40th week of 2017 patent applcation highlights part 13 |
Patent application number | Title | Published |
20170281815 | Fabric Sterilization Tote Apparatus and Related Methods - A fabric sterilization tote apparatus and related methods of using and manufacturing the same is provided. The apparatus includes a flexible, bacteria-impenetrable material formed into a closable container, the closable container having a base, at least four sidewalls, and a cover, wherein an interior area of the closable container is defined by the base, the at least four sidewalls, and the cover. A bacteria-impenetrable closure is positioned between the cover and at least one of the four sidewalls, wherein the bacteria-impenetrable closure controls a sealing of the interior area of the closable container from an exterior atmosphere. In use, a medical instrument sterilization tray with the at least one medical instrument may be placed within the fabric sterilization tote apparatus after completion of a sterilization process. | 2017-10-05 |
20170281816 | Method of Using a Sterilization Wrap System - A method of using a sterilization wrap system including a permeable material having barrier properties and having a first surface and a second opposing surface, the exterior panel being substantially opaque or having a first level of translucence, and an interior panel including a permeable material having barrier properties and having a first surface and a second opposing surface, the interior panel having a level of translucence that is higher than the translucence of the exterior panel, the panels being joined together over at least a portion of their surfaces. Also disclosed is inspection of the sterilization wrap system for exterior panel breaches by looking for light passing through a panel facing the viewer. | 2017-10-05 |
20170281817 | Method of Using a Sterilization Wrap System - A method of using a sterilization wrap system including a permeable material having barrier properties and having a first surface and a second opposing surface, the exterior panel being substantially opaque or having a first level of translucence, and an interior panel including a permeable material having barrier properties and having a first surface and a second opposing surface, the interior panel having a level of translucence that is higher than the translucence of the exterior panel, the panels being joined together over at least a portion of their surfaces. Also disclosed is inspection of the sterilization wrap system for exterior panel breaches by looking for light passing through a panel facing the viewer. | 2017-10-05 |
20170281818 | DEODORIZING GLOVE HOLDER FOR ATHLETIC GLOVES AND OTHER EQUIPMENT - A deodorizer for insertion into athletic and other equipment, having an outer housing that is infused with an antimicrobial agent and that has ventilation holes, and containing a moisture absorbing deodorizer within the outer housing. The deodorizer absorbs moisture that allows bacteria to grow and the antimicrobial infused outer housing kills existing bacteria, thereby reducing bacteria and odor. | 2017-10-05 |
20170281819 | Scent Dispensation - A scent dispenser may comprise a vial retaining mechanism, a heating element, vial sensor, and a controller. The vial retaining mechanism includes a vial coupling that removeably retains a vial containing a scented solution. The includes a wick extending from a cavity of the vial through an opening of a neck of the vial. The heating element is shaped to receive and heat the wick of the vial. The vial sensor includes an array of sensor pads that are arranged in alignment with the vial retained by the vial coupling. The controller is electrically coupled to the heating element and electrically coupled to the array of sensor pads. The controller regulates a temperature level of the heating element, and receives signals from the array of sensor pads and processing the signals to determine a fluid level of the vial. | 2017-10-05 |
20170281820 | SOLID AIR FRESHENER - The present invention relates to a solid pressed air freshener and odor neutralizer composition which can include greater than 10% fragrance. The air freshener comprises a fragrance; preferably the fragrance is impregnated within a water soluble substrate made from a foamed vegetable starch, a surfactant and a solidifier. The solid formulations break down easily in the presence of water and may be sprayed, within the area to be freshened. | 2017-10-05 |
20170281821 | DIFFUSER WITH INTERCHANGEABLE COVER - Apparatuses, systems, and methods are disclosed for a complete diffuser and a two-part decorative diffuser cover. The two-part decorative diffuser cover has an inner cavity shaped to receive the complete diffuser. One part of the two-part decorative diffuser cover is removable couple to the complete diffuser. The two-part decorative diffuser cover forms a single decorative structure when both parts of the two-part decorative diffuser cover are joined together. | 2017-10-05 |
20170281822 | PEST CONTROL SYSTEM AND METHOD - A system for integrated pest management in an environment includes devices positioned within the environment. The devices each include a communications facility that enables transmitting signals to and receiving signals from a network device. The system further includes a network to provide communication between the network device to the devices. The network device receives communication and control functions from a remote computer for distribution to the devices. The system further includes a sensor positioned within the environment to transmit sensor data to the remote computer. The sensor is configured to detect and transmit a parameter for the environment to the remote computer. The system further includes a controller to control the emission of a fluid from a source of the fluid in fluid communication with the devices. The controller is configured to set or adjust an operation parameter of the devices in response to the sensor data. | 2017-10-05 |
20170281823 | APPARATUS AND METHODS FOR OZONE GENERATION AND DEGRADATION - Devices and methods for sterilizing an enclosed space using ozone are disclosed herein. Various embodiments of the devices and methods also provide for accelerated degradation of the ozone upon sterilization. In some embodiments, a disclosed sterilization unit includes a first housing defining an ozone generation cavity, an ozone generator disposed within the ozone generation cavity, a second housing defining an ozone degradation cavity, and an ozone degrader disposed within the ozone degradation cavity. The sterilization unit of various embodiments is configured to cycle air between the enclosed space and the ozone generation cavity during an ozone generation cycle to sterilize the enclosed space; similarly, the unit is further configured to cycle air between the enclosed space and the ozone degradation cavity during an ozone degradation cycle to return the air within the enclosed space to safe ozone levels. | 2017-10-05 |
20170281824 | Anti-Microbial Medical Materials and Devices - The present disclosure relates generally to materials and medical devices impregnated with antimicrobial compounds. More specifically, the materials are medical matrix materials comprising nanopores or nanochannels in which the antimicrobial compounds are disposed. In other embodiments, medical matrix materials comprises nanomaterials and antimicrobials distributed throughout the material. The materials described herein are useful for a broad spectrum of medical devices and consumer products. The present disclosure further provides methods of making the antimicrobial materials and medical devices disclosed herein. | 2017-10-05 |
20170281825 | COMPOSITIONS AND METHODS FOR WOUND HEALING - The present invention relates, in part, to sutures which promote wound closure and/or healing. In particular, the present invention provides fibrin microthread sutures that mimic the mechanical behavior of a target tissue thereby reducing, for example, scarring, inflammation, and cell death at the ligature site, including monofilament sutures. | 2017-10-05 |
20170281826 | Biohybrid for the Use Thereof in the Regeneration of Neural Tracts - The invention relates to a biohybrid for the use thereof in the regeneration of neural tracts, comprising an implantable tubular hybrid structure which is degradable and biocompatible and characterized in that it comprises three layers of different porosity: an inner layer a), an intermediate layer b) and an outer layer c), with uninterrupted connection among them, the three layers consisting of the same porous hydrogel based on cross-linked hyaluronic acid, a biohybrid comprising the hybrid tubular structure described, which can contain a fibrous material, preferably poly-L-lactic acid, to a method for producing said tubular hybrid structure and said biohybrid, and to the use of same for regenerating neural tracts in diseases that affect the central nervous system, preferably Parkinson's disease. | 2017-10-05 |
20170281827 | MATERIAL COMPOSITIONS, APPARATUS AND METHOD OF MANUFACTURING COMPOSITES FOR MEDICAL IMPLANTS OR MANUFACTURING OF IMPLANT PRODUCT, AND PRODUCTS OF THE SAME - A coated powder composite may include a core particle of Ca or an alloy thereof, or of Mg or an alloy thereof. One or more coating layers may be disposed about the core particle, cladding the core particle. The coated powder composite may be biodegradable. | 2017-10-05 |
20170281828 | THREE-DIMENSIONAL BIOPRINTED ARTIFICIAL CORNEA - An artificial cornea is fabricated by separately culturing live stromal cells, live corneal endothelial cells (CECs) and live corneal epithelial cells (CEpCs), and 3D bioprinting separate stromal, CEC and CEpC layers to encapsulate the cells into separate hydrogel nanomeshes. The CEC layer is attached to a first side of the stromal layer and the CEpC layer to a second side of the stromal layer to define the artificial cornea. | 2017-10-05 |
20170281829 | BONE REGENERATION USING BIODEGRADABLE POLYMERIC NANOCOMPOSITE MATERIALS AND APPLICATIONS OF THE SAME - A biocompatible structure includes one or more base structures for regeneration of different tissues. Each base structure includes alternately stacked polymer layers and spacer layers. The polymer layer includes a polymer and tissue forming nanoparticles. The polymer includes polyurethane. The tissue forming nanoparticles includes hydroxypatites (HAP) nanoparticles, polymeric nanoparticles, or nanofibers. The spacer layer includes bone particles, polymeric nanoparticles, or nanofibers. The weight percentage of tissue forming nanoparticles to the polymer in the polymer layer in one base structure is different from that in the other base structures. A method of producing the biocompatible structure includes forming multiple base structures stacked together, coating the stacked multiple base structures, and plasma treating the coated structure. | 2017-10-05 |
20170281830 | IGF-I FOR MYOCARDIAL REPAIR - Provided herein are methods for treating an individual having (suffering from) an acute myocardial infarction and drug eluting stents useful for treating such individuals. These methods include treating an individual by introducing, such as by surgically inserting, at a site of an acute coronary artery occlusion upstream of the site of acute myocardial infarction, a drug eluting stent (DES) that is capable of eluting from 25 pg to 950 pg of IGF-I directly into the coronary circulation. The treatment is specifically directed to stimulation of repair or survival of damaged cardiac muscle or left ventricular remodeling. | 2017-10-05 |
20170281831 | LUBRICIOUS COATING FOR MEDICAL DEVICE - Embodiments of the disclosure include lubricious coatings. In an embodiment the disclosure includes a lubricious coating for a medical device including an acrylic acid polymer, an acrylamide copolymer comprising at least one photoreactive group, and a cross-linking agent comprising at least two photoreactive groups. The coating can be used on a catheter surface to facilitate its movement in the body. | 2017-10-05 |
20170281832 | COMPOSITE STENT HAVING MULTI-AXIAL FLEXIBILITY AND METHOD OF MANUFACTURE THEREOF - A bioabsorbable composite stent structure, comprising bioabsorbable polymeric ring structures which retain a molecular weight and mechanical strength of a starting substrate and one or more interconnecting struts which extend between and couple adjacent ring structures. The ring structures can have a formed first diameter and being radially compressible to a smaller second diameter and re-expandable to the first diameter. The ring structures can comprise a base polymeric layer. The interconnecting struts can be formed from a polymer blend or co-polymer of poly-L-lactide (PLLA) and an elastomeric polymer. The interconnecting struts each can have a width that is less than a circumference of one of the ring structures. The adjacent ring structures can be axially and rotationally movable relative to one another via the interconnecting struts. The interconnecting struts can also be bioabsorbable. | 2017-10-05 |
20170281833 | MULTI-LAYER BIODEGRADABLE DEVICE HAVING ADJUSTABLE DRUG RELEASE PROFILE - Methods and apparatus for a biodegradable multi-layer device suitable for medical applications are provided, wherein the device is formed from multiple film-layers configured to have different characteristics from one another such as different release profiles for therapeutic agents, adhesive properties, stiffness properties, and solubility properties. The film-layers may include a solid fibrinogen component. A device having multiple film-layers may take a non-adherent form during delivery to a target location within or on tissue, and thereafter may be exposed to moisture to take an adherent form on the tissue. The device may include a number of additives, including materials to improve the mechanical properties of the device, or one or more therapeutic or contrast agents. | 2017-10-05 |
20170281834 | CHLORHEXIDINE GLUCONATE COMPOSITIONS, RESIN SYSTEMS AND ARTICLE - Compositions containing chlorhexidine gluconate solubilized in hydrophobic vehicles are described. Resin systems containing such chlorhexidine gluconate compositions, including adhesives and articles incorporating such resin systems, including medical articles such as drapes are also described. | 2017-10-05 |
20170281835 | NEEDLE SURFACE FOR REDUCED COAGULATION AND METHOD FOR SAME - A medical needle may include a lumen coating configured to reduce surface energy of the lumen-facing/lumen defining surface, in a manner effective to slow and/or reduce coagulation of biomaterial (particularly blood) that contacts the needle lumen surface. Such a coating may include a hydrophobic coating such as a silane and/or siloxane material on at least the needle lumen surface. The coating reduces a surface energy of coated needle regions below the surface energy of uncoated regions, and particularly reduces the polar component of the surface energy in the coated needle regions. The needle may be a metallic biopsy needle with the coating comprised by at least a distalmost length of sample-collection lumen. | 2017-10-05 |
20170281836 | SUSPENSION DEVICE OF A DRAINAGE CONTAINER - A suspension device for a drainage container has, on a first side, a first fastening unit for mounting and fastening the drainage container on the suspension device. On a second side, a second fastening unit is present for mounting and fastening the suspension device on a rail. The first fastening unit is arranged in a first fastening part, and the second fastening unit is arranged in a second fastening part. The suspension device further comprises a weighing part with a weighing element, wherein the weighing part is connected or can be connected to the first fastening part and to the second fastening part so as to measure, with the weighing element, a relative displacement, such that a filling quantity of the aspirated body fluid in the drainage container can be determined. | 2017-10-05 |
20170281837 | SYSTEM AND KIT FOR THE COLLECTION AND PROCESSING OF AMNIOTIC FLUID AND PLACENTAL ASPIRATE - Disclosed is a system for the collection, processing and reuse of amniotic fluid and placental aspirate at a C-section site. The system includes a canister positioned along the vacuum line through which the amniotic fluid and placental aspirate is suctioned. The canister has a coil whereby the heavier cellular components, including stem cells, platelets and growth factors, are separated coincident with the surgical procedure. The canister has a port whereby the heavier cellular material can be removed from the canister. The heavier cellular material can be then applied to the wound site of the cesarean section patient. The system disclosed allows for the processing of the amniotic fluid and placental aspirate to take place in the same room as the surgical procedure. A kit and method are also provided. | 2017-10-05 |
20170281838 | NEGATIVE PRESSURE WOUND CLOSURE DEVICES AND METHODS - Systems, devices, and methods of the present application can accelerate and reduce medical complications associated with healing of non-planar wounds such as amputation wounds. The devices and methods utilize a collapsing structure and negative pressure to cause the shaped wound to preferentially close. The structure can accommodate movement over curved tissue surfaces, which can utilize scales or interleaved elements to provide efficient wound closure along arcuate paths. This structure can enable gradual closure from the deepest portion of the wound to the shallowest portion. | 2017-10-05 |
20170281839 | IRRIGATION AND ASPIRATION DEVICE AND METHOD - An irrigation and aspiration system is disclosed. The system can be configured to aspirate and irrigate alone, sequentially or concurrently. The system can be configured to aspirate and irrigate the nasal cavity. The system can be manually controlled. The system can have removable and easily cleanable reservoirs for aspirant and irrigant. | 2017-10-05 |
20170281840 | FLANGED HEART TISSUE BLOCKER - An apparatus for protecting heart tissue from an implanted inlet element of a blood pump. The apparatus includes a flange member having a first radially constricted configuration and a second radially expanded configuration, the flange member being biased in its second radially expanded configuration. The flange member defines an opening there through sized to receiving the inlet element of the blood pump. A retaining element extending from the flange member is included, the retaining element being flexible and sized to be disposed about at least a portion of the inlet element. | 2017-10-05 |
20170281841 | CRENELLATED INFLOW CANNULA - A blood pump including a housing defining a fluid flow path, an upstream end, a downstream end, and an outlet at the downstream end. A rotor is disposed within the housing and within the fluid flow path, the rotor being rotatable independent of the housing in a first direction and configured to pump blood downstream toward the outlet. The housing defines an inflow cannula at the upstream end, the inflow cannula defining a proximal end proximate the rotor and an opposite distal end. The inflow cannula defines a major longitudinal axis and minor longitudinal axis, the distal end of inflow cannula defines a plurality of slots radially disposed about the distal end, the plurality of slots being at least one from the group consisting of sloped in the first direction with respect to the major longitudinal axis and angled in the first direction with respect to the minor longitudinal axis. | 2017-10-05 |
20170281842 | AXIAL FLOW BLOOD PUMP WITH RADIALLY OFFSET ROTOR - A blood pump including a housing defining a proximal end, a distal end, and a first axis extending from the proximal end to the distal end. A ferromagnetic rotor is disposed within the housing and configured pump blood in a direction along the first axis. A stator is disposed within housing and around the ferromagnetic rotor, the stator is configured to apply a magnetic force causing rotation of the ferromagnetic rotor, the stator being eccentric to the rotor. | 2017-10-05 |
20170281843 | A DEVICE FOR GENERATING BILATERAL PRESSURE IMPULSES - Disclosed is an electromechanical device generating bilateral pressure impulses, wherein the alternative and specular movement of the homologous cursors (CV, CO), pacing one of the Cartesian axes, exclusively manages mobile cores (NEM) of electromagnets (EM) with planned solicitation, for supplying the necessary mechanical energy for the correct working of operating machines of different kinds, and in particular of a permanent artificial heart. | 2017-10-05 |
20170281844 | Dialysis Service Box - A dialysis service box for centralized control and plumbing arrangement of a dialysis machine is disclosed. The dialysis service box includes a plumbing arrangement having a supply inlet for supplying a fluid to the dialysis machine, a backflow preventer for preventing retrograde flow through the plumbing arrangement, a trap primer for maintaining a trap seal designed to prevent waste gases from flowing into the dialysis service box and a waste connection for allowing waste from the dialysis machine to exit. The dialysis service box can be universally installed to operate, control and adjust any dialysis machine that requires supply connection, waste connection, backflow preventer and trap primer, or any combination of the foregoing. | 2017-10-05 |
20170281845 | PERITONEAL DIALYSATE FLUID GENERATION SYSTEM - Systems and methods of generating peritoneal dialysate are provided. The systems and methods use a water purification module, a sterilization module and concentrates to prepare a bolus of peritoneal dialysate from source water for use with an non-integrated cycler. | 2017-10-05 |
20170281846 | PERITONEAL DIALYSATE FLUID GENERATION SYSTEM WITH INTEGRATED CYCLER - Systems and methods of generating peritoneal dialysate and using the peritoneal dialysate with an integrated cycler are provided. The systems and methods use a water purification module, a sterilization module and concentrates to prepare peritoneal dialysate from source water and infuse the prepared peritoneal dialysate into a patient with an integrated cycler. Optional dialysate storage containers are provided for storage of the peritoneal dialysate prior to use. | 2017-10-05 |
20170281847 | REGENERATIVE PERITONEAL DIALYSIS SYSTEM - Systems and methods of generating and regenerating peritoneal dialysate are provided. The systems and methods use a dialysate regeneration module, a sterilization module and concentrates to prepare peritoneal dialysate from used peritoneal dialysate or source water. An optional integrated cycler for direct infusion of the generated peritoneal dialysate is included. Optional dialysate storage containers are provided for storage of the peritoneal dialysate prior to use. | 2017-10-05 |
20170281848 | APPARATUS FOR PERFORMING PERITONEAL ULTRAFILTRATION - An apparatus for ultrafiltration of a patient being overhydrated due to congestive heart failure, comprising a tube set including a connector for connection to a patient line for access to the peritoneal cavity of the patient. A flow pump is arranged for addition and removal outflow and inflow (recirculation) of fluid from/to the peritoneal cavity. An osmotic agent peristaltic pump is arranged for replenishment of glucose solution to the fluid added to the peritoneal cavity for promoting ultrafiltration. The glucose is replenished intermittently for keeping a concentration of glucose substantially constant in the peritoneal cavity. The flow pump comprises a pressure chamber with rigid walls and a flexible pump bag arranged therein. An air pump pressurizes the chamber for outflow of fluid from the peritoneal cavity by a sub pressure and inflow of fluid to the peritoneal cavity by an overpressure, which pressures are maintained within safe limits. | 2017-10-05 |
20170281849 | BLOOD PURIFICATION SYSTEM - A blood purification system that is capable of notifying any changes in the patient's condition on the basis of noninvasive vital sings of the patient that are observed during the blood purification treatment. An external information-processing apparatus includes an external input device into which a vital sign detected by a detecting device is inputtable in real time; a checking device capable of checking whether or not the vital sign inputted in real time into the external input device satisfies a predetermined condition; and an external output device capable of outputting, if it is determined by the checking device that the vital sign satisfies the predetermined condition, a result of the checking or checked information including the vital sign leading to the result of the checking to a blood purification apparatus. The checked information outputted from the external output device is displayable on a display included in the blood purification apparatus. | 2017-10-05 |
20170281850 | ARTIFICIAL DIALYSIS DEVICE - A filter CF | 2017-10-05 |
20170281851 | IRRIGATION AND ASPIRATION DEVICE AND METHOD - An irrigation and aspiration system is disclosed. The system can be configured to aspirate and irrigate alone, sequentially or concurrently. The system can be configured to aspirate and irrigate the nasal cavity. The system can be manually controlled. The system can have removable and easily cleanable reservoirs for aspirant and irrigant. | 2017-10-05 |
20170281852 | DELIVERING AND/OR RECEIVING MATERIAL WITH RESPECT TO A SUBJECT SURFACE - The present invention generally relates to receiving bodily fluid through a device opening. In one aspect, the device includes a flow activator arranged to cause fluid to be released from a subject. The flow activator may be actuated in a deployment direction by a deployment actuator, which may in turn cause fluid release from a subject. The flow activator may also be moved in a retraction direction by a retraction actuator. In one aspect, the device may include a vacuum source that may help facilitate fluid flow into the opening of the device and/or may help facilitate fluid flow from the opening to a storage chamber. In one aspect, an effector may enable fluid communication between the opening and the vacuum source and may do so in response to actuation of the flow activator. | 2017-10-05 |
20170281853 | SYRINGE ASSEMBLY - A syringe assembly includes a plunger assembly, a syringe body, and a needle. The plunger assembly includes a plunger rod, a spring, a plunger base, and a plunger plug. The plunger rod includes a first end member having a first stepped part positioned in an inner wall thereof, a second end member, and a first accommodating room. The plunger base includes a plunger body, a projection, a second stepped part, a plunger member, and a locating member. The plunger body is received in the first accommodating room, and the projection abuts against the first end member. The spring is arranged around the plunger body and positioned between the first stepped part and the second stepped part. The plunger plug is mounted to the second end member, and defines a fixing groove. The syringe body includes a needle cannula, a needle base, a fixing pole, and a fixing valve. The plunger assembly is received in the needle cannula. The needle base is mounted to the needle cannula. The fixing valve is received in the needle base. The fixing pole is received in the fixing valve and protrudes out of the needle base. The needle is received in the fixing pole. The syringe assembly of the present invention is prevented from reuse and accidently damage because the needle can retract into the plunger rod using restoring force of the spring. | 2017-10-05 |
20170281854 | Auto-Injector Apparatus - An auto-injector apparatus includes a flexible container containing a liquid medicant, a needle communicated with a container, a housing with a container being received in the housing, a pump disposed in the housing and positioned to engage the flexible container and expel the medicant from the container through the needle upon relative movement between the pump and the container, and a main drive spring operably associated with the needle to extend the needle from a first needle position wherein the needle is completely received in the housing to a second needle position wherein the needle protrudes from the housing. The pump may be a roller. | 2017-10-05 |
20170281855 | ILLUMINATING MEDICAL INFUSION PUMP - Disclosed are various embodiments for medical infusion pumps comprising an integrated source of illumination for illuminating an illuminating medical infusion line. | 2017-10-05 |
20170281856 | TRANSFORMABLE INTRAVENOUS POLE AND BOOM COMBINATION AND METHOD THEREOF - An intravenous (IV) pole docking system for supporting medical equipment having a mast engaged to a base, the base having legs to support the mast and a lifting mechanism engaged to the base and the mast for moving the base along the mast in combination with an extension arm meant to reduce the IV pole footprint. The boom/IV pole system can reduce excess obstacles in and around hospital bed, surgical rooms and the like. | 2017-10-05 |
20170281857 | SYRINGE PUMP AND DRIVE HEAD ASSEMBLY THEREFOR - A syringe pump usable with a syringe having a barrel and a plunger, the plunger having a plunger flange, comprises a barrel retaining mechanism for holding the barrel, and a drive mechanism having a drive head assembly for driving the plunger along its axis. The drive head assembly comprises a flange retaining mechanism for retaining the plunger flange to the drive head assembly, and a load measuring device for measuring compressive force on the plunger flange, the load measuring device being movable within the drive head assembly transverse to the axis. The syringe pump comprises a self-centering mechanism having a pushing component which is arranged to move the load measuring device within the drive head assembly until the pushing component abuts against the plunger flange, such that a center of the load measuring device is aligned with the axis. | 2017-10-05 |
20170281858 | Infusion System for the Controlled Delivery of Therapeutic Agents - Embodiments of the invention provide infusion systems for the intravenous or other delivery of drugs and other therapeutic agents to a patient including a human or mammal. The therapeutic agents may be dissolved in solution or comprise the solution itself. Embodiments of the systems can utilize a chemical reaction to predictably drive a flow of drug(s) through a catheter or other flow path and into the patient. More specifically, the reaction may include an acid-base reaction or any other reaction that produces a gaseous substance. The gas is produced and contained in an expandable drive balloon when the acid-base reactants are combined with a liquid. As the gas is produced, the drive balloon expands to exert pressure on a separately-contained drug reservoir which, in turn, pushes drug(s) from the reservoir into the flow path where the drug is ultimately delivered to the patient in a controlled and predetermined manner. | 2017-10-05 |
20170281859 | Drive Mechanism for Drug Delivery Pumps with Integrated Status Indication - A drive mechanism includes a housing, a piston adapted to impart movement to a plunger seal within a drug container, a plurality of biasing members disposed in parallel, and a retainer. The biasing members are disposed to release energy to cause movement of the piston from a retracted first position to the extended second position, the piston bearing against the plunger seal to dispense medicine. The retainer is disposed to maintain the biasing members in the energized position and to release the biasing members to permit the piston to dispense the medicine. The drive mechanism may also include an end-of-dose indicator to identify at least one of when the sleeve assembly is disposed subjacent a window in the housing the relative motion of the sleeve assembly with reference to the window or another reference component, the stoppage of such motion, and the rated or change of rate of motion. | 2017-10-05 |
20170281860 | Apparatus, Systems and Methods for an Infusion Pump Assembly - A system for delivery of a volume of infusible fluid. The system includes a controller configured to calculate a trajectory for delivering infusible fluid, the trajectory comprising at least one volume of fluid, and determine a schedule for delivering the at least one volume of fluid according to the trajectory, wherein the schedule comprising an interval and a volume of infusible fluid for delivery. The system also includes a volume sensor assembly for determining the at least one volume of fluid delivered, wherein the controller recalculates the trajectory based on the volume of fluid delivered. | 2017-10-05 |
20170281861 | MEDICAMENT DELIVERY DEVICE WITH ROTATABLE HOUSING ON A BASE - A medicament delivery device ( | 2017-10-05 |
20170281862 | INJECTABLE COMPOSITIONS AND METHODS OF PREPARATION AND USE THEREOF - Compositions useful for tissue resection procedures and related methods of preparing the compositions are discussed. The composition may comprise gellan gum, at least one salt, and water. In some aspects, the composition may be prepared by combining the gellan gum, the salt(s), and the water to form a mixture, heating the mixture, introducing the mixture into a reservoir, and allowing the mixture to cool while inside the reservoir to form a gel. The gel may have a continuous, three-dimensional structure, and may be solid or quasi-solid. The composition may be biocompatible and injectable from the reservoir through a needle coupled to the reservoir to the target site of a patient. | 2017-10-05 |
20170281863 | Infusion Set and Inserter Assembly - A two-stage infusion set inserter system is disclosed. The inserter system includes an inserter assembly including a housing including a rotatable button assembly comprising ramps and and tab indents and a non-rotatable portion of housing, a sliding component comprising sliding component tabs, a needle carrier connected to an introduction needle, the needle carrier slidably movable from a starting position to an injection position and then to a second ending position, a sliding component spring, and a needle spring, wherein the rotatable button assembly rotates from a locked to an unlocked position, wherein when force is applied onto the rotatable button assembly, the sliding component and needle carrier are forced downward by the sliding component spring, and wherein when the needle carrier reaches the injection position, the needle spring forces the needle carrier upward towards the second ending position. | 2017-10-05 |
20170281864 | Wireless Communication for On-Body Medical Devices - Apparatus, systems and methods for the wireless communication of medical devices in an on-body fluid delivery system are disclosed. A system for on-body fluid delivery includes a primary patch pump adapted to attach a first infusion cannula to a user and to perform a plurality of primary patch pump functions, and a secondary patch pump adapted to attach a second infusion cannula to a user. The secondary patch pump is further adapted to perform a plurality of secondary patch pump functions substantially similar to the plurality of primary patch pump functions if an error condition associated with the primary patch pump is determined. | 2017-10-05 |
20170281865 | Process and system for fluid management during reinjection of adipose tissue - The invention is a process and system, consisting of a reinjection pump, connecting tubing, a reinjection cannula and a recipient site, with fluid management features including a peristaltic pump head and controls for pressure limits, flow rates and flow distribution wherein the process of controlling the reinjected fat and fluid is unique because of the control of flow rates, pressures, matching cannula hole sizes, and maintaining a closed continuous system where the harvesting and reinjection is done all together with a completely closed system. The process utilizes a method and control system to manage pressure levels during reinjection procedures of viable soft tissue. Although this case specifically relates to its use in the reinjection of adipose fat and other tissue back into the body during liposuction procedures, it can be applied to any medical procedure of introducing or re-introducing materials into the body. | 2017-10-05 |
20170281866 | PHARMACEUTICAL INJECTION SYSTEM, PORTABLE TERMINAL, PHARMACEUTICAL INJECTION DEVICE, HEALTH CARE WORKER-USE INFORMATION TERMINAL, AND METHOD FOR CONTROLLING PHARMACEUTICAL INJECTION SYSTEM - With the pharmaceutical injection system in an embodiment, pharmaceutical injection amount setting conditions for setting a pharmaceutical injection amount are inputted to a portable terminal ( | 2017-10-05 |
20170281867 | REGULATING ENTRY INTO A CLOSED-LOOP OPERATING MODE OF AN INSULIN INFUSION SYSTEM - An electronic controller for an insulin infusion device includes at least one processor device and at least one memory element that cooperate to provide a processor-implemented closed-loop initiation module. The initiation module is operated to obtain a most recent calibration factor for a continuous glucose sensor, the most recent calibration factor representing a first conversion value applicable to convert a first sensor value to a first blood glucose value. The initiation module also obtains a prior calibration factor for the sensor, and calibration timestamp data for the most recent calibration factor and the prior calibration factor. The initiation module regulates entry into a closed-loop operating mode of the insulin infusion device, based on the most recent calibration factor, the prior calibration factor, and the calibration timestamp data. | 2017-10-05 |
20170281868 | PEN-TYPE INJECTOR - A pen includes a carpule having a longitudinal axis, a first end with a dispensing opening closable by a closure part, a second end via which at least one stopper can be inserted in the direction of the longitudinal axis, and an interior that is tightly closed by the closure part and the at least one stopper. A pen housing has a central axis, receives the carpule, and has a piston rod that interacts with the at least one stopper and a drive for moving the at least one stopper within the interior of the carpule, wherein the second end of the carpule can be inserted into the housing. The drive element moves the carpule into the housing in the direction of the longitudinal axis, which is arranged coaxially to the central axis of the housing, when the drive is activated; and in the process the piston rod is held in a fixed position with respect to the longitudinal direction of the housing such that the piston rod, which is engaged in the second end of the carpule, moves the at least one stopper within the interior of the carpule in the direction of the first end of the carpule. | 2017-10-05 |
20170281869 | Applicator - There is provided an applicator for ejecting together with a gas a mixed liquid obtained by mixing a first liquid and a second liquid which are different from each other in composition. The applicator includes a first liquid flow path through which the first liquid flows; a second liquid flow path through which the second liquid flows; a gas flow path through which the gas flows; a confluence section in which the first liquid and the second liquid merge; and a backflow preventing section that prevents backflow of the first liquid and prevents backflow of the second liquid. | 2017-10-05 |
20170281870 | Applicator - There is provided an applicator including: a first liquid flow path through which a first liquid containing fibrinogen passes; a second liquid flow path through which a second liquid containing thrombin passes; a confluence section in which the first liquid and the second liquid merge with each other to form a mixed liquid; and a gas flow path through which a gas for jetting the mixed liquid passes. At least part of a wall portion defining the confluence section is composed of a gas-permeable membrane that is impermeable to the mixed liquid and permeable to the gas. | 2017-10-05 |
20170281871 | AUTO-INJECTOR SYSTEMS AND METHOD FOR DELIVERING CYST MEDICATION ON DEMAND - An auto-injector device including a syringe, a needle arranged in the vicinity of a first end of the syringe, and a plunger arranged within the syringe. A volume within the syringe between the plunger the needle accommodates medicine, such that movement of the plunger toward the needle dispenses medicine through the needle. A selection assembly configurable by a user to adjust an amount of medicine dispensed by the auto-injector device and depth to which the medicine is delivered. Also, a method for treating a skin lesion or skin disorder utilizing the auto-injector and a kit for patient administered treatment. | 2017-10-05 |
20170281872 | Dual-Dose Syringe System - An dual-dose syringe system is an apparatus that includes a tubular housing and a plunger. The tubular housing attaches onto a variety of syringe and needle assemblies and mounts the plunger within the syringe. The tubular housing prevents the plunger from simply traversing into the syringe. The tubular housing includes a first lateral-half portion and a second lateral half-portion that snaps onto each other and encloses a syringe. The tubular housing further includes a key slot that engages the plunger. The plunger includes a plurality of cross bars that predetermine two doses. Each of the plurality of cross bars is positioned perpendicular to a corresponding adjacent bar, forcing a user to purposefully twist the plunger in order to administer a dose. The apparatus further includes at least one spring-loaded barb that prevents the reuse of the apparatus. | 2017-10-05 |
20170281873 | MEDICAL SYRINGE, GASKET TO BE USED FOR SYRINGE, AND GASKET PRODUCTION METHOD - Laminated gasket free from liquid drug leakage. A gasket ( | 2017-10-05 |
20170281874 | Drug Delivery Device and Method for a Drug Delivery Device - A drug delivery device ( | 2017-10-05 |
20170281875 | APPARATUS AND KITS FOR FLUID INFUSION - An infusion device includes a housing with an interior chamber sized and configured to hold at least a flange and plunger of a syringe, a trigger held by the housing, and a lever in communication with the trigger and including an upwardly extending cam with a cam path having an upper end. The cam is in communication with the flange of the syringe. In response to actuation of the trigger to dispense fluid from the syringe, the upper end of the cam travels upward above the syringe and longitudinally toward a dispensing end of the syringe to linearly translate the plunger of the syringe in a first direction to dispense fluid from the syringe. To refill fluid into the syringe, the upper end of the cam travels downward and longitudinally away from the dispensing end of the syringe to linearly translate the plunger in a second direction to intake fluid. | 2017-10-05 |
20170281876 | Method and Apparatus for Manufacturing, Filling and Packaging Medical Devices and Medical Containers - Medical devices such as medical containers can be formed of glass and annealed which produces a clean device having a low bio-burden, or formed by plastic molding which produces a clean device. The clean devices are immediately transferred to a controlled environment such as a clean room or localized area to avoid the need to maintain cleanliness levels in an entire room. Syringe tip closures can be introduced into the housing assembly, where syringe barrels and tip closures are cleaned with filtered ionized air and the tip closures are coupled to the barrels. The syringe barrels can be filled with a substance and a closure member attached. While still in the housing assembly the syringe barrels can be formed into an array and placed in a clean outer container, which is then closed and sealed. | 2017-10-05 |
20170281877 | Skin Sensors and Automatic Injectors for Injectable Syringes Having Skin Sensors - A skin sensing system for a drug delivery device includes a control unit and a skin sensor comprising one or more electrodes. The skin sensor may be configured to store a threshold value associated with skin sensing, receive one or more sensed signal values | 2017-10-05 |
20170281878 | SEGMENTED SAFETY COVER FOR NEEDLE DELIVERY - A segmented safety cover may include a proximal segment combined with a needle hub; a needle cannula that extends from the proximal needle hub to a distal sharpened end; a distal end cap with a hollow bore through which the needle cannula passes; a centrally mounted toggle locking mechanism, separating the proximal needle hub from the distal end cap; the toggle locking mechanism is torsion spring assisted; a proximal cover segment is connected to the hub via a proximal hinge and a distal cover segment is connected to the end cap via a distal hinge; said proximal cover segment and said distal cover segment of said toggle locking mechanism being configured with abutting faces when the segmented safety cover is in a safety mode; and wherein the proximal hinge, abutting faces and distal hinge are in line in the safe mode. | 2017-10-05 |
20170281879 | Medical Liquid Warmer with Auxiliary Temperature Sensor - An auxiliary sensor can be used to measure the temperature of individual products in a heating cabinet. By arranging the temperature sensor with respect to the low mass thermal conductors and insulators, the sensor can be focused on the product to obtain the proper temperature irrespective of the immediate environment whether it is at room temperature or even within the heating cabinet. | 2017-10-05 |
20170281880 | AEROSOL OR SPRAY DEVICE, SPRAY NOZZLE UNIT AND METHOD OF MANUFACTURING THE SAME - A method for manufacturing an spray device includes assembling at least one spray nozzle plate into a thermoplastic holder, while controlling the temperature of the spray nozzle plate and/or the holder and as a result at least locally plastically deforming the holder permanently. After the thermoplastic deformation of a seat of the holder, a diameter of the seat of the holder upstream of the spray nozzle plate exceeds a diameter of the seat of the holder downstream of the nozzle plate. The thermoplastic holder may have a tapered seat, where the smallest cross section of the tapered seat is smaller than the spray nozzle plate, where a widest side of the tapered seat is pointing towards a supply side of the liquid. | 2017-10-05 |
20170281881 | COUNTERBALANCED NASAL BULB ASPIRATOR - A nasal bulb aspirator that can be sized to fit the needs of infants through adults and is designed to ensure that the tip remains hygienically intact by a one-way valve and a counterbalance system that prevents the tip from touching surrounding surfaces, thereby limiting cross contamination from possibly resistant pathogens. | 2017-10-05 |
20170281882 | INHALATION DEVICE - An inhalation device ( | 2017-10-05 |
20170281883 | LIQUID TANK, ATOMIZER AND ELECTRONIC CIGARETTE HAVING SAME - An exemplary liquid tank for an atomizer includes a bottom part, a liquid outlet, a first air inlet, a first porous liquid blocking element, and a top part. The bottom part has a first end and an opposite second end, and defines a liquid chamber for containing tobacco liquid. The liquid outlet is defined in the second end. The first air inlet is defined in the first end, so that external air can enter the liquid chamber via the first air inlet. The first porous liquid blocking element covers the first air inlet. The first porous liquid blocking element is capable of preventing the tobacco liquid in the liquid chamber from flowing out via the first air inlet, and allows air to pass through. The top part is detachably connected to the first end. The top part and the bottom part cooperatively clamp the first liquid blocking element therebetween. | 2017-10-05 |
20170281884 | Aerosol Forming Device For Use In Inhalation Therapy - The present disclosure relates to the inhalation delivery of aerosols containing small particles. Specifically, it relates to a device that forms drug containing aerosols for use in inhalation therapy. In a device aspect of the present disclosure, a device for delivering drug containing aerosols for inhalation therapy is provided. The device includes a housing and an airway that has a gas/vapor mixing airway. The airway further includes a subassembly, which has a metallic substrate coated on its surface with a composition comprising a drug. | 2017-10-05 |
20170281885 | AEROSOL INHALATION DEVICE - Actuators for a pressurised metered dose inhalers containing (a) a housing adapted to receive an aerosol canister containing a pressurised medicament formulation, (b) a nozzle block defining the receptacle for the aerosol canister valve stem, the expansion chamber or sump, the nozzle channel its external aperture, and (c) a mouthpiece portion comprising a central rounded opening of a defined width and distance from the nozzle aperture and a cylindrical recess, whose central axis is aligned with the central longitudinal axis of the mouthpiece portion and with the central longitudinal axis of the nozzle channel, provide a significant reduction in the non-respirable coarse fraction of the emitted aerosol medicament via inertial impaction and retention in the actuator rather than in the oro-pharynx, with consequent less associated side effects and oral candidiasis in the patient. In addition, the presence of the central rounded opening has minimal, negligible impact on the fine particle dose of the delivered aerosol particles. | 2017-10-05 |
20170281886 | INHALER - An inhaler, preferably for insertion into a nostril, in particular a horse's nostril, with an inhalation valve, which has a movable valve element, whereby the valve element is designed in an annular manner and has an outer edge and an inner edge, whereby the valve element is fastened at the outer edge, the inner edge forms the boundary of an indentation of the valve element, and the inhalation valve has a valve body seat that corresponds to the inner edge. | 2017-10-05 |
20170281887 | SYSTEM AND METHOD FOR USE OF ACOUSTIC REFLECTOMETRY INFORMATION IN VENTILATION DEVICES - The present disclosure relates to a system and method for use of acoustic reflectometry information in ventilation devices. The system and method includes a speaker to emit sound waves into an intubated endotracheal tube (“ETT”) and a microphone to detect returning acoustic reflections. In addition, the system and method includes a reflectometry device in communication with a ventilation device for analyzing timings and amplitudes of the returning acoustic reflections to determine a size of a passageway around an ETT tip, location and size of ETT obstructions, and relative movement of the ETT tip within a trachea. The reflectometry device is also configured to determine a resistance parameter representative of resistance to actual flow of air through the ETT based upon a function of the diameter of the ETT, length of the ETT, and percent obstruction of the ETT, where the resistance parameter is used to calculate the tracheal pressure. | 2017-10-05 |
20170281888 | ORAL MEDICAL APPARATUS - An oral medical apparatus includes a flexible tube with a first portion adjacent a proximal end of the tube and a second portion adjacent to the first portion. A support is located within the upper portion to prevent compression or collapse of the upper portion of the tube. The oral medical apparatus can accommodate a rigid connector that may be directly coupled to an anesthesia breathing circuit or a medical breathing device. | 2017-10-05 |
20170281889 | CPAP PRESSURIZED GAS PERMEABLE MASK CUSHION - The present invention relates to a patient-contacting element ( | 2017-10-05 |
20170281890 | CATHETER GUIDE STRUCTURE - A catheter guide structure is disclosed. Provided are a first guide module provided with an oxygen supply opening, a second guide module connected to the first guide module, and having an internal space that is opened only when the advancement of the catheter into the first guide module is necessary, and a third guide module connected to the second guide module to guide the advancement of the catheter into the first guide module. Accordingly, efficiency is ensured for the process of inserting a catheter in a respiratory system of a patient to suction foreign substances such as sputum present in the respiratory system of the patient assisted by the respirator and the process of removing the catheter such that nursing treatment for the patient can be provided with speed and efficiency. Further, according to the present disclosure, cleaning and sterilization inside and outside the catheter can be performed with ease. | 2017-10-05 |
20170281891 | TRACHEA MONITORING TUBE AND ENDOTRACHEAL CATHETER INCORPORATING THE SAME - A trachea monitoring tube and an endotracheal catheter incorporating the same are characterized in that the trachea monitoring tube is located outside a breathing tube of the endotracheal catheter. More specifically, the breathing tube has a first end portion and a second end portion, the latter of which is inserted into a patient's respiratory duct during use; and the trachea monitoring tube has a monitoring end fixed to the breathing tube and spaced from the first end portion of the breathing tube by a predetermined distance. An endoscope can be inserted into the trachea monitoring tube in order to observe from outside the breathing tube how the breathing tube is inserted into the patient's respiratory duct. | 2017-10-05 |
20170281892 | TRACHEA CANNULA - A trachea cannula comprises a cannula body ( | 2017-10-05 |
20170281893 | METHOD AND APPARATUS FOR MANAGING MOISTURE BUILDUP IN PRESSURISED BREATHING SYSTEMS - A vent in a patient interface has an air-permeable porous portion having an entry surface and an exit surface. The entry surface is formed of or coated with a hydrophobic material or hydrophilic material. The exit surface is formed of or coated with the other of the hydrophobic material and the hydrophilic material. | 2017-10-05 |
20170281894 | HEADGEAR FOR A RESPIRATORY MASK - A headgear for a respiratory mask has first and second straps configured to be connected to each other by first and second buckles. The straps are configured to overlap in a region that contacts the rear of a user's head. The overlapping regions of the first and second straps can be positioned in a bifurcated configuration to improve stability on a user's head. The first and second buckles can feature a glider end through which one of the first and second straps can slide and a strap attachment end to which the other strap is permanently connected. In some embodiments, the first and second buckles have two components that are pivotally connected to allow adjustment of the headgear size whilst in a bifurcated configuration. | 2017-10-05 |
20170281895 | COUPLING AND SUPPORTING OF APPARATUS ON THE FACE AND NECK - Apparatus ( | 2017-10-05 |
20170281896 | APPARATUS AND METHOD FOR FILTERING LIQUID PARTICLES FROM INSPIRATORY GAS FLOW OF A PATIENT BREATHING CIRCUIT AFFILIATED WITH A VENTILATOR AND/OR NITRIC OXIDE DELIVERY SYSTEM - The present disclosure relates to a filter apparatus for filtering liquid from a gas, the apparatus having a first housing having a gas inlet and a gas outlet; a first filter media disposed in the first housing; a second filter media disposed in the housing; and a second housing forming a first collection basin disposed in the flow path between the first filter media and the second filter media, so that a path is defined for the gas flowing from the inlet, through the first filter media, past the collection basin, through the second filter media, and to the outlet. The present disclosure also relates to a method of passing a gas through a coalescing filter media and through a hydrophobic filter media. | 2017-10-05 |
20170281897 | DEVICE FOR PROVIDING SUPPLEMENTAL OXYGEN TO A SUBJECT - According to one aspect, there is provided a device ( | 2017-10-05 |
20170281898 | GAS WITHOUT VENT FOR PATIENT INTERFACE - A gas washout vent, and a patient interface with the gas washout vent, configured to allow patient-exhaled CO | 2017-10-05 |
20170281899 | INFANT SLEEP INDUCING DEVICE - An infant sleep inducing device that in application, simulates the vibrations that occur in an automobile to soothe a restless infant. The infant sleep inducing device generally comprising a playback device connected to an amplifier, a tactile transducer, a battery source, a housing that defines an inner chamber, and a mounting bracket. A top panel is releasably attached to the housing and includes a central opening. The playback device, amplifier, and battery source are contained within the inner chamber in such a way as to define a recessed portion in the inner chamber. The recessed portion is aligned with the central opening of the top panel. The tactile transducer is received within the recessed portion and a head of the transducer is aligned to project through the central opening of the top panel and is in direct contact with a surface area, such as a surface portion of the infant carrier to transmit physical vibrational impulses to the surface area. | 2017-10-05 |
20170281900 | PERSONALIZED AUDITORY-SOMATOSENSORY STIMULATION TO TREAT TINNITUS - Timed stimulation of both somatosensory system and auditory system is controlled, in such a manner, that an individual's brain activity is altered through spike-timing dependent plasticity, thereby reducing or removing tinnitus. | 2017-10-05 |
20170281901 | STORAGE CASE - A storage case accommodates a plurality of medical elongated bodies, which are assembled when used, and includes a plurality of pipe bodies wound to form a ring-like shape that are connected to each other in order to accommodate each of the medical elongated bodies, and a package case that collectively accommodates the plurality of connected pipe bodies. At least two of the pipe bodies are disposed side by side so as to overlap each other in a state in which the center axes of winding are deviated, and the pipe bodies have opening portions arranged so that the medical elongated bodies can be assembled within the storage case using no more than two hands. | 2017-10-05 |
20170281902 | ACCOMMODATION TOOL - An accommodation tool is disclosed with which an operator can easily wind and accommodate a flexible medical elongated body. An accommodation tool winds and accommodates the flexible medical elongated body, for example, a guide wire. The accommodation tool has an inner wall, an outer wall, and an interlock wall. The guide wire is wound around the inner wall. The outer wall defines an accommodation space for accommodating the guide wire between the inner wall and the outer wall, and that is disposed further outward in a radial direction from a centroid of the accommodation tool than the inner wall. The interlock wall interlocks one end portion of the inner wall and one end portion of the outer wall with each other. | 2017-10-05 |
20170281903 | Left Heart Vent Catheter - A method for venting the left ventricle of a patient's heart includes the step of providing a left heart vent catheter that includes an elongate tube having a hollow passageway. The catheter is provided with a plurality of openings and a balloon near the distal end. The balloon can be inflated after the catheter is in place so as to engage a desired part of the heart such as the aortic valve or tricuspid valve and thereby prevent undesired withdrawal of the catheter. The openings near the distal end permit fluid to be withdrawn from the heart through the hollow passageway. After the surgical procedure has been completed, the balloon can be collapsed and the catheter can be withdrawn. | 2017-10-05 |
20170281904 | Method and Apparatus for Intra-Aortic Substance Delivery to a Branch Vessel - A renal flow system injects a volume of fluid agent into a location within an abdominal aorta in a manner that flows bi-laterally into each of two renal arteries via their respectively spaced ostia along the abdominal aorta wall. A local injection assembly includes two injection members, each having an injection port that couples to a source of fluid agent externally of the patient. The injection ports may be positioned with an outer region of blood flow along the abdominal aorta wall perfusing the two renal arteries. A flow isolation assembly may isolate flow of the injected agent within the outer region and into the renals. The injection members are delivered to the location in a first radially collapsed condition, and bifurcate across the aorta to inject into the spaced renal ostia. A delivery catheter for upstream interventions is used as a chassis to deliver a bilateral local renal injection assembly to the location within the abdominal aorta. | 2017-10-05 |
20170281905 | TORQUE DEVICES FOR USE WITH INTRAVASCULAR DEVICES AND ASSOCIATED SYSTEMS AND METHODS - Torque devices for use with intravascular devices and associated systems and methods are disclosed. In some embodiments, a torque device for use with an intravascular device includes a first component having a body defining a tapered opening for receiving a proximal portion of the intravascular device, a first arm extending from the body, and a second arm extending from the body; and a second component movably coupled to the first component, wherein the second component is movable relative to the first component between an open position where the torque device is configured to slidably receive the proximal portion of the flexible elongate member between the first and second arms of the first component and a closed position where the torque device fixedly engages the proximal portion of the flexible elongate member between first and second arms of the first component. | 2017-10-05 |
20170281906 | PERIPHERAL INTRAVENOUS CATHETER WITH WINGED GRIP - A PIVC includes a catheter adapter having a catheter that extends distally from the catheter adapter, and an introducer needle that inserts through the catheter. The introducer needle has a grip component at a proximal end of the introducer needle. The grip component extends outwardly and distally to form a winged grip adjacent the catheter adapter when the introducer needle is inserted within the catheter. The grip component can be rotatable within the catheter adapter to allow repositioning of the winged grip with respect to the catheter adapter. | 2017-10-05 |
20170281907 | TWO-PART INSERTION TOOL AND METHODS - Embodiments herein include an insertion tool for inserting a medical device into another medical device, such as a hemostasis sealing valve, and related methods. In an embodiment, an insertion tool includes a guide sheath and a protection tube. The guide sheath can include a flared proximal end. The guide sheath can further include a central lumen. The guide sheath can further include a locking notch disposed on the inner surface between the proximal end and the distal end. The protection tube can include a flared proximal end. A portion of the protection tube can be situated within the central lumen of the guide sheath. The flared proximal end of the protection tube can be sized to fit within the locking notch and can have an outer diameter larger than portions of the inner surface immediately adjacent to the locking notch. Other embodiments are also included herein. | 2017-10-05 |
20170281908 | VASCULAR ACCESS CONFIGURATION - One embodiment is directed to a system for creating translumenal vascular access, comprising a dilator adaptor member having proximal and distal ends and defining a dilator adaptor lumen therethrough, wherein the dilator adaptor lumen is defined by an inner diameter profile sized to accommodate insertion of one or more portions of a guidewire, and wherein the dilator adaptor is further defined by an outer diameter profile sized to accommodate at least partial insertion of the proximal end of the dilator adaptor into a dilator member lumen formed through a dilator member, the dilator member being coupleable to an introducer catheter member through an introducer member lumen formed through the introducer member. | 2017-10-05 |
20170281909 | MEDICAL DEVICES AND METHODS OF MANUFACTURING SAME - A method of forming a fenestrated tubular support member includes determining a first iso-stiffness curve corresponding to a first function of beam length versus ring width for the first stiffness; determining a second iso-stiffness curve corresponding to a second function of beam length versus ring width for the second stiffness; determining an iso-volume curve corresponding to a third function of beam length versus ring width for a given fenestration volume; identifying a first intersection point where the iso-volume curve intersects the first iso-stiffness curve; and identifying a second intersection point where the iso-volume curve intersects the second iso-stiffness curve. The first section ring width and first section beam length are determined from the first intersection point, and the second section ring width and second section beam length are determined from the second intersection point. | 2017-10-05 |
20170281910 | GUIDEWIRE DEVICE WITH DEPLOYABLE DISTAL END PORTION, SYSTEMS AND METHODS THEREOF - Devices, methods and systems are provided for delivering a guidewire to a target location within an anatomic structure. In one embodiment, a guidewire includes a guidewire body and a deployable guidewire end portion. The deployable guidewire end portion is coupled to a distal end of the guidewire body, the deployable guidewire end portion having a self-expandable structure moveable between a constricted position and an expanded position. With this arrangement, the guidewire end portion, in the expanded position, includes a distal most side surface sized and configured to a traumatically position and brace the guidewire end portion against tissue at the target location. | 2017-10-05 |
20170281911 | ANATOMICAL STRUCTURE ACCESS - A method of accessing a hollow anatomical structure (HAS) of a patient includes puncturing the patient's skin with a needle, upon which is disposed a cannula. A tip portion of the needle is inserted into the HAS. A distal portion of the cannula is advanced distally along the needle, until the distal portion of the cannula is in the HAS. The needle is removed from the HAS while the distal portion of the cannula remains in the HAS. A guide wire is inserted into the HAS via the cannula. The cannula is removed from the HAS while at least a portion of the guide wire remains in the HAS. | 2017-10-05 |
20170281912 | DRUG COATED BALLOON - A balloon catheter includes an inflatable balloon defining an inner and an outer surface. A first biocompatible layer that includes hyaluronic acid is releasably disposed on the outer surface of the balloon. A second drug containing layer is disposed on the first biocompatible layer. The second drug containing layer includes paclitaxel and urea. | 2017-10-05 |
20170281913 | DELIVERY SYSTEM FOR ACTIVE AGENT COATED BALLOON - Embodiments herein include delivery systems for active agent coated balloons and related methods. In an embodiment, a delivery system can include a tunneling sheath and a balloon catheter. The tunneling sheath can include a tubular shaft having an outer diameter and defining a lumen. The tunneling sheath can include a proximal collar defining a lumen. The balloon catheter can include a balloon catheter shaft disposed within the tubular shaft. The balloon catheter shaft can include a lumen for the passage of a fluid therein. The balloon catheter can include an expandable balloon disposed on the balloon catheter shaft. The balloon catheter shaft can include an active agent layer disposed on the expandable balloon. The position of the expandable balloon can be configured to be stationary relative to the tubular shaft as the delivery system is passed through a blood vessel of a patient. Other embodiments are also included herein. | 2017-10-05 |
20170281914 | LOCALIZED TREATMENT OF TISSUES THROUGH TRANSCATHETER DELIVERY OF ACTIVE AGENTS - Embodiments herein include catheters and methods for the localized treatment of tissues through transcatheter delivery of active agents. In an embodiment, a method herein can include inserting a catheter into the lumen of a blood vessel. The catheter can include an inflatable balloon, a first lumen within the shaft for delivering a fluid to inflate the balloon, an active agent delivery port, and a second lumen disposed within the shaft for delivering the active agent composition through the shaft to the active agent delivery port. The method can include inflating the balloon to at least partially occlude the flow of blood through the blood vessel. The method can include ejecting the active agent composition from the active agent delivery port into the blood vessel. In an embodiment, a catheter for treating a localized region of the body with an active agent composition is included. Other embodiments are also included herein. | 2017-10-05 |