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

Abstract: The application discloses a flexible strap for retaining protective eyewear on a wearer's head. The strap includes an energy absorbing material which is configured to deform to absorb kinetic energy on impact and which is held in contact with a first outer layer. A method of manufacture of the strap is also disclosed.

Abstract: In various embodiments, a device for inserting an implant on a human or animal body may be provided. The device may include an operable portion configured to make an incision on the human or animal body and configured to hold the implant for insertion on the human or animal body. The device may further include an actuator mechanism coupled to the operable portion, the actuator mechanism configured to move the operable portion along a first axis and configured to vibrate the operable portion along a second axis substantially perpendicular to the first axis.

Abstract: Apparatus and associated methods for a hydrogel wound covering membrane may include a backing layer and a release liner each having high pliability for permitting the membrane to be folded without pinching a sandwiched hydrogel layer thereby preventing its thinning in folded regions. In an illustrative embodiment, the hydrogel layer may annularly circumscribe a central wound region of the membrane. The thickness of the annulus may be selected to prevent water from penetrating the annulus for water exposures of a predetermined length of time. In some embodiments, a gauze may be affixed to a central portion of the membrane for gentle contact with a wound when the membrane is affixed to a wounded person. The membrane may advantageously maintain a substantially uniform hydrogel thickness when folded or rolled, so as to permit secure annular adhesion circumscribing a wound when unfolded or unrolled and applied.

Abstract: A thin absorbent composite is provided wherein a nonwoven support sheet is hydro-entangled with a carded fiber web to provide a nonwoven substrate. The nonwoven substrate is coated with an absorbent layer comprising microfibrillated cellulose-coated superabsorbent polymer particles. A cover layer is placed above the absorbent layer to provide the absorbent composite. A process for manufacturing the absorbent composite and an absorbent article containing the absorbent composite are also provided.

Abstract: A method for producing a multi-layered absorbent articles is disclosed. At least two of the layers include a colored region.

Abstract: A substrate assembly is mechanically deformed to form various products. In part, the substrate assembly may advance toward a bonder apparatus. The bonder apparatus rotates about a longitudinal axis and includes a plurality of manifolds. The plurality of manifolds allow for substrate assemblies including different process product pitches to be processed on a single bonder apparatus.

Abstract: The present invention provides a method and apparatus for increasing the number of articles processed over a distance traveled in the machine direction of an assembly line. In particular, the orientation of the long dimension of the article is provided transverse to the machine direction, thus process rug the articles side-by-side instead of end-to-end.

Abstract: An absorbent article may be constructed by printing on a web that forms a portion of the side panels using a first printing method; and by printing on a backsheet using a second printing method. Seams may be formed by attaching the side panels to a chassis and by attaching the side panels to each other to form a waist opening and leg openings.

Abstract: A wearable absorbent article includes a conductor arrangement. Including a plurality of elongate conductors, each conductor extending along an extension direction. At least some of the conductors have different lengths from each other in the respective extension directions. Those of the at least some of the conductors which have larger lengths in the respective extension directions have lower electrical resistances per unit length than those of the at least some of the conductors which have smaller lengths in the respective extension directions.

Abstract: An absorbent article (1) includes a permeable front-side sheet (3), a back-side sheet (2), an absorber (4) disposed between the permeable front-side sheet and the back-side sheet, and an embossment (10) formed in the front surface of the permeable front-side sheet (3). The embossment (10) includes bent parts (30) at which an embossment direction abruptly changes. An outer edge of each of the bent parts (30) is an angled part (31), and an inner edge of each of the bent parts (30) is a curved part (32).

Abstract: A male incontinence device is configured to contain urine and/or blood involuntarily expelled from the penis of a wearer. In some implementations, the male incontinence device may be easily donned and removed for disposal. In this way, both ambulatory and non-ambulatory wearers may be fitted with the male incontinence device.

Abstract: The male incontinence wrap system is a disposable absorbent pad designed to be wrapped around the male genital member of a person suffering from incontinence. The pad is wrapped around the male genital and secured by a first adhesive strip and then folded back at the end and held in place by a second adhesive strip, an elastic band, or both. An adhesive peel-and-stick strip attaches the absorbent pad assembly around the user to prevent sliding. At least one fold crease can be included extending between first and second edges and aids in the folding and forming of a pouch-shaped interior volume.

Abstract: The present invention relates generally to a sanitary pad with a crevice mound and a method of using same. More particularly, the invention encompasses a sanitary pad having at least one crevice mound or male portion or raised padded projection, and where the at least one crevice mound physically and partially penetrates an area near and around a human orifice, such as, anal crevice area, vaginal crevice area, to intercept, collect, and retain any bodily fluid that maybe being discharged from the human orifice around the vaginal and/or anal area. The invention also provides a method of using the inventive sanitary pad with at least one crevice mound, where the crevice mound is placed near or adjacent a human orifice, such as, anus, vagina, to at least capture at least a portion of a human bodily fluid coming out of the human orifice around the anal and/or vaginal area.

Abstract: The present invention generally relates to absorbent articles and in particular to a absorbent articles demonstrating controlled deformation and enhanced fluid wicking in the longitudinal direction of the absorbent articles.

Abstract: A carded staple fiber nonwoven having a basis weight of between about 45 grams per square meter (gsm) and about 150 gsm, includes a blend of absorbing fibers, stiffening fibers and filler fibers. The carded staple fiber nonwoven is non-heat stiffened, has an air permeability of between about 100 m3/m2/min and about 500 m3/m2/min, and a pore radius mode of between about 60 ?m and about 120 ?m.

Abstract: An absorbent core assembly for use in a product for absorbing a liquid is disclosed. The core assembly has a first section and a second section. The first section is a quilted porous material that contains a slow acting but high absorption capacity SAP therein. The, second section is a quilted porous material that contains a fast acting but lower absorption capacity SAP therein. The first and second sections are in fluid communication with each other, whereupon a liquid which is exposed to the core assembly flows through the first section to the fast acting SAP in the second section to be absorbed quickly and rapidly by the fast acting SAP therein, while the slow acting SAP desorbs or takes liquid away from the fast acting SAP as well as absorbing the liquid itself to thereby trap the liquid in the core assembly.

Abstract: A disposable undergarment including an absorbent core assembly and methods of making the same is disclosed. The undergarment includes a chassis holding the core assembly. The chassis includes a front section, a crotch section and a rear section. The core assembly is located in the crotch section, with portions of it extending into the front and rear sections. A large plurality of closely spaced elastic threads extends across the full width of the undergarment in the front and rear sections. The elastic threads are broken in the areas of the core assembly. The core assembly includes a first section of a slow acting but high absorbency SAP in pockets thereof and an underlying second section of a fast acting but lower absorbency SAP in pockets thereof.

Abstract: A gurney cover that can be quickly deployed from an integrated pocket to protect a mattress or patient area of a gurney with the undployed gurney cover contained within the integral pocket.

Abstract: An equipment mounting system includes a quick mount track (11) with tapered edges (3611, 3612) couple to a surface or structure. The quick mount track includes a backing plate (15), one or more mounting points positioned such that any forces exerted on a mount (50) coupled to the quick mount track is transferred directly through the quick mount track to the one or more mounting points. The quick mount track also includes a flush mounting surface (3610) that creates and maintains a seal between the quick mount track and the surface, and a chase (3605) is disposed in the quick mount track and defined by the flush mounting surface. A plurality of diamond contoured target regions (13) and a plurality of half diamond contour regions in the backing plate aid in coupling the mount to the quick mount track.

Abstract: A convertible transport system including a seat portion, a back support portion, and a pivoting mechanism coupled to the seat portion and to the back support portion. The pivoting mechanism is configured to adjust and lock the back support portion relative to the seat portion, the pivoting mechanism having three operative states: a free pivoting state allowing the back support portion to pivot relative to the seat portion about an axis; a ratcheting state allowing the back support portion to only pivot toward the seat portion about the axis; and a locking state in which the pivoting mechanism is locked to thereby prevent a pivoting movement of the back support portion relative to the seat portion.

Abstract: A retrofitable drive assembly attaches and detaches quickly, easily, and reversibly from a conventional, manually powered wheelchair and is employed to convert the manually powered wheelchair into an electrically powered wheelchair. The drive assembly includes a plurality of wheel troughs, each adjustably sizeable to receive therein a rear push wheel of the manually powered wheelchair, regardless of the wheelchair's size and its rear push wheels' dimensions. In addition, the drive assembly includes two drive wheels positioned towards a front end of the drive assembly and a single caster-wheel assembly positioned towards a rear end of the drive assembly.

Abstract: Mobility device for physically disabled people 1, comprising a chassis 10 with at least one motor for maneuvering the online mobility device 1; a pivot arm 20, which at its lower end 22 is pivotably connected to the chassis 10; and a pelvis support 40, which is connected to an upper end 23 of the pivot arm 30; wherein a physically disabled person 2 can sit with the pelvis support 40 attached to its body, can move around with the mobility device 1 in a standing position on the chassis 10, and can change on its own from sitting to standing position, wherein all elements of the mobility device 1 except the elements directly contacting the body of the person 2 extending above pelvis height h of the sitting person 2 can be lowered or moved to or below this height h. The present invention further comprises a method for connecting of a sitting physically disabled person 2 and for fixing of the person 2 for standing position once is motor-driven mobility device 1.

Abstract: The invention relates to an on-site medical gas production plant (100) comprising a unit (50) for purifying gas, such as air, a first compartment (A) for storing purified gas, and a main gas line (10) fluidically connecting the gas purification unit (50) to the said first storage compartment (A). It furthermore comprises an actuated valve (304) arranged on the main gas line (10) upstream of the first storage compartment (A), and furthermore connected to the secondary purifying device (306), as well as an operating device (4) which controls at least the actuated valve (304), and at least a gas analysis device (D2) in fluid communication with the main line (10), and which is in communication with said operating device (4).

Abstract: Providing a surgical support instrument for the alignment of the lower extremities comprising modular elements which provides an excellent and not invasive tool that may allow to obtain a 90 degree angle on the foot's sole vs. full leg (upper thigh, knee, leg, ankle and foot) and vice versa, as well as 90 degrees on the foot's sole vs. lower leg (lower leg, ankle and foot) and vice versa. The term patient's lower extremities alignment mainly refers to, but not exclusively, Ankle, Foot and Knee, and such alignment may help the surgeon to achieve a higher success rate on the surgery procedure.

Abstract: In one aspect, an orthosis for increasing range of motion of a body joint generally includes first and second dynamic force mechanisms for simultaneously applying a dynamic force to body portions on opposite sides of a body joint.

Abstract: A device for treating or preventing lower back pain that is simpler and less costly than previous similar devices. Among the features of the device are a leg rest height adjustment arrangement that is simple to operate and provides substantially continuous height adjustment, a leg rest folding mechanism that pivotally couples the leg rest to a leg rest support shaft to place the leg rest in operative and storage positions, and a flexible cover that does not substantially change its length during height adjustment.

Abstract: A collapsible wheeled walker with two side frames and two height adjustable upper body supports. The apparatus includes a seat that is slidably attached to the two side frames and is movable between a front position to facilitate an ample walking space inside the frames and a rear position for a user to sit. The apparatus may include an X-folder that facilitates collapsing the walker to a small footprint for storage and transportation. It may also include a left forearm gutter and a right forearm gutter as part of the upper body supports that give the user an upright walking posture for health benefits.

Abstract: A rolling walker comprises a frame, a seat supported by that frame, and a backrest supported by the frame. By one approach the backrest is configured to selectively move between a first position that provides back support for a person sitting in the seat facing in a forward direction and a second position that provides back support for a person sitting in the seat facing in a rearward direction. If desired, this backrest can be comprised of a material (such as a memory foam material) that biases the backrest towards that first position when the backrest is in the first position and that biases the backrest towards the second position when the backrest is in the second position.

Abstract: A lip suction device. A rigid hollow form has an opening at a first end of the rigid hollow form and a cavity therein extending from the first end to a second end of the rigid hollow form. The rigid hollow form has an outer surface and a thickness at the opening between the outer surface and a surface of the cavity. The opening has an edge with a rounded shape, across the thickness at the opening, which is configured to form a substantially air-tight seal between a user's face and the edge when the rigid hollow form is pressed against the user's face near the user's lips. The rigid hollow form is configured so that when the user draws air into the user's mouth after forming a substantially air-tight seal, the user's lips are drawn into the rigid hollow form towards the second end of the rigid hollow form.

Abstract: We disclose methods and medical device systems for selectively recruiting a nerve fiber type within a cranial nerve, a peripheral nerve or a spinal root. Such a method may comprise applying a first pressure, a heating, and/or a cooling to a second location of the nerve, the pressure, heating, or cooling sufficient to substantially block at least one of activation or conduction in at least one fiber population through the second location of the nerve for a blocking time period; and applying an electrical signal to a first location during the blocking time period.

Abstract: A roller which an individual may use to perform a variety of self-applied exercises for massage, myofascial release and other exercises. The roller is cylindrical having a resilient outer surface on which are a plurality of axially spaced, circumferentially extending bands of similar projections which manipulate the body of the individual when the individual rolls against the surface of the roller. The projections are equally circumferentially spaced in each band extending around the cylindrical body. The material and shape of the projections are selected to provide greater resistance to bending or flexing to forces applied axially than to tangentially applied forces.

Abstract: A massage ball having a plurality of adjacent foam layers including at least one first density foam layer, at least one second density foam layer and at least one third density foam layer, and a glue layer between each adjacent foam layer thereby adhering together the plurality of foam layers. A density of the first density foam layer is different from a density of the second density foam layer which is different from a density of the third density foam layer. The massage ball may also include a solid core in the center thereof.

Abstract: An ergonomic and two-hands operated device for exercising a male genital organ is disclosed. The device comprises a fixed member and a movable member. The device further includes a first mounting bracket and a second mounting bracket arranged to provide structural support for maintaining a spaced parallel relationship between the fixed member and the movable member. The device further includes a pair of handles to control the open and closing of the device. The device further includes squeezing means arranged to symmetrically compress and adapt to fit the shape of the male genital organ in a centered position. The squeezing means is adapted to provide a sealed grip around the male genital organ free of pinch points.

Abstract: A device for treating sleep apnea by discriminating between successive sleep stages of a patient includes a generator configured to produce stimulation pulses, a stimulator that receives the stimulation pulses produced by the generator and delivers stimulation to the patient, a sensor configured to measure a biological parameter of the patient, and a controller. The controller is configured to determine a state of the patient based on the biological parameter, perform a sleep analysis based on the state of the patient, activate the generator to trigger production of the stimulation pulses, determine a variation of the biological parameter subsequent to the production of the stimulation pulses, determine a response of the patient to the stimulation pulses according to the variation of the biological parameter, and determine a sleep stage of the patient based on the response.

Abstract: The invention relates to a method for controlling the intensity of the massaging motion of a massage device including at least one preferably elongated massage section with at least one wall that forms the outer surface of the massage section and having at least one electric drive device. The drive device has an electric motor unit, at least some sections of which are operatively connected either directly or indirectly to the wall in order to generate a massaging motion. A control assembly, which is connected to the electric motor unit, is provided to control the intensity of the massaging motion. The current electric power draw of the at least one electric motor unit is advantageously determined periodically or continuously, the electric power draw that has been determined is compared to at least one predefined reference power value and the intensity of the massaging motion is controlled depending on the result of said comparison.

Abstract: An example skincare device includes a main body having a first side, a second side, an intermediate portion, a groove, a light source, a motor, a temperature control unit, and a user control configured to control one or more of the light source, motor, and temperature control unit. The skincare device can provide heat, cool, light, and/or vibrational therapy to a user's skin.

Abstract: A method of treating a mental disorder of a patient includes 1) generating, by an electroacupuncture device implanted beneath a skin surface of the patient at or near an acupoint corresponding to at least one of a trigeminal nerve and an occipital nerve of the patient, stimulation sessions at a duty cycle that is less than 0.05, and 2) applying, by the electroacupuncture device, the stimulation sessions to at least one of the trigeminal nerve and the occipital nerve by way a central electrode and an annular electrode located on the electroacupuncture device in accordance with the duty cycle.

Abstract: An adjustable acupoint and organ pressing device includes a rod, a first pressing member mounted on one end thereof, and an adjustment unit mounted on the other end thereof and provided with a second pressing member facing the first pressing member. The adjustment unit includes a frame and an adjustment handle hingedly connected to the frame with a spring in between. The adjustment unit also includes a fine-adjustment handle hingedly connected to the frame with a fine-adjustment plate and a fine-adjustment spring in between for fine adjustment.

Abstract: The glass containers described herein have at least two performance attributes selected from resistance to delamination, improved strength, and increased damage resistance. In one embodiment, a glass container may include a body having an inner surface, an outer surface and a wall thickness extending between the outer surface and the inner surface. At least the inner surface of the body may have a delamination factor less than or equal to 10. A tenacious inorganic coating may be positioned around at least a portion of the outer surface of the body. The outer surface of the body with the tenacious inorganic coating may have a coefficient of friction less than or equal to 0.7.

Abstract: In embodiments, a delamination resistant glass pharmaceutical package includes a glass body formed from a Type 1 Class glass composition according to ASTM Standard E438-92, the glass body having a wall portion with an inner surface and an outer surface. The glass body may have at least a class A2 base resistance or better according to ISO 695, at least a type HGB2 hydrolytic resistance or better according to ISO 719 and Type 1 chemical durability according to USP <660>. An interior region of the glass body may extend from about 10 nm below the inner surface and have a persistent layer homogeneity. The glass body may also have a surface region extending over the inner surface and having a persistent surface homogeneity such that the glass body is resistant to delamination.

Abstract: A container for collecting, transporting, storing, delivering and dispensing fluid. The container has a hollow tube with an outer circumference diameter and is configured to receive a plunger. A collection adaptor and a dispensing adaptor provide interchangeable coupling of a variable volume container such as a syringe with a collection device such as a breast pump and a dispensing device such as a nipple. The container also has a circumferential seal assembly secured at one end of the hollow tube. The seal assembly outer diameter is substantially similar to the hollow tube outer diameter.

Abstract: The presently disclosed subject matter is directed to a device for dispensing a mixture of a first composition (e.g., an anesthetic) and a second composition (e.g., a diluent buffer, a second drug, or a solution). The device comprises a plunger that slidably engages with the interior of the device barrel at a first end. The second end of the device barrel includes a flexible container configured to house one or more solutions (e.g., sodium carbonate). The flexible container comprises a membrane positioned adjacent to the interior of the barrel. The flexible container can be manipulated by the user, rupturing the membrane. In this way, the first and second solutions are intermixed within the interior of the barrel, and can be administered to a patient.

Abstract: An improved oral administration coupler for delivery of fluids such as medications and nutritional fluids. Example oral administration couplers have a first end with an applicator for oral delivery to an infant, and a second end with a coupling compatible with an enteral fluid delivery syringe. A fluid delivery conduit extends in fluid communication from the first end to the second end, to deliver fluid from the syringe to the infant. In some example embodiments, the coupler is configured for back-of-mouth delivery, and can comprise a generally elongate and at least partially flexible tube or straw.

Abstract: The invention relates to an arrangement for packing drug portions into dispensing packages. A dispensing machine includes a plurality of storing and metering stations having a plurality of drug portions, a packing device that receives the drug portions dispensed by the storing and metering stations and places them into dispensing packages, and a control device. Each storing and metering station includes a stationary part fixed to a frame, a removable part containing a refillable reservoir and has an information memory for storing an identifier of the removable part. A reading device for reading the information memory is functionally assigned to the stationary part. Each information memory contains a memory location for a filling code.

Abstract: A storage and dispensing container comprises a housing including a bottom end and a peripheral wall upstanding on the bottom end and having an opening, the bottom end and the peripheral wall defining, in a combination with each other, a generally open top end and a hollow interior of the housing; one or more compartments defined within the hollow interior and having a bottom wall thereof spaced apart from an interior surface of the bottom end; a tray member movable between a retracted position and an extended position; and a writing implement holder being sized and shaped to receive a writing implement therewithin.

Abstract: An occlusion clearing device for a patient has a housing with a motor(s) that generates repetitive motion, which is reciprocating, rotational or both. A clearing stem including a sheath that has a lumen, wherein aspiration is conducted through the sheath lumen. A wire is located in the sheath lumen and receives repetitive motion from the controller. The sheath terminates in a sheath end having at least one sheath opening. The wire terminates in a wire tip, which may be flat, helical, or tubular. The wire tip is positioned within the sheath end, in proximity to the sheath opening(s), and movement of the wire tip and/or sheath end relative to each other creates shearing forces that break up an adjacent occlusion.

Abstract: A feeding tube position confirmation device 102, operable to confirm the position of a predetermined portion of a medical feeding tube in a predetermined portion of a human or animal body, the position confirmation device comprising an optical waveguide 106 dimensioned to be insertable into the lumen of the feeding tube, the optical waveguide having a sensing distal end 108 comprising a distal end material and a sensing material mixed with the distal end material, the sensing material operable to provide a change in optical properties at the distal end 110 of the optical waveguide dependent on the environment to which the sensing distal end 108 of the waveguide is exposed. The sensing material may comprise a reflective material. Methods of manufacture and use of such devices are also described.

Abstract: There is provided an oral biofilm inhibitor having an exceptional inhibitory effect on oral biofilm formation. It is an oral biofilm inhibitor comprising a curable composition containing an antimicrobial agent, wherein a compressive strength of a cured product formed by curing the composition is 150 MPa or less, and a content of the antimicrobial agent is 0.001 to 3% by weight. An oral biofilm inhibitor thus obtained is used for inhibiting biofilm formation in an oral cavity by applying a curable composition containing an antimicrobial agent to a dental defect site for allowing the composition to cure at the dental defect site, and then disintegrating the cured composition.

Abstract: The invention relates to a polymerizable dental material containing a catalyst paste (A) and a base paste (B), wherein the catalyst paste (A) contains at least one organic peroxygen compound, at least one radically polymerizable organic (meth)acrylic monomer and at least one filler, and wherein the base paste (B) contains at least one radically polymerizable organic (meth)acrylic monomer, an amine as co-initiator of the radical polymerization, at least one filler and at least one salt-like, water-soluble, powdery reduction agent dispersed therein, wherein the catalyst paste (A) and/or the base paste (B) contains at least one phase transfer catalyst that is selected from the group consisting of the ammonium, phosphonium and/or sulfonium salts that contain an inorganic or organic anion, provided that the phase transfer catalyst—in the event of organic anions—contains only those having 1-4 carbon atoms, and that anions of sulfinic acids are precluded.