26th week of 2012 patent applcation highlights part 61 |
Patent application number | Title | Published |
20120165694 | BREATH AND BREATH CONDENSATE ANALYSIS SYSTEM AND ASSOCIATED METHODS - A system for collecting an exhaled breath sample and exhaled breath aerosol from a subject includes a condensation chamber having an outer wall defining an interior space. The outer wall has an inlet port and an outlet port therethrough in fluid communication with the interior space. The inlet port is placeable in fluid communication with an exhaled breath sample of the subject. A condensation element is positioned within the condensation chamber interior space and has a shape tapering downwardly toward a bottom tip thereof. A condensation of fluid on the condensation element is enhanced through various elements. A collection area is positioned within the condensation chamber's interior space beneath the condensation element bottom tip. The collection area is for collecting condensate accumulating on an outer surface of the condensation element and dropping from the tip thereof. | 2012-06-28 |
20120165695 | EEG MONITORING APPARATUS AND METHOD FOR PRESENTING MESSAGES THEREIN - An EEG monitoring apparatus ( | 2012-06-28 |
20120165696 | METHOD FOR ASSESSING THE SUSCEPTIBILITY OF A HUMAN INDIVIDUAL SUFFERING FROM A PSYCHIATRIC OR NEUROLOGICAL DISORDER TO NEUROMODULATION TREATMENT - Method for assessing the susceptibility of a human individual suffering from a psychiatric or neurological disorder, in particular with depressed mood as a predominant feature, to neuromodulation treatment, in particular repetitive Transcranial Magnetic Stimulation (rTMS), the method comprising: a) Providing a dataset comprising electroencephalographic (EEG) activity and Event Related Potentials (ERP) data of said human individual; b) Assessing the susceptibility of said human individual to neuromodulation treatment based on said dataset. | 2012-06-28 |
20120165697 | SAMPLE COLLECTING DEVICE - A sampling device for collecting a bodily fluid, the device comprising a membrane penetration device including a membrane penetrating element for penetrating a membrane to release a bodily fluid and a collecting element adapted to take up the bodily fluid, the collecting element being engaged with the membrane penetration device. | 2012-06-28 |
20120165698 | CONTROL DEVICE FOR A MEDICAL TEST SYSTEM - The invention concerns a control device for a medical test system which has a lancing element that can be inserted into body tissue to collect body fluid and a lancing drive for the lancing element. A sensor element for body fluid is arranged on the lancing element and a control unit is coupled to the sensor element for detecting a fault when collecting body fluid. In order to improve the success rate, the control unit actuates the lancing drive for an automatic puncture repetition in less than 1 second when a fault, e.g., inadequate wetting of a detection field, occurs. | 2012-06-28 |
20120165699 | Method and Apparatus for Collecting and Preparing Biological Samples for Testing - A kit and a method are disclosed for collecting and preparing a biological sample for testing where the sample is to be mixed with a buffer prior to being tested. | 2012-06-28 |
20120165700 | INTESTINAL PERISTALSIS DETECTING DEVICE AND SYSTEM AND METHOD THEREOF - An intestinal peristalsis detecting device comprises a radio frequency (RF) signal generator, an antenna, and a mixer. After the RF signal generator sends a pulse signal, the antenna receives the pulse signal and emits a pulse electromagnetic wave to an organism. Thereafter, the antenna receives a response pulse electromagnetic wave reflected from the organism to generate a response pulse signal. The mixer couples with the RF signal generator and the antenna to mix the pulse signal and the response pulse signal. | 2012-06-28 |
20120165701 | Intramedullary locked compression screw for stabilization and union of complex ankle and subtalar deformities - This invention describes an implant to fuse the bones of the ankle and subtalar joints together. The method includes steps of producing an implant to apply compressive forces across the bones of the ankle or the bones of the subtalar joint. In one embodiment, the invention includes a method that uses images such as radiographs preoperatively to determine the length and width of the disclosed implant or any other implant based on each patient's unique anatomy, that will properly allow coaptation of the ends of the prepared tibia and talus at the ankle joint or the prepared talus and the calcaneus at the subtalar joint. The implant is inserted from the bottom of the foot through a predetermined hole in the calcaneus extending through the talus into the diaphysis of the tibia. When properly seated in the bones, the implant is locked to the bones by screws. | 2012-06-28 |
20120165702 | CARDIAC TISSUE ELASTICITY SENSING - A system and method are provided for assessing the compliance of internal patient tissue for purposes of catheter guidance and/or ablation procedures. Specifically, the system/method provides for probing internal patient tissue in order to obtain force and/or tissue displacement measurements. These measurements are utilized to generate an indication of tissue elasticity. In one exemplary embodiment, the indication of elasticity is correlated with an image of the internal tissue area and an output of this image including elasticity indications is displayed for a user. | 2012-06-28 |
20120165703 | Preempt Muscle Map Screen - Some embodiments of the invention provide a software generated series of tests or screens to determine skeletal muscle balance as related to muscle strength and muscle flexibility. In some embodiments, a color coded muscle map illustrating the findings of the screens, is generated. The findings of the screens compile an exercise program, specifically tailored to the individual's general health and fitness state, as well as to the specific shortcomings identified in the screen. The invention also provides, in some embodiments, an exercise program adherence tracking calendar which monitors both completed exercises and exercise effectiveness as measured by changes in screen results. | 2012-06-28 |
20120165704 | APPARATUS FOR CONTROLLING REHABILITATION ROBOT - An apparatus for controlling a rehabilitation robot providing walking assistance to a user is disclosed. The apparatus includes a command perceiving unit for receiving a explicit walking command mode of a user based on a conscious adjustment signal, a motion sensing unit for sensing action of the user, a biometric sensing unit for sensing a biometric state of the user, and a host control module for analyzing walking steps and perceiving intent to walk by using the walking command perceived by the command perceiving unit and the action sensed by the motion sensing unit, thereby controlling the rehabilitation robot. The apparatus for controlling a rehabilitation robot further includes a wearing-type suit having the apparatus disposed thereon. | 2012-06-28 |
20120165705 | SYSTEM AND METHOD FOR DETECTING AN EPILEPTIC SEIZURE IN A PRONE EPILEPTIC PERSON - A system for detecting an epileptic seizure in a prone person, comprising:
| 2012-06-28 |
20120165706 | System For Determining The Position Of A Knee Prosthesis - The present invention provides a method for determining a position of a joint prosthesis using a computer assisted orthopedic surgery system in support of an arthroplasty surgery. The method includes attaching a first locatable element to a first bone on one side of a joint, providing a sensor having a second locatable element and moving the sensor in proximity of the joint to locate a plurality of positions of the sensor relative to the first locatable element using a tracking device. The method further includes selecting a generic model of a joint, determining the generic model in response to the plurality of positions located using the tracking device to generate a deformed model, determining a position for a joint prosthesis on the deformed model, and outputting on a display the determined position upon the deformed model. | 2012-06-28 |
20120165707 | NON-INVASIVE TRACKING OF BONES FOR SURGERY - The described method for determining at least orientation of a pelvic bone in space and for tracking movement of the pelvic bone using a computer assisted surgery (CAS) system includes removably attaching, in a non-invasive manner, at least one reference marker, in communication with the CAS system, to a skin surface covering the pelvic bone. Registering at least orientation readings of the reference marker is then performed with respect to a fixed reference in a reference coordinate system, following which at least an orientation of the pelvic bone in the reference coordinate system is determined using the orientation readings of the reference marker. These steps are repeated to update the orientation readings while tracking the pelvic bone in space. | 2012-06-28 |
20120165708 | Massage Apparatus and Method of Use - The present invention relates to a device for therapeutic and/or prophylactic massage, in particular massage of mammalian eyelids, having a body housing a heater in thermal communication with a massaging bobbin, the bobbin having a plurality of massaging elements extending therefrom. In use, the bobbin heats the eyelid and rotates such that a massaging force is exerted on the eyelid perpendicular to the lash line. This force can be used to express material from blocked sebaceous glands of the mammalian eyelid. As such, also disclosed herein is a method for treating disorders of the mammalian eyelid, such as inflammation, using the device of the invention. | 2012-06-28 |
20120165709 | LOCOMOTION ASSISTING DEVICE AND METHOD - A method of controlling an exoskeleton bracing system to walk includes identifying an expected current stance, receiving a tilt signal from a tilt sensor, and receiving a ground force signal from ground force sensors. Motorized joints are actuated to forwardly extend a leg brace when the expected stance includes standing with the leg braces together, the tilt signal indicates tilting forward, and the ground force signal indicates leaning on an opposite leg brace. Motorized joints are actuated to extend a trailing leg brace forward beyond a forwardly extended leg brace when the expected stance includes a forwardly extended leg brace and a trailing leg brace, the tilt signal indicates tilting forward, and the ground force signal indicates leaning on the forwardly extended leg brace. Motorized joints are actuated to converge both leg braces to a standing stance when the ground force signal indicates leaning on a trailing leg brace. | 2012-06-28 |
20120165710 | Handheld Facial Massage and Microcurrent Therapy Device - A Handheld Facial Massage and Microcurrent Therapy Device. The device includes a massage feature that enables the user to provide motorized agitation to a skin-contacting attachment selected from a group of detachable elements. The detachable skin-contacting element includes bristle brushes, massage sponges, smooth and rough applicators, among others. In addition to the motorized agitation from the attachment, the device also includes the ability to apply rejuvenating micro-current therapy to the skin. Both the motorized agitation and micro-current generation are independently user-adjustable in order to achieve the optimum treatment for each individual. Versions of the device that include galvanic current application as well as ultrasonic skin stimulation are available. The device is compact and easy to use so that the non-professional user can self-treat with professional results. | 2012-06-28 |
20120165711 | SUPRAPATELLAR EXTERNAL COUNTERPULSATION APPARATUS - An external counterpulsation apparatus has an efficient cuff and bladder system. Embodiments of this system generally allow effective treatment at lower pressures and a reduced total body surface area being compressed. An accurate and reliable combination of automatic and preset timing for inflation and deflation of the bladder system is used to simplify use of the apparatus. | 2012-06-28 |
20120165712 | CERVICAL COLLAR WITH INDEPENDENT HEIGHT AND CIRCUMFERENCE ADJUSTABILITY - An adjustable cervical collar designed to accommodate a broad range of prospective wearers with unique physical attributes, and to restrict the movements of the wearer's cervical spine, including rotation, flexion, extension, and lateral bending. The cervical collar includes a front portion and back portion, which may be adjusted in relation to one other to vary the circumference of the cervical collar. The front portion includes upper and lower plastic portions which may be adjusted to vary the height of the cervical collar, and a front thoracic extender which may be adjusted to achieve a desired restrictiveness of flexion movement. The back portion includes occipital and back thoracic extenders which may be adjusted to achieve a desired restrictiveness of extension movement. The adjustable features may be operated independently of one another. The adjustable features include locking means to ensure that the cervical collar is securely applied to the wearer. | 2012-06-28 |
20120165713 | ORTHOPEDIC DEVICE - An orthopedic device has an elongate, tubular body defining a patella opening located generally at a center portion of the tubular body. A patella buttress including a buttress pocket is located on the tubular body and about the patella opening. The buttress pocket has various stretchability characteristics relative to the tubular body. A buttress element is associated with the buttress pocket. | 2012-06-28 |
20120165714 | ORTHOPEDIC DEVICE - An orthopedic device has a main body panel including a longitudinal length with a curved cross-section, and opposed lateral and medial sides. A posterior panel is secured to the lateral and medial sides of the main body panel, and is sized longitudinally shorter than the main body panel in a non-stretched condition. The posterior panel is secured to the main body panel in a pretensioned condition and spans the longitudinal length of the main body panel along the lateral and medial sides thereof. | 2012-06-28 |
20120165715 | DRAINING WOUND DRESSING - A wound dressing is made of multiple layers and includes a collection chamber that is in fluid communication with a drainage channel. When applied over a wound, the wound dressing provides protection for the wound while allowing air and fluids to evacuate from the wound through the collection chamber and out through the drainage channel. The wound dressing can include a valve that restricts air and fluids from entering the wound, which is beneficial for treating pneumothorax. | 2012-06-28 |
20120165716 | Self Adhesive Bandage Embodying Light Infused Photodynamically Sanitized Permeable Absorbent Pad Outer Surface - A Band-Aid type self-adhesive bandage whose absorbent pad outer surface is photodynamically sanitized while maintaining standard absorbency performance. | 2012-06-28 |
20120165717 | MEDICAL COMPRESSION PRODUCT, SYSTEM UTILIZING SUCH PRODUCT, AND PROGRAM FOR USE THEREWITH - A medical compression product (“MCP”) for applying pressure to a limb of a patient may include one or more sensors integrally united therewith for measuring information indicative of the pressure applied by the MCP. The sensors may be permanently or removably attached to the MCP, and the sensors may be grouped into particular predetermined regions. The sensors may communicate (e.g., by use of wires or wirelessly) with a computer system that provides information to the user regarding the application of the MCP. The MCP may include bandages in the form of elongated fabric strips and tubular hosiery products. Wires connected to the sensors and communicating with the computer system may be aligned along or transverse to the longitudinal dimension of the bandage. | 2012-06-28 |
20120165718 | TUBE SET FOR A BLOOD HANDLING APPARATUS AND BLOOD HANDLING APPARATUS COMPRISING A TUBE SET - A tube set for a blood handling apparatus, in particular an extracorporeal blood handling apparatus with an extracorporeal blood circuit or an apparatus for peritoneal dialysis, and a blood handling apparatus that has such a tube set are described. The tube set includes a device for collecting particles provided in a tube line portion of the tube set downstream of the tube portion placed in the occluding hose pump. The device for collecting particles prevents retention of solid substances that are possibly contained in the dialysis fluid, substituate or peritoneal solution. The tube set also has a device for limiting the pressure in the tube line portion between the occluding hose pump and the device for collecting particles. The device for limiting the positive pressure prevents an excessive positive pressure from building up in the tube line when fluid flow through the device for collecting particles is reduced or interrupted. | 2012-06-28 |
20120165719 | ACOUSTIC ACCESS DISCONNECTION SYSTEMS AND METHODS - An access disconnection system includes: an arterial line; a venous line; a transmitter configured to transmit a sound wave in one of the arterial and venous lines when connected to a patient; a receiver configured to receive the sound wave from the other of the arterial and venous lines when connected to the patient; and electronic circuitry coupled to at least one of the transmitter and receiver, the circuitry configured to send a disconnection output indicative of a change in the sound waves received by the receiver from the transmitter sufficient to expect that an access disconnection of one of the arterial line and venous lines has occurred. | 2012-06-28 |
20120165720 | INTRAOCULAR SHUNTS - The present invention generally relates to different types of intraocular shunts. | 2012-06-28 |
20120165721 | SYSTEMS FOR DEPLOYING INTRAOCULAR SHUNTS - The present invention generally relates to systems for deploying intraocular shunts without the use of an optical apparatus that contacts an eye, such as a goniolens. In certain embodiments, systems of the invention include a locking mechanism, and a device configured to hold and deploy an intraocular shunt, in which a distal portion of the device is movable within a proximal portion of the device and the distal portion of the device is configured to mate with the locking mechanism to prevent movement of the distal portion when the locking mechanism is engaged. | 2012-06-28 |
20120165722 | DEVICES AND METHODS FOR IMPLANTING A SHUNT IN THE SUPRACHOROIDAL SPACE - The invention generally relates to devices and methods for implanting a shunt in the suprachoroidal space of an eye. In certain aspects, devices of the invention include a housing, a deployment mechanism at least partially disposed within the housing, and a flexible hollow shaft coupled to the deployment mechanism, in which the shaft holds an intraocular shunt, and is configured to self-guide the shunt along a scleral spur of an eye as the shunt is deployed from the shaft. Such a device may be inserted into an eye and used to deploy a shunt within the eye such that a proximal portion of the shunt receives fluid from an anterior chamber of an eye and a distal portion of the shunt directs the fluid to the suprachoroidal space. | 2012-06-28 |
20120165723 | METHODS FOR IMPLANTING A SOFT GEL SHUNT IN THE SUPRACHOROIDAL SPACE - The invention generally relates to methods for implanting a soft gel shunt in the suprachoroidal space. In certain embodiments, methods of the invention involve inserting into the eye a hollow shaft configured to hold a soft gel intraocular shunt, deploying the soft gel shunt from the hollow shaft such that the shunt forms a passage from the anterior chamber of the eye to the suprachoroidal space of the eye, and withdrawing the hollow shaft from the eye. | 2012-06-28 |
20120165724 | HYDRAULIC VITRECTOMY PROBE - Hydraulic vitrectomy probes and methods and systems associated therewith are discussed. Example hydraulic vitrectomy probes may include a pressure multiplier that is operable to output a hydraulic pressure at a multiple of a received pneumatic pressure. Because of the incompressible nature of liquid, hydraulic vitrectomy probes are, among other things, more responsive, may be operated at higher cutting rates, provide improved patient safety, and have a form factor (e.g., size and/or shape) that may be more easily maneuvered by a surgeon. | 2012-06-28 |
20120165725 | DISSECTION HANDPIECE WITH ASPIRATION MEANS FOR REDUCING THE APPEARANCE OF CELLULITE - A dermatological skin treatment device is provided. The device comprises a handpiece and a cutting tool, wherein the tool is inserted through the conduit and percutaneously inserted into a tissue disposed within a recessed area of the handpiece. The device and method cut the fibrous structures under the skin that cause cellulite at an angle substantially parallel to the surface of the skin and replace these structures with a non-cellulite forming structure by deploying a highly fibrous mesh through a single needle hole to create a highly fibrous layer directly or through wound healing processes. A tool is provided to aspirate excess fluid and tissue from the treatment area. | 2012-06-28 |
20120165726 | SYSTEM AND METHOD FOR DELIVERING A SUBSTANCE TO A BODY CAVITY - A system and method for creating a medicated atmosphere in an organ, or body cavity is disclosed. The system includes a flexible aerosolization catheter that can be manipulated during use, a device for the introduction of the aerosolization catheter, a medication delivery apparatus configured to control delivery of a medication to the catheter, a gas delivery apparatus in communication with the catheter, a gas pressure relief apparatus configured to relieve pressure in the organ or body cavity, and a central controller The method includes providing insufflation gas and an aerosol of medication to an organ or body cavity while controlling overall pressure in the organ or cavity. The method may also include re-entering a patient through at least one port to apply gas and an aerosolized medicament, in either a post-operative procedure or in a chemotherapy context. | 2012-06-28 |
20120165727 | Spray For Fluent Materials - Certain embodiments relate to a sprayer or other medical apparatus for applying a biocompatible coating in situ. Such an apparatus may have a first conduit connected to a first exit opening and a second conduit connected to a second exit opening to deliver a first composition through the first conduit and a second composition through the second conduit to mix the first composition and the second composition outside both the first conduit and the second conduit. The first composition may be, e.g., a precursor to a material formed after the mixing of the first composition and the second composition. The first exit opening and the second exit opening may be approximately adjacent to each other and define an angle that is less than about 140 degrees. | 2012-06-28 |
20120165728 | COMMUNICATION PROTOCOL THAT SUPPORTS PASS-THRU COMMUNICATION - A private extension of the IEEE 11073 standard for enabling pass-thru communication between a external computing device and a medical device via a diabetes management device is disclosed herein. Within this context, a diabetes management system for configured to allow pass thru communication is described. The system includes a diabetes management device in communication with a external computing device and the first medical device. A pass-thru module of the diabetes management device uses a set of pass-thru commands for establishing a pass-thru communication path and enabling communication between the external computing device and the first medical device, and wherein the set of pass-through commands is defined in compliance with a communication protocol defined in accordance with IEEE standard 11073-20601. | 2012-06-28 |
20120165729 | BREAST ATTACHMENT - The invention relates to a breast attachment, in particular a flexible insert for a breast pump or a nipple shield, wherein the insert or shield applies a positive massaging effect on a breast mimicking the natural stimulation of a baby breast feed— | 2012-06-28 |
20120165730 | BREASTFEEDING SHIELD - The breastfeeding shield is configured for comfort and to facilitate the breastfeeding of an infant. The shield is formed of a soft thermoplastic elastomeric, e.g., silicone rubber or the like, and has a major portion closely conforming to the major contours of the female human breast. The major portion is relatively thin, the portion covering the areola being relatively thick and the nipple portion having an intermediate thickness. The hollow nipple includes reinforcing and spacing ribs therein to preclude contact with the natural nipple due to suction and resulting blockage of milk flow. One embodiment is configured for use by full term infants, and another embodiment has a smaller nipple extension for use by premature infants. Different sizes may be provided to suit the nursing mother. The shield is removably secured to the breast by disposable or reusable low-stick adhesive materials. | 2012-06-28 |
20120165731 | COMPOSITIONS AND METHODS FOR TREATING JOINTS - Methods and compositions are disclosed for an intra-articular injection for the treatment of osteoarthritis. The methods and compositions comprising combinations of hyaluronic acid and a bone morphogenetic protein, like rhGDF-5, can be useful for any synovial joint, including the knee, shoulder, hip, ankle, hands, spinal facet, or temporomandibular joint, both for the relief of pain and for slowing disease progression. | 2012-06-28 |
20120165732 | BALLOON CATHETER COMPRISING A ZERO-PROFILE TIP - Described herein is a balloon catheter with a zero-profile tip—that is, a balloon catheter having a distal tip that does not extend beyond the boundary of the cavity that will be created by the balloon when inflated—and further described herein are methods for the manufacturing of same. Several embodiment feature a method for inverting the distal end of an inflatable balloon structure, said inflatable balloon structure having a middle region, a first end region with a first opening, and a second end region with a second opening, said method comprising: (1) centrally inverting the second end region of the inflatable balloon structure and passing it through the first opening; (2) permanently fixing the inverted second end region to prevent un-inversion; and (3) returning the second end region back through the first opening. | 2012-06-28 |
20120165733 | MONITORING THE SEATING STATUS OF A FLUID RESERVOIR IN A FLUID INFUSION DEVICE - A device for delivering fluid to a user includes a housing, a drive motor assembly in the housing, a force sensor, and an electronics module. The drive motor assembly regulates delivery of fluid by actuating a piston of a fluid reservoir, and the force sensor generates output levels in response to force imparted thereto during, for example, fluid delivery operations. The electronics module processes the output levels of the force sensor to assess the operating health of the force sensor, to check for occlusions in the fluid delivery path, and to monitor the seating status of the fluid reservoir. | 2012-06-28 |
20120165734 | DEVICE FOR AT LEAST ONE OF INJECTION OR ASPIRATION - Devices, systems, and associated methods that facilitate the injection and/or aspiration of precisely controlled volumes of fluids at precisely controlled rates are provided. In some implementations, an apparatus may include a syringe and a lead screw connected to a plunger of the syringe. A ratchet gear may be connected to the lead screw. A mechanism may also be included to oscillate a frame in a direction perpendicular to a longitudinal axis of the lead screw such that one or more pawls of the frame engage the teeth of the ratchet gear in a manner that results in rotation of the ratchet gear in a single direction for controlled linear displacement of the plunger. | 2012-06-28 |
20120165735 | Devices and Methods for Reducing Electrical Noise in an Irrigated Electrophysiology Catheter System - An irrigation system for use with an irrigated electrophysiology catheter includes a peristaltic pump and an irrigation tube. The pump generally includes a pump clamp and a rotor, which are spaced apart to provide a tubing channel therebetween. The irrigation tube is inserted into the tubing channel. At least one of the pump clamp and the irrigation tube is treated to reduce surface adhesion therebetween. This advantageously minimizes perturbations to the double layer, which reduces a noise signal that might otherwise couple to and distort an electrogram signal. | 2012-06-28 |
20120165736 | MEDICATION INFUSION SET - An infusion set is provided for use in delivering fluid through a cannula, which is housed on a cannula housing, to a selected subcutaneous infusion site on a patient. The fluid is generally a medication, e.g., insulin. The cannula is in fluid communication with a fluid passageway surrounded by a projection on the cannula housing that includes one or more rail-like extensions acting as guides. A connector connects the cannula housing to a fluid delivery system, e.g., an infusion pump. The connector includes a needle, one or more guide arms that slide over the rail-like extensions to guide the needle into the self-sealing septum, and one or more locking arms, with barbs at the end, to connect with corresponding recesses in the cannula housing. An introducer having one or more similar guide arms and locking arms, and a longer needle, may be used to insert the cannula into the patient. | 2012-06-28 |
20120165737 | DEVICES AND METHODS FOR MAINTAINING AN ASEPTIC CATHETER ENVIRONMENT - Devices and methods for maintaining an aseptic catheter environment. In at least one exemplary embodiment of a device for maintaining an aseptic catheter environment of the present disclosure, the device comprises a first housing and a second housing, the first housing and the second housing coupled to one another by way of at least one coupler, the first housing and the second housing configured to engage one another when in a closed configuration and to define an interior space when in the closed configuration, and at least one aperture and/or notch defined within at least one of the first housing and the second housing, the at least one aperture and/or notch sized and shaped to allow at least part of a catheter to be positioned therethrough. | 2012-06-28 |
20120165738 | Method for Manufacturing a Composite Work Piece for a Drug Delivery Device and Composite Work Piece for a Drug Delivery Device - Method for manufacturing a composite work piece for a drug delivery device, comprising the steps: Providing a first work piece part | 2012-06-28 |
20120165739 | Spindle and Bearing Combination and Drug Delivery Device - An improved spindle and bearing combination for a drug delivery device is provided that has a first connection between the spindle ( | 2012-06-28 |
20120165740 | Medicament Identification System for Multi-Dose Injection Devices - A dynamic identification system for a multi-dose injection device includes a dose dial sleeve ( | 2012-06-28 |
20120165741 | Dose Button for a Drug Delivery Device and Method for Manufacturing a Dose Button - The present invention relates to a drug delivery device ( | 2012-06-28 |
20120165742 | DRUG DELIVERY DOSE SETTING MECHANISM WITH VARIABLE MAXIMUM DOSE - A method and system for proving a drug delivery device having a variable maximum dose. The drug delivery device comprising a first tubular member and a second tubular member rotatably coupled to the first tubular member. A maximum stop component is operatively coupled to the first tubular member and the second tubular member such that the maximum stop component is movable from a first position to a second position. The first position defines a first maximum dose that may be set by a user of said drug delivery device and the second position defines a second maximum dose that may be set by the user of said drug delivery device. | 2012-06-28 |
20120165743 | Dose Setting Mechanism for Priming a Drug Delivery Device - A method and system for priming a drug delivery device are provided. The drug delivery device includes a forced priming feature that requires the user to move the dose dial sleeve ( | 2012-06-28 |
20120165744 | RESETTABLE DRUG DELIVERY DEVICE - A resettable dosing mechanism comprises a dose button and a dial grip operatively coupled to the dose button. A spindle acts on a bung of a cartridge and a driver is operatively coupled between the dose button and the spindle. During an injection of the dose, the dose button moves in an axial direction to cause the spindle to administer the dose. During resetting of the dose setting mechanism, the spindle is retracted back into the dose setting mechanism. An advantageous resetting mechanism is described. | 2012-06-28 |
20120165745 | CAP LOCK - A needle assembly for a medical device comprising a needle cannula which is mounted in a hub connectable to a medical device, and which needle assembly comprises releasable locking means which co-operates with the connection means of the hub such that the needle cap is locked to the hub when the releasable locking means is not released. Once the locking means is released by activation of the connection means, the needle cap is unlocked from the hub. The activation of the locking means is preferably done automatically when the needle assembly is attached to the medical device. | 2012-06-28 |
20120165746 | PEN CAP - The present invention refers to a pen cap, being capable of covering a distal end of a drug delivery device comprising at least one protruding element located inside the pen cap which prevents that the rim of an outer needle cap, while being a protective casing for the needle at the distal end of the drug delivery device, can get stuck within a part of the pen cap if the user puts the pen cap on the drug delivery device. The inner diameter of the pen cap is reduced by means of the at least one protruding element, such that the inner diameter of the pen cap is smaller than the largest outer diameter of the outer needle cap. Furthermore, the invention relates to a drug delivery device comprising a pen cap with the described protruding elements. | 2012-06-28 |
20120165747 | Pen-Type Injector With Ergonomic Button Arrangement - A hand-held injection device ( | 2012-06-28 |
20120165748 | DOSE SETTING MECHANISM FOR A DRUG DELIVERY DEVICE - A dose setting mechanism of a drug delivery device and a respective method of assembling said dose setting mechanism. The dose setting mechanism includes an inner housing having a helical groove along an external surface of the housing. The inner housing includes a rotational stop member near one end of the helical groove. The dose setting mechanism also includes a dial sleeve rotatably engaged with the helical groove of the inner housing. When a user rotates the dial sleeve to select a dose, the rotational stop member prevents the user from selecting a dose greater than a pre-defined maximum selectable dose. | 2012-06-28 |
20120165749 | Dosing Mechanism for a Drug Delivery Device - A maximum settable dose feature is disclosed that is set by a user or health care professional one time that prevents future injections from exceeding the desired maximum dose. The feature includes a locking band ( | 2012-06-28 |
20120165750 | Drug Delivery Device Inner Housing Having Helical Spline - A dose setting mechanism for a drug delivery device is disclosed. The mechanism comprises an outer housing and an inner housing having an external groove and a helical spline. The inner housing helical spline guides a driver to dispense a set dose. A dial sleeve is disposed between the outer and inner housing and is rotatably engaged with the inner housing. When a dose is set, the dial sleeve is rotated and translates away from both the outer housing and the inner housing. | 2012-06-28 |
20120165751 | DOSE SETTING MECHANISM FOR A DRUG DELIVERY DEVICE - The invention relates to a dose setting mechanism, which is operable to be coupled to a medication cartridge and which comprises means that prevent the user from setting a dose greater than the remaining medication in the cartridge. The dose setting mechanism comprises a shaft. A helical groove having a first pitch is provided along a first portion of the shaft. The dose setting mechanism further comprises a nut member disposed on the helical groove of said shaft. During dose setting, the shaft is rotated relative to the nut member while the nut member traverses along the groove from a distal end of the shaft towards a proximal end of the shaft. The mechanism further comprises means preventing a user of said dose setting mechanism from setting a dose of said medication that is greater than said remaining medication in said cartridge, said means comprising a second pitch provided along a second portion of said shaft, wherein said first pitch is different from said second pitch, wherein said second pitch is preferably greater than said first pitch. | 2012-06-28 |
20120165752 | Dose Reset Mechanism - A dose reset mechanism for a medicament delivery device with a housing and a medicament container includes a dose setting member in the housing for setting a dose when it is rotated and for resetting the dose when it is rotated in the opposite direction. The dose setting member has a drive member connected to a plunger rod such that when the drive member rotates, the rod moves axially; and a connection member between the dose setting member and the drive member. A ratchet mechanism enables the connection member to rotate when the dose setting member rotates for setting a dose but not to move in the opposite direction. At least one dose reset member and at least one blocking member are connected to the ratchet mechanism such that the connection member and drive member are released when a dose knob is turned in the opposite direction. | 2012-06-28 |
20120165753 | Medicament Delivery Device - The present invention relates to a medicament delivery device ( | 2012-06-28 |
20120165754 | SYRINGE PISTON WITH FIN-SHAPED CIRCUMFERENTIAL SEALING ELEMENT - Syringe pistons for a fluid syringe, and related sealing elements, are presented here. A syringe piston includes a piston body having a fluid end, an actuator end, and an outer seal-retaining surface between the fluid end and the actuator end. The syringe piston may utilize a piston sealing sleeve or a piston sealing cover. The sleeve can be coupled to the piston body around the outer seal-retaining surface, the piston sealing sleeve having a fin-shaped fluid seal element to form an interference fluid seal with an interior wall of a syringe barrel. The sealing cover can be coupled overlying the tip of the piston body. The cover has a fin-shaped fluid seal element to form an interference fluid seal with an interior wall of a syringe barrel. | 2012-06-28 |
20120165755 | SYRINGE PISTON WITH FINNED SEALING COVER - Syringe pistons for a fluid syringe, and related sealing elements, are presented here. A syringe piston includes a piston body having a fluid end, an actuator end, and an outer seal-retaining surface between the fluid end and the actuator end. The syringe piston may utilize a piston sealing sleeve or a piston sealing cover. The sleeve can be coupled to the piston body around the outer seal-retaining surface, the piston sealing sleeve having a fin-shaped fluid seal element to form an interference fluid seal with an interior wall of a syringe barrel. The sealing cover can be coupled overlying the tip of the piston body. The cover has a fin-shaped fluid seal element to form an interference fluid seal with an interior wall of a syringe barrel. | 2012-06-28 |
20120165756 | COAXIAL GUIDE CATHETER FOR INTERVENTIONAL CARDIOLOGY PROCEDURES - A coaxial guide catheter to be passed through guide catheter having a first lumen, for use with interventional cardiology devices that are insertable into a branch artery that branches off from a main artery. The coaxial guide catheter is extended through the lumen of the guide catheter and beyond the distal end of the guide catheter and inserted into the branch artery. The device assists in resisting axial and shear forces exerted by an interventional cardiology device passed through the second lumen and beyond the flexible distal tip portion that would otherwise tend to dislodge the guide catheter from the branch artery. | 2012-06-28 |
20120165757 | Sheaths - Disclosed are sheaths that comprise a first sheath member having a first passageway, a first length, and a first proximal end defined by a first valve apparatus configured to seal the first passageway, the first passageway having a first passageway diameter at a location in the first passageway; and a second sheath member coupled to the first sheath member, the second sheath member having a second passageway and a second length, the second passageway having a second passageway diameter at a location in the second passageway; where the first passageway and the second passageway are separate from each other and not co-axial, the first length is different from the second length, and the first and second sheath members are positioned beside each other for a portion of their first and second lengths. | 2012-06-28 |
20120165758 | SANITARY APPARATUS FOR INTESTINAL CLEANSING - A sanitary apparatus for intestinal cleansing to be attached to a water faucet (R), includes a faucet filter ( | 2012-06-28 |
20120165759 | WATERPROOF STRETCHABLE OPTOELECTRONICS - Described herein are flexible and stretchable LED arrays and methods utilizing flexible and stretchable LED arrays. Assembly of flexible LED arrays alongside flexible plasmonic crystals is useful for construction of fluid monitors, permitting sensitive detection of fluid refractive index and composition. Co-integration of flexible LED arrays with flexible photodetector arrays is useful for construction of flexible proximity sensors. Application of stretchable LED arrays onto flexible threads as light emitting sutures provides novel means for performing radiation therapy on wounds. | 2012-06-28 |
20120165760 | DRUG ELUTING IMPLANT - Described herein is an implantable medical device that has one or more surfaces that include one or more shallow recesses configured to receive a drug delivery composition comprising a polymeric matrix and one or more biologically active agents. In one embodiment, one or more surfaces comprise a frictional surface. In a more particular embodiment, the implantable medical device comprises a stem configured for insertion into a bone of a patient, wherein the stem comprises one or more surfaces that include one or more shallow recesses configured to receive a drug delivery composition comprising a matrix and one or more biologically active agents. The drug delivery composition can be a durable drug delivery matrix, a biodegradable drug delivery matrix, or a combination thereof. Methods of making such an implant are also provided. | 2012-06-28 |
20120165761 | DRUG ELUTION THERAPY APPARATUS AND METHOD FOR TREATING BLOOD VESSELS - A drug therapy elution system and method for treating blood vessels. The system includes an enclosed receptacle containing the drug therapy for treating the damaged blood vessel. The system also includes one or more conduits that permit elution of the drug therapy from the enclosed receptacle into the damaged blood vessel wall. The system also includes one or more fixation mechanisms that can secure the enclosed receptacle to the blood vessel wall. | 2012-06-28 |
20120165762 | TRANSDERMAL DRUG DELIVERY DEVICE INCLUDING AN OCCLUSIVE BACKING - A transdermal drug delivery system for the topical application of one or more active agents contained in one or more polymeric and/or adhesive carrier layers, proximate to a non-drug containing polymeric backing layer which can control the delivery rate and profile of the transdermal drug delivery system by adjusting the moisture vapor transmission rate of the polymeric backing layer. | 2012-06-28 |
20120165763 | EYE MEDICATION APPLICATION DEVICE - A one piece eye medication application device allows the user to easily align the medication bottle with the inner corner of the eye, preventing the human reaction of blinking and keeping the medication in the eye. The device includes a one piece elongated member having an integrated ring with an opening. | 2012-06-28 |
20120165764 | SYSTEMS AND METHODS FOR CONTROLLING OPERATION OF A REDUCED PRESSURE THERAPY SYSTEM - Negative pressure wound therapy apparatuses and dressings, and systems and methods for operating such apparatuses for use with dressings are disclosed. In some embodiments, controlling the delivery of therapy can be based on monitoring and detecting various operating conditions. An apparatus can have a controller configured to monitor the duty cycle of a source of negative pressure and, based on the monitored duty cycle, determine whether a leak is present. The controller can be configured to provide an indication that a leak is present. For example, the controller can be configured to suspend and/or pause the delivery of therapy, and to restart the delivery of therapy due to a timeout, request from a user, etc. In addition, the controller can be configured to pause and/or restart the delivery of therapy upon a request from the user, such as in response to the user operating a switch. | 2012-06-28 |
20120165765 | REDUCED-PRESSURE, LINEAR-WOUND TREATMENT SYSTEMS - A system for treating a linear wound on a patient has a closing dressing bolster for placing on the patient's epidermis over the linear wound, a sealing subsystem for providing a seal over the closing dressing bolster and the patient, and a reduced-pressure subsystem for delivering reduced pressure to the sealing subsystem. The sealing subsystem and reduced pressure subsystem are operable to deliver reduced pressure to the closing dressing bolster. The closing dressing bolster is operable under reduced pressure to develop a inward closing. The closing dressing bolster may include one or more closing members on each side of a center wound area to create the inward closing when under reduced pressure. A compressive force may also be developed. Other systems and methods are presented. | 2012-06-28 |
20120165766 | ACTIVATION OF BONE AND CARTILAGE FORMATION - Provided is a method of activating osteogenic or chondrogenic activity at a site in a subject in need thereof. Also provided is a method of treating a bone or cartilage defect in a subject. Additionally, the use of a reduced pressure apparatus for treating a bone or cartilage defect adjacent to dura mater, periosteum, or endosteum is provided. Further provided is a composition for treating a bone or cartilage defect. Also, the use of a reduced pressure apparatus and a biocompatible scaffold for the manufacture of a composition for treating a bone or cartilage defect adjacent to dura mater, periosteum or endosteum is provided. | 2012-06-28 |
20120165767 | OSTOMY BARRIER SEAL - An ostomy barrier seal comprising an open-ended conical base | 2012-06-28 |
20120165768 | MALE URINE COLLECTOR - A male urine collector is provided. The bag comprises an elongate urine collecting bag sized to be worn on a lower part of a male user. The bag comprising a proximal end with a penis receiving opening for receiving a penis of a male user and, a distal end configured to be closed to collect urine discharged from the user's penis in the bag and to be selectively opened to discharge the collected urine from the bag. The male urine collector comprises at least one thin pliable opening ring disposed around and attached to the proximal end of the bag to open the penis receiving opening. | 2012-06-28 |
20120165769 | Sanitary Napkin with Braid - The present invention relates to a sanitary napkin whose securing means includes a braid of absorbent material. The braid structure maximizes absorbency, while minimizing bulk and thus allows the pad to be comfortably held in place during use, in much the same way that the popular thong underwear are held. | 2012-06-28 |
20120165770 | Absorbent article with stimulation composite - A stimulation material is partially bonded to a pressure-sensitive adhesive to form a stimulation blend. The stimulation blend, with or without pressure-sensitive adhesive, may be juxtaposed between two substrates to form a stimulation composite. When the pressure-sensitive adhesive is present within the stimulation composite, there are regions of the adhesive that do not contain a significant amount of stimulation material. By arranging regions of stimulation blend with respect to the pressure-sensitive adhesive regions, a pattern defined by the stimulation blend is formed. This pattern may deliver a stimulation effect that is at least as effective as using one-hundred percent stimulation blend within the stimulation composite, it not more effective. The stimulation composite may be cut into countless varieties of pledget shapes for use in personal-care absorbent articles. | 2012-06-28 |
20120165771 | Absorbent Articles With Multiple Active Graphics - Absorbent articles are disclosed that have been printed with active graphics alone or in combination with permanent graphics. The active graphics may be used, for instance, as a wetness indicator on an absorbent article. In accordance with the present disclosure, the active graphics include at least one disappearing graphic and at least one appearing graphic. The disappearing graphic and appearing graphic allow for complete scene changes on the article and also allow for the illusion of movement of objects in the scene. | 2012-06-28 |
20120165772 | MOISTURE DETECTING MODULE AND A RECEIVING UNIT - The invention relates to a moisture detecting module for monitoring a moisture state of a napkin. The module comprises a moisture sensitive sensor and a moisture non-permeable layer covering the sensor. The moisture non-permeable layer is arranged for attachment to a napkin surface that, during use of the napkin by a person, is facing towards the person's skin such that the moisture sensitive sensor contacts the napkin surface. The moisture detection module is a RLC circuit that acts as a RF-tag thereby transmitting moisture information to a remote reading device. | 2012-06-28 |
20120165773 | ABSORBENT CORE AND ABSORBENT ARTICLE - An absorbent core comprising a gelling region and a thickening region, as well as an absorbent article containing the absorbent core. The absorbent core formed from at least two layers. The absorbent core has in an upper layer gelling region comprising a gelling agent that contains a polysaccharide capable of thickening in the presence of a polyvalent metal ion and a substance that can supply a polyvalent metal ion, and has in a lower layer, thickening region comprising a thickening agent. | 2012-06-28 |
20120165774 | DISPOSABLE WEARING ARTICLE - In a disposable wearing article, a first waist region is elasticized and formed of an inner sheet and an outer sheet. The non-skin-facing side of the outer sheet is formed substantially over its entire area with a plurality of thermocompression-bonded spots regularly and intermittently arranged at predetermined intervals. The outer sheet has non-thermocompressed regions surrounded by a plurality of thermocompression-bonded spots. A fibrous layer lying at least on the outer surface of said outer sheet is formed of thermal adhesive crimped fibers which are bonded together by thermocompression-bonding treatment in the thermocompression-bonded spots. The outer sheet and the inner sheet are bonded to each other by adhesive applied on at least one of respective opposite surfaces thereof so that the crimped fibers in the non-thermocompressed regions may protrude outward in a thickness direction of the outer sheet as the inner sheet contracts in the direction of the transverse axis Q. | 2012-06-28 |
20120165775 | Creped Tissue Product with Enhanced Retention Capacity - An absorbent composite material may be manufactured by applying a flexible absorbent binder polymer (FAB), also referred to herein as a flexible superabsorbent, during the creping step of conventional tissue manufacturing. As such, the costly process of applying FAB to a substrate by spraying or printing followed by drying may be eliminated. The creping step has the additional advantage of improving the flexibility and softness of the FAB treated fibrous web. | 2012-06-28 |
20120165776 | Disposable Diaper with Reduced Bulk - A disposable diaper is disclosed having reduced bulk, especially in the back waist region. Due to an opaque topsheet and a backsheet having a relatively high percentage of printed surface area, the diaper has reduced see-through even in those areas of the back waist region where no absorbent core is comprised. | 2012-06-28 |
20120165777 | Absorbent incontinence article with improved closure system - An absorbent incontinence diaper ( | 2012-06-28 |
20120165778 | PERSONAL WEAR ABSORBENT ARTICLE WITH DISPOSAL TAB - An absorbent article includes a front waist region, a back waist region and a crotch region. The front and back waist regions are permanently attached or releasably attachable to each other by an article fastening system to define a wear configuration of the absorbent article. The article is configurable from the wear configuration to a disposal configuration. A disposal tab has an attachment region attached to one of the sides of the article and extends a greatest length La along at least a portion of a length Lp of one of the sides. A tab region extends transversely outward from the attachment region a greatest distance Dt and is attachable to the article in at least the disposal configuration of the article. The attachment region has a first surface attached to one of the sides of the article and a second surface that defines part of the article fastening system. | 2012-06-28 |
20120165779 | AIR-FILTERING VIAL ADAPTORS AND METHODS - In certain embodiments, a vial adaptor for removing liquid contents from a vial comprises a housing and a bag. In some embodiments, an initial volume of a regulating fluid can be contained within the bag. In some embodiments, the regulating fluid flows into the vial as liquid is removed from the vial via the adaptor, thereby regulating pressure within the vial. In some embodiments, a vial adaptor is coupled with the vial in order to remove the liquid. In some embodiments, as the liquid is removed from the vial via the adaptor, the bag expands, and in other embodiments, the bag contracts. | 2012-06-28 |
20120165780 | MONITORING THE OPERATING HEALTH OF A FORCE SENSOR IN A FLUID INFUSION DEVICE - A device for delivering fluid to a user includes a housing, a drive motor assembly in the housing, a force sensor, and an electronics module. The drive motor assembly regulates delivery of fluid by actuating a piston of a fluid reservoir, and the force sensor generates output levels in response to force imparted thereto during, for example, fluid delivery operations. The electronics module processes the output levels of the force sensor to assess the operating health of the force sensor, to check for occlusions in the fluid delivery path, and to monitor the seating status of the fluid reservoir. | 2012-06-28 |
20120165781 | TARGETED APHERESIS FOR THE TREATMENT OF RHEUMATOID ARTHRITIS - This invention uses “targeted apheresis” to treat rheumatoid arthritis patients. “Targeted Apheresis” is a process whereby the RF and immune complexes responsible for causing the disease symptoms are selectively removed from the blood by passing the blood through a cartridge containing immobilized IgG. The RF and immune complexes are bound out and the cleaned blood is returned to the patient Removal of circulating RF and immune complexes will ameliorate the symptoms of rheumatoid arthritis. | 2012-06-28 |
20120165782 | PHARMACEUTICAL COMPOSITION OF AN IONTOPHORESIS - It is an object of the present inventions to produce a pharmaceutical composition for the iontophoresis wherein a drug stability is excellent, and it is easy to blend and fill up when manufactured and it is possible to manufacture at low cost. A pharmaceutical composition for an iontophoresis according to the present invention, is characterized in that the composition contains a nonionic synthetic polymer, betamethasone sodium phosphate and solvent. Furthermore, in a preferred embodiment of a pharmaceutical composition for an iontophoresis according to the present invention, the composition is characterized in that the nonionic synthetic polymer is polyvinyl alcohol (PVA). Furthermore, in a preferred embodiment of a pharmaceutical composition for an iontophoresis according to the present invention, the composition is characterized in that the mixing amount of the polyvinyl alcohol (PVA) is 0.5 to 30.0 percent by weight. | 2012-06-28 |
20120165783 | DEVICE FOR AT LEAST ONE OF INJECTION OR ASPIRATION - Micro-volume devices, systems, and associated methods that facilitate the injection or aspiration of precisely controlled volumes of materials at precisely controlled rates are provided. In one embodiment, a micro-volume device includes a syringe and a lead screw connected to a plunger of the syringe. A mechanical interface is connected to the lead screw and includes a first set of cams adjacent a proximal portion and a second set of cams adjacent a distal portion. A mechanism is configured to oscillate a structure in a direction parallel to a longitudinal axis of the lead screw such that one or more projections of the structure to alternatively engage cams of the first and second sets of cams in a manner that results in rotation of the mechanical interface in a single direction for highly controlled linear displacement of the plunger. | 2012-06-28 |
20120165784 | AUTOMATIC NEEDLE GUARD - A device for selectively protecting a needle includes an adapter holding the needle and a guard engaging the adapter for relative movement therebetween. Further, the device includes a means for guiding movement between the adapter and the guard. Structurally, the guiding means includes a “V” shaped slot in the guard and a radially-extending boss on the adapter. The boss is received in the slot to limit relative movement between the guard and the adapter. Specifically, in a first position of the device, the boss is in a first leg of the slot and the needle partially extends beyond the guard. In a second position, the boss is held at the apex of the slot and the needle fully extends beyond the guard. In a third position, the boss is in the second leg of the slot and the needle is retracted into the guard to protect the needle. | 2012-06-28 |
20120165785 | Catheter System for a Needle Injector with an Automatic Needle/Barrier Extension - A catheter system includes a positioning catheter for receiving an injection needle into its lumen. The injection needle incorporates a web member mounted directly onto its shaft. As the injection needle is moved in a distal direction to exit from the lumen of the catheter, the web member is biased to transition from a folded configuration, and into a flared configuration. Specifically, this transition occurs when the injection needle is deployed more than a predetermined distance “d” beyond the distal end of the catheter. In its flared configuration, the web member is disk-shaped and is oriented perpendicular to the needle. Thus, it acts as a barrier to limit the depth of insertion of the needle into target tissue of a patient, to a depth less than “d”, and to prevent perforation of the target tissue by the catheter tip. | 2012-06-28 |
20120165786 | LIPID COATING FOR MEDICAL DEVICES DELIVERING BIOACTIVE AGENT - The present invention relates compositions for delivering therapeutic agents from a medical device including an expandable and collapsible structure and methods employing them. A lipid coating including one or more fatty acids increases the amount of therapeutic agent released from the device at the delivery site. The therapeutic agent can be in a matrix including a hydrophilic polymer or an amphiphilic polymer. Release and adhesion coatings can also facilitate delivery of therapeutic agent. | 2012-06-28 |
20120165787 | COMPOSITIONS AND METHODS FOR TREATING JOINTS - Compositions and methods are provided for treating joint conditions, such as osteoarthritis and/or the pain associated therewith. The compositions and methods utilize a first component, namely hyaluraonic acid (“HA”), in combination with a lyophilized second component that is effective to at least temporarily reduce the viscosity of the HA. In an exemplary embodiment, the second component is one or more glycosaminoglycans (“GAG”), such as chondroitin sulfate (“CS”), including CS4 and/or CS6, dermatan sulfate, heparin, heparan sulfate, and keratan sulfate. The composition can optionally include other joint supplements, such as glucosamine (“GlcN”) | 2012-06-28 |
20120165788 | MEDICAL DEVICE DELIVERY CATHETER - Apparatus for delivering a medical device to a location in a patient's body includes an elongate catheter body having a proximal end and a distal end, a pod coupled with the distal end of the catheter body and adapted to house the medical device during delivery to the location and to open to release the medical device, and at least one distal actuator coupled with at least one of the pod and the medical device. The distal actuator is adapted to promote opening of the pod. A method involves advancing a pod at the distal end of an elongate catheter to the location within the body and activating an actuator coupled with the pod and/or the medical device to cause the pod to open. Opening the pod releases the medical device. | 2012-06-28 |
20120165789 | Spring Action Wire Guide - A medical wire guide may include a mandrel and a cannula disposed about a portion of the mandrel. A spring may be coupled with the mandrel. The spring may be placed in a loaded state in response to relative displacement between the mandrel and the cannula. Upon release from the loaded state, the spring is configured to bias the mandrel in a distal direction relative to the cannula. | 2012-06-28 |
20120165790 | CATHETER ASSEMBLY AND A METHOD AND SYSTEM FOR PRODUCING SUCH AN ASSEMBLY - A catheter assembly is disclosed, comprising a catheter, such as a urinary catheter, which at least a partly is provided with a hydrophilic coating. The catheter assembly further comprises a wetting fluid. The receptacle is in direct contact with the hydrophilic coating of the catheter over essentially the entire length of the part of the catheter being provided with the hydrophilic coating. This may e.g. be achieved by using a shrink wrap material. In order to accomplish adequate wetting, channels or the like may be provided on the inner surface of the receptacle or the outer surface of the catheter. | 2012-06-28 |
20120165792 | Pill Catchers - Devices and related methods arc provided for the controlled delivery of a therapeutic to a targeted location within a body. More particularly, methods and devices are provided for controlling the rate of passage of an orally administered pill through a body, as well as for controlling the delivery of a therapeutic within the pill at a specific location within the body. Various types of devices, generally referred to herein as “catchers,” are provided that can actively catch a pill as it passes through a body. The catcher can hold the pill at a specific location within the body until a predetermined event occurs, such as partial or complete. administration of a therapeutic within the pill. The catcher can then release the pill upon command and/or upon the occurrence of the predetermined event to allow the pill to pass out of the body. In other embodiments, various types of pills are provided that can actively engage a catcher and remain engaged with the catcher until a predetermined event occurs. | 2012-06-28 |
20120165793 | Pill Catchers - Devices and related methods are provided for the controlled delivery of a therapeutic to a targeted location within a body. More particularly, methods and devices are provided for controlling the rate of passage of an orally administered pill through a body, as well as for controlling the delivery of a therapeutic within the pill at a specific location within the body. Various types of devices, generally referred to herein as “catchers,” are provided that can actively catch a pill as it passes through a body. The catcher can hold the pill at a specific location within the body until a predetermined event occurs, such as partial or complete administration of a therapeutic within the pill. The catcher can then release the pill upon command and/or upon the occurrence of the predetermined event to allow the pill to pass out of the body. In other embodiments, various types of pills are provided that can actively engage a catcher and remain engaged with the catcher until a predetermined event occurs. | 2012-06-28 |
20120165794 | Pill Catchers - Devices and related methods are provided for the controlled delivery of a therapeutic to a targeted location within a body. More particularly, methods and devices are provided for controlling the rate of passage of an orally administered pill through a body, as well as for controlling the delivery of a therapeutic within the pill at a specific location within the body. Various types of devices, generally referred to herein as “catchers,” are provided that can actively catch a pill as it passes through a body. The catcher can hold the pill at a specific location within the body until a predetermined event occurs, such as partial or complete administration of a therapeutic within the pill. The catcher can then release the pill upon command and/or upon the occurrence of the predetermined event to allow the pill to pass out of the body. In other embodiments, various types of pills are provided that can actively engage a catcher and remain engaged with the catcher until a predetermined event occurs. | 2012-06-28 |