Abstract: A condom, container and applicator for a condom, in which the condom is provided in a longitudinally expandable cup having a peel-off lid. The cup is typically formed of plastic material. The side wall of the container is expandable, and can include accordion-like pleats to allow for longitudinal expansion of the cup. The condom is placed in the cup such that it can be directly applied to the penis while still in the cup, and the cup used as an applicator to unroll the condom over at least the head of the penis by expanding the side wall of the cup. The disclosure also relates to a dispenser for storing and dispensing the condom containers.

Abstract: The invention relates to electronic contact lens systems, methods for fabrication thereof, and uses thereof for treatment of ophthalmic diseases and conditions, for example, meibomian gland dysfunction.

Abstract: Embodiments include methods and systems for treating back pain associated with a nerve. A needle of a cryogenic system may be inserted beneath a skin surface. The needle may include an electrically conducting structure at least partially surrounded by an electrical insulator for conducting electrical energy. The needle may include an outer lumen and an inner lumen extending distally within the outer lumen, the inner lumen include a distal opening open to the outer lumen. The needle may be positioned at a desired location in proximity to the nerve, and a cooling therapy including cooling cycles and thawing periods may be performed to cool tissue at the desired location. The cooling therapy may sufficiently reduce the back pain.

Abstract: An ocular surgical apparatus is provided, including a surgical control device such as a foot pedal configured to be employed to control at least one ocular surgical parameter, and a controller configured to receive a series of values from the surgical control device and evaluate the series of values provided from the surgical control device, the series of values provided using a buffer comprising a detection area and an exclusion area. Presence of a desired value in the detection area and an absence of a contrary indication in the exclusion area is determined by the controller to indicate a switch associated with the surgical control device is requested by a user of the surgical control device.

Abstract: As shown in the drawings for purposes of illustration, a method and system for making physical modifications to intraocular targets is disclosed. In varying embodiments, the method and system disclosed herein provide many advantages over the current standard of care. Specifically, linear absorption facilitated photodecomposition and linear absorption facilitated plasma generation to modify intraocular tissues and synthetic intraocular lenses.

Abstract: Disclosed is a wound dressing material comprising a substrate, about 2.5% to about 8% by weight of a bicarbonate, and a film-forming agent, the film-forming agent serving as a binder for said bicarbonate to said substrate, the film-forming agent and the bicarbonate being present in a ratio of between 1:2 and 2:1 with respect to one another. Also disclosed are a method for preparing a wound dressing material and a method for treating a wound.

Abstract: Systems, kits, methods of manufacturing, and a sealing member for creating a sealed space are described. The sealing member can include a film layer and a first adhesive layer coupled to the film layer. The sealing member can also include a second adhesive layer coupled to the first adhesive layer. A plurality of apertures may extend through the second adhesive layer. Each aperture can expose at least a portion of the first adhesive layer through the second adhesive layer. A plurality of polymer particles may be disposed in the first adhesive layer. The polymer particles can be configured to dissolve in response to interaction with a switching solution.

Abstract: In one embodiment, an array of packages may comprise three or more different sizes of disposable absorbent articles. The Product Length-to-Waist Silhouette of a second absorbent article may be equal to or less than a Product Length-to-Waist Silhouette of a first absorbent article. And the Product Length-to-Waist Silhouette of a third absorbent article may be equal to or less than a Product Length-to-Waist Silhouette of a second absorbent article. And, an Array Average Product Length-to-Waist Silhouette of first and second packages of the array may be from about 1.1 to about 0.3. Further, an Array Average Product-Hip-to-Side Silhouette may be from about 1.0 to about 1.7.

Abstract: A sensor system for detecting a property of or within an absorbent article may comprise an absorbent article and a sensor. The absorbent article may comprise a garment-facing layer and an absorbent assembly. The sensor may be disposed in and/or on the absorbent article. The sensor may be separable from the absorbent article. The sensor may be configured to sense a change in condition within the absorbent article.

Abstract: An absorbent article having a wearer-facing side and garment-facing side, the article comprising: —a nonwoven topsheet on the wearer-facing side, wherein the topsheet has a first color which is not white and comprises thermal bonds; a backsheet on the garment facing-side; an absorbent core between the topsheet and the backsheet; optionally an acquisition layer; and a visual signal disposed on the topsheet or a layer of the article under the topsheet; wherein the visual signal comprises a first portion having a first appearance and a second portion having a different second appearance. The topsheet has an opacity index of at least 28% as measured by the opacity index test as described herein and the visual signal is visible on the wearer-facing side of the article.

Abstract: Absorbent cores for use in absorbent articles are presented. The absorbent cores include a low-density zone that is surrounded by zones having a higher density than that of the low-density zone. The low-density zone aids in fluid absorption, distribution and storage.

Abstract: A method of making an absorbent composite that includes a first fabric, a second fabric, and particles positioned between the two fabrics and absorbent articles made from the absorbent composite. The particles are secured between the two fabric using adhesive, thermal plastic or combinations thereof. The fabrics are bonded together in a manner that limits particle movement between the fabrics. The bond pattern may define pockets or other shapes. In applications in which the bond pattern forms pockets, the particles may be positioned in the pockets. The particles may be SAP particles or other particles with advantageous properties.

Abstract: A package containing a stack of folded disposable absorbent articles, the package being formed of a flexible polymeric film defining a cuboid package having top and bottom surfaces and rear, front, first and second side walls. One or more folding tabs are provided proximal the top surface and extending along a width of one or both of the first and second side walls. Each folding tab has a height of between about 10 mm and about 50 mm in a direction perpendicular to the length of the folding tab and comprises a higher bending stiffness than the flexible polymeric film.

Abstract: According to one embodiment, an absorbent article includes a moisture-impervious outer layer, an inner layer substantially co-extensive with the outer layer, and an absorbent layer interposed between the outer layer and the inner layer. The inner layer is treated with at least one antimicrobial booster. The absorbent layer is treated with at least one antimicrobial agent.

Abstract: An adhesive cover and method of use in which the cover is well-suited to effectively cover a temporary tattoo utilized in radiation therapy treatments. The cover includes a transparent, flexible layer with an optional rigid layer releasably adhered thereto. The first, flexible layer has a lower adhesive surface, an upper low-adhesion surface and a predefined peripheral edge. The second, rigid layer has a lower surface releasably adhered to the upper low-adhesion surface of the first layer, an opposing upper exposed surface, and a peripheral edge cooperative with the predefined peripheral edge of the first layer to preserve the integrity of the first layer during handling and application. The second layer is removed from the first layer only after the first layer is adhered to a patient's skin.

Abstract: A gown dispenser system has a plurality of gowns, each having a back region, the gowns folded and stacked back region facing up, such that, pulling on the back region of a gown on top of the stack removes that gown from the stack and exposes the back region of the next gown in the stack, an enclosure containing the stack of gowns, the enclosure having an opening exposing the back region of the gown at the top of the stack, enabling a user to grasp the exposed back region and pull the topmost gown from the enclosure, exposing the next gown in the stack. Gowns are drawn from the enclosure one-at-a-time, at need.

Abstract: Patient handling devices for transporting patients in health care settings are disclosed herein. The patient handling devices may include a support member and a torso support member. The patient handling device includes at least one articulating joint that is coupled to the support member and the torso support member. The articulating joint is selectable to arrest or allow articulation of the respective torso support member or the lower extremities support member relative to the support member through a variety of orientations.

Abstract: In one embodiment, a wheelchair includes a drive wheel, a motor coupled to the drive wheel, and a user input device. The motor, in one embodiment, is configured to rotate the drive wheel. The user input device may be configured to send a signal for controlling a motor parameter. The wheelchair, in one embodiment, includes a caster wheel and a castor sensor configured to sense a caster angle. In one embodiment, a controller is configured to receive the signal for controlling the motor parameter and a signal from the caster sensor and to determine a first turn rate parameter of the wheelchair based upon the received signal from each of the input device and the caster sensor.

Abstract: A patient support system comprises a patient support apparatus for patients. The patient support apparatus comprises a support structure and a patient support surface supported by the support structure. The patient support apparatus also comprises movable members. One or more rotary actuators are coupled to the movable members. The rotary actuator comprises a gear assembly with a cycloidal drive arranged to drive movement of the movable member. The gear assembly also restricts back drive torque from backdriving the movable member.

Abstract: A novel foot support device includes a first sidewall adapted to engage the lateral side of a first foot, a second sidewall adapted to engage the lateral side of a second foot, and a backwall adapted to engage both the plantar region of the first foot and the plantar region of the second foot. In a particular embodiment, the first sidewall includes an inclined interior surface, the second sidewall includes an inclined interior surface, and the backwall includes an inclined interior surface. In another particular embodiment, the foot support device includes sidewalls and a backwall that can flatten and pivot relative to one another, facilitating a collapsible foot support device.

Abstract: Embodiments of the invention thus define a system and methods for moving a patient into a medical treatment/imaging apparatus. By appropriate use of relatively narrow guides, a bed can be held securely both prior to movement onto the apparatus and while on the apparatus. By use of relatively wide guides, the bed is allowed a degree of lateral play to ensure a smooth transition on to the apparatus.

Abstract: Extracorporeal membrane oxygenation systems and methods of use are disclosed. Several publications and patent documents are cited throughout the specification in order to describe the state of the art to which this invention pertains. Full citations of these references can be found throughout the specification. Each of these citations is incorporated herein by reference as though set forth in full.

Abstract: An upright extension for personal walkers for supporting users of personal walkers in an upright position includes a cross-member. The cross-member is removably coupled to a cross-brace of a walker. The cross-member has a first end and a second end orientated opposite each other. A coupler removably couples the cross-member to the cross-brace. A pair of lateral members extends rearwardly from each of a one of the first and second ends. Each of the pair of lateral members has a support attached to a distal end with regard to the cross-member. Each of the supports extends outwardly away from the pair of lateral members. Each of a pair of vertical members extends upwardly from a one of the lateral members adjacent to a one of the first and second ends. Each of the pair of vertical members has a grip and an armrest extending rearwardly.

Abstract: An exoskeleton subassembly is provided. The exoskeleton subassembly includes first and second exoskeleton parts, and a connecting assembly that connects the first and second exoskeleton parts. The connecting assembly includes a guide, a pin, and a limiting device. The guide is fixedly mounted on one part, and a pin fixedly mounted on the other part and slidably mounted inside the guide. The limiting device allows rotation of the pin with respect to the guide when the pin is in a first position, and to oppose the rotation when the pin is in a second position. The limiting device includes an elastic element engaged with the first part when the pin is in the second position. The elastic element exerts on the first part an elastic return force opposing relative rotation between the first and second parts both in two opposite directions of rotation.

Abstract: A linkage mechanism including a base, a first linkage, a second linkage and a driving element is provided. The first linkage has a first end portion and a second end portion opposite to each other, and the first end portion is pivoted to the base. The second linkage has third end portion and a fourth end portion opposite to each other, wherein the third end portion is coupled to the base, and the second end portion and the fourth end portion are coupled with each other. The driving element is coupled to at least one of the second end portion and the fourth end portion, and is configured to drive the first linkage and the second linkage to move relative to the base. A walking aid device is also provided.

Abstract: An apparatus and system for manipulating soft tissue may include a support member and a raised member. The support member includes a support surface disposed between a first end of the support member and a second end of the support member. The support member is elongated in a lengthwise direction between the first end of the support member and the second end of the support member. The raised member includes an outer surf ace disposed opposite an inner surface. The inner surf ace is supportable by the support surface of the support member. The outer surf ace of the raised member is configured to rotate along at least a portion of a user's body in response to movement of the raised member along the user's body. The raised member is repositionable along the support surf ace of the support member in the lengthwise direction.

Abstract: The invention provides for a medical apparatus (100, 200, 300) for treating cells of a subject comprising at least one transducer (102, 224) with a vibrating surface (116). The transducer further comprises an applicator (118, 600) for attaching the vibrating surface to an outer surface of the subject (108, 218). The transducer is operable to vibrate at a frequency between 10 Hz and 1000 Hz. The medical apparatus further comprises a controller (104, 222, 230) for controlling the vibration of the transducer. The controller is operable for causing the transducer to vibrate for greater than a predetermined period of time for treating the cells. The predetermined period of time is greater than one hour.

Abstract: The present disclosure concerns an adjustable bed facility including a system for executing a computer-based safety-action during a motor-actuated adjustable bed position adjustment, comprising an adjustable bed facility comprising a computer-based controller, an actuator, and a sensor, the computer-based controller providing control of adjustable bed position adjustments, the actuator configured to adjust a height of the adjustable bed facility upon receiving a height-adjustment command from the computer-based controller, and the sensor for determining an actuator action parameter measured value of the actuator, the computer-based controller in communicative connection with the sensor to monitor and compare the motor action parameter measured value to an actuator action parameter normal operation value range, and when the controller determines the monitored motor action parameter measured value is outside the range of the actuator action parameter normal operation value range the controller sends a safety-ac

Abstract: A label includes (a) a base segment, (b) a first lobe segment comprising at least one protruding member and a pull tab, (c) a second lobe segment comprising at least one protruding member, (d) a first cutout segment, (e) a second cutout segment, (f) a first perforation forming a boundary between the base and first lobe segments, (g) a second perforation forming a boundary between the base and second lobe segments, and (h) a third perforation forming a boundary between the first lobe segment and its at least one protruding member. The first and second lobe segments are connected to the base segment and opposed to one another. The first and second cutout segments separate the at least one protruding member of the first and second lobe segments, respectively, from the base segment. The label comprises at least (A) a facesheet layer and (B) an adhesive layer.

Abstract: A cartridge for use with a beneficial agent delivery device having a fillable reservoir. The cartridge includes a reconstitution, unit dose package having first and second compartments, and a fitment. The first compartment contains at least a first constintuent of the beneficial agent. The second compartment contains at least a second constituent of the beneficial agent. The fitment is disposed on the package for interfacing the package to the fillable reservoir.

Abstract: Provided is a medicine feeding apparatus including: a medicine feeder body configured to feed medicine; and a medicine passage configured to guide the medicine fed by the medicine feeder body to a packaging material configured to package the medicine. The medicine passage includes: an inlet that is configured to allow the medicine to enter from above therethrough; an outlet that is configured to allow the medicine to exit downward therethrough; and a communication part that is configured to communicate the inlet and the outlet with each other. The inlet and the outlet are provided as separate bodies from each other. The communication part is provided as a separate body from the inlet and the outlet and is connected to the inlet and the outlet so as to be positionally adjustable.

Abstract: A pliers having an upper jaw supporting a cutting blade chamber near the tip of the pliers and fixed crushing protrusions closer to a pivot of the pliers. The cutting blade chamber includes a depressed basin with a slot for receiving and retaining a releasable cutting blade. The arcuate concave cutting edge of the blade is aligned to a pill-holding cavity in the lower jaw of the pliers such that, when the pliers are manually closed, the blade cuts an installed pill in half. The fixed crushing protrusions are mounted on a convex semi-cylindrical shell, and are aligned to pill holding cavities in a concave semi-cylindrical crushing basin in the lower jaw of the pliers such that, when the pliers are manually closed, pills in the cavities are crushed.

Abstract: Pill sorting devices are described herein that include a cavity formed from a bottom, a front, a first side wall, and a second side wall, a channel formed at the intersection of the first side wall and the second side wall, and a delivery channel within the front and first side wall or the within the front and the second side wall, wherein the delivery channel is offset from the channel. The pill sorting, counting, and dispensing device can be useful for people with arthritis or poor sight, or could be used commercially in pharmacies or industrially. Methods of making and using the pill sorting, counting, and dispensing devices are also described.

Abstract: Patients with substance abuse problems may be prescribed regular medication that dulls the positive effects of the substance. However, one of the largest challenges for substance abuse patients is that many do not regularly take their medication as they want to experience the high of the substance. Accordingly, systems and methods have been developed for medication sessions that distract the patient from taking the medicine by incorporating the reminder and other med actions in close temporal proximity.

Abstract: A baby bottle assembly for bottom venting includes a bottle having a top closure member adapted for releasable engagement with a top portion of the bottle, and a bottom closure member adapted for releasable engagement with a base portion of the bottle. The bottom closure member has a base panel with a raised portion having an air passage therethrough and a top sealing surface. A diaphragm is positionable between the bottom closure member and the base portion. The diaphragm has a disc, at least one moveable sealing element for sealingly engaging the top sealing surface, and an air passage extending under the at least one moveable sealing element into the liquid chamber. The diaphragm is moveable between a sealed position and an unsealed position. The moveable sealing element when in the sealed position prevents liquid contained within a liquid chamber of the bottle from entering the air passage. When in the unsealed position, the diaphragm allows bottom venting of the bottle.

Abstract: A male connector (1) includes a luer portion (10) connected to the upstream end of a tube (8) used in enteral feeding, and a lock portion (20) that is removably attached to the luer portion. The luer portion (10) includes a tubular male luer (11) in which a channel (17) in communication with the tube (8) is formed. The lock portion (20) has a hollow tubular shape and is open at two ends, and includes female threading (21) that opposes the male luer on the inner circumferential face of the lock portion (20). The male luer (11) is inserted into the lock portion (20). Rotation prevention mechanisms (16, 26) that engage with one another are provided on the luer portion (10) and the lock portion (20) such that the lock portion (20) does not rotate relative to the luer portion (10).

Abstract: The present invention relates to a makeup cosmetic composition containing capsules containing pigments in an inner layer thereof and, more specifically, to a makeup cosmetic composition, which contains a pigment in an inner layer and blocks a pigment from an external environment, thereby preventing pigment discoloration caused by the external environment, and contains capsules readily broken so as to enable color to show when applied to the skin, thereby showing color when applied to the skin even though the color of a formulation is nearly colorless and having an excellent skin coloring ability.

Abstract: An aluminum-free antiperspirant/deodorant composition is disclosed. The aluminum-free antiperspirant/deodorant composition may include an oil-in-water emulsion base and an antiperspirant active dispersed in the oil-in-water emulsion base. The antiperspirant active may be primarily an amino acid, calcium carbonate and optionally a zinc-based antiperspirant active and the oil-in-water emulsion base may include an emulsifier having a mixture of steareth-2 and steareth-20; a plant-based oil, a polyol, and water. The zinc-based antiperspirant active may be free of zinc oxide-amino acid-halide complexes, amino acid-halides, and chelated zinc oxide complexes.

Abstract: The present invention relates to a composition and method for stabilisation of compounds including retinoids using the synergistic effects of beta-carotene and sodium polyaspartate.

Abstract: The present invention relates to non-aerosol shaving compositions which are free of propellants, and methods of preparing and using such shaving composition. In particular, the present invention relates to a non-aerosol, propellant-free composition comprising: (i) at least two C14 to C16 carboxylic acids or an alkali metal salt thereof; (ii) at least one compound of general Formula (I) R—O—[—CH2CH2O—]n—CH2CO2H??(I) or an alkali metal salt thereof, wherein R represents a saturated, straight- or branched-chain C10 to C18 alkyl group; and n represents an integer between 4 and 12; (iii) polyvinyl pyrrolidone; and (iv) water.

Abstract: The present invention a process for straightening the hair, using a composition comprising at least one carboxylic acid of the formula (I): R—CO—COOH Formula (I) The process of the invention is characterized in that it involves the treating of the hair with the composition and the drying of the treated hair under conditions of mechanical tension and hot air flow having a temperature of 60-140° C.

Abstract: An emulsifier-free composition includes in a water phase a hydroxy acid system that includes alpha hydroxy, a blend of low pH, high electrolyte compatible thickeners and in an oily phase one or a combination of emollient oils. The composition has a pH in the range from about 1 to about 5.0 and is essentially free of emulsifiers and comprises a gel cream architecture.

Abstract: Described are methods and uses of TRPV3 agonists for the treatment of conditions associated with TRPV3 pathophysiology such as acne, psoriasis, dermatitis, would healing, the inhibition of hair growth, anxiety or depression. Peptides comprising all or part of the C-terminal portion of soricidin are shown to activate TRPV3 cation channel activity and/or promote wound healing in keratinocytes.

Abstract: The present disclosure relates to compositions capable of absorbing UVA and UVB light. In particle, the present disclosure relates to UV screening compositions comprising at least a portion of LITE-1 polypeptides which are capable of absorbing UV light (e.g., UV-A and/or UV-B light).

Abstract: The present invention discloses a synergistic composition comprising 3-O-ethyl-ascorbic acid and tetrahydrocurcuminoids for use as a skin lightening agent. The invention also discloses a method of inhibiting melanin biosynthesis and tyrosinase activity in mammalian skin cells using a composition comprising 3-O-ethyl-ascorbic acid and tetrahydrocurcuminoids.

Abstract: Provided are personal care compositions including (a) hydrophobic ester oil, (b) at least one of a nonionic or anionic surfactant, and (c) one or more polymers containing polymerized structural units of (i) 79 to 95.74 weight % of C4-C8 (meth)acrylate monomers, (ii) 0.5 to 5 weight % of (meth)acrylic acid monomer, (iii) 3.75 to 14 weight % of (methoxy) poly(ethylene glycol) methacrylates, and (iv) 0.01 to 2 weight % of at least one crosslinker.

Abstract: Disclosed are hair styling compositions comprising at least two latex polymers chosen from acrylate and polyurethane polymers, wherein at least one latex polymer is a film-forming polymer. Methods of styling the hair are also disclosed.

Abstract: The disclosure relates to compositions, films, and methods for improving the appearance of the skin. Compositions comprise at least one thermoplastic elastomer, at least one adhesive polymer, and at least one filler. Methods comprise applying the compositions to the skin to tighten the skin or hide skin imperfections, by forming a film on the skin.

Abstract: Multilayer thin film devices that include a bioactive agent for elution to the surrounding tissue upon administration to a subject are provided. The multilayer thin film devices are useful as medical devices, such as ocular devices. Also provided are methods and kits for localized delivery of a bioactive agent to a tissue of a subject, and methods of preparing the subject devices. The multilayer thin film medical device includes a first layer, a bioactive agent and a second layer. The first and the second layers may be porous or non-porous. The devices have a furled structure, suitable for administration to a subject.

Abstract: The present invention relates to an ophthalmic aqueous composition containing PGF2? analogues for treating ocular hypertension and glaucoma, to a method for treating ocular hypertension and glaucoma by administering said composition to a subject in need of such treatment, and to a method for increasing aqueous solubility and stability of PGF2? analogues in an aqueous composition.