Abstract: A method for connecting at least two structural parts of an orthopedic component, wherein the structural parts are retained in an orienting device while oriented in relation to each other, an intermediate space thus being formed between the structural parts. The orienting device and the structural parts together form a cavity, which has a flow connection to at least one feed connection, via which an adhesive for adhesively bonding the structural parts is introduced into the cavity.

Abstract: A battery pack including a case, a battery included in the case and relatively movable with respect to the case, a generator attached to the battery and including a generation axis, and a rotation member connected to the generation axis, wherein the rotation member is configured to act a torque enabling the generation axis to be rotatable when the battery is moved is disclosed.

Abstract: A system for conscious sensory feedback for a body extremity without sensation or a body extremity prosthesis is disclosed, as well as methods for conscious sensory feedback based on said system; a glove, a sock and a body extremity prosthesis comprising said system; and use of the system.

Abstract: A brim attachment for a prosthetic socket includes a cuff section defining an upper portion of the brim attachment and is arranged to extend about and upwardly from a socket opening. The cuff section is configured to move between tensioned and relaxed positions, wherein the tensioned position the cuff section is arranged to fold away from the socket opening, wherein the relaxed position the cuff section is arranged to extend above the socket opening and generally concentric with an outer surface of the socket. An interface section defines a lower portion of the brim attachment and is arranged to extend along a surface of the socket. The brim attachment may include a seal element protruding toward a central axis of the socket.

Abstract: The present disclosure provides a stent graft comprising (a) a self-expandable stent structure having a first end and a second end, wherein the self-expandable stent structure defines a lumen, (b) at least one restraint configured to be coupled to an exterior surface of the stent graft in a compressed condition, and wherein the at least one restraint is configured to be broken to permit the stent graft to transition to an expanded condition, and (c) a first plurality of anchoring projections coupled to the exterior surface of the stent graft adjacent to the first end of the self-expandable stent-structure.

Abstract: A woven, self-expanding stent device has one or more strands and is configured for insertion into an anatomical structure. The device includes a coupling structure secured to two different strand end portions that are substantially aligned with each other. The two different strand end portions include nickel and titanium. The coupling structure is not a strand of the device.

Abstract: A monolithic device comprising an ultra-dense stent cell pattern including a plurality of structural members that diverts the majority of blood flow without restricting blood flow completely. The method of making medical devices comprises vapor depositing an initial film onto a substrate, laser cutting a device pattern through the initial film, electropolishing the patterned device while disposed on the substrate, and releasing the patterned device from the substrate.

Abstract: Some embodiments relate in part to endovascular prostheses and delivery catheter systems and methods for deploying same. Embodiments may be directed more specifically to graft bodies having self-expanding members, including inflatable graft bodies, and catheters and methods for deploying same within the body of a patient.

Abstract: A kit for placing a bypass between two body vessels (R, L) of a patient comprises two catheters (10, 11), two guide wires (30, 31) moveable within one of the catheters (10, 11) each and a bypass element delivery system (52, 53, 8) for holding a bypass element (6, 7). The bypass element delivery system (52, 53, 8) is moveable along the first guide wire (30) and the bypass element delivery system (52, 53, 8) is capable of releasing and setting free the bypass element (6, 7). The kit further comprises an expansible element (40) being capable of connecting with the bypass element delivery system (52, 53, 8), of moving the bypass element delivery system (52, 53, 8) towards the opposite end of the first guide wire (30) and of setting the bypass element delivery system (52, 53, 8) free. The inventive kit enables an atraumatic placement of a bypass.

Abstract: A stent delivery system can include a core member, an introducer sheath, and a microcatheter. The core member can have a first section and a second section distal to the first section. The second section can have a bending stiffness per unit length that is less than a bending stiffness per unit length of the first section. The introducer sheath can have a lumen configured to receive the core member therethrough. The introducer sheath can have a length of at least about 80 cm. The microcatheter can have a lumen and a proximal end configured to interface with a distal end of the introducer sheath for delivering the core member into the microcatheter lumen.

Abstract: Methods and systems for detecting wall breach in inflatable prostheses rely on intrusion of a body fluid or inflation medium to electrically alter a signaling circuit. In one embodiment, an open portion of a circuit is closed to enable or modify a transmitted signal In another embodiment, electrical current is generated to power an electrical transmission.

Abstract: The present disclosure provides a support device for a gastrointestinal implant. The support device may include a lumen configured to extend through a submucosal tunnel and a mouth located at a proximal end of the lumen and in fluid communication with the lumen. The mouth may be configured to face proximally within a gastrointestinal tract to receive GI contents, and the mouth may be configured to direct the GI contents into the lumen. The support device may further include a support structure, where the lumen extends through the support structure, and where the support structure is configured to apply an outward radial force on an inner wall of the gastrointestinal tract. An artificial tunnel may extend distally from the support structure, may form at least a portion of the lumen, and may be configured to extend through the submucosal tunnel.

Abstract: The present application describes an implant system useable for positioning an implant device such as a device useful for restricting passage of ingested food into the stomach. In one embodiment, the disclosed system includes a plurality of anchors that may be coupled to tissue within the stomach, or to a tissue tunnel formed by plicating stomach wall tissue. The anchor includes a loop. During use, the implant device is inserted through the loop and expanded such that it retains its position within the loop until removed. Instruments for implanting and explanting the implant device are also described.

Abstract: A garment includes a longitudinal arch support configured for supporting a longitudinal arch of a foot; and a transverse arch support that extends from the longitudinal arch support and is configured for supporting a transverse arch of the foot.

Abstract: Described herein are systems and devices for providing an orthopedic walking brace having a housing and a sole with a curved distal surface. The housing is configured to encompass and immobilize a patient's ankle against flexion. The distal surface of the sole has a posterior region, a mid region, and an anterior region. The posterior region is configured to lie under a heel portion of the patient's foot, and the mid region is configured to lie under a center portion of the patient's foot. The anterior region is configured to lie under an anterior metatarsal and toe portion of the patient's foot, and has an Anterior-Posterior curvature that increases from a posterior side of the anterior region toward a middle portion of the anterior region and decreases from the middle portion toward an anterior side of the anterior region.

Abstract: A limb support coupler including a flexible body having opposing flexible body first and second faces, the flexible body conformingly embeddable within a limb support; and a connector outwardly extending from the flexible body first face. Further, a limb support coupler whereby the flexible body conformingly embeds within the limb support to dispose the flexible body first and seconds faces in adjacent generally parallel relation to respective limb support external and internal surfaces.

Abstract: To provide a shoulder brace for non-surgical treatment which is capable of immobilizing an upper arm of a patient in an extremity position where the upper arm hangs down along the trunk in treatment for acromioclavicular joint dislocation or distal clavicle fracture, for the purpose of promoting the activities of daily living of the patient and relieving the uneasiness/discomfort of the patient who has the shoulder brace for non-surgical treatment on. The shoulder brace for non-surgical treatment includes a strap utilized for reduction, the strap forming a loop made in series by: a section which runs down vertically from the front of the acromioclavicular joint toward the ulnar side of the forearm; a section which runs across a forearm trough; a section which runs up from the radial side of the forearm windingly across the front of the upper arm to the back of the shoulder; and a section which runs across from the back to the front over the shoulder pad and reaches to the acromioclavicular joint part.

Abstract: A disposable urinary funnel for assisting a male user to prevent splattering of urine stream, the urinary funnel comprises a foldable, elongate tubular housing with an inlet at a first open end and an outlet at a second open end. The urinary funnel further comprises at least two loops attached externally to sidewalls of the first open end, for holding the funnel by placingfingers into the loop and positioning the inlet around the male reproductive organ while urinating from a standing position.

Abstract: The present invention relates to an oral device for treatment of sleep disordered breathing that includes an upper body in which at least a part of upper teeth is housed; a lower body in which at least a part of the lower teeth is housed; at least one or more elastic members that connect the upper body and the lower body to provide the elastic force in a direction in which the upper body and the lower body come closer to each other; and a support jaw that protrudes downward from the rear end of the upper body to support the rear end of the lower body. Thus, according to the present invention, it is possible to prevent the sleep disordered breathing such as an obstructive sleep apnea syndrome that may occur during sleep, enable a patient to more comfortably wear, and minimize the discomfort in a state of wearing.

Abstract: The present invention provides devices for cooling and heating an individual's neck. Devices of the invention include two heating and cooling members that each a contoured surface for resting against a side of a user's neck and are coupled together via a bridge portion. The members each include a temperature assembly. The temperature assembly includes a heating and cooling module positioned against the contoured surface of the member. The temperature assembly may also include a heat sink, a fan, or both. The device further includes a controller for controlling the temperature assembly.

Abstract: Production of sterile therapeutic medium such as sterile surgical slush for use in surgery. A sterile slush container with a sterile sleeve assembly so that the outside of the sterile slush container remains sterile after placement in a non-sterile slush making machine so that the sterile slush container may be returned to the sterile field after removal of the sterile slush container from the sleeve assembly.

Abstract: Cold plates through which refrigerant flows define a slot between them that can receive a cassette through which sterile working fluid with a relatively low flow rate flows from an intravascular heat exchange catheter. The working fluid from the catheter is heated or cooled by heat exchange with the cold plates through the walls of the cassette to maintain the sterility of the working fluid. On the other hand, high flow rate working fluid chambers surround the cold plates and non-sterile working fluid from an external heat exchange pad flows through the high flow rate working fluid chambers to exchange heat through direct contact with the cold plates.

Abstract: An energy harvesting, heat managing, multi-effect therapeutic garment, defining an inner surface and an outer surface, seamlessly knitted using a predetermined number of yarns is provided. The yarns for constructing the therapeutic garment are selected from a yarn that absorbs, stores, and releases heat energy through a phase change, yarns that convert heat energy and ultra violet radiation energy into far infrared radiation energy and radiate the far infrared radiation energy to other yarns and to a wearer's body part, a yarn that adsorbs moisture from the wearer's body part and/or ambient environment and generates heat energy through an exothermic reaction, a heat insulting and hydrophobic yarn, and a heat conductive yarn that maintains a uniform temperature within the yarns. The yarns of the therapeutic garment are bundled and knitted to create a uniform surface area distribution of the yarns that contact each other and cover the wearer's body part.

Abstract: Apparatus for controlling a body temperature with a controller. The controller is adapted to control the body temperature by controlling at least two different body temperature adaption devices, wherein one body temperature adaption device is an infusion device (200); and wherein at least one further body temperature adaption device (300) is different from the one body temperature adaptation device and, preferably, not an infusion device.

Abstract: The present invention pertains to a cassette capture mechanism for uniting a cassette with a console to prevent jamming or damage to the console and/or cassette. The cassette capture mechanism comprises a cassette receptacle, an axial translation linkage, a first sensor apparatus, and a second sensor apparatus. The cassette receptacle is configured to couple with a cassette having a positioning surface. The axial translation linkage is configured to couple the cassette with the cassette receptacle. The first sensor apparatus is configured to detect alignment of the cassette in a horizontal plane with respect to the cassette receptacle when the cassette is initially coupled with the cassette receptacle; and the second sensor apparatus is configured to detect activation of the first sensor apparatus and detect alignment of the cassette in a vertical plane with respect to the cassette receptacle.

Abstract: The present invention relates to a device for permanently changing the color of the iris, such as from brown to blue. The invention is a system that includes a slit lamp microscope, a source of intense pulsed light (IPL), optical tracking and measuring systems, and a device that prevents the application of light to the pupil. The IPL provides a simultaneous application of a range of wavelengths, rather than the single wavelength typically applied by lasers. In a preferred embodiment, the IPL is applied as annular ring, striking only the iris and not the pupil or the sclera. Air or liquid cooling can be used to prevent the eye from overheating.

Abstract: The present invention includes a device and method for treatment of retinal detachment, ocular hypertension and glaucoma, and increasing an amplitude of accommodation. The device includes a tapered, mesh tube that within a sclera, expands to deform the sclera, and when placed within the posterior sclera for the treatment of a retinal tear, the device expands deforming the sclera so that the retinal pigment epithelium comes in contact with the retinal tear to seal the tear. For the treatment of ocular hypertension, glaucoma and to increase the amplitude of accommodation, the device is placed within the anterior sclera over the posterior plicata of the ciliary body, which upon expansion causes the underlying ciliary body to deform, resulting in traction on the trabecular meshwork and deformation of the ciliary body, which causes lowering of intraocular pressure, and increases the amplitude of accommodation in patients with ocular hypertension or decreased accommodation.

Abstract: A lacrimal duct tube includes: a pair of tubular members that each have at one end an opening communicating with a lumen and have in a wall a hole for guiding a lacrimal duct tube operative instrument to the lumen; and a connection member that connects the other ends of the tubular members. Surfaces of the tubular members include a hydrophilic-coated portion and a non-coated portion without the hydrophilic coating. It is preferred that the lumen in the vicinity of the opening includes an engagement portion for engagement with a tip of the lacrimal duct tube operative instrument, and the non-coated portion is formed without overlapping with the surface of the tubular member at the position of the engagement portion. The lacrimal duct tube can be used favorably for various lacrimal duct obstruction treatments. In the case of using a sheath such as in sheath guided endoscopic probing, the lacrimal duct tube can be easily inserted into the sheath and be firmly fixed to the sheath.

Abstract: Treatment validation techniques include generating a modified treatment target from an original treatment target using a modification process, and comparing induced aberrations provided by the original and modified treatment targets, so as to verify the modified treatment target or the modification process. In some cases, a modification process may include a deconvolution process, a low pass filter process, a scaling process, or an adjustment process. The induced aberrations may include high order aberrations, such as spherical aberration.

Abstract: Providing neuroprotective therapy for glaucoma includes generating a micropulsed laser light beam having parameters and characteristics, including pulse length, power, and duty cycle, selected to create a therapeutic effect with no visible laser lesions or tissue damage to the retina. The laser light beam is applied to retinal and/or foveal tissue of an eye having glaucoma or a risk of glaucoma to create a therapeutic effect to the retinal and/or foveal tissue exposed to the laser light beam without destroying or permanently damaging the retinal and/or foveal tissue and improve function or condition of an optic nerve and/or retinal ganglion cells of the eye.

Abstract: A method for providing vision correction to a patient. The method includes: (a) measuring the degree of vision correction needed by the patient and determining the location and shape of refractive structures that need to be positioned within the cornea to partially correct a patient's vision; (b) directing and focusing femtosecond laser pulses in the blue spectral region within the cornea at an intensity high enough to change the refractive index of the cornea within a focal region, but not high enough to damage the cornea or to affect cornea tissue outside of the focal region; and (c) scanning the laser pulses across a volume of the cornea or the lens to provide the focal region with refractive structures in the cornea or the lens. Again, the refractive structures are characterized by a change in refractive index, and exhibit little or no scattering loss.

Abstract: A fixed structure for the constricting band of snow goggles includes a goggle frame, a constricting band and a fastening member combined together. The goggle frame has two sides respectively provided with an insert slot and a hooking portion; the constricting band has two sides respectively fixed with a fastening body of the fastening member, and the fastening member consists of a hooking seat and the fastening body. In assembling, the hooking seat is inserted in the insert slot of the goggle frame and clasped with the hooking portion and then, the fastening body at the two sides of the constricting band is inserted in the hooking seat and positioned therein. Thus, the fixed structure for the constricting band of snow goggles can be stably combined and impossible to fall off.

Abstract: The present patent application discloses a weld mask, which has a weld cap, a protection plate, a filter and a press block. The weld cap has a through-hole. A scaleboard pedestal is installed on the edge of the through-hole. The scaleboard pedestal raises towards the inside of the weld cap and encompasses the through-hole. The protection plate, the filter and the press block are installed in the scaleboard pedestal successively. A raised snap-gauge is installed on the outside of the scaleboard pedestal. The snap-gauge includes a hole. An elastic snap joint is installed on the edge of the press block. The snap joint includes a hook and a reducible resilient trip. The top and bottom of the resilient trip connect with the press block and the hook respectively.

Abstract: An improved hearing protection device intended to be inserted into an external auditory meatus of a user, having a housing structure, a passive tuning element, and a passive, nonlinear acoustic filter. The tuning element and the acoustic filter may be supported in series by the housing structure. The tuning element may be or include a diaphragm, a resonator, or both. The housing structure may support a diaphragm of the tuning element at its circumference, and may provide cavities on both sides of the diaphragm. In some embodiments electronic components are included in the hearing protection device to counteract insertion loss provided by the passive element, and restore natural hearing for low to moderate sound pressure levels. Communications devices may also be incorporated into the hearing protection device.

Abstract: Disclosed herein are several embodiments of a negative pressure appliance and methods of using the same in the treatment of wounds. Some embodiments are directed to improved fluidic connectors or suction adapters for connecting to a wound site, for example using softer, kink-free conformable suction adapters.

Abstract: A device for cutting a web of material comprises movement means for moving a web of material to be cut, defining a feed path for the web at least partly rotatable about a central axis and equipped with at least one conveyor mounted around the central axis, at least one cutting head equipped with a laser source and an optical system configured to direct the laser beam towards a cutting zone, where the optical system of the cutting head comprises at least one directing member located inside the conveyor to direct the laser beam away from the central axis towards the cutting zone.

Abstract: A method for producing a low density perforated web material having a thickness of at least 0.20 mm, comprising the steps of: providing a layer of low density material having a maximum overall weight per square meter of 75 g/m2 or less; and processing the low density material between two rollers pressing onto each other to obtain a low density perforated web material, wherein a first roller has protrusions to perforate the low density material, and a second roller rotates at a different speed from that of the first roller and has projecting parts with contact areas arranged to perforate the material with the protrusions, the contact areas being spaced by recesses to receive the material and having larger contact face dimensions than the protrusions, the recesses leaving an impression in relief on the low density polymer material.

Abstract: A process for making a composite web is disclosed. The composite web can be incorporated into an absorbent article. A volume of ink is applied to the composite web such that when the composite web is incorporated into the absorbent article, a visual signal is produced.

Abstract: A tampon produced by a method of multiple successive passes of a needle through a fiber web in a manner such that the tampon is afforded a desirable structural configuration and optimized characteristics, including tensile strength, relative absorbency, linear density, and thickness.

Abstract: Remotely detecting the presence of urine or feces in a diaper of an infant or adult using a disposable sensor placed inside the diaper, in conjunction with a permanent device that is capable of wirelessly transmitting data to a mobile device or base station is disclosed. The permanent device can also be capable of measuring temperature and body movements. This additional information can be used in conjunction with the detection of urine or feces to identify patterns.

Abstract: An absorbent article including features facilitating toilet training of a wearer is provided. The article includes at least a first appearing graphic that changes from an initial, less visible state to a subsequent, more visible state in the absence of wetness, thereby to provide positive encouragement to a child during toilet training. The appearing graphic becomes less visible if subjected to liquid. A wetness sensation member may also be provided to give tactile, negative sensation to the child, thereby giving feedback received by at least two different senses. Additionally or alternatively, a second appearing graphic, different from the first appearing graphic, may be provided to increase a child's interest in the toilet training process. The first and second appearing graphics may become visible at different times, thereby providing a sequential or spaced reveal of the image.

Abstract: A feminine hygiene article comprises a topsheet, a backsheet and an absorbent core disposed therebetween. The feminine hygiene article has two longitudinal side edges. Each longitudinal side edge has a notch that extends from the longitudinal side edge towards the absorbent core. Each notch is disposed between a front portion transverse centerline and rear portion transverse centerline of the feminine hygiene article.

Abstract: The present disclosure is directed to disposable absorbent articles and arrays of disposable absorbent articles which are designed to fit a range of wearers having different physiological, psychological and cognitive needs which can be impacted by product form and level of engagement required during application as well as by the final appearance fit and function of the article.

Abstract: A cover that is sized to secure over an appendage of an animal, such as a human is provided. The cover includes a tubular sidewall. The sidewall has a closed bottom end and an open top end formed by an upper rim. The sidewall further includes a first inner edge and a second inner edge formed along a length of the tubular sidewall and terminating at the upper rim. A first connector releasably connects the first inner edge and the second inner together, forming a water tight seal along the length of the tubular sidewall.

Abstract: Disclosed herein is a dispenser for adhesive fabrics or tapes, such as bandages or other adhesive medical fabrics or correction tapes. The dispenser has a case in which a supply reel and a take-up reel are mounted. A belt having adhesive fabrics or tapes thereon extends from the supply reel through one or more openings to the exterior of the case, and thence to a take-up reel. The supply reel and the take-up reel are coupled so that the belt is wrapped around the take-up reel as it is unwound from the supply reel and advances to move an adhesive fabric or tape to the exterior of the case for dispensing. The dispenser may optionally have an activation device that allows a user to extend a portion of an adhesive fabric outside the dispenser and dispense and apply the adhesive fabric to a human skin with one hand.

Abstract: A patient support includes bearings, a litter frame supported relative to the bearings, an elevating mechanism for changing the elevation of the litter frame relative to the bearings at an elevating mechanism speed, and a user interface operable to vary the elevating mechanism speed.

Abstract: A patient transfer device is utilized to transport infant patients between locations within a hospital environment. The patient transfer device includes a center, support section and a pair of side sections that can be moved into contact with each other to surround the infant patient. The first and second side sections each include a handle that can be brought into close proximity to each other and can be grasped by a single hand of a clinician. The patient transfer device includes a heart rate sensor positioned to provide a heart rate measurement of the patient when the patient is received on the patient transfer device. The patient heart rate can be displayed on either an integrated display or wirelessly transmitted to an external display device. In this manner, the heart rate of the infant can be continuously monitored during transport.

Abstract: A mobility securement system, and method for securing a wheelchair or other mobility device, and its passenger, within a public or private vehicle. In various embodiments, the system includes one or two attachment members, one or two vehicle anchor assemblies and, potentially, at least one fixed or moveable bumper, and may further include a barrier. A tensioning assembly is operably connected to at least one attachment member and vehicle anchor assembly. One or more moveable bumpers are configured to articulate to in turn apply a force against the mobility device, and one attachment member may be hidden behind a stored position of a moveable bumper.

Abstract: A robot system for assisting a patient in standing up and/or sitting down is provided. The robot system includes the following elements. A drive mechanism executes a drive pattern for assisting the patient in standing up and/or sitting down. An instruction input device receives an instruction to cause the drive mechanism to execute the drive pattern. A state acquirer acquires an execution state of the drive mechanism which is executing the drive pattern. A controller decides whether or not to cause the drive mechanism to execute the instruction received by the instruction input device, on the basis of the execution state acquired by the state acquirer, and controls the driving of the drive mechanism.

Abstract: A synchronized motion control system for a double electric bed includes two control devices attached to two electric single beds of the double electric bed respectively. Each electric single bed has a driver circuit and a motor. Each control device has a Hall sensor for generating a Hall signal of the motor, a microcontroller electrically connected with the Hall sensor for generating a rotation number signal according to the Hall signal, and a communication unit electrically connected with the microcontroller. The communication units are electrically connected with each other. The microcontroller of one of the control devices compares the two rotation number signals to generate a difference signal. The motor corresponding to the larger rotation number signal is decelerated according to the difference signal, so as to make the two electric single beds perform synchronized motion.