| 19th week of 2013 patent applcation highlights part 50 |
| Patent application number | Title | Published |
|---|
| 20130116598 | I.V. INFUSION OR BLOOD COLLECTION APPARATUS - An I.V. infusion or blood collection apparatus comprises an I.V. infusion set ( | 2013-05-09 |
| 20130116599 | FLUID DIVERSION MECHANISM FOR BODILY-FLUID SAMPLING - An apparatus includes a housing, a flow control mechanism, and an actuator. At least a portion of the flow control mechanism is movably disposed within the housing. The apparatus further includes an inlet port and an outlet port, and defines a fluid reservoir. The outlet port is fluidically coupled to a second fluid reservoir and is fluidically isolated from the first fluid reservoir. The actuator is configured to move the flow control mechanism between a first configuration, in which the inlet port is placed in fluid communication with the fluid reservoir such that the fluid reservoir receives a first flow of bodily-fluid, and a second configuration, in which the inlet port is placed in fluid communication with the outlet port. | 2013-05-09 |
| 20130116600 | Method and Apparatus for Treating Pelvic Pain - A method and apparatus for treating self-treating internal muscles and trigger points related to pelvic pain in women and men. The apparatus includes a rod having a handle attached to a straight portion at a first end of the rod and a pressure applicator attached to a second end of the rod, where a first curved portion is disposed between the straight portion of the rod and the second end of the rod. In the method of the present invention, a trigger point is located in the patient's pelvic floor, the patient inserts the apparatus either vaginally or rectally to allow contact of the pressure applicator of the apparatus with the pelvic floor, and pressure is applied to the trigger point using the apparatus. | 2013-05-09 |
| 20130116601 | METHOD AND DEVICE FOR NON-INVASIVE AND SELECTIVE DETERMINATION OF BIOMECHANICAL, CONTRACTILE AND VISCOELASTIC PROPERTIES OF SURFACE SKELETAL MUSCLES - The subject of this invention is a measurement method and device for selective and non-invasive determination of biomechanical, contractile and viscoelastic properties (BCVP) of skeletal muscles, muscle parts, tendons and ligaments (subjects of measurements) performed in situ (examine the phenomenon exactly in place where it occurs) by measuring the force at the skin surface above the subject of measurement. The essential parts included of the measurement device include a measurement sensor with a suitably shaped sensor tip, a microprocessor and a supporting part. The innovative measurement device is shaped in such a way that when positioned on the skin surface, the sensor tip is pressed into the skin. Any suitable force or pressure meter can be used to measure the force at the skin surface above the subject of measurement, where the sensor tip position is not affected by the measuring force. | 2013-05-09 |
| 20130116602 | AUTOMATIC ORIENTATION CALIBRATION FOR A BODY-MOUNTED DEVICE - In order to eliminate the need of tiresome and complex calibration procedures for posture-detecting devices, means are provided for determining an orientation of a body-mounted or implanted device ( | 2013-05-09 |
| 20130116603 | Methods and Apparatus for Intracranial Ultrasound Delivery - A method for delivering ultrasound energy to a patient's intracranial space involves forming at least one hole in the patient's skull, advancing at least one ultrasound delivery device at least partway through the hole(s), and transmitting ultrasound energy from the ultrasound delivery device(s). According to various embodiments, ultrasound delivery devices may be advanced into the epidural space, one or both ventricles and/or an intracerebral space of the patient's brain. In alternative embodiments, one or multiple holes may be formed in the skull, and any number of ultrasound delivery devices may be used. Intracranial ultrasound delivery may be used in diagnostic or therapeutic treatment of ischemic stroke, head trauma, atherosclerosis, perfusion disorders and other acute or chronic neurological conditions. | 2013-05-09 |
| 20130116604 | CONTROLLED-SUSPENSION STANDING DEVICE FOR MEDICAL AND VETERINARY USE - The present invention relates to the field of supporting arrangements, devices or systems for the rehabilitation and treatment of patients or animals suffering from motor disabilities resulting from surgery, chronic disorders, accidents and the like. More specifically, the present invention refers to aerial or overhead supporting arrangements, devices or systems that allow the patient or animal under treatment to remain suspended. | 2013-05-09 |
| 20130116605 | ROTATOR CUFF THERAPY DEVICE - A rotator cuff therapy device assists a user in accomplishing orbital motion of the user's arm to provide a therapeutic effect that strengthens and rehabilitates the arms, shoulders, and related joints and tissues. The device may be adjustable so that an unevenly-weighted rotatable portion can be moved along a desired path with varying speed and effort according to a pre-selected friction setting, and while being held in different positions relative to the user's body. This allows the device to be used by people with varying degrees of dexterity, strength, or injury, while targeting different tissues for therapy. | 2013-05-09 |
| 20130116607 | Blood Salvage Sleeve - A blood salvage sleeve comprises an outer surface forming a generally tubular structure with an open end and a closed end and configured for enclosing at least a portion of a patient's limb. An inner membrane is joined to the inner surface of the tubular structure. The inner membrane comprises a plurality of inflatable chambers. The inflatable chambers are disposed along a length of the tubular structure. A plurality of pressure release valves connects adjacent inflatable chambers. A plurality of one-way valves is connected to the inflatable chambers. A vent tubing conducts the released gas. An inlet tubing is connected to at least a first inflatable chamber proximate the open end, in which a pressurized gas, supplied through the inlet tubing, sequentially inflates the plurality of inflatable chambers. | 2013-05-09 |
| 20130116608 | SHRINK-TUBE MEDICAL AND PROTECTIVE DEVICE - A therapeutic, supportive, or protective device is fabricated from a material capable of contracting in response to interacting with heat, cold, a chemical reagent, electromagnetic energy, or mechanical energy. The device is positioned over an anatomical joint or other body part and via a “shrink fit,” conforms to the part, providing a customizable fit. | 2013-05-09 |
| 20130116609 | SUPPORTER - A supporter includes a small number of members and has a simple fitting method. It can give an intraperitoneal pressure rise effect to a supporter wearer, attain retroflexion suppression, and stabilize the sacroiliac joint. The supporter includes a base material which is formed of a knitted fabric by warp knitting and in which a knitting direction of the knitted fabric is set to be a longitudinal direction. Stretchability in the longitudinal direction is given, while stretchability in a short direction is suppressed. It has a back-supporting section that is a central portion of the base material, projection sections provided by projecting upward both end portions disposed on both sides of the back-supporting section, and curved sections each making the vicinity of the boundary between the back-supporting section and each of the projection sections. Each curved section is curved into a shape of approximate “ | 2013-05-09 |
| 20130116610 | ORTHOPEDIC COMPONENT FOR USE WITH AN ORTHOPEDIC BRACE - An orthopedic component for use in orthopedic device includes a rigid frame and a flexible subshell connected to and extending flexibly outwardly from the rigid frame. The subshell may have a shell body and a perimeter edge portion defining a lip extending outwardly from a surface of a shell body and defining a clearance between the shell body and the lip. The subshell may include a plurality of slots and ventilated padding is used in combination with the slots. A tightenable fastener may be adjustably secured to the rigid frame and extend through an opening on the subshell, wherein the first side portion of the subshell is adjustable in location relative to the rigid frame. | 2013-05-09 |
| 20130116611 | SUPPORT FOR HUMAN JOINTS - A support for human joints is disclosed having first and second rods which are connected to each other via articulation means which permits reciprocal rotation of the two rods about a rotation pin. The support includes locking means having a flexible cable which limits rotation between the two rods in an angular direction. The support has first fixing means for fixing a first end of the cable to the first rod or to the articulation means, and second fixing means for fixing a second end of the cable to the second rod or to the articulation means. The first fixing means also has a plurality of hooks. The first end of the flexible cable forms a loop suitable to engage selectively with one of the hooks to vary the anchorage position of the first end of the cable with respect to the first rod. | 2013-05-09 |
| 20130116612 | WEARABLE LIGHT THERAPY APPARATUS - Optical rods which transmit light exteriorly of their length are coupled to one or more lasers at ends. The optical rods are mounted on various carriers or as part of an optical bandage to provide therapeutic light to a portion of a human body. The lasers may be activated at various times in a 24-hour period, while the optical rods are worn by a user. | 2013-05-09 |
| 20130116613 | VETERINARY DRESSING WRAP - A veterinary dressing wrap for positioning and holding a medical dressing on a wound site located on the leg of an animal providing both protection for the leg as well as breathability and moisture control at the wound site. | 2013-05-09 |
| 20130116614 | Methods and Apparatus for Providing an Arteriovenous Fistula - Methods and apparatus for creating an artificial arteriovenous fistula between an artery and an adjacent vein are disclosed. Methods include utilizing a hollow spiral shunt that defines a fluid passageway between a proximal port and a distal port thereof. The spiral shunt is loaded within a delivery device that is transversely advanced through a wall of the artery. A piercing end of the spiral shunt is than exposed and the delivery device is rotated to pierce an opposing wall of the artery and a wall of the adjacent vein with the spiral shunt piercing end. Rotation of the delivery device corkscrews the spiral shunt through the walls of the artery and the vein in order to position the spiral shunt to fluidly connect the artery and vein. Once so positioned, the spiral shunt is released to be deployed between the artery and vein lumens thereby forming an artificial arteriovenous fistula therebetween. | 2013-05-09 |
| 20130116615 | Inflatable cuff with built-in drug delivery device for dynamic drug therapy response to blood pressure incidents - An inflatable cuff in a blood pressure-measurement system is integrated with a drug delivery device. The drug delivery device is configured to automatically deliver a drug dermally or transdermally to the individual in response to the measured blood pressures. | 2013-05-09 |
| 20130116616 | ENHANCEMENT OF PENETRATION AND ACTION - The present invention relates, inter alia, to dermal systems comprising at least one light source and at least one pharmaceutically and/or cosmetically active ingredient. The dermal systems can be employed in order to enhance the penetration and action of the pharmaceutically and/or cosmetically active ingredient. | 2013-05-09 |
| 20130116617 | NEEDLE ASSEMBLY FOR MIXING OF SUBSTANCES - In one aspect of the invention, a needle assembly is provided, including: a body having a proximal end, a distal end, and a channel located therebetween, the body being configured to be mounted to an injector; a needle fixed to the body, the needle having proximal and distal ends, the distal end extending distally from the distal end of the body and being formed for insertion into a patient, the proximal end of the needle being in communication with the channel; and, a filter disposed in the channel proximally of the proximal end of the needle. Advantageously, a needle assembly is provided which permits mixing of at least two substances in preparation for injection, without modification to the associated injector. | 2013-05-09 |
| 20130116618 | CATHETER INCLUDING A BARE METAL HYPOTUBE - Catheter and methods for designing, making, and using catheters are disclosed. An example catheter is a balloon catheter. The balloon catheter may include a proximal shaft. The proximal shaft may be a bare metal hypotube having a skew value of −1.0 to −2.5. A midshaft may be attached to the proximal shaft. A distal shaft may be attached to the midshaft. A balloon may be coupled to the distal shaft. An inflation lumen may be defined that extends from the proximal shaft, through the midshaft, and into the distal shaft. The inflation lumen may be in fluid communication with the balloon. | 2013-05-09 |
| 20130116619 | SAFETY SYRINGE - A safety syringe includes a barrel, a plunger, and a needle hub. The barrel is extended axially and includes a first tube portion, a second tube portion extended from an end of the first tube portion, and a first folded ring flexibly branched and formed on an inner side of the first tube portion and disposed around the axis, such that after the first folded ring is unfolded, the first folded ring is bounded and extended from the first tube portion towards the second tube portion, and includes a movable first flexible portion. The plunger includes a rod extended along the axis. The needle hub is detachably installed in second tube portion. The plunger can be moved to an injecting position, a limit position, and a disposal position with respect to the needle hub. | 2013-05-09 |
| 20130116620 | AIR TRAP FOR INTRAVENOUS PUMP - An intravenous pump system includes an intravenous pump having an air bubble detector, a separate air trap module and a patient line. The air trap module is connectable to a set interface upon which the pump can operate. The air trap module includes an air chamber capable of receiving fluids and air, a plurality of valves controlling the flow of the fluids and air, and an air vent. The patient line is connectable to the air trap module and to a patient. The air trap module includes an actuator to control the state of the valves to enable, at least during a venting mode, the pump to push air out of the air chamber via the vent without disconnecting the patient from the patient line. | 2013-05-09 |
| 20130116621 | BACTERIUM-BASED MICROROBOT INCLUDING MAGNETIC PARTICLES - Provided is a bacterium-based microrobot, wherein bacteria are attached to a part of a surface of a microstructure including at least one or more magnetic particle, for actuating a bacterium-based microrobot more effectively. | 2013-05-09 |
| 20130116622 | MEDICAL DEVICE - A medical device includes a catheter having an opening formed in a side portion of the catheter, an infusion tubing extending within the catheter along an axial direction of the catheter; an infusion needle disposed at a distal portion of the infusion tubing, a connecting part which bendably connects the infusion needle to the distal portion of the infusion tubing, and a bending unit by which the infusion needle located inside the catheter so as to face the opening is bent at the connecting part at essentially a right angle with respect to the distal portion of the infusion tubing. | 2013-05-09 |
| 20130116623 | PERISTALTIC INFUSION PUMP WITH LOCKING MECHANISM - A medical device includes an interface unit body, which is configured to hold a portion of a flexible infusion tube. A hinge insert is fixed to the interface unit body and is configured to engage a hinge receptacle, which defines a hinge axis, on an infusion pump. A catch insert is fixed to the interface unit body and is configured to lock onto a catch receptacle on the infusion pump upon rotation of the mechanical interface unit about the hinge axis while the hinge insert engages the hinge receptacle, so as to bring the tube into engagement with a peristaltic mechanism of the infusion pump in order to enable the peristaltic mechanism to propel a fluid through the tube. | 2013-05-09 |
| 20130116624 | HOLDER FOR AN INJECTION SYRINGE - The present invention relates to a holder for an injection syringe ( | 2013-05-09 |
| 20130116625 | Medicament Delivery Device - Provided is a medicament delivery device ( | 2013-05-09 |
| 20130116626 | Medical Needle Safety Devices - A safety device for shielding the sharp tip of a medical needle has a needle mount which either directly supports a medical needle, or indirectly supports the needle for instance where the needle is provided as a part of a syringe. A sleeve is carried directly or indirectly on the needle mount and is slidably movable to a needle shielding position where the sleeve surrounds the needle sharp tip. A spring including forwardly projecting spring blades when sufficiently loaded acts on an internal conical surface of the sleeve to drive the sleeve to its shielding position and a locking mechanism then locks the sleeve in that position. A camming mechanism serves to load the spring blades in the course of the use of the safety device such that thereafter the interaction of the blades with the conical surface urges the sleeve to its shielding position, the camming mechanism being activated by movement of the sleeve to expose the needle for use. | 2013-05-09 |
| 20130116627 | Syringe Having Reduced Static Friction - A syringe comprising a cylinder and a plunger arranged in the latter has a sealing element which, with a contact region, abuts an inner wall of the cylinder and seals an annular gap between the plunger and an inner wall of the cylinder. The contact region has a front section which, in the rest state, abuts the inner wall of the cylinder with an abutment pressure. The plunger is connected to the sealing element in such a way that the sealing element does not follow an initial movement of the plunger out of the rest state and such that the sealing element follows a continued movement of the plunger. The abutment pressure between the sealing element and the inner wall in the front section of the contact region decreases during the initial movement. With the syringe, less force is required in order to overcome the static friction between the sealing element and the inner wall of the cylinder. | 2013-05-09 |
| 20130116628 | Recycled Resin Compositions And Disposable Medical Devices Made Therefrom - Syringe plunger rods comprising an elongate body formed from a composition comprising one or more of virgin material, a sterilization-stable recycled resin and a biobased compositions are described. Plunger rods comprising a plurality of ribs, some of which may have a plurality of openings, are also described. The plunger rods requiring less material while maintaining sufficient structural integrity to function properly. | 2013-05-09 |
| 20130116629 | CONNECTOR FOR A FLUID TRANSPORT LINE OF A MEDICAL DEVICE - A connector for a fluid transport line of a medical device including: a first body having a first access port, a second access port, and a first fluid path extending through the first body and directly connecting, for fluid transport, the first access port and second access port; a second body, mountable to the first body, having a third access port, the second body being movable with respect to the first body between (i) a main operating position in which the first fluid path is interrupted and in which a second fluid path is defined and enabled from the first access port to the third access port, and (ii) an auxiliary operating position in which the first fluid path is enabled and in which the second fluid path is interrupted. | 2013-05-09 |
| 20130116630 | LARGE-VOLUME BOLUS PATIENT CONTROLLED DRUG ADMINISTRATION DEVICE - A device for dispensing fluid to a patient enabling either or both of a continuous flow, as well as successive, large-volume boluses. A first reservoir provides a source of fluid under pressure. A bolus flow path provides for the delivery of a bolus dose of fluid and an optional continuous flow path provides a continuous flow rate of fluid. Both flow paths are in fluid communication with the source of fluid. A bolus delivery system in fluid communication with the bolus flow path receives fluid from the first reservoir, expands to pressurize fluid, stores the pressurized fluid, and dispenses the pressurized fluid while avoiding bolus refill until enabled to expand in a subsequent delivery cycle. An actuator releases fluid from the bolus delivery system such that when actuated by the patient, fluid is permitted to flow out of the bolus reservoir to the patient without further action by the patient. | 2013-05-09 |
| 20130116631 | SAFETY NEEDLE ASSEMBLY WITH CORRECT MEDICATION CONNECTION - An adapter is placed between the needle and a conventional fluid store, or medical line. The end of the adapter that connects to the needle assembly is formed to have a configuration that is complementary to that of the hub of the needle assembly, so that the adapter and the needle hub may be readily mated to each other. The other end of the adapter is formed to have another configuration, for example a conventional luer, that is readily connectable to a conventional fluid store, such as a syringe that has a conventional luer. The adapter is formed by inter-fitting two elements to effect an integral locking mechanism to prevent the uncoupling of the fluid store and the adapter, once they are securely coupled. | 2013-05-09 |
| 20130116632 | FLANGED SEALING ELEMENT AND NEEDLE GUIDE PIN ASSEMBLY FOR A FLUID INFUSION DEVICE HAVING A NEEDLED FLUID RESERVOIR - A sealing assembly for a fluid infusion device includes a base plate, a reservoir port receptacle, a flow base component, and a needle sealing element. The receptacle receives the reservoir port, and has proximal and distal ends, and a needle entry in the distal end to receive a hollow needle of a fluid reservoir. The flow base component has an inlet structure defining a fluid chamber, and a needle guide pin protruding therefrom. The end of the guide pin fits within the hollow needle. The needle sealing element has a proximal flange adjacent to the inlet structure, a distal flange opposite the proximal flange, a neck section between the flanges, and a needle opening extending through the neck section. The needle sealing element is positioned within the port receptacle such that the neck section surrounds the end section of the needle guide pin. | 2013-05-09 |
| 20130116633 | ENHANCED ULTRASOUND VISUALIZATION OF INTRAVASCULAR DEVICES - Methods and devices for providing improved ultrasound visibility of medical devices intended for intravascular use are described. The inclusion of gas/solid boundary regions within a medical devices improves the resolution of the device under ultrasound visualization. Gas/solid boundary regions may be provided through the use of embedded gas-filled microlumens, microwells, or enclosed pockets within the medical device. | 2013-05-09 |
| 20130116634 | INTRAVASCULAR DRUG ELUTION-TYPE CATHETER - When the intravascular drug elution-type catheter is inserted into a blood vessel, the elastically deformable portion is formed into a deflated shape and accommodated in the first lumen of the catheter body. When the top end side of the catheter body reaches near a damaged blood vessel wall, the shaft is inserted into the catheter body, the elastically deformable portion is pushed out from the first lumen of the catheter body to elastically return to an inflated shape from the deflated shape, and then the drug holding film presses the blood vessel wall. Thus, the drug eluted from the drug holding film can be infiltrated into the blood vessel wall, The state where the drug holding film is pressed against the blood vessel wall can be maintained without blocking the blood flow toward the peripheral side. | 2013-05-09 |
| 20130116635 | WOUND TREATMENT DEVICE - A wound treatment device comprises a wound surface contacting plug and a cover for covering the wound surface and the plug, wherein said plug consists of a flat textile isolating material comprising at least one first surface layer, one second surface layer and one intermediate space arranged between said surface layers. At least the first surface layer is provided with a biocompatible surface and a structure which enables a liquid to pass and prevents a wound tissue from growing in said structure. The intermediate space is provided with isolating threads elastically holding the first surface layer and the second surface layer at a certain distance from each other. | 2013-05-09 |
| 20130116636 | Ostomy Appliance and Method - An ostomy appliance includes a translucent receptacle for releasably securing to the stoma flange with the gathered ostomy pouch located within the receptacle. No or negligible pressures are applied to the stoma which remains clear and healthy. The user may use the receptacle during times of physical or personal activity when additional discreteness is desired. The pouch may be made of a material having a thermochromatic ink which changes color with heat such that the user may visually inspect and identify when waste is present in the pouch. | 2013-05-09 |
| 20130116637 | CONTROL CIRCUIT AND METHOD FOR NEGATIVE PRESSURE WOUND TREATMENT APPARATUS - A negative pressure wound therapy apparatus can include a wound dressing, a fluid collection container, a vacuum pump comprising a pump motor, and tubing. Additionally, the apparatus can include a pressure sensor that measures a pressure in the tubing. One or more tubes can channel a fluid between the wound dressing, the fluid collection canister, and the pump. In addition, first and second control circuits can be provided for controlling the pump motor without using a processor. The first control circuit can generate a difference signal between a desired pressure input and a pressure sensor input, and can further generate a motor control signal responsive to the difference signal. Moreover, a second control circuit can provide an override signal based at least in part on the difference signal and at least one reference signal. The override signal beneficially overrides the motor control signal to prevent the pump motor from stalling. | 2013-05-09 |
| 20130116638 | REDUCED-PRESSURE TREATMENT SYSTEMS WITH RESERVOIR CONTROL - A reduced-pressure system for delivering reduced pressure for medical purposes to a desired site and to receive fluids in one instance includes a reservoir having an interior space operable to contain the fluids. A reduced-pressure delivery conduit is placed in fluid communication with the interior space for delivering the reduced pressure to the desired site. A source conduit and a pressure sensor conduit are placed in fluid communication with the interior space. A pressure sensor is placed in fluid communication with the pressure sensor conduit. A reduced-pressure source is placed in fluid communication with the source conduit. A reduced-pressure control unit is associated with the pressure sensor and the reduced-pressure source and is operable to receive pressure data from the pressure sensor and supply data from the reduced-pressure source and to determine when a reservoir-full/blockage condition exists. Other systems and methods are presented. | 2013-05-09 |
| 20130116639 | REDUCED-PRESSURE, MULTI-ORIENTATION, LIQUID-COLLECTION CANISTER - A liquid-collection canister includes a liquid collection chamber defined by at least one wall and a first and second gas-communication pathway formed within the at least one wall. A first aperture is positioned between the first gas-communication pathway and the liquid collection chamber to allow gaseous communication between the liquid collection chamber and the first gas-communication pathway. A second aperture is positioned between the second gas-communication pathway and the liquid collection chamber to allow gaseous communication between the liquid collection chamber and the second gas-communication pathway. A first and a second liquid-air separator are positioned over the first aperture and the second aperture, respectively, to substantially prevent liquid passing through the first and second apertures. | 2013-05-09 |
| 20130116640 | LAMINAR DRESSINGS, SYSTEMS, AND METHODS FOR APPLYING REDUCED PRESSURE AT A TISSUE SITE - A system for applying a reduced pressure at a tissue site includes a reduced pressure source, a porous pad in fluid communication with the reduced pressure source, and a drape positionable over the porous pad to seal the porous pad at the tissue site. The porous pad includes a plurality of channel walls to form a plurality of channels between the channel walls. The channel walls are substantially liquid impermeable to prevent movement of a liquid through the channel walls but are gas permeable to allow movement of a gas through the channel walls as reduced pressure is applied at the tissue site. The liquid impermeability of the channel walls and the application of reduced pressure causes flow of the liquid to occur through the plurality of channels. | 2013-05-09 |
| 20130116641 | PROVISION OF WOUND FILLER - A process of manufacturing a wound dressing filler and/or wound dressing. | 2013-05-09 |
| 20130116642 | OSTOMY PORT GAS RELEASE MECHANISM - Controlled or automatic release of gas from ostomy ports. In some embodiments a gap is selectively formed between a cap and a body of an ostomy port. In some embodiments, a dedicated gas exhaust lumen is provided as part of the port. Optionally, the gas release uses a filter to reduce odor. | 2013-05-09 |
| 20130116643 | OSTOMY POUCH APPARATUS WITH CLOSABLE OPENING - An ostomy pouch apparatus including a first and second sheets of flexible sheet material having perimeter edge portions and respective broad surface portions, the first and second sheets joined at the perimeter edge portions to form a pouch having an interior portion between the first and second sheets. The apparatus includes a waste admitting opening on the broad surface portion of the first sheet for admitting and subsequently removing a waste holding bag disposed within the interior portion of the pouch, and a coupling disposed about the waste admitting opening for connecting to a flange secured to a waste releasing opening on a patient. At least one of the broad surface portions of the pouch includes a closable opening for admitting a waste holding bag, and that reduces the risk of spillage of the contents of the waste holding bag as it is removed from the pouch. | 2013-05-09 |
| 20130116644 | Non-Tacky Wetness Indicator Composition for Application on a Polymeric Substrate - The invention describes a color-developing composition that contains at least three major components: (1) a leuco dye or a combination of leuco dyes, (2) an color-developer or a combination of color-developers that can form colored complexes with the leuco dyes, and (3) a desensitizer to temporarily remove the effect of the developer so the leuco dye appears in its colorless form. An optional binder may be included so that the composition may be applied to a substrate as an ink. The ink composition may be applied to synthetic polymeric substrates and other substrates that are incorporated into absorbent articles or personal care products. | 2013-05-09 |
| 20130116645 | Absorbent Foam Tape And Related Methods Thereof - A foam tape having an adhesive layer for positioning against a tissue surface, a porous layer including a plurality of pores adapted to absorb fluid, a breathable layer configured to allow the passage of vapor therethrough, and an optional release layer is disclosed. The foam tape may be utilized as a wound dressing or in a compression bandage system. | 2013-05-09 |
| 20130116646 | ABSORBENT ARTICLE WITH DUAL CORE - An absorbent article. The absorbent article includes a topsheet having a body contacting surface, a backsheet joined to said topsheet, and an absorbent core disposed between the topsheet and the backsheet, wherein the absorbent core has an upper layer and a lower layer. | 2013-05-09 |
| 20130116647 | TUCKED FASTENER FOR IMPROVED FASTENER PERFORMANCE - An absorbent garment has a chassis. A first region of the chassis includes a first panel and at least one first side panel. A second region of the chassis includes a second panel and at least one second side panel. A resilient fastening component is permanently attached to an inner surface of the at least one first side panel and releasably attached to an outer surface of the at least one second side panel. At least one of the first region and the second region is folded at least twice such that at least portions of the at least one first side panel and the at least one second side panel are positioned between the first and second panels and the resilient fastening component is tucked between the folded absorbent assembly and lies in a plane parallel to a plane in which a first part of the absorbent assembly lies. | 2013-05-09 |
| 20130116648 | RUBBER STOPPER FOR MEDICAL TREATMENT - This invention is a rubber stopper for medical treatment, which is obtained by molding a resin composition containing a component (A): at least one of a block copolymer having at least two of a polymer block P containing a vinyl aromatic compound as the core and at least one of a polymer block Q containing a conjugated diene as the core and a hydrogenated block copolymer thereof, a component (B): a hydrocarbon-based softening agent for rubbers, and a component (C): a polyolefin-based resin, wherein the resin composition contains a specified amount of the component (C) based on the total amount of the component (A) and the component (B), and the resin composition has a specified molecular weight distribution. | 2013-05-09 |
| 20130116649 | Method and System For The Safety, Analysis and Supervision of Insulin Pump Action and Other Modes of Insulin Delivery in Diabetes - An insulin delivery supervisor (IDS) with a safety analysis and supervision function that can reside between the insulin request and the insulin delivery and can intercept any excessive insulin requests before the insulin was delivered. The IDS can be implemented in any system based on insulin pump or pen and will work with either SMBG or CGM modes of blood glucose monitoring. | 2013-05-09 |
| 20130116650 | DIALYSIS APPARATUS AND METHOD FOR CONTROLLING A DIALYSIS APPARATUS - Dialysis apparatus including a blood treatment unit having a dialysate chamber and a blood chamber separated by a semipermeable membrane, a dialysate circuit presenting a supply line and a discharge line connected to the blood treatment unit, a preparation device for preparing a dialysate containing a substance present in the blood too and a regulator regulating the concentration of the substance in the dialysate. A blood circuit to circulate extracorporeal blood through the blood chamber; a controller that determines a value representative of the concentration of the substance in the blood and are programmed for driving the regulator as a function of the determined value representative of the substance concentration in the blood such that the substance concentration in the dialysate tends towards the substance concentration in the blood. | 2013-05-09 |
| 20130116651 | CATHETER AND METHOD - The presently disclosed subject matter relates to a catheter and method. The catheter can be configured as a guiding catheter with a flexible shaft section, a hub disposed at a proximal portion of the shaft section, and a strain relief section that surrounds a predetermined proximal-side range of the shaft section. A distal end of the strain relief section can be moved along an axial direction of the shaft section at least toward the side where the hub is located. | 2013-05-09 |
| 20130116652 | CATHETER CANNULA WITH ANCHORING ELEMENTS, CATHETER INCLUDING THEREOF, AND/OR CATHETERIZATION METHOD USING - Catheter cannula, catheter, and catheterization method, for administering a fluid or/and substance to, or for draining a fluid or/and substance from, a treatment space of a body vessel, duct, or cavity. In some embodiments the cannula includes: an elongated flexible tube mountable on a needle, and having an invasive section and a non-invasive section; and at least one anchoring element protruding from, a surface of the invasive section in a manner such that an operative configuration of each anchoring element increases outer circumferential diameter of the cannula to an extent less than lumen diameter of the body vessel, duct, or cavity, at the treatment space, thereby anchoring the invasive section to inside the body vessel, duct, or cavity, at the treatment space. The catheter includes a needle and the cannula mounted thereupon. | 2013-05-09 |
| 20130116653 | INTRAVENOUS INFUSION DEVICE WITH DRIP CHAMBER AND ELASTIC FLOAT - An intravenous infusion device ( | 2013-05-09 |
| 20130116654 | Aortic Occlusion Catheter - An cardioplegic fluid delivery catheter includes an expandable member for occluding the ascending aorta of a patient. A length of the catheter allows the distal end to be within the ascending aorta while the proximal end extends from a peripheral artery. The delivery catheter has a multi-lumen construction with a primary lumen extending configured to allow a cardioplegic fluid to be delivered to the aorta. Secondary lumens provide for balloon inflation and aortic root pressure monitoring. The delivery catheter includes a shaft having a pre-determined curve profile at a distal end of the delivery catheter. The pre-determined curve profile generally corresponds to the curve of the bottom surface of the aortic arch. The shaft may be eccentric to the expandable member such that retraction of the shaft causes a distal tip to be parallel within the ascending aorta. | 2013-05-09 |
| 20130116655 | BALLOON ASSEMBLIES HAVING CONTROLLABLY VARIABLE TOPOGRAPHIES - Various embodiments provide a device comprising a balloon disposed at least partially along a template, the template including an aperture, wherein the template has a substantially cylindrical portion that resists deformation in a radial direction, wherein the balloon expands radially during inflation, wherein a portion of the balloon at least partially protrudes about the aperture. Other embodiments are directed toward balloons having textured surfaces. | 2013-05-09 |
| 20130116656 | Nose Bleeding Stopper. - The present invention discloses a nose plug device comprising a compressible material to exert a pressure on bleeding areas in inner wall of nostril. The present nose plug device can further comprise a bio-lubricant coating to help in device removal. | 2013-05-09 |
| 20130116657 | METHOD AND DEVICE - The invention relates to a method and device for treating or preventing or suppressing a disease or condition in a non-human animal. The method comprises the steps of providing a single delivery device containing two components for sequential delivery from the delivery device. A first component is delivered from the single delivery device into a teat canal of a non-human animal and subsequently the second component is delivered from the single delivery device into the teat canal. The components are delivered without substantial mixing of the components. | 2013-05-09 |
| 20130116658 | APPARATUS FOR REMOVING CHEMOTHERAPY COMPOUNDS FROM BLOOD - A filter apparatus for removing small molecule chemotherapy agents from blood is provided. The filter apparatus comprises a housing with an extraction media comprised of polymer coated carbon cores. Also provided are methods of treating a subject with cancer of an organ or region comprising administering a chemotherapeutic agent to the organ or region, collecting blood laded with chemotherapeutic agent from the isolated organ, filtering the blood laden with chemotherapeutic agent to reduce the chemotherapeutic agent in the blood and returning the blood to the subject. | 2013-05-09 |
| 20130116659 | MEDICAL DEVICE WITH BI-COMPONENT POLYMER FIBER SLEEVE - An elongate medical device having a longitudinal axis and a surface; and a continuous, helical bi-component fiber wound around at least a portion of the surface of the medical device along its longitudinal axis, wherein the bi-component fiber has a cross-section with a generally flattened side and an inner core encased in a sheath, and wherein the inner core is aligned about the medical device. | 2013-05-09 |
| 20130116660 | WOUND TREATMENT APPARATUS EMPLOYING REDUCED PRESSURE - An apparatus for stimulating healing of a wound, includes a porous pad adapted to contact a surface of the wound on an affected part of a body. An envelope for receiving the porous pad and the affected part of the body is provided, and the envelope includes a re-sealable opening that permits the wound to be inspected. A connector is fluidly connected to an interior of the envelope and to a source of negative pressure. | 2013-05-09 |
| 20130116661 | SYSTEM AND METHOD FOR REDUCED PRESSURE CHARGING - A reduced pressure treatment system includes a compressible chamber positionable beneath a foot of a user and being movable between an expanded position and a compressed position. The compressible chamber includes an inlet and an outlet. An inlet valve is in fluid communication with the inlet to prevent fluid within the compressible chamber from exiting the inlet, and an outlet valve is in fluid communication with the outlet to prevent fluid from entering the compressible chamber through the outlet. A biasing member is disposed within the compressible chamber to bias the compressible chamber toward the expanded position, and a manifold is positionable at a tissue site and in fluid communication with the inlet of the compressible chamber. | 2013-05-09 |
| 20130116662 | METHOD FOR MANUFACTURING OF A TUBULAR OBJECT FOR INSERTION INTO A BODY PASSAGEWAY - Disclosed are a method and an apparatus for manufacturing a medical tubular object, such as a catheter, for insertion into a body passageway. The method comprises the steps of extruding a tube by pushing tube material though an extrusion nozzle and cutting the extruded tube at a predetermined length. Further, an initial part of the extruded tube is advanced onto a tapered mandrel arranged adjacent the extrusion nozzle such that a flared end is formed, and after a predetermined length of the extruded tube has been advanced onto the tapered mandrel, the tapered mandrel is moved away from the extrusion nozzle to prevent that the rest of the extruded tube is expanded by the tapered mandrel. | 2013-05-09 |
| 20130116663 | Systems and methods for dynamic drug therapy response to blood pressure incidents - A dermal or transdermal drug-delivery skin patch has a blood pressure sensor structurally integrated or built into it. The skin patch when attached to a skin portion of an individual determines a blood pressure of the individual and in response needle-lessly delivers a treatment drug to the individual if necessary. | 2013-05-09 |
| 20130116664 | IMPLANTABLE DRUG PUMPS AND REFILL DEVICES THEREFOR - Implanted drug pump devices can be refilled via a fill port in the drug reservoir that includes a self-resealable septum. | 2013-05-09 |
| 20130116665 | IMPLANTABLE DRUG PUMPS AND REFILL DEVICES THEREFOR - Implanted drug pump devices can be refilled with a refill needle inserted through a fill port in the drug reservoir of the drug pump device. Proper needle insertion may be verified visually or using electrical, magnetic, optical, acoustic, or other suitable sensing mechanisms. | 2013-05-09 |
| 20130116666 | IMPLANTABLE DRUG PUMPS AND REFILL DEVICES THEREFOR - A system for refilling the drug reservoir of an implanted drug pump device may facilitate wireless data exchange between the refill system and the implanted device, e.g., to verify proper drug selection prior to commencement of the refill process. | 2013-05-09 |
| 20130116667 | SYSTEM FOR CONTROLLED ADMINISTRATION OF A SUBSTANCE FROM A HUMAN-BODY-IMPLANTED INFUSION DEVICE - A system for the controlled administration of a substance by means of an infusion device implanted in the human body is described. The system has an implantable unit for detecting a shortage or an excess of such substance or a physiological parameter correlatable to the shortage or excess of such substance, an infusion group of this substance implantable in the peritoneal cavity and having a central control unit for processing data received from the detection unit, and energy storage means to power such infusion group. The system also has a carrier of such substance adapted to be ingested, and a refilling device for refilling the infusion group with such substance. | 2013-05-09 |
| 20130116668 | SURGICAL INSTRUMENT HAVING FORCE FEEDBACK CAPABILITIES. - A surgical instrument. The surgical instrument has a force delivery system which communicates a changing force to a user of the surgical instrument when a limit of a surgical function is reached. A sensor senses position of a moving element to communicate a signal to the force delivery system. In various embodiments, the system generates a vibratory force to signal the user. | 2013-05-09 |
| 20130116669 | A SURGICAL METHOD USING FEEDBACK CAPABILITIES. - The surgical method using force delivery and communicating a vibratory force to a user of the surgical instrument when a limit of a surgical function is reached. | 2013-05-09 |
| 20130116670 | RETINAL LASER SURGERY - Various systems, processes, and computer program products may be used to perform retinal laser surgery. In particular implementations, systems, processes, and computer program products may include the ability to identify retina blood vessels from a retina image and determine a retina location needing therapy and not substantially intersecting a retina blood vessel. The systems, processes, and computer program products may also include the ability to generate a command to activate a retinal laser when a beam from the retinal laser will be aligned with the therapeutic location. | 2013-05-09 |
| 20130116671 | STEERABLE LASER PROBE - A steerable laser probe may include a handle, an actuation lever, an optic fiber, and a housing tube. The housing tube may have a first housing tube portion having a first stiffness and a second housing tube portion having a second stiffness. The second stiffness may be greater than the first stiffness. The optic fiber may be disposed within the housing tube and within an inner bore of the handle. An actuation of the actuation lever about a pivot pin of the handle may gradually curve the optic fiber. An actuation of the actuation lever about the pivot pin of the handle may gradually straighten the optic fiber. | 2013-05-09 |
| 20130116672 | GRID PATTERN LASER TREATMENT AND METHODS - Embodiments of the invention provide systems and methods for treating the retina and/or other areas of a patient's eye. The procedures may involve using one or more treatment beams (e.g., lasers) to cause photocoagulation or laser coagulation to finely cauterize ocular blood vessels and/or prevent blood vessel growth to induce one or more therapeutic benefits. In other embodiments, a series of short duration light pulses (e.g., between 5-15 microseconds) may be delivered to the retinal tissue with a thermal relaxation time delay between the pulse to limit the temperature rise of the target retinal tissue and thereby limit a thermal effect to only the retinal pigment epithelial layer. Such procedures may be used to treat diabetic retinopathy, macular edema, and/or other conditions of the eye. The treatment beam may be delivered within a treatment boundary or pattern defined on the retina of the patient's eye. | 2013-05-09 |
| 20130116673 | Microscope Magnification Sensor - Devices, systems and methods for scaling the size and/or position of a marker on a magnified image of an object. In preferred embodiments, the object is an eye that is undergoing laser eye surgery. The eye is viewed through a magnification system or microscope and an image of the eye is presented on a display. One or more markers are present on the image, each identifying a specific target location or landmark on the eye. When a desired magnification setting is selected, the image is scaled accordingly. In addition, one or more of the markers is scaled in size and/or position to reflect the magnification setting. This allows the marker to maintain identification of the target location while reflecting the selected magnification level. | 2013-05-09 |
| 20130116674 | SYSTEM AND METHOD FOR TREATING VISION REFRACTIVE ERRORS - Disclosed is a computer-implemented method for correcting refractive errors in a living eye using a laser vision correction system that involves first calculating an amount of sphere based on preoperative manifest refraction and higher order aberrations data associated with the eye, and then correcting for the calculated amount of sphere by ablating at least a portion of the eye. The preoperative manifest refraction may include preoperative manifest sphere, preoperative spherical equivalent, regular astigmatism, and oblique astigmatism, and the preoperative higher-order aberrations may include 4th-order spherical and 3rd root mean square. Other factors may also be used to adjust the calculated amount of sphere. A device readable medium for storing the calculation and instructions for operating a laser vision correction system for practicing the method is also disclosed, as is a method of treating refractive errors. | 2013-05-09 |
| 20130116675 | System and Method for Correcting Higher Order Aberrations with Changes in Intrastromal Biomechanical Stress Distributions - A method for correcting higher order aberrations in an eye requires Laser Induced Optical Breakdown (LIOB) of stromal tissue. In detail, the method identifies at least one volume of stromal tissue in the eye, with each volume defining a central axis parallel to the visual axis of the eye. Thereafter, a pulsed laser beam is focused to a focal spot in each volume of stromal tissue to cause LIOB of stromal tissue at the focal spot. Further, the focal spot is moved through the volume of stromal tissue to create a plurality of incisions centered about the respective central axis of the volume. As a result, a predetermined selective weakening of the stroma is caused for correction of the higher order aberration. | 2013-05-09 |
| 20130116676 | METHODS OF CONDITIONING SHEET BIOPROSTHETIC TISSUE - Methods for the conditioning of bioprosthetic material employ bovine pericardial membrane. A laser directed at the fibrous surface of the membrane and moved relative thereto reduces the thickness of the membrane to a specific uniform thickness and smoothes the surface. The wavelength, power and pulse rate of the laser are selected which will smooth the fibrous surface as well as ablate the surface to the appropriate thickness. Alternatively, a dermatome is used to remove a layer of material from the fibrous surface of the membrane. Thinning may also employ compression. Stepwise compression with cross-linking to stabilize the membrane is used to avoid damaging the membrane through inelastic compression. Rather, the membrane is bound in the elastic compressed state through addition cross-linking. The foregoing several thinning techniques may be employed together to achieve strong thin membranes. | 2013-05-09 |
| 20130116677 | SYSTEMS AND METHODS FOR TREATMENT OF PREMENSTRUAL DYSPHORIC DISORDERS - An endoscopic procedure for the parasympathetic and sympathetic denervation of the nerves of the ovaries and uterus for management of endocrine dysphoric disorders. The tissues of selected inferior mesenteric and pelvic nerves are heated via introduction of radiofrequency energy at sufficient power and time to induce complete or partial nerve blockade while leaving the supporting tissue structurally intact. In some embodiments, the suspensory ligament of the ovary, the ovarian ligament, and/or the uterosacral ligament are heated to a range of 45° C. to 65° C. for a period of about 5 seconds to about 60 seconds. | 2013-05-09 |
| 20130116678 | IMPEDANCE MEDIATED CONTROL OF POWER DELIVERY FOR ELECTROSURGERY - A method of controlling electrosurgical power delivery is based on a comparison of sensed tissue impedance to various impedance threshold values. Energy is delivered to tissue in a sealing cycle as a series of pulses. A pulse has a profile with a preset energy starting value that increases at a ramping rate to a preset end value. Sensed impedance data are monitored throughout each pulse and compared to each of an impedance threshold value for RF setpoint, an impedance threshold value for cumulative time, and an impedance threshold value for energy cutback. Based on sensed impedance during a pulse, the profile of a subsequent pulse can be modified. In the event of a high impedance event that reflects low tissue presence, energy may be cutback. A sealing cycle is stopped when a cumulative amount of time with an impedance value over the impedance cumulative time threshold value reaches a limit. | 2013-05-09 |
| 20130116679 | ENERGY DELIVERY SYSTEMS AND USES THEREOF - The present invention relates to comprehensive systems, devices and methods for delivering energy to tissue for a wide variety of applications, including medical procedures (e.g., tissue ablation, resection, cautery, vascular thrombosis, treatment of cardiac arrhythmias and dysrhythmias, electrosurgery, tissue harvest, etc.). In certain embodiments, systems, devices, and methods are provided for delivering energy to difficult to access tissue regions (e.g. peripheral lung tissues), and/or reducing the amount of undesired heat given off during energy delivery. | 2013-05-09 |
| 20130116680 | ELECTROSURGERY IRRIGATION PRIMER SYSTEMS AND METHODS - Systems and methods are provided for priming or purging an electrosurgical fluid irrigation system. The electrosurgical system can include a high frequency power supply, a fluid delivery system, a handheld device having one or more electrodes, and one or more connectors for connecting the handheld device to the fluid delivery system and the RF generator. The electrosurgical system may be configured to deliver RF current and irrigation fluid until a threshold current level is detected, which is indicative of a continuous flow of fluid at the electrode and purging completion. The systems and methods of purging an electrosurgical system may further include dynamically controlling an RF output and fluid delivery system in accordance with varied parameters of detected threshold current levels. | 2013-05-09 |
| 20130116681 | System for Automatic Medical Ablation Control - A system provides heart ablation unit control. The system includes an input processor for acquiring electrophysiological signal data from multiple tissue locations of a heart and data indicating tissue thickness at the multiple tissue locations. A signal processor processes the acquired electrophysiological signal data to identify location of particular tissue sites of the multiple tissue locations exhibiting electrical abnormality in the acquired electrophysiological signal data and determines an area of abnormal tissue associated with individual sites of the particular sites. An ablation controller automatically determines ablation pulse characteristics for use in ablating cardiac tissue at an individual site of the particular tissue sites in response to the acquired data indicating the thickness of tissue and determined area of abnormality of the individual site. | 2013-05-09 |
| 20130116682 | Non-Stick Conductive Coating for Biomedical Applications - The present disclosure provides a plasma system including a plasma device having at least one electrode; an ionizable media source coupled to the plasma device and configured to supply ionizable media thereto; a precursor source configured to supply at least one monomer precursor to the plasma device; and a power source coupled to the at least one electrode and configured to ignite the ionizable media at the plasma device to form a plasma effluent at atmospheric conditions, wherein the plasma effluent polymerizes the at least one monomer precursor to form a hydrophobic, electrically-conductive polymer. | 2013-05-09 |
| 20130116683 | MEDICAL SYSTEM AND METHOD OF USE - Medical instruments and systems for applying energy to tissue, and more particularly relates to systems for ablating or damaging structures in a body or vessel wall to alter electrical conduction therein to cause an intended therapeutic effect. Variations include devices and methods for generating a high pressure flow of a liquid media and/or a vapor media to treat the targeted tissue by the application of mechanical energy, thermal energy or chemical energy to such targeted tissue. | 2013-05-09 |
| 20130116684 | PFO CLOSING DEVICE - A PFO closing device for bringing the septum primum and the septum secundum into contact with each other and joining them together includes a clamping mechanism and energy supplying device. The clamping mechanism includes a needle part for puncturing the septum primum, and a clamping member for cooperating with the needle part in clamping therebetween tissue of the septum primum and the septum secundum. The energy supplying device supplies energy for joining the tissues clamped by the needle part and the clamping member. The clamping mechanism is mounted in a catheter so as to be protrudable from and retractable into the catheter. | 2013-05-09 |
| 20130116685 | APPARATUSES FOR RENAL NEUROMODULATION AND ASSOCIATED SYSTEMS AND METHODS - Methods and apparatus are provided for renal neuromodulation using a pulsed electric field to effectuate electroporation or electrofusion. It is expected that renal neuromodulation (e.g., denervation) may, among other things, reduce expansion of an acute myocardial infarction, reduce or prevent the onset of morphological changes that are affiliated with congestive heart failure, and/or be efficacious in the treatment of end stage renal disease. Embodiments of the present invention are configured for percutaneous intravascular delivery of pulsed electric fields to achieve such neuromodulation. | 2013-05-09 |
| 20130116686 | ENERGY TREATMENT DEVICE - An energy treatment device includes a probe in which a suction path is defined inside along a longitudinal axis to a distal surface portion. The probe includes a first protrusion protruding an outer peripheral distal end of an outer peripheral portion toward a first perpendicular direction perpendicular to the longitudinal axis and perpendicular to open/close directions of the jaw. The distal surface portion includes an inclined plane in which it goes toward a distal direction side as it goes from the first perpendicular direction toward a second perpendicular direction that is opposite to the first perpendicular direction, the inclined plane extending from a first end position, located to the first perpendicular direction side of a first root position of a first protrusion, to a second end position, located to the second perpendicular direction side of the suction path. | 2013-05-09 |
| 20130116687 | OSTIAL RENAL NERVE ABLATION - A catheter including an elongated shaft having a distal end and a proximal end, where the catheter includes a thermal element at the distal end thereof. The thermal element may be used in an ablation procedure or other procedure to heat a tissue adjacent a vessel. In some instances, the thermal element may be positioned in a first vessel and may operate to heat tissue adjacent a second vessel or adjacent an ostium between the first vessel and the second vessel. Further, the catheter may include an expandable portion on which the thermal element may be connected or positioned. The expandable portion(s) may comprise a basket or cage, a balloon, a memory shape and formable portion, and/or other mechanical expanders. | 2013-05-09 |
| 20130116688 | ABLATION CATHETER - Devices, systems and methods are disclosed for the mapping of electrical signals and the ablation of tissue. Embodiments include an ablation catheter that has an array of ablation elements attached to a deployable carrier assembly. The carrier assembly can be transformed from a compact, linear configuration to a helical configuration, such as to map and ablate pulmonary vein ostia. | 2013-05-09 |
| 20130116689 | SYSTEMS AND METHODS FOR LIMITING JOINT TEMPERATURE - Joint temperature monitoring and control systems and methods are described herein in which the temperature of a fluid within a body or joint space is determined and/or monitored despite the energy generated during treatment by an ablation probe. One or more temperature sensors are positioned along the probe proximally of the electrode assembly and measure the temperature of an electrically conductive fluid without being overly influenced by the surgical effect occurring proximate the electrode assembly. The controller coupled to the probe can also be configured to set temperature limits and treatment times as well as moderating joint temperature by altering the electrically conductive fluid flow. | 2013-05-09 |
| 20130116690 | Endoscopic Vessel Sealer and Divider for Large Tissue Structures - An endoscopic bipolar forceps includes a housing having a shaft affixed thereto, the shaft including jaw members at a distal end thereof. The forceps also includes a drive assembly which moves the jaw member relative to one another for manipulating tissue and a knife assembly for cutting tissue disposed between jaw members. The forceps also includes a knife lockout mechanism operatively connected to the drive assembly. Movement of the drive assembly moves the knife lockout mechanism from a first orientation in obstructive relationship with the knife bar to prevent movement thereof to a second position which allows selective, unencumbered movement of the knife assembly to cut tissue disposed between the jaw members. | 2013-05-09 |
| 20130116691 | APPARATUS FOR SECURING AN ELECTROPHYSIOLOGY PROBE TO A CLAMP - An apparatus for use with a clamp including a base member configured to be secured to the clamp and at least one energy transmission device carried by the base member. An apparatus for use with a clamp and a probe that carries at least one energy transmission device including a base member configured to be secured to the clamp and an engagement device associated with the base member and configured to engage the probe. A clamp including first and second clamp members, at least one of which is malleable, and a movement apparatus that moves at least one of the first and second clamp members relative to the other. A surgical system including a clamp with first and second clamp members and a device that removably mounts at least one electrode on at least one of the first and second clamp members. | 2013-05-09 |
| 20130116692 | EXTERNAL FIXATION - An orthopedic external fixation system may include a distal bar having a curvature that varies along its length, an uncurved proximal bar, a plurality of proximal embedding members, and a plurality of distal embedding members. The proximal and the distal embedding members, sized and shaped for embedding in bone, may attach directly or indirectly to the proximal bar and the distal bar, respectively. | 2013-05-09 |
| 20130116693 | STRAIGHT INTRAMEDULLARY FRACTURE FIXATION DEVICES AND METHODS - A straight intramedullary bone fracture fixation device is provided with an elongate body having a longitudinal axis for deployment in a long bone, such as a clavicle. Methods of repairing a fracture of a bone are also disclosed. One such method comprises inserting a bone fixation device into an intramedullary space of the bone to place at least a portion of an elongate body of the fixation device on one side of the fracture and at least a portion of a hub on another side of the fracture, and engaging an inner surface of the intramedullary space to anchor the fixation device to the bone. Various configurations and designs may be used in combination with other fixation device components. | 2013-05-09 |
| 20130116694 | TELESCOPING SCREW FOR FEMORAL NECK FRACTURES - A bone fixation system includes a bone fixation device, including a first element having a first channel extending therethrough and a second element including a proximal portion sized and shaped to be received within the first channel such that the longitudinal axes of the first and second elements are substantially coaxial and a distal portion including a bone engaging structure, a proximal end of the second element slidably locked within the first channel such that the first and second elements are longitudinally movable relative to one another between a permitted range of motion. The system also includes a driving tool, including an outer sleeve and an inner sleeve slidably received therethrough, a distal end of the outer sleeve configured to engage the proximal end of the first element to prevent relative rotation therebetween, a distal end of the inner sleeve configured to engage the proximal end of the second element. | 2013-05-09 |
| 20130116695 | CABLE BUTTON - The present disclosure includes a method for reducing a bone fracture and an apparatus such as a cable button for use with a bone plate, the cable button including cable button threads, a plurality of cable button apertures, a hex socket, and a hex opening. The present disclosure also includes a method for reducing a bone fracture and an apparatus such as a cable button for use with a bone plate, the cable button including a plurality of legs, where a leg includes a protrusion, where the protrusion engages the bone plate, and the cable button defines at least one cable button aperture. | 2013-05-09 |
| 20130116696 | Lean Electrolyte for Biocompatible Plasmaelectrolytic Coatings on Magnesium Implant Material - The present disclosure is directed, at least in part, to a method of producing ceramic layers on magnesium and its alloys, a magnesium implant with a ceramic layer made by the method, and a magnesium implant having a biocompatible ceramic layer substantially free of material which impairs the biocompatibility of said biocompatible ceramic layer. In an exemplary embodiment, the method of producing ceramic layers on magnesium and its alloys, includes (a) immersing an implant and a metal sheet into the aqueous electrolyte bath, said aqueous electrolyte bath including: ammoniac, diammonium hydrogen phosphate and urea, and wherein the implant is made of magnesium or its alloy; (b) performing a anodic oxidation by passing a current between the implant, the metal sheet and through the aqueous electrolyte bath, wherein the implant is connected to a positive pole of a current source and the metal sheet is connected to a negative pole of the current source; (c) applying a current density selected to form sparks on said implant, to thereby form a ceramic layer on said implant. | 2013-05-09 |
| 20130116697 | ARTHROPLASTY DEVICES AND RELATED METHODS - Methods and apparatuses for forming customized arthroplasty jigs are disclosed. Some of the apparatuses may comprise a plurality of rapid production machines and an automated mechanical system. The automated mechanical system may be configured to transport a first arthroplasty jig blank to a first rapid production machine and a second arthroplasty jig blank to a second rapid production machine. The first rapid production machine may be configured to form a first arthroplasty jig from the first arthroplasty jig blank, and the second rapid production machine may be configured to form a second arthroplasty jig from the second arthroplasty jig blank, the second arthroplasty jig having a different configuration from the first arthroplasty jig. | 2013-05-09 |
| 20130116698 | DEVICES AND METHODS FOR PERFORMING KNEE ARTHROPLASTY - Methods and devices for performing knee arthroplasty including but not limited to bicruciate retaining knee arthroplasty are provided. Methods and devices for preparing a proximal tibia for a tibial implant are also provided. These methods and devices, in at least some embodiments and uses, facilitate decreasing the complexity of knee arthroplasty procedures such as bicruciate retaining procedures while maintaining, if not improving on, the safety, accuracy and/or effectiveness of such procedures. | 2013-05-09 |
