Abstract: [Problem] The present invention provides a preparation jig for a tympanic membrane regenerating agent and a preparation vessel for a tympanic membrane regenerating agent enabling simple preparation of a tympanic membrane regenerating agent. [Solution] A preparation jig for a tympanic membrane regenerating agent (1a) and a preparation vessel for a tympanic membrane regenerating agent (1A) each include: a vessel (3A) including housing walls (6, 7) forming an interior space (S1) housing a medicinal solution support (2), and including an opening (6h) opening in one direction and formed in the housing walls (6, 7); and a holding portion (4A) disposed in the interior space (S1). The deep side of the interior space (S1) is a housing portion (S3) housing the medicinal solution support (2) holding a medicinal solution. The opening (6h) side of the interior space (S1) is an installation space (S2) in which the holding portion (4A) is disposed.

Abstract: A knit hemostatic bandage provided herein can include a continuous rayon fiber and a continuous glass fiber. The knit hemostatic bandage can have a gauge of between 10 and 30 stitches per inch. The knit hemostatic bandage can have a Young's modulus of elasticity of less than 50 MPa.

Abstract: A method and system for tailoring a compression garment having a first lateral end and a second lateral end. A first tension tab releasably attachable to the compression garment; wherein the first tension tab includes at least a first indicator and a second indicator on an outer surface. The first tension tab being attachable to the compression garment and the first strap being attachable onto the compression garment adjacent or over at least a portion of the first tension tab with a first strap covering a first part of the first tension tab and terminating at a first strap end that exposes a second portion of the first tension tab. A first tension tab setting indicates whether the end of the first strap terminates adjacent or over the first indicator or the second indicator of the first tension tab.

Abstract: Scar formation is inhibited by simultaneously applying a vertical force and a lateral compression to the wound site during the healing process. Apparatus for applying such simultaneous forces can include a backing and a tissue displacement device. The backing holds the tissue displacement device over the wound. The tissue displacement device may be expanded to both apply the vertical force against the wound and to draw the backing radially or laterally inward to apply the desired compression forces to the wound.

Abstract: Silicone gels are described that are adhesive to the skin. The gels are able to be used in particular for articles that are adhesive to the skin for medical or paramedical use.

Abstract: The present invention relates to a dispenser for the silicone sheeting and the adhesive anchors and method for treating sites, such as wounds or closed incisions, using the silicone sheeting and anchors. The silicone sheeting may be provided in the form of a roll, which includes a leader. The silicone sheeting may be cut from the roll, or may be of precut sizes. Adhesive anchors may be cut from a roll or may be of precut sizes. The dispenser allows for easy access to silicone sheeting for wound treatment and adhesive anchors for securement of the silicone sheets, especially in high tension areas of the body.

Abstract: A method for inspecting absorbent articles is provided. The inspection is performed using an inspection algorithm generated with a convolutional neural network having convolutional neural network parameters. The convolutional neural network parameters are generated by a training algorithm. Based on the inspection, characteristics of the absorbent articles, such as defects, can be identified. Absorbent articles having identified characteristics can be rejected, or other actions can be taken.

Abstract: A method for inspecting absorbent articles is provided. The inspection is performed using an inspection algorithm generated with a convolutional neural network having convolutional neural network parameters. The convolutional neural network parameters are generated by a training algorithm. Based on the inspection, characteristics of the absorbent articles, such as defects, can be identified. Absorbent articles having identified characteristics can be rejected, or other actions can be taken.

Abstract: The present invention provides an applicator improved so that the entirety of the tampon may be reliably inserted into vagina. A raised portion is located on an exterior surface of an inner tube in the vicinity of a rear end thereof and put in a slidable contact with a part of an interior surface of an outer tube. The raised portion has an outer shape having a width dimension gradually increasing rearward from an apex located on a front end.

Abstract: The invention provides an absorbent article comprising an indication means for indicating the presence of bodily exudates, the indication means comprising a color-changing indication means, wherein the absorbent article and the indication means form one integral unit, the article further comprising a indication device, which comprises a housing and a connection means, such that the indication device can be attached to the absorbent article and be detached from the absorbent article, wherein the indication device comprises a color sensor.

Abstract: Sensor devices and systems for monitoring the basic needs of an infant comprising feeding, sleeping, and/or voiding (urinating and/or defecating) are described herein.

Abstract: Sensor devices and systems for monitoring the basic needs of an infant comprising feeding, sleeping, and/or voiding (urinating and/or defecating) are described herein.

Abstract: A disposable pant-type absorbent article, such as a pant diaper, a sanitary pant or incontinence pant is described. The disposable pant-type absorbent article has a longitudinal direction (Y) and a transverse direction (X). The disposable pant-type absorbent article is adapted for a male user. A method for manufacturing such a disposable pant-type absorbent article is also described.

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: Patient support apparatuses, such as beds, cots, stretchers, recliners, or the like, include control systems with one or more image, radar, and/or laser sensors to detect objects and determine if a likelihood of collision exists. If so, the control system controls the speed and steering of the patient support apparatus in order to reduce the likelihood of collision. The control system may be adapted to autonomously drive the patient support apparatus, to transmit a message to a remote device indicating whether it is occupied by a patient or not, and/or to transmit its route to the remote device. The remote device may determine an estimate of a time of arrival of the patient support apparatus at a particular destination and/or determine a distance of the patient support apparatus from the particular destination.

Abstract: A vehicle, such as a car, camper or van including a seat, is mounted in the vehicle, with a seat surface; and a carrier arranged close to the seat and mounted in the vehicle, and provided with a drive for adjusting the carrier between a first position, in which an edge of the carrier runs parallel to the main direction of travel of the vehicle and lies in line with and adjoins the seat surface of the seat, and a second position in which, relative to the first position, this edge of the carrier is arranged at a distance from the seat surface in a direction transversely of the seat surface. The invention further relates to a carrier with a drive.

Abstract: A mobile chair apparatus is described that comprises a drive assembly that preferably includes one or more moveable foot pedals, and drive wheels which rotate in response to rotation of the foot pedals by the mobile chair occupant, and a steering assembly which comprises two steering wheels and at least one tiller, configured such that forward and backward movement of said tiller will translate into movement of both steering wheels, wherein the drive assembly and the steering assembly concurrently enable the mobile chair occupant to propel and steer the mobile chair apparatus without assistance from another person.

Abstract: A disclosed vehicle wheel assembly includes a plurality of wheels, a plurality of rotary drive modules each having a respective rotation axis, and a plurality of rotatable arms, wherein each arm is arranged to extend radially from a rotation axis of a respective rotary drive module to couple the respective rotary drive module to a respective wheel. Each rotary drive module is operable to drive rotation of a respective rotatable arm about the rotation axis of the drive module, to thereby rotate a respective wheel about the rotation axis. A control module can sense stepped terrain, and control each rotary drive module to enable a vehicle to travel over the stepped terrain.

Abstract: A wheelchair including a supporting frame and moving means configured to allow the movement of the wheelchair, the supporting frame having a seating area for a user of the wheelchair, the wheelchair including first actuation means configured to translate the seating area laterally and externally with respect to the supporting frame and, at least partially, with respect to the moving means, in a transfer configuration of the user, supporting means being operationally associated with the seating area, being able to be activated in the transfer configuration of the seating area to support the seating area with respect to the ground, the seating area being defined, in the transfer configuration, by a main seat and a secondary seat able to be activated in the transfer configuration of the seating area to increase the extension of the main seat.

Abstract: A patient support apparatus comprises a support structure and a first side rail. The support structure comprises a base and a patient support surface for supporting a patient. A side rail connector is coupled to the support structure. The first side rail is removably coupled to the support structure by the side rail connector. The first side rail is configured to be removable from the support structure and interchanged with a second side rail. The second side rail is configured to be removably coupled to the support structure by the side rail connector.

Abstract: A patient support apparatus for use in ambulating a patient to a floor surface. A patient support deck is operatively attached to a base and has a seat section, a leg section, and a pair of foot sections. The patient support deck is operable between a bed configuration and a chair configuration. In the bed configuration, the seat section, leg section, and foot sections support the patient in a flat position. In the chair configuration, the seat section supports the patient in a seated position, the leg section is articulated adjacent to the floor surface, and the foot sections are articulated relative to the leg section and out of support of the patient. A handle to facilitate patient ambulation is coupled to each of the foot sections, and the handles are arranged to facilitate patient ambulation when the patient support deck is in the chair configuration.

Abstract: An aspirator includes a pump, a detecting unit, and a control unit. The pump is driven by a piezoelectric element and has a suction portion and a discharge portion. The detecting unit includes a current detector and a regulator, and detects a closed state of the suction portion. The control unit includes the regulator and a voltage controller, and regulates an output voltage for the piezoelectric element in accordance with the closed state of the suction portion detected by the detecting unit.

Abstract: A system for cooling a pressurized hyperbaric chamber without pressure change includes an air compressing unit, an air cooling unit, and an air discharging hose. The pressurized hyperbaric chamber, the air compressing unit, the air cooling unit, and the air discharging hose are in fluid communication with each other. A flow of output warm air from the pressurized hyperbaric chamber is withdrawn and discharged into the air cooling unit by the air compressing unit. A heat exchanger of the air cooling unit then removes heat energy from the flow of output warm air to convert the flow of output warm air into a flow of input cold air, as the heat exchanger is in fluid communication with stored ice water within an insulated reservoir of the air cooling unit. The flow of input cold air is then discharged back into the pressurized hyperbaric chamber through the air discharging hose.

Abstract: A surgical frame and a method for use thereof facilitates transfer of a patient from and to a surgical table/gurney. The surgical table includes a main beam positionable such that a surgical table/gurney with patient laying thereon can be positioned under the main beam. The main beam includes componentry for supporting a patent thereon, and the main beam can be rotated, raised/lowered, and tilted upwardly/downwardly to afford positioning and repositioning of the main beam to facilitate transfer of a patient from the surgical table/gurney to the main beam and transfer from the main beam to the surgical table/gurney.

Abstract: A patient support structure for supporting a patient in a supine position for surgery and a method for use of the patient support structure is provided. The patient support structure includes at least a head support portion. The head support portion includes at least one base portion, a first arm portion, a second arm portion, and a head harness, where the first arm portion and the second arm portion are adjustable inwardly/outwardly and upwardly/downwardly, and the head harness is supported by the first arm portion and the second arm portion.

Abstract: A training device suppresses unintended operation of an operation rod when executing an operation mode in which operation of the operation rod is controlled based on a force applied to the operation rod. The training device includes the operation rod, a motor, a force detector, a rotation information output sensor, a first command calculator, and a force corrector. The operation rod moves a limb. The motor operates the operation rod in a direction of degree of freedom. The force detector detects a force component and outputs a force component signal. The rotation information output sensor detects an operation position of the operation rod in a corresponding direction of degree of freedom. The force corrector calculates a corrected force component value based on operation positions of the operation rod and force component signal. The first command calculator calculates a first motor control command based on the corrected force component value.

Abstract: A standing-up assistance apparatus includes a first sensor that measures a muscle potential of a lower leg of a user, a second sensor that measures a knee angle of the user, a processor that determines whether starting to assist the user in a standing-up motion from a seated state is possible, based on, at least, the measured muscle potential and the measured knee angle, and outputs an instruction signal if the processor determines that starting to assist the user in the standing-up motion is possible, and an assistance mechanism. The assistance mechanism starts assisting the user in the standing-up motion when the assistance mechanism receives the instruction signal from the processor.

Abstract: Provided is a pelvis fixing device including a rear fixing module including a driving module mounting portion, the rear fixing portion configured to enclose a side surface and a rear surface of a waist of a user, and a front fixing module including a soft layer and a hard layer configured to enclose a front surface of the waist of the user, wherein the hard layer is connected to the rear fixing module to form a closed loop around the waist of the user.

Abstract: There is provided an assistance apparatus in which when assistance provided to a user in walking is to be stopped, a motor reduces a tension of a first wire and a tension of a second wire, which couple an upper-body belt and a left knee belt to each other on or above a front part and a back part of a body of the user, to less than a second threshold value during a first stop period in a gait phase of a left leg of the user, the first stop period being a period from a period included in a first period and including a timing at which the left leg shifts from a stance phase to a swing phase to a start period of a second period, and reduces a tension of a third wire and a tension of a fourth wire, which couple the upper-body belt and a right knee belt to each other on or above the front part and back part of the body of the user, to less than the second threshold value during a second stop period in a gait phase of a right leg of the user, the second stop period being a period from a period included in a third pe

Abstract: According to one implementation an apparatus is provided that comprises: one or more support plates with which there are associated massage units, the one or more support plates being secured to and facing an abdominal wall of the body of a patient; massaging heads integrated in the massage units for performing an abdominal massage on the patient, wherein at least two massaging heads are applied such that they are adjacent to at least one section out of an ascending section, transverse section or descending section of the colon of the patient thereby to apply a localized force generating a pressure on the colon section in a direction normal to the abdominal area, wherein the at least two massaging heads are synchronized; and control means for controlling the magnitude and timing of the localized force.

Abstract: The present invention discloses a deep vein thrombosis (“DVT”) device that is portable, tubeless, and battery-operated, which ensures that the patient will have maximum mobility during recovery. The DVT device provides a pneumatically controlled bladder portion, which is actuated by an electronically controlled air pump, where the pump/bladder combination is enclosed in a “pocket” of a wrap or cuff during use. All pump, battery, and control components are protectively housed in a plastic case that is permanently attached to the bladder portion. Once the pump/bladder combination is placed in the “pocket” the wrap or cuff will be sealed. The wraps or cuffs are single use, disposable garments designed to provide an absorbent barrier during use, where the bladder portion and air pump remain clean during use and can be reused by the patient or hospital staff. Tabs or extensions may be used to secure the pump/bladder combination after insertion into the “pocket” of the wrap or cuff.

Abstract: Generally, a system for soothing a baby during imaging by an imaging device is provided. The system can include: a capsule incubator for positioning the baby within the imaging device, the capsule incubator can include: a bottom portion having an inner surface, a bed positioned on top of the inner surface for positioning the baby thereon, and one or more members coupled to the bottom portion that are positioned in a first position to open the capsule incubator and a second position to close the capsule incubator; a vibrational device including a vibrational element that extends from outside of the capsule incubator into the capsule incubator and is coupled to the bed to cause the bed to vibrate with a predetermined vibrational frequency, thus causing the baby to vibrate with the predetermined vibrational frequency.

Abstract: A massage unit includes a base member, a treatment element driven unit, and a slide mechanism. A lower portion of the treatment element drive unit is fitted to the base member to be rotatable about a first rotation axis. One end of the slide mechanism is fitted to a lower portion of the base member. The other end of the slide mechanism is fitted to the treatment element drive unit. At least one of the following structures is adopted: a structure where the one end of the slide mechanism is fitted to a lower portion of the base member to be rotatable about a second rotation axis; and a structure where the other end of the slide mechanism is fitted to the treatment element drive unit to be rotatable about a third rotation axis.

Abstract: A vibrating ingestible capsule includes a housing having a longitudinal axis, and having a vibrating agitator adapted such that, in a first vibrating mode of operation, the housing exerts vibrations on an environment surrounding the capsule. A power supply disposed within the housing is adapted to power the vibrating agitator. A temperature sensor provides temperature information signals with respect to a temperature in an environment surrounding the vibrating ingestible capsule over a period of time.

Abstract: Systems and methods related to the field of cardiac resuscitation, and in particular to devices for assisting rescuers in performing cardio-pulmonary resuscitation (CPR) are described herein. The system includes an applicator device configured to provide ACD CPR treatment to a patient's chest according to a plurality of phases at least one sensor configured to be coupled to the patient's chest and to measure at least one parameter related to the ACD CPR treatment and information for determining whether at least one transition point of the ACD CPR treatment has been reached; and one or more processors configured to provide a feedback signal based on a parameter for administering ACD CPR treatment to the patient's chest according to a desired treatment protocol.

Abstract: A pharmaceutical pack and the method for making the same are provided. The pharmaceutical pack includes a blister layer and a lidding sheet disposed over the blister layer. The blister layer defines at least one opening. The lidding sheet includes a first layer and optionally a second layer. The first layer includes at least one hologram, and is disposed on the second layer, which is a plastic film. The blister layer and the lidding sheet define at least one cavity so as to hold at least one pharmaceutical dosage form therein.

Abstract: A child-resistant medication container assembly that includes a blister card including a plurality of compartments each configured to support a dosage of medication, and a puck including a body portion, a recess that defines a partition wall in the body portion, and a plurality of openings defined in the partition wall. Each opening corresponds to one of the plurality of compartments in the blister card. The assembly further includes a carton including a first wall opposite a second wall. An access opening is defined in the first wall and a plurality of perforations are defined in the second wall. The access opening is sized to provide access to the plurality of compartments, and each perforation corresponds to one of the plurality of compartments in the blister card.

Abstract: Medical vials and bottles containing medications dispensable syringes and needles are interfaced to replaceable caps having alcohol infused wipes therein to sterilize the rubber hubs through which the needles will be inserted into the vials to draw out the medication therefrom.

Abstract: A drug delivery device includes a capsule, a logic circuit disposed within the capsule, and an actuator connected to the logic circuit and configured to expose an interior of the capsule to an exterior of the capsule upon activation by the logic circuit.

Abstract: A feeding system for medical patients comprises a storage assembly, dispensing assembly, and extension set including, in part, a reservoir, a pump, a feeding tube, a check valve and an adapter. The reservoir is configured to hold at least one feeding of nutritional substance. The dispensing assembly is connected to the storage assembly and pumps the at least one feeding of nutritional substance from the reservoir to the feeding tube connected to an outlet of the pump. The check valve unit is connected to a second end of the feeding tube by means of a check valve connection point and is configured to allow the flow of nutritional substance in only one direction. The at least one feeding of nutritional substance is passed through the adapter unit connected to the check valve unit.

Abstract: Disclosed is a microemulsion of oil-in-water type including, preferably consisting of, by weight relative to the total weight of microemulsion: •70% to 94% of water, •1% to 15% of at least one hydrophobic fragrancing substance, •4% to 20% of at least one preferably volatile solvo-surfactant, and •0.1% to 15%, preferably 1% to 13%, of at least one hydrotropic agent or at least one surfactant selected from anionic surfactants, cationic surfactants, amphoteric surfactants and non-ionic surfactants. The solvo-surfactant is selected from monoalkylated glycerol derivatives of following formula (I): wherein the “alkyl” group is a linear or branched alkyl group including from 1 to 8 carbon atoms, and R and R? are each independently H or a linear or branched alkyl group including from 1 to 5 carbon atoms, with the proviso that R is different from R?, and mixtures thereof.

Abstract: The present invention relates to a method for producing a multi-capsule, the method including steps of: (a) preparing a coating solution by mixing purified water, titanium dioxide, mica, a hydrophobic polymer, cellulose gum, and sucrose; and (b) drying the coating solution prepared in step (a) while spraying the coating solution through a spray nozzle of a fluid bed dryer after introducing a spherical seed of a colorant component for a cosmetic; or a starch or sucrose spherical seed coated with a functional component into the fluid bed dryer, a multi-capsule produced by the method, and a cosmetic composition containing the multi-capsule as an active component.

Abstract: The subject of the present disclosure is a blonding agent for changing the natural color of keratinic fibers, in particular human hair, which contains a) sodium percarbonate, b) sodium chloride and further from 0 to about 8% by weight of water. Furthermore, the present disclosure relates to a method for blonding human hair.

Abstract: The invention relates to cosmetic processes and compositions for depigmenting, lightening and/or whitening keratin materials, in particular the skin, which comprises the application of a cosmetic composition comprising thiopyridinone compounds to keratin materials.

Abstract: A cationic compatible metal oxide and oral care compositions containing the metal oxide are disclosed. Preferably, the oral care compositions contain a cationic compatible metal oxide and a cationic ingredient, such as for example, a cationic antibacterial agent such as cetyl pyridinium chloride (“CPC”). The cationic compatible metal oxide, e.g. silica, comprise metal oxide particles having a substantially negative surface charge and a vitamin deposited onto or reacted with the surface of the metal oxide particles in an amount sufficient to provide a substantially positive surface charge on the metal oxide particle. Processes for making and using the vitamin modified metal oxide in oral care compositions are also disclosed.

Abstract: A method of preparing a fine oil-in-water emulsion comprising an oil phase based on silicone and/or hydrocarbon oils, in which the oil phase particles have an average particle size of 150 nm or less. The emulsion is stabilized by a carboxy-modified silicone in combination with a C16 to 22 higher alcohol; a nonionic surfactant having a POE chain and an HLB of 5 to 10; and a dihydric glycol. The emulsions can be prepared without the use of a high-pressure emulsifying apparatus.

Abstract: An aqueous cleansing composition comprising a cationic surfactant, a nonionic surfactant, and a thickener comprising an alkoxylated methyl glucose ether, wherein a weight ratio of cationic surfactant to nonionic surfactant is greater than 0.9:1. The combination of the cationionic:nonionic surfactant ratio with the alkoxylated methyl glucose ether thickener provides the composition with cold weather stability. Cold weather stability is observed when the composition remains transparent after cold storage.

Abstract: Compositions and methods for amelioration of skin laxity and body contour are provided. Provided herein are compositions comprising a combination of peptides.

Abstract: The present invention relates to a non-cellulosic polysaccharide derivative: i) having a mean average molecular weight (Mw) from about 100,000 g/mol, preferably from about 150,000 g/mol and more preferably from about 200,000 g/mole to about 2,000,000 g/mol, preferably to about 1,800,000 g/mol and more preferably to about 1,400,000 g/mole; and ii) containing at least one cationic group, with a cationic degree of substitution (DScat.)extraction, from about 0.20 to about 0.30.

Abstract: A subject of the present invention is to provide a cosmetic for unevenness correction which has an excellent effect of concealing wrinkles and pores and correcting skin unevenness and has good compatibility with a makeup cosmetic. The present inventors have found that the cosmetic for unevenness correction which conceals wrinkles and pores and has good compatibility with a makeup cosmetic at the time of application can be easily provided by using a polyacrylate water-absorbing polymer having a specific water absorption capacity, but not a water-soluble macromolecule having a thickening effect commonly used in cosmetics, and they thus have completed the present invention.