Abstract: Introduced here are apparatuses and systems for mitigating contact pressures applied to a human body by the surface of an object, such as a chair, bed, or table. A pressure-mitigation apparatus can include a series of chambers whose pressure can be individually varied. When placed between a patient and a contact surface, the pressure-mitigation apparatus can vary the contact pressure on a specific anatomical region of the patient by controllably inflating and/or deflating one or more cell. Moreover, a pressure-mitigation system can be readily integrated into a conventional treatment regimen for a variety of different conditions.

Abstract: A used feminine hygiene product disposal pad includes an outer cover, a middle absorbent layer, an inner containment layer, and a drawstring component. The outer cover is held by the user when grasping the used feminine hygiene product, the middle absorbent layer absorbs moisture or fluid from the used feminine hygiene product, and the inner containment layer comes into direct contact with the used feminine hygiene product being grasped and wraps around the hygiene product. The drawstring component is used to securely tie the disposal pad around the used feminine hygiene product.

Abstract: The present invention is a disposable absorbent undergarment, such as an adult brief or baby diaper, having an exterior surface designed to provide improved attachment for one or more fastener members, thereby resulting in improved closure and securement of the undergarment to a wearer.

Abstract: The invention relates to a medical vehicle (1) comprising a compartment (2) with a medical imaging system (3), wherein the medical imaging system (3) comprises at least one system support sensor (4). The system support sensors (4) augment the vehicle's own sensors and/or replace equivalent sensors in the vehicle. The medical vehicle (1) is configured to obtain sensor readings from the at least one system support sensor (4) during operation of the medical vehicle (1), analyze the sensor readings and provide feedback based on the analyzed sensor readings. The invention further relates to a corresponding method for operating a medical vehicle (1).

Abstract: The Electric Motor Medical Chair with Hand Brake is propelled by FIG. 4 L & R electric motors configuration. It is designed to be control and stop by FIG. 2 L & R which will turn left, right, back, and forward. The feet can rest in FIG. 6. The front wheel as in FIG. 5 gives it better control. The chair in FIG. 3 is equipped to turn out for mounting and will adjust for comfort. It's Powered by FIG. 1 Lithium battery. The Electric Motor Medical Chair with Joystick is propelled by FIG. 3 L & R electric motors. The footrest in FIG. 5 for comfort while traveling and the Joystick in FIG. 1 will turn left, right, back and forward. The wheelie bar as in FIG. 6 is for slops and balance while inclined.

Abstract: A wheel lock for a wheelchair is provided. The wheel lock comprises a supporting member configured to attach to a frame of the wheelchair adjacent to a wheel of the wheelchair. The wheel lock also comprises a brake shoe mechanically coupled to the supporting member and configured to be movable between a first directional configuration and a second directional configuration, and a brake pad mechanically coupled to the brake shoe. The wheel lock comprises a lever mechanically coupled to the brake shoe and configured to move the brake shoe between the first directional configuration and the second directional configuration. When the brake shoe is in the first directional configuration, the brake pad does not contact the wheel of the wheelchair. When the brake shoe is in the second directional configuration, the brake pad is configured to mechanically couple to the wheel of the wheelchair to prevent the wheel from rotating.

Abstract: A patient support apparatus includes a frame. The frame includes a first track and a second track. An articulated deck is coupled to the frame. The articulated deck includes a head section, a seat section, a thigh section, and a foot section. The seat section includes a stationary frame coupled to the frame and a moveable frame that is moveable relative to the stationary frame. The moveable frame includes a first roller that moves along the first track and a second roller that moves along the second track when the moveable frame moves relative to the stationary frame.

Abstract: A hospital bed includes a frame, a plurality of extendable patient support panels mounted to the frame, and a slide mechanism. Each patient support panel includes a central section and at least one coplanar side section selectively movable laterally towards and away from the central section, where the at least one coplanar side section is slidably connected to the corresponding central section. The slide mechanism allows sliding movement of the at least one side section relative to the corresponding central section.

Abstract: A patient transport system including a patient transport apparatus. The patient transport apparatus may include a support structure having a lift assembly having a powered lift actuator to raise and lower the patient transport apparatus. The patient transport apparatus includes a primary user input device for operating the lift assembly when a state of charge of a battery is above a predetermined threshold. The patient transport system may further include a backup system including a backup user input device for operating the lift assembly when the state of charge of the battery is below the predetermined threshold.

Abstract: The present disclosure provides an adjustable support apparatus configured for a bed. The adjustable support apparatus includes at least one handrail attachment, each of the at least one handrail attachment includes a fixing assembly configured for fixing a corresponding handrail attachment of the at least one handrail attachment to the bed and a handrail component telescopically connected to the fixing assembly and located at a side edge of the bed, and configured for providing lateral support to patients; and a pedal element telescopically connected and arranged in sequence with the handrail component, configured to be attached below an approximate center of the bed edge of the bed.

Abstract: An alternate pressure mattress system and methods of use may include an air mattress having a plurality of first air cells and a plurality of second air cells adjacent to the plurality of first air cells. A control housing is configured to exhaust air from within the air cells; deflate the plurality of first air cells for a first predetermined period of time; inflate the plurality of second air cells to a desire high pressure; deflate the plurality of first air cells to a desired low pressure; hold the desired high pressure and the desired low pressure for a second predetermined period of time. The pressure within the air cells may be alternated by swapping inflation and deflation of the plurality of first air cells and the plurality of second air cells and repeating the above steps. Methods of alternating the pressure within an air mattress are described.

Abstract: A trauma gurney includes a base connected to a frame by a vertical adjustment mechanism. The base is configured that it can be maneuvered over a receiving table. The frame holds a detachable platform suitable for the positioning of a patient thereon. Actuation of the adjustment mechanism allows the frame to be lowered and the patient platform to be detached. The patient platform is configured to be non-interfering with various procedures such as MRI procedures so the patient platform can remain with the patient after the patient has been transferred without adverse effects to the procedures. The patient platform can also be reattached to the frame after it has been removed. The trauma gurney beneficially allows a patient to be transferred from the gurney to another surface, such as for imaging, without requiring a conventional lateral transfer. Similarly, the trauma gurney allows a patient to be transferred back to the gurney.

Abstract: A surgical table including a first platform portion and a second platform portion that are independently moveable relative to one another is provided. A first portion of a patient can be supported by the first platform portion and a second portion of the patient can be supported by the second platform portion, and the first platform portion and the second platform portion can be adjusted relative to one another to correspondingly adjust positions/orientations of the first portion and the second portion of the patient. To illustrate, using a first end portion supporting the first platform portion, the first platform portion can be rotated about a vertical axis and moved side to side to adjust the position/orientation thereof relative to the second platform portion, and using a second end portion supporting the second platform portion, the second platform portion can be moved toward and away from first platform portion.

Abstract: A massage apparatus capable of adjusting the position of an arm massage unit includes a body massage unit configured to massage at least a part of a body of a user, the arm massage unit disposed on a side portion of the body massage unit and configured to massage an arm of the user, and a lifting and lowering unit disposed on a lower portion of the arm massage unit and configured to adjust a position of the arm massage unit.

Abstract: An articulating footplate assembly for a gait training system is disclosed. The footplate assembly can include a footplate base configured to support a user's foot and a lower leg support assembly configured to extend along a portion of the user's leg. The lower leg support assembly can include a footplate base connector attachable to the footplate base and a pivoting mechanism. The pivoting mechanism can comprise a pivot point and a rotation selection device configured to selectively permit rotation about the pivot point, the rotation selection device comprising a plurality of discrete rotation settings, and each rotation setting being configured to permit rotation about the pivot point along a corresponding predetermined angular distance.

Abstract: The present invention allows a subject to enjoy a sense of accomplishment of improvement in a gait function while viewing and listening to motion advice for improving the gait function when the subject participates in rehabilitation through gait motion using a wearable motion support apparatus.

Abstract: Provided is an ankle joint rehabilitation training device, wherein the device acquires an actual movement parameter of a patient by a sensor assembly, determines a parameter difference according to the actual movement parameter and an application movement parameter by a controller, and adjusts the application movement parameter according to the parameter difference and the actual movement parameter, finally generates a movement instruction, and drives a foot support to move by the motor according to the movement instruction, so as to perform the rehabilitation training on the patient's foot. Since the current movement ability of the patient is considered in the process of rehabilitation training, the rehabilitation training is more suitable to personal condition of the patient, meanwhile, the rehabilitation training also considers the application movement parameter corresponding to the target rehabilitation strategy.

Abstract: By normalizing and comparing a first signal pattern of a biological potential signal of a subject and a second signal pattern of a biological potential signal corresponding to a healthy subject, a gait function of the subject is recognized as temporal change based on similarity obtained from the comparison result.

Abstract: The present disclosure describes a vision training device with high training efficiency for the ciliary muscle. In an example, a vision training device includes a housing having at least one eyepiece unit corresponding to an eye of a user, a display that displays a target image in front of a fixation axis of the user, a lens arranged between the eyepiece unit and the display unit, a movable unit capable of moving at least one of the display and the lens along the fixation axis, and a control unit that sets at least one training range within a movable range of the display and the lens and controls the movable unit such that at least one of the display and the lens is moved within the training range.

Abstract: The present invention provides a device with a pressure control system and methods for controlling the application of negative pressure to an external surface of an individual for creating and/or maintaining patency of the upper airway passage. The device is configured to fit under the chin of a subject at an external location corresponding approximately with the subject's internal soft tissue associated with the neck's anterior triangle. The pressure control system contains control module elements that may include circuit board elements, digital output barometer elements, sensor elements, processing elements and memory elements to optimize device function and safety of the device through regulation of the flow rate of the air pump.

Abstract: A system and method for promoting angiogenesis and adipogenesis in soft tissue using a tissue enlargement apparatus. The tissue enlargement apparatus includes an interface configured for affixation to the soft tissue. A force generating device is coupled to the interface by a connecting tube for applying mechanical forces to the soft tissue. A processor is coupled to the force generating device and is configured to apply intermittent cyclical patterns of the mechanical forces to the soft tissue to promote angiogenesis and adipogenesis in soft tissue. The intermittent cyclical patterns are based on at least one of duration, frequency, and intensity of the mechanical forces.

Abstract: Systems and methods for treating fluid stasis employ an airstream to move static fluid to one or more natural drainage areas for static fluid. A system for treating fluid stasis includes an airstream nozzle and an airflow generator for supplying an airflow to the airstream nozzle. The airflow nozzle is configured to output an airstream configured to be directed onto a patient to induce shear-thinning of static fluid and movement of static fluid toward one or more natural drainage areas for static fluid.

Abstract: A therapeutic, fitness and sports enhancement device which includes a cylindrically shaped body having a predetermined density and predetermined diameter, the body including a plurality of projections of a predetermined shape. One or more of the predetermined density and the predetermined diameter in combination with the predetermined shape of the projections optimize mobilization of soft tissue structures of the human body.

Abstract: Disclosed is a massager with better adsorption effect, falling within the technical field of adult health care products. The massager with better adsorption effect includes a massage head and a handle. The handle includes a housing, a control key and a driving assembly, the driving assembly being arranged in the housing and the control key being connected to the driving assembly, and a soft tongue portion, an upper lip and a lower lip are arranged on the massage head. The driving assembly includes a driving circuit board, a telescopic motor and a mounting frame, the mounting frame including a lantern ring, a connecting rod, a limit rod, an upper driving plate and a lower driving plate. The present disclosure has a simple structure and a humanization design, and the human-imitation action is close to the real action effect of human beings, which brings a better experience to a user.

Abstract: A built-in inflation mechanism for a sex toy and an inflating method thereof are provided. The built-in inflation mechanism for the sex toy includes a fixing sleeve, a piston sleeve, and a three-way guide pipe disposed in a main body. An air cavity is defined in a top end of the main body, an upper end of the piston sleeve is disposed at a bottom portion of the air cavity, and the upper end of the piston sleeve is communicated with the bottom portion of the air cavity through at least one air injection hole. A one-way air injection valve plate is disposed on the upper end of the piston sleeve and covers the at least one air injection hole. A spring is disposed between the piston sleeve and the fixing sleeve, and the spring is configured to drive the piston sleeve to elastically move upward.

Abstract: A system is disclosed. The system has an accessory control module, comprising computer-executable code stored in non-volatile memory, a processor, a user device of a human viewer, a viewer accessory configured to communicate with the user device, the viewer accessory including a first motor or a first heater, a model device of a human model, and a model accessory configured to communicate with the model device, the model accessory including a second motor or a second heater. The accessory control module, the processor, the user device, the viewer accessory, the model device, and the model accessory are configured to provide a chat communication application between the human viewer and the human model configured to provide chat between the human viewer via the user device and the human model via the model device.

Abstract: The present disclosure relates to a medical vibratory stimulation device comprising: a wearable part that is worn on a target site of the body; a plurality of vibration elements which are arranged in the wearable part to apply vibratory stimuli to the target site of the body; and a control unit which individually controls the plurality of vibration elements so that the plurality of vibration elements sequentially apply vibratory stimuli from the distal portion to the proximal portion of the target site of the body.

Abstract: An immersive stimulation system generates audio (such as music) and a vibration signal that causes a stimulation device to vibrate synchronously with the audio. The vibrations may be synchronized with respect to amplitude and frequency such that frequency components of the vibrations adapt in coordination with time-dependent frequency distributions of the audio. The immersive stimulation system may include a control device for generating the audio and vibration signals and a stimulation device that produces the vibrations based on the vibration signal. The stimulation device may include one or more voice coil transducers to produce the vibrations and a detachable vibratory unit that may have different form factors depending on the desired usage of the stimulation system.

Abstract: A medical device system for providing sensor data capture includes a medical device that may include one or more removably coupled sensor hubs and that includes a display to provide sensor data and at least one data interface (DI) port that may be a sensor-agnostic DI (SA-DI) port and a data transfer cable that may be compatible with the sensor-agnostic DI port and includes a first electromechanical connector configured to detachably couple to the SA-DI port and a second electromechanical connector configured to couple to the sensor and that includes a cable memory and processor configured to execute stored software to format sensor data according to a protocol of the SA-DI port, an authentication circuit, and a cable isolation device to limit patient leakage current flow from the medical device to the sensor and to electrically isolate the authentication circuit from the cable processor and the cable memory.

Abstract: A head-up CPR board and method for using the same. The head-up CPR board gradually elevates the chest of a patient to a 15-degree angle and the head of the patient to a 30-degree angle. While CPR is being performed on the patient, a wedge insert is slowly and incrementally inserted beneath an incline portion of the head-up CPR board. By slowly elevating the patient, the head-up CPR board facilitates venous drainage through gravity and promotes improved circulation of oxygenated blood, leading to better neurological outcomes when Return of Spontaneous Circulation (ROSC) occurs in cardiac arrest patients. By significantly enhancing cerebral brain blood flow, cerebral perfusion, and coronary perfusion, this can have a profound impact on the overall recovery and neurological well-being of patients. The head-up CPR also reduces pulmonary vascular resistance. This dual benefit contributes to better oxygenation and circulation, further improving patient outcomes.

Abstract: A portable massage support device includes a frame that has a pair of first members each hingedly coupled to a pair of second members and a support bracket pivotally coupled to the pair of first members. A leg cushion is attached to the pair of second members to rest upon a user's thighs when the user is seated in a chair and a torso cushion is slidably disposed on the pair of first members to orient the user in a preferred orientation to receive a back massage. A face cushion bracket is removably attachable to the torso cushion and a face cushion is coupled to the face cushion bracket to support the user's face when the user is seated in the chair.

Abstract: A clamping massage device includes an outer shell, a dynamic component, connecting components and massage arms. The dynamic component includes a motor and a cam connected to the motor. The connecting components include a push plate and connecting rods connected to the push plate, the push plate is disposed corresponding to the cam. The massage arms are disposed respectively corresponding to the connecting rods, and the massage arms are at least partially exposed to the outer shell. A height of the motor in the vertical direction is disposed to 12 millimeters (mm)-17 mm, and a straight distance from the output end to the fixed end is disposed in a range of 23 mm-32 mm. The device achieves purpose of pressing and clamping massage by driving the massage arms to open and close through the dynamic component, while achieving a more human-like technique and better massage effects.

Abstract: A flexible multi-chamber bag for storing and reconstituting parenteral nutrition solutions is disclosed. The flexible multi-chamber bag comprises a first peelably sealing wall and a second peelably sealing wall between the two polymer films extending from the top edge to the bottom edge and separating the first bag into a first chamber between the first peelably sealing wall and the second peelably sealing wall, a first space between the left edge and the first peelably sealing wall, a second space between the second peelably sealing wall and the right edge; a third peelably sealing wall extending from the left edge to the first peelably sealing wall to separate the first space to form a third chamber and a fourth chamber; and a fourth peelably sealing wall extending from the right edge to the second peelably sealing wall to separate the second space to form a second chamber and a fifth chamber.

Abstract: An apparatus, comprising an environmental control element configured to control at least one environmental condition of a substance contained within a chamber, the environmental control element includes a thermal insulator configured to provide a thermal shield to the substance and a phase change material (PCM) configured to thermally regulate at least one environmental condition. The environmental control element is configured to control the environmental condition without use of an external power source, thereby allowing the apparatus to be thermally self-recharging.

Abstract: The present application discloses a sealing valve and an anesthetic bottle. The sealing valve includes a valve body and a valve core. The valve body is provided with a first end, a second end and a channel. The end surface of the first end and/or the inner wall surface of the channel are provided with a first right angle portion and a second right angle portion, the valve core is arranged in the channel, and the outer wall surface of the valve core is convexly arranged with an engagement ring. The engagement ring is provided with a conical surface and an annular groove. The conical surface can abut against the first right angle portion and the second right angle portion to close the channel, or separate from the first right angle portion and the second right angle portion to open the channel.

Abstract: Transfer devices with vial adapter and/or an infusion set for reducing overdosing/underdosing of an infusion bag are provided. The transfer device provides user-controlled fluid transferring between an infusion liquid container and a drug-containing container. In one aspect, the transfer device provides user-controlled venting that can be used during liquid transfer between the infusion liquid container and a drug-containing container.

Abstract: A nursing bottle is provided for reducing tooth decay in a user. Embodiments provide a nursing bottle having a first chamber for containing a first liquid to feed an infant, such that the first liquid dispenses through lateral openings of a nipple. The bottle includes a second chamber sealed by a stopper having an extension extending into a nipple. Once the infant has fed on a volume of first liquid, a second liquid dispenses from the second chamber through the extension to a central opening of the nipple. The second liquid rinses the first liquid from the teeth of the infant during feeding, reducing sugars that cause tooth decay.

Abstract: The invention relates to the application of photon energy to energize dental materials to enhance their physical handling characteristics, efficacy, ability to be delivered, reactivity, polymerization, and/or post-cure mechanical properties, among other attributes.

Abstract: The present invention provides an alumina workable body for dental use that exhibits excellent translucency, strength, and linear light transmittance as a sintered body after sintering. The present invention relates to an alumina workable body for dental use with D1 and D2 that are different from each other, where D1 is the post-sintering average crystal grain size at a first point falling within an interval from one end P to 25% of the entire length on a straight line extending along a first direction from said one end P to the other end Q of the alumina workable body for dental use, and D2 is the post-sintering average crystal grain size at a second point falling within an interval from said other end Q to 25% of the entire length.

Abstract: A detergent product containing a detergent composition is provided.

Abstract: The present invention relates to a method for increasing sun protection factor (SPF) of a UV filter composition, use of hybrid metal oxide particles for increasing SPF of a UV filter composition and UV filter compositions comprising the hybrid metal oxide particles.

Abstract: The present invention relates to solidified, oil-in-water dispersion or emulsion deodorant or antiperspirant stick compositions. Disclosed is a deodorant or an antiperspirant stick composition in the form of an oil-in-water dispersion or emulsion, comprising: i) at least one lipophilic material having a melting point higher than 50° C.; ii) at least one nonionic emulsifier having a HLB value from 1 to 11 within an oil-in-water emulsifier mixture with an average HLB value in the range of from 6.8 to 11; iii) an aqueous cosmetically acceptable carrier; wherein said composition comprises at least 8% of said lipophilic material by weight of the composition; wherein said composition comprises higher than 50 wt % of water by weight of the composition; wherein said lipophilic material has a straight alkyl chain comprising at least 20 carbon atoms.

Abstract: An oil-in-water emulsion cosmetic composition includes at least one superabsorbent polymer, at least one water soluble emollient, and at least one thickener.

Abstract: Oral care compositions are disclosed herein. In accordance with an aspect, provided is an oral care composition having a whitening agent; potassium nitrate, wherein about 80% or more of the total amount of potassium nitrate has a particle size of about 150 ?m or less; water in an amount of about 8 wt. % or less or about 3 wt. % or less, wherein all weight percentages are based on the total weight of the oral care composition.

Abstract: A tobacco and nicotine-free oral pouched product for dental and oral care is provided. The oral pouched product includes a saliva-permeable pouch enclosing an oral formulation including tooth re-mineralizing agent. Also described is a tobacco and nicotine-free oral pouched product for use as a medicament.

Abstract: An alcohol-free lotion for the topical application having antiseptic properties is made by combining an aqueous phase comprising formaldehyde and at least one humectant with an oil phase comprising at least one surfactant and at least one oil; wherein the at least one humectant is present in the aqueous phase in the range of from 30 to 75 wt. %., wherein formaldehyde is present in the aqueous phase in the range of from about 1.0 to 20.0 wt. %; wherein the surfactant is present in the oil phase in the range of from about 30 to 60 wt. %; wherein the aqueous phase to oil phase ratio is from about 10:1 to 4:1; and wherein the lotion free of the odor of formaldehyde.

Abstract: Various preservatives and compositions incorporating these preservatives as well as various methods of using these preservatives and compositions are described. For example, various compositions that include cosmetic and pharmaceutical compositions containing a preservative such as 3-(heptyloxy)propane-1,2-diol and one or more other ingredients (e.g., natural ingredients) are described.

Abstract: Suggested is a fragrance according to formula (Ia) and/or (Ib).

Abstract: Provided are a novel cosmetic compounding agent capable of imparting superior properties such as a water and moisture retention property to a cosmetic for use on the hair and skin; a cosmetic using the cosmetic compounding agent; and a method for producing the cosmetic. The cosmetic compounding agent of the present invention contains an organic ammonium salt having a hydrogen-bonding functional group(s) in a cation and/or an anion.

Abstract: Provided is a nanoemulsion which has stability and to which preservative efficacy is imparted, in a bacterial contamination environment. This object is attained by a nanoemulsion which has an average particle diameter of 30 nm or less, has a particle size distribution index of 0.14 or less, does not contain particles of 100 nm or more, and contains, as a preservative, at least one selected from an organic acid (salt) and a biguanide-based compound.