Abstract: A bone implant composition and methods thereof include bone material made into various implant shapes including a cylinder having an outermost layer and an inner layer completely surrounded by the outermost layer. The bone implant compositions and methods include a bag or cylindrical tube made from a bone material which may be filled with additional bone material.

Abstract: A temporary spacer device for a joint of the human body such as a knee joint includes a first component or femoral component, adapted to be constrained to a bone or to the femoral bone of a patient, at the joint of the human body; a second component or tibial component, adapted to be constrained to a bone or tibial bone of a patient, at the joint of the human body, and at least one stem having a proximal end, wherein the first component or femoral component and/or the second component or tibial component include at least one housing seat for the proximal end of the at least one stem, adapted to allow the inclination and/or rotation of the at least a stem with respect to an insertion axis of the proximal end into the at least one housing seat.

Abstract: A tibial implant may include a plurality of implant subunits. The implant subunits may be configured for individual insertion within a wedge-shaped-void of the tibia. The implant subunits may further be configured for assembly in order to provide an implant substantially covering an exposed portion of cortical bone formed when performing a surgical osteotomy. Methods and kits for insertion and assembly of implants are further described.

Abstract: An orthopedic implant having a titanium or titanium alloy body with a plurality of surfaces. The orthopedic implant is produced according to a process comprising the steps of: (a) additively building the orthopedic implant; and then (b) mechanically, chemically, or mechanically and chemically eroding one or more surfaces of the orthopedic implant to (i) remove alpha case from, and (ii) impart an osteoinducting roughness including micro-scale structures and nano-scale structures into, the one or more surfaces.

Abstract: There is provided an acetabular cup liner for a total hip replacement (THR) prosthesis comprising an inner surface with a hemispherical portion having a radius of curvature. The hemispherical portion is disposed about a centerline and it intersects a hemisphere plane perpendicular to the centerline so that the intersection of the hemispherical portion and the plane define a circle having a radius equal to the radius of curvature. The liner further comprises a capture portion continuous with the hemispherical portion that has the same radius of curvature as the hemispherical portion and connects with the hemispherical portion at the hemispherical plane along a first arc of the circle on the plane, and extends a first distance out of the plane. The liner further comprises an insertion portion continuous with the hemispherical portion. The insertion region is connected with the hemispherical portion along a second arc of the circle on the plane.

Abstract: Disclosed is a distal radio ulnar joint prosthesis system, and the method of use for the same, the system comprising an ulnar stem component, and ulnar head component, a set screw, and a sigmoid notch component, the system providing a prosthesis for replacement of the distal radio ulnar joint to restore the pronation-supination motion of the forearm as well as stability between the ulna and radius; a DRUJ prosthesis adapted for rotational alignment of the replacement joint along the axis of forearm rotation; a DRUJ prosthesis which allows for the use of a number of different sized heads having differing geometries; a DRUJ prosthesis adapted for variable pivoting alignment between the replacement distal ulnar head and the ulna; and a DRUJ prosthesis adapted for adjustment in the alignment between the articulating surface of the ulnar head and the sigmoid notch.

Abstract: Intervertebral devices and systems, and methods of their use, are disclosed having configurations suitable for placement between two adjacent vertebrae, replacing the functionality of the disc therebetween. Intervertebral devices and systems contemplated herein are implantable devices intended for replacement of a vertebral disc, which may have deteriorated due to disease for example. The intervertebral devices and systems are configured to allow for ample placement of therapeutic agents therein, including bone growth enhancement material, which may lead to better fusion between adjacent vertebral bones. The intervertebral devices and systems are configured for use in minimally invasive procedures, if desired.

Abstract: A joint spacer for therapeutically maintains separation of bones of a joint. A frame defines a longitudinal axis extending between distal and proximal ends. A carriage is slideably retained within the frame and has at least one ramped surface and a threaded portion. An actuator screw is threadably engaged with the threaded portion, and bears against said frame to cause the carriage to slideably move within the frame when the actuator screw is rotated. A first endplate engages a bone of the joint, and has at least one ramped surface that is mateable with the ramped surface of the carriage.

Abstract: An intervertebral implant may include a superior exterior surface, an inferior exterior surface, a first exterior lateral surface, and a second exterior lateral surface. The first and second exterior lateral surfaces may be substantially transverse to the superior and inferior exterior surfaces. The implant may further include a first curved end wall at a first longitudinal extremity of the body. The first curved end wall may include a bore configured to receive a first shaft of a tool. Additionally, the implant may include a second curved end wall at a second longitudinal extremity of the body and an elongated slot extending from a portion of the first curved end wall to a portion of the first exterior lateral surface.

Abstract: An intervertebral implant includes an insertion end, an opposing engagement end, and first and second opposed main surfaces configured to contact respective adjacent vertebral endplates. Each of the first and second main surfaces has an anterior edge, a posterior edge, and extends between the insertion and engagement ends. Anterior and posterior walls are formed between the first and second main surfaces and along the respective anterior and posterior edges and converge at the insertion and engagement ends. A slot is formed at the engagement end and extends continuously between and at least partially along the anterior and posterior walls. A post is positioned within the slot, spaced from at least one of the anterior and posterior walls and extending at least partially between the first and second main surfaces. The post includes a plurality of exposed facets and is configured for engagement with a pivotable insertion instrument.

Abstract: An apparatus and a method are provided for performing cartilage allograft implant surgeries. The apparatus comprises an allograft plug kit comprising one or more grafts configured to treat osteochondral defects in various bone joint locations in a patient's body. Each of the grafts comprises a cartilage layer coupled with a bone portion. The cartilage layer comprises a thickness selected to closely match the thickness of existing cartilage at an implant location. The bone portion comprises surface features configured to encourage the patient's bone tissue to grow into the bone portion, thereby accelerating incorporation of the graft into the patient's bone. An instrument kit comprises a multiplicity of instruments configured for implantation of the grafts into the patient's body, including at least a graft inserter, a guidewire, a reamer, and a size gauge.

Abstract: The present invention provides a three-dimensional bioprinter for fabricating cellular constructs such as tissues and organs using electromagnetic radiation (EMR) at or above 405 nm. The bioprinter includes a material deposition device comprising a cartridge for receiving and holding a composition which contains biomaterial that cures after exposure to EMR. The bioprinter also includes an EMR module that emits EMR at a wavelength of about 405 nm or higher. Also provided is a bioprinter cartridge which contains cells and a material curable at a wavelength of about 405 nm or greater. The cells are present in a chamber and are extruded through an orifice to form the cellular construct.

Abstract: A prosthetic leg knee joint includes a thigh connection part that is provided on the thigh side, a lower leg part that is provided rotatably around a knee shaft connected to the thigh connection part, a four-bar link mechanism that sets an instant center S whose relative position with respect to the thigh connection part is substantially constant regardless of the relative position between the thigh connection part and the lower leg part, and a braking unit that brakes the movement of the lower leg part in accordance with the relative position between the instance center S set by the four-bar link mechanism and the lower leg part.

Abstract: A method for controlling a change of resistance in an artificial joint of an orthosis, an exoskeleton or prosthesis of a lower extremity. The artificial joint has an upper part and a lower part which are secured on each other so as to be pivotable about a pivot axis, a damper unit is secured between the upper part and the lower part in order to provide a resistance to flexion or extension of the artificial joint, and the damper unit is assigned an adjusting mechanism via which the resistance is changed when a sensor signal of a control unit assigned to the adjusting mechanism activates the adjusting mechanism. The resistance is changed as a function of the position and/or length of the measured or calculated leg tendon and/or the time derivatives thereof.

Abstract: A tunable actuator joint module of a robotic assembly comprises an output member and an input member, where the output member is rotatable about an axis of rotation. A primary actuator (e.g., a motor) is operable to apply a torque to rotate the output member about the axis of rotation. A quasi-passive elastic actuator (e.g., rotary or linear pneumatic actuator) comprising an elastic component is tunable to a joint stiffness value and is operable to selectively release stored energy to apply an augmented torque to assist rotation of the output member and to minimize power consumption of the primary actuator. The tunable actuator joint module comprises a control system having a valve assembly controllably operable to switch the quasi-passive elastic actuator between an elastic state and an inelastic state during respective portions of movement of the robotic assembly (e.g., a hip or knee joint of an exoskeleton). Associated systems and methods are provided.

Abstract: A tunable actuator joint module of a robotic assembly comprises an output member and an input member, where the output member is rotatable about an axis of rotation. A primary actuator (e.g., a motor) is operable to apply a torque to rotate the output member about the axis of rotation. A quasi-passive elastic actuator (e.g., rotary or linear pneumatic actuator) comprising an elastic component is tunable to a joint stiffness value and is operable to selectively release stored energy to apply an augmented torque to assist rotation of the output member and to minimize power consumption of the primary actuator. The tunable actuator joint module comprises a control system having a valve assembly controllably operable to switch the quasi-passive elastic actuator between an elastic state and an inelastic state during respective portions of movement of the robotic assembly (e.g., a hip or knee joint of an exoskeleton). Associated systems and methods are provided.

Abstract: The invention is an air hammock for a prosthetic with dynamic conformity to better match to the underlying limb shape in real-time through a combination of structural support members with modularly adjustable compliant members thereby creating an air hammock for a prosthetic by suspending the limb within the socket without pressure on the bottom of the residual limb.

Abstract: An endovascularly deployed prosthetic includes a portion for being positioned within an ascending aorta. The prosthesis includes a replacement aortic valve on a proximal end thereof. The prosthesis includes an increased diameter portion that seals against the aorta at a more distal portion, and a pair of conduits extend from the increased diameter portion to the coronaries for fluidly coupling the coronaries to the prosthesis.

Abstract: An endovascularly deployed prosthetic includes a portion for being positioned within an ascending aorta. The prosthesis includes a replacement aortic valve on a proximal end thereof. The prosthesis includes an increased diameter portion that seals against the aorta at a more distal portion, and a pair of conduits extend from the increased diameter portion to the coronaries for fluidly coupling the coronaries to the prosthesis.

Abstract: A hand-held device is used to deliver and hydrate a temporary polymeric implant having a length, an outer surface and a cross-section, with a disruptable cover over the implant. A lumen may pass through the entire length, the lumen having a surface forming an equivalent diameter in the polymeric stent. The temporary polymeric implant includes a first aqueous-swellable, biocompatible and biodegradable composition (e.g., polymer) having a thickness. The aqueous-swellable and biodegradable polymer retaining structural integrity for at least 1 hours up to thirty days when swollen and kept moist by a moist aqueous environment. Barrier layers of biodegradable polymer(s) may be used to prevent migration of liquids into the lumen.

Abstract: A hand orthosis having a cuff for fixing the hand orthosis to a wrist joint or a lower arm of a wearer of the hand orthosis, at least one carrier element, and at least one hand support element that can be fixed to the carrier element. The hand support element includes a contour that is designed to be symmetrical to a longitudinal axis of the hand support element and includes a thumb support area on both sides of the longitudinal axis.

Abstract: A hand orthosis having a cuff for fixing the hand orthosis to a wrist joint or a lower arm of a wearer of the hand orthosis, at least one support brace that extends radially or ulnarly next to a hand of the wearer in the direction of an extension of the lower arm, at least one carrier element arranged on the support brace, and a functional element detachable fixed to the carrier element.

Abstract: A modular device is configured to provide different levels of knee extension to a patient by being moveable between an assembled or “rest” configuration and a detached or “therapy” configuration. The device includes a proximal section with an inclined upper surface and a separate distal section with an inclined upper surface. When attached, the proximal and distal sections form a single continuous incline for supporting a patient's leg. At least one of the sections also includes an ankle supporting cavity that holds the patient's ankle and heel and provides greater stretching/extension of the patient's knee.

Abstract: An artificial stoma device includes a hollow first unit and a second unit that are adapted to be respectively inserted into an upstream section and a downstream section of an intestine via an opening of a skin tissue and via a radial side opening of the intestine. The first unit has inlet and outlet portions. The inlet portion has an inlet opening at a distal end thereof that is adapted for facing the upstream section of the intestine. The outlet portion is connected to the inlet portion, and has an outlet opening that is opposite to and in spatial communication with the inlet opening and that is adapted to be exposed from the skin tissue via the opening. The inlet portion, the outlet portion and the second unit are molded as one piece.

Abstract: Enhanced convenience of use is achieved due to the fact that the gas collector, which includes a device for the anus gas discharge, a tube connected to the said device with its first end, and a gas collection container connected to the second end of the tube, is characterized by the fact that the first end of the tube is connected to the gas relief device detachably to allow the first end of the tube and the anus gas relief device to be disconnected by applying force along the tube. The force aimed at disconnecting the first end of the tube and the gas relief device can be to 5-7 kg. The gas collection container has a gas relief valve. This makes it possible for the user to release gases in a desired, ventilated location.

Abstract: The present invention relates to a mask-shaped skin treatment device and system. The device comprises one or more coupling agent detectors configured to detect presence of coupling agent on one or more skin portions of a user and one or more heating elements configured to cause local heating of one or more skin portions of the user. The one or more heating elements are configured to cause heat selectively based on the presence of coupling agent measured by the one or more coupling agent detectors.

Abstract: A device for altering an optical and/or mechanical property of a lens that is implanted in an eye, the device including a laser device, which has a laser beam source that provides a pulsed laser beam and an optical unit, which impinges on the implanted lens with the pulsed laser beam. The device also includes a control device, which controls the laser device such that the optical and/or mechanical property of the lens is altered on the basis of non-linear interaction between the laser beam and the lens material.

Abstract: A corneal cross-linking system includes a light source configured to emit a photoactivating light. The system includes a spatial light modulator configured to receive the photoactivating light from the light source and provide a pixelated illumination. The spatial light modulator defines a maximum area for the pixelated illumination. The system includes a controller configured to cause the spatial light modulator to project a first pixelated illumination onto the cornea to photoactivate a cross-linking agent applied to a treatment area. The first pixelated illumination has an area that is smaller than the maximum area defined by the spatial light modulator. The controller is configured to determine movement of the cornea. In response to the movement, the controller controls the spatial light modulator to project a second pixelated illumination to the treatment area based on a translation and/or transformation of the first pixelated illumination to continue photoactivating the cross-linking agent.

Abstract: An example multi-fiber, multi-spot laser probe comprises a plurality of fibers extending from a proximal end of the laser probe to at least near a distal end of the laser probe, where the proximal end of the laser probe is configured to be coupled to a laser source via an adapter interface, and a cannula having a distal end and surrounding the plurality of fibers along at least a portion of the laser probe at or near the distal end of the laser probe, where a distal end of each of the plurality of fibers is angle-polished so that the distal end of each fiber is angled relative to a longitudinal axis of the cannula and relative to a plane perpendicular to the longitudinal axis of the cannula. Additional embodiments employ lensed fibers, a distal window, ball lens, lens array, or faceted wedge.

Abstract: A welding hood for protecting an operator's face comprising a face protective shield having a concave rearward side for receiving the operator's face, a viewing opening extending through the shield, wherein the viewing opening is located in a position in front of the eyes of the operator while the hood is fixed to the operator's head. The welding hood includes an eye box located adjacent the viewing opening. The eye box has walls framing the viewing opening and extend inwardly from the rearward side of the shield. The walls are configured for blocking reflective arc flashes and/or light from entering the operator's field of view during welding. The welding hood has sidewalls of varying width and a neck attachment for added protection. The welding hood also includes a lens located within the viewing opening and at least one strap for securing the welding hood to the operator's head.

Abstract: A welding helmet can record a welding time based on an arc intensity detected by a sensor mounted on the helmet. A configured level is compared with the arc intensity detected by the sensor to determine a welding duration. Individual welding times from multiple welding instances can be accumulated over a period of time to provide a total welding time for an operator. The total welding time may be stored in the welding helmet.

Abstract: Systems, apparatus, and methods are described for delivering a therapeutic substance to the tympanic membrane of an ear of a subject, including a reservoir configured to contain the therapeutic substance and a delivery interface by which the therapeutic substance is delivered to the tympanic membrane.

Abstract: The present disclosure discloses a noise-reducing earmuff, comprising: an earmuff shell forming an earmuff cavity; a separator being installed in the earmuff cavity and forming an independent chamber; and a conduit being installed on the separator, the conduit being provided with an opening at each of the two ends thereof; wherein one of the openings being located in the chamber, and the other extending out of the chamber and being located in the earmuff cavity; wherein the chamber and the conduit form a low-frequency resonator whose resonance frequency is equivalent to a corner frequency of a low-pass filter formed by the earmuff.

Abstract: A product for monitoring the condition of a wound comprises: (a) a sample application zone; (b) a reaction zone downstream of the sample application zone comprising protease-sensitive polymers; (c) coloured particles; and (d) a viewing zone downstream of the sample application zone and reaction zone. The sample application zone transmits fluid towards the viewing zone. Cleavage of the polymers by protease activity present in applied wound fluid results in carriage of the coloured particles with the wound fluid to the viewing zone thereby providing a visual indication of protease activity in the viewing zone. A product for monitoring the condition of a wound comprises a matrix that absorbs wound fluid. The matrix comprises cross-linked and protease-sensitive polymers forming a reaction zone on/in the matrix, and, coloured particles.

Abstract: Sealing members and methods of manufacturing the same are described. A first film layer and a second film layer each having a first side and a second side can be provided. A first adhesive can be coupled to the second side of the first film layer to form a first adhesive layer. A second adhesive can be coupled to the second side of the second film layer to form a second adhesive layer, and a third adhesive can be coupled to the first side of the second film layer to form a third adhesive layer. One or more perforations can be formed through the third adhesive layer, the second film layer, and the second adhesive layer. A first side of the third adhesive layer can be coupled to a second side of the first adhesive layer.

Abstract: In order to provide an elastic medical tape having an especially excellent elastic function and a high effect of alleviating persistent skin irritation during application duration caused by an application-duration shrink force, and applicable to skin that hypersensitively reacts to even insignificant irritation, disclosed is a medical tape for alleviating persistent skin irritation during application duration caused by an application-duration shrink force of an elastic base member of an elastic medical tape, the medical tape including: an elastic base member portion (1) having an elastic function; an adhesive portion (2) having a function of applying and holding the elastic base member portion (1) to skin; and an anti-expansion portion (3) having a function of preventing expansion of the elastic base member portion, the anti-expansion portion (3) overlying the elastic base member portion (1), wherein, after in a manufacturing process, the elastic base member portion (1) and the anti-expansion portion (3) are

Abstract: A stretchable structure of an absorbent article has a first sheet layer made of a nonwoven fabric; a second sheet layer made of a nonwoven fabric and opposed to one side surface of the first sheet layer; and a plurality of elongated elastically stretchable members provided along the stretchable direction at intervals from each other between the first sheet layer and the second sheet layer. The first sheet layer and the second sheet layer have sheet bonded portions bonded via a hot melt adhesive disposed in a striped pattern that is intermittent in the longitudinal direction of the elastically stretchable members and continuously elongated in the direction intersecting with the elastically stretchable members, and either one of the first sheet layer and the second sheet layer is made of a low-adhesion nonwoven fabric having lower peel strength with respect to the hot melt adhesive than the other sheet layer.

Abstract: A method for producing an underpants-type disposable diaper including a stretchable region stretchable at least in one direction in an outer body. The stretchable region is formed by stacking an elastic film between a first sheet layer composed of a nonwoven fabric and a second sheet layer composed of a nonwoven fabric. When the elastic film is stretched in the stretching and contracting direction, the first sheet layer and the second sheet layer are joined via through holes formed in the elastic film at a large number of sheet bond portions arranged at intervals in each of a stretching and contracting direction and a direction orthogonal thereto, and in the sheet bond portions, the first sheet layer and the second sheet layer (20B) are joined at least by a melted and solidified material of the elastic film among the first sheet layer and the second sheet layer.

Abstract: A disposable absorbent article may include a chassis that includes a topsheet, a backsheet, and an absorbent core disposed between the topsheet and the backsheet; and a leg gasketing system. The leg gasketing system may include an inner cuff and an outer cuff; the inner cuff may include an inner cuff folded edge and an inner cuff material edge and the outer cuff may include an outer cuff folded edge and an outer cuff material edge such that the web of material is folded laterally inward to form the outer cuff folded edge and folded laterally outward to form the inner cuff folded edge. The leg gasketing system may also include a leg gasketing system pocket with an opening on an inboard longitudinal edge of the pocket.

Abstract: In order to prevent degradation of appearance, prevent a decrease in flexibility, and improve non-elasticity in a non-stretchable region in an elastic film stretchable structure, the invention is characterized by having an elastic film stretchable structure (20X) formed by stacking an elastic film (30) between a first sheet layer (20A) and a second sheet layer (20B), wherein a region having the elastic film stretchable structure (20X) includes a non-stretchable region (70) and a stretchable region (80) provided at least at one side of the non-stretchable region (70) in a stretching and contracting direction, the stretchable region (80) being stretchable in the stretching and contracting direction, the first sheet layer (20A) and the second sheet layer (20B) are joined via through holes (31) penetrating the elastic film (30) at the large number of sheet bond portions (40) arranged at intervals, and the non-stretchable region (70) does not have a section in which the elastic film (30) linearly continues along t

Abstract: In order to prevent degradation of appearance, prevent a decrease in flexibility, and improve non-elasticity in a non-stretchable region in an elastic film stretchable structure, the invention is characterized by having an elastic film stretchable structure (20X) formed by stacking an elastic film (30) between a first sheet layer (20A) and a second sheet layer (20B), wherein a region having the elastic film stretchable structure (20X) includes a non-stretchable region (70) and a stretchable region (80) provided at least at one side of the non-stretchable region (70) in a stretching and contracting direction, the stretchable region (80) being stretchable in the stretching and contracting direction, the first sheet layer (20A) and the second sheet layer (20B) are joined via through holes (31) penetrating the elastic film (30) at the large number of sheet bond portions (40) arranged at intervals, and the non-stretchable region (70) does not have a section in which the elastic film (30) linearly continues along t

Abstract: A rising portion of a rising gather includes a main region having a first part extending toward the center in the width direction, a second part extending outward in the width direction from the tip of the first part, in the middle of the front-back direction including a crotch portion, and a support region composed of only a third part extending toward the center in the width direction, between the main region and a back fallen portion. The main region has a first gather elastic member attached to a tip end of the second part along the front-back direction. The support region has a second gather elastic member attached to the tip end of the third part along the front-back direction. The base edge side of the third part is a non-stretchable portion, and the third part has a layer that follows the second part of the main region.

Abstract: A three-dimensional sheet material can be provided with a pattern of various material treatments. The material treatments can include a pattern of embossments and a pattern of apertures. The three-dimensional sheet material can be utilized in a personal care absorbent article including, but not limited to, diapers, training pants, incontinence products, feminine hygiene products such as sanitary napkins and panty liners, as well as other absorbent article such as bandages and wound dressings.

Abstract: An absorbent article in the form of a feminine hygiene pad is disclosed. The article includes a topsheet formed of a section of formed nonwoven web material having an ordered arrangement of zones, each zone comprising one or more attenuated regions adjacent to one or more built-up regions, wherein the attenuated regions have a first average basis weight and the built-up regions have a second average basis weight. Through configuration of the regions and the ordered arrangement, inclusion of melt additive to the resin(s) from which the filaments are spun and/or application of a surfactant to a surface of the topsheet, the topsheet may be imparted with a Rewet of no greater than 0.50 g and an Acquisition Time of no greater than 25 seconds, balancing competing topsheet performance characteristics in a manner acceptable or preferable for consumers/users.

Abstract: An absorbent article is disclosed. The article includes a topsheet formed of a section of formed nonwoven web material having an ordered arrangement of zones, each zone comprising one or more attenuated regions adjacent to one or more built-up regions, wherein the attenuated regions have a first average basis weight and the built-up regions have a second average basis weight, wherein the first average basis weight is less than the second average basis weight, the difference in basis weights corresponding to disposition of the filaments according to the ordered arrangement. The attenuated region(s) may include a plurality of discrete low bulk portions arranged in a pattern disposed along a longitudinal axis of the article, which facilitate z-direction movement of fluid through the topsheet and inhibit spreading of a fluid stain along the topsheet in the x and y directions.

Abstract: An absorbent core comprising: a front portion; a back portion; a middle portion positioned between the front portion and the back portion; and a longitudinal axis extending along a length of said core and crossing said front, middle and back portions, the absorbent core having a width extending perpendicular to said length and a perimeter comprising at least two opposing ends and at least two opposing sides positioned between said ends, said core being a multi-layer core comprising at least two distinct core layers, wherein a first core layer comprises a channel having a first shape and a second core layer comprises a further channel having a second shape and wherein the first and second core layers are disposed one on top of the other such that a third channel shape is formed along said core length and width, and wherein said first and second shapes are substantially the same and are different to said third shape.

Abstract: A self-propelled track drive module for an emergency stretcher, includes a left-side track drive unit and a right-side track drive unit. A frame, having a front end and a rear end, is disposed between the left-side track drive unit and the right-side track drive unit. The frame has a mounting structure for receiving an emergency stretcher and for releasably securing the emergency stretcher to the frame. The mounting structure is configured to support the emergency stretcher such that rolling wheels of the emergency stretcher do not contact a ground surface therebelow when the emergency stretcher is in a mounted condition.

Abstract: The present disclosure provides a chair with a rotatable armrest, comprising a seat body, which is provided with an armrest, a backrest and a rotating member; wherein the backrest is arranged at a position on one end portion of the seat body, the rotating member is fixed on one end of the seat body near the backrest, the armrest is rotatablely connected with the seat body through the rotating member, and the armrest is capable of rotating roughly horizontally with respect to the seat body. According to the present disclosure, a user can leave the chair from one side of the seat body, moreover, when the user is leaving the chair, the rotated armrest can still provide help for the user.

Abstract: A system for use with an inflatable device includes an air output and a nozzle at a distal end of the air output. The nozzle includes a lip extending radially from the nozzle and configured to retain the nozzle in a port of the inflatable device. The lip has a non-circular shape around the nozzle.

Abstract: A person relocation device includes sheet which defines a person space for a person. The sheet includes a left lateral strap, a right lateral strap, a head end strap and a foot end strap. Each strap is attached to the sheet only at a perimeter thereof and does not extend into the person space. The straps are adapted to be connected to a hoist so that when all of the straps are so connected and tensioned by the weight of the person the sheet suspends the person in a seated posture.