Abstract: An apparatus for mounting surgical rails to a litter having a pair of parallel poles includes a surgical rail fixed to a clamp. The clamp is fixed to one of the parallel poles. A cross bar extends between the clamp and a second clamp fixed to the other of the parallel poles.

Abstract: A collar with a relieved area (3) strategically placed in-between the upper and lower wheelchair leg-rest attachments (2) so a leg-rest can still be removed and installed and where the leg-rest locking arm (6) can lock into place unimpeded. A second collar (4) attached directly below the lower wheelchair leg-rest attachment (2). Both collars (3 and 4) are locked into place using flat-head screws (5). Collars (3 and 4) are of sufficient size to extend horizontally beyond the typically exposed mainframe leg-rest attachments (2). When installed at both leg-rest attachment areas (2) the invention protects a wheelchair user from a laceration injury.

Abstract: A patient support includes a frame, a patient support surface supported at the frame, a display incorporated into the frame, and a user interface incorporated into the frame. The patient support frame includes a controller incorporated into the frame, which has a plurality of prompts stored therein. The user interface is in communication with the controller and may be used to select a selected prompt from the plurality of prompts stored in the controller. When a prompt is selected, the controller generates a display image or text associated with the selected prompt at the display in response to a passage of time or an input to provide a visual prompt to the user.

Abstract: A user module for a patient support apparatus is provided. The user module has a user interface operably coupled thereto. The user interface includes an input device and an output device. The output device includes a visual display including textual and non-textual elements. The non-textual elements include enhanced, graphical, and animated portions relating to one or more operational features of the patient support or to a person positionable on the patient support. The input device includes one or more touch sensors corresponding to defined regions of the visual display.

Abstract: The present disclosure describes an operating table with an operating table column and a patient bearing surface arranged on the operating table column, wherein the operating table column comprises a column cladding with at least two rigid components arranged one above the other. The operating table column is designed and configured so that all movable parts of the operating table running inside the operating table column are completely covered laterally. An intermediate space extends from the upper edge of the two components of the column cladding arranged one above the other as far as the patient bearing surface, the intermediate space being a bellows-free space.

Abstract: A device for supporting recovery of an injured upper extremity of a subject includes a support member and a retainer. The support member has an inclined surface for supporting at least a first portion of the injured upper extremity at an angle of elevation. The retainer is for immobilising at least a second portion of the injured upper extremity on the support member.

Abstract: A patient support apparatus includes a base, a seat supported by the base and a backrest pivotable between an upright position and a reclined position. In one embodiment, a backrest support member is coupled to the backrest and is adapted to move between a stowed position in which the backrest support member does not support the backrest and a deployed position in which the backrest support member does support the backrest. Movement to the deployed position occurs in response to activation of an emergency control. In other embodiments, the base includes a portion that moves into an extended position underneath the backrest when the backrest is in the reclined position. Movement of the base portion to the extended position also occurs in response to activation of an emergency control.

Abstract: Users of body bags know and live with the technical issues that come with the reality of the manipulation of the corpse of a deceased animal or human. The simple and efficient design of this body bag is free of unnecessary structures, is expandable to adapt to various body shapes depending on species and size through two expandable gussets, is leak proof through glued side folds, presents an aperture that allows access to the entire corpse through a closable flap, is permanently identifiable through a printed identification area, is the only bag necessary for transportation, storing and disposal and is compact, sturdy, and economical. With this invention, technical issues are addressed while bringing an even more dignified look to the corpse of the deceased in the body bag for the family, the public and the professionals involved in the process.

Abstract: A pressurizing device includes a main body and a pressurizing mechanism having a controlling assembly and a pressing assembly arranged on the controlling assembly and movable relative to the main body. The controlling assembly has a base body arranged on the main body and a controlling member having a pivot portion and a driving portion, the pivot portion is pivoted to the base body so that the controlling member is swingable between pressurizing and releasing positions, and the pressing assembly has a controlled portion comovable with the driving portion and a pressurizing portion for pressing an object. When the controlling member swings toward the pressurizing position, the driving portion drives the controlled portion to make the pressurizing portion press the object; when the controlling member swings toward the releasing position, the driving portion drives the controlled portion to depressurize the object.

Abstract: A compression therapy apparatus for applying therapeutic compression to a limb includes a bandage having a trunk, a first end, a second end, and a compression line between the first end and the second end. The apparatus also includes a plurality of compression control members disposed on the trunk along the compression line. Each compression control member defines a compression zone and is adapted to independently control a therapeutic compression associated with the compression zone. The plurality of compression control members are configured to provide a substantially continuous compression profile along the compression line.

Abstract: The described knee rehabilitation device can include any suitable component. In some implementations, however, it includes a sitting surface that is configured to support a user; a knee arm that comprises a leg coupling mechanism, that is pivotally coupled to the rehabilitation device, and that is configured to pivot through a range of motion; and a drive mechanism that is configured to force the knee arm through the range of motion. In some cases, the drive mechanism includes a first hard stop that prevents the knee arm from extending past a first set point, and the drive mechanism further includes a second hard stop that prevents the knee arm from being retracted past a second set point. In some cases, the device is further configured to be programmed to electronically limit the knee arm's range of motion. Other implementations are discussed.

Abstract: A portable urinal mounting assembly selectively connectable to a walker having a pair of side support assemblies including upper and lower support braces. The mounting assembly comprises an body sleeve adapted to receive a portable urinal. Front left and right straps and rear left and right straps are attached to the body sleeve. Each of the front and rear left and right straps have an end portion including an attachment device. The end portions of the straps are arranged and designed to be removably secured to the upper and lower support braces of the pair of side support assemblies.

Abstract: A magnetic conveyance system comprising a support structure having a ferromagnetic capacity and a trolley moveable upon the support structure in a plurality of directions. The trolley may include a trolley frame and at least one attractor cell disposed on the trolley frame. The at least one attractor cell may comprise a housing and at least one magnet, at least one friction reducing load spreading device, and a load transfer member disposed within the housing. The magnet may provide a magnetic attraction force between the trolley and the support structure. The friction reducing load spreading device may comprise a plurality of bearing balls circulating within a reservoir and a channel formed by the load transfer member disposed within the housing. The load transfer member may also include a bearing surface wherein a portion of the plurality of bearing balls is disposed between the bearing surface and the support structure.

Abstract: Apparatus and method using two couplings connecting a wheelchair to a walker for safely assisting a patient regaining their ability to walk. Physical therapists use the walker to train patients on walking to build strength, endurance, and balance. The couplings provide a fixed gap between the wheelchair and walker and keeps the wheelchair close to the patient. The patient can easily sit in the wheelchair, and the presence of the wheelchair minimizes the risk of falling, allows the patient to rest when fatigued, provides a sense of security, and eliminates a need for an assistance to push the wheelchair behind the patient.

Abstract: A method includes receiving an input indicative of at least one factor that contributes to the development of pressure ulcers; determining a risk score as a function of the input; comparing the risk score to a previous risk score; and at least one of activating a therapy configured to reduce the magnitude of the factor and notifying a caregiver if the risk score is greater than the previous risk score.

Abstract: A massage system includes a seat having a first surface, a first massage assembly beneath the first surface and including a first matrix of inflatable bladders, and an interface including a touchscreen. The system further includes a controller displaying an image of the matrix on the touchscreen, receiving a touch input from the touchscreen, interpreting the touch input as an indication of a desired massage sequence, and causing the first massage assembly to implement the desired massage sequence.

Abstract: A head mounted display (HMD) device including a display configured to display content; a communication processor configured to communicate with a massage chair; and a controller configured to acquire information about an urgency degree of the displayed content, and transmit a control command to the massage chair for controlling the massage chair to perform a massage corresponding to the urgency degree.

Abstract: A method of controlling a compression device controls a vent phase of a compression device having an inflatable bladder capable of being pressurized for applying compression to a part of a subject's body. The method includes delivering pressurized fluid from a source of pressurized fluid to a first inflatable bladder disposed about a portion of the subject's body and venting the pressurized fluid from the first inflatable bladder by opening a first valve. The method further includes monitoring fluid pressure in the first inflatable bladder during the venting of the first inflatable bladder. Based at least in part on the monitored fluid pressure, the first valve is selectively closed and selectively reopened to control fluid pressure in the first inflatable bladder to remain within a desired residual pressure range.

Abstract: A method of controlling a compression device controls a vent phase of a compression device having an inflatable bladder capable of being pressurized for applying compression to a part of a subject's body. The method includes delivering pressurized fluid from a source of pressurized fluid to a first inflatable bladder disposed about a portion of the subject's body and venting the pressurized fluid from the first inflatable bladder by opening a first valve. The method further includes monitoring fluid pressure in the first inflatable bladder during the venting of the first inflatable bladder. Based at least in part on the monitored fluid pressure, the first valve is selectively closed and selectively reopened to control fluid pressure in the first inflatable bladder to remain within a desired residual pressure range.

Abstract: The first embodiment of a handheld personal muscle massage device has an arm rest that reacts the compressive massage force against the forearm to allow higher massage forces than would otherwise be possible. Additionally, the roller is extended from the location of the hand to facilitate massage of areas of the lower leg without the person having to bend over to administer massage effort. The second embodiment has the same attributes as the first embodiment, with the added attribute of an adjustable angle between the two structural frameworks to allow massage access to body areas that are not accessible by the device of the first embodiment. Additionally, the device of the second embodiment folds into itself for compact storage.

Abstract: A portable roller massager includes an elongate center shaft having a longitudinal axis extending between a first end and a second end, a roller section rotatably positioned about an outer surface of the elongate center shaft and extending not entirely between the first and second ends, a first handle member movably attachable to the first end of the elongate center shaft, and a second handle member movably attachable to the second end of the elongate center shaft. The elongate center shaft, roller section, first handle member, and second handle member cooperate to form a portable roller massager for massaging and treating a person's muscles.

Abstract: A phallic vibrator is provided for stimulating female genitalia, the vibrator comprising one or more speakers, a microphone, a transmitter, and a receiver for facilitating interactive connectivity with a remotely situated user during vibratory function.

Abstract: Disclosed is a hydrotherapy method suitable for diagnosis and treatment of a subject, as well as headgear suitable for use during hydrotherapy diagnosis and treatment.

Abstract: Disclosed are an apparatus, a method, and/or a system of targeted myofascial release through use of a rolling track. In one or more embodiments, an apparatus for targeted myofascial release of a human body, muscles, and fascia includes a rolling track with one or more supports forming a support contour permitting a ball to roll along the rolling track while the body exerts force against the ball. The support contour transitions into a rolling surface so the ball can be guided out of the rolling track for the rolling surface and then guided back in. A friction means such as a lip and/or friction surface retains the ball in the rolling track. The rolling track is securable relative to the rolling surface via a mount. The adjustment track may have two or more adjustment positions for repositioning along the rolling surface and/or a pivot to adjust a track orientation.

Abstract: A massage device sized and shaped to be individually applied to the user's skin or clothing in order to apply pressure to selected trigger points on the body, the device having a base formed of a first compliant material, and a dome-shaped body extending from the base and formed of a second compliant material that is harder and less compliant than the first compliant material. In addition, a flexible filament having a substantially planar surface can be used to support one or more massage devices and apply the massage devices to selected trigger points on the body.

Abstract: Embodiments of dermatological cell treatment are described generally herein. Other embodiments may be described and claimed.

Abstract: A bubble manufacturing container 20 of the present invention includes: a container body 21 having an opening portion; and a rubber stopper 221 provided on the opening portion of the container body 21. The rubber stopper 221 is constituted so that the bubbles 1 of an inside of the container body 21 are able to be taken by piercing an injection needle. It is preferred that the bubble manufacturing container 20 has a fastening portion 222 provided on the rubber stopper 221, having an opening and sealing the container body 21 with the rubber stopper 221. Furthermore, it is preferred that the container body 21 mounts a weight portion.

Abstract: A single-use bag (32) and dispensing system (30) for storage of liquid or frozen media and for dispensing the media are disclosed. A single-use bag (32) is composed of materials that can withstand the temperatures required for dry heat sterilization and, further, includes specialized clamps (40, 140) that accommodate the materials and construction techniques necessary for constructing the single-use bag (32) for restriction and isolation of flow from the single-use bag (32).

Abstract: A connector for a medical container comprises a connector element to be attached to the medical container for providing a port to the medical container. The connector element comprises a head section and a pinch-off section adjoining the head section. The head section comprises an opening and the pinch-off section encloses an inner lumen being in fluid connection with the opening of the head section for proving a fluid path through the connector element. The pinch-off section is flexibly deformable for pinching off the fluid path. A closure element is attachable to the head section for closing the opening of the head section, and a pierceable membrane element is held between the head section of the connector element and the closure element. A deflection element extends from the head section towards the inner lumen for deflecting a needle of a delivery device when piercing the membrane element.

Abstract: A containment and transfer device for use with highly active or sensitive compounds, comprising a sleeve or a bag with one or more flexible walls, a first sanitary clamp, an endcap, a second sanitary clamp and a compression clamp. The sleeve or bag has a first end for connection to a container, and a second end for (a) connection to a storage or mixing vessel at the discharge location, or (b) connection to an endcap for transportation. The flexible walls surround and define an internal passageway in that permits compounds in the first end of the sleeve or bag to pass into the second end of the sleeve or bag. The compression clamp compresses the flexible walls of the sleeve or bag together to produce a barrier across the internal passageway, preventing the highly active or sensitive compound from flowing into the second end of the sleeve or bag during packing, transporting and discharging the device.

Abstract: The present invention relates to a sealing device to seal a container, the sealing device including: a tip that defines an internal passage leading to an opening and is designed to allow connection to a collection member such as an enteral syringe, a non-return valve that is associated with the tip and is designed to open during collection of the contents of the container using the collection member, at least one air-return port, and an antibacterial filter associated with said at least one port.

Abstract: The disclosure encompasses systems and methods for performing high temperature and high humidity curing of tablets using air flow delivered from a recirculating air handler to a pan coater of a tablet coating device. The recirculating air handler may be integrated into a preexisting tablet coating device so that the air flow may be delivered by the preexisting air handler or by the recirculating air handler as desired.

Abstract: A pill crushing device pulverizes pills and then transfers the pulverized pills out of the device with minimal transfer loss and spillage. The device includes a pill chamber and may include a storage portion. The pill chamber forms a threaded connection with the storage portion that enables detachment. The storage portion stores the pill and operates the crushing mechanism. The pill is pulverized in the pill chamber. The pill chamber is disposed beneath the storage portion. A first spoon retains the pill and carries the pulverized pill out of the chamber along a longitudinal opening of the pill chamber. An optional second spoon detachably attaches to the first spoon to carry supplemental compositions to the pulverized pill.

Abstract: An automatic medicine retrieving device includes a medicine tray, a medicine box, and a driving mechanism. The medicine tray includes a bearing plate defining an exit port and a medicine separating member rotatably positioned on the bearing plate. The medicine separating member has medicine separating areas and a positioning area. Medications in the form of pills are positioned on the bearing plate and received in the medicine separating areas. The medicine box is opposite to the exit port. The driving mechanism drives the medicine separating member to rotate from being opposite to the exit port, bringing the medicine separating area to a position opposite to the exit port. A pill in the medicine separating area then passes through the exit port to fall into an accepting mechanism.

Abstract: Techniques provided herein are directed toward accurately determining when an item is removed from a blister pack by utilizing capacitive sensors. The capacitive sensors may be positioned on each blister of the blister and may detect the presence of the skin of the finger and/or the whether the blister has been deformed, which can occur when an item is removed from the blister. Some embodiments may determine whether skin was detected at the time of extraction to determine whether extraction was intentional.

Abstract: A feeding assembly generally comprises a container having an open top and defining a liquid chamber therein for holding a liquid. A collar assembly defines a closure for the open top of the container upon assembly with the container. The collar assembly includes a collar releasably securable to the container and a nipple coupled to the collar and having an opening through which liquid exits the feeding assembly during feeding. A vent assembly is positionable at least in part on the open top of the container and is configured to facilitate venting of the container to atmosphere as liquid exits the feeding assembly during feeding. The vent assembly is disposed intermediate the container and the nipple and has a vent tube through which air is able to flow from external of the feeding assembly to the container during feeding.

Abstract: The present disclosure provides a method for producing a customised teat product for a subject, the method includes the initial step of performing a 3D scan of at least a nipple region of the subject's breast to create a 3D model of the nipple region. In the next step, a 3D product model for a teat product is created, incorporating a teat that corresponds in shape to at least the nipple region of the subject, based on the 3D model of the nipple region. In the final step, a physical teat product is generated based on the 3D product model using an additive or subtractive manufacturing apparatus.

Abstract: Devices and methods for delivering non-pathogenic, intestinally beneficial bacteria to a patient having a feeding tube. Examples of non-pathogenic, intestinally beneficial bacteria that could be used include Bifidobacterium species and Lactobacillus species. In one embodiment, the bacteria is contained in a bacteria infusion device that comprises: (a) an internal chamber; (b) an outlet in communication with the internal chamber; and (c) the non-pathogenic, intestinally beneficial bacteria contained in the internal chamber. Another embodiment is a feeding tube comprising a flexible tubing and coating on the outer surface of the flexible tubing. The coating comprises an antimicrobial agent. Also disclosed are methods of administering a non-pathogenic, intestinally beneficial bacteria to a patient.

Abstract: A hygienic pacifier includes a multi-durometer faceplate defining a nipple access opening and a substantially spherical shield joining a nipple to the faceplate and being movable between a recoiled storage position in which the shield substantially surrounds the nipple and an extended use position in which at least a portion of the nipple projects through the nipple access opening and is exposed for use. The nipple access opening is pliable to facilitate withdrawal of a bulbous core of a mold used to form an interior of the shield during a molding process.

Abstract: A pacifier and a method of making a pacifier. Two or more separate silicone-based materials are joined together with a compression mold such that the pacifier defines a unitary structure where gaps and related crevices associated with multi-piece pacifier construction are avoided while still permitting artwork, differing colors or other aesthetically-pleasing indicia. In one form, one grade of silicon may be utilized in a region of the pacifier that is placed within a baby's or child's mouth, while another grade of silicone material may be used in a region of the pacifier that is not normally associated with placement within a baby's or child's mouth. The aesthetically-pleasing indicia that is formed in or on the pacifier is achieved without recourse to painting, labels, appliques, embossing, decals, stickers or other affixable or markable medium.

Abstract: A method for producing elliptical, needle-shaped, or rod-shaped polymer particles satisfying (1)-(3) below includes a step in which a synthesis solution including water, a mixed solvent of a hydrophilic organic solvent and a hydrophobic organic solvent, a polymeric stabilizer, a polymerization initiator, and an unsaturated monomer is heated, and, at least after the heating has started, the pH of the synthesis solution is adjusted to 5-9 inclusive to perform solution polymerization: (1) the average (LAV) length (L) in a two-dimensional projection diagram obtained by irradiating the particles with light from a direction orthogonal to the longitudinal direction is 0.1-80 ?m; (2) the average (DAV) breadth (D) in the two-dimensional projection diagram obtained by irradiating the particles with light from the direction orthogonal to the longitudinal direction is 0.05-40 ?m; and (3) the average (PAV) aspect ratio (L/D) calculated from the length (L) and the breadth (D) is 1.5-30.

Abstract: The present disclosure describes and enables a method of lengthening the appearance of a subject's eye lashes through use of a cellulosic fiber in combination with transplanting gel and a system therefor. The disclosed process and system allows a user to lengthen their eyelashes through use of an only semisynthetic naturally derived fiber such as rayon, which allows a user to avoid use of a fully synthetic fiber such as nylon. The method of the present disclosure comprises applying mascara to a subject's eyelashes and then applying the fibers with a brush while the mascara is still wet. In some cases a transplanting gel is applied first (which may comprise mascara) and then mascara can be applied after the fibers have been applied to the subject's eyelashes. In additional cases, the fibers have also been treated prior to use.

Abstract: A composition for preventing hair loss or promoting hair growth comprising Decanal or pharmaceutically acceptable salt thereof as an active ingredient is provided. In particular, the composition relates to a quasi-drug, a cosmetic composition, a health functional food composition, and a pharmaceutical composition for preventing hair loss or promoting hair growth, which exhibits an excellent and stable effect on hair growth and hair growth, even while comprising a natural compound which has no side effect even in long-term administration in a chronic disease as an active ingredient.

Abstract: Antifibrinolytic agents are administered to a human individual to treat fine lines, wrinkles and overall skin tone of the face and body, as well as inflammation and tissue degradation effects.

Abstract: The invention relates to a new composition in the form of a translucent, advantageously transparent, gel, without triethanolamine, comprising at least a fatty body in the form of an oleic acid an aqueous phase; and a base or a mixture of bases. The invention also relates to compositions, advantageously cosmetic compositions, comprising said gel base, such as a shaving gel. The invention also relates to a method for preparing said gel base, a shaving method, the use of said gel base and a shaving kit.

Abstract: The present invention relates to non-aerosol shaving compositions which are free of propellants, and methods of preparing and using such shaving composition. In particular, the present invention relates to a non-aerosol, propellant-free composition comprising: (i) at least two C14 to C16 carboxylic acids or an alkali metal salt thereof; (ii) at least one compound of general Formula (I) R—O—[—CH2CH2O—]n—CH2CO2H??(I) or an alkali metal salt thereof, wherein R represents a saturated, straight- or branched-chain C10 to C18 alkyl group; and n represents an integer between 4 and 12; (iii) polyvinyl pyrrolidone; and (iv) water.

Abstract: The present invention is directed to a composition comprising a combination of surfactants for cleansing keratin fibers, a method for cleansing, use of the composition for cleansing, and kit-of-parts thereof. It has been found that the combination of two anionic surfactants, an amphoteric surfactant, and a diol compound provide a rich foam and superior color retention on pre-colored hair.

Abstract: A hair dye removal composition includes a cleansing agent, a humectant, a rheology modifier, arginine, cysteine, and aminomethyl propanol. The cleansing agent includes between approximately 60 wt % to approximately 80 wt % of the hair conditioning composition, the humectant includes between approximately 10 wt % to approximately 20 wt % of the hair conditioning composition, the rheology modifier includes between approximately 2 wt % and approximately 10 wt % of hair conditioning composition, the arginine includes between approximately 0.05 wt % and approximately 0.8 wt %, the cysteine includes between approximately 0.02 wt % and approximately 0.08 weight %, and the aminomethyl propanol includes between approximately 1 wt % and approximately 6 wt % of the hair conditioning composition. The cleansing agent may include sulfated castor oil, the humectant may include propylene glycol, and the rheology modifier may include acrylates/steareth-20 methacrylate copolymer.

Abstract: A cosmetic composition is disclosed comprising a synthetic optical brightener and a naturally-derived optical brightener. Both brightener classes absorb and emit light at different wavelengths and possess in combination a superior effect. The combination enhances color brilliance on keratin fibers under daylight and artificial light conditions.

Abstract: An aqueous shear-thinning personal care composition comprising: (a) at least 3 wt % of a sulfonate compound of general formula where R1 represents a C8-22 alkyl group alkyl group; R2 represents a C1-4 alkyl group; each of R3, R4 and R5 independently represents a hydrogen atom or a C1-4 alkyl group; and M+ represents a sodium or potassium cation; (b) at least 3 wt % of an amphoteric or zwitterionic surfactant; (c) at least 10 wt % of water; and (d) at least 0.5 wt % of an additional component in the form of particles or droplets suspended in the composition. The composition is stable in an aqueous environment and can be formulated with a wide range of additional components.