10th week of 2014 patent applcation highlights part 72 |
Patent application number | Title | Published |
20140066842 | MICRONEEDLE DEVICES AND METHODS - A medical device, comprising: an array of microneedles, and a coating disposed on the microneedles, wherein the coating comprises: a local anesthetic selected from the group consisting of lidocaine, prilocalne, and a combination thereof; and a local anesthetic dose-extending component selected from the group consisting of alpha 1 adrenergic agonists, alpha 2 adrenergic agonists, and a combination thereof; wherein the local anesthetic is present in an amount of at least 1 wt-% based upon total weight of solids in the coating, and wherein the dose-extending component/local anesthetic weight ratio is at least 0.0001; a medical device, comprising an array of dissolvable microneedles, the microneedles comprising: a dissolvable matrix material; at least 1 wt-% of a local anesthetic selected from the group consisting of lidocaine, prilocalne, and a combination thereof; and a local anesthetic dose-extending component selected from the group consisting of alpha 1 adrenergic agonists, alpha 2 adrenergic agonists, and a combination thereof; wherein the dose-extending component/local anesthetic weight ratio is at least 0.0001, and wherein wt-% is based upon total weight of solids in all portions of the dissolvable microneedles which contain the local anesthetic; a method of extending a topically delivered local anesthetic dose in mammalian tissue using the devices; and methods of making the devices are provided. | 2014-03-06 |
20140066843 | MICRONEEDLE DEVICES AND METHODS - A medical device, comprising: an array of microneedles, and a coating disposed on the microneedles, wherein the coating comprises: a local anesthetic selected from the group consisting of lidocaine, prilocaine, and a combination thereof; and a local anesthetic dose-extending component selected from the group consisting of tetracaine, ropivacaine, bupivacaine, procaine and a combination thereof; wherein the local anesthetic is present in an amount of at least 1 wt-% based upon total weight of solids in the coating, and wherein the local anesthetic and dose-extending component are in a non-eutectic weight ratio; a medical device, comprising an array of dissolvable microneedles, the microneedles comprising: a dissolvable matrix material; at least 1 wt-% of a local anesthetic selected from the group consisting of lidocaine, prilocaine, and a combination thereof; and a local anesthetic dose-extending component selected from the group consisting of tetracaine, ropivacaine, bupivacaine, procaine and a combination thereof; wherein the local anesthetic and dose-extending component are in a non-eutectic weight ratio, and wherein wt-% is based upon total weight of solids in all portions of the dissolvable microneedles which contain the local anesthetic; a method of extending a topically delivered local anesthetic dose in mammalian tissue using the devices; and methods of making the devices are provided. | 2014-03-06 |
20140066844 | FLUID COMPONENT ANALYSIS SYSTEM AND METHOD FOR GLUCOSE MONITORING AND CONTROL - Disclosed are methods and apparatuses for determining analyte concentration in a sample such as bodily fluid. Systems and methods disclosed herein can also include a treatment dosing system to infuse or inject a treatment dose (e.g. insulin, dextrose, etc.) and provide glycemic control. The dose of the treatment drug may be based on the patient's calculated sensitivity to treatment dosing, for example. The dose of the treatment drug may be based on the concentration of the analyte or the average value for the concentration of the analyte and/or the rate of change of the value of the concentration of the analyte. Delivery of the treatment drug can be cut off if the determined analyte concentration indicates that continued delivery would be harmful to the patient. | 2014-03-06 |
20140066845 | INJECTION DEVICE HAVING AN ANGLED TIP PORTION - In one embodiment, the handheld injection device includes a first housing having a first axis and a second housing having a second axis. In one embodiment, the second housing is configured to support a needle. In one embodiment, the first axis and a second axis form an adjustable angle between about 180 degrees and about 90 degrees. | 2014-03-06 |
20140066846 | BENEFICIAL AGENT DISPENSER - A dispensing device for use with a beneficial agent has a dispensing package, a dispenser disposed on an end portion of the dispensing package, and an actuator movably disposed along at least a portion of the package between a pre-dispensing state and a dispensing state. One arrangement also provides a beneficial agent dispenser having a dispensing port, an elongate portion and a plunger that is movably disposed relative to a tubular wall of the elongate portion during a dispensing stroke to partially penetrate a separable barrier and expel the beneficial agent through the dispensing port. | 2014-03-06 |
20140066847 | FOOT IMPLANT AND METHOD FOR TREATING A FOOT - A silk mesh used for treating plantar fasciitis and a method of treating plantar fasciitis. The silk mesh optionally comprises a low dose corticosteroid. The method of treating plantar fasciitis comprises inserting a silk, biocompatible surgical mesh over the plantar aspect of the foot to treat plantar fasciitis. | 2014-03-06 |
20140066848 | APPARATUSES AND METHODS FOR MEDICATION ADMINISTRATION - A rectal medication administration device includes a tube, a balloon, a first valved port, and a second valved port. The tube includes a first lumen, a second lumen, and a plurality of holes extending from the first lumen therethrough. The balloon is proximal to the holes, is in communication with the second lumen, and is configured to be inflated to hold the tube in place within a patient's rectum. The first valved port is in communication with the first lumen and opens when connected to a first syringe or infusion set to provide medication transmission therethrough and closes when the first syringe or infusion set is withdrawn. The second valved port is in communication with the second lumen and opens when connected with a second syringe or infusion set to provide fluid to inflate the balloon and closes when the second syringe or infusion set is withdrawn. | 2014-03-06 |
20140066849 | WARMER FOR MEDICAL TREATMENT - A warmer for medical treatment includes a heater including a resist pattern for generating heat on front and back surfaces of the heater, a partition and cover respectively disposed on the front and back surfaces of the heater to surround the heater, thereby forming a passage, through which a fluid flows, together with the heater. The warmer also includes a first connection part for introducing the fluid into the passage, a second connection part for discharging the fluid from the passage, a pore defined in the cover, a filter disposed on an inner surface of a portion of the cover in which the pore is defined, and an air discharger coupled to the cover to discharge air contained in the fluid through the filter and the pore. | 2014-03-06 |
20140066850 | INFUSION PUMP PRESSURE PLATE ADAPTER SYSTEM - A medical infusion pump pressure plate adapter system and components that include a tube set, a control module and a reusable adapter plate in various embodiments. The tube set having a fluid tube for supplying fluid, medication, or nutrients, and an interface card component having a generally flat top surface portion fixed to the exterior surface of the fluid tube at an intermediate location of the fluid tube. The control module having a processor and a chassis with a pumping mechanism for pumping fluid through the fluid tube. Further, the reusable adapter plate has a first end pivotally mounted to the chassis of the control module for long-term pivotal retention and a second end selectively mounted to chassis of the control panel. The reusable adapter plate contains a recessed feature configured for receipt of the interface card component of the tube set. | 2014-03-06 |
20140066851 | MEDICAL DEVICE WITH MEMBRANE KEYPAD SEALING ELEMENT, AND RELATED MANUFACTURING METHOD - A device for delivering fluid to a user includes a housing, a drive motor assembly in the housing, other internal components in the housing, and a keypad external to the housing. The device includes a number of features and elements that enhance its operation, manufacturability, reliability, and user-friendliness. These features and elements include a shock absorbing element for a battery of the device, a keypad actuator layer that overlies a keypad assembly and forms a water resistant seal with the housing, and an offset element for a piezoelectric speaker that is located inside the housing. | 2014-03-06 |
20140066852 | HIGH SHEAR APPLICATION IN DRUG DELIVERY - In this disclosure, methods and systems for drug delivery utilizing high shear are disclosed. In an embodiment, a method comprises (1) subjecting a therapeutic fluid containing a drug to high shear; and (2) obtaining a processed therapeutic fluid, wherein the processed therapeutic fluid contains the drug in nano-size. In an embodiment, a method comprises (1) subjecting a drug carrier and a therapeutic fluid containing a drug to high shear; and (2) obtaining a processed therapeutic fluid, wherein the processed therapeutic fluid contains the drug carrier loaded with the drug. In an embodiment, a method comprises (1) applying high shear to a drug carrier and a therapeutic fluid containing a drug; (2) obtaining a processed therapeutic fluid, wherein the processed therapeutic fluid contains the drug-loaded carrier; and (3) modifying the drug-loaded carrier with a targeting moiety to obtain a modified drug-loaded carrier. | 2014-03-06 |
20140066853 | CONTAINER FOR AN ANAL IRRIGATION SYSTEM - An anal irrigation system includes a tube attachable between an anal probe and a container, and a displaceable pump element. The container includes an exterior wall, an inner wall that defines an inside perimeter of the container, and a bridge piece connected between the exterior wall and the inner wall such that a reservoir space is formed between the exterior wall and the inner wall. The inside perimeter of the container provides a containment space within the container that is sized to contain the tube and the anal probe. An opening is formed in the container and communicates with the reservoir space. The reservoir space is configured to contain irrigation liquid. The displaceable pump element is located in the reservoir space, where the displaceable pump element is adapted to increase pressure in the irrigation liquid. | 2014-03-06 |
20140066854 | CATHETER TUNNELER WITH LARIAT MEMBER - A tunneler device is provided which includes a handle, a shaft supported on distal end of the handle, and a body positioned on a distal end of the shaft. The body supports an extension segment and a lariat member. The lariat member includes a rod that supports a capturing element. The capturing element is at least partially positioned about a perimeter of the extension segment in a spaced apart relationship with the extension segment, wherein the extension segment and the capturing element define an annular channel dimensioned to receive a catheter. | 2014-03-06 |
20140066855 | INTEGRATED MICRONEEDLE ARRAY AND A METHOD FOR MANUFACTURING THEREOF - The invention relates to a method of manufacturing of a microneedle array comprising the steps of selecting a soft production mold comprising a set of microscopic incisions defining geometry of the microneedles, said soft production mold being capable of providing the microneedle array integrated into a base plate; using a filler material for abundantly filling the microscopic incisions of the soft production mold thereby producing the microneedle array with pre-defined geometry integrated into the base plate; wherein for the filler material a water or alcohol based ceramic or polymer-ceramic slurry is selected. The invention further relates to a microneedle array 16, a composition comprising a microneedle array, a system for enabling transport of a substance through a barrier and a system for measuring an electric signal using an electrode. | 2014-03-06 |
20140066856 | MEDICAL ARTICLE SECUREMENT SYSTEMS COMPRISING A BRACKET AND A FLAP - A medical article securement system comprising a bracket and a flap for securing a medical article. The bracket can include a base, and an arm coupled to the base and extending generally parallel to the first major surface of the base. The arm can be spaced a distance from the first major surface of the base to define a channel under the arm that can be dimensioned to receive at least a portion of the medical article. The flap can include a fixed end, and a free end that is movable with respect to the bracket between a first position in which the flap is not positioned over the bracket, and a second position in which at least a portion of the flap is positioned over the bracket to further inhibit movement of the medical article. The fixed end of the flap can be coupled to the bracket. | 2014-03-06 |
20140066857 | Pre-Filled Syringe Identification Tag - An assembly includes a pre-filled syringe including a barrel with a first end and a second, open end, a plunger disposed within the barrel and spaced between the first end and the second, open end, a product disposed in the barrel between the first end of the barrel and the plunger, and an outwardly-directed rim disposed about the barrel at the second, open end. In addition, the assembly includes an identification tag secured to the outwardly-directed rim of the barrel of the syringe with an outwardly-facing surface of the tag overlying the second, open end of the barrel, the tag having an identifier disposed on the surface of the tag, the identifier including data regarding the pre-filled syringe, the product disposed in the barrel, or both. | 2014-03-06 |
20140066858 | VACUUM-OPERATED RETRACTABLE SAFETY SYRINGE - Vacuum-operated safety syringes designed to prevent an accidental needle prick, where the needle of the syringe is retracted after use into a vacuum created within the hollow plunger and/or the syringe barrel of the syringe. Retraction of the needle assembly is accomplished from minimal moving parts according to an exceedingly simple design. In some embodiments, one or more one-way valves prevent airflow into the interior of the syringe barrel and thereby maintain the vacuum that is created during the act of injection. In some embodiments, the plunger of the safety syringe is manufactured to be pre-conditioned at negative pressure. | 2014-03-06 |
20140066859 | ELASTIC SEAL MEMBER FOR PREFILLED SYRINGE - In a prefilled syringe including an elastic seal member to be pierced with a needle for use to eject a protein pharmaceutical preparation therefrom, the elastic seal member ensures smooth and reliable piercing thereof with the needle while reliably preventing an active substance of the protein pharmaceutical preparation from being adsorbed thereon. When a protective film ( | 2014-03-06 |
20140066860 | VOLUME MONITORING DEVICE - An apparatus includes a syringe housing and a plunger slidably received within the syringe housing. A plunger magnet is secured to the plunger. A potentiometer housing is fixed to the syringe housing and includes a potentiometer disposed therein. A wiper magnet is also disposed within the potentiometer housing. Movement of the plunger magnet causes a corresponding movement of the wiper magnet. | 2014-03-06 |
20140066861 | ACTIVE VALVE FOR DRUG DELIVERY - The present invention inter alia relates to a valve arrangement comprising at least two ports, a valve body and a valve piston, wherein the valve piston is at least partially movably arranged in the valve body, wherein the valve arrangement is configured to disable a fluid flow between the at least two ports in a first position of the valve piston in the valve body and to enable the fluid flow in a second position of the valve piston in the valve body, and wherein at least one port of the valve arrangement is arranged in the valve piston and at least one port of the valve arrangement is arranged in the valve body. | 2014-03-06 |
20140066862 | ERGONOMIC SYRINGE SYSTEMS - Ergonomic syringe systems provide attachments that may be used to allow users to dispense or draw in fluid with increased operator comfort and reduced risk of repetitive strain injuries. The disclosure describes supports for holding syringes that permit one-handed operation, handles that are removably attachable to syringe plungers and hand supports that are removably attachable to syringe barrels. | 2014-03-06 |
20140066863 | Cartridge Holder and Method for Assembling a Cartridge Unit for a Drug Delivery Device - A cartridge holder for retaining a cartridge comprising a distal end and a proximal end being spaced apart from one another in the direction of an axis, an interior which is suitable to receive and retain a cartridge in a cartridge retaining section of the interior, and a main part and at least one protrusion which is moveably connected to the main part. The protrusion is arranged to define the radial extension of a subsection of the interior, wherein the subsection is arranged at an axial position which is further away from the distal end than the cartridge retaining section. Furthermore, the protrusion is arranged to vary the radial extension of the subsection when the protrusion is moved with respect to the main part. Moreover, a method for securing a cartridge in a cartridge holder is proposed. | 2014-03-06 |
20140066864 | MICRO NEEDLE AND MICRO NEEDLE DEVICE - The micro needle includes a needle and a body. The needle includes an inclined part including an inclined outer wall, a straight part including a straight outer wall, and a recess having a certain depth along the inclined or straight outer wall. The body is coupled to the needle to move or support the needle. The micro needle apparatus includes a micro needle head part, an infrared generator part, and a power supply part. The micro needle head part includes a plurality of micro needles having front ends protruding out of the micro needle head part. When the micro needles are pressed against a skin, the micro needles arrive at a dermis of the skin. The infrared generator part generates an infrared or far infrared ray to the skin through an inside or outside of the micro needle. The power supply part supplies energy required for the infrared generator part to generate the infrared or far infrared ray. | 2014-03-06 |
20140066865 | PATCH PREPARATION - The present invention provides a patch preparation that has an extremely low moisture permeability, has a sufficient ODT effect, is excellent in drug releasability, and has a preferred handleability. The patch preparation of the present invention includes a support; and a pressure-sensitive adhesive layer containing an adherent polymer and a drug on one surface of the support, wherein: the support has a polyester base layer, an inorganic oxide layer, and a polyester nonwoven fabric layer in the stated order; the polyester base layer has a thickness of 1.0 μm to 16 μm; and the pressure-sensitive adhesive layer is laminated on the polyester base layer. | 2014-03-06 |
20140066866 | METHOD FOR HANDLING ADHESIVE LAMINATE SECTIONS - A method of handling an adhesive laminate, wherein the adhesive laminate is provided releasably adhered to a first web, comprising a plurality of cut or punched sections and wherein adjacent sections of the adhesive laminate remain joined to one another in the longitudinal direction of the web through one or more tie points. A first supporting structure and a second supporting structure adjacent to the first supporting structure are provided. The first web is led over the first supporting structure. A second web is provided and led over the second supporting structure, wherein the second web is oriented such that the release surface of the second web faces the first supporting structure. A leading portion of a first section of adhesive laminate from the first web is attached to the release surface of the second web and the second web is advanced such that the first section of the adhesive laminate is detached from a second section of adhesive laminate and the leading edge of the second section of adhesive laminate is adhered to the second web in a spaced apart configuration from the trailing edge of the first section of the adhesive laminate. A transdermal drug delivery device prepared by such a method. | 2014-03-06 |
20140066867 | DRESSINGS AND METHODS FOR TREATING A TISSUE SITE ON A PATIENT - Dressings, systems, and methods for treating a tissue site on a patient involve allowing liquids from the tissue site or a priming fluid to evaporate and exit the dressing through a liquid-impermeable, vapor-permeable membrane. The dressing is able to process more liquids than would otherwise be possible without evaporation and potentially to create reduced pressure. Other dressings, systems, and methods are disclosed. | 2014-03-06 |
20140066868 | MECHANICAL WOUND THERAPY FOR SUB-ATMOSPHERIC WOUND CARE SYSTEM - A mechanical wound therapy (MWT) system includes a connection for a vacuum source, which is routed through an airtight covering to a porous material positioned over the wound. The porous material may be a tubing network interspaced by a netting material constructed of biologically inert or bioabsorbable material. Alternatively, the porous material may be a layered unified dressing in which layers of mesh, netting or thin perforated film are separated and fixedly attached to functional elements of the dressing (e.g., irrigation tubing) or spacers. The vacuum and irrigation systems may be completely separated. An airtight sealing layer or foldable adhesive sealing layer may seal the dressing and facilitate sealing the dressing to the wound margins. Additional modular devices such as a wound approximating system, positive pressure bladders and adjuvant therapy modules as well as enhanced monitoring technology can be added to synergistically increase the capabilities of each dressing. | 2014-03-06 |
20140066869 | DEODORISING COMPOSITION - The present invention relates to an absorbent article, such as a sanitary towel, impregnated or coated with a deodorizing composition comprising a buffering component, a deodorizing agent, and an antimicrobial agent. Such deodorizing compositions help to reduce or eliminate odours emanating from the bodily fluids absorbed into the article during use. | 2014-03-06 |
20140066870 | Color-Changing Composition And Material - The present disclosure relates to a color-changing composition and to a substrate having the color-changing compositions disposed thereon. The color-changing composition includes a leuco dye, a color-developer and a desensitizer. The color-changing composition changes from a colorless or largely colorless composition to color upon being wetted with an aqueous liquid. The color-changing composition remains colorless or largely colorless prior to exposure to high relative humidity conditions. | 2014-03-06 |
20140066871 | Anatomically Conforming Vaginal Insert With Cover - An anatomically-conforming vaginal insert is formed from a composition, wherein the composition includes a material that is introduced into a vaginal canal as a viscous material at a first temperature and after insertion into the vaginal canal becomes a semi-solid at a second temperature greater than the first temperature, wherein the first temperature is about 20° C. and the material has increased solidity at the second temperature as compared to the first temperature, and wherein the composition is disposed within a over sheet. The vaginal insert can be formulated with a withdrawal device, and the withdrawal device can be attached to the cover sheet. | 2014-03-06 |
20140066872 | Nonwoven Fabrics Comprised of Individualized Bast Fibers - Nonwoven textile fabrics in accordance with the present invention are formed primarily of individualized bast fibers substantially free of pectin. The nonwoven fabric can include staple fibers to a lesser extent than the individualized bast fibers. Individualized bast fibers include fibers derived from the flax and hemp plants. The nonwoven textile fabric is formed into a web while in a dry state and subsequently bonded to produce a nonwoven fabric. | 2014-03-06 |
20140066873 | CRIMPED CONJUGATED FIBER AND NON-WOVEN FABRIC COMPRISING THE FIBER - It is an object of the present invention to obtain crimped conjugated fibers having excellent crimp properties. The present invention provides a crimped conjugated fiber having a crimpable cross-sectional configuration, wherein a cross section of the fiber includes at least two portions: a portion (a) and a portion (b); the portion (a) includes an olefin polymer (A) and the portion (b) includes an olefin polymer (B); the olefin polymer (A) differs from the olefin polymer (B) in at least any one of Mz/Mw, melting point and MFR; and a specific fatty acid amide is added to the olefin polymer (A) and/or the olefin polymer (B). The present invention also provides a non-woven fabric including said crimped conjugated fiber. | 2014-03-06 |
20140066874 | Absorbent Article With Highlighted Active Barrier - An absorbent article is configured for controlled deformation when insulted by a user and includes an absorbent body having a body-facing surface, a garment-facing surface, and a first graphic visible at the body-facing surface; and a deformable top component positioned adjacent to the body-facing surface, the top component having a longitudinal direction, a transverse direction, a longitudinally-extending centerline, a transverse-extending centerline, and a peripheral edge, wherein the top component includes an attached region and a cantilevered region, and wherein the cantilevered region includes a translucent portion through which the first graphic is at least partially visible. The article also includes a fluid shrinkable string attached to the deformable top component in a pattern capable of providing forces to the top component when insulted by a user. | 2014-03-06 |
20140066875 | Absorbent Article With Highlighted Passive Barrier - An absorbent article includes an absorbent core, a garment-facing surface, a body-facing surface, a first graphic visible at the body-facing surface, and a top component affixed to the article body and including an attached region and a cantilevered region, wherein the cantilevered region includes a translucent portion through which the first graphic is at least partially visible. The translucent portion can include a second graphic, wherein the first graphic and the second graphic combine to form the appearance of a third graphic. The article can also include a baffle forming at least part of the garment-facing surface, wherein the baffle includes a baffle graphic, and wherein at least a portion of the article body is translucent such that the baffle graphic is visible at the body-facing surface such that the first graphic and the baffle graphic combine to form the appearance of a fourth graphic. | 2014-03-06 |
20140066876 | ABSORBENT ARTICLE - An absorbent article package ( | 2014-03-06 |
20140066877 | Stretch Laminate, Method Of Making, And Absorbent Article - A stretch laminate includes a first layer including a skinned or skinless elastomer film, the first layer having a surface, and a second layer including a nonwoven material, the second layer having a basis weight of less than about 25 gsm and a surface that is attached to the surface of the first layer. The elastomer film has a strength of an engineering tensile strength, at an engineering strain rate of about 600/s, of at least one of about greater than about 14 MPa for a plain specimen or about greater than about 7 MPa for a notched specimen. A method of making the stretch laminate and an absorbent article having at least one region defined by the stretch laminate are also provided. | 2014-03-06 |
20140066878 | DIAPERS HAVING A ZONED NON-ATTACHABLE BACK SHEET AND METHODS OF MANUFACTURING SAME - According to one embodiment, an absorbent article to be worn about a wearer has a front portion and a back portion. The absorbent article includes an outer layer, an inner layer that is substantially co-extensive with the outer layer, an absorbent layer and one or more fasteners, which are located on the back portion of the absorbent article. The absorbent layer is interposed between the outer layer and the inner layer to form the absorbent article. The outer layer has a central portion between two side portions. The central portion of the outer layer is treated with a chemical to substantially inhibit attachment of the one or more fasteners to the central portion of the outer layer. The one or more fasteners secure the back portion to the outer layer of the front portion. Specifically, the one or more fasteners are configured to secure the back portion to a region of the outer layer which is not treated with the chemical. | 2014-03-06 |
20140066879 | Dispense Interface Assembly - The invention is related to an apparatus comprising an inner body of a dispense interface and a manifold, wherein the inner body comprises a recess configured to receive a distal needle from a distal end of the inner body, a first fluid reservoir and a second fluid reservoir, and wherein the manifold comprises a filling block configured to redirect flow, a fluid groove arrangement configured to provide a fluid connection to the filling block, wherein the inner body and the manifold are assembled such that there is formed a channel providing a fluid connection from the first fluid reservoir and the second fluid reservoir, respectively, via the fluid groove arrangement and the filling block to the recess. The invention is further related to a drug delivery device comprising an apparatus of the aforementioned kind | 2014-03-06 |
20140066880 | Selectively Controlling Fluid Flow Through A Fluid Pathway - Systems and methods for controlling fluid delivery via a manually administrable medication container to a patient through a fluid delivery pathway are provided. The systems and methods described herein incorporate rules-based clinical decision support logic to drive a flow control valve within a flow pathway based on a determination of whether or not an IV fluid connected to an input port on the pathway is appropriate for patient administration by considering such factors as patient-specific clinical circumstances, current medical orders, and accepted delivery protocols. Related apparatus, systems, methods and articles are also described. | 2014-03-06 |
20140066881 | CARDIAC RESUSCITATION METHODS AND KITS - The invention provides methods of improving circulation in a subject undergoing a cardiac resuscitation protocol, reducing the risk of stroke in a subject undergoing a cardiac resuscitation protocol, improving the efficacy of cardiac resuscitation in a subject undergoing a cardiac resuscitation protocol, and providing cardiac resuscitation to a subject having cardiac arrest. Also provided are kits including a composition containing at least one vasoconstrictor formulated for systemic administration, and a composition containing at least one vasodilator formulated for nasal administration. | 2014-03-06 |
20140066882 | MEDICAL ARTICLE SECUREMENT SYSTEMS COMPRISING INDICIA AND METHODS OF USING SAME - A medical article securement system comprising indicia and methods of using same. The indicia can include a representation of a medical article, such that the indicia mimics the appearance of the medical article and provides a visual cue for coupling the medical article to the medical article securement system. The systems can further include a bracket that can comprise the indicia. Methods can include orienting the medical article relative to the medical article securement system in an orientation that matches the indicia, and coupling the medical article to the medical article securement system. | 2014-03-06 |
20140066883 | GLUCOSE ALTERATION METHODS - According to some embodiments, a method of treating a subject having diabetes or symptoms associated with diabetes is provided. The method includes delivering a neuromodulation catheter within a vessel (e.g., hepatic artery) having surrounding nerves that innervate the liver (e.g., sympathetic nerves of the hepatic plexus). The method may also include modulating (e.g., disrupting, ablating, stimulating) the nerves by mechanical compression, energy delivery, or fluid delivery. | 2014-03-06 |
20140066884 | SENSOR MODEL SUPERVISOR FOR A CLOSED-LOOP INSULIN INFUSION SYSTEM - An electronic device includes a processor architecture and a memory element that stores instructions that, when executed by the processor architecture, perform a method of controlling an insulin infusion device for a user. The method operates the device in a closed-loop mode to deliver insulin to the user, obtains current insulin-delivered data and current glucose sensor data for the user, and processes historical insulin-delivered data and historical sensor data, to obtain predicted sensor glucose values for a historical time period. The method continues by calculating a difference between the current sensor glucose value and a predicted current sensor glucose value for the most recent sampling period. An alert is generated when the difference exceeds a threshold error amount. | 2014-03-06 |
20140066885 | SAFEGUARDING MEASURES FOR A CLOSED-LOOP INSULIN INFUSION SYSTEM - Processor-implemented methods of controlling an insulin infusion device for a user are provided here. A first method obtains a current insulin on board (IOB) value that estimates active insulin in the user, and compensates a calculated insulin infusion rate in response to the obtained IOB value. A second method supervises the operation of a glucose sensor by obtaining and processing insulin-delivered data and glucose sensor data for the user. An alert is generated if the second method determines that a current glucose sensor value has deviated from a predicted sensor glucose value by at least a threshold amount. | 2014-03-06 |
20140066886 | GENERATION OF TARGET GLUCOSE VALUES FOR A CLOSED-LOOP OPERATING MODE OF AN INSULIN INFUSION SYSTEM - A 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 start-up module. The start-up module is operated to initiate a closed-loop mode of the infusion device and to obtain a most recent sensor glucose value for the user. The start-up module also calculates a difference between the most recent sensor glucose value and a target glucose setpoint value. When the difference is less than or equal to a threshold value, the closed-loop insulin infusion rate is adjusted over time, based on a fixed final target glucose value that is derived from the target glucose setpoint value. When the difference is greater than the threshold, the infusion rate is adjusted over time, based on a dynamic final target glucose value that decreases over time toward the target glucose setpoint value. | 2014-03-06 |
20140066887 | SAFEGUARDING TECHNIQUES FOR A CLOSED-LOOP INSULIN INFUSION SYSTEM - Processor-implemented methods of controlling an insulin infusion device for a user are provided here. A first method obtains and analyzes calibration factors (and corresponding timestamp data) for a continuous glucose sensor, and regulates entry into a closed-loop operating mode of the infusion device based on the calibration factors and timestamp data. A second method obtains a most recent sensor glucose value and a target glucose setpoint value for the user at the outset of the closed-loop mode. The second method adjusts the closed-loop insulin infusion rate over time, in response to the sensor glucose value and the setpoint value. A third method calculates an upper insulin limit that applies to the insulin infusion rate during the closed-loop mode. The insulin limit is calculated based on a fasting blood glucose value of the user, a total daily insulin value of the user, and fasting insulin delivery data for the user. | 2014-03-06 |
20140066888 | 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. | 2014-03-06 |
20140066889 | GENERATION AND APPLICATION OF AN INSULIN LIMIT FOR A CLOSED-LOOP OPERATING MODE OF AN INSULIN INFUSION SYSTEM - A controller for an insulin infusion device includes a processor device and a memory element that cooperate to provide a processor-implemented closed-loop insulin limit module. The insulin limit module is operated to obtain: a fasting blood glucose value of a user; a total daily insulin value of the user; and fasting insulin delivery data that is indicative of insulin delivered to the user during a fasting period. The insulin limit module calculates a maximum insulin infusion rate for the user based on the fasting blood glucose value, the total daily insulin value, and the fasting insulin delivery data. The maximum insulin infusion rate is applicable during a period of closed-loop operation of the insulin infusion device. | 2014-03-06 |
20140066890 | USABILITY FEATURES FOR INTEGRATED INSULIN DELIVERY SYSTEM - Various systems and methods for improving the usability of continuous glucose monitors and drug delivery pumps are described. | 2014-03-06 |
20140066891 | Devices and Methods for Modulating Medium Delivery - Devices, systems and methods for controlling, regulating, altering, transforming or otherwise modulating the delivery of a substance to a delivery site. The devices, systems and methods optimize the delivery of the substance to an intended site, such as a vessel, vascular bed, organ and/or other corporeal structures, while reducing inadvertent introduction or reflux substance to other vessels, vascular beds, organs, and/or other structures, including systemic introduction. | 2014-03-06 |
20140066892 | INSULIN ON BOARD COMPENSATION FOR A CLOSED-LOOP INSULIN INFUSION SYSTEM - An electronic controller for an insulin infusion device includes a processor architecture and at least one memory element. The memory element stores executable instructions that, when executed by the processor architecture, provide an insulin on board (IOB) compensation module to estimate a current IOB value that indicates an amount of active insulin in the body of the user, calculate an IOB rate based at least in part on the estimated current IOB value, determine an adjusted insulin infusion rate based at least in part on the calculated IOB rate and an uncompensated insulin infusion rate, select a final insulin infusion rate for the device, and provide the selected final insulin infusion rate to regulate delivery of insulin by the device. | 2014-03-06 |
20140066893 | Roller Clamp - A roller clamp includes at least two opposing and spaced apart side walls, a guide wall, a further wall opposite the guide wall defining an aperture therethrough, a hollow body and a roller. The hollow body has a body aperture therethrough. The roller comprises a roller wheel having two axial projections protruding from a center of each side of the roller. Each side wall is provided with an opposing guide groove on the interior surface thereof. The two axial projections of the roller wheel are slidingly seated in the guide grooves so that the roller can move in the aperture of the further wall as the projections slide in the grooves. At least one respective long edge of each corresponding guide groove is provided with at least one notch. The resulting at least one pair of corresponding notches can at least partially seat the two projections. | 2014-03-06 |
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. | 2014-03-06 |
20140066895 | ANATOMIC DEVICE DELIVERY AND POSITIONING SYSTEM AND METHOD OF USE - An anatomic device delivery and positioning system has a stabilizing guide wire for placement of a catheter or other medical device or material into a vessel or cavity of a tissue or organ within a body of a living subject into which the guide wire is insertable. The guide wire includes an elongated member having a proximal end and a distal end, the proximal end to extend out of the body and the distal end to extend into the body, the distal end having an expandable portion that expands from a compressed condition when inside of a delivery tube or catheter to an expanded condition when outside of the delivery tube or catheter. A method is also disclosed of performing a percutaneous procedure within a vessel or cavity of a tissue or organ of a subject using the guide wire, particularly but not exclusively involving a heart procedure. | 2014-03-06 |
20140066896 | INFLATABLE MEDICAL DEVICES - An inflatable structure for use in biological lumens and methods of making and using the same are disclosed. The structure can have an inflatable balloon encircled by a shell. The shell can have proximal and distal tapered necks, longitudinally-oriented flutes, and apertures at the proximal and distal ends of the shell. The apertures can be recessed in the flutes in the necks. The shell can also have fiber reinforced walls. | 2014-03-06 |
20140066897 | RETRACTABLE SHEATH DEVICES, SYSTEMS, AND METHODS - The invention is directed to delivery medical devices that enable consistent “on-demand” delivery of therapeutic agents to a vessel. The medical device of the current invention comprises retractable sheath comprising neckable elements. The medical device of the current invention comprises an expandable member, a hydrophilic coating comprising at least one therapeutic agent about the expandable member or structural layer and a retractable outer sheath with a selectively permeable microstructure. The design and methods disclosed herein ensures that therapeutic agent delivery occurs essentially only during retraction of the outer sheath, minimizing coating and/or therapeutic agent loss to the bloodstream and providing controlled delivery to the treatment site. | 2014-03-06 |
20140066898 | RETRACTABLE SHEATH DEVICES, SYSTEMS, AND METHODS - The invention is directed to delivery medical devices that enable consistent “on-demand” delivery of therapeutic agents to a vessel. The medical device of the current invention comprises retractable sheath comprising neckable elements. The design and methods disclosed herein ensures that therapeutic agent delivery occurs essentially only upon necking of the outer sheath, minimizing coating and/or therapeutic agent loss to the bloodstream and providing controlled delivery to the treatment site. | 2014-03-06 |
20140066899 | HEMOSTASIS VALVE AND SYSTEM FOR GUIDE CATHETER CONTROL - A combined hemostasis valve and drive mechanism is provided. The hemostasis valve has a valve body with a first and second leg. The first leg has a proximal port, a distal port and a lumen extending between the proximal port and the distal port. At least one valve is located in the lumen adjacent the proximal port to permit an interventional device to be passed therethrough. The second leg extends at an angle relative to the first leg and is in fluid communication with the first leg. A rotating male luer lock connector is rotatably connected to the first leg proximate to the distal port. It is configured to secure a guide catheter and has a driven member. The drive mechanism has a drive member removably interfacing with the driven member and a motor operatively connected to the drive member. The motor rotates the guide catheter about its longitudinal axis in a first direction and opposing second direction in response to rotation of the motor in a first direction about an axis of the motor and an opposing second direction about the axis of the motor, through rotation of the drive member, driven member and rotating male luer lock connector. | 2014-03-06 |
20140066900 | SYSTEM FOR GUIDE CATHETER CONTROL - A system for the advancement or retraction of a guide catheter has a base member, support, linear actuator and bedside support. The base member has a hemostasis valve affixed which includes a valve body with a first leg having a proximal port, a distal port and a lumen with a linear axis extending between the proximal port and the distal port. At least one valve is located in the lumen adjacent the proximal port to permit an interventional device to be passed therethrough. The valve body has a second leg extending at an angle relative to the first leg and has a lumen in fluid communication with the lumen of the first leg. The support is affixed to the base member such that it functions to move the base member and its affixed valve in concert with the movement of the linear actuator along its linear axis. The liner actuator to which the support is affixed has a linear axis along which it may be advanced or retracted in a continuous or incremental manner. The bedside support is slidingly affixed to the linear actuator to allow the linear actuator to move relative to the bedside support. | 2014-03-06 |
20140066901 | Systems, Devices and Methods for Providing Therapy with Image Guidance - Systems, devices, and methods comprising an instrument for treating an anatomical opening such as a paranasal sinus. | 2014-03-06 |
20140066902 | DEVICE AND A SYSTEM FOR DELIVERY OF BIOLOGICAL MATERIAL - The present invention provides a device and a system for the delivery of biological material across the biological tissue. The device may be for the programmed delivery of biological material through a needle or a micro-needle or micro-needles or biodegradable micro-needles. | 2014-03-06 |
20140066903 | Drainage System for Cerebrospinal Fluid - The object of providing a cerebrospinal fluid drainage system | 2014-03-06 |
20140066904 | Packaged Catheter Assembly - The present invention relates to a packaged catheter assembly comprising: a catheter assembly comprising a catheter shaft and a catheter sleeve mounted on the catheter shaft; and packaging for the catheter assembly, in which the catheter assembly is packaged, wherein the packaging is openable from one end thereof and wherein the catheter sleeve is mounted on a distal end of the catheter shaft, and wherein the distal end of the catheter shaft and the catheter sleeve are disposed at or towards the openable end of the packaging. | 2014-03-06 |
20140066905 | Catheter Grip and Catheter Assembly - A catheter grip and catheter assembly are provided. The catheter grip includes a body portion adapted to extend circumferentially around a catheter shaft of the catheter assembly to facilitate gripping of the catheter shaft by a user. The catheter grip also includes a head portion through which the catheter shaft can be fed and a biasing mechanism. The biasing mechanism biases the body portion and the head portion away from one another. | 2014-03-06 |
20140066906 | System and apparatus for delivering a laser beam to the lens of an eye - A system and apparatus for increasing the amplitude of accommodation and/or changing the refractive power and/or enabling the removal of the clear or cataractous lens material of a natural crystalline lens is provided. Generally, the system comprises a laser, optics for delivering the laser beam and a control system for delivering the laser beam to the lens in a particular pattern. There is further provided a range determining system for determining the shape and position of the lens with respect to the laser. There is yet further provided a method and system for delivering a laser beam in the lens of the eye in a predetermined shot pattern. | 2014-03-06 |
20140066907 | STEERABLE LASER PROBE - A steerable laser probe may include an actuation structure, a nosecone fixed to the actuation structure by one or more links and one or more link pins, a flexible housing tube, and an optic fiber disposed in the flexible housing tube and the actuation structure. A compression of the actuation structure may be configured to gradually curve the flexible housing tube and the optic fiber. A decompression of the actuation structure may be configured to gradually straighten the flexible housing tube and the optic fiber. | 2014-03-06 |
20140066908 | System and method for improving the accommodative amplitude and increasing the refractive power of the human lens with a laser - A system and method for increasing the amplitude of accommodation and/or changing the refractive power of lens material of a natural crystalline lens is provided. Generally, there is provided methods and systems for delivering a laser beam to a lens of an eye in a plurality of patterns results in the increased accommodative amplitude and/or refractive power of the lens. There is further provided a system and method of treating presbyopia by increasing both the flexibility of the human lens and the depth of field of the eye. | 2014-03-06 |
20140066909 | DEVICE AND PROCEDURE TO TREAT PRESBYOPIA - A treatment apparatus for surgical correction of presbyopia or defective eyesight in an eye of a patient. The treatment apparatus includes a laser device configured to treat lens tissue of the eye by irradiation of pulsed laser radiation with the laser radiation being focused on target points arranged in a pattern within the lens. An interface supplies measurement data on parameters of the eye and/or defective-eyesight data on the eyesight defect to be corrected in the eye, and defines a volume located within the lens using the supplied measurement data and defective-eyesight data, the volume being defined so as to achieve the desired correction of presbyopia or defective eyesight when removed. | 2014-03-06 |
20140066910 | MEDICAL DEVICES AND METHODS INCORPORATING FRUSTRATED TOTAL INTERNAL REFLECTION FOR ENERGY-EFFICIENT SEALING AND CUTTING OF TISSUE USING LIGHT ENERGY - A medical instrument includes two jaw members, at least one of which creates conditions of frustrated total internal reflection at a tissue-contacting surface when tissue is grasped between the two jaw members. The first jaw member may include an optical element having a tissue-contacting surface. The medical instrument also includes a light source that provides a light beam for sealing tissue. The light source is positioned so that the light beam is totally internally reflected from an interface between the tissue-contacting surface and air when tissue is not grasped by the jaw members. When tissue is grasped by the jaw members, at least a portion of the light beam is transmitted through that portion of the tissue-contacting surface that is in contact with the tissue. The light source may be movably coupled to a jaw member to scan the light beam and/or to change the incident angle based on optical properties of the tissue. | 2014-03-06 |
20140066911 | MEDICAL DEVICES AND METHODS INCORPORATING FRUSTRATED TOTAL INTERNAL REFLECTION FOR ENERGY-EFFICIENT SEALING AND CUTTING OF TISSUE USING LIGHT ENERGY - A medical instrument includes two jaw members, at least one of which creates conditions of frustrated total internal reflection at a tissue-contacting surface when tissue is grasped between the two jaw members. The first jaw member may include an optical element having a tissue-contacting surface. The medical instrument also includes a light source that provides a light beam for sealing tissue. The light source is positioned so that the light beam is totally internally reflected from an interface between the tissue-contacting surface and air when tissue is not grasped by the jaw members. When tissue is grasped by the jaw members, at least a portion of the light beam is transmitted through that portion of the tissue-contacting surface that is in contact with the tissue. The light source may be movably coupled to a jaw member to scan the light beam and/or to change the incident angle based on optical properties of the tissue. | 2014-03-06 |
20140066912 | STEERABLE LASER PROBE - A steerable laser probe may include an actuation structure, a nosecone fixed to the actuation structure by one or more links and one or more link pins, a housing tube having a first housing tube portion with a first stiffness and a second housing tube portion with a second stiffness, and an optic fiber disposed in the housing tube and the actuation structure. A compression of the actuation structure may be configured to gradually curve the housing tube and the optic fiber. A decompression of the actuation structure may be configured to gradually straighten the housing tube and the optic fiber. | 2014-03-06 |
20140066913 | ABLATION DEVICE AND METHOD FOR ELECTROPORATING TISSUE CELLS - A method and system for producing deep lesions without the production of high heat. The method generally includes ablating target tissue cells with a device in communication with an energy generator programmable to ablate tissue using heat energy, electroporation, or a combination thereof. The system generally includes a medical device having a plurality of electrodes at a distal end, and an energy generator in communication with the plurality of electrodes, the generator programmable to deliver alternating current energy between approximately 100 volts RMS and approximately 2000 volts RMS or greater. The generator is further programmable to deliver energy in unipolar mode, bipolar mode, and a combination thereof. | 2014-03-06 |
20140066914 | CRYOTREATMENT DEVICES AND METHODS OF FORMING CONDUCTION BLOCKS - Cryotreatment devices and methods of ablating tissue within the body are disclosed. A cryotreatment device in accordance with an exemplary embodiment of the present invention includes an elongated member having one or more needle-like ablation tips configured to induce necrosis at a target site within the heart. A cooling fluid such as a cryogen may be injected through a lumen extending into the distal portion of the device. The ablation tips can be configured to pierce and ablate surrounding tissue, blocking electrical stimuli that can cause fibrillations or other arrhythmias of the heart. The device may also include means for controlling the transmural depth at which the ablation tips are inserted into the cardiac tissue. Methods of forming a contiguous line of conduction block in accordance with the present invention are also disclosed. | 2014-03-06 |
20140066915 | RENAL RF ABLATION SYSTEM WITH A MOVABLE VIRTUAL ELECTRODE AND RELATED METHODS OF USE - Tissue ablation devices and methods for using tissue ablation devices are disclosed. A tissue ablation device may include an elongate guide member having a distal section defined by a sidewall defining a lumen and having a plurality of openings. The distal section may have a helical shape in a released configuration. The tissue ablation device also may include an electrode having a distal end slideable within the distal section of the guide member. The electrode catheter may have an ablation element disposed thereon. | 2014-03-06 |
20140066916 | HEPATIC NEUROMODULATION DEVICES - According to some embodiments, a method of treating a subject having diabetes or symptoms associated with diabetes is provided. The method includes delivering a neuromodulation catheter within a vessel (e.g., hepatic artery) having surrounding nerves that innervate the liver (e.g., sympathetic nerves of the hepatic plexus). The method may also include modulating (e.g., disrupting, ablating, stimulating) the nerves by mechanical compression, energy delivery, or fluid delivery. | 2014-03-06 |
20140066917 | COOL RF ELECTRODE - Systems and methods for ablating tissue in the living body can include a cool electrode. | 2014-03-06 |
20140066918 | APPARATUS FOR TRANSCUTANEOUSLY TREATING TISSUE - An apparatus for transcutaneously treating tissue beneath a skin surface using radiofrequency energy. The apparatus includes an electrode assembly supported by a handpiece. The electrode assembly includes an electrode configured to transfer the radiofrequency energy through the skin surface to the tissue. A force sensor, which is located in the handpiece, is configured to detect an amount of force applied by the electrode against the skin surface. | 2014-03-06 |
20140066919 | TREATMENT OF NON-ALCOHOLIC FATTY LIVER DISEASE - According to some embodiments, a method of treating a subject having diabetes or symptoms associated with diabetes is provided. The method includes delivering a neuromodulation catheter within a vessel (e.g., hepatic artery) having surrounding nerves that innervate the liver (e.g., sympathetic nerves of the hepatic plexus). The method may also include modulating (e.g., disrupting, ablating, stimulating) the nerves by mechanical compression, energy delivery, or fluid delivery. | 2014-03-06 |
20140066920 | NERVE MODULATION TO TREAT DIABETES - According to some embodiments, a method of treating a subject having diabetes or symptoms associated with diabetes is provided. The method includes delivering a neuromodulation catheter within a vessel (e.g., hepatic artery) having surrounding nerves that innervate the liver (e.g., sympathetic nerves of the hepatic plexus). The method may also include modulating (e.g., disrupting, ablating, stimulating) the nerves by mechanical compression, energy delivery, or fluid delivery. | 2014-03-06 |
20140066921 | BALLOON CATHETER NEUROMODULATION SYSTEMS - According to some embodiments, a method of treating a subject having diabetes or symptoms associated with diabetes is provided. The method includes delivering a neuromodulation catheter within a vessel (e.g., hepatic artery) having surrounding nerves that innervate the liver (e.g., sympathetic nerves of the hepatic plexus). The method may also include modulating (e.g., disrupting, ablating, stimulating) the nerves by mechanical compression, energy delivery, or fluid delivery. | 2014-03-06 |
20140066922 | HEPATIC DENERVATION SYSTEMS - According to some embodiments, a method of treating a subject having diabetes or symptoms associated with diabetes is provided. The method includes delivering a neuromodulation catheter within a vessel (e.g., hepatic artery) having surrounding nerves that innervate the liver (e.g., sympathetic nerves of the hepatic plexus). The method may also include modulating (e.g., disrupting, ablating, stimulating) the nerves by mechanical compression, energy delivery, or fluid delivery. | 2014-03-06 |
20140066923 | GASTRODUODENAL ARTERY NEUROMODULATION - According to some embodiments, a method of treating a subject having diabetes or symptoms associated with diabetes is provided. The method includes delivering a neuromodulation catheter within a vessel (e.g., hepatic artery) having surrounding nerves that innervate the liver (e.g., sympathetic nerves of the hepatic plexus). The method may also include modulating (e.g., disrupting, ablating, stimulating) the nerves by mechanical compression, energy delivery, or fluid delivery. | 2014-03-06 |
20140066924 | NEUROMODULATION METHODS USING BALLOON CATHETER - According to some embodiments, a method of treating a subject having diabetes or symptoms associated with diabetes is provided. The method includes delivering a neuromodulation catheter within a vessel (e.g., hepatic artery) having surrounding nerves that innervate the liver (e.g., sympathetic nerves of the hepatic plexus). The method may also include modulating (e.g., disrupting, ablating, stimulating) the nerves by mechanical compression, energy delivery, or fluid delivery. | 2014-03-06 |
20140066925 | Vibrating Erogenic Stimulator Glove - A vibrating erogenic stimulator glove has an elastic textured surface with a geometric pattern of raised bumps, ridges or other protrusions. A vibration system is embedded within the elastic glove, and an electrical switch controls the electrical connection between a battery and the vibration motors. | 2014-03-06 |
20140066926 | FABRIC ELECTRODE HEAD - An electrode head is disclosed that utilizes electrically conductive or dissipative fabric to exchange electrical energy with tissue. This electrode head may be used for any appropriate application, such as a catheter electrode, a return electrode, or the like. Any appropriate function may be provided by this electrode head, such as tissue ablation, tissue mapping, or providing an electrical ground. | 2014-03-06 |
20140066927 | ELECTROSURGICAL SYSTEM - An electrosurgical system can include an electrosurgical generator, a feedback circuit or controller, and an electrosurgical tool. The feedback circuit can provide an electrosurgery endpoint by determining the phase end point of a tissue to be treated. The electrosurgical system can include more than one electrosurgical tool for different electrosurgical operations and can include a variety of user interface features and audio/visual performance indicators. The electrosurgical system can also power conventional bipolar electrosurgical tools and direct current surgical appliances. | 2014-03-06 |
20140066928 | BATTERY PACK ATTACHED TO A CABLE - An article comprising: (i) a handheld device including (a) a housing, (b) a powered element within the housing: (ii) a battery pack, wherein the handheld device is connected by an external cable to a functional system, wherein the battery pack is attached to the external cable, and wherein the battery pack supplies power to the powered element. | 2014-03-06 |
20140066929 | BI-POLAR SURGICAL INSTRUMENT - A surgical device is disclosed that comprises a shaft member and a pair of electrodes. The shaft member has a pair of electrode channels that open at the distal end of the shaft member, wherein the electrode channels are positioned adjacent to one another. The pair of electrodes are configured to deliver energy, and one of the pair of electrodes are configured to be disposed in each electrode channel such that distal ends of each of the electrodes are arranged to protrude from the distal end of the shaft member. The shaft member further includes at least one lumen opening at the distal end of the shaft member. | 2014-03-06 |
20140066930 | BI-POLAR SURGICAL INSTRUMENT - A surgical device is disclosed that comprises a sleeve member, a shaft member and a pair of electrodes. The shaft member extends distally of the sleeve member and has a pair of electrode channels that open at the distal end of the shaft member, wherein the electrode channels are positioned adjacent to one another. The pair of electrodes are configured to deliver energy, and one of the pair of electrodes are configured to be disposed in each electrode channel such that distal ends of each of the electrodes are arranged to protrude from the distal end of the shaft member. An irrigation annulus is formed about the electrodes. The shaft member further includes at least one lumen opening at the distal end of the shaft member. | 2014-03-06 |
20140066931 | EXTERNAL FIXATION - External fixation systems, and methods for immobilizing joints or fractured bones. An external fixation system may include one or more clamp assemblies connected to one or more rod assemblies at polyaxial joints. Each rod assembly may be length adjustable, and may include a one-way locking mechanism to provisionally lock the length of the rod assembly, and additional locking mechanisms to permanently lock the length of the rod assembly. The system may be deployed pre-assembled as a unit to immobilize a joint or fracture. Another external fixation system further includes a spanning member extending transverse to the rod assemblies. Two or more external fixation systems may be deployed in a stacked configuration on one set of bone pins to immobilize two joints and/or fractures. The systems may be provided in kits including guiding instrumentation, bone pins and pin clamping assemblies for connecting the bone pins to the external fixation systems. | 2014-03-06 |
20140066932 | Intramedullary Fixation Assembly - Intramedullary fixation assemblies ( | 2014-03-06 |
20140066933 | Devices, Apparatuses, Kits, and Methods for Repair of Articular Surface and/or Articular Rim - Embodiments of devices, apparatuses, kits, and methods for repairing and/or augmenting the articular surface and/or articular rim of a joint (e.g., repairing the anterior glenoid rim after an anterior shoulder dislocation). | 2014-03-06 |
20140066934 | Bi-Cruciate Knee System - A tibial tray configured for use in a bi-cruciate retaining knee procedure can include a medial portion, a lateral portion, and an anterior connecting portion. The medial portion can have a medial superior bearing opposing surface, a medial inferior bone opposing surface, and a medial connecting surface. The lateral portion can have a lateral superior bearing opposing surface, a lateral inferior bone opposing surface, and a lateral connecting surface. The anterior connecting portion can connect the medial and lateral portions and cooperate with the medial and lateral portions to define a slot therebetween. The medial and lateral connecting surfaces can be formed on converging planes from respective inferior surfaces to superior surfaces of the tibial tray. | 2014-03-06 |
20140066935 | Joint Arthroplasty Devices and Surgical Tools - Disclosed herein are methods, compositions and tools for repairing articular surfaces repair materials and for repairing an articular surface. The articular surface repairs are customizable or highly selectable by patient and geared toward providing optimal fit and function. The surgical tools are designed to be customizable or highly selectable by patient to increase the speed, accuracy and simplicity of performing total or partial arthroplasty. | 2014-03-06 |
20140066936 | PATIENT SELECTABLE JOINT ARTHROPLASTY DEVICES AND SURGICAL TOOLS - Disclosed herein are methods, compositions and tools for repairing articular surfaces repair materials and for repairing an articular surface. The articular surface repairs are customizable or highly selectable by patient and geared toward providing optimal fit and function. The surgical tools are designed to be customizable or highly selectable by patient to increase the speed, accuracy and simplicity of performing total or partial arthroplasty. | 2014-03-06 |
20140066937 | PATIENT SPECIFIC IMPLANT POSITIONING - Instrument that is made to match the perimeter shape of a Patient Specific Knee Implant (PSKI) with features for locating holes in the distal femur such that the posts or lugs in the femoral implant locate the femoral implant centered medial-laterally within an acceptable degree of precision to prevent overhang of either the medial or lateral side of the femoral implant over the perimeter of the distal femur bone resections. Patient specific implant technology, in which a three-dimensional model of at least a portion of a bone is accessed and a three-dimensional solution volume is defined based on resection cuts used in fitting an implant on the portion of the bone. An outline representation of at least a portion of an outer surface of a periphery of the resultant bone volume is determined and the outline representation is used in one or more operations related to instrument matching. | 2014-03-06 |
20140066938 | PATIENT-SPECIFIC PARTIAL KNEE GUIDES AND OTHER INSTRUMENTS - A surgical kit for unicompartmental knee arthroplasty includes a unitary patient-specific unicompartmental tibial guide and a tibial drill template and other instruments. The tibial guide has a patient-specific body with an inner surface preoperatively configured to nestingly conform and mate in only one position with an anterior portion and a proximal portion of one compartment of a tibial bone of a specific patient. The tibial guide includes a drill guide portion preoperatively configured for drilling first and second anterior holes into the tibial bone for guiding a horizontal tibial resection. The tibial guide includes a vertical resection guide portion preoperatively configured for guiding a vertical resection through the tibial bone before the horizontal resection. | 2014-03-06 |
20140066939 | METHOD AND APPARATUS FOR DISTRACTING A JOINT - A method for creating space in a joint formed at the convergence of two bones, comprising applying force to a body part so as to separate the two bones from one another by a distance which is greater than the distance that they are normally separated from one another when the joint is in a healthy state, whereby to distract the joint and create an intrajoint space; inserting an assembly of three balloons into the intrajoint space while the assembly is in a contracted condition; expanding the assembly of three balloons within the intrajoint space; and reducing the force applied to the body part so that the joint is supported on the assembly of three balloons, with the two bones remaining separated from one another by a distance which is greater than the distance that they are normally separated from one another when the joint is in a healthy state. | 2014-03-06 |
20140066940 | ASSISTANT DEVICE AND GUIDING ASSEMBLY FOR PERCUTANEOUS SURGERY - An assistant device for percutaneous puncture is disclosed. The assistance device includes a fixing element, a first rotatable element, a supporting element and a second rotatable element. The fixing element has a first rail, and the first rotatable element is slidably disposed on the first rail. The supporting element is connected to the first rotatable element. The second rotatable element is slidably disposed on the supporting element and has a puncture restraint pore. | 2014-03-06 |
20140066941 | ANTERIOR SPINAL INTERBODY FUSION DELIVERY SYSTEM - A surgical instrument is disclosed comprising a base having a tray, a first member and a second member. A first and second top arm are coupled near the proximal end of the base. At least one bottom finger is coupled to the distal end of the first member and at least one top finger is coupled to the distal end of the first top arm. At least a first lifting arm is located between the first member and the first top arm, said lifting arm comprising a cam for engaging the first top arm. Rotation of an adjustment member positioned near the proximal end of the first member engages at least one lifting arm. As the lifting arm moves towards the distal end of the first member, the cam engages and lifts the first top arm, displacing the first top finger to a separation distance from the bottom finger. | 2014-03-06 |