Abstract: The invention relates to a device for receiving an intraocular lens, comprising a first and a second half-shell which are connected to each other in an articulated manner by a first joint and which can be moved relative to each other from an open position into a closed position. The half-shells form an open chamber in the open position and an enclosed chamber in the closed position. A covering element is pivotally arranged on the longitudinal side of the first of the two half-shells covering element covering the open chamber in the open position and being positioned substantially outside of the enclosed chamber in the closed position. A movable or pivotal stopper can be provided which delimits the open chamber in the ejection direction of the lens in the open position and is positioned substantially outside of the enclosed chamber laterally to the ejection passage in the closed position.

Abstract: Apparatuses, tools and kits are directed to fluid manipulations in relation to a paranasal sinus through a paranasal sinus access implant device (906) that provides fluid communication between the lacrimal apparatus in the orbit and a paranasal sinus. An implant device has a proximal head and a conduit distal of the head, with the conduit having a first longitudinal portion having a larger minimum wall thickness than a minimum wall thickness of a second a second longitudinal portion of the conduit located distal of the first longitudinal portion. A paranasal sinus fluid manipulation tool (900) has an engagement structure (904) insertable into the palpebral fissure to engage a head of the implant device.

Abstract: Intraocular pressure can be reduced by insertion of an intraocular shunt in the eye such that it forms a drainage pathway between the anterior chamber and a region of lower pressure. A hollow shaft that holds an intraocular shunt can be advanced through the anterior chamber. The sclera can be penetrated with the hollow shaft. A beveled tip of the shaft can be oriented such that a beveled surface thereof faces toward the Tenon's capsule when the beveled tip passes out of the sclera. After the beveled tip passes out of the sclera, at least a portion of the shunt can be advanced from the hollow shaft.

Abstract: An ocular implant adapted to be disposed within Schlemm's canal of a human eye with a body extending along a curved longitudinal central axis in a curvature plane, a first strut on one side of the implant and a second strut on an opposite side of the implant, the circumferential extent of the first strut with respect to the plane of curvature being greater than the circumferential extent of the second strut with respect to the plane of curvature. The invention also includes methods of using the implant.

Abstract: Configurations are described for conducting ophthalmic procedures to address cataract-related clinical challenges. In one embodiment, a one-piece patient contact interface may be utilized to couple a diagnostic and/or interventional system to a cornea of a patient; in another embodiment, a two-part configuration may be utilized; in another embodiment, a liquid interface two-part embodiment may be utilized.

Abstract: Embodiments of this invention generally relate to ophthalmic laser procedures and, more particularly, to systems and methods for photorefractive keratectomy. In an embodiment, an ophthalmic surgical laser system comprises a laser source generating a pulsed laser beam and a laser delivery system delivering the pulsed laser beam to a cornea of an eye. A patient interface couples to and constrains the eye relative to the laser delivery system. A controller controls the laser delivery system to perform an anterior surface volume dissection on the cornea.

Abstract: An ophthalmic laser treatment apparatus includes: an aiming optical system configured to irradiate an aiming beam to a patient's eye; a laser irradiation optical system configured to irradiate a laser beam for treatment to the patient's eye; a shift unit configured to make a shift of a focus shift position corresponding to a focus position of the laser beam to a posterior or anterior position with respect to a focus position of the aiming beam; a selection receiving unit configured to receive an instruction to select any one of a plurality of treatment modes; and a control unit configured to control operations of the ophthalmic laser treatment apparatus. The control unit sets a value of a parameter related to irradiation of the laser beam, the parameter including a parameter related to the shift of the focus shift position, according to the treatment mode selected with the selection receiving unit.

Abstract: An apparatus for covering a left eye and a right eye of a human, includes: a first eye piece configured for covering a left eye of a human; and a second eye piece configured for covering a right eye of the human; wherein the first eye piece and the second eye piece are configured for preventing transmission of visible light; and wherein at least one of the first eye piece and the second eye piece comprises a region that is transparent for electromagnetic radiation with a wavelength range outside a visible range.

Abstract: A wound dressing product comprising: a substrate layer having an upper surface and a lower surface; a tacky silicone coating composition present on said upper surface and on said lower surface; and upper and lower release sheets covering said substrate and said tacky silicone coating composition on said upper and lower surfaces, respectively, and adhered to said surfaces by said tacky silicone coating composition, wherein said upper surface is less tacky than said lower surface whereby said upper release sheet can be removed from said upper surface more readily than said lower release sheet can be removed from said lower surface. Also provided are methods for making such dressings.

Abstract: A device or structure for fitting on the bottom of an equine leg cast to protect the cast from abrasion and wear, to aid in keeping the cast clean and, in one aspect, to provide a shaped molded rocker bottom that allows the leg cast hoof to rock forward or back, allowing the equine to find a naturally comfortable position. A method of applying the device to an equine leg cast. The device or structure consist, in general, of a solid member having a top face and a bottom face and having malleable straps attached to the solid member and extending from at least two sides of the solid member, which straps are made of material and sized to be capable of being bent or folded upward in a plane perpendicular to the top face of the solid member to attach to an equine leg cast.

Abstract: It is aimed to provide a composite sheet manufacturing device and a composite sheet manufacturing method capable of maintaining high cutting performance of a cutter by suppressing the adhesion of an adhesive of an adhesive surface to the cutter. A first sheet (42) introduced to between a cutter roller (2) and an anvil roller (3) is cut into strips (42a) while these rollers (2, 3) are rotated relative to each other, adhesive surfaces (a) of the strips (42a) are adhered onto a second sheet (43) for compounding, and at least one of a cutter (12) of the cutter roller (2) and the anvil roller (3) is cooled by a refrigerant by a cooling unit (20, 21).

Abstract: It is aimed to provide a conveying device for absorbent articles capable of precisely sorting an absorbent article between a main conveyance path and a branch path and a conveyance method using the same. A path switching means includes a belt conveying unit with a conveying belt arranged along an annular path and configured to circulate along the annular path to be able to convey an absorbent article and a path switching mechanism configured to switch a conveyance path specified by the conveying belt between a path along which the absorbent article is transferrable from an upstream conveying mechanism to a downstream conveying mechanism and a path along which the absorbent article is guided along a sampling path from the upstream conveying mechanism.

Abstract: A personal hygiene product with a digital element is described. In one embodiment, a conductive sensor assembly is disposed within the personal hygiene product that includes one or more moisture sensors that generate a resistive signal indicative of saturation of the personal hygiene product when in wetting contact with menstrual fluid.

Abstract: A pull-on garment (1) includes an outer cover (3) forming an outer surface of the garment, both lateral side edge portions of the outer cover in a front body portion F and both lateral side edge portions of the outer cover in a back body portion R being joined to each other to form a pair of side seals (4), a waist opening (8), and a pair of leg openings (9). Each of the side seals (4) includes a seal edge portion (41) where the edge portion (3F) of the outer cover (3) in the front body portion F and the edge portion of the outer cover (3) in the back body portion R are bonded to each other by a continuous linear fusion-bonded portion (40) extending in a longitudinal direction of the side seal (4). In a cross-section orthogonal to a direction in which the side seal (4) extends, the fusion-bonded portion (40) includes a narrow section (4F) which is formed at a middle portion thereof in the thickness direction Q and of which a width W along the inner-to-outer direction P is small.

Abstract: An absorbent body forming satisfactory connections while webs are conveyed at a high speed includes at least two sheets of nonwoven fabric overlapping each other; connections at which the nonwoven fabric sheets are connected together; and an absorbent material disposed between the nonwoven fabric sheets at a small region encircled by the connections. When seen in a direction perpendicular to a main surface of the nonwoven fabric sheets, a plurality of the connections is formed with spaces therebetween on each side of imaginary polygons compartmentalizing the nonwoven fabric sheets and neighboring each other, and the connection is formed at least on a middle part of the sides common to the imaginary polygons neighboring each other. The connections are formed sequentially, and simultaneously arranged in a row parallel to each other, and the minimum number of connections per row is at least 45% of the maximum number of connections per row.

Abstract: An incontinence pad includes an absorbent body provided between a liquid permeable topsheet and a backsheet, a concave groove formed in a surface of the absorbent body on the liquid permeable topsheet side and extending along an approximately longitudinal direction of the groove, and a highly compressed portion formed in a bottom surface of the concave groove. The highly compressed portion includes a sloping element in a unit portion formed by dividing the concave groove in a longitudinal direction thereof and crossing the concave groove from one side edge to the other side edge, and is formed into a pattern obtained by repeatedly inverting the highly compressed portion of the unit portion in the longitudinal direction.

Abstract: An absorbent article is provided that comprises a front waist region, a back waist region, a crotch region disposed between the front waist region and the back waist region, a front waist end edge, a back waist end edge, a longitudinal axis extending from a mid-point of the front waist end edge to a mid-point of the back waist end edge, a first longitudinally extending side edge, a second longitudinally extending side edge, an exterior surface, an interior surface, a topsheet, a backsheet, and an absorbent core disposed between the backsheet and the topsheet. A portion of the front waist region and a portion of the back waist region are joined in a surface to surface relationship to form a pant comprising a first permanent side edge seam and a laterally opposed second permanent side edge seam. The first and second permanent side edge seams define an initial waist opening circumference and a pair of leg openings.

Abstract: A manual wheelchair propulsion device (FIGS. 5, 6 & 7), attached to wheelchairs through the axles of the rear wheels (FIGS. 14, 15, 16 & 17), attached through the wheel winder unit with a quick release head with ball Joint to lock in position (FIGS. 1, 2) to an adaptable socket either manufactured into the axle of the wheelchair wheel or attached rigidly with supports later (FIGS. 14, 15 & 17) with a retractable arm (FIGS. 5 & 6) with eight gears and one neutral (FIGS. 3, 12 & 13) used in a circular motion to manually propel ones self.

Abstract: A bed (1) comprising, a base part, with a patient support base (10) arranged above the base part, and including a position configurable patient support (19), four telescopic elevator columns (5), mounted on said base part. The four elevator columns (5) are arranged as a first and a second pair of telescopic elevator columns (5). The bed (1) has two cross-beams (8) for supporting the patient support base (10). An operator housing (9) is mounted on at least one of said cross-beams (8). The operator housing (9) comprises means for configuring said position configurable patient support (19). The operation housing (9) and said patient support base (10) comprising mutually releasable connection means.

Abstract: A patient support apparatus includes a patient support surface to support a patient. The patient support surface has at least one air bladder that is inflated and/or deflated to achieve a turn assist function and/or a therapy function of the patient support surface. A graphical user interface (GUI) is configured to receive user inputs from a caregiver to initiate the turn assist or therapy functions. The patient support apparatus has control circuitry coupled to the GUI. The GUI is controlled by the control circuitry to display information indicating that the patient is improperly positioned on the patient support surface for either the turn assist function or the therapy function. Alternatively or additionally, the control circuitry indicates that the patient is improperly positioned for raising a head section of a bed frame.

Abstract: An electric actuator system for hospital and care beds (1, 20) for adjusting e.g. the lying surface of the bed (1, 20). The actuator system is connected to one or more light sources (19, 23, 24), which may be switched on if a change in the patient's movement pattern and/or position in the bed (1, 20) is registered. The electric actuator system may thus help the patient navigate around the room.

Abstract: A bariatric patient management system includes a single-wheel drive system having bi-directional variable speed control through use of a variable control joystick. The single-wheel drive system is disposed on an underside of the bariatric patient management system and engages a floor surface when the bariatric bed is in a lowermost position. The bariatric patient management system further includes a removable headboard having a disconnect feature for disconnecting the variable control joystick from the single-wheel drive system when the headboard is removed. A plurality of three-setting casters is used in conjunction with the single-wheel drive to allow the bariatric patient management system to be manually turned when transported from one location to another. The bariatric patient management system further includes an improved trapeze boom that allows for additional access to a patient adjacent the headboard of the bariatric patient management system.

Abstract: A memorial object including inner cremation contents, and a housing structure for housing the inner cremation contents, the housing structure being made of at least a first fluid, wherein the housing structure is maintainable in a predetermined solid shape only upon maintenance of the housing structure under a freezing temperature of the first fluid. Preferably the fluid is water. The invention provides a sustainable method of making a dissolvable memorial object or urn by transforming water into solid shape of ice encapsulating cremation ashes.

Abstract: The present invention relates to the technical field of massagers and provides a head massager and a helmet size adjusting structure thereof.

Abstract: An exoskeleton device includes a plurality of braces that are each attachable to a part of a user. A plurality of joints connects adjacent braces. Each joint is controllable to bend or unbend so as to cause the exoskeleton device to change between an erect configuration and a sitting configuration. At least one support column is extendible from a brace. A length of the support column is adjustable. A controller is configured to adjust the length of the support column in coordination with the bending or unbending of a joint to provide support for the exoskeleton device when in the sitting configuration.

Abstract: A lower extremity orthosis is configured to be coupled to across at least one joint of a person for gait assistance and can incorporate knee, thigh, hip and ankle/foot assistive orthotic devices which can be used in various combinations to aid in the rehabilitation and restoration of muscular function in patients with impaired muscular function or control.

Abstract: There is provided a walker apparatus having a pair of spaced-apart, upright frame members. The walker apparatus includes a seat operatively connected to the upright frame members. The walker apparatus has a backrest cantilevered from the frame members. The backrest has at least one opening extending therethrough for permitting a user's vision past the backrest when the user grips the upright frame members.

Abstract: Your applicants, Gail B. Rehmert (formerly Dreybus) and Colby D. Rehmert desire to be granted a Utility Patent for the hereinafter described improvements and enhancements to her former U.S. Pat. No. 4,312,333, a Tactile Stimulating Mechanism, granted Jan. 26, 1982. Goal of device is to relax, soothe, and calm the body and reduce stress. This modified enhanced application, renamed Tactile Sensory Stimulator, is an improvement allowing the device to reduce stress, while able to adjust to a user's large or small body type while in horizontal position. This mechanism creates a relaxing and sensitive touch over user's body by three adjustable wand assemblies holding filaments changed in figure to include light plastic orbed bendable units which do not weigh over 1-2 ounces each. This configuration of filaments creates very gentle pressure as all strands move in a rotational, reversible 360 degree orbit over the user body.

Abstract: Described herein are devices, systems and method for treating inflammatory disorders by modulating a subject's inflammatory reflex. The method may include the step of non-invasively stimulating the inflammatory reflex (e.g., the vagus nerve, the splenic nerve, the hepatic nerve, the facial nerve, and the trigeminal nerve) of a subject in a manner which significantly reduces proinflammatory cytokines in the subject and/or provides a therapeutically effective treatment for the subject. Devices for non-invasively stimulating the inflammatory reflex may include a movable tip or actuator that is controlled to mechanically stimulate the ear. The devices may be hand-held or wearable, and may stimulate the cymba conchae region of the subject's ear.

Abstract: An acoustic foetal stimulation device comprising a capsule (2) enclosing the means of emitting (10) acoustic stimulation signals, manufactured in a biocompatible (hygienic) maternal and with a size and shape suitable for removable insertion in the vagina, in a position adjacent to the foetus, and an extraction cord (20) for removing the device (1). The means of emitting (10) the acoustic signals comprises a playback system (12, 13) for a predetermined acoustic stimulation signal, complete with control software and a speaker (11), and a means of wireless communication with the exterior using a remote control to give instructions to the playback system via an RF wireless signal.

Abstract: A wearable mobile terminal is provided that includes a base provided in an insole of a shoe, a pressure sensing unit provided in the base to sense a pressure selectively applied when a user walks, an acupressure unit provided to apply an acupressure to the user's foot, when the pressure is applied to the pressure sensing unit; and a wireless communication unit synchronized with an external mobile terminal.

Abstract: A vial holder is provided to protect a user's hand from needle sticks. The holder includes a handle and a shield attached to a distal end of the handle. An opening is formed in the distal end of the handle to receive a vial. The vial is placed through the opening and into a passageway of the handle with the upper end of the vial exposed. A user grasps the handle which holds the vial in a stabilized manner. A needle may then safely approach the vial in which inadvertent slippage or movement of the needle results in contact with the needle against the shield and not contact with the user's hand.

Abstract: People can damage their medicines by taking them outside in hot or cold weather. On the other hand, some people need to carry their medicines with them wherever they go (even if the weather is extremely hot or cold). Specially constructed storage systems can protect medicines from damage due to hot and cold weather without requiring bulky structures or expensive components that consume electricity to regulate temperature.

Abstract: A closed fluid transfer system for fluidly interconnecting a syringe to any one of a patient I.V. set, a vial and an I.V. bag, is provided and includes a first adapter defining a lumen and supporting a seal across a first end of its lumen, the first adapter supporting a rear end of a needle within the lumen, wherein the seal is movable relative to the needle such that a tip of the needle penetrates through the seal; and a second adapter defining a lumen and supporting a seal across a first end of its lumen; wherein when the second adapter is coupled to the first adapter, the second adapter seal abuts the first adapter seal and moves the first adapter seal relative to the tip of the needle such that the tip of the needle penetrates through the abutting first adapter seal and second adapter seal.

Abstract: A rotary die system that includes first and second axially aligned, coacting rotary dies positioned adjacent one another. Each die includes a working surface having a plurality of recesses defined therein. The recesses in the first die are each configured to align with a recess in the second die to form a product cavity upon coaction of the first and second dies. The product cavity is configured to receive a product. Each recess in at least one of the first or second dies includes a pin therein that is configured to puncture a film that at least partially surrounds the product.

Abstract: The invention addresses the problem of providing a medication cassette, which in addition to being capable of smooth automated dispensing despite being capable of storing large amounts of medication, allows accurate ascertainment of whether the medication has run out or is jammed. This medication cassette is provided with: a cylindrical body in which the medication is stored; a first rotating body capable of reciprocating movement inside the cylindrical body in the direction of the shaft center thereof; a second rotating body disposed on the outer circumference of the cylindrical body; a conveyed medication-detecting element for detecting medication that has been conveyed by the second rotating body; and a control for moving the first rotating body upward when a medication detection signal is not output from the conveyed medication-detecting element.

Abstract: A medication dispensing assembly includes a housing that has a plurality of wells therein and each of the wells may contain pills. A dispensing unit is coupled to the housing and the dispensing unit may assign a unique user to each of the wells corresponding to the pills contained within each of the wells. The dispensing unit selectively dispenses the pills from each of the wells according to a pre-determined dispensing schedule.

Abstract: An infant bottle (10) method and kit, wherein the bottle comprising: a disposable bag (20), for containing a beverage (30, 44, 46); a foldable bag frame (16), for deploying therein the disposable bag (20) at a deployed state of the foldable bag frame (16), wherein a folded state thereof occupies less space than an unfolded state thereof; and a teat (14), for covering the disposable bag (20) in a sealed manner, thereby resulting in a compact infant bottle (10) at a folded state of the foldable bag frame (16), and sealable upon deployment.

Abstract: The present invention provides a dental color tone adjustment material kit that has improved properties in terms of surface drying and of discoloration after curing and that enables adjustment to a desired color tone. The present invention relates to a dental color tone adjustment material kit including: a primer composition (A) including an acid group-containing polymerizable monomer (a) and a volatile organic solvent (b); and a dental color tone adjustment material B including a polymerizable monomer (d), a polymerization initiator (e), particle aggregates (f) that are chain aggregates of ultrafine filler particles having an average primary particle diameter of 1 to 50 nm, titanium dioxide (g), and a pigment (h). The monomer (a) accounts for 0.05 to 45 weight % of the primer composition (A), and the organic solvent (b) accounts for 55 to 99.95 weight % of the primer composition (A).

Abstract: The invention relates to the use of polymer particles in the form of filaments formed by block copolymers, as viscosifiers or agents that modify the rheology of organic or aqueous solutions. More specifically, the invention relates to the use of said crosslinked filamentous polymer particles for improving the resistance to heat ageing of an organic or aqueous solution.

Abstract: Fibrous structures containing one or more particles, and methods for making same are provided.

Abstract: A cosmetic composition is disclosed comprising particle active; opacifying particles having a refractive index of at at least 1.7 and cosmetically acceptable carrier. The particle active comprises (i) water-insoluble shell component comprising inorganic material and having a refractive index of from 1.3 to 1.8; and (ii) core component comprising volatile liquid and having a refractive index of at least 1.2.

Abstract: A composition is provided to apply to the skin, hair, or external mucosa of a human or animal, and a method for using the composition. The composition includes for example a composition for application to skin, hair or external mucosa comprising: a) dispersed submicron particles of hydrophobic agent(s) having average particle size from 100 nm to 999 nm; b) an aqueous-solvent fluid; and c) rheological modifying agent(s); wherein the aqueous-solvent fluid is 10% to 95% wt. of one or more water miscible solvent(s), 4.99% to 89.99% wt. water, and 0.01% to 10% wt. of the rheological modifying agent(s); and wherein the hydrophobic agents comprise 0.01 to 70% wt. of the skin, hair or mucosal composition; and wherein the composition is substantially surfactant-free.

Abstract: The invention relates to stabilised multiple emulsions comprising the compounds a), b) and c), methods for the stabilisation of multiple emulsions and the use of multiple emulsions as skin protection products, in particular for protection against aqueous noxa, where: a) at least one aliphatic unbranched diol with 2 to 4 carbon atoms in the hydrocarbon chain, b) at least one further branched or unbranched aliphatic diol with 4 to 12 carbon atoms in the hydrocarbon chain that is different from a), whereby the hydrocarbon chain may be interrupted by an oxygen atom, c) at least one single-value aliphatic alcohol with 12 to 30 carbon atoms in the hydrocarbon chain.

Abstract: It has emerged that blonding pastes of relatively high oil content that have been thickened by specific polymers are especially table when the persulfates employed satisfy certain criteria. Blonding tablets including, based on their weight, 10 to 70 wt % of peroxydisulfate(s), 0 to 30 wt % of oil(s) and 1 to 20 wt % of disintegrant(s) made from cellulosic material that before being admixed to components a) and b) and before tableting has been compacted and takes the form within the tablet of compacted granules with a density of 0.3 to 1.5 g/cm3 exhibit increased chemical and physical stability and can be mixed readily with oxidant preparations to produce blonding compositions with stable viscosity.

Abstract: Process for heat treating precipitated silica to improve stability. Oral care compositions comprising such heat treated precipitated silica abrasives and a stannous ion source.

Abstract: The present invention provides personal care compositions having efficient perfume blooms or bursts. The personal care compositions include shampoo and body wash compositions, and comprise perfume materials having high perceived odor intensity at low concentrations of perfume materials.

Abstract: Disclosed are methods and uses for conditioning the scalp against the onset, return or worsening of symptoms associated with dandruff, comprising applying glycerol or a composition comprising glycerol to the scalp of an individual.

Abstract: A oral care composition comprising 20% to 75% of water by weight of the composition; 25% to 60% of a calcium-containing abrasive by weight of the composition; 0.1% to 15%, of a polyethylene glycol (PEG) by weight of the composition; and 0.001% to 5% of a flavorant composition by weight of the oral care composition.

Abstract: Disclosed are compositions in the form of fluid O/W (oil-in-water) or two-phase liquid emulsions for reshaping keratin fibre, comprising: a) at least one dicarbonyl compound of formula (I), or the hydrates or salts thereof: wherein: R represents hydrogen; a carboxyl group; a straight or branched C1-C6 alkyl group optionally substituted by at least one hydroxy or carboxy group or halogen, preferably Br; optionally substituted phenyl; optionally substituted benzyl; an indole or imidazolylmethyl group or the tautomers thereof of formula wherein * represents the part connected to the rest of the molecule. b) at least one lipid selected from a liquid, semisolid or solid hydrocarbon or an ether; c) at least one ethoxylated or non-ethoxylated fatty alcohol.