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23rd week of 2016 patent applcation highlights part 7
Patent application numberTitlePublished
20160158011INTRACARDIAC DEVICE TO CORRECT MITRAL REGURGITATION - A device structured to suppress mitral regurgitation by restricting prolapse of a mitral valve leaflet and including a base correspondingly dimensioned to the mitral valve and including a central portion, structured to allow blood flow there through and a peripheral portion or ring connected to the central portion in substantially surrounding relation thereto. An operative position of the base includes the central portion disposed in overlying, movement restricting relation to at least one of the valve leaflets and the ring concurrently anchored adjacent or directly to the native annulus of the mitral valve. The physical characteristics of the base facilitate its movement with and conformance to the mitral valve during diastole and systole cycles of the heart.2016-06-09
20160158012VALVE CUFF SUPPORT - A prosthetic heart valve includes a stent having a collapsed condition and an expanded condition. The stent has a proximal end, a distal end and a plurality of cells, each cell being formed by a plurality of struts. A valve assembly is secured to the stent and includes a cuff and a plurality of leaflets. The plurality of leaflets are attached to the cuff adjacent an underwire that extends about the perimeter of the cuff.2016-06-09
20160158013PROSTHETIC MITRAL VALVE - A prosthetic mitral valve with a compressible and expandable stent that, when expanded, is circumferentially oval, elliptical, or D-shaped, with a major axis and a minor axis ratio of from about 3:4 to about 4:5. Embodiments of the stent comprise three commissure posts disposed towards an outflow end and three curved cusp regions between adjacent commissure posts. Three flexible leaflets are attached to the commissure posts in a tri-foil configuration. Embodiments of the prosthetic mitral valve include an atrial ring disposed at the inflow end of the stent.2016-06-09
20160158015BONE IMPLANT - Provided is an implant receiving apparatus (2016-06-09
20160158016JOINT REPLACEMENT COMPONENT WITH INTEGRATED FIXATION PADS - In one embodiment, a prosthetic component includes a plurality of fixation pads coupled to a body portion. The fixation pads may be formed of a first material suitable for attachment to bone, and the body portion may be formed of a second material different from the first material and suitable to provide a bearing surface for a joint.2016-06-09
20160158017SELF-CENTERING, ANTI-SEIZING ACETABULAR LINER - A liner adapted for insertion into an acetabular shell for use in hip arthroplasty. The liner includes a concave inner surface adapted to engage a femoral head. The liner also includes an outer surface adapted to engage the acetabular shell and a rim that extends between the inner surface and the outer surface. The outer surface includes a locking section extending from the rim, a composite-curved section extending from the locking section at a first transition point, and a dome section extending from the composite-curved section, wherein at the first transition point, the composite-curved section is tangential to the locking section.2016-06-09
20160158018Prosthesis for Partial and Total Joint Replacement - A prosthetic joint is secured to the bones forming the original joint by utilizing strictly mechanical fasteners, for example, a threaded rod engaging a tapped intramedullary canal. Cross locking members may be provided. The need for bone cement is avoided. The prosthetic joint may be used to replace one end of one bone forming the joint, utilizing the naturally occurring end of the other bone. Alternatively, both bone ends may be replaced with prosthetic joint portions. The decision to replace one or both bone ends may be made mid-surgery. The prosthetic joint portions are secured together utilizing ligament reconstruction members made from portions of the patient's tendons or allograft tendons. A bearing forming the interface between the two joint portions is designed to wear in order to protect the remaining components from wear, and to be easily replaced in relatively simple future surgeries.2016-06-09
20160158019TIBIAL BASEPLATE WITH ASYMMETRIC PLACEMENT OF FIXATION STRUCTURES - An orthopaedic knee prosthesis is provided including a tibial baseplate component having a distal, bone-contacting surface with one or more fixation structures extending distally therefrom, in which the fixation structures are asymmetrically arranged within the baseplate periphery.2016-06-09
20160158020ARTIFICIAL KNEE JOINT IMPLANT - Provided is an artificial knee joint implant with which the balance between ligaments can be properly adjusted. An artificial knee joint implant includes a plurality of types of tibial plates-having tibia-side sliding faces that slide against femoral components and respectively having at least either the tibia-side sliding faces at different positions with respect to a tibia in a state where the tibial plates are fixed to a tibial tray attached to a tibia, or the tibia-side sliding faces in different shapes.2016-06-09
20160158021HUMERAL ARTHROPLASTY - Arthroplasty components include an articular surface and a bone-facing surface. The bone-facing surface includes a concave arrangement of planar surfaces which converge as they approach a middle portion of the articular surface. Instruments and implantation methods are also disclosed.2016-06-09
20160158022ATTACHMENTS FOR ORTHOPEDIC IMPLANTS - Apparatuses, kits, and methods for cementing an orthopedic implant to a bone, post attachment, are disclosed in some aspects of the present disclosure. A kit can include a prosthetic component and a cement applicator. The prosthetic component can include an attachment profile that corresponds to a mating profile formed on or in a bone. The cement applicator can be configured to apply a bone cement between the bone and the prosthetic component following alignment between the prosthetic component and the bone or another prosthetic component. The kit can also include a bone cement. A method can include positioning the prosthetic component adjacent to the bone, aligning the prosthetic component relative to the bone or another prosthetic component, and applying a bone cement between the bone and the aligned prosthetic component.2016-06-09
20160158023MULTI-PIECE INTERVERTEBRAL IMPLANTS - Intervertebral implants for implanting into an intervertebral space are provided. The implants can comprise one or more layers that are operably attached to one another. An implant can comprise a first layer having a first mating surface that mates with a second mating surface of a second layer. The first mating surface and the second mating surface can have features that allow them to complement each other. The implants can include one or more bore holes for receiving a fixation member. The bore holes can be horizontal, vertical or diagonal. In some cases, the bore holes will be blind bore holes.2016-06-09
20160158024Interbody Fusion Implant and Related Methods - An implant for spinal fusion includes a base member, a closure member, pins, and recesses. The base member includes a U-shaped configuration with an open end defined by first and second free ends of first and second side walls extending away from an end wall. The closure member is configured to form an enclosed interior when coupled with the base member. The closure member includes first and second overlapping portions configured to engage the first and second free ends. First and second pins are embedded in a respective one of the first and second free ends. First and second recesses are formed in a respective one of the first and second overlapping portions. The pins cooperate with the recesses to align and frictionally couple the base member with the closure member.2016-06-09
20160158025ADJUSTABLE TOTAL DISC REPLACEMENT DEVICE - Disclosed is an implantable artificial intervertebral disc joint replacement device for implantation between adjacent vertebral bodies. The device allows selective positioning of a disc implant element and comprises translatable surfaces, a mechanism for translation, a means for bone attachment, and an integrated disc implant. The device can be used in the lumbar, thoracic, and cervical regions of the spine in single or multi-level configurations. When implanted in a patient, the device includes an upper (cranial) component and a lower (caudal) component attached to the vertebral body above and below the replaced intervertebral disc respectively, with the joint implant integrated into the translatable surfaces. Following implantation, precise positioning of the joint implant within the intervertebral space with respect to the spinal axis is then adjusted based upon the particular anatomical and functional needs of the individual patient to satisfy spinal range of motion and stability requirements.2016-06-09
20160158026Devices and Methods for Tissue Engineering - A resorbable tissue scaffold fabricated from bioactive glass fiber forms a rigid three-dimensional porous matrix having a bioactive composition. Porosity in the form of interconnected pore space is provided by the space between the bioactive glass fiber in the porous matrix. Strength of the bioresorbable matrix is provided by bioactive glass that fuses and bonds the bioactive glass fiber into the rigid three-dimensional matrix. The resorbable tissue scaffold supports tissue in-growth to provide osteoconductivity as a resorbable tissue scaffold, used for the repair of damaged and/or diseased bone tissue.2016-06-09
20160158027ALIGNMENT GUIDE - An alignment guide is provided having a shaft having a longitudinal axis. The guide includes a housing configured to be attached to the shaft and rotatable about a first axis substantially perpendicular to the longitudinal axis. The housing includes a base and a plate. The base is attached to the shaft, and the plate is rotatable about the first axis relative to the base. The guide also includes a guide arm having a first portion and a second portion, the first portion being attached to the housing and extending from the housing along a second axis, the second portion extending from the first portion at a first predetermined angle.2016-06-09
20160158028MODULAR PROXIMAL BODY TRIAL - A trial system for determining a suitable proximal body implant for hip replacement surgery comprises a separator instrument, a trial body attachable to a distal stem, and an insert. The insert is positioned within the trial body to receive the separator instrument. As the separator instrument is rotated about its axis, a ramp element of the insert guides a pin of the separator instrument, so as to separate the trial body from the distal stem. Additional apparatus, methods, and systems are disclosed.2016-06-09
20160158029POWERED AND PASSIVE ASSISTIVE DEVICE AND RELATED METHODS - Systems and methods for assistive devices for replacing or augmenting the limb of an individual, such devices comprising a joint and a powered system; the powered system having a first configuration in which the powered system rotates the joint by applying power to the joint, and a second configuration that allows for rotation of the joint without actuation of the powered system.2016-06-09
20160158030PROSTHETIC FOOT - A stable shock absorbing prosthetic foot that transfers energy between heel strike and toe-off. A toe plate is separated from one or more other plates by a bumper assembly located at each of the toe end and heel end of the foot. Certain embodiments of the shock absorbing foot of the present invention are designed for use with a prosthetic ankle. A torsion adapter may also be used to attach a prosthetic foot of the present invention to the remainder of a prosthesis.2016-06-09
20160158031Quasi-Active Prosthetic Joint System - A prosthetic joint device includes a foot portion and a main body pivotally coupled to the foot portion at a first joint. A first compliant member is coupled to the main body and foot portion. A first clutch is coupled to the first compliant member. An actuator is coupled to the first clutch to lock and unlock the first clutch and engage and disengage the first compliant member. A control system is coupled to the actuator to control the actuator based on a gait activity. The first clutch is locked to engage the first compliant member. A second compliant member is coupled to the main body and foot portion. A sensor is coupled to the prosthetic joint device to measure a physical state of the prosthetic joint device. The engagement and disengagement of the first compliant member is timed based on the physical state of the prosthetic joint device.2016-06-09
20160158032Quasi-Active Prosthetic Joint System - A prosthetic joint device includes a foot portion and a main body pivotally coupled to the foot portion at a first joint. A first compliant member is coupled to the main body and foot portion. A first clutch is coupled to the first compliant member. An actuator is coupled to the first clutch to lock and unlock the first clutch and engage and disengage the first compliant member. A control system is coupled to the actuator to control the actuator based on a gait activity.2016-06-09
20160158033Powered prosthetic devices using EMG-based locomotion state classifier - Real-time control of a prosthetic device using EMG-based locomotion state classification computes a histogram [2016-06-09
20160158034METHOD AND APPARATUS OF A LINER INTERFACE WITH NEURAL RECEPTORS - A liner interface and method of making the liner interface comprising attaching non-compressible deformable electrically conductive receptors to an inner surface of a fabric layer, placing the fabric layer into a female part of a molding machine, axially deforming the deformable receptors from their initial thickness with a male part of the molding machine, injecting a molten gel elastomer into the molding machine to completely surround and adhere to the receptors and inner surface of the tubular fabric layer, allowing the molten gel to cure, and removing the male part from the molding machine and allowing the axially deformed receptors to axially expand beyond the inner surface of the cured liner interface.2016-06-09
20160158035Adaptable Socket System, Method, and Kit - An adjustable socket system, method, and kit for use with prosthetic devices or orthotic, orthopedic, or exoskeletal support devices that includes a paddle and a compressing device coupled to the paddle. The paddle is chosen from a plurality of paddles of different shapes in such a way that the paddle inner surface is substantially coextensive with a soft tissue area overlying skeletal structures. The compressing device presses the paddle against the soft tissue area in order to minimize the motion of the paddle relative to the underlying skeletal structures without causing discomfort to the user or compressing areas not in contact with the paddle, allowing compressed tissue to flow into uncompressed areas. The system, method, and kit can include an external tool, sensors, actuators, and controllers, to assist fitting and for adjustment after fitting. A stabilizer can be added to resist the bending force on the paddle.2016-06-09
20160158036METHOD OF MANUFACTURING IMPLANTS - A method of manufacturing a tubular medical implant, such as a stent, includes introducing a liquid polymer material into an axial lumen of an elongate metal tube, the metal tube having an inner wall defining the lumen; allowing the polymer material to solidify within the metal tube lumen, the solidified polymer forming a high friction surface in contact with the inner wall of the metal tube; securing the metal tube, including the solidified polymer material therein, to a collet of a laser etching system; and laser etching a predetermined pattern of openings in the metal tube.2016-06-09
20160158037BIODEGRADABLE DOUBLE STENT - A biodegradable double stent is used for various organs such as a biliary tract, an esophagus, an airway and a ureter. A biodegradable stent having a hollow cylindrical body woven out of a separate wire made of biodegradable polymer so as to have a plurality of rhombic spaces is fixed to an intermediate portion of a primary stent having a cylindrical body. When administered into the organ, the biodegradable stent has its original function of expanding the organ, and is firmly supported in the inner wall of a narrowed passage of the organ by pressurizing the inner wall of the narrowed passage of the organ. After a predetermined time period has elapsed, the biodegradable stent is gradually degraded away by bodily fluids, thereby enabling the primary stent to be easily removed from the organ.2016-06-09
20160158038FLOW DIVERSION DEVICE - A flow diversion device for the treatment of intracranial aneurysms and other medical conditions is disclosed. The flow diversion device may include a generally tubular wire stent frame formed from a plurality of zig-zag shaped wire elements that are coupled together. The device further includes a base layer of graft material coupled to the wire stent frame and surrounding at least a portion thereof, the wire stent frame maintaining the base layer in an open condition. In some embodiments, the base layer may be formed of porous graft material having a plurality of pores formed thereon to provide a passageway for a small blood flow to maintain the long term patency of important small side branches, while also reducing blood flow to the aneurysm to promote occlusion and avoid potential rupture.2016-06-09
20160158039MEDICAL DEVICE FOR INSERTING INTO A HOLLOW ORGAN OF THE BODY - The invention relates to a medical device for inserting into a hollow organ of the body. The device has a compressible and expandable lattice structure made of webs, which are integrally connected to each other by web connectors and which bound closed cells of the lattice structure, wherein the web connectors each have a connector axis extending between two cells which, in a longitudinal direction of the lattice structure, are adjacent to each other. During the transition of the lattice structure from the production state to a compressed state, the web connectors rotate in such a way that an angle between the connector axis and a longitudinal axis of the lattice structure changes, in particular increases, during the transition of the lattice structure from a completely expanded production state to a partially expanded intermediate state.2016-06-09
20160158040INFLATABLE BALLOON STENT - An illustrative stent may comprise an elongated tubular balloon having a first end and a second end and an intermediate region disposed therebetween. The elongated tubular balloon may have an inner wall and an outer wall, the inner wall and the outer wall connected at the first end and the second end to define an enclosed inflation chamber between the inner wall and the outer wall. The stent may further include an inflation valve.2016-06-09
20160158041MAGNETIC HANDLE ASSEMBLY FOR PROSTHESIS DELIVERY DEVICE - A prosthesis delivery comprising a rotatable inner cannula and a prosthesis releasably coupled to a proximal end of the inner cannula is disclosed. The inner cannula has a first position in which the prosthesis is retained on the cannula and a second position in which the prosthesis is released. At least one magnet is disposed on the inner cannula. A handle assembly is disposed about a distal portion of the inner cannula, the handle assembly comprising a rotary collar having at least one magnet disposed on the inner surface thereof, wherein the at least one magnet disposed on the rotatable inner cannula and the at least one magnet disposed on the inner surface of the rotary collar comprise a magnetic attraction. The magnetic attraction translates torque from rotation of the rotary collar to rotate the inner cannula from the first position to the second position to thereby release the prosthesis.2016-06-09
20160158042TWISTED STENT - A stent is disclosed and can include a stent body having a longitudinal axis. The stent body can also have a network of struts that can define a plurality of cells defined between interconnected struts. Each of the plurality of cells includes a major axis that is angled with respect to the longitudinal axis to form a cell angle, b.2016-06-09
20160158043INTERNAL ILIAC PRESERVATION DEVICES AND METHODS - A system for internal iliac preservation includes a catheter having a distal catheter portion and a proximal catheter portion; a first guidewire having a proximal portion extending from the proximal catheter portion, a distal portion and a medial portion disposed between the proximal portion and the distal portion; a first outer sheath slidably disposed over distal catheter portion; and an integrated second delivery system disposed within the outer sheath at the distal catheter portion. The integrated second delivery system includes a second guidewire; an expandable stent-graft disposed over a lumen of the second guidewire, and a slidable connector slidably disposed over the medial portion of the first guidewire, where the second guidewire is slidably engaged with the slidable connection to permit movement of the integrated second delivery system along the first guidewire when the first outer sheath is retracted from distal catheter portion.2016-06-09
20160158044Systems And Methods For Treating A Carotid Artery - Systems and methods are adapted for treating the carotid artery. The systems include interventional catheters and blood vessel access devices that are adapted for transcervical insertion into the carotid artery. Embodiments of the systems and methods can be used in combination with embolic protection systems including blood flow reversal mechanisms, arterial filters, and arterial occlusion devices.2016-06-09
20160158045DELIVERY DEVICE WITH AN EXPANDABLE POSITIONER FOR POSITIONING A PROSTHESIS - A prosthesis delivery device comprises a cannula having an expandable positioning device disposed at the proximal end thereof. A prosthesis is retained on the cannula distal of the expandable device. Expansion of the expandable device retains and centers the delivery device and the prosthesis carried thereon in the vessel and allows repositioning of the prosthesis without contacting the proximal end of the prosthesis with the vessel walls prior to deployment.2016-06-09
20160158046FLOW REGULATION VALVE FOR CONTROLLING INFLATION RATE OF A BALLOON DEPLOYING A SCAFFOLD - An apparatus and method for controlling inflation pressure, pressurization rate, and volumetric flow rate of a balloon during deployment of a stent or scaffold is disclosed.2016-06-09
20160158047TWO PRONGED HANDLE - Medical device delivery systems and methods of using the same are disclosed. Some of the delivery systems may include a catheter having a proximal end, a distal end, and a sheath. A bifurcated gripping member may be disposed on the proximal end of the catheter and the bifurcated gripping member may include a first gripping prong and a second gripping prong. A deployable prosthesis may be disposed on the distal end of the catheter.2016-06-09
20160158048RELEASABLE VASCULAR DEVICE CONNECTION - A medical device, for insertion into an anatomical vessel, can include a sheath, a delivery wire, and a frame or vessel-engaging member. The delivery wire can have a first stop, a second stop, and a coupling area between the first and second stops. The coupling area can be disposed within and movable relative to the sheath. The frame or vessel-engaging member can have a matrix of cells, first and second tapered sections, and interlocking members. The interlocking members can be attached to the tapered sections. The interlocking members can be releasably coupled to the delivery wire at the coupling area with the interlocking members surrounded and held in the coupling area by the sheath. The interlocking members can be movable relative to the sheath, and the interlocking members can separate from each other when the interlocking members are positioned distal to the sheath.2016-06-09
20160158049DELIVERY SYSTEM FOR A SELF EXPANDING STENT - A system for delivering a stent from a catheter sheath in a longitudinal direction comprising: a thumbwheel mounted on an axle, the axle being supported by opposite walls of a housing; a first pinion mounted on the axle; a second pinion mounted on the axle, whereby rotation of the thumbwheel causes rotation of the first pinion and rotation of the second pinion; a first rack, enageable with the first pinion at a first surface of the first pinion, the first rack being operably connected with a stent-engaging member; a second rack, engageable with the second pinion at a second surface of the second pinion, the second surface being disposed in a direction diametrically opposite the first surface, the second rack being operably connected with a sheath configured to confine the stent.2016-06-09
20160158050DELIVERY DEVICE HANDLE ASSEMBLY FOR THE SEQUENTIAL DEPLOYMENT OF A PROSTHESIS - A prosthesis delivery device and method of using the same is described. The delivery device comprises a rotatable inner cannula extending from a proximal end to a distal end with a prosthesis releasably coupled to the proximal end. A delivery handle assembly is disposed at the distal end of the delivery device. The handle comprises a first handle disposed about the inner cannula, a rotary dial rotatably disposed about a distal end of the first handle and a second handle disposed about at least a portion of the distal end of the first handle. The second handle is longitudinally moveable relative to the first handle between a first position wherein the sheath is coaxially disposed about the prosthesis and rotation of the rotary dial is prevented, and a second position wherein the sheath is retracted distally to expose at least a portion of the prosthesis and rotation of the dial is permitted.2016-06-09
20160158051METHODS AND DEVICES FOR TREATING OBESITY, INCONTINENCE, AND NEUROLOGICAL AND PHYSIOLOGICAL DISORDERS - Methods and devices are disclosed that provide therapeutic benefit and treatment for a variety of neurologic and physiologic conditions that include obesity, urinary incontinence, and sensory system disorders.2016-06-09
20160158052Medical Device and Application Thereof - A duodenal internal covering membrane is disclosed herein. The covering membrane is made of a biocompatible biodegradable or non-biodegradable material and/or hydrophobic material and mainly comprises an elastic ampulla and a tubular portion. The ampulla contains biocompatible bionic microarray adhesive piece capable of realizing strong adhesion through a force exerting direction without pricking into an intestinal tissue and capable of being easily detached and recovered. The adhesive piece has good stability, strong adaptability to material and appearance, good self-cleaning property, no injuries and pollution to the intestinal tissue and can be adhered and detached repeatedly. The adhesive piece can realize mutual support with other parts in the functions. When contents in the intestinal duct move, because there is no traction force which is nearly perpendicular, the internal covering membrane cannot be detached. When the duodenal bulb expands, as the internal covering membrane has no opposite traction force which is nearly perpendicular, the internal covering membrane cannot be detached either. When recovery is performed, the detachment and recovery can be easily realized by force exerting which is nearly perpendicular. The duodenal internal covering membrane can be prepared into a medical device for preventing and treating obesity and diabetes without injuring the intestinal tissue.2016-06-09
20160158053DEVICE FOR MITIGATING PLANTAR FASCIITIS - A device includes a truss structure, an upper anchor, and an actuator. The upper anchor is proximally located from the truss structure and the actuator couples a posterior portion of the truss structure to a posterior portion of the upper anchor. The actuator is designed to provide assistive force to urge heel lift during ambulation such that the tension in the plantar fascia is reduced.2016-06-09
20160158054ADJUSTABLE CERVICAL COLLAR - An embodiment of an adjustable cervical collar system includes a collar body and a chin support structure assembled together, about respective pivots at opposed ends, for pivotal movement about a pivot axis so that the angle subtended by the collar body and chin support structure can be adjusted. The collar body and chin support structure can be locked in a selected position by a locking mechanism. A release mechanism permits the wearer to release the locking mechanism using one hand, and the angular position of the chin support structure relative to the collar body is changed manually. When the release mechanism is released, the locking mechanism automatically locks the chin support in the new position. A neck strap is detachable from the chin support structure and the collar body, and its length is also adjustable.2016-06-09
20160158055Stabilization Table and System - A stabilization system configured to be arranged on a floor comprising a table having generally flat surface having a longitudinal axis for receiving a human body having a first hole, a second hole, and third hole within the flat surface, each hole having a hole shape with a generally vertical inner surface and configured to receive a bolster connector, a bolster comprising a bolster connector having an outer shape corresponding to the hole shape, the bolster connector configured to be reversibly engaged by one of the holes, a generally flat surface generally perpendicular to the table surface when the bolster connector is engaged by one of the holes.2016-06-09
20160158056LEAK DETECTION SENSOR FOR A STOMA POUCH AND PROCESS FOR MAKING SAME - A leak detection sensor includes a pair of electrodes, each electrode being coated with an electrically insulating coating having fractures formed therein having a breadth of less than 500 nm, whereby a current can flow between the electrodes when the electrodes are exposed to an electrically conductive fluid. An alarm is activatable in response to current flowing between the electrodes.2016-06-09
20160158057OSTOMY APPLIANCE WAFER HAVING AN ABSORBENT LAYER LOCATED BETWEEN A FIRST ADHESIVE AND A SECOND ADHESIVE - An ostomy appliance wafer is provided with a stoma-receiving hole formed through the wafer. The wafer includes a backing layer, and an absorbent layer located between a first adhesive and a second adhesive. The first adhesive is disposed over the backing layer to define a peripheral edge area, a central area surrounding the hole, and an intermediate area of the wafer that is located between the peripheral edge area and the central area. The absorbent layer is disposed on the first adhesive either in A) the central area of the wafer, B) the intermediate area of the wafer, or C) the central area and the intermediate area of the wafer. The second adhesive is disposed over both a portion of an outer edge area of the absorbent layer and a portion of the first adhesive peripheral to the outer edge area of the absorbent layer.2016-06-09
20160158058CONTACT LENS AND OPHTHALMIC TREATMENT DEVICE HAVING SAME - A contact lens, according to the present invention, comprises: a housing having a light-incident part on which a therapeutic beam oscillated from a beam generation part is incident, and a light-emitting part for guiding the therapeutic beam incident from the light-incident part to an eyeball; a first sensing part arranged between the light-incident part and the light-emitting part so as to sense the reaction occurring in a healing site of the eyeball on which the therapeutic beam is irradiated; and a second sensing part arranged in a region of the light-emitting part spaced from the first sensing part so as to sense whether contact has been made with the eyeball.2016-06-09
20160158059MEMS DEVICE AND METHOD FOR DELIVERY OF THERAPEUTIC AGENTS - Embodiments of an implantable device for delivering a therapeutic agent to a patient include a reservoir configured to contain a liquid comprising the therapeutic agent, and a cannula in fluid communication with the reservoir. The cannula is shaped to facilitate insertion thereof into a patient's eyeball.2016-06-09
20160158060OPHTHALMIC SHUNT AND METHOD - An ophthalmic shunt includes a seal or septum through which multiple injections of the therapeutic agent can be made as needed, thereby avoiding repeated injury to the sclera. The therapeutic agent is temporarily carried in a tube connected to the septum. The therapeutic agent release may be rapid or sustained over a period of time.2016-06-09
20160158061TECHNIQUE FOR SETTING ENERGY-RELATED LASER-PULSE PARAMETERS - A method for energy setting of pulsed, focused laser radiation is provided. In the method, a relationship between a threshold pulse energy required for causing irreversible damage in a material and a pulse duration is established. The relationship allows for obtaining a threshold pulse energy for each of a plurality of pulse durations, including one or more pulse durations in a range between 200 fs and smaller. The relationship defines a decreasing threshold pulse energy for a decreasing pulse duration in the range between 200 fs and smaller. For a given pulse duration in the range between 200 fs and smaller, an associated threshold pulse energy is determined based on the established relationship. The pulse energy of the laser radiation is set based on the determined associated threshold pulse energy.2016-06-09
20160158062SYSTEM AND METHOD FOR PROVIDING PRESSURIZED INFUSION - The present invention relates generally to providing pressurized infusion of liquids and, more particularly, is directed to providing a stable and pressurized flow of irrigation fluid to the eye during surgery.2016-06-09
20160158063INTRAOCULAR SHUNT MANUFACTURE - An intraocular shunt can be manufactured using a system that includes a liquid bath and a wire, which is moved through the bath. When moved through the bath, the wire is coated with a material, such as gelatin. For example, the liquid bath can have a top layer, including water, and a bottom layer, including gelatin. The coated wire passes through an aperture formed in a plate component of the system. The gelatin can be dried on the wire in a humidity-controlled space, thereby forming the shunt.2016-06-09
20160158064MASK WITH A COMFORT ELEMENT - An eye protective mask designed for the practice of outdoor sports, for example, includes an eye protective screen, a frame supporting the screen, and a comfort element affixed to the frame. The comfort element includes a nasal portion configured to come into contact with a portion of the user's nose, and a frontal portion configured to come into contact with a portion of the user's forehead. The material used for the nasal portion has different mechanical compression properties from the material used for the frontal portion, such that the maximum compression, or stroke, of the material of the nasal portion caused by a predetermined compressive force is greater than the compression of the material of the frontal portion caused by the same predetermined compressive force.2016-06-09
20160158065RING COMPRESSION BANDAGE - A toroidal compression bandage includes: a soft fibrous material, defined by an absorbency of a predetermined amount; a compression bandage form comprised of soft fibrous absorbent material in a rolled, wrapped form and of a shape defined by a circle revolved in three-dimensional space about a circular axis coplanar with the circle, wherein the axis of revolution does not touch the rotated circle, to define a torus ring compression bandage; an aperture defined within a center area of the torus ring compression bandage as it is formed, the aperture having a predetermined diameter and configured for placement directly over a trauma wound to avoid contact with the trauma wound; and a compression surface defined on an underside of the torus ring compression bandage, the compression surface configured for circumferential placement around the trauma wound to avoid direct contact of the trauma wound, and for absorption placement around the trauma wound.2016-06-09
20160158066NEGATIVE PRESSURE WOUND DRESSING - A negative pressure wound dressing is provided. The negative pressure wound dressing sequentially includes a backing layer, a water blocking layer, an absorbent layer and a wound contacting layer. Wherein, the backing layer includes a connecting aperture for fluidly communicating to a negative pressure source. The wound contacting layer includes a surface layer for wound contacting and a plurality of chambers containing a medication, wherein openings of the chambers are disposed on the surface layer for releasing the medication contained in the chamber. The medication can be prevented from being suctioned to the absorbent layer and can be released toward the wound to enhance the wound healing by using the negative pressure wound dressing.2016-06-09
20160158067REDUCED-PRESSURE, WOUND-CLOSURE AND TREATMENT SYSTEMS AND METHODS - A reduced-pressure, wound closure system is presented that generates a closing force on a surface wound and optionally provides reduced pressure to a body cavity or tissue site. The sealed contracting member, when placed under reduced pressure, generates the closing force. One illustrative system includes a first attachment member and a second attachment member, a sealed contracting member coupled to the first attachment member and the second attachment member, and wherein the closing force is generated between the first attachment member and the second attachment member when reduced pressure is supplied to the sealed contracting member. Other systems and methods are presented.2016-06-09
20160158068FOAM DRESSING WITH INTEGRAL POROUS FILM - Wound dressings and wound inserts comprising a porous film layer and at least a channel, wound inserts of forming wound inserts comprising a porous film layer and at least a channel, and wound-treatment wound inserts.2016-06-09
20160158069Method and Apparatus for Applying an Elastic Material to a Moving Substrate in a Curved Path - Aspects of the methods and apparatuses relate to making elastic laminates, and more particularly, methods and apparatuses for applying elastic material in a curved path onto an advancing substrate. The elastic material may be in various forms, such as for example, elastic strands and/or ribbons. Apparatuses and methods disclosed herein may also provide for the application of viscous fluids, such as adhesives, in pre-determined patterns to the elastic material while being positioned on an advancing substrate.2016-06-09
20160158070TAMPON TEST METHOD AND APPARATUS - A method for in vitro testing of an absorbent article includes the steps of inserting the absorbent article into a radiolucent simulated body cavity, placing the radiolucent simulated body cavity into a radiolucent pressure chamber, placing the radiolucent pressure chamber into a radiological device, pressurizing the radiolucent pressure chamber to a predetermined pressure, providing test liquid through the test liquid port and to the absorbent article, acquiring data relating to the absorbent article and the test liquid via the radiological device and an associated computing device, and analyzing the acquired data. The radiological pressure chamber includes a simulated body cavity arranged and configured to accommodate the absorbent article, a test liquid port, and a pressure control system. The radiolucent test device has at least one radio scanning element rotatable about radiolucent test device support having the pressure chamber disposed thereon.2016-06-09
20160158071APPARATUS AND METHOD FOR ANALYSING EVENTS FROM SENSOR DATA BY OPTIMISATION - The present invention relates to sensor signal analysis. It relates particularly, but not exclusively, to methods, systems and devices for monitoring and processing the sensor signals to determine automatically characteristics of events represented by the sensor signals. The present invention is particularly, but not exclusively, related to methods, systems and devices for monitoring moisture in absorbent articles such as diapers, incontinence garments, dressings and pads resulting from wetness events caused by, for example, urinary and/or faecal incontinence. In an embodiment, the invention includes a method for processing sensor signals representing an event in an absorbent article. The method comprises: receiving sensor signals from a sensor representing one or more events in an absorbent article; and processing the sensor signals to determine a characteristic of at least one event in the absorbent article. One such characteristic can include the volume of a voiding event such as a urinary incontinence event. In another embodiment, the method includes carrying out a learning phase including the steps of: receiving sensor signals representing one or more events in each of one or more absorbent articles; receiving observation data indicative of a cumulative characteristic of the one or more events in each absorbent article; and identifying an optimal mathematical model describing a relationship between the sensor signals and the observation data. Such events can include urinary incontinence events occurring in absorbent articles such as diapers. Observation data can be measured cumulative volume of a cycle of voiding events occurring in a diaper.2016-06-09
20160158072ABSORBENT ARTICLE WITH A WAISTBAND AND LEG CUFFS HAVING GATHERS - A disposable absorbent article comprising a first waist region, a second waist region, a crotch region disposed between the first waist region and second waist region; a first waist edge and a second waist edge; and a first longitudinal edge and a second longitudinal edge; the disposable absorbent article comprising a waistband and a leg gasketing system, wherein the waistband has a first gather count and the leg gasketing system has a second gather count such that the ratio of the first gather count to the second gather count is from about 0.75 to about 1.25.2016-06-09
20160158073Disposable Absorbent Pants With Advantageous Stretch And Manufacturability Features, And Methods For Manufacturing The Same - A disposable absorbent pant that includes a central chassis and a belt structure is disclosed herein.2016-06-09
20160158074ABSORBENT ARTICLE - In an absorbent article a three-dimensional opening hole mesh sheet, having a face which faces skin of a wearer of the absorbent article and a reverse or opposite side face within the absorbent article, is combined with an absorber which includes an air-laid pulp non-woven fabric. The mesh sheet has an array of mechanically embossed concave portions forming protrusions on the skin-facing face of the mesh sheet and recesses on the reverse or opposite face, i.e., the unexposed face inside the absorbent article.2016-06-09
20160158075CORE ASSEMBLY FOR ABSORBING LIQUIDS - An absorbent core assembly for use in a product for absorbing a liquid is disclosed. The core assembly has a first section and a second section. The first section is a quilted porous material that contains a slow acting but high absorption capacity SAP therein. The, second section is a quilted porous material that contains a fast acting but lower absorption capacity SAP therein. The first and second sections are in fluid communication with each other, whereupon a liquid which is exposed to the core assembly flows through the first section to the fast acting SAP in the second section to be absorbed quickly and rapidly by the fast acting SAP therein, while the slow acting SAP desorbs or takes liquid away from the fast acting SAP as well as absorbing the liquid itself to thereby trap the liquid in the core assembly.2016-06-09
20160158076FOLDING STRETCHER - A rescue device includes at least two parallel columns defining a core section. The columns are located in a substantially flat plane with each column lying adjacent at least one other column. Each column includes rods, a connection device, and at least one sleeve. Each rod is located within a sleeve and the rods are connectable in series by the connection devices to form a column. The rescue device further includes at least one linking element. Each sleeve is connected to at least one linking element.2016-06-09
20160158077EMERGENCY VEHICLE PATIENT TRANSPORT SYSTEMS - Emergency vehicle patient transport systems are disclosed. In one embodiment, an emergency vehicle patient transport system includes: a loading passage providing access to an interior of an emergency vehicle; one or more tracks coupled to a floor of the emergency vehicle, a ceiling of the emergency vehicle, a wall of the emergency vehicle or combinations thereof wherein, a travel path is delineated by the one or more tracks; and a chair slidingly engaged with the one or more tracks, and vertically positioned between the floor and the ceiling. The chair locks in one or more set positions. And, the one or more set positions are selected from a group consisting of an airway care position, an extended airway care position, a procedural care position, a responder position, a patient care position, and a patient load position.2016-06-09
20160158078TWO-WHEELED SELF-BALANCING WHEELCHAIR - A two-wheeled self-balancing wheelchair is provided, including: a housing having support brackets which are mounted directly below rotary shafts of the motors located at both sides of the bottom side of the housing, rotary shafts of the motors which are drawn out from the housing, and wheels which are mounted to the rotary shafts and rotate in a way as to read an inclination angle of a rider's body; a saddle frame which is mounted on the upper part of the housing; and multipoint supports mounted at the front and rear of the support brackets, each of the multipoint supports having a first hinge part and a second hinge part which are formed at the front ends of the multipoint support to be able to rotate by bolts and are connected with each other through a connection bar and a third hinge part.2016-06-09
20160158079Inverted pendulum type vehicle - Electric locomotion means comprising a dynamically stabilised vehicle (2016-06-09
20160158080STANDING-UP ASSIST TOOL AND WALKING SUPPORT DEVICE - The present invention is provided with a support mechanism for an armrest part that includes a gas spring. The support mechanism supports the armrest part in a state of being able to change a posture between an ordinary posture and a forward-tilt posture when the gas spring is locked, and the support mechanism supports the armrest part so as to make the armrest part move with forming an arc from a sitting corresponding position to a standing corresponding position that is located at a forward upper position when the gas spring is unlocked. A gas spring switch part that does not obstruct the locked state of the gas spring when the armrest part is in the ordinary posture and that releases the locked state of the gas spring at a time when the armrest part is in the forward-tilt posture is arranged between the gas spring and the armrest part.2016-06-09
20160158081Actuator System - Adjustable article of furniture comprising at least one adjustable element and furnished with an actuator system comprising at least one electrically driven linear actuator with an electrical motor and an electrical controller with an operation device, wherein the system in equipped with a battery pack for operating the system during mobile situations, where a mains supply is not readily available. The battery pack is equipped with a frontend, which allows for the battery pack to be retrofitted on existing actuator systems, without compromising the functionality of the actuator system in connection with charging of the battery. Moreover, the frontend is adapted to facilitate continued viewing of remaining power on the battery pack even though the technology of the battery pack is replaced, e.g. from lead battery to lithium ion battery.2016-06-09
20160158082Multimodality Medical Procedure Mattress-Based Device - A mattress system is provided that is optimized for the hospital setting and includes a guiderail system that accepts a variety of accessories for attachment thereto. The guiderail system may have integrated data lines, power lines, gas lines, and/or fluid lines. Also provided are radioabsorbant shields, trays and other components designed for optimal use with the mattress system.2016-06-09
20160158083PATIENT SUPPORT WITH ENERGY TRANSFER - A patient support including a base; a patient support surface supported by the base; an electrically powered device; a rechargeable power storage device for powering the electrically powered device; and a receiving coil electrically coupled to the rechargeable power supply for inductive coupling with a transmitting coil. The receiving coil is for recharging the rechargeable power supply when the receiving coil is inductively coupled to the transmitting coil.2016-06-09
20160158084METHODS FOR AMBULATORY OXYGEN THERAPY - The present invention provides a topical oxygen therapy system for treating chronic non-healing wounds. The system is configured to be extremely portable, allowing patients to be completely ambulatory during treatment. The topical oxygen therapy system includes an oxygen source and a wound dressing capsule. The oxygen source includes a miniature compressed oxygen cylinder and a miniature pressure regulator that delivers oxygen through an outlet tube to the interior of the wound dressing capsule. The oxygen source may be attached directly to or integrated into the wound dressing capsule. Alternatively, the oxygen source and wound dressing capsule may be separate modules connected by a flexible tube.2016-06-09
20160158085INCUBATOR - An incubator is provided that prevents damage to the arm of an operator when an arm abuts against the upper end segment of a baby guard relatively hard while inserting the arm into an infant accommodation space. The walls of the baby guards around the infant accommodation space have bent segments that are sufficiently strong to serve as a guard structure on the periphery of the infant accommodation space. Each of the bent segments in the upper end segments of the walls includes an inclined segment and a substantially horizontal segment integrally connected to a distal end of the inclined segment. At least some of the walls can pivot between upward and downward positions, thereby closing or revealing cassette trays.2016-06-09
20160158086Systems, Devices and Methods for Exercising the Lower Limbs - The present invention relates to devices and methods for exercising the lower limbs, in particular for exercising lower limbs. The devices are suitable for training the lower limbs of persons suffering from paraplegia or hemiplegia or musculoskeletal disorders in general. In some aspects, the present invention relates to powered articulated systems (ASs) and to the rehabilitation by aid of said ASs. The parallel or hybrid ASs of the invention are based on a parallel or hybrid, lambda-type framework and are controlled by a data processing unit. The ASs are preferably controlled by a closed-loop, real time control system.2016-06-09
20160158087PORTABLE HUMAN EXOSKELETON SYSTEM - A portable human exoskeleton system (2016-06-09
20160158088Suspension-Based Walking Assistance Aide Apparatus - A walking assistance device configured to permit the independent movement of an individual via simulated weight reduction is described. The device is configured to partially suspend a portion of a user's weight via a suspension system, facilitating the movement of a user with experiencing difficulty walking without assistance. The suspension system of the device preferably employs at least one cable in communication with a pulley system, an electric lifting actuator, and a harness. The harness of the device is configured to affix to the legs and torso of the user, and connects to at least one cable of the pulley system via at least one hook. The lifting actuator engages the pulley system, enabling the user to control the percentage of weight lifted. A frame houses the suspension system of the device, and is configured to move laterally via wheels on the bottom of the frame of the device.2016-06-09
20160158089SENSORY FURNITURE SYSTEM FOR TREATMENTS, METHOD OF USE, AND METHOD OF MANUFACTURE - A sensory lounging chair system and method of use. The system generally includes a frame, a pump, air tubes connecting the pump to a pair of inflatable air tubes, pressure release valves, piping and hardware, a pressure sensor, and a fabric cover. In a preferred embodiment, the pump and pressure sensor are powered by a power supply connected to a terminal board, which in turn is connected to the pump and the pressure sensor. The fabric cover provides a comfortable barrier between the occupant and the air tubes, which initially are usually deflated or less than fully inflated. As the pressure in the air tubes increase, deep touch pressure is applied to the occupant's body in the places where the air tubes are in contact with the occupant. Deep touch pressure is thus applied to the occupant via contact with the tubes through the fabric cover.2016-06-09
20160158090SENSORY UPRIGHT CHAIR FOR APPLYING DEEP TOUCH PRESSURE AND METHOD OF USE - A sensory upright chair system to provide deep touch pressure to a person and method of use. The system includes a frame, a pump, a pair of inflatable air tubes, a pressure release valve, hoses and hardware, a pressure sensor, and a fabric cover. The pump and pressure sensor are connected to a power supply, and connected to the air tubes and pressure release valve via hoses and hardware. Switching on the power supply provides controlled inflation to the air tubes. A user sits in the chair between deflated air tubes. As the pressure in the air tubes increase, deep touch pressure is applied to the occupant's body where the air tubes contact the occupant. The fabric cover provides a comfortable barrier between the occupant and the air tubes. Deep touch pressure is thus applied to the occupant via contact with the tubes through the fabric cover.2016-06-09
20160158091SYSTEM FOR RESPIRATORY DISORDER THERAPY WITH SELECTION OF STIMULATION STRATEGIES - The disclosure relates to a system including a processor configured to generate stimulation control signals in response to a detection of a respiratory disorder. The system further includes at least one kinesthetic effector with a vibrating electromechanical transducer applied to a site on a patient's skin for delivering a kinesthetic stimulation energy determined by the control signals. The processor is further configured to determine the effectiveness of a stimulation by detecting a disappearance of the respiratory disorder. The processor is further configured to determine a therapy by selecting a stimulation strategy among several stimulation strategies according to a type of expected or detected disorder.2016-06-09
20160158092SYSTEM FOR RESPIRATORY DISORDER THERAPY WITH STABILIZATION CONTROL OF STIMULATION - The disclosure relates to a system including a processor configured to generate stimulation control signals in response to a detection of a respiratory disorder. The system further includes at least one kinesthetic effector with a vibrating electromechanical transducer applied to a site on a patient's skin for delivering a kinesthetic stimulation energy determined by the control signals. The processor is further configured to determine the effectiveness of a stimulation by detecting a cessation of the respiratory disorder. The processor is further configured to extend the stimulation control signals for a determined duration following the cessation of the respiratory disorder.2016-06-09
20160158094HEATING AND COOLING MAT ASSEMBLY - A heating and cooling mat assembly includes a mat having a bottom wall, a top wall and a perimeter wall. A conduit is positioned in the man and has fluid therein. A pump is in fluid communication with the conduit to pump the fluid through the conduit. A heat emitter is thermal communication with the liquid in the conduit. The heat emitter warms the liquid when the heat emitter is turned on. A cartridge is removably couplable to the mat. The cartridge includes a pair of first ports. The conduit is in fluid communication with a pair of second ports. Each of the first ports is removably coupled to one of the second ports to fluidly couple the conduit to the cartridge. The cartridge is fillable with a cold fluid so that the conduit is cooled when the pump is turned on and the cartridge is coupled to the conduit.2016-06-09
20160158095SOUND THERAPY SYSTEMS AND METHODS FOR RECALIBRATING THE BODY'S ELECTROMAGNETIC FIELD - A sound treatment system includes an audio system for transmitting tones of predetermined frequencies through a plurality of outputs. A sound transmitting device is electrically connectable to one or more of the outputs, and includes a speaker for transmitting the tones received. The speaker is adjacent to crystal which is vibrationally responsive to the tones. A method of using the system includes generating tonal segments of predetermined duration, modulating the frequencies, and compiling these into an audio program. One or more sound transmitting devices are placed on desired locations of the body, and their inputs connected to corresponding outputs of the audio system. The generating step includes compiling selected predetermined frequencies into an audio program to generate the tonal segments, as well as modulating tones of one or more desired frequencies to generate the tonal segments.2016-06-09
20160158096VIBRATING MASSAGE ROLLER - A vibratory massage roller is provided for therapeutic massage, intimate massage, physical therapy, yoga, physical conditioning, and general well-being. The massage roller and method for balancing the massage roller, increasing the overall utility and therapeutic value so as to more efficiently massage a subject through resort to a vibrational roller having a tubular casing containing a motor housed in the center of the tubular casing, a central axle projecting from the motor, a plurality of eccentric propellers, positioned at different points along the central axle, the tubular casing vibrationally linked to the axle by the plurality of eccentric propellers via a plurality of housing supports and an optional surface casing extending over a length of the vibratory roller.2016-06-09
20160158097Device, System and Method for Facilitating Breathing Via Simulation of Limb Movement - A device, system and method for increasing air intake by a subject is described. The device includes a vibration motor and a control unit for controlling vibrational motion output by the vibration motor. The methods include positioning the vibration motor on one or more limbs of a subject, and stimulating nerves in the limbs via the generated vibrational motion, whereby the stimulated nerve signals the brain to increase breathing rate or air intake by the subject. Accordingly, the device of the present invention activates nerve fibers that carry kinesthetic cues from the limbs in a pattern that simulates normal limb motion, and thus triggers inherent reflexes that increase ventilation in response to such motion.2016-06-09
20160158099ELBOW DUAL COMPRESSION ARMBAND WITH INTERCHANGEABLE COMPRESSION PLATFORM - Apparatus for applying pressure, heat, cold or accu-pressure to a limb, comprises band members, at least a portion of which are elastic. A tab element, at least a portion of which is stiff and plastic, forms a catch for receiving and holding various treatment modalities. A shield, at least a portion of which is thin, flexible and smooth, prevents the user from becoming uncomfortable during treatment. A safety tab, at least a portion of which is stiff and plastic prevents the apparatus from coming undone, and thereby facilitates securement of the armband around the affected area. A pocket element receives various treatment modalities. A rectangular frame, at least a portion of which is stiff and plastic, connects band members and forms a cuff-like apparatus.2016-06-09
20160158100Slidable Pill Organizer and Dispenser - A device is provided for storing, organizing, and accessing prescription pills that comprises a pill tray and tray lid engaged in a slidable configuration. The pill tray possesses upward protrusions on opposing ends of its flat base, while the tray lid possesses linear channels on opposing ends of its flat body. With the tray lid placed over the pill tray, the channels of the lid meet the protrusions of the tray to engage in a male/female sliding configuration. The pill tray contains an array of pill chambers that is covered and uncovered by sliding the tray lid along this channel configuration. The pills are placed within the pill chambers of the pill tray, and viewable through holes found on the tray lid once it has covered the pill tray. Each viewing hole corresponds to a pill chamber.2016-06-09
20160158101SYRINGE FOR AND METHOD OF DELIVERING A VOLUME OF SOLUTION - Methods and apparatuses are disclosed with regard to syringe-transfer of a solution or other fluid within a carpule. One embodiment includes an apparatus that is a non-standard carpule barrel having a top portion, a bottom portion, and a barrel portion therebetween. The top portion includes an opening for receiving a syringe plunger and at least a first portion of a connection mechanism for connecting to an upper portion of the syringe. The bottom portion includes another opening capable of holding a bottom end of the carpule, wherein the carpule may be a standard carpule or a non-standard carpule. The barrel portion is located between the top portion and bottom portion, wherein the barrel portion includes a cradle, and wherein the cradle has a length capable of holding a standard carpule or a non-standard carpule and a width greater than the standard carpule.2016-06-09
20160158102FLEXIBLE, FLAT POUCH WITH PORT FOR MIXING AND DELIVERING POWDER-LIQUID MIXTURE - A pouch for mixing and dispensing a composition including a pouch body and a port body. The pouch body includes opposing, first and second major flexible walls sealed to one another along respective peripheries thereof to define an internal chamber and a pouch perimeter. The pouch body has a C-like shape. The port body projects from the first wall and is fluidly open to the internal chamber. With this configuration, various components, such as a powder component and a liquid component, can be mixed by a user's hand(s) in pressing the walls in a kneading fashion, with the resultant composition being dispensed through the port body. In some embodiments, the pouch is provided to a user with a powder component pre-loaded in the internal chamber.2016-06-09
20160158103METHOD FOR HANDLING MEDICINAL AGENT CONTAINER - There is provided a method for handling a medicinal agent container that allows reduction of the time and effort of an operator handling the medicinal agent container. The method for handling a medicinal agent container includes the steps of: setting a container in a container holding body capable of holding a plurality of containers, the container being capable of being filled with a medicinal agent; filling the medicinal agent of interest into the container held by the container holding body; sealing the container; and wrapping the container held by the container holding body and the container holding body into one package.2016-06-09
20160158104SYSTEMS FOR FILLING A FLUID INFUSION DEVICE RESERVOIR - A transfer device for filing a fluid reservoir of a fluid infusion device with a fluid is provided. The transfer device comprises a first end to couple to a source of the fluid, and a second end to couple to a pressurizing device. The transfer device also comprises a body interconnecting the first end and the second end, and having an end to couple to the fluid reservoir. The body defining at least one fluid flow path between the source of the fluid, the pressurizing device and the fluid reservoir to enable the filling of the fluid reservoir with the fluid2016-06-09
20160158105DEVICES, SYSTEMS AND METHODS FOR FILLING A SYRINGE WITH A MEDICATION - Devices, systems and methods for automatically positioning a syringe in a target orientation suitable for withdrawing medication from a container, and for filling the syringe with the medication. The device comprises a syringe conveyor, which is configured to receive the syringe in an initial orientation, and to bring the syringe to a target orientation by being translated and rotated while holding the syringe in a steady orientation relative to the syringe conveyor. The device further comprises a supporting module, configured to support the syringe conveyor while allowing a translation and a rotation thereof. The device comprises a syringe holder configured to hold the syringe, and a gripper coupled to the syringe holder. The gripper is configured to engage the plunger and to enable the automatic displacement2016-06-09
20160158106Sealable Pill Organizer and Dispenser - A device is provided for storing, organizing, and dispensing prescription pills that comprises a clamshell container configured to house a sealable pill tray and sliding card. The pill tray contains an array of pill chambers that are covered by an adhesive seal composed of foil or paper. The clamshell container comprises a top portion and a bottom portion, the top portion having an array of pill holes that correspond with the chambers of the pill tray. The top of the sliding card has markings corresponding to the pill chambers beneath it and slides over the pill tray and beneath the top portion of the clam shell. Pills are placed within the pill holes on top of the sliding card. When the sliding card is removed, the pills fall through the pill holes and into the pill chambers of the pill tray.2016-06-09
20160158107PRESCRIPTION MEDICATION SECURITY AND DISPENSING SYSTEMS - A prescription drug monitoring/dispensing device ensures prescription medication housed within is taken only as directed, and not abused or sold on the streets. The device serves as an intricately guarded casing that may only dispense the preprogrammed dosage amounts at preset times, as directed by a prescribing physician. The device may include a housing having a biometric finger scanner and a display screen in communication therewith, a loading tube capable of holding a pill therein, a rotating hub in communication with the loading tube, a rotating disc in communication with the loading tube, and an exit port capable of dispensing the pill out from the housing.2016-06-09
20160158108AUTOMATED MEDICATION DISPENSING AND RELATED APPLICATIONS THEREOF - Automated medication dispensing devices, kits, systems, methods, and related applications thereof, such as using computer readable (e.g., NFC [near field communication], or QR) standards for monitoring and verifying patient and caregiver activities and health related data-information. The medication dispensing device includes: a housing having a sliding mechanism configured to receive, hold, and release a removably slidable medication holder containing a plurality of individual medication holding compartments. The medication holder for dispensing medication includes: a receptacle (as either a disposable blister pack, or a reusable medication tray) containing a plurality of individual medication holding compartments, and having one side configured with one or more outward facing holes or an outward facing external handle to facilitate removably sliding the medication holder into and out of a medication dispensing device.2016-06-09
20160158109ELECTRONIC PILL BOX WITH DETACHABLE DAY MODULE - An electronic pill box for receiving a blister pack having a plurality of dosettes pre-loaded with doses of medication. The pill box includes a base module having a plurality of receptacles that receive the dosettes of the blister pack. The number of receptacles is sufficient to hold about a month of medication. A day module is engaged with the base module but is detachable therefrom. Individual dosettes are detached from the blister pack and loaded into receptacles in the day module. The base module and day module include capacitance sensors for determining if a dose of medication has been removed at the required time. The day module also includes a light sensor assembly that verifies whether the dosettes loaded into the day module's receptacles are the correct dosettes for the time of day a particular dose of medication should be taken.2016-06-09
20160158110Adapter Assembly for Enteral Feeding and Method of Making - An adapter assembly includes a tapered connector including a central passage and a tapered outer surface for sealing with a tube or bottle. A male connector for connection to a female connector to fluidly communicate the female connector with the tube or bottle is coupled with the tapered connector. A method of forming such an adapter assembly is also disclosed.2016-06-09
20160158111NASOGASTRIC TUBE - A system comprising a nasogastric tube comprising a nasogastric location element, a feeding mechanism, a suction mechanism configured to sealingly draw an inner wall of an esophagus against said nasogastric tube, and a gastric decompression mechanism.2016-06-09
20160158112PLUSH ANIMAL SHAPED TOY WITH PACIFIER - A plush animal shaped toy for intellectually stimulating, entertaining, and calming an infant-toddler, comprising at least: one rattle mechanism; one squeeze mechanism; a sound box to emit a recorded voice and/or melody; and a detachable pacifier with cover attached via Velcro-like material near the animal's mouth. The toy may further comprise visual symbols printed, stitched, or patched on the exterior animal surface, such as letters of the alphabet or numeric numbers. Exemplary embodiments comprise: a caterpillar; an elephant; a lamb; a monkey; and a puppy; and the sound box emits the ABC song when the designated animal's paw, hoof, or mid-section is pressed. The rattle mechanism is housed within the animal's head, and the squeeze and press mechanism and sound box are housed within the animal's body. A “Press” patch is sewn onto a hoof or paw bottom, or midsection and connected to the sound box via a wire.2016-06-09
20160158113PACIFIER - The present invention provides a pacifier having a mouthpiece, a shield and an attachment. The shield defines an aperture and the mouthpiece and attachment are removeably connectable through the aperture thereby to hold the shield in place. Alternatively, the mouthpiece and shield may be connected in such a manner that they cannot be detached and reattached, and the shield and attachment are removeably connectable. Further alternatively, the mouthpiece and the shield are removeably connectable, and the shield and attachment are removeably connectable.2016-06-09
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