Abstract: The specification relates to a mobile exerciser. The mobile exerciser can include a mobile exerciser frame; a foot rest assembly attached to the mobile exerciser frame having a working position and a stored position; and a pedal assembly attached to the mobile exerciser frame having a working position and a stored position. The mobile exerciser can be converted from a push mode to a pedal mode by moving the foot rest assembly into a stored position and the pedal assembly into a working position and the mobile exerciser can be converted from a pedal mode to a push mode by moving the foot rest assembly into a working position and the pedal assembly into a stored position.

Abstract: An auxiliary drive device for a wheelchair has at least one electrically driven drive wheel and a coupling mechanism for coupling the auxiliary drive device to the wheelchair. The coupling mechanism includes a movable locking element which is movably supported in the coupling mechanism. The movable locking element can be in a locking position in which it causes locking in a positive-locking manner so that the auxiliary drive device is coupled to the wheelchair and, by operation of a handle, the locking element can be moved in a release position in which uncoupling of the auxiliary drive device from the wheelchair is possible.

Abstract: An auxiliary drive device for a wheelchair has at least one electrically driven drive wheel and a coupling mechanism for coupling the auxiliary drive device to the wheelchair. The electrically driven drive wheel is supported at a steering shaft and freely pivotable with respect to the auxiliary drive device. The steering shaft is arranged such that, when the auxiliary drive device is coupled at a wheelchair ready to be operated, a castor is provided for the electrically driven drive wheel.

Abstract: Disclosed is a device for converting a manual wheelchair into an electronic wheelchair is provided. The device includes a joystick, a communication unit, a motor, a retractable friction roller, an engagement unit and a power source. The joystick is operably connected to a communication unit. The communication unit is operably connected to a motor. The motor includes an axle connected to a rotor. The retractable friction roller is mounted on the axle. The roller is placed in contact with a wheel of a manual wheelchair. The engagement unit is attached to the manual wheelchair to detachably attach the friction roller and the wheel. The power source is operably connected to the motor and the joystick.

Abstract: A modular power base for a wheelchair, the modular power base includes a leg module. The leg module includes an upper leg portion comprising a distal end and a proximal end. The proximal end is configured to be detachably and rotatably coupled to a seat portion of the wheelchair. The leg module also includes a lower leg portion having a first end and a second end, the first end of the lower leg portion being rotatably coupled to the distal end of the upper leg portion. The leg module also includes a first wheel rotatably coupled to the distal end of the upper leg portion and to the first end of the lower leg portion and a second wheel rotatably coupled to the second end of the lower leg portion.

Abstract: A swing arm assembly for a foldable wheelchair consisting of a camber tube and adapters is disclosed. The adapters mount to the frame of the wheelchair and receive the ends of the camber tube. One end of the camber tube is pinned into an adapter such that it pivots. The other end is pinned in an adapter using a quick release pin. The camber tube improves the stability of the foldable wheelchair. When desired to fold the wheelchair, the quick release pin is removed and the camber tube is rotated approximately 90 degrees, thereby allowing the wheelchair to fold. The adapters may be mounted to the wheelchair frame or to stub axles if used. The swing arm assembly adds substantial stiffness and stability to a folding wheelchair.

Abstract: An articulating assembly for an adjustable bed has side supports received on side rails of a bed frame. A first axle extends between the side supports and a second axle extending between the side supports defining a fixed center section. An upper body support frame has a first torque tube concentrically received on the first axle. A thigh support frame has a second torque tube concentrically received on the second axle. A first actuator assembly supported in the center section is operably attached to rotate the first torque tube to articulate the upper body support frame over a range of positions from a horizontal unarticulated position to a fully articulated position. A second actuator assembly supported in the center section is operably attached to rotate the second torque tube to articulate the thigh support frame over a range of positions from a horizontal unarticulated position to a fully articulated position.

Abstract: A method of determining a lifting event of a person lifting apparatus is provided. The method includes receiving one or more of (i) current load information from a current measuring device that is indicative of current drawn by an actuator operatively connected to a lifting strap of the person lifting apparatus; (ii) strap position information from a position sensor that is indicative of a paid out length of the lifting strap of the person lifting apparatus; and (iii) weight information from a weight sensor that is indicative of a load supported by the lifting strap of the person lifting apparatus. A computing device comprising a processor using logic is used to identify at least one of a raising event, a repositioning event and a lowering event based on the one or more of the current load information, strap position information and weight information.

Abstract: A patient lift system includes a motor and a drum. The drum is operably coupled to the motor. The drum can be selectively driven to rotate by the motor. A housing surrounds at least the motor and the drum. A load-bearing member is provided that includes a first end and a second end. The first end of the load-bearing member can be operably coupled to at least one of the housing and the drum. The second end of the load-bearing member can be operably coupled to a patient support assembly. An electrically conductive member can be positioned within the load-bearing member. A user interface is configured to actuate the patient support assembly in vertical and horizontal directions.

Abstract: A person lifting apparatus includes a first lifting strap feeding device including a first drum and a first lifting strap wound on the first drum. A second lifting strap feeding device includes a second drum and a second lifting strap wound on the second drum. A controller is communicatively coupled to the first lifting strap feeding device and to the second lifting strap feeding device. The controller includes logic that controls operation of the first lifting strap feeding device and the second lifting strap feeding device based on a comparison of current draws of the first lifting strap feeding device and the second lifting strap feeding device.

Abstract: A patient isolation unit (PIU) for use in marine rescues. The PIU of this invention is useful to safely transport personnel exposed to, or potentially exposed to, an identified and/or known infectious agent or chemical warfare agent (CWA) on marine vessels and/or aircraft such as Coast Guard boasts, cutters and aircraft. The PIU has a generally tapered tubular shape compatible with wire rescue baskets conforming in shape to the human body and into which an injured, sick, or disabled person can be safely strapped, such as the Stokes litter rescue basket for hoisting and fit in rotary wing aircraft.

Abstract: An anatomy table for use in autopsies and dissections comprises a base and an immersion storage tank arranged in the base. The anatomy table further comprises a dissection lid arranged on the base, wherein the dissection lid covers the immersion storage tank in its closed position. The table also comprises a hinge secured between the dissection lid and a top edge of the base, wherein the dissection lid rotates about the hinge between a first and second position, wherein the first position allows for access to the body stored in the anatomy table immersion storage tank while the second or closed position of the dissection lid allows for dissecting to occur directly on top of the anatomy table. This may allow for a two in one table to be arranged within a lab, such that autopsy work and dissection or cutting may be performed with the same piece of equipment, wherein two pieces of equipment are usually used within the lab for these procedures.

Abstract: An integrated and modular air and lighting plenum that is the primary directional lighting mounting apparatus and laminar flow diffuser of an HVAC system in a healthcare setting. The plenum provides laminar air flow from the ceiling to the room in which it is located in accordance with HVAC requirements for healthcare environment settings, by using a plurality of cylindrical airflow outlets. The use of cylindrical airflow outlets promotes laminar airflow by reducing sharp boundaries that induce turbulence (e.g., the corners of rectangular or square outlets) and creates a highly sterile environment around the patient and staff in the operating room. The surgical lights used in the integrated air and lighting plenum allow the beam direction, spot size, focal point, brightness, and color temperature of the emitted light to be controlled.

Abstract: A patient warming system for stabilizing and/or heating and cooling a patient includes a plurality of solid-surface sections arranged for attachment to a surgical table and a warming pad layer comprising a plurality of warming pads configured for removable connection to the plurality of solid-surface sections. At least one of the plurality of solid-surface sections includes a power connector for connection to an external power source. Each warming pad of the plurality of warming pads includes a foam insulation layer, a distributed heating element layer having a warming-pad power connection for connection to the power connector, an isothermal layer, and a flexible waterproof layer. Power supplied to the warming-pad power connection of the distributed heating element layer of the respective warming pad can be used to provide a user-selected uniform temperature over the surface of the flexible waterproof layer in order to prevent hot spots.

Abstract: A medical support arm may include a holding end, a coupling end, a coupling-end pivot joint for swiveling the support arm about a pivot axis (A1) and tilting the support arm about a tilt axis (A2), and a clamping mechanism with which the pivot joint can be locked or released as desired. The pivot joint allows the support arm to rotate exclusively about the tilt axis (A2) and the pivot axis (A1). A tilting device may have a tilting element and a cylindrical sliding surface on which the tilting element is seated. A pivot mechanism can have a guide ring and at least one ring guide surface that receives the guide ring. A tilting element, as part of the clamping mechanism, may be provided as a gripper clamp that secures both the tilting device and the pivot mechanism against rotation by clamping the central body.

Abstract: Provided is a sporting apparatus for automatically adjusting cervical vertebrae, which automatically moves while a user rests or sleeps with the apparatus, so as to ensure a user naturally maintains a good lying position. The sporting apparatus includes a rail assembly, a swing panel including a roller part inserted into the rail assembly to slidably move, and a support body which is coupled to and stably placed on an upper surface of the swing panel and on which a user's neck and head are stably placed. The apparatus makes an internal movement of an upper cervical vertebral portion to realign the cervical vertebrae, thereby inducing alignment and balance of the user's neck to be automatically achieved, and also inducing alignment and balance exercise of the head, a cervical vertebral portion, and an upper thoracic vertebral portion to be naturally conducted.

Abstract: A method and apparatus for assisting walking of a user is provided. Information related to a motion of a user wearing a walking assistance apparatus is measured by an inertial measurement unit (IMU), a gait phase of the user corresponding to the measured information is predicted using data learned in advance through machine learning, an assistance torque to be provided to the user is determined based on the predicted gait phase, and a driver is controlled to output the assistance torque.

Abstract: The disclosure belongs to the technical field of lower limb exoskeleton, and specifically discloses a hip-knee passive exoskeleton device based on clutch time-sharing control, comprising a waist support subassembly, connection subassemblies, thigh subassemblies, clutch subassemblies, shank subassemblies and elastic member subassemblies, the waist support subassembly is configured to be connected to the waist, the connection subassemblies are configured to include two connection subassemblies which are arranged in bilateral symmetry on two sides of the support subassembly, the thigh subassemblies are configured to include two thigh subassemblies which are respectively connected to the two connection subassemblies, the clutch subassemblies are configured to include two clutch subassemblies which are respectively mounted on the two thigh subassemblies, the shank subassemblies are configured to include two shank subassemblies which are arranged in bilateral symmetry below the two thigh subassemblies, the elastic

Abstract: The present invention provides a plurality of training modes for an electric walking rehabilitative device, including: constant speed mode, adaptive speed mode, strengthening push/pull mode, weight bearing mode, high frequency disturbance random speed mode, low frequency perturbation variable speed mode, direction control by handle push/pull forces mode, and slope mode, to improve the user's walking speed, muscle strength, balance, speed adjustment, direction control and slope walking.

Abstract: The foam generator for inverted compression receptacles according to the present invention is configured such that liquid contents pumped by an internal pressure as a result of directly compressing an inverted compression receptacle (100), having the liquid contents stored therein, are mixed with air in a gas-liquid mixing chamber (S) and, at the same time, directly discharged in the form of foam. That is, direct compression of the inverted compression receptacle (100) allows the liquid contents to be instantly discharged in the form of foam, thereby further improving product responsiveness. In particular, the present invention is capable of further improving the convenience of use thereof, since the contents can be discharged in the form of foam by directly compressing the inverted compression receptacle (100) merely with one hand.

Abstract: A unitary manipulation instrument for use by a practitioner on soft tissue of a person formed of a pair of planar sections, each section including an outer tissue engaging surface. The sections are interconnected and each section is located in a different spatial plane such that the sections are oriented at 90 degrees one with respect to the other.

Abstract: This document describes devices for mitigating or eliminating alopecia (hair loss) resulting from chemotherapy treatments and methods for their use. For example, this document describes headband devices that deliver localized pressure to portions of the patient's scalp to cause physical obstructions of scalp arterial circulation to mitigate alopecia. In some embodiments, localized pressure is exerted on frontal arteries, temporal arteries, and/or occipital arteries to reduce the blood flows therethrough.

Abstract: A system for mechanical stimulation of nasal tissues of a patient comprises a catheter assembly connected to a fluid flow generator. The catheter assembly comprises a generally oblong inflatable catheter defining at least one catheter volume and the catheter is configured to assume a shape suitable for insertion into a nasal cavity and to assume a shape suitable for stimulating a nasal tissue. The catheter assembly also comprises a tube part comprising at least one lumen configured to establish fluid flow connection between said fluid flow generator and catheter. Preferably, the catheter assembly comprises at least one vent for releasing fluid or permitting fluid to escape from the generated fluid flow. The fluid flow generator of previous aspects of the invention is configured to generate at least one of a smooth continuous flow, an oscillating flow and a pulsating flow.

Abstract: A therapeutic device includes sensors for collecting biometric health-related parameter information, such as a person's vital signs, during a therapy session for a particular user. A therapeutic program includes an artificial intelligence learning algorithm that uses the biometric health-related information for a particular user acquired during one or more training periods to customize therapeutic parameter values of a therapeutic program to deliver a specialized massage/therapy session that minimizes detriment, and maximizes benefit, to a user by comparing biometric health-related information collected during a therapy session to criteria that corresponds to the health-related information. Biometric health-related information may be stored to a database either local or remote relative to the therapeutic device.

Abstract: Disclosed embodiments provide a pressure field stimulation device having an arm adaptable in shape. Embodiments of the improved stimulation device include a cup, a driver, and an arm. The arm is flexible in such a way that it holds its position when bent. The adaptable arm may be a handle, a member insertable into the vagina or rectum, or a connection member between the pressure field stimulator and another stimulator. In use, a user positions a rim of the cup such that an opening to the cavity is over an area to be stimulated (e.g., the clitoris). A sealed-, or substantially-sealed, chamber is formed by the cavity walls and the user's skin (surrounding the clitoris). A pressure field is generated in the chamber, providing sexual stimulation to the clitoris. The user can adjust the placement of the cup by bending the arm.

Abstract: A percussive massage appliance has a general Y-shape, with first and second handle portions being suitable for being held by first and second hands, respectively, of a user, with the percussive massage head reciprocating along an axis that lies in a major arc defined by the two handle portions. One use for the device is so that a user can grip the device with both hands while delivering a percussive massage to his own lower back muscles. The device has a rotation mechanism such that the user can rotate the reciprocation axis through an arc of about 120 degrees relative to the handles, and an extension handle mates with one of the handle portions, providing great versatility to the user.

Abstract: Embodiments of the improved stimulation device include a cup and a driver. The cup has a cavity surrounded by a rim. The driver comprises a plate disposed on an underside of the cup, a cam disposed adjacent to the plate, and a motor mechanically coupled to the cam. The driver is configured to intermittently vary a volume of the cavity of the cup from a first volume to a second volume without returning the cup from the second volume to the first volume. In some embodiments, the cup returns from the second volume to the first volume, in between intermittent varying from the first volume to the second volume, due to the resilient nature of the material of the cup and/or the configuration of the cup. This varying of the volume between the first and second volumes creates a pressure field in a chamber formed by the cavity and a user's skin.

Abstract: Disclosed embodiments provide an improved stimulation device. Embodiments of the improved stimulation device include a cup and a driver. The cup has a cavity surrounded by a rim. In use, a user positions the rim such that an opening to the cavity is over an area to be stimulated (for example, the clitoris). A sealed-, or substantially-sealed, chamber is formed by the cavity walls and the user's skin (surrounding the clitoris). A pressure field is generated in the chamber without generating a pressure below a reference pressure, which is gauge pressure reading of zero. In some embodiments, this is achieved by a driver configured to vary a volume of the cavity in such a way that the varied volume is not larger than an initial volume. In some embodiments, the stimulation device is a sex toy. In some embodiments, the stimulation device is a medical device.

Abstract: Disclosed embodiments provide an improved stimulation device, including a cup and a driver. The cup has a cavity surrounded by a rim. In use, a user positions the rim such that an opening to the cavity is over an area to be stimulated (for example, the clitoris). A sealed- or substantially-sealed, chamber is formed by the cavity walls and the user's skin (surrounding the clitoris). A driver is configured to vary a volume of a cavity of a cup from a first volume to a second volume. The cup returns from the second volume to the first volume, in between intermittent varying from the first volume to the second volume, due to a buckle region wall of the cup springing out. The varying of the volume creates a pressure field in the chamber. The springing out produces a “thud” force, also used intechangably with “thump” force.

Abstract: Embodiments of the invention relate to a pressure field stimulation device including a sheath having an integrated cup. The sheath and cup are together formed of (or consist of) a single piece of material. The pressure field stimulator has a cup and a driver, where the driver is configured to vary a volume of the cup. The pressure filed stimulator has a housing that has an opening therein with an edge on which a portion of the cup rests when installed. The sheath is tightly bound to the housing such that a driver can make contact with the cup. In some embodiments, the pressure field stimulator has a shaft portion, which may include a second stimulation device. The sheath can be bound over the shaft portion as well as the pressure field stimulator housing.

Abstract: An adjustable stimulation device is provided. Embodiments comprise a stimulator having a roller disposed adjacent a sheath. The roller presses the sheath against the G-spot or prostate of the user, providing stimulation. An arm having a first end is mechanically coupled to the shaft. A position of the stimulator and the arm with respect to one another is adjustable. The arm is flexible such that it holds its shape when bent. The shape of the arm is adjustable. The arm is adaptable into a plurality of shapes. In some embodiments, there is a handle or a second stimulator attached to a second end of the arm.

Abstract: Disclosed embodiments provide a massager having at least one expandable chamber. In some embodiments, there is provided an expandable shaft chamber that is inflatable to push a stimulator towards the G-spot of the user to increase contact pressure in that area. This inflation can also allow for a hands-free experience by expanding the width of the shaft inside the vagina for a snug fit tight against the vaginal or rectum walls. In some embodiments, there is provided an expandable ring chamber that is inflatable to securely hold a massager device inside the vagina or rectum, allowing for a hands-free experience.

Abstract: Described herein is a pad for administering a cardiac massage, including: a first layer configured for being applied on the chest of a patient; and a second layer coupled to said first layer, the second layer being configured for receiving an action by an operator administering the cardiac massage, where said first layer is made of a material having an average value of the transmitted force, in an impact test at ambient conditions according to EN1621-1 at an energy of 10 J, lower than 25 kN.

Abstract: A hot plasma disease treatment system includes a mutually connected control system and at least one power supply system, the control system and the power supply system respectively being connected to and controlling a medium gas modulation system, at least one cooling system, at least one hot plasma generator, at least one plasma processing apparatus, a plasma treatment cabin, a detection feedback system, and a tail gas processing system, the medium gas modulation system being connected to the hot plasma generator, the cooling system being arranged on the hot plasma generator, the hot plasma generator and the plasma processing apparatus being connected, the plasma processing apparatus and the plasma treatment cabin being connected, and the plasma treatment cabin and the tail gas processing system being connected.

Abstract: An improved portable massage device includes a first housing including a plurality of acupressure protrusions formed on an upper surface thereof and spaced apart from each other. The portable massage device further includes a battery supplying power, a motor connected to the battery to be turned on/off, and a rotating member mounted to surround the motor. In addition, the portable massage device includes a shield plate provided on the rotating member, at least one magnet detachably attached to the shield plate so that the shield plate vibrates when the motor rotates, a case accommodating the motor, a first switch connected to and controlling the battery to be turned on/off, and a second housing detachably combined with the first housing. The battery and the case are accommodated in the first housing or the second housing.

Abstract: A method includes performing, by a processor: providing a database that contains records corresponding to a plurality of drug product packaging systems, the records in the database being accessible through a common database management system, receiving a packaging order for at least one drug product, evaluating at least one criterion for fulfilling the packaging order, and identifying one of the plurality of drug product packaging systems to package the at least one drug product based on evaluating the at least one criterion.

Abstract: A medication bottle includes an outer container wall, an inner container wall and a fluid, such as an aversive liquid, located between the walls. In another aspect, the fluid is located within separate compartments or channels located between the walls where the walls contact or are secured to each other. A further aspect provides a removeable cap including multiple sensors, at least one of which is a biometric sensor.

Abstract: A storage device having a cylindrical housing with a first end, a second end and cylindrical side, wherein the ends are closed and the cylindrical side has one or more apertures. There is a cylindrical cover for each of the one or more apertures that slidably fit over the cylindrical side of the cylindrical housing and able to slide about the cylindrical side exposing or covering the one or more apertures.

Abstract: A plastic container product, in particular produced by a blow molding, filling and sealing method, comprising a container body (10) having a content of the container and an adjoining head part (12) which delimits an extraction area (14), which is closed by a head membrane (16), which has a connecting seam (38), which passes through a plane (20) spanned by the head membrane (16) and separates at least two penetrable areas (22, 24) on the free end face (26) of the head membrane (16) from each other for extracting the content of the containers, characterized in that the connecting seam (38) seen on the free end face (26) of the head membrane (16) has a course of the seam (36) at least partially deviating from a fictitious rectilinear course (32) extending within this plane (20), which is longer than the rectilinear course (32) and at least partially comprises the penetrable areas (22, 24).

Abstract: The present disclosure relates to aseptic connectors with integrated wireless connectivity. For example, an example system may include a removable clamp configured to secure a first portion of an aseptic connector to a second portion of the aseptic connector. The removable clamp may include a housing, a controller disposed within the housing, a rechargeable battery disposed within the housing, a wireless radio disposed within the housing, and a sensor plug receptacle configured to receive a sensor plug coupled to a sensor of the aseptic connector. The controller may be configured to determine a sensor output of the sensor and to transmit the output using the wireless radio.

Abstract: In some embodiments, a medical fluid connector is configured to receive an emitter of therapeutic agents to be emitted into a fluid pathway within the connector, the medical fluid connector comprising a proximal female end, an intermediate region, a distal male end, and a fluid pathway extending from the proximal female end, through the intermediate region, to the distal male end. A retaining structure is positioned within the intermediate region. The retaining structure is configured to securely receive an emitter of one or more therapeutic agents in a position and orientation where the fluid pathway is configured to convey fluid moving longitudinally through the fluid pathway directly into a proximal region of the emitter, around one or more lateral surfaces of the emitter, and toward the distal male end.

Abstract: A medication compounding system is described that is capable of receiving one or more medications and diluents and that includes an array of moveable transfer cartridges to access a medication container and to transfer medication. The transferred medication may be joined with a diluent to form a compounded medication. The resulting compounded medication may then be directed to a filling port where a compounded medication container may be coupled. A second medication container may align with a second transfer cartridge to transfer a second medication. Because the device may comprise one or more medications and diluents, a series of compounded medications may be created using an individual transfer cartridge for each medication.

Abstract: A single-use nesting cup for use with mechanical comminution devices having a spinning drive mechanism for pulverizing pills into powder is disclosed. Each cup has a textured base surface that provides for a more efficient grinding and crushing of pills inserted between two such cups when an upper cup is spinningly brought to bear down on a bottom cup. The textured surface of each cup base has a symmetric three-dimensional wave design with each wave arcing along a curve from an outer cylindrical wall of the cup spiraling in toward a center point of the base of each cup. The crest and troughs of each wave act as grinding edges while the overall symmetric wave design acts to maintain the one or more pills and it's powdered form in the center of the bottom cup.

Abstract: A dispenser device for dispensing fluids is described. The dispenser can include a reservoir cap that can directly attach to and replace the screw top cap of traditional screw top bottle. The reservoir cap includes an air reservoir that can facilitate movement of the fluid through the device. The reservoir cap is coupled to a dispenser that is configured to receive the fluid from the cap. The dispenser can be detached from the cap and used to directly dispense the fluid.

Abstract: A computerized pill intake reminder device is disclosed. The computerized pill intake reminder device is used for storing pills, detecting the number of pills in each pouch of the blister pack, inventory management, reminding users to take their medication on time, alerting by providing an audible or a visual alarm if the medications are not taken on time and as a secondary mechanism alerting their caregiver if the user has not responded to the alert and taken the medication on time. The device includes a top housing and a bottom housing that can be rotated about each other to form a closed and sealed module. It also includes a processor that is communicatively coupled through an electronic circuit to a plurality of electronic components housed within the pill intake reminder device. These include a speaker, microphone, infrared sensors, cameras, LED lights, microphone, RFID scanner, non-volatile memory, transmitter, and a receiver. The LED lights can be programmed with various colors.

Abstract: Improved feeding set connectors and cassettes are disclosed for use with peristaltic infusion pumps for safely delivering enteral nutritional fluids to a patient. The connectors provide an easy to use “pump-to-set” integration or “keying” system for specific reusable infusion pumps and their matching feeding sets, and can be utilized by medical professionals having various skill levels. The inventive feeding set cassettes can prevent accidental free flow of enteral fluids into a patient, even upon inadvertent release of the connector from the pumping mechanism.

Abstract: A feeding set for use with a peristaltic enteral feeding pump to deliver nutritional liquid fluid to a patient includes a container having nutritional liquid. A conduit assembly includes tubing placeable in fluid communication with the container and adapted for mounting on the enteral feeding pump. The tubing provides a fluid pathway for delivering the nutritional liquid from the container to a patient when the tubing is mounted on the enteral feeding pump. An identification member is mounted on the conduit assembly and has at least one characteristic of a nutritional liquid associated with the feeding set represented by the identification member. The identification member is positioned on the conduit assembly so as to permit automatic identification by the enteral feeding pump of the at least one characteristic of the nutritional liquid upon mounting the conduit assembly on the enteral feeding pump.

Abstract: The present invention relates to a dental composition comprising a specific radically polymerizable compound and a radical initiator system. Furthermore, the present invention relates to the specific radically polymerizable compound and its use in a dental composition. The specific radically polymerizable compound of the present invention has an allyl (meth)acrylamide group and a phosphoric acid ester group.

Abstract: A dental composition comprising doped T1O2 nanoparticles, and a curable resin material, wherein the curable resin material comprises a polymer precursor component, and wherein the dopant may be one or more of, for example, N (nitrogen), Ag (silver), F (fluorine), P (phosphorus), and P04 (phosphate). A method of using the dental composition in a dental application. The dental composition may be antibacterial in the absence of visible light or UV light.

Abstract: A method for manufacturing a colored sheet for coloring an object by adhesion to the object includes, a coloring step of applying by spraying, a first coating fluid containing first microparticles for coloring to a thin film of a print receiver body which has a sheet-shaped support body and the thin film, the thin film being peelably held on the sheet-shaped support body to serve as a base material of an adhesive sheet which is to be adhered to the object, and a restricting step of applying by spraying, before the coloring step, a second coating fluid for restricting the first microparticles from penetrating the thin film to a location where the first coating fluid is to be applied.