Abstract: An inserter for treating glaucoma can comprise a housing, a needle, a plunger, a slider component, and a drive component. The drive component is disposed within a cavity of the housing and rotatable within the cavity to result in movement along a longitudinal axis of the inserter to the needle and the plunger upon rotation of the drive component. The slider component is coupled to the housing and slidable along an elongate groove of the drive component such that movement of the slider component along the axis rotates the drive component within the housing.

Abstract: An inserter for treating glaucoma can comprise a housing, a needle, a plunger, a slider component, and a drive component. The drive component is disposed within a cavity of the housing and rotatable within the cavity to result in movement along a longitudinal axis of the inserter to the needle and the plunger upon rotation of the drive component. The slider component is coupled to the housing and slidable along an elongate groove of the drive component such that movement of the slider component along the axis rotates the drive component within the housing.

Abstract: Devices and methods of implanting an intraocular shunt into an eye can be used to deliver the shunt to a location within the sclera. Some methods involve creating an opening in the sclera, and positioning a shunt in the anterior chamber of the eye such that the shunt terminates via the opening in the intrascleral space, thereby facilitating fluid flow through both the opening and the intrascleral space.

Abstract: An intraocular shunt can be manufactured using a system that includes a liquid bath and a wire, which is moved through the bath. The wire can be moved through a first liquid bath to produce a first tubular layer of drug-infused gelatin. Further, the wire can be moved through a second liquid bath to produce a second tubular layer of drug-free gelatin. The first and second tubular layers can be dried on the wire in a humidity-controlled space, thereby manufacturing a drug-loaded gelatin shunt.

Abstract: A surgical laser system can include a laser source configured to generate a laser beam. The system can also include a scanning delivery system that can be configured to direct the laser beam to an ocular target region and scan the laser beam along a scan pattern in the ocular target region of an eye. The system can further include a system controller in communication with the scanning delivery system. The system controller can be configured to control the scanning delivery system to scan the laser beam along the scan pattern to create a pattern of cuts for relaxing ophthalmic tissue in the ocular target region. Each cut of the pattern of cuts can extend only partially through the ophthalmic tissue.

Abstract: An ophthalmic endoprobe system comprises an optical fiber configured to transmit light energy along an optical axis. The system further comprises a first scanning element rotatable relative to the optical fiber and arranged to receive at least a portion of the transmitted light energy. The first scanning element includes a diffractive optical element. The system also comprises a second scanning element rotatable relative to the first scanning element and arranged to receive at least a portion of the transmitted light energy from the first scanning element.

Abstract: An imaging-based laser system can include a laser-beam system, configured to generate and scan a beam of laser pulses with an adjustable laser-power parameter to points of a scan-pattern in an eye, and an imaging-based laser-controller, configured to image a layer in the eye, to control the scanning of the beam of laser pulses to the points of the scan-pattern, and to control a laser-power parameter of the laser pulses according to the distance of the points of the scan-pattern from the imaged layer.

Abstract: An apparatus for controlled perforation and aspiration of the inner ear.

Abstract: The present invention is directed to a resorbable hemostatic nonwoven felt suitable for use in laparoscopic procedures and to methods for manufacturing said felt.

Abstract: An article comprising a macroporous wound-packing material and a microcorrugated microporous wound-contact layer is provided. The wound packing material is coupled to and/or substantially surrounded by the wound-contact layer. The average pore diameter of the microporous layer is less than or equal to about 90 m. A method of treating a wound using a microcorrugated microporous wound-contact layer and a macroporous wound packing material is also provided.

Abstract: A reduced pressure tissue treatment system includes an applicator having an aperture, a first pad section, and a second pad section substantially covering the aperture and positioned substantially adjacent the first pad section. A fabric layer is located at least partially between the second pad section and the drape, and the fabric layer includes a woven or non-woven fabric made from a fiber material. A drape substantially covers the first pad section, the second pad section, the fabric layer, and the applicator. A reduced pressure source is in fluid communication with at least one of the first pad section and the fabric layer for providing reduced pressure to the aperture.

Abstract: An orthosis chosen from a venous support orthosis and an elastic venous compression orthosis, the orthosis including a ribbed top and a leg part, the ribbed top including an intermediate part extending the leg part, the stitch being different on each side of the boundary separating the leg part and the intermediate part, a welt extending the intermediate part and of a height less than 1.5 cm.

Abstract: The present disclosure relates to absorbent articles and methods for assembling absorbent articles with components having printed graphics with masked zones having alternatingly arranged printed regions and unprinted regions. Various substrates and/or components to be incorporated into manufactured absorbent articles include graphics with the masked zones positioned and/or printed in such a manner so as to functionally reduce noticeable visible results of imprecise and/or inconsistent manufacturing operations performed in areas where the graphics are located. In some configurations, substrates and/or components include graphics with masked zones positioned in regions that are subject to bonding, cutting, and/or folding transformations during the assembly process, such as for example, along inner edges of front and/or back belts and/or leg openings.

Abstract: The present invention relates to a method and apparatus for forming a composite structure, preferably for use in an absorbent structure used within the personal hygiene industry, such as for instance feminine hygiene garments, baby diapers and pants and adult incontinence garments. The present invention preferably provides a method and apparatus for depositing and positioning particulate materials in a desired pattern onto a moving carrier layer. The method allows accurate forming of a pattern of particulate material clusters at high production speed having improved attachment properties, with reduced raw material usage and relative low cost. The present invention foresees in the need for improved thin, flexible, lightweight absorbent structure having optimal absorption, distribution and retention.

Abstract: A process of forming a shaped, dimensionally stable tampon includes the steps of: radially compressing a tampon blank to form a dimensionally stable intermediate pledget having an intermediate pledget diameter and a longitudinal axis; placing the intermediate pledget into a hollow carrier and inserting the intermediate pledget and hollow carrier into a mold; urging the intermediate pledget into the mold via a ram bearing on an end of the intermediate pledget contained within the hollow carrier and withdrawing the hollow carrier from the mold to permit the exposed end of the intermediate pledget to substantially fill the mold and to form the shaped, dimensionally stable tampon; removing the shaped, dimensionally stable tampon from the mold; and enclosing the shaped, dimensionally stable tampon in a primary package that conforms to the shape thereof. The mold has an access opening through which the hollow carrier can be withdrawn.

Abstract: Provided is a tampon applicator having one or more insertion indicators to gauge and/or control the insertion depth of a tampon. The one or more insertion indicators may be located on the tampon applicator barrel, plunger, tampon, removal string, or any combinations thereof. As a result of the one or more insertion indicators, a woman can adjust the insertion depth of the tampon to her body's requirements ensuring leakage protection, comfort, or both.

Abstract: Sensor arrangement and method for monitoring a person with a sensor arrangement, which includes measuring electronics and a sensor structure that can be fitted onto a base. The sensor structure includes at least one sensor, and the arrangement determines, by the data measured by the measuring electronics and the sensor, a change in the moisture of the base and the presence of a person on the base.

Abstract: The present disclosure relates to absorbent articles and methods for assembling absorbent articles with components having printed graphics with masked zones having alternatingly arranged printed regions and unprinted regions. Various substrates and/or components to be incorporated into manufactured absorbent articles include graphics with the masked zones positioned and/or printed in such a manner so as to functionally reduce noticeable visible results of imprecise and/or inconsistent manufacturing operations performed in areas where the graphics are located. In some configurations, substrates and/or components include graphics with masked zones positioned in regions that are subject to bonding, cutting, and/or folding transformations during the assembly process, such as for example, side seam regions.

Abstract: The present disclosure relates to absorbent articles and methods for assembling absorbent articles with components having printed graphics with masked zones having alternatingly arranged printed regions and unprinted regions. Various substrates and/or components to be incorporated into manufactured absorbent articles include graphics with the masked zones positioned and/or printed in such a manner so as to functionally reduce noticeable visible results of imprecise and/or inconsistent manufacturing operations performed in areas where the graphics are located. In some configurations, substrates and/or components include graphics with masked zones positioned in regions that are subject to bonding, cutting, and/or folding transformations during the assembly process, such as for example, along outer edges of front and/or back waist regions.

Abstract: Absorbent articles herein may include components having graphics including unmasked and masked zones, wherein the masked zones are defined by alternating arranged printed and unprinted regions. The masked zones give the appearance that the graphics fade or gradually transition from areas of relatively high print intensities in the unmasked zones to areas of relatively low print intensities. In addition, the graphics may be printed with relatively constant print densities in both masked and unmasked zones, and thus, avoid many of the unintended negative effects and difficulties associated with printing graphics with faded zones of print intensities. As such, substrates and/or components to be incorporated into manufactured absorbent articles include graphics include masked zones that may be positioned and/or printed in such a manner so as to functionally reduce noticeable visible results of imprecise and/or inconsistent assembly operations performed in areas where the graphics are located.

Abstract: An article including a front region, a back region, and a chassis. The chassis may include an absorbent core having a front end edge and a back end edge. The front region and the back region may extend laterally outward beyond side edges of the chassis. The front region and the back region may abut to form a first seam and a second seam. At least one of the front region and the back region may include an elastic member. A first outer nonwoven layer of the front region and a second outer nonwoven layer of the back region may be folded to form an upper edge in the front and back regions such that a distal end of each of the first and second outer nonwoven layer may be disposed between the upper edge and the front and back end edges of the absorbent core, respectively.

Abstract: An absorbent article in which an absorbent body is provided between a liquid permeable topsheet and a backsheet, includes an absorbent body emboss provided from a front surface side of the absorbent body before stacking the liquid permeable topsheet to surround an area corresponding to a body fluid expelling portion; and a front surface emboss, formed separately from the absorbent body emboss and not to overlap the absorbent body emboss, provided from a front surface side of the liquid permeable topsheet.

Abstract: A power ambulance cot having a cot control system operably connected to a cot actuation system to control independent raising and lowering of front and back legs thereof, and which detects a presence of a signal requesting a change in elevation of a support frame thereof and causes the cot actuation system to raising or the lowering of the front and/or back legs automatically upon detecting a condition during loading/unloading a patient from an emergency vehicle or transporting the patient up or down an esculator and methods thereafter are disclosed.

Abstract: A reconfigurable portable load bearing structure which can be configured into an extended load bearing configuration or a collapsed configuration, comprising of a first, second and third plurality of rail segments that are each rotatably coupled together and a plurality of support segments or pads which are configured to selectively couple and latch into one of a plurality of positions on said first, second and third plurality of rail segments.

Abstract: A patient transport apparatus transports a patient over a surface. The patient transport apparatus comprises a base and support wheels coupled to the base. An auxiliary wheel assembly is coupled to the base to influence motion of the patient transport apparatus over the surface to assist caregivers. The auxiliary wheel assembly comprises auxiliary wheels and an actuator operably coupled to the auxiliary wheels. A controller adjusts the actuator based on input from a sensing system so that frictional forces acting between the auxiliary wheels and the surface are sufficient for steering and maneuvering of the patient transport apparatus, without sacrificing stability of the patient transport apparatus.

Abstract: Embodiments according to the present invention include a load transitioning mechanism which enables attachment and release of at least one ground-contacting adaptive implement, such as a multi-terrain caster wheel assembly, a motorized wheel, or a ski; embodiments further enable reversible reconfiguration of the wheelchair by a user between a.) an original load-bearing configuration utilizing the conventional forward caster wheels of the wheelchair, and b.) a modified load-bearing configuration utilizing the ground-contacting adaptive implement.

Abstract: The travelling apparatus according to exemplary embodiments includes front wheels, which are driving wheels, an upper frame, first linear motion mechanisms configured to be extendable and retractable and couple the front wheels to the upper frame, middle wheels configured to be disposed at a back of the front wheels, second linear motion mechanisms configured to be extendable and retractable and couple a riding part to the middle wheels, rear wheels configured to be disposed at a back of the middle wheels, lower links configured to couple the middle wheels to the rear wheels, respectively, rear links configured to couple the lower links to the upper frame, and a third linear motion mechanism configured to change an angle between the upper frame and the rear links.

Abstract: A suspension for a vehicle is provided. The suspension includes, for example, a frame, at least one drive assembly and at least one caster pivot arm. The at least one drive assembly and the at least one caster pivot arm are pivotally connected to the frame at a common pivot axis such that the drive assembly and the front caster pivot arm are pivotable relative to one another.

Abstract: A transport chair is provided that includes a base frame, a seat assembly pivotally mounted to the base, and a footrest assembly pivotally mounted to the base frame, the footrest assembly being associated with the seat assembly so as to pivot in unison with the seat assembly until the seat assembly is pivoted forward to an extent at which the footrest assembly contacts the floor or ground, at which point the footrest assembly does not pivot further upon further forward pivoting of the seat assembly. Further embodiments of the transport chair allow the seat assembly to recline, alone or in unison with a leg rest assembly, while the footrest remains in position.

Abstract: A shower stretcher assembly (10) includes a frame (22) which supports a platform (20) consisting of three mattress support panels (50-54), and a headboard (16) and foot board (18). The support panels (50-54) define a back rest section (30), a seat section (31) and a foot section (32). The seat section (31) is of flexible material to more closely conform to the shape of a person lying thereon. The stretcher assembly (10) is provided with side barriers (68) at each head and foot end, the side barriers (68)arranged to move between a raised vertical position, a raised position extending outwards from the frame, and a lowered position in which they lie alongside the frame so as to be below the level of the mattress of the stretcher. The side barriers present substantially vertical walls to accommodate a water-resistant mattress with side walls (28).

Abstract: A patient support system comprises a patient support apparatus for patients. The patient support apparatus also comprises an actuatable device that perform one or more predetermined functions on the patient support apparatus. A controller is provided to control the rate of operation of the actuatable devices based on a user input or a patient condition.

Abstract: A patient support system includes a scale system, an air system, and a lift system. The patient support system also includes a control system configured to graphically communicate information about the scale system, the air system, and the lift system to a user.

Abstract: A patient support system comprises a patient support apparatus for patients. The patient support apparatus comprises a base and a patient support surface supported by the base. The patient support apparatus also comprises side rails that move between raised and lowered positions. One or more actuators are coupled to each of the side rails. A controller communicates with the actuators to raise and lower the side rails, either without any manual assistance from the user, or with manual assistance from the user.

Abstract: Inflatable mattress apparatus includes a mattress provided with a plurality of inflatable cells (A, B); a manifold unit (V1-V4) connected to the plurality of cells, wherein the manifold (V1-V4) couples the cells into a plurality of individual sets of cells; and a control unit connected to the manifold, the control unit being operable to provide substantially simultaneous inflation and deflation of cells (A, B) in each set of cells over a period, and time offset inflation and deflation of cells in different sets of cells. The apparatus can provide the same benefits of a 1 of 2? system with reduced movement of the entire surface at any point in the cycle, less air moving at any given time and thus a reduction in the audible noise produced in any pump supplying the air and the associated airflow in the mattress. The arrangement provide other benefits too.

Abstract: A circulating hot water nursing machine includes a main unit and a working head, wherein a water tank support, a clean water tank, a small water pump and a PTC heater are arranged on the main unit; a heating tank is arranged at a lower part of the water tank support, the clean water tank is arranged at an upper part of the water tank support, a shunt valve is arranged on the water tank support, a water inlet of the shunt valve is connected with the heating tank and the clean water tank, and a water outlet of the shunt valve, the small water pump, the PTC heater and the heating tank are connected successively; a control system and a main power supply are arranged on the main unit, and the small water pump, the PTC heater and the shunt valve are connected with the main power supply.

Abstract: A combination massage table with one or more resistance bands (hereinafter, a combination table) is disclosed. In some embodiments, the combination table may comprise: a massage table; the one or more resistance bands; and a means for attaching the one or more resistance bands to the massage table; such that a client using the combination table receives at least one improved health benefit as compared against massage therapy without any resistance band use. Furthermore, methods for using the combination table are disclosed.

Abstract: Body containment constructions, materials, and methods of use for bio-cremation processes are disclosed. Preferably, the containment constructions of the present invention provide the functionality of liquid containment and also the functionality of body presentment for viewing purposes, if desired, in addition to bio-degradability. Advantageously, liquid containment is provided in a body containment construction that is sufficiently liquid impervious, allows for body transport by sufficient structural support, and is decomposable within the time period for a bio-cremation process. More preferably, the containment construction will dissolve or decompose within a normal procedural time period without leaving any component remaining from the containment construction.

Abstract: The present invention is concerned with a massage device for the treatment of skin. The device comprises a body and an applicator for contacting the skin of a user. The applicator is mounted on the body. Further, a drive unit is provided for generating a translational back-and-forth movement of the applicator along a first axis having an amplitude of 0.2 mm to 1.5 mm. Finally, the amplitude can be varied between two different operation modes of the device.

Abstract: A therapeutic compression garment made from body and band portions wherein at least one of the body and spine portions is narrower or wider across its mid-section than at either or both of its top and bottom edges such that the garment assumes a non-planar shape when the body and spine portions are attached together.

Abstract: An apparatus and method for rehabilitating a joint of a user is provided. The apparatus includes a modular frame configured to support the joint in a predefined position. A plurality of pulleys are adjustably coupled to one or more locations on the modular frame. A plurality of cords pass through the plurality of pulleys and couple to opposing ends of a boot. The boot surrounds a portion of the user distal to the joint. The plurality of cords permit a user to actuate the joint through a full range of motion. The user may selectively apply either a resistive force or an assistive force through the one or more cables to affect the joint through its range of motion.

Abstract: The present application relates to a bodycare device (10) for performing a skincare procedure on a periorbital area of a subject. The bodycare device (10) has a treatment head (30) with a treatment surface (37) having a curved profile and a surface roughness Ra between 1 ?m and 4 ?M. A driver is configured to cause a rotational motion and an axial vibratory motion of the treatment head (30). The present application also relates to a treatment head (30) for a bodycare device (10) for performing a skincare procedure on a subject.

Abstract: A detection system for patient therapy devices is provided. A controller is coupled to the detection system. The controller determines a desired operational parameter based on the type of patient therapy device detected.

Abstract: A method of treating knee abnormalities includes securing the portion of the leg above the knee to a stationary object and securing the portion of the leg below the knee to a movable support. A force is applied to the movable support to stretch the knee joint. Apparatus for carrying out the method is also disclosed.

Abstract: Apparatuses, such as massage rollers, for partially enclosing a rotatable spherical object are disclosed herein. A massage roller may include a housing formed from a base and cap that, when coupled together, partially enclose a spherical object. The spherical object, such as a stone, of the massage roller may be rubbed on an individual to provide a massage. As the massage roller is rubbed onto the individual, the spherical object may rotate within the housing.

Abstract: Ejaculation promotion apparatuses. Apparatuses for promoting ejaculation may include a sensory component coupled to a shaft at or near a first end of the shaft, a bar coupled to the shaft at or near a second end of the shaft, a rail coupled to the bar to permit the bar to move along the length of rail, a pin coupled to a wheel and inserted through a slot of the bar, and a motor coupled to the wheel. A housing includes the bar, the rail, the pin, and the wheel. Operation of the motor rotates the wheel, which moves the pin between two ends of the slot. Movement of the pin between the two ends of the slot moves the bar between two ends of the rail. Movement of the bar between the two ends of the rail moves a portion of the shaft in and out of the housing.

Abstract: A system and method for slowing down degeneration of central nervous system caused by Parkinson's disease, which comprises an energy wave generator has an energy wave's frequency control mode. The energy wave's frequency control mode includes multiple controls for acting the energy wave generator to generate and emit energy waves each with a corresponding energy density. The energy density is calculated by a corresponding base frequency, a sweep bandwidth of the corresponding base frequency, an emission rate and a total time of emission in a duty cycle, so that the energy waves with the corresponding energy densities effecting on the body of animals or human to slow down degeneration of central nervous system caused by Parkinson's disease.

Abstract: The present disclosure relates to a device for generating shock waves that comprises an interchangeable applicator head for generating shock waves for treatment of human or animal bodies, which applicator head comprises a reflection or focusing mechanism, two electrode tips for producing a spark gap, and a membrane, which together with the reflection or focusing mechanism encloses a fluid medium that is designed to generate a plasma when a voltage between 1 kV and 30 kV is applied. According to the disclosure, the applicator head is electrically and mechanically connected to a hand-held apparatus in a detachable manner.

Abstract: A device for the determination of at least one compression parameter during administration of cardiopulmonary resuscitation (CPR) on a patient comprising: a field generator, a field detector, and a processor. Position information and the compression parameter are determined from the field detected by the field detector. One of the field generator and the field detector is a position sensor and the other is a reference sensor.

Abstract: A cardio-pulmonary compression device includes a motor (11) having a rotating portion, and a ball nut (12) mounted on the rotating portion and configured to rotate with the rotating portion. A ball screw (13) is received in the ball nut such that rotation on the ball nut advances and/or retracts the ball screw in accordance with a direction of the motor. A pad assembly (15) is coupled to an end portion of the ball screw such that longitudinal motion of the ball screw imparts a compression cycle to a patient.

Abstract: The present invention relates to a package (7) for pharmaceutical blister packs (12) comprising means (11) for removing the protecting foil of the blister packs. The package protects the blister packs (12) and at the same time provides an easy and convenient way of opening the blister pack for people at all level of ability and dexterity.