and an opening biased in a sealed position. Securing the first connector to the second connector enables transitioning the proximal end opening of the waste transport device and the waste collection device opening to unsealed positions. | 04-03-2014 |
20140088518 | Ureteral Access Sheath - In one embodiment, an access sheath includes a sheath assembly including sheath tubing, the sheath tubing having a main lumen and a secondary lumen that extends along the length of the main lumen, the main lumen being large enough to receive an endoscope. | 03-27-2014 |
20140081316 | Removable Embolus Blood Clot Filter and Filter Delivery Unit - A blood filter includes a hub, a plurality of legs, and a plurality of arms. Each of the legs includes a hook at a distal end thereof, a first linear segment extending substantially parallel to a hub longitudinal axis, a second linear segment extending obliquely with respect to the longitudinal axis at a first angle, and an intermediate linear segment coupled to the first and second segments, the intermediate segment extending obliquely with respect to the longitudinal axis at a second angle less than the first angle. Each of the arms has a free end closer to the longitudinal axis than the hook of each of the legs. The free ends of the arms are spaced radially transverse to the longitudinal axis at substantially the same radial distance. | 03-20-2014 |
20140081219 | Access Port Identification Systems and Methods - An access port for subcutaneous implantation is disclosed. Such an access port may comprise a body for capturing a septum for repeatedly inserting a needle therethrough into a cavity defined within the body. Further, the access port may include at least one feature structured and configured for identification of the access port subsequent to subcutaneous implantation. Methods of identifying a subcutaneously implanted access port are also disclosed. For example, a subcutaneously implanted access port may be provided and at least one feature of the subcutaneously implanted access port may be perceived. Further, the subcutaneously implanted access port may be identified in response to perceiving the at least one feature. | 03-20-2014 |
20140067045 | Bend-Capable Stent Prosthesis - A stent is described, which includes a plurality of stenting rings, each stenting ring including a plurality of struts and points of inflection, each point of inflection connecting adjacent struts, the points of inflection of adjacent stenting rings facing each other along an axis parallel to a longitudinal axis of the stent in a radially expanded stenting disposition while the stent is in an unbent configuration. Adjacent stenting rings are connected by connectors extending from a point of inflection on one stenting ring to a facing point of inflection on another stenting ring, the connectors being linear along an entire length thereof and parallel to the longitudinal axis of the stent, each of the connectors having a length shorter than a length of each of the struts. | 03-06-2014 |
20140066894 | Self-Sealing Pad for a Needle-Based Infusion Set - A safety needle assembly of an infusion set is disclosed. The needle assembly is configured to prevent fluid/vapor escape therefrom so as to reduce or prevent fluid exposure to a clinician using the needle assembly. In one embodiment, the needle assembly comprises a handle portion including a needle extending therefrom, the needle defining a lumen for passage of a fluid therethrough. The needle assembly also includes a safety assembly defining a needle hole through which the needle initially extends. The safety assembly is selectively and axially slidable along the needle in order to shield a distal tip of the needle and prevent user contact therewith. A fluid isolation component is included in the safety assembly for isolating fluid escape from the needle. In one embodiment, the fluid isolation component includes a self-sealing pad that prevents needle leakage when the distal tip is shielded by the safety assembly. | 03-06-2014 |
20140066805 | BIOPSY DEVICE - A biopsy device is disclosed. The biopsy device includes a chamber having a body having a distal end and a proximal end, wherein the proximal end includes an inlet. The biopsy device further includes a vacuum generator for generating negative and positive pressure and at least one first recessed area and at least one second recessed area. The first recessed area extends along an inner wall of the body, proximate the proximal end of the body of the chamber. The first recessed area is configured to release pressure within the chamber. The second recessed area extends along the inner wall of the body, proximate the distal end of the body of the chamber. The second recessed area is configured to release pressure within the chamber. | 03-06-2014 |
20140058437 | Removable Embolus Blood Clot Filter - A removable blood clot filter includes a number of locator members and anchor members disposed radially and extending angularly downward from a hub. The locator members include a number of linear portions having distinct axes configured to place a tip portion approximately parallel to the walls of a blood vessel when implanted and to apply sufficient force to the vessel walls to position the filter near the vessel centerline. The anchor members each include a hook configured to penetrate the vessel wall to prevent longitudinal movement due to blood flow. The hooks may have a cross section sized to allow for a larger radius of curvature under strain so that the filter can be removed without damaging the vessel wall. | 02-27-2014 |
20140058354 | Huber Needle Safety Enclosure - A method of using a safety enclosure for a needle, the needle including an aft end and a fore end together forming a right angle, the fore end including a sharp outer end. The method includes providing a safety enclosure including a needle housing and a panel unit, the needle housing having a finger pad, orienting the safety enclosure in a desired location for insertion of the needle, and applying pressure to the finger pad sufficient to cause penetration of the needle at the desired location and to move the panel unit to the installation position. | 02-27-2014 |
20140058193 | Adjustable Tissue Support Member - An adjustable single-incision sling system, includes a tissue support portion, a first tissue anchor, and a second tissue anchor. The first tissue anchor connects to the tissue support portion via a first arm, which spaces the first tissue anchor from the tissue support portion a fixed first distance. The second tissue anchor connects to the tissue support portion via a second arm, which has a free end passing through the second tissue anchor spacing the second tissue anchor from the tissue support portion a variable second distance, such that movement of the free end with respect to the second tissue anchor decreases the second distance. | 02-27-2014 |
20140046261 | Magnetic Element-Equipped Needle Assemblies - A guidance system for assisting with the insertion of a needle into a patient is disclosed. The guidance system utilizes ultrasound imaging or other suitable imaging technology. In one embodiment, the guidance system comprises an imaging device including a probe for producing an image of an internal body target, such as a vessel. One or more sensors are included with the probe. The sensors sense a detectable characteristic related to the needle, such as a magnetic field of a magnet included with the needle. The system includes a processor that uses data relating to the sensed characteristic to determine a 3-D position of the needle. The system includes a display for depicting the position of the needle. A needle assembly including a hub, cannula, and magnetic element is also disclosed, wherein a magnetic axis of the magnetic element is configured to be coaxially or otherwise aligned with the needle cannula. | 02-13-2014 |
20140033790 | Stent - A radially expansible annular stent is disclosed. The stent comprises a plurality of stenting turns around a lumen centred on a longitudinal axis. Adjacent turns of the stent are joined by connector struts. The stent annulus has a wall thickness related to the material from which it is formed. The radial thickness of the connector struts is smaller than that of the stent annulus. A method of making such a stent is also disclosed. The method includes cutting the connector struts from a tubular workpiece with a laser beam. The laser beam is aimed so as to be offset from a longitudinal axis of the workpiece to provide the reduced radial thickness of the connector struts. | 02-06-2014 |
20140031752 | Catheter Placement Device and Method - An insertion tool for inserting a catheter into a body of a patient is disclosed. The insertion tool unifies needle insertion, guidewire advancement, and catheter insertion in a single device. In one embodiment, the insertion tool comprises a housing in which at least a portion of the catheter is initially disposed, a hollow needle distally extending from the housing with at least a portion of the catheter pre-disposed over the needle, and a guidewire pre-disposed within the needle. A guidewire advancement assembly is also included for selectively advancing the guidewire distally past a distal end of the needle in preparation for distal advancement of the catheter. In one embodiment a catheter advancement assembly is also included for selectively advancing the catheter into the patient. Each advancement assembly can include a slide or other actuator that enables a user to selectively advance the desired component. | 01-30-2014 |
20140025096 | IMPLANTABLE MESH PROSTHESES AND METHOD OF MANUFACTURING SAME - Implantable prostheses for reinforcing and repairing defects in a muscular or tissue wall and a method for fabricating the prostheses that minimizes wasted mesh material and reduces the labor and time required for fabrication. The prosthesis may include a plug body formed of surgical mesh material having a closed end, a larger open end, and a cavity extending therebetween, and a filler body formed of the surgical mesh material comprising a plurality of petals extending radially outwardly from and spaced laterally about a common base disposed in the plug body with the common base attached to the closed end of the plug body. The plug bodies are cut as circular pieces, and the filler bodies are cut as hour-glass shaped pieces from the same sheet of material so as to leave virtually no wasted mesh material. The filler pieces may be attached to the plug body piece by welding. | 01-23-2014 |
20140025042 | Solid-Body Catheter Including Lateral Distal Openings - A split-tip catheter for placement within the vasculature of a patient and for use in hemodialysis or other suitable procedures is disclosed. In one embodiment, the split-tip catheter includes a catheter body that defines a first lumen and a second lumen. The catheter body further comprises a split distal region, including a venous segment and an arterial segment. The venous segment includes a recess extending proximally of a nose portion; and a lateral opening in fluid communication with the first lumen. The arterial segment also includes a lateral opening, is separate from the venous segment, and is removably seatable in the recess provided by the venous segment. In one embodiment, the distal region is un-split, but includes symmetrically opposed lateral openings, as well as distal openings, in communication with the first and second lumens for providing a functional stagger for blood flow in both forward and reverse catheter flow directions. | 01-23-2014 |
20130345791 | Bendable Stent - A stent includes a matrix of struts. The matrix of struts may be disposed parallel to one another in a non-expanded disposition. A plurality of loops along the longitudinal axis may be formed by the matrix of struts. In one aspect, a plurality of cusps in each loop of the plurality of loops connects adjacent struts, the plurality of cusps including tied cusps and free cusps. The tied cusps of one loop can be connected to the tied cusps of an adjacent loop by a bridge extending therebetween. In one aspect, the adjacent struts connected by a tied cusp have different lengths. In one aspect, at least one free cusp in each loop joins two struts of approximately equal length. | 12-26-2013 |
20130345788 | Low Friction Vascular Implant Delivery Device - A vascular implant delivery device is disclosed and can include a body and a syringe attachment formed in the body. Further, the device can include an outer sheath extending from the body. The outer sheath can include a distal end that can be configured to receive a vascular implant. The device can also include at least three implant support structures that can extend radially inward from the distal end of the outer sheath. The implant support structures can be configured to support and guide a vascular implant moving through the outer sheath. Additionally, the device can include an inner carrier catheter slidably disposed within the outer sheath. | 12-26-2013 |
20130338759 | Helical Stent Having Improved Flexibility and Expandability - A stent includes a central portion of helically wound undulations formed of struts, cylindrical end portions, and transition zones between the helical portion and the cylindrical portions. According to a first aspect of the invention, the torsional flexibility of the stent is maximized by having bridges connecting adjacent winding be interrupted by the maximum possible number of undulations. In one embodiment, each winding includes nineteen undulations around the circumference, bridges are provided every five undulations. According to a second aspect of the invention, uniform opening of the transition zone is achieved by altering the width, and thereby the flexibility, of a series of struts in accordance with their lengths. Specifically, the long transition zone struts are made wider. | 12-19-2013 |
20130338503 | Apparatus and Methods for Detection of a Removable Cap on an Ultrasound Probe - An ultrasound imaging device including the ability to determine when a component, such as a removable probe cap, is attached to a portion of an ultrasound probe. Such a cap is employed in one embodiment to act as a spacer component to provide a standoff for the probe head. Detection of probe cap attachment to the ultrasound probe enables the resultant ultrasound image to be adjusted automatically by the ultrasound imaging system. In one embodiment, an ultrasound imaging system comprises an ultrasound probe, a cap or other component that is attachable to the probe, and a component attachment detection system for detecting attachment of the component to the probe. Once the cap is detected, an aspect of an ultrasound image produced by the imaging system is modified, such as cropping the image to remove undesired portions of the cap, such as the spacer component. | 12-19-2013 |
20130324851 | Low Power Ultrasound System - A low power ultrasound system for use in sonography applications, including vascular imaging, is disclosed. In one embodiment, the low power ultrasound system comprises a base unit that includes an image processor and a display. An ultrasound probe is operably connected to the base unit. The probe includes a head portion including an array of crystal transducers. A plurality of pulser/receiver modules that cause the transducers to emit ultrasonic transmit pulses are also included in the probe. The pulser/receiver modules are further configured to receive analog signals relating to ultrasonic echo receive pulses detected by the transducers. The probe includes a singular low noise amplifier that amplifies the analog signals, and an analog-to-digital converter that converts the analog signals to a digital signal. A wireless interface is included for enabling the digital signal to be wirelessly transmitted from the probe to the image processor of the base unit. | 12-05-2013 |
20130317592 | Device for Catheter Sheath Retraction - A device for moving an elongate member relative to an elongate body through which it extends, the device including a housing, a mover, and a pre-mover. The housing is connectable to the elongate body. The mover is associated with the housing and is connectable to the elongate member for moving the elongate member relative to the housing. The pre-mover is associated with the housing and is connectable to the elongate member for adjusting the elongate member in preparation for moving the elongate member with the mover. | 11-28-2013 |
20130296897 | SELF ADHERING IMPLANTABLE MESH PROSTHESIS WITH REDUCED INSERTION PROFILE - The present invention is an implantable adhesive mesh prosthesis for reinforcing and/or repairing a defect in tissue that is easy to roll into a small diameter cylinder or other low-profile shape for passing through a trocar, incision, or other surgical instrument. More specifically, the adhesive may be applied to the mesh material in a pattern that leaves a significant portion of the surface area of the mesh material free of adhesive. In one embodiment, the adhesive is applied only near the outer perimeter of the mesh product. In another embodiment, the adhesive is applied in spots over all or a portion the surface of the mesh product. In yet another embodiment, the adhesive is applied in parallel lines on the surface of the mesh product and the mesh may be rolled up around an axis parallel to the lines of adhesive. | 11-07-2013 |
20130280346 | Infusates with Enhanced pH Stability Under Ethylene Oxide Sterilization - Normal saline and other infusate solutions for infusion into the body of a patient during medical treatment are disclosed. In particular, infusates are disclosed that are formulated to resist changes to the pH of the solution when subjected to sterilization procedures that employ ethylene oxide gas. In one embodiment, a buffered infusate suitable for disposal in a syringe or other container is disclosed. The syringe is sterilizable using ethylene oxide. The buffered infusate comprises an aqueous solution that is disposed in the syringe and is suitable for infusion into a body of a patient. A buffer component is added to the aqueous solution to form a buffered solution. The buffer component is configured to resist a change in the pH of the buffered solution upon exposure of the buffered solution to the ethylene oxide during sterilization of the syringe. | 10-24-2013 |
20130248386 | METHOD AND APPARATUS FOR REHYDRATION OF LYOPHILIZED BIOLOGIC MATERIALS - The present invention is a method and an apparatus for packaging lyophilized implants and other medical devices. In accordance with the invention, a lyophilized implant may be packaged for delivery to the surgical site in a sealed, flexible/expandable, sterile inner pouch. The inner pouch may be further packaged within an outer, sterile package. The inner pouch contains a resealable port through which rehydration liquid may be introduced into the inner pouch without opening the inner pouch. The inner pouch may be made of a flexible, substantially non-stretchable material so that the pouch can expand only to a predetermined maximum size to accept a predetermined volume of rehydration liquid. After rehydration, any excess rehydration liquid within the pouch may be removed via the same port. Next, the pouch is opened via a second opening to expose the implant for removal from the package. | 09-26-2013 |
20130245574 | Assemblies for Identifying a Power Injectable Access Port - An assembly for identifying a power injectable vascular access port, including a vascular access port and an identification feature. The port is structured for power injection and includes a housing and a septum together defining a reservoir. A radiographic feature incorporated into the port is perceivable via x-ray following subcutaneous implantation, the radiographic feature identifying the port as suitable for flowing fluid at a fluid flow rate of at least 1 mL/sec therethrough. A structural feature of the port is perceivable via palpation following subcutaneous implantation, the structural feature identifying the port as suitable for accommodating a pressure within the reservoir of at least 35 psi. The identification feature is separated from the port and confirms that the port is both suitable for flowing fluid at a rate of at least 1 mL/sec therethrough and suitable for accommodating a pressure within the reservoir of at least 35 psi. | 09-19-2013 |
20130245452 | Needle Guides for a Sonographic Imaging Device - An medical device guide system includes a probe configured for imaging portions of a patient's body, a first guide connector extending from a first surface of the probe, the first guide connector including a first mounting surface, and a guide removably mountable to the first guide connector. The guide may include a first cavity shaped to receive the first mounting surface and a first channel disposed on a top surface of the guide opposite the first cavity, the first channel angled at a first angle with respect to a longitudinal axis of the probe and configured to guide a medical device to a targeted depth in the patient's body. | 09-19-2013 |
20130245434 | Integrated System for Intravascular Placement of a Catheter - An integrated catheter placement system for accurately placing a catheter within a patient's vasculature is disclosed. In one embodiment, the integrated system comprises a system console, a tip location sensor for temporary placement on the patient's chest, and an ultrasound probe. The tip location sensor senses a magnetic field of a stylet disposed in a lumen of the catheter when the catheter is disposed in the vasculature. The ultrasound probe ultrasonically images a portion of the vasculature prior to intravascular introduction of the catheter. The ultrasound probe includes user input controls for controlling use of the ultrasound probe in an ultrasound mode and use of the tip location sensor in a tip location mode. In another embodiment, ECG signal-based catheter tip guidance is included in the integrated system to enable guidance of the catheter tip to a desired position with respect to a node of the patient's heart. | 09-19-2013 |
20130245431 | User Interface and Methods for Sonographic Display Device - A user interface for a sonographic device is disclosed that displays a sonographic image and at least one reference object corresponding to a catheter size. The reference object may be scaled in proportion to the sonographic image. In addition, the user interface may further display a plurality of vertical lines and a plurality of horizontal lines arranged in a grid-like pattern and placed over the sonographic image. The size of both the sonographic image and the at least one reference object may change in proportion to a chosen insertion depth. A display device, a sonographic device and corresponding methods are also disclosed. | 09-19-2013 |
20130231640 | DEPOSITION OF A SILVER LAYER ON A NONCONDUCTING SUBSTRATE - Methods for the deposition of silver-comprising films on nonconducting substrates, and, more particularly, to deposition of such films that are very thin, are provided. The surface of nonconducting substrates is modified with a superabsorbent polymer to increase silver deposition when compared to a non-modified surface. Also provided are films produced using a swelling agent, whereby porosity of the surface of the nonconducting substrate is increased, thereby permitting increased silver deposition when compared to an unmodified surface. | 09-05-2013 |
20130226141 | Reduced Friction Catheter Introducer and Method of Manufacturing and Using the Same - Tear-away sheath introducers for catheters, methods for making such introducers, and methods for using such introducers are described. A splittable sheath introducer may include a sheath, a hub disposed at a proximal end of the sheath, a valve included with the hub, and a valve actuator movable from a first position to a second position, the valve actuator opening the valve when in the second position. The valve actuator may include a retaining member that enables the valve actuator to be retained by a portion of the hub when the sheath introducer is split apart. | 08-29-2013 |
20130226106 | Access Port Identification Systems and Methods - An access port for subcutaneous implantation is disclosed. Such an access port may comprise a body for capturing a septum for repeatedly inserting a needle therethrough into a cavity defined within the body. Further, the access port may include at least one feature structured and configured for identification of the access port subsequent to subcutaneous implantation. Methods of identifying a subcutaneously implanted access port are also disclosed. For example, a subcutaneously implanted access port may be provided and at least one feature of the subcutaneously implanted access port may be perceived. Further, the subcutaneously implanted access port may be identified in response to perceiving the at least one feature. | 08-29-2013 |
20130225991 | Access Port Identification Systems and Methods - A power-injectable access port includes a housing defining an internal cavity and including a plurality of suture apertures, a needle-penetrable septum captured by the housing enabling needle access to the internal cavity, a stem having a lumen in fluid communication with the internal cavity, the stem configured for coupling to a catheter, and a radiopaque identification feature observable via imaging technology subsequent to subcutaneous implantation of the port, the feature indicating that the port is suitable for power injection. | 08-29-2013 |
20130225990 | Access Port Identification Systems and Methods - An access port for subcutaneous implantation is disclosed. Such an access port may comprise a body for capturing a septum for repeatedly inserting a needle therethrough into a cavity defined within the body. Further, the access port may include at least one feature structured and configured for identification of the access port subsequent to subcutaneous implantation. Methods of identifying a subcutaneously implanted access port are also disclosed. For example, a subcutaneously implanted access port may be provided and at least one feature of the subcutaneously implanted access port may be perceived. Further, the subcutaneously implanted access port may be identified in response to perceiving the at least one feature. | 08-29-2013 |
20130218260 | Bend-Capable Tubular Prosthesis - A tubular prosthesis having a succession of turns around a longitudinal axis includes connectors between adjacent turns distributed around the circumference of the prosthesis. Each turn includes struts interspersed by inflection zones located at the axial ends of each turn such that, when the prosthesis expands radially, gaps open up between adjacent struts of each of the turn. The inflection zones are distributed regularly around the circumference so that the gaps are substantially the same size as each other around the circumference of the turn. The prosthesis may include a turn that exhibits a stagger zone within which the gap between adjacent struts is of an individual size different from that common to the other gaps of that turn. The inflection zones in that turn that lie circumferentially next to the stagger zone are displaced out of facing relationship with corresponding zones of inflection in the adjacent turn. | 08-22-2013 |
20130218108 | Waste Management System - A waste management system and method of use. The waste management system includes a waste transport device and a waste collection device. The waste transport device includes a generally tubular body, a distal end section configured for disposition and maintenance in a patient's rectum, and a proximal end section including a first connector biased in a sealed position. The waste collection device includes a second connector. The first connector is transitioned to an unsealed position when the first connector is secured to the second connector. | 08-22-2013 |
20130218106 | Automated Method of Pooling Elimination with a Biological Fluid Collection System - A drainage and/or collection system for biological fluids includes at least one conduit for transporting a biological fluid from a catheter to a collector device and a gas pressure source configured to feed a gas into the at least one conduit between the catheter and the collection device. The gas causes the biological fluid arranged in the at least one conduit to drain into the collection device. A method includes inserting a catheter, draining a fluid into a collector device via a conduit, and introducing gas into the conduit so as to force fluid remaining in the conduit into the collection device. | 08-22-2013 |
20130217999 | Systems and Methods for Positioning a Catheter - A method for displaying a position of a medical device, such as a catheter, during insertion thereof into a patient. In one example embodiment, the method includes obtaining a first set of detected position data relating to a location marker, such as a permanent magnet, then determining a possible first position thereof. A first confidence level relating to a match between the first set of detected position data and a first set of predicted position data is assigned. A determination is made whether the first confidence level meets or exceeds a first threshold. If the first confidence level meets or exceeds the first threshold, a determination is then made whether the first position of the location marker is within a first detection zone. If the first position of the location marker is within the first detection zone, the first position of the location marker is displayed. | 08-22-2013 |
20130190616 | MULTIPLE IMAGING MODE TISSUE MARKER - An intracorporeal marker for marking a site within living tissue of a host having a body of porous hydroxyapatite whose physical properties permit the body to be distinguished from human soft tissue under visualization using ultrasonic and radiation imaging modalities. | 07-25-2013 |
20130184562 | BIOPSY MARKER WITH IN SITU-GENERATED IMAGING PROPERTIES - An intracorporeal marker, for marking a site within living tissue of a host, includes an outer body portion of biodegradable material. An inner body portion is located in the outer body portion. The inner body portion includes biological material that becomes calcified in the living tissue of the host over time. An agent interacts with the biological material to promote calcification of the biological material of the inner body portion in the living tissue of the host. | 07-18-2013 |
20130172733 | Systems and Methods for Radiographically Identifying an Access Port - An access port for subcutaneous implantation is disclosed. Such an access port may comprise a body for capturing a septum for repeatedly inserting a needle therethrough into a cavity defined within the body. Further, the access port may include at least one feature structured and configured for identification of the access port subsequent to subcutaneous implantation. Methods of identifying a subcutaneously implanted access port are also disclosed. For example, a subcutaneously implanted access port may be provided and at least one feature of the subcutaneously implanted access port may be perceived. Further, the subcutaneously implanted access port may be identified in response to perceiving the at least one feature. In one embodiment, an identification feature is included on an insert that is incorporated into the access port so as to be visible after implantation via x-ray imaging technology. | 07-04-2013 |
20130165773 | Access Port Identification Systems and Methods - An access port for subcutaneous implantation is disclosed. Such an access port may comprise a body for capturing a septum for repeatedly inserting a needle therethrough into a cavity defined within the body. Further, the access port may include at least one feature structured and configured for identification of the access port subsequent to subcutaneous implantation. Methods of identifying a subcutaneously implanted access port are also disclosed. For example, a subcutaneously implanted access port may be provided and at least one feature of the subcutaneously implanted access port may be perceived. Further, the subcutaneously implanted access port may be identified in response to perceiving the at least one feature. | 06-27-2013 |
20130150827 | MEDICAL DEVICE SECUREMENT SYSTEM - A securement device, system, and method for use with a medical article. The securement device, system, or method may include a body that has a top surface and a bottom surface. The bottom surface has an adhesive compound thereon. A resilient retainer formed from a soft, tacky elastomeric gel or foam is supported by the bottom surface of the body. The resilient retainer receives and secures a medical device. The medical device is secured to the skin of a patient upon affixing the bottom surface to the patient via the adhesive compound. | 06-13-2013 |
20130116571 | Ruggedized Ultrasound Hydrogel Insert - A ruggedized hydrogel product that is formulated to withstand the effects of high-energy sterilization procedures, such as gamma beam and electron beam sterilization, without significant structural degradation is disclosed. This enables the hydrogel product to be suitable for use in medical applications where sterile components are required. In one embodiment a ruggedized hydrogel product is disclosed and comprises a gel component, water for hydrating the gel component, and at least one free radical absorber component that is capable of absorbing free radicals produced when the hydrogel product is sterilized via a high-energy sterilization procedure. The free radical absorber component in one embodiment includes potassium metabisulfite and ascorbic acid. The ruggedized hydrogel product can be included with an ultrasound probe to provide an acoustically transparent interface between the probe and the skin of a patient. | 05-09-2013 |
20130102950 | Graft-Catheter Vascular Access System - A vascular access device, for implantation at least partially below the skin of a patient to provide an arteriovenous fistula, includes a graft portion coupled to a catheter portion. The graft portion is sutured to an opening in an artery while the catheter portion is inserted into a vein so that its end lies within the vein downstream from the point of entry into the vein. The device may be comprised of ePTFE with an outer polyurethane coating or the graft portion may comprise ePTFE with an outer polyurethane coating and the catheter portion may comprise polyurethane. There may also be an inner polyurethane coating. Alternatively, the device may be comprised entirely of polyurethane. | 04-25-2013 |
20130102889 | Systems and Methods for Ultrasound-Based Medical Device Assessment - Systems and methods for assisting the placement of a catheter within the body of a patient through the use of an ultrasound imaging system are disclosed. In particular, the systems and methods described herein enable a clinician to determine, prior to insertion of the medical device, how much of the device will be disposed within the vessel, thus enabling the clinician to choose a catheter with suitable length. In one embodiment, an ultrasound imaging system for assisting with placement of the medical device comprises a console, a probe for producing an image of a target location, and a processor. The processor provides to a user proximity information relating to the anticipated proximity of the medical device to the target location prior to insertion of the medical device. A display is included for depicting the image, target location depth, and the proximity information of the medical device to the target location. | 04-25-2013 |
20130102860 | Drains for Use in Medical Applications and Methods of Using the Same - A drain for use in medical applications may include an elongated conduit configured to be implanted in a body cavity, wherein the conduit has a proximal end and a distal end. The conduit may include at least one channel configured to drain fluid from the body cavity and at least one lumen extending from the proximal end to the distal end of the conduit. The lumen may be at least partially surrounded by the at least one channel and may be separated from the at least one channel by a wall. At least one hole in the wall may be configured to provide fluid communication between the lumen and the at least one channel. | 04-25-2013 |
20130098398 | Insert for a Microbial Scrubbing Device - The microbial scrub brush in one embodiment employs an insert that is impregnated with an anti-bacterial disinfectant and that is housed within a housing of alcohol-compatible material and sealed over by a removable lid. The insert is maintained in sterile condition until ready for use. After removal of the lid, the insert is moved over the end of a female luer or other portion of a medical device and rotated in order to clean the exterior surface as well as the interior luminal surface of the device. In one embodiment, the insert includes a base from which extends an outer wall that defines a chamber. A plurality of complaint fingers extend from the base into the chamber. A plurality of wipers extend radially inward from the outer wall into the chamber to enable the cleansing of both the exterior surface and an interior surface of the medical device. | 04-25-2013 |
20130096607 | Embolus Blood Clot Filter and Delivery System - A blood filter delivery system for delivering a filter into a vein includes an introducer and a push rod with a spline member disposed along the push rod. The spline member has a main body, and first and second boss portions spaced apart along the longitudinal axis to provide a gap for retaining anchor member of the filter during delivery via the introducer. | 04-18-2013 |
20130096585 | Blood Vessel Transecting and Anastomosis - Method and device for cutting a blood vessel using a cutting tool from within the blood vessel. A first cut portion of the blood vessel is fused to a second blood vessel to provide a flow channel therebetween. | 04-18-2013 |
20130090721 | Highly Flexible Stent and Method of Manufacture - Preferred embodiments of a stent with a high degree of flexibility are shown and described. The stent can include a continuous helical winding having interconnected struts joined at vertices, and having bridges connecting sections of the helical winding to each other. An annular ring can be provided at one or both ends of the helical winding, and the annular ring can have extensions extending to connect to the helical winding. One of the extensions can connect to a bridge and another extension can connect to a vertex. The struts at the ends of the helical winding can have strut lengths that differ from the strut lengths of the struts in a central portion of the winding between the ends of the winding. | 04-11-2013 |
20130090719 | Highly Flexible Stent and Method of Manufacture - Preferred embodiments of a stent with a high degree of flexibility are shown and described. The stent can include a continuous helical winding having interconnected struts joined at vertices, and having bridges connecting sections of the helical winding to each other. An annular ring can be provided at one or both ends of the helical winding, and the annular ring can have five extensions extending to connect to the helical winding. One of the extensions can connect to a bridge and another extension can connect to a vertex. The struts at the ends of the helical winding can have strut lengths that differ from the strut lengths of the struts in a central portion of the winding between the ends of the winding. | 04-11-2013 |
20130090716 | Delivery System for a Self-Expanding Implant - The present disclosure provides a delivery system for a self-expanding implant ( | 04-11-2013 |
20130090614 | Corporeal Drainage System - A corporeal drainage system and a method of draining fluid from a bodily cavity. The corporeal drainage system includes a connection tube and a fluid receptacle in fluid communication with the connection tube. The fluid receptacle creates a negative pressure in the system by transitioning from a collapsed configuration to an expanded configuration. The system may include an activation member to initiate transitioning of the fluid receptacle. | 04-11-2013 |
20130085523 | Non-Entangling Vena Cava Filter - A method of treating a patient includes providing an implantable vessel filter including a plurality of legs and a center-post, inserting the filter into a delivery assembly, and deploying the filter at a desired location in a patient's body. One or more of the legs may have a hook at a distal end thereof and the center-post includes a grooved distal section to receive the hooks. The filter legs transition from a compressed configuration to an expanded configuration during deployment. | 04-04-2013 |
20130085436 | Tip Configurations for Multi-Lumen Catheter - Multi-lumen catheters with improved tip configurations, including a triple-lumen catheter which may be useful for apheresis. In one variation, the catheter has three lumens with distal openings angularly spaced apart and staggered axially with respect to one another. In another variation, the catheter has two lumens exiting distally and one centrally positioned lumen exiting proximally. A third variation is a catheter with a single distal opening and two proximal openings. The staggered lumen openings along the axial length of the catheter may decrease recirculation while maximizing flow rates. | 04-04-2013 |
20130079863 | Loading and Delivery of Self-Expanding Stents - A method of deploying a stent includes providing a delivery system with the stent loaded in a reduced diameter configuration between an inner catheter and an outer sheath, the stent including a covering positioned on a luminal wall surface thereof, the inner catheter including a radially outwardly extending protrusion that extends into the covering but does not intersect a plane along the stent luminal wall surface, advancing the delivery system to a stenting site, and withdrawing the outer sheath to deploy the stent at the stenting site. | 03-28-2013 |
20130079752 | Solid-Body Catheter Including Lateral Distal Openings - A split-tip catheter for placement within the vasculature of a patient and for use in hemodialysis or other suitable procedures is disclosed. In one embodiment, the split-tip catheter includes a catheter body that defines a first lumen and a second lumen. The catheter body further comprises a split distal region, including a venous segment and an arterial segment. The venous segment includes a recess extending proximally of a nose portion; and a lateral opening in fluid communication with the first lumen. The arterial segment also includes a lateral opening, is separate from the venous segment, and is removably seatable in the recess provided by the venous segment. In one embodiment, the distal region is un-split, but includes symmetrically opposed lateral openings, as well as distal openings, in communication with the first and second lumens for providing a functional stagger for blood flow in both forward and reverse catheter flow directions. | 03-28-2013 |
20130072901 | Fixation and Protection of an Implanted Medical Device - Fixation and protective components for use with implantable medical devices, such as access ports and catheters, are disclosed. In one embodiment, a protective sleeve is employed about a catheter so as to distribute compressive loads and ensure patency of the catheter lumen, even in areas prone to pinch-off. A catheter assembly in one embodiment thus comprises an elongate catheter tube that defines at least one lumen. A protective mesh sleeve is disposed about an external portion of the catheter tube so as to cover at least a portion of the longitudinal length of the catheter tube. The protective sleeve is configured to distribute a compressive load on the catheter tube so as to ensure patency of the at least one lumen of the catheter tube. | 03-21-2013 |
20130071550 | Self-Sealing PTFE Graft with Kink Resistance - A self-sealing vascular graft, including a substrate with a sealant layer and several optional additional layers, is described. The substrate can be ePTFE and the material used for the sealant and additional layers can be polyurethane. The sealant layer and additional layers may include one or more base layers, one or more foam layers, beading of different sizes and shapes, and ePTFE tape. A flared cuff may be integral to one or both ends of the substrate or may be attached to one or both ends. Various methods of making a self-sealing vascular graft are also described, including methods of disposition, methods of forming, methods of bonding and methods of attaching. | 03-21-2013 |
20130066329 | Medical Retrieval Devices - A medical retrieval device may include an elongated member having first and second end portions and a middle portion. The elongated member may be configured such that the first and second end portions are proximal one another and extend substantially parallel to one another along a longitudinal axis. The middle portion may have an unconstrained basket configuration. A first sheath may be configured to receive at least a portion of the first end portion, and a second sheath may be configured to receive at least a portion of the second end portion. At least one of the first and second sheaths may be movable relative to the middle portion so as to constrain the middle portion in an elongated configuration. | 03-14-2013 |
20130060116 | Integrated System for Intravascular Placement of a Catheter - An integrated catheter placement system for accurately placing a catheter within a patient's vasculature is disclosed. In one embodiment, the integrated system comprises a system console, a tip location sensor for temporary placement on the patient's chest, and an ultrasound probe. The tip location sensor senses a magnetic field of a stylet disposed in a lumen of the catheter when the catheter is disposed in the vasculature. The ultrasound probe ultrasonically images a portion of the vasculature prior to intravascular introduction of the catheter. The ultrasound probe includes user input controls for controlling use of the ultrasound probe in an ultrasound mode and use of the tip location sensor in a tip location mode. In another embodiment, ECG signal-based catheter tip guidance is included in the integrated system to enable guidance of the catheter tip to a desired position with respect to a node of the patient's heart. | 03-07-2013 |
20130048516 | Enhanced Pre-Wetted Intermittent Catheter With Lubricious Coating - A pre-wetted intermittent catheter apparatus including a container, a conduit positioned within the container, and a wetting fluid disposed within the container. The container may have a proximal end section, a distal end section, and a middle section connecting the proximal end section to the distal end section. The middle section may have a plurality of pleats along a collapsible section, the collapsible section having a first expanded length and a second collapsed length less than the first expanded length. The conduit may have a proximal end fixed to the proximal end section, a distal end slidably positioned with respect to the container at the distal end section, and a coating disposed on an outer surface thereof. | 02-28-2013 |
20130030413 | Sacrificial Catheter - A sacrificial catheter assembly and method of use for placing a functional catheter within the body of a patient, such as into the patient's vasculature, is disclosed. In one embodiment, the sacrificial catheter assembly comprises a sacrificial catheter including an elongate body that defines a longitudinally extending lumen. A stylet is removably received within the lumen of the sacrificial catheter such that the catheter and stylet can be advanced together to a target destination within the body of the patient. The sacrificial catheter is configured so as to then be proximally slid over the stylet to remove the sacrificial catheter from the body while the stylet remains in place at the target destination. A functional catheter can then be distally slid over the stylet to place the functional catheter at the target destination. The stylet can then be removed from the body of the patient. | 01-31-2013 |
20120330242 | Vascular Access Port with Integral Attachment Mechanism - An implantable port with an integral attachment mechanism. The implantable port includes one or more suture needles enclosed within a port body, the suture needle(s) coupled to a movable member such that movement of the movable member results in movement of the suture needle(s) out of the port body and into the tissue of a body into which it is implanted. The movable member can be a cam or tensioning member that rotates about a central port axis. The movable member can be coupled to a gear to permit movement of the movable member following implantation of the port within a subcutaneous pocket. | 12-27-2012 |
20120323140 | SINGLE-INSERTION, MULTIPLE SAMPLE BIOPSY DEVICE WITH INTEGRATED MARKERS - The present invention provides for exemplary embodiments of a single-insertion, multiple sample biopsy device. Exemplary embodiments of a single-insertion, multiple sampling device with integrated marker release. | 12-20-2012 |
20120310260 | IMPLANTABLE MESH PROSTHESES AND METHOD OF MANUFACTURING SAME - Implantable prostheses for reinforcing and repairing defects in a muscular or tissue wall and a method for fabricating the prostheses that minimizes wasted mesh material and reduces the labor and time required for fabrication. The prosthesis may include a plug body formed of surgical mesh material having a closed end, a larger open end, and a cavity extending therebetween, and a filler body formed of the surgical mesh material comprising a plurality of petals extending radially outwardly from and spaced laterally about a common base disposed in the plug body with the common base attached to the closed end of the plug body. The plug bodies are cut as circular pieces from a sheet of the surgical mesh material while the filler bodies are cut as a plurality of hour-glass (or dog-bone) shaped pieces with arcuate side edges, wherein the hour-glass shaped filler pieces are cut from the same sheet of material between adjacent circular plug body pieces so as to leave virtually no wasted mesh material. The filler pieces may be attached to the plug body piece by welding. | 12-06-2012 |
20120310219 | Medical Device with Elastomeric Bulb - A drainage catheter including a body, a drainage lumen extending between the body proximal end and the body distal end, the drainage lumen including a distal fluid inflow port and a proximal fluid drain coupling, and an inflation lumen extending between the body proximal end and the body distal end, conveying inflating fluid from a proximal fluid supply element to a distal fluid acceptor balloon, the proximal fluid supply element adjacent the proximal fluid drain coupling. A sleeve may be secured about the proximal fluid supply element and the proximal fluid drain coupling to provide a fluid impervious coating. | 12-06-2012 |
20120302969 | Overmolded Access Port Including Anchoring and Identification Features - An access port for providing subcutaneous access to a patient is disclosed. In one embodiment, the port includes an internal body defining a fluid cavity that is accessible via a septum. A compliant outer cover including silicone is disposed about at least a portion of the body. A flange is included with the port body and is covered by the outer cover. The flange radially extends about a perimeter of the port body proximate the septum so as to impede penetration of a needle substantially into the outer cover in instances where the needle misses the septum. The flange can further include both an anchoring feature for securing the outer cover to the port body and an identification feature observable via x-ray imaging technology for conveying information indicative of at least one attribute of the access port. The outer cover provides a suitable surface for application of an antimicrobial/antithrombotic coating. | 11-29-2012 |
20120281021 | User Interface and Methods for Sonographic Display Device - A user interface for a sonographic device is disclosed that displays a sonographic image and at least one reference object corresponding to a catheter size. The reference object may be scaled in proportion to the sonographic image. In addition, the user interface may further display a plurality of vertical lines and a plurality of horizontal lines arranged in a grid-like pattern and placed over the sonographic image. The size of both the sonographic image and the at least one reference object may change in proportion to a chosen insertion depth. A display device, a sonographic device and corresponding methods are also disclosed. | 11-08-2012 |
20120259296 | Systems and Methods for Identifying an Access Port - An access port for subcutaneous implantation is disclosed. Such an access port may comprise a body for capturing a septum for repeatedly inserting a needle therethrough into a cavity defined within the body. Further, the access port may include at least one feature structured and configured for identification of the access port subsequent to subcutaneous implantation. Methods of identifying a subcutaneously implanted access port are also disclosed. For example, a subcutaneously implanted access port may be provided and at least one feature of the subcutaneously implanted access port may be perceived. Further, the subcutaneously implanted access port may be identified in response to perceiving the at least one feature. In one embodiment, an identification feature is engraved or otherwise defined by the access port, so as to be visible after implantation via x-ray imaging technology. | 10-11-2012 |
20120259290 | Drug Delivery System - Apparatuses and methods for coating and/or loading a medical device with a therapeutic agent prior to or during the placement of the medical device within the patient's body. In one variation, the medical device is coated and/or loaded with a therapeutic agent while the device is positioned in a delivery apparatus. In another variation, the delivery apparatus comprises a reservoir for retaining a therapeutic agent. The user may release the therapeutic agent from the reservoir prior to or during the placement of the device to coat and/or load the device with the therapeutic agent. | 10-11-2012 |
20120253322 | Connection System for Multi-Lumen Catheter - A catheter connection system and a method of connecting the catheter connection system to a catheter. The catheter connection system includes a hub assembly and a collar. The hub assembly includes a cannula extending from a distal end thereof, and a collet defining an inner surface spaced apart from the cannula to permit passage of a catheter wall between the body and the cannula. | 10-04-2012 |
20120253177 | Radiation Containing Seeds and Method for High Visibility Magnetic Imaging - A radioactive seed and method for making a radioactive seed with selective magnetic imaging characteristics are provided. The seed includes a housing which may include a metal shell for at least partially enclosing a radioactive material. The shell encloses a rod having a nickel layer with a phosphorous content, wherein the phosphorous content includes a level of phosphorous sufficient, when the seed is implanted in tissue, to provide a magnetic resonance image of the seed while substantially eliminating gross artifacts in the magnetic resonance image. | 10-04-2012 |
20120253110 | Adjustable Tissue Support Member - A tissue support system including an implantable tissue support member is described. The tissue support member includes a tissue support portion, a first arm having a first end joined to a first end of the tissue support portion, a second arm having a first end joined to a second end of the tissue support portion, the second arm defining a lumen, a first tissue anchor fixed to a second end of the first arm, a second tissue anchor slidably positioned over the second arm, and a locking member disposed in the lumen of the second arm between the second tissue anchor and a second end of the second arm. | 10-04-2012 |
20120226244 | Septum Feature for Identification of an Access Port - An access port for providing subcutaneous access to a patient, and a method of identifying a subcutaneously implanted access port. The access port includes a body capturing a septum that covers a cavity defined by the body, and a pattern of protrusions extending from an outer surface of the septum away from the cavity, the pattern of protrusions detectable through palpation to indentify the access port as a power-injectable port. | 09-06-2012 |
20120220984 | Catheter Connection Systems - A catheter connector system, including a catheter hub and a coupling member. The catheter hub includes a cannula portion connected to a housing portion and a distal interface including a tapered seal post fixed to the housing portion, a deformable sealing element surrounding the tapered seal post, and a retention collar surrounding the sealing element. The coupling member includes an opening to receive the distal interface, an inwardly extending portion to engage the retention collar, and an actuating member to engage the deformable sealing element. | 08-30-2012 |
20120220942 | Medical Component Insertion Device Including a Retractable Needle - An insertion device for use in assisting with the placement of a medical device within the body of a patient is disclosed. For example, the insertion device can be employed to assist with the placement of an introducer, which provides a conduit for insertion of a catheter into the body. In one embodiment, the insertion device comprises a needle that is removably disposed within a bore defined by the medical device, and a needle retraction assembly. The needle retraction assembly can position the needle in any one of a first position wherein a distal tip of the needle is disposed a predetermined distance distal to a distal end of the medical device, a second position wherein the needle distal tip is disposed distal but proximate to the distal end of the medical device, and a third position wherein the needle distal tip is retracted within the medical device bore. | 08-30-2012 |
20120220854 | Integrated System for Intravascular Placement of a Catheter - An integrated catheter placement system for accurately placing a catheter within a patient's vasculature is disclosed. In one embodiment, the integrated system comprises a system console, a tip location sensor for temporary placement on the patient's chest, and an ultrasound probe. The tip location sensor senses a magnetic field of a stylet disposed in a lumen of the catheter when the catheter is disposed in the vasculature. The ultrasound probe ultrasonically images a portion of the vasculature prior to intravascular introduction of the catheter. The ultrasound probe includes user input controls for controlling use of the ultrasound probe in an ultrasound mode and use of the tip location sensor in a tip location mode. In another embodiment, ECG signal-based catheter tip guidance is included in the integrated system to enable guidance of the catheter tip to a desired position with respect to a node of the patient's heart. | 08-30-2012 |
20120215063 | PELVIC FLOOR REPAIR SYSTEM - Described herein are devices and methods comprising a system for tissue reinforcement, such as stabilization of fascial structures of the pelvic floor in vaginal wall prolapse. The surgical treatment can provide a mechanical support or bridging material for a fascial defect. An implant with four arms, for example two proximal arms and two distal arms, can provide post-surgical adjustability of the graft position, enabling tension free placement of the implant. In addition, a four-point fixation of the implant with apical support can ensure a suitable anatomical repair. Furthermore, instrumentation is disclosed herein, including an introducer device capable of fixing a wide variety of materials, such as mesh arms and suture, to tissue. | 08-23-2012 |
20120209221 | Multi-Lumen Catheter Including an Elliptical Profile - A multi-lumen catheter including an elliptical cross-sectional profile configuration that enhances fluid flow rate while minimizing the average diameter of the catheter body is disclosed. In one embodiment the catheter comprises an elongate catheter tube defining a plurality of lumens. At least a portion of the longitudinal length of the catheter tube defines an elliptical cross section, in turn defined by a major axis and a minor axis. A ratio of the major axis to the minor axis of the elliptical catheter tube cross section is between about 1.3 and about 1.4 in one embodiment. The catheter body can define two, three, or more lumens, in one embodiment. | 08-16-2012 |
20120191071 | Infusion Apparatuses and Methods of Use - An exemplary infusion system for accessing an implanted device is disclosed comprising an insertion assembly, a hub comprising a sealable path configured to receive at least a portion of the insertion assembly, a flexible catheter attached to the hub and configured to receive at least a portion of the insertion assembly, and an extension tube attached to the hub. The hub may comprise a manifold element configured to provide fluid communication between the flexible catheter and the extension tube. The hub may also comprise a septum configured to seal the sealable path upon removal of the insertion assembly from the flexible catheter. The extension tube may also be configured to receive at least a portion of the insertion assembly. Exemplary methods of providing a fluid communication path to an implanted device are also disclosed. | 07-26-2012 |
20120184985 | Removeable Embolus Blood Clot Filter and Filter Delivery Unit - A blood clot filter is collapsible toward a longitudinal axis into a collapsed configuration for insertion into a blood vessel, and is radially expandable outwardly from the longitudinal axis to an expanded configuration for contact with the inner wall of the blood vessel at two longitudinal spaced locations. A first plurality of spaced, elongate arms, in the expanded configuration, curve outwardly away from the longitudinal axis toward the leading end of the filter to form a first filter basket and to center a hub at the trailing end of the filter within the vessel. A second plurality of spaced elongate legs angle outwardly away from the longitudinal axis toward the leading edge of the filter in the expanded configuration to form a second filter basket opening toward the leading end. The ends of these legs include hooks to bend and straighten in response to withdrawal force. | 07-19-2012 |
20120184922 | Huber Needle Safety Enclosure - A safety enclosure for a Huber needle includes a needle housing and a panel unit. The panel unit includes a series of planar panels assembled in an enclosing arrangement defining an enclosed area and is movable between an installation position where the sharp outer end of the Huber needle projects from the panel unit and a safety position where the sharp outer end is covered by the panels. The Huber needle has an aft end and a fore end connected by a bend with the fore end including a sharp outer end. | 07-19-2012 |
20120184913 | Valved Sheath Introducer for Venous Cannulation - A valved sheath introducer for venous cannulation, including a valve, sheath, handle and cap. The valve is configured to permit safe introduction and removal of medical instruments through the sheath introducer. The valve may have one or more anchoring members and a thickened central portion through which a slit is formed. The central portion may have one or more concave surfaces and the slit can be angled with respect to the top surface of the valve. The cap is attached to the handle, compressing a portion of the valve therebetween. | 07-19-2012 |
20120180791 | Ventilator Attachment Fitting Usable on an Endotracheal Tube Having an Integrally Formed Suction Lumen and Method of Making And/Or Using the Same - A ventilation connector ( | 07-19-2012 |
20120165679 | Selectable Angle Needle Guide - A needle guide assembly for inserting a needle into the body of a patient in order to access a subcutaneous target, such as a vessel, is disclosed. In one embodiment, the needle guide assembly comprises a needle guide body that is configured to at least indirectly and removably attach to an image producing device, such as an ultrasound probe. The needle guide body defines at least first and second elongate guide channels. Each guide channel defines a unique insertion angle with respect to a longitudinal axis of the ultrasound probe. Further, each guide channel is configured to accept needles of differing gauges. | 06-28-2012 |
20120143304 | TRANSLUMINAL DELIVERY SYSTEM - There is disclosed herein a transluminal delivery system for a self-expanding luminal prosthesis, the system comprising an inner catheter component ( | 06-07-2012 |
20120143303 | DEVICE TO RELEASE A SELF-EXPANDING IMPLANT - A device to release from an implant bed in the device a self-expanding implant by pulling back proximally, the length of the implant, a rolling membrane with an inner sleeve that extends distally to the distal end of the implant and an outer sleeve that extends proximally, from the distal end of the inner sleeve, the outer sleeve, during said release, pulling the distal end of the inner sleeve back proximally over the abluminal surface of the remainder of the inner sleeve, proximal of its distal end, the device having a slitter, that is caused to move proximally contemporaneously with the outer sleeve, to slit the inner sleeve progressively, starting at a distal point in the inner sleeve, and progressing proximally along the length of the inner sleeve. | 06-07-2012 |
20120132212 | Endotracheal Tube with Multi-Mode Valve and Method of Using Same - An endotracheal tube for intubation within a patient's trachea. The endotracheal tube includes an elongated tube having a main lumen, an auxiliary lumen, a proximal end, and a distal end. An inflatable cuff is arranged on the elongated tube between the proximal and distal ends. A multi-mode valve is arranged on the elongated tube. A method for tracheal intubation of a patient is also disclosed. | 05-31-2012 |
20120123407 | METHOD OF PROMOTING TISSUE ADHESION - The present invention provides methods and devices for promoting tissue adhesion, which utilizes the healing process and scar tissue formation to bond two tissue surfaces together. A tissue injury is accomplished by destroying the mucosal layer of tissue. After the injury is initiated, the tissue is preferably held in close contact by a tissue apposition means such as a suture, staple or clip device placed adjacent to the treatment site. The tissue injury may be initiated by electrical/radiofrequency energy; chemical or mechanical means integrated with the tissue apposition device or delivered by a separate instrument such as an electrocautery catheter through an endoscope. As scar tissue created by the injury forms, the tissue surfaces become bonded together in a permanent union. | 05-17-2012 |
20120116323 | Catheter Assembly, Catheter Systems Including Same, and Method of Manufacture - A catheter assembly includes a catheter, a tubular structure affixed to an exterior surface of the catheter, and a stabilizing cuff affixed to, and at least partially embedded within, the tubular structure. The tubular structure may include a tapered surface extending from an end of the tubular structure to an exterior surface of the catheter. A method of manufacturing a catheter assembly may include positioning a tubular structure about a catheter, positioning a stabilizing cuff near the tubular structure, and partially embedding at least a portion of the stabilizing cuff within the tubular structure while shaping the tubular structure to form a tapered surface. A temporary sleeve may be positioned about the tubular structure prior to shaping the tubular structure. The tubular structure may also be preformed to include a tapered end prior to positioning the tubular structure about the catheter. | 05-10-2012 |
20120116154 | SELF-ANCHORING SLING AND INTRODUCER SYSTEM - A system for supporting the urethra using an introducer needle, the ends of which are flattened and which have openings therethrough, a handle having a latch mechanism which engages the opening in the flattened portion of the first end of the introducer needle, an implant, and a connector joining the end of the implant to the flattened portion of one of the ends of the introducer needle. These components are used to draw the implant into position, either through vaginal or abdominal incisions, to form a U-shaped loop beneath the urethra. The ends of the implant are adjusted to provide proper support for the urethra. The implant can have slits that open under applied tensile force. | 05-10-2012 |
20120108950 | BIOIMPEDANCE-ASSISTED PLACEMENT OF A MEDICAL DEVICE - A system and method for guiding a catheter or other medical device to a desired target destination within the vasculature of a patient via bioimpedance measurements is disclosed. The target destination in one embodiment includes placement of the catheter such that a distal tip thereof is disposed proximate the heart, e.g., the junction of the right atrium and superior vena cava. In one embodiment the method for guiding the catheter comprises introducing the catheter into a vessel of the patient, the catheter defining a lumen through which fluids can be infused into the vasculature of the patient. The catheter is advanced toward a target destination within the vasculature. A first impedance value based on intravascular detection of at least one electrical property related to a first tissue surface of the vessel is calculated to enable determination of the proximity of a distal end of the catheter to the target destination. | 05-03-2012 |
20120108890 | Sling Anchor System - The present disclosure is generally directed to surgical articles useful for implanting support members in patients. The articles disclosed herein include a support member, such as a sling for urinary incontinence, tissue anchors, filamentary elements for associating the support member with the anchors, and introducer needles for placing the anchors in a patient. The support members can also be configured for use in pelvic floor repair, such as for treating cystoceles, rectoceles, and enteroceles. | 05-03-2012 |
20120103140 | Tool for Removing Object from the Body of a Patient - A tool for removing a discrete object from the body of a human or animal patient includes a single length of Nitinol tubing and a sheath. The tubing includes a tool head section at a distal end of the tubing and a shaft section extending from a proximal end of the tubing to the tool head section. The tool head section includes a slitted section and a non-slitted section. The non-slitted section is disposed at a distal most end of the tubing. The slitted section includes a plurality of longitudinal slits forming a plurality of strands. | 05-03-2012 |
20120095319 | Guidewire-Assisted Catheter Placement System - A catheter assembly for providing precise placement of a catheter distal end at a desired location within the patient vasculature is disclosed. In one embodiment, the catheter assembly comprises a catheter including an elongate body that defines a proximal end, a distal end, and a lumen extending therebetween. A guidewire is also included and is configured for being received within the lumen of the catheter and for guiding the catheter through the patient vasculature. The guidewire includes a plurality of depth markings along at least a portion of a length of the guidewire. The depth markings indicate a distance between a distal end of the guidewire and an insertion site through which the guidewire passes into the patient vasculature. The guidewire further includes a modified tip configured for assisting in guidewire advancement through the vasculature, and a proximal end orientation feature that indicates the orientation of the modified tip. | 04-19-2012 |
20120089115 | Reduction of Recirculation in Catheters - A catheter tip designed to reduce the outflow velocity and/or directional momentum of fluid being infused by a catheter having such a tip. In one variation, a plurality of channels is provided at the distal portion of the catheter to increase the outflow cross-sectional area. In another variation, the diameter of the catheter at its distal portion where the fluid exits is increased. In yet another variation, a bullet-shaped nose is implemented which may decrease turbulence at the distal end of catheter tip. The low velocity outflow catheter tip may also be implemented on a dual lumen catheter, such as a hemodialysis catheter, to reduce recirculation rate. Various device configurations and methods for such implementations are also disclosed. | 04-12-2012 |
20120089070 | Catheter Assembly Including Triple Lumen Tip - A catheter assembly for use in accessing a vasculature of a patient during renal replacement or other therapies is disclosed. In one embodiment, the catheter assembly includes a catheter body that defines first and second lumens. The catheter body defines a distal tip region that includes a venous lateral opening that is in fluid communication with the first lumen and an arterial lateral opening that is in fluid communication with the second lumen. | 04-12-2012 |
20120083869 | DELIVERY SYSTEM FOR A PROSTHESIS - The invention provides a delivery system for a prosthesis, said delivery system comprising a catheter shaft with a distal end, a proximal end and a longitudinal axis, a space for a prosthesis with a distal end and a proximal end, the space being at the distal end of the catheter shaft, a sheath with a proximal end and a distal end, the sheath being disposed at the distal end of catheter shaft so as to surround the space, a pusher element attached to the distal end of the catheter shaft and arranged at the proximal end of the space for abutting prosthesis, a pull element with a longitudinal axis, the pull element running the length of the catheter shaft and having a distal end attached to the proximal end of the sheath and a proximal end for pulling the pull element proximally, thereby retracting the sheath proximally relative to the prosthesis space, and at least one fixation element having a proximal end and a distal end and being disposed within a flexible portion of the length of the shaft that lies between the proximal end of the sheath and the proximal end of the catheter shaft. The fixation element serves to limit a radial distance between the axis of the pull element outside the shaft and the axis of the catheter shaft along the length of the fixation element whenever a tensile stress in the pull element results in an endwise compressive stress on the shaft and a tendency of the shaft to bow, relative to the pull element. | 04-05-2012 |
20120065663 | EMBOLUS BLOOD CLOT FILTER AND DELIVERY SYSTEM - A blood filter delivery system for delivering a filter into a vein includes an introducer and a push rod with a spline member disposed along the push rod. The spline member has a main body, and first and second boss portions spaced apart along the longitudinal axis to provide a gap for retaining anchor member of the filter during delivery via the introducer. | 03-15-2012 |
20120065587 | SYSTEMS FOR ISOLATION OF A NEEDLE-BASED INFUSION SET - A safety needle assembly of an infusion set for infusing fluids into a subcutaneously implanted access port is disclosed. The needle assembly is configured to prevent fluid/vapor escape therefrom so as to reduce or prevent fluid exposure to a clinician using the needle assembly. In one embodiment, the needle assembly comprises a handle portion including a needle extending therefrom, the needle defining a lumen for passage of a fluid therethrough. The needle assembly also includes a safety assembly defining a needle hole through which the needle initially extends. The safety assembly is selectively and axially slidable along the needle in order to shield a distal tip of the needle and prevent user contact therewith. A fluid isolation component is included in the safety assembly for isolating fluid escape from the needle to prevent exposure to a clinician. | 03-15-2012 |
20120061001 | Vascular Graft with Kink Resistance After Clamping - A self-sealing vascular graft with kink resistance is described. The vascular graft includes a substrate that can be ePTFE, having a self-sealing region that may include several layers of material. The central section of the vascular graft may be constructed differently from surrounding self-sealing regions, in order to provide kink resistance following the clamping of the graft. Also described is a graft with a flared cuff attached to one or both ends, the attachment or transition region including reinforcement beading. | 03-15-2012 |
20120059321 | TUNNELER FOR BI-DIRECTIONAL TUNNELING - A tunneler for producing a subcutaneous tunnel in connection with the placement of a catheter within a body of a patient is disclosed. In one embodiment, the tunneler comprises an elongate tunneler member and a sheath. The tunneler member includes a handle on its proximal end and a tapered distal end. The sheath defines an elongate lumen inside which the tunneler member is initially received. The tunneler member is configured to define a tunnel through subcutaneous tissue while disposed in the sheath, then is removable from the sheath lumen thereafter. The sheath is configured to remain within the tunnel so that a catheter can be inserted through the sheath within the tunnel. The sheath is splittable in one embodiment so as to enable its removal from the tunnel while leaving the catheter in place. | 03-08-2012 |
20120059304 | SPLIT-TIP CATHETER INCLUDING LATERAL DISTAL OPENINGS - A split-tip catheter for placement within the vasculature of a patient and for use in hemodialysis or other suitable procedures is disclosed. In one embodiment, the split-tip catheter includes a catheter body that defines a first lumen and a second lumen. The catheter body further comprises a split distal region, including a venous segment that defines a distal portion of the first lumen and an arterial segment that defines a distal portion of the second lumen. The venous segment includes a recess extending proximally of a nose portion; and a lateral opening in fluid communication with the first lumen. The arterial segment is separate from the venous segment and is removably seatable in the recess provided by the venous segment such that it “nests” therein. The arterial segment also includes a lateral opening in fluid communication with the second lumen. | 03-08-2012 |
20120046562 | RECONFIRMATION OF ECG-ASSISTED CATHETER TIP PLACEMENT - Reconfirmation of the position of a catheter intravascularly placed with the assistance of ECG signals of the patient is disclosed, thus assisting in determination of subsequent catheter displacement within the patient vasculature. In one embodiment a method for reconfirming a position of an indwelling medical device within a body of a patient comprises first placing the medical device within the body of the patient using ECG signals of the patient. A first ECG signal profile relating to an initial position of the indwelling medical device after initial placement of the medical device is stored. A second ECG signal profile relating to the position of the indwelling medical device at a time subsequent to initial placement of the medical device is then acquired. The first ECG signal profile is compared with the second ECG signal profile to determine whether displacement of the indwelling medical device has occurred. | 02-23-2012 |
20120041419 | TRIMMABLE CATHETER INCLUDING DISTAL PORTION STABILITY FEATURES - A catheter tube for insertion into a body of a patient is disclosed. The catheter tube includes a distal portion that remains stable during fluid infusion into the patient, thus reducing or eliminating whipping of the catheter distal tip, even during power injection. In one embodiment, the catheter tube defines at least one lumen and is formed from a tube material that defines a proximal portion and a distal portion of the catheter tube. The catheter tube is configured such that the arithmetic product of an elastic modulus and an area moment of inertia for at least a portion of the distal portion of the catheter tube defined by the catheter tube material is greater relative the arithmetic product of an elastic modulus and an area moment of inertia for at least a portion of the proximal portion of the catheter tube. | 02-16-2012 |
20120035550 | SAFETY NEEDLE WITH POSITIVE FLUSH - A needle assembly including a positive flush mechanism for use with a vascular access port. The needle assembly is configured to supply fluid to the port and to provide a positive flush to overcome negative pressures in the port that can potentially occur during withdrawal of the needle from the port. | 02-09-2012 |
20120022580 | MEDICAL DEVICE REMOVAL SYSTEM - A medical device removal system includes a vessel filter repositioning or removal device to remove and/or reposition a medical device, such as a vessel filter. The system includes a gripper to grip a medical device that is located within a body vessel, and a detector, linked to the gripper, to detect the proximity of the medical device to the gripper. The system may also include an output to indicate a signal from the detector. | 01-26-2012 |
20120018073 | SYSTEMS AND METHODS FOR RADIOGRAPHICALLY IDENTIFYING AN ACCESS PORT - An access port for subcutaneous implantation is disclosed. Such an access port may comprise a body for capturing a septum for repeatedly inserting a needle therethrough into a cavity defined within the body. Further, the access port may include at least one feature structured and configured for identification of the access port subsequent to subcutaneous implantation. Methods of identifying a subcutaneously implanted access port are also disclosed. For example, a subcutaneously implanted access port may be provided and at least one feature of the subcutaneously implanted access port may be perceived. Further, the subcutaneously implanted access port may be identified in response to perceiving the at least one feature. In one embodiment, an identification feature is included on a molded insert that is incorporated into the access port so as to be visible after implantation via x-ray imaging technology. | 01-26-2012 |
20110315305 | SELECTIVE ADHERENCE OF STENT-GRAFT COVERINGS - A method for making a radially expandable stent-graft, including positioning a radially expandable stent member concentrically over a first polymeric member, locating a second polymeric member concentrically over the stent member and first polymeric member, and joining the first polymeric member to the second polymeric member through interstices of the stent member at selective locations to form slip planes between the first and second polymeric members. The slip planes accommodate movement of the stent between the polymeric members to facilitate compression of the stent graft to a low profile. | 12-29-2011 |
20110313293 | SUPPORT AND COVER STRUCTURES FOR AN ULTRASOUND PROBE HEAD - A probe cap for use with an ultrasound probe including a head portion and an acoustic surface is disclosed. In one embodiment, the probe cap includes a body that defines a cavity sized for releasably receiving the head portion of the probe therein. The probe cap body further defines a hole that is proximate the acoustic surface of the head portion. A compliant spacer component is disposed in the hole. The spacer component can include a hydrogel and provides an acoustic path between the acoustic surface and a tissue surface of a patient. The spacer component includes a skin contact surface that defines a concavity and is deformable against the tissue surface. Additional embodiments disclose various probe cap and accompanying needle guide designs for use in assisting a clinician with ultrasound probe use and needle insertion into a patient. | 12-22-2011 |
20110301689 | Stent Delivery Device - A delivery device is provided for delivering a stent device. The stent device ( | 12-08-2011 |
20110288567 | IMPLANTABLE PROSTHESIS - An implantable prosthesis is provided for repairing an anatomical defect, such as a tissue or muscle defect, that promotes tissue of muscle ingrowth into the prosthesis and subsequently strengthens the area of the defect. The prosthesis is easy to manipulate and may be designed to minimize the incidence of postoperative adhesions between a portion of the prosthesis and surrounding tissue or organs. The prosthesis may include one or more layers of biologically compatible material that is suitable for repairing a defect. The prosthesis may include a support assembly to facilitate manipulation and deployment of the prosthesis. The support assembly may include a stiffening member that is surrounded by material that separates the stiffening member from the layer of material. The stiffening member may be located in a sleeve of material, such as mesh fabric. The stiffening member may be formed from a resorbable material. | 11-24-2011 |
20110287398 | DEMONSTRATION MANNEQUIN FOR SIMULATING CATHETER MALPOSITION - A demonstration mannequin for simulating insertion of a catheter or other medical device into the body of a patient is disclosed. The mannequin is useful for training clinicians in the placement of a catheter into the patient's vasculature and includes the ability to provide a malposition scenario in which the catheter is deviated from an intended path within the vasculature, resulting in a simulated malposition thereof. In one embodiment, the mannequin comprises a torso body portion and a simulated vasculature disposed within the body. The simulated vasculature is accessible by a medical device, such as a catheter, which can be advanced within the simulated vasculature. The mannequin further includes at least one diversion element that selectively obstructs a portion of the simulated vasculature to block advancement of a distal end of the catheter along an intended path and instead causes diversion of the catheter, thus simulating a catheter malposition scenario. | 11-24-2011 |
20110284024 | ASSISTIVE DEVICE FOR A MICROBIAL SCRUB BRUSH - A system and device for assisting with the cleansing of a medical component with a scrub brush is disclosed. In one embodiment, an assistive device for use with the scrub brush is disclosed. The scrub brush includes an insert disposed therein, the insert including a cleansing substance such as CHG or alcohol. The assistive device comprises a housing, a motor, a head removably supporting the scrub brush, and an interface interconnecting the motor and the head. The interface is a shaft that enables back-and-forth rotation or other movement of the head and scrub brush relative to the medical component so as to cleanse the medical component. | 11-24-2011 |
20110282311 | WASTE MANAGEMENT SYSTEM - A waste management system includes a waste transport device and a waste collection device. The waste management system may include a securement device for maintaining the position of the waste transport device following insertion. The waste transport device may include a modular medication delivery apparatus with a disposable delivery device for delivering medication to the patient following insertion of the waste transport device. | 11-17-2011 |
20110282285 | CATHETER PLACEMENT DEVICE AND METHOD - An insertion tool for inserting a catheter into a body of a patient is disclosed. The insertion tool unifies needle insertion, guidewire advancement, and catheter insertion in a single device. In one embodiment, the insertion tool comprises a housing in which at least a portion of the catheter is initially disposed, a hollow needle distally extending from the housing with at least a portion of the catheter pre-disposed over the needle, and a guidewire pre-disposed within the needle. A guidewire advancement assembly is also included for selectively advancing the guidewire distally past a distal end of the needle in preparation for distal advancement of the catheter. In one embodiment a catheter advancement assembly is also included for selectively advancing the catheter into the patient. Each advancement assembly can include a slide or other actuator that enables a user to selectively advance the desired component. | 11-17-2011 |
20110276015 | ACCESS PORT IDENTIFICATION SYSTEMS AND METHODS - An access port for subcutaneous implantation is disclosed. Such an access port may comprise a body for capturing a septum for repeatedly inserting a needle therethrough into a cavity defined within the body. Further, the access port may include at least one feature structured and configured for identification of the access port subsequent to subcutaneous implantation. Methods of identifying a subcutaneously implanted access port are also disclosed. For example, a subcutaneously implanted access port may be provided and at least one feature of the subcutaneously implanted access port may be perceived. Further, the subcutaneously implanted access port may be identified in response to perceiving the at least one feature. | 11-10-2011 |
20110275930 | SYSTEMS AND METHODS FOR IDENTIFYING AND LOCATING AN IMPLANTED DEVICE - A system for identifying an attribute of an implanted medical device, such as an access port is disclosed. In one embodiment, the identification system comprises a marker included with the implanted medical device, wherein the marker relates to an attribute of the implanted medical device. An external detection device is also included, comprising a signal source that emits an incident electromagnetic signal for impingement on the marker of the implanted medical device, a detector that detects a return signal from the marker resulting from impingement of the incident electromagnetic signal, and a user interface for conveying information relating to the attribute based on detection of the return signal. In the case of an implantable access port, for instance, the described system enables information, such as the ability of the port to withstand power injection of fluids therethrough, to be ascertained even after the port has been subcutaneously implanted within the patient. | 11-10-2011 |
20110257677 | REMOVABLE EMBOLUS BLOOD CLOT FILTER - A removable blood clot filter includes a number of locator members and anchor members disposed radially and extending angularly downward from a hub. The locator members include a number of linear portions having distinct axes configured to place a tip portion approximately parallel to the walls of a blood vessel when implanted and to apply sufficient force to the vessel walls to position the filter near the vessel centerline. The anchor members each include a hook configured to penetrate the vessel wall to prevent longitudinal movement due to blood flow. The hooks may have a cross section sized to allow for a larger radius of curvature under strain so that the filter can be removed without damaging the vessel wall. | 10-20-2011 |
20110245806 | REINFORCED MULTI-LUMEN CATHETER AND METHODS FOR MAKING SAME - Methods for manufacturing multi-lumen catheter tubes are disclosed. The described methods may be employed to manufacture a reinforced catheter tube suitable for use in power injectable and torqueable multi-lumen catheters, for example. In one embodiment, a method for manufacturing a multi-lumen catheter tube comprises first clamping a flexible sheet of catheter tube material between first and second mandrels. The mandrels may be D-shaped, or may include another suitable cross sectional profile. The first and second mandrels are rotated with respect to the flexible sheet so as to wrap the flexible sheet about the mandrels. Adjacent portions of the flexible sheet are joined along a longitudinal length thereof to define a closed catheter tube including first and second lumens. The first and second lumens may conform to the D-shaped profile of the respective mandrels. | 10-06-2011 |
20110238042 | Drainage Catheter with One-Way Valve - Systems and methods that serve to drain a bodily fluid are provided The medical device includes a lumen connecting between the proximal end and the distal end The lumen is preferably adapted to drain fluid from the distal end to the proximal end The device may also include a pressure sensitive valve adapted for insertion and placement in the lumen The pressure-sensitive valve may be pressure sensitive wherein, when pressure at the inflow port rises to a predetermined threshold, the pressure-sensitive valve opens The lumen may also be configured whereby, when pressure at the inflow port drops to a second predetermined threshold, the pressure-sensitive valve closes In some embodiments, the valve may be unidirectional and not sensitive to any substantial pressure threshold but may open at any substantially non-zero pressure applied in the appropriate direction. | 09-29-2011 |
20110230842 | VASCULAR ACCESS PORT WITH INTEGRAL ATTACHMENT MECHANISM - An implantable port with an integral attachment mechanism. The implantable port includes one or more suture needles enclosed within a port body, the suture needle(s) coupled to a movable member such that movement of the movable member results in movement of the suture needle(s) out of the port body and into the tissue of a body into which it is implanted. The movable member can be a cam or tensioning member that rotates about a central port axis. The movable member can be coupled to a gear to permit movement of the movable member following implantation of the port within a subcutaneous pocket. | 09-22-2011 |
20110196341 | DEFLATION INDICATOR FOR A MEDICAL DEVICE BOLSTER - A deflation indicator system for visually indicating an inflation status of a balloon-type or other inflatable internal bolster of a medical device is disclosed. The indicator system enables an observer to ascertain from an external vantage point whether the internal bolster of the indwelling device is inflated. In one embodiment, the medical device comprises an elongate body defining a lumen, and an inflatable internal bolster for securing a portion of the medical device within the patient. A deflation indicator is also disclosed, including a flexible membrane in fluid communication with the internal bolster. The membrane is included in an external portion of the medical device. The membrane assumes a first concavely-shaped position when the internal bolster is deflated. Correspondingly, the membrane assumes a second convexly-shaped position when the internal bolster is inflated. The positions of the membrane are externally observable to indicate the inflation status of the internal bolster. | 08-11-2011 |
20110192008 | REINFORCED MULTI-LUMEN CATHETER - A reinforced multi-lumen catheter and method of manufacturing the same. An assembly for manufacturing the multi-lumen catheter includes a proximal catheter body substrate including a septum, a first and second distal catheter body substrate, a first and second mandrel, a reinforcing element and a sleeve. The reinforcing element is positioned over the proximal catheter body substrate and at least a proximal region of the first and second distal catheter body substrates. | 08-11-2011 |
20110178425 | MULTI-FUNCTIONAL AND MODULAR URINE COLLECTION SYSTEM - Multi-functional urine collection devices, embodiments of which can include a self-expanding container having a receptacle for receiving urine from the tubing, a pump for moving urine through the tubing and into a receptacle, extendable tubing that may be shortened and/or lengthened, and/or one or more meters for monitoring, measuring, transmitting or storing a characteristic from the urine. | 07-21-2011 |
20110172604 | HYBRID GUIDEWIRE - A hybrid guidewire, a method for manufacturing the hybrid guidewire including co-extruding a core inside a sheath in bulk, cutting the core and sheath to a desired length, and shaping a distal and proximal portion of the guidewire depending on the desired application. | 07-14-2011 |
20110166638 | FLEXIBLE STRETCH STENT-GRAFT - A stent device includes a first graft member, a second graft member and a stent frame defining a central axis. The frame has an abluminal surface engaged with the first graft member and a luminal surface engaged with the second graft member such that the first graft member and the second graft member encapsulates the stent frame along the length of the central axis. The stent frame includes a configuration where the stent frame is disposed on a curvature such that the abluminal surface has a radius of curvature of approximately 20 millimeters about a center of the curvature and the luminal surface defines a substantially constant effective cross-sectional area at any portion generally transverse to the central axis of the stent frame disposed about the curvature. | 07-07-2011 |
20110144485 | SYSTEM AND METHOD FOR MARKING BODY CAVITIES - A surgical method, including inserting an internal viewing device via a ureter into a first calyx of a kidney, inspecting the first calyx with the internal viewing device, and determining whether the first calyx contains one or more stones. If the first calyx does contain one or more stones, it is marked with a first marking material, but if the first calyx does not contain one or more stones, it is marked with a second marking material different from the first marking material. | 06-16-2011 |
20110137402 | STENT DEVICE DELIVERY SYSTEM WITH A HEAT SHRINK RESISTANT SUPPORT MEMBER - A stent device delivery system and method of making. The stent device delivery system includes a stent device and an outer sheath overlaying the stent device in a radially compact, delivery configuration of the stent device. The system also includes a pull member for pulling proximally on to retract the outer sheath, wherein a portion of the outer sheath is heat shrunk radially onto a relatively heat shrink resistant support member in order to capture a distal portion of the pull member radially between the outer sheath and the heat shrink resistant support member. | 06-09-2011 |
20110137401 | STENT DEVICE DELIVERY SYSTEM WITH AN OUTER SHEATH POLYMERIC REINFORCEMENT LAYER - A stent device delivery system and method of making. The stent device delivery system includes a stent device and an outer sheath overlaying the stent device in a radially compact, delivery configuration of the stent device. The outer sheath may include a first layer of polymeric material and a reinforcement layer of polymeric material that are laminated together. | 06-09-2011 |
20110137400 | STENT DEVICE DELIVERY SYSTEM WITH A VARYING RADIAL PROFILE PULL MEMBER - A stent device delivery system and method of making. The stent device delivery system includes a stent device, an outer sheath overlaying the stent device in a radially compact, delivery configuration of the stent device, and a pull member. The outer sheath may include a first layer and a reinforcement layer that are laminated together, a portion of the pull member captured radially between the first layer and the reinforcement layer. At least a partial length of the captured portion of the pull member may be formed with a varying radial profile. | 06-09-2011 |
20110137396 | STENT DEVICE DELIVERY SYSTEM WITH INWARDLY TAPERING STENT BED - A stent device delivery system and method of making. The stent device delivery system includes a stent device, an outer sheath overlaying the stent device in a radially compact, delivery configuration of the stent device, and an inner catheter extending axially and radially within a lumen of the stent device. The inner catheter provides a stent bed upon which the stent device is located so that a radially inner surface of the stent device engages a radially outer surface of the stent bed. The stent bed may define an inwardly tapering profile, narrowing in radius from a distal portion of the stent device to a proximal portion of the stent device. | 06-09-2011 |
20110118677 | OVERMOLDED ACCESS PORT INCLUDING ANCHORING AND IDENTIFICATION FEATURES - An access port for providing subcutaneous access to a patient is disclosed. In one embodiment, the port includes an internal body defining a fluid cavity that is accessible via a septum. A compliant outer cover including silicone is disposed about at least a portion of the body. A flange is included with the port body and is covered by the outer cover. The flange radially extends about a perimeter of the port body proximate the septum so as to impede penetration of a needle substantially into the outer cover in instances where the needle misses the septum. The flange can further include both an anchoring feature for securing the outer cover to the port body and an identification feature observable via x-ray imaging technology for conveying information indicative of at least one attribute of the access port. The outer cover provides a suitable surface for application of an antimicrobial/antithrombotic coating. | 05-19-2011 |
20110112629 | IMPLANTABLE MEDICAL DEVICES WITH FLUORINATED POLYMER COATINGS, AND METHODS OF COATING THEREOF - An implantable medical device including an expandable stent with an amorphous fluoropolymer coating, and methods of coating the stent. The amorphous fluoropolymer coating may be optically transparent and resistant to chemical corrosion. | 05-12-2011 |
20110112516 | MEDICAL DEVICE WITH ELASTOMERIC BULB - A drainage catheter including a body, a drainage lumen extending between the body proximal end and the body distal end, the drainage lumen including a distal fluid inflow port and a proximal fluid drain coupling, and an inflation lumen extending between the body proximal end and the body distal end, conveying inflating fluid from a proximal fluid supply element to a distal fluid acceptor balloon, the proximal fluid supply element adjacent the proximal fluid drain coupling. A sleeve may be secured about the proximal fluid supply element and the proximal fluid drain coupling to provide a fluid impervious coating. | 05-12-2011 |
20110098801 | STENT WITH A BIO-RESORBABLE CONNECTOR - A helical stent having bio-resorbable connecting members connecting sections of the stent. The connecting members provide various spring rates or spring constants to the stent, and permit a change in the flexibility of the stent subsequent to implantation while maintaining the unitary design of the stent. | 04-28-2011 |
20110098680 | PRE-MOLDED BIFURCATION INSERT - A catheter assembly including a coaxial catheter and insert, and method of making. The catheter assembly includes a coaxial catheter, an insert, and a hub. The coaxial catheter includes an inner lumen and an outer lumen. The insert includes first and second passageways, the first passageway defined from a first opening on a distal end of the insert to a second opening on a proximal end of the insert, the second passageway branching from the first passageway to a third opening. A portion of the insert distal end is received in a proximal opening of the outer lumen, and a proximal section of the inner lumen extends through the first passageway. The hub is molded over the insert and a proximal section of the outer lumen. | 04-28-2011 |
20110098679 | CONNECTION SYSTEM FOR MULTI-LUMEN CATHETER - A catheter connection system and a method of connecting the catheter connection system to a catheter. The catheter connection system includes a hub assembly and a collar. The hub assembly includes a cannula extending from a distal end thereof, and a collet defining an inner surface spaced apart from the cannula to permit passage of a catheter wall between the body and the cannula. The collet includes a proximal barb on an outer surface and the collar includes an attachment barb on an inner surface, engagement of the respective barbs acting to provide a permanent connection between the collar on the collet, while permitting free rotation of the collar about the collet. | 04-28-2011 |
20110098653 | CONNECTOR SYSTEM FOR A PROXIMALLY TRIMMABLE CATHETER - A catheter connector system for a subcutaneously placed catheter and method of attaching a catheter to extracorporeal medical equipment. The catheter connector system and method enables proximal trimming of the placed catheter and facilitates precise positioning of both distal and proximal ends of a catheter. The method includes sliding a boot and dilator combination over a portion of a catheter extending from a venipuncture site until a distal end of the boot is positioned in the venipuncture site, removing the dilator from the boot, and trimming a portion of the catheter extending from a proximal end of the boot. A bifurcation assembly may be attached to the proximal end of the boot following trimming of the catheter. | 04-28-2011 |
20110030726 | INSERT FOR A MICROBIAL SCRUBBING DEVICE - The microbial scrub brush in one embodiment employs an insert that is impregnated with an anti-bacterial disinfectant and that is housed within a housing of alcohol-compatible material and sealed over by a removable lid. The insert is maintained in sterile condition until ready for use. After removal of the lid, the insert is moved over the end of a female luer or other portion of a medical device and rotated in order to clean the exterior surface as well as the interior luminal surface of the device. In one embodiment, the insert includes a base from which extends an outer wall that defines a chamber. A plurality of complaint fingers extend from the base into the chamber. A plurality of wipers extend radially inward from the outer wall into the chamber to enable the cleansing of both the exterior surface and an interior surface of the medical device. | 02-10-2011 |
20100331823 | PROXIMALLY TRIMMABLE CATHETER INCLUDING PRE-ATTACHED BIFURCATION AND RELATED METHODS - A proximally trimmable catheter is disclosed. In one embodiment, the catheter includes a multi-lumen catheter tube, one or more extension tubes, and a hub for fluidly connecting the two. In a first unlocked state, the hub is axially slidable along the catheter tube. The hub includes tube pins that are in fluid communication with the extension tubes. A cutting member is positioned to longitudinally cut the catheter tube during axial sliding of the hub along the catheter tube such that distal portions of the tube pins remain disposed within the lumens of the catheter tube. When positioned as desired, the hub is locked into a second locked state and is no longer axially slidable along the catheter tube. The tube pins are fluidly sealed within the lumens of the catheter tube as to establish fluid communication between the extension tubes and the lumens via the tube pins. | 12-30-2010 |
20100324657 | LOCKED SEGMENTS PUSHABLE STENT-GRAFT - An implantable prosthesis includes a scaffold with a plurality of expandable segments axially spaced apart along a substrate, adjacent segments connected by one or more support members when the prosthesis is in a collapsed configuration and disconnected when the prosthesis is in an expanded configuration. | 12-23-2010 |
20100298921 | BEND-CAPABLE TUBULAR PROSTHESIS - Stent exhibiting a succession of turns around the axis, adjacent turns being connected by connector portions distributed around the circumference of the prosthesis, each of the turns being made up of struts that extend the length of the turn and are interspersed by inflection zones located at the axial ends of each of the turns. When the prosthesis expands radially, gaps open up between adjacent struts of each of the turns, the inflection zones being distributed regularly around the circumference so that the gaps are substantially the same size as each other around the circumference of the turn, characterised in that at least every second turn exhibits a stagger zone within which the said gap between adjacent said struts is of an individual size different from that common to the other gaps of that second turn. | 11-25-2010 |
20100286656 | SAFETY NEEDLE WITH POSITIVE FLUSH - A safety needle device and method of supplying fluid to a vascular access port is described. The device may include a base member, a handle member, and a compressible member positioned between the handle member and a compression plate. The compressible member is coupled to a proximal end of a needle. Following the delivery of fluid to a vascular access port, the needle is removed by moving the handle member away from the base member, which collapses the compressible member, flushing fluid into the vascular access port to substantially replace a volume of the needle. | 11-11-2010 |
20100280805 | METHOD FOR MEASURING RECIRCULATION IN CATHETERS - A system and method for measuring recirculation of blood in a catheter designed for implantation in a human is described. In one variation, the system comprises an artificial circulatory system and an ultrasonic detection device for measuring and comparing the density of a circulated blood simulant with a later introduced bolus saline. The system may be configured to simulate a human heart by providing the flow, pressure and dimensions of a typical human heart. In addition to simulating the circulatory system of a normal human heart, the system may also be configured to simulate particular negative conditions of a patient, such as stenotic condition, which would affect the recirculation measurement. | 11-04-2010 |
20100280596 | IMPLANT DELIVERY DEVICE - Disclosed is a system for delivering self-expanding stents to stenting sites within the body, which minimizes trauma to the affected tissue of the patient yet, at the same time, offers the medical practitioner a robust and simple system for stent placement. These technical effects are achieved by providing a catheter which receives the stent at its proximal end and guides it to the stenting site. The catheter serves as a guide catheter and has a tapered distal tip from which the stent emerges at the site of stenting. A stent pusher can be used which abuts the proximal end of the stent inside the guide catheter. The tapered tip can be molded and can be integral with the catheter shaft or bonded to it. The guide catheter can include a figurated portion towards its distal tip. The system has particular application to stenting the carotid artery. | 11-04-2010 |
20100268321 | DRUG-RELEASING GRAFT - A method of incorporating drugs into an implantable medical device. In one variation, water insoluble drugs are used to form crystals within the porous structure of the device. Upon implantation, the drug crystals dissolve slowly and release the drug into the surrounding tissue. In one example, a water insoluble drug is crystallized within the pores of an ePTFE vascular graft. | 10-21-2010 |
20100268165 | SYSTEMS AND METHODS FOR RADIOGRAPHICALLY IDENTIFYING AN ACCESS PORT - An access port for subcutaneous implantation is disclosed. Such an access port may comprise a body for capturing a septum for repeatedly inserting a needle therethrough into a cavity defined within the body. Further, the access port may include at least one feature structured and configured for identification of the access port subsequent to subcutaneous implantation. Methods of identifying a subcutaneously implanted access port are also disclosed. For example, a subcutaneously implanted access port may be provided and at least one feature of the subcutaneously implanted access port may be perceived. Further, the subcutaneously implanted access port may be identified in response to perceiving the at least one feature. In one embodiment, an identification feature is included on a molded insert that is incorporated into the access port so as to be visible after implantation via x-ray imaging technology. | 10-21-2010 |
20100262226 | RADIALLY EXPANSIBLE STENT - There is disclosed herein a radially expansible stent formed from a tube, comprising a continuous spiral of tube material with a plurality of turns ( | 10-14-2010 |
20100249903 | STENT - A radially expansible annular stent is disclosed. The stent comprises a plurality of stenting turns around a lumen centred on a longitudinal axis. Adjacent turns of the stent are joined by connector struts. The stent annulus has a wall thickness related to the material from which it is formed. The radial thickness of the connector struts is smaller than that of the stent annulus. A method of making such a stent is also disclosed. The method includes cutting the connector struts from a tubular workpiece with a laser beam. The laser beam is aimed so as to be offset from a longitudinal axis of the workpiece to provide the reduced radial thickness of the connector struts. | 09-30-2010 |
20100249655 | Tip-Shapeable Guidewire - A guidewire for partial placement within a body of a patient is disclosed. The guidewire is employed to assist in the insertion of a medical device into the body, such as the placement of a catheter into the patient's vasculature. In one embodiment, the guidewire defines an elongate body that includes a distal segment. The distal segment includes a shape memory material that enables at least a portion of the distal segment to be deformed by a user prior to placement of the guidewire in the body of the patient. The shape memory material enables the guidewire to maintain the deformation of the distal segment portion after being deformed by the user. | 09-30-2010 |
20100242620 | FATIGUE TEST SYSTEM AND METHOD OF TESTING OF TUBULAR IMPLANT STRUCTURES - A fatigue test system for repetitively deforming a substantially tubular implant structure which is within a radial range and within an axial range expandable and contractable and which has at least a first and a second end, wherein the system comprises at least a first and second part which are controllably moveable relative to each other, and a first and a second fixture assembly for fixing the first end to the first part and the second end to the second part, so that the system controls in use the position of each of the first and second end of the tubular implant structure. | 09-30-2010 |
20100234679 | PELVIC IMPLANT SYSTEMS AND METHODS - Systems and methods for implanting pelvic implants ( | 09-16-2010 |
20100222664 | CATHETER ASSEMBLY INCLUDING ECG SENSOR AND MAGNETIC ASSEMBLIES - A stylet for use in guiding a distal tip of a catheter to a predetermined location within the body of a patient. In one embodiment the stylet is configured for use within a lumen of the catheter and comprises a core wire, an ECG sensor, and a magnetic assembly. The ECG sensor senses an ECG signal of a patient when the stylet is disposed within the lumen of the catheter and the catheter is disposed within the body of the patient. The magnetic assembly includes at least one element capable of producing a magnetic or electromagnetic field for detection by a sensor external to the patient. In another embodiment, the stylet includes a pre-shaped distal segment that is deflected with respect to a more proximal portion of the stylet, which in turn causes a distal segment of the catheter to be deflected when the stylet is received within the lumen. | 09-02-2010 |
20100211161 | Bendable Stent - A stent formed by slitting a tube to create a matrix of struts, the slitted tube being radially expandable to a stenting disposition in which the struts exhibit a zig-zag pattern in successive loops around the circumference of the stent, the zig-zag pattern exhibiting a cusp between any two adjacent struts, with selected tied cusps of any one loop being connected by a bridge to a facing cusp of the adjacent loop and with intervening free cusps, characterised by lengthwise staggering of circumferentially adjacent said slits within said loops, wherein any two struts that are contiguous with a said tied cusp are of different lengths and any strut that extends from one free cusp to another free cusp has the same length as any other such strut such that, in the said stenting disposition, the free cusps of adjacent loops are circumferentially displaced from each other. | 08-19-2010 |
20100211026 | ACCESS PORT IDENTIFICATION SYSTEMS AND METHODS - An access port for subcutaneous implantation is disclosed. Such an access port may comprise a body for capturing a septum for repeatedly inserting a needle therethrough into a cavity defined within the body. Further, the access port may include at least one feature structured and configured for identification of the access port subsequent to subcutaneous implantation. Methods of identifying a subcutaneously implanted access port are also disclosed. For example, a subcutaneously implanted access port may be provided and at least one feature of the subcutaneously implanted access port may be perceived. Further, the subcutaneously implanted access port may be identified in response to perceiving the at least one feature. | 08-19-2010 |
20100204569 | SYSTEM FOR PLACEMENT OF A CATHETER INCLUDING A SIGNAL-GENERATING STYLET - An integrated catheter placement system for accurately placing a catheter within a patient's vasculature is disclosed. In one embodiment, the integrated system comprises a system console, a tip location sensor unit for temporary placement on the patient's chest, and an ultrasound probe. The tip location sensor senses a field produced by a stylet disposed in a lumen of the catheter when the catheter is disposed in the vasculature. The ultrasound probe ultrasonically images a portion of the vasculature prior to introduction of the catheter. ECG signal-based catheter tip guidance is included to enable guidance of the catheter tip to a desired position with respect to a node of the patient's heart. The stylet includes an electromagnetic coil that can be operably connected to the sensor unit and/or console through a sterile barrier without compromising the barrier. The stylet can also be wirelessly connected to the sensor unit and/or console. | 08-12-2010 |
20100200017 | MICROBIAL SCRUBBING DEVICE - The microbial scrub brush in one embodiment employs an insert of foam material that is impregnated with an anti-bacterial disinfectant that is housed within a housing of alcohol compatible material and sealed over by a removable lid. The insert is maintained in sterile condition until ready for use. After the removal of the lid, the insert of foam material is moved over the end of a female luer or other portion of a medical device and rotated in order to clean the exterior surface as well as the interior luminal surface of the device. In one embodiment, the insert includes a plurality of resilient fingers that substantially occupy a cross sectional area of the cavity to enable the cleansing of both the exterior surface and an interior luminal surface of the medical device. | 08-12-2010 |
20100198040 | Methods and apparatus for assessing and improving electrode contact with cardiac tissue - Embodiments of the invention relate to methods for assessing and/or improving contact between an electrophysiology catheter and tissue, and catheters for performing the methods. One embodiment relates to a catheter comprising a braided conductive member coupled to the distal end of a shaft, wherein the braided conductive member comprises a plurality of pressure sensitive wires. Another embodiment relates to a catheter comprising a braided conductive member having a plurality of sectors and coupled to the distal end of a shaft, and a balloon assembly constructed and arranged to selectively apply distal pressure to one or more sectors of the braided conductive member. | 08-05-2010 |
20100179637 | TRANS-LUMINAL SURGICAL DEVICE - A device for trans-luminal delivery of a self-expanding stent or other surgical device and which is designed for rapid exchange over a guidewire has a guidewire lumen that adjacent its proximal exit port lies side-by-side with the line of the shaft of the device. A sleeve which surrounds and confines the stent has a proximal end that is shaped around the guidewire exit port to show in profile a shape reminiscent of the nose of a dolphin. In preferred embodiments, the sleeve also has a tapered distal tip that is withdrawn proximally over the length of the stent to release it, progressively, from its distal end. The configuration delivers simplicity of design, enhanced performance and reliability in use. | 07-15-2010 |
20100174310 | NON-ENTANGLING VENA CAVA FILTER - An implantable vessel filter including an elongated body coupled proximally to a hub, and including a grooved distal section. A first set of legs coupled proximally to the hub have a first length, each of the first set of legs translating from a collapsed state in a filter compressed configuration to an extended state in a filter expanded configuration. A second set of legs coupled proximally to the hub have a second length longer than the first length, each of the second set of legs including a hook positioned at a distal end thereof, each of the second set of legs translating from a collapsed state in the filter compressed configuration to an extended state in the filter expanded configuration, each hook received in the grooved distal section in the filter compressed configuration and penetrating a wall of a vessel in the filter expanded configuration. | 07-08-2010 |
20100168835 | STENT DELIVERY DEVICE WITH ROLLING STENT RETAINING SHEATH - A delivery device for delivering a stent device that is expandable from a radially reduced, delivery configuration to a radially expanded, deployed configuration. A retaining sheath is disposed over the stent device for maintaining the stent device in the delivery configuration. A pull line to be pulled upon is provided to retract the retaining sheath in a rolling manner such that the retaining sheath is folded back on itself to provide a radially inner sheath of the retaining sheath, a radially outer sheath of the retaining sheath and a fold portion therebetween. The retaining sheath may be made of a cold drawn plastic at least along the path of travel of the fold portion in retracting the retaining sheath from over the stent device. | 07-01-2010 |
20100160787 | NEEDLE GUIDES FOR A SONOGRAPHIC IMAGING DEVICE - Needle guide systems for a sonography device are disclosed. The needle guide systems include both fixed and adjustable and fixed needle guides. In one embodiment, the needle guide includes a needle guide body that is rotatably mounted to a probe of a sonography device. A plurality of needle channels is disposed on a surface of the needle guide body. Each needle channel can be selectively rotated into position to guide a needle into a body of a patient at a predetermined needle insertion angle. If another needle insertion angle is desired, the needle guide is rotated to place a new needle channel defining the desired needle insertion angle into position. | 06-24-2010 |