Abstract: Provided herein is a probe for treating an eye of a patient. In one or more embodiments, the probe includes a body, and a tubular element having a main lumen extending from the body, the tubular element comprising a distal end. The probe further includes a visualization optical fiber within the main lumen, the visualization optical fiber adapted to emit an illumination provided by at least one of a plurality of light sources connected to the visualization optical fiber. In some embodiments, the probe further includes an optical switching system (e.g., a time-division multiplexor) operable with the plurality of light sources, wherein the optical switching system is adapted to independently control each of the plurality of light sources. By providing time-division multiplexing between different surgical light sources, quasi-simultaneous illumination delivery through the same optical path may be achieved.

Abstract: A laser eye surgery system produces a treatment beam that includes a plurality of laser pulses. An optical coherence tomography (OCT) subsystem produces a source beam used to locate one or more structures of an eye. The OCT subsystem is used to sense the distance between a camera objective on the underside of the laser eye surgery system and the patient's eye. Control electronics compare the sensed distance with a pre-determined target distance, and reposition a movable patient support toward or away the camera objective until the sensed distance is at the pre-determined target distance. A subsequent measurement dependent upon the spacing between the camera objective and the patient's eye is performed, such as determining the astigmatic axis by observing the reflection of a plurality of point source LEDs arranged in concentric rings off the eye.

Abstract: A dressing for negative pressure wound therapy includes an absorbent layer comprising a gelling absorbent material for absorbing exudate, a peripheral adhesive skin contact layer comprising a hydrocolloid adhesive and defining a window through which the absorbent layer is able to contact a wound, and a cover layer that is water impermeable and air permeable. The cover layer defines an aperture to be used with a pump assembly to provide negative pressure to a wound site.

Abstract: Ultrasonic welding is performed by passing a first sheet layer, a second sheet layer, and an elastic film interposed therebetween in a stretched state in a machine direction between an anvil roll having a large number of protrusions and an ultrasonic horn. The anvil roll includes a region having the protrusions and in the region. A site, in which welding is performed by one ultrasonic horn, has a portion in which an area rate of the protrusions changes in a roll circumferential direction and a roll length direction. A difference between a maximum value and a minimum value in a change of the area rate of the protrusions in the roll circumferential direction is 4.5% or less, and a difference between a maximum value and a minimum value in a change of the area rate of the protrusions in the roll length direction is 1.5% or less.

Abstract: The methods herein relate to assembling an elastic laminate with a first elastic material and a second elastic material bonded between first and second substrates. During assembly, an elastic laminate may be formed by positioning the first and second substrates in contact with stretched central regions of the first and second elastic materials. The elastic laminates may include two or more bonding regions that may be defined by the various layers or components of the elastic laminate that are laminated or stacked relative to each other. In some configurations, a first plurality of ultrasonic bonds are applied to the elastic laminate to define a first bond density in the first bonding region, and a second plurality of ultrasonic bonds are applied to the elastic laminate to define a second bond density in the second bonding region, wherein the second bond density is not equal to the first bond density.

Abstract: An absorbent article processing device includes a cutter roll and an anvil roll. The cutter roll includes a roll main body; a blade protruding in a radial direction in a first angular range of a part of a circumferential direction of the roll main body; a first bearer protruding in the radial direction in a second angular range of a part of the circumferential direction including at least the first angular range and being in contact with the anvil roll, and being cut out in an angular range excluding the second angular range at a first end portion in an axial direction of the roll main body; and a second bearer provided around the entire circumference or a part of the circumferential direction and being in contact with the anvil roll at the second end portion in an axial direction of the roll main body.

Abstract: A stretchable structure is provided with an elastic member provided between a first sheet layer and a second sheet layer. A stretchable region and a non-stretchable region are alternatively repeated three or more regions from end to end in the stretching direction of the stretchable structure. Both ends are the stretchable region. Both of the ends have an adhesive region of a hot melt adhesive, where the elastic member is adhered to the first sheet layer and the second sheet layer, in a spread state, intervals between adhesive regions adjacent in the stretching direction are all the same, twice of a stretching direction length of the adhesive region positioned on both ends in the stretching direction of the stretchable structure and a stretching direction length of the adhesive region positioned at an end portion on the non-stretchable region side of the stretchable region are all the same.

Abstract: A system and method for detecting biofluid is disclosed, specifically utilizing a signaling element and a reader, wherein the signaling element comprises a sensing element, an impedance measuring circuit, an oscillator circuit, an acoustic transducer, and a power supply source, while the reader device comprises a microphone and a processor.

Abstract: A moisture management apparatus monitors an area for moisture events and wirelessly transmits moisture-related information to one or more notification devices. An embodiment of the moisture management apparatus includes a substrate and one or more sensors supported by the substrate. The sensor(s) emit wireless signals indicative of the moisture-related information. A sensor event communication system forwards the sensor signals to another device, such as a notification device. The sensor event communication system may monitor other types of patient events. Portions of the moisture management apparatus and/or the moisture event communication system may be embodied in a patient support apparatus, such as a bed.

Abstract: A method for manufacturing an absorbent article, said method comprising guiding a first sheet material along a rotating member, wherein a surface of said rotating member is provided with a pattern with at least one suction zone and at least one non-suction zone; applying an absorbent material on said first sheet material on the rotating member; locally removing the absorbent material applied on at least one attachment portion of the first sheet material located above the at least one non-suction zone, such that at least one remaining portion of the first sheet material located above the at least one suction zone is covered with absorbent material and substantially no absorbent material is present on the at least one attachment portion; applying a second sheet material on top of the absorbent material on the first sheet material.

Abstract: An absorbent garment that includes a longitudinal axis and a lateral axis. The absorbent garment also includes a front region, a back region and a crotch region, with the crotch region being disposed between the front region and the back region. The crotch region includes an absorbent assembly. The absorbent garment further includes a front panel in the front region, wherein the front panel includes an inner layer, an outer layer and a front longitudinal end; a back panel in the back region, wherein the back panel includes an inner layer, an outer layer and a back longitudinal end. The front panel and the back panel each include a stranded elastic area between their inner and outer layers. The front panel also includes a stretch banded area disposed between the inner and outer layers. The stretch banded area is disposed adjacent the front longitudinal end.

Abstract: A patient transfer apparatus is provided and includes a frame, a seat assembly coupled to the frame, and a track assembly coupled to the frame. The track assembly includes a moveable track for traversing stairs and a motor configured to drive the track. The apparatus further includes a control system. The control system includes a controller configured to control the motor and to adjust a speed of the apparatus based on an occupancy of the seat assembly upon traversing the stairs based on a current to the motor upon traversing stairs.

Abstract: A mounting unit for adjustably mounting an add-on piece to a frame, in particular of a wheelchair, includes at least one drum receiving unit having at least one aperture and female thread. The drum receiving unit is an integral part of the frame or adapted to be attached to the frame. At least one drum assembly has at least one hole and a male thread. At least one bolt is part of the add-on piece or adapted to be mounted therewith to hold the add-on piece. The drum receiving unit is adapted to receive the drum assembly. The female thread mates with the male thread and allows an alignment of the position of the hole with respect to the aperture, such that the bolt can be inserted through the aperture at least partly into the hole. The drum receiving unit with the drum assembly and/or the drum assembly with the bolt comprises a detachable form fit connection. At least one of the drum receiving unit, the drum assembly and/or the bolt comprises a detachable force fit connection with respective mating component.

Abstract: The present invention relates to a wheelchair improvement kit and a manual wheelchair. The improvement kit includes an anti-tip device including a pair of multifunction tube assemblies. Each multifunction tube assembly includes a mount tube configured for pivotally mounting one on each side of the wheelchair, a slide tube slidably engaged to the mount tube where both ends of the slide tube extend beyond the mount tube, a slide tube brake engaging or releasing the position of the slide tube relative to the mount tube, and an extendable pole inserted into the top of the slide tube. The top of the extendable pole is fitted with a hand grip. The anti-tip device further includes a pair of guide tubes configured for mounting one on each side of the wheelchair. When the multifunction tube assembly is used as the anti-tip device, the slide tube passes through the guide tube.

Abstract: A patient turning device attaches to side rails of a bed on one end in at least two spaced apart locations. Straps of the device are then placed under a patient and/or patient is placed on top of such straps. Between two of the straps are connecting straps extending perpendicular thereto, such as where the first straps are horizontal and the connecting straps are vertical. Connected to some of the vertical and/or horizontal straps are removable windows which are material which fills in at least some of the area between the first straps, connects to at least some of the connecting straps, and are removably and replacably connected to cover (fill in) some of this area between the straps. This allows for access to a patient's back after rotating the patient, in embodiments of the disclosed technology.

Abstract: A patient support device including a patient support board including of at least two board sections, wherein at least one of the at least two board sections may be pivoted with respect to another of the board sections around a pivot axis by a pivoting mechanism. The pivoting mechanism includes two ratchets that may be latched in mutually opposite directions of rotation around the pivot axis and at least one operator control device. At least one of the two ratchets may be moved from a latched state into an open state and/or vice versa by the at least one operator control device.

Abstract: In one aspect, the present disclosure provides a patient repositioning sheet including an inflatable sheet having a lower layer and an upper layer that are urged apart with inflation of the inflatable sheet. The patient repositioning sheet further includes at least one inflatable support, such as an inflatable wedge. The inflatable wedge has a wedge surface that extends obliquely to the upper layer of the inflatable sheet with the inflatable wedge inflated.

Abstract: An apparatus for transferring a patient or other body comprises a housing, a deck at least partially disposed within the housing, and a continuous belt disposed about the deck. The housing is formed with first and second sides coupled to first and second ends, and a panel attached to the sides and ends to provide structural rigidity to the apparatus. The deck is coupled to the housing, and the continuous belt circulates around the deck to transfer a body from a first surface at a first side of the housing to a second surface at a second side of the housing.

Abstract: A medical examination table includes a base assembly, a table assembly, a table actuation assembly, a wheel assembly, and an actuating mobility assembly. The base assembly configured to support the medical examination table in a first mobility configuration. The table actuation assembly is configured to raise and lower the table assembly relative to the base member to thereby transition the table assembly between a lowered position and a raised position. The wheel assembly is configured to support the medical examination table in a second mobility configuration. The actuating mobility assembly is configured to cooperate with the table actuation assembly to thereby actuate the wheel assembly relative to the base assembly to thereby transition the medical examination table between the first mobility configuration to the second mobility configuration.

Abstract: A soft, inflatable, single use, repositioning device for ob/gyn/pelvic examination and procedures, more particularly, to single time use and/or partially reusable pillow like device. A flat collapsible/inflatable-expandable, repositioning and lifting apparatus for medical and ob/gyn examination and procedures and, more particularly, to a reposition and lift device, with a single or more than one, inflatable compartment. Various attachments may be provided, such as foot stirrups, sleeves, and handles, and optional accessories, with built in compressed gas cartridge, and/or a reusable pump for air source through connector. The device repositions, orient and raises the patient's lower back and the buttocks from supine, flat position to dorsal lithotomy and Trendelenburg position on a flat hospital bed to carry out an exam or a procedure, without moving a patient to a special exam room or using another table.

Abstract: A power assistive device (100) for hand rehabilitation that provides training of a combined movement of finger flexion-extension and forearm supination-pronation to a user. The power assistive device (100) includes a hand brace (102) and a base (104). The hand brace (102) includes finger driving units (206) that adjustably connect to a platform (202, 204), actuators (208) that connect to the finger driving units (206), and force sensors (232) that connect to the finger driving units (206) and the bottom of the hand brace (102) and detect force signals generated by movement of the hand brace (102).

Abstract: A suit type exoskeleton adjustable to a user's body size includes a wire, a wearing portion worn on a part of the user's body to assist with physical strength, a controller removably coupled to an outer surface of the wearing portion and coupled to an end of the wire, and a driver coupled to an opposite end of the wire and configured to provide power to the wire. A suit type exoskeleton for knee power assistance is characterized by use of the suit type exoskeleton which is adjustable to a user's body size for their knee.

Abstract: A joint actuator assembly includes a motor, a rotating driving member driven by the motor for driving a driven component, and a transmission assembly located between the motor and the rotating driving member that provides speed reduction from the motor to the rotating driving member. The rotating driving member comprises a magnetic coupling including a plurality of magnetic elements that are configured to magnetically couple with an opposing magnetic coupling of the driven component. The actuator and driven component may be combined into a mobility device including a magnetic coupling system having a first magnetic coupling on the actuator that magnetically couples to a second magnetic coupling on the driven component. The magnetic coupling system includes plurality of magnetic elements located as part of one or both of the first and second magnetic couplings. The first and second couplings have opposing mating surfaces that join together in a coupled position.

Abstract: Apparatuses, systems and methods associated with a travel assistance system. A wearable personal navigation device may include a communication system, an indicator, and a processor coupled to the communication system and the indicator. The processor may be configured to generate a request for a navigation path from a location to a destination and transmit the request to a node of the network. The processor may be configured to determine the direction of travel from the location of the user based on a first navigation path received from the node of the network in response to the request, wherein the first navigation path includes at least one modification from a second navigation path, wherein the modification is based on data received by the network from a remote device that indicates an object, and cause the indicator to indicate the direction of travel. Other embodiments may be described and/or claimed.

Abstract: An upright massage tub can be converted into a standard bathtub. The upright massage tub is designed so as users can safely and easily enter the tub in a step/sit motion, sitting themselves upright in a natural, ergonomic position (at approximately a standard chair height). This upright design is also better for user assistants, putting them in a better ergonomic position while they assist users in bathing. This upright massage tub design also includes a vertically adjustable hub, housing a water jet that can deliver a proximity source of water-jet flow.

Abstract: A vibration therapy device that includes a housing that includes a handle portion, a head portion and a module seat defined on the head portion, an electrical source, a motor positioned in the housing, a switch for activating the motor, a push rod assembly operatively connected to the motor and configured to reciprocate in response to activation of the motor, and a therapy module removably secured to the module seat. The distal end of the push rod assembly is configured to removably receive a reciprocating attachment thereon. The therapy module at least partially surrounds the distal end of the push rod assembly.

Abstract: A vibration appliance includes a vibration-isolation structure which substantially reduces vibration felt by the user at the handle. The vibration motor is mounted to a vibration plate which carries the massage node. The vibration plate floats within the vibration appliance housing, being suspended by a flexible, elastomer membrane having contours such as curves or folds in it that provide freedom of movement of the vibration plate relative to the housing to which the flexible membrane is mounted. This arrangement can be thought of as the motor and vibration node being mounted on a flexible diaphragm that can move freely as if mounted to the housing by a bellows-like arrangement.

Abstract: A bath system comprises a tub and a fluid injection system. The tub has a jet orifice, and the fluid injection system is fluidly coupled to the jet orifice. The fluid injection system comprises a conduit, a heat source, an air supply source, and a fluid injector. The conduit has an opening. The heat source is coupled to an outer portion of the conduit external to the opening. The air supply source is fluidly coupled to the conduit, and is configured to provide a flow of air to the central opening. The fluid injector is configured to provide water to the flow of air to produce a combined flow of air and water. The heat source and the conduit are cooperatively configured to heat the combined flow of air and water in the opening before the combined flow enters the tub through the jet orifice.

Abstract: A liner for use with a basin to contain a liquid features a plurality of bodies of flexible plastic. Portions of an inner face of a first body of flexible plastic are joined to corresponding portions of an inner face of a second body of flexible plastic, through which a plurality of openings are formed, to provide a multi-layer body of flexible plastic. Other portions of the inner face of the first body of flexible plastic are not joined to corresponding other portions of the inner face of the second body of flexible plastic, defining an air conduit between the first body of flexible plastic and the second body of flexible plastic for guiding pressurized air substantially from an air discharge apparatus.

Abstract: A bioprocess vessel includes a flexible bag or substantially rigid container that defines an interior volume and having a bottom surface, the bottom surface being open or containing an aperture therein for the passage of fluid. A pump is secured to the bottom surface of the flexible bag or substantially rigid container. In some embodiments is secured directly to the flexible bag or substantially rigid container. In other embodiments, the pump is secured indirectly the flexible bag or substantially rigid container using, for example, a port that extends through the aperture on the bottom surface. The port or flanged surface may also be integrated into the pump, which is secured to the vessel. An optional mixing adaptor may be provided inside the interior volume of the flexible bag or substantially rigid container and at least partially covers the inlet that leads to the pump.

Abstract: The present technology is a device for delivering a medicinal agent to a breastfeeding child. One embodiment comprises a first portion configured to be positioned on the breast during breastfeeding a second portion having an agent region and a sealing region. The agent region is configured to house the agent during breastfeeding and has a first cross-sectional area. The sealing region has a second cross-sectional area at least great enough to surround and engage a circumference of the nipple but less than the first cross-sectional area. When the device is positioned on the breast and the child is breastfeeding, the device is configured such that the nipple extends through the sealing region into the agent region and the portion of the delivery device at the sealing region contacts the nipple, thereby reducing or preventing the flow of breast milk and/or the agent through the sealing region to the first portion.

Abstract: A method for manufacturing a colored sheet for coloring an object by adhesion to the object includes, a coloring step of applying by spraying, a first coating fluid containing first microparticles for coloring to a thin film of a print receiver body which has a sheet-shaped support body and the thin film, the thin film being peelably held on the sheet-shaped support body to serve as a base material of an adhesive sheet which is to be adhered to the object, and a restricting step of applying by spraying, before the coloring step, a second coating fluid for restricting the first microparticles from penetrating the thin film to a location where the first coating fluid is to be applied.

Abstract: A system, computer readable medium and method for selective brightening of hair, the method may include or may be preceded by applying at least one photosensitive material to the hair. The method may also include forming at least one pattern of brightened hair by illuminating the hair by at least one pattern of illumination.

Abstract: A whitening dentifrice composition includes a blue coloring agent, a zinc salt, and an orally acceptable vehicle. The blue coloring agent is selected from the group consisting of a blue pigment and a blue dye. The blue pigment has a blue to blue-violet color with a hue angle in the CIELAB system ranging from 200 degrees to 320 degrees. The whitening dentifrice composition provides a greater whitening benefit to a tooth surface in comparison to a dentifrice composition that does not contain the zinc salt.

Abstract: Compositions, such as personal care compositions, and methods for selectively inhibiting the growth of a detrimental bacteria and promoting the growth of a beneficial bacteria are disclosed. The composition may include a base and one or more fatty alcohols. The one or more fatty alcohols may be present in an amount effective to selectively inhibit the growth of at least one detrimental Gram-positive bacteria and promote the growth of at least one beneficial Gram-positive bacteria on skin. The detrimental Gram-positive bacteria may include Corynebacterium, and the beneficial Gram-positive bacteria may include Staphylococcus.

Abstract: A composition provides a protective barrier and includes glyceryl dibehenate, tribehenin, and glyceryl behenate, a surfactant that includes glyceryl stearate, one or more fatty compounds, and one or more triglyceride. The composition optionally includes a hydrating agent and may be essentially free of or is devoid of one or more of petrolatum, mineral oil and water. The composition provides occlusivity and hydration effects that are comparable to compositions that include one or more of petrolatum, mineral oil and lanolin.

Abstract: Provided is a composition containing the following components (A), (B) and (C) and suppressing formation of scum during cleansing, wherein a weight ratio of (A)/(B) is 0.2-5 and a weight ratio of ((A)+(B))/(C) is 0.01-10: (A) N-lauroyl glycine or a salt thereof (B) N-myristoyl glycine or a salt thereof (C) N-acyl acidic amino acid having an acyl group having 8 to 24 carbon atoms, or a salt thereof.

Abstract: The present disclosure relates to a cosmetic composition for blocking fine dust. The composition according to the present disclosure can fundamentally prevent problems due to fine dust by reducing the attachment rate of fine dust attached to skin.

Abstract: The present disclosure provides biophotonic topical compositions and methods useful in phototherapy. In particular, the biophotonic topical compositions of the present disclosure are substantially resistant to leaching such that very low amounts of chromophore(s) present in the biophotonic composition leach out of the composition. The biophotonic compositions and the methods of the present disclosure are useful for promoting wound healing and skin rejuvenation, as well as treating acne and various skin disorders.

Abstract: The subject of the present disclosure is a process for dyeing keratinous material, in particular human hair, including the following steps: Application of an agent (a) to the keratinous material, wherein the agent (a) is at least one organic silicon compound selected from silanes having one, two or three silicon atoms, said organic silicon compound including one or more hydroxyl groups and/or hydrolysable groups per molecule, and said agent (a) further including at least one oligoalkylsiloxane, and Application of an agent (b) to the keratinous material, the agent (b) including at least one colorant compound selected from the group including pigments and/or direct dyes. A second object of the present disclosure is a multi-component packaging unit which contains the two agents (a) and (b) in two separately assembled containers.

Abstract: A surfactant composition comprising a sugar-based surfactant comprising a C8-C16 alkyl glucoside, a C8-C16 alkyl polyglucoside, or a combination of a C8-C16 alkyl glucoside and a C8-C16 alkyl polyglucoside; a C8-C18 amphodiacetate; a C8-C16 acyl sarcosinate, a C8-C16 acyl glutamate, a C8-C16 acyl glycinate, or a combination thereof; and optionally a C8-C14 acyl lactylate, wherein the composition is free of sulfated anionic surfactants.

Abstract: The present invention may provide an oil in water (O/W) cosmetic composition having water resistance and ease of facial cleansing, using an A-B-A type triblock copolymer which is included in the cosmetic, and thus may adjust the surfactant power. Further, it is possible to provide a method for imparting water resistance and ease of facial cleansing, using the A-B-A type triblock copolymer.

Abstract: The present invention relates to a transdermal delivery complex using a metal-organic framework (MOF) and nanocellulose. In addition, the present invention relates to a cosmetic composition comprising the transdermal delivery complex and a method for preparation of a transdermal delivery complex.

Abstract: A method of treating skin by reducing tumor necrosis factor alpha (TNF-?) activity or matrix metalloproteinase enzyme (MMP-1) activity in a person's skin is disclosed. The method can include topically applying a composition that includes an effective amount of an extract of Brachychiton acerifolius to the person's skin to reduce TNF-? activity or MMP-1 activity in the skin.

Abstract: Provided is a male cleanser including a skin conditioner, a solvent, a humectant, a viscosity increasing agent, a surfactant, a preservative, a chelating agent, and perfume, wherein the skin conditioner includes a Maca root extract, a natural extract, niacinamide, glyceryl acrylate/acrylic acid copolymer, hyaluronic acid, arginine, hydrolyzed collagen, sucrose distearate, hydrogenated lecithin, and dimethicone.

Abstract: A fermented extract of aerial parts of Citrus aurantium and the process for obtaining it. The fermented extract may be added to a cosmetic composition. Also, the use of a fermented extract of Citrus aurantium to combat skin ageing, and also as an antioxidant active agent, to prevent/reduce oxidative stress and/or to detoxify the skin.

Abstract: The present disclosure is directed to a method for producing an olive branch extract having a high oleuropein content. The method includes crushing at least a portion of dried olive branch and extracting olive branch extract from the crushed olive branch with an extraction solvent. The olive variety is at least one selected from Lucca, Mission, and Nevadillo Blanco. The added branch amount of olive branch to the extraction solvent is 10% by weight or more, the extraction solvent is 30% to 50% 1,3-butylene glycol, and the extraction is performed at a temperature in a range of 70° C. to 80° C.

Abstract: The application provides pharmaceutical compositions comprising stable concentrated solutions of antioxidant free norepinephrine bitartrate for injection dispensed in glass containers and methods of providing such solutions to a subject.

Abstract: Provided herein are sustained release biodegradable intracanalicular insert comprising a hydrogel and cyclosporine, methods of treating or preventing an ocular disease in a subject in need thereof by administering such inserts as well as methods of manufacturing such inserts.

Abstract: This invention relates to a chocolate or chocolate substitute composition or product comprising (a) at least compound to be delivered to a subject; (b) a chocolate or chocolate substitute matrix and at least (i) a masking agent or (ii) a firming agent, wherein the composition or product is substantially stable.