Abstract: The system of the preferred embodiments is an ear treatment device including: an electrical power supply; an electric heater coupled in electronic communication to the electrical power supply; a spray nozzle coupled to a fluid passageway; a fluid reservoir coupled to the opposite end of the fluid passageway from the spray nozzle; at least one of I) a pump, II) an ultrasonic mist generator, and III) a vapor generator designed to cause the fluid from the reservoir to flow through the fluid passageway and out of the spray nozzle; wherein the electric heater is adapted to heat the fluid in at least one of A) the reservoir, B) the fluid passageway, and C) the spray nozzle; wherein the nozzle is adapted to spray the fluid into the ear canal of a user. Preferably the ear treatment device of the preferred embodiments is designed to treat earaches in a user, and possibly to assist in the promotion of drainage of fluid from a user's middle ear and in some cases to treat ear infections.

Abstract: An instrument comprises a handpiece, a boss member, a cylindraceous cam body, a linearly movable member, a cam follower, and a braking member. The cam body is rotatably supported in the handpiece and includes an exterior cam feature. The cam follower couples the linearly movable member with the cam feature of the cam body. The cam feature and the cam follower cooperatively drive the linearly movable member linearly in response to rotation of the cam body within the handpiece. The braking member extends about at least a portion of the exterior of the cam body and is positioned to progressively engage the boss member as the cam body rotates within the handpiece. The braking member and the boss member thus cooperate to provide gradual braking of the cam body. The instrument is operable to deploy a pressure equalization tube in the tympanic membrane of a patient.

Abstract: Disclosed herein is a hydrogel wound dressing having a wound-contact side and a non-wound-contact side wherein the rate of moisture evaporation from said non-wound contact side is faster than the rate of moisture evaporation from said wound contact side, thereby causing said dressing to curl toward said non-wound contact side upon drying. Optionally, the hydrogel wound dressing can be comprised of two materials having different rates of moisture evaporation bonded together to form a bilayer structure.

Abstract: The disclosed invention is a device and method of use for gauze utilized in the treatment of hemorrhage. In an embodiment the device combines clotting factor concentrator gauze and urea in order to slow hemorrhage and prevent hemorrhage induced coagulopathy. In an embodiment, the gauze is comprised of a first layer comprised of gauze and a second layer embedded with urea. The urea reacts spontaneously when it comes into contact with water, and undergoes an endothermic reaction. This endothermic reaction cools the smaller blood vessels exposed from soft tissue trauma, causing enhanced platelet activity as well as vasoconstriction to minimize the bleeding that occurs before and after the clotting cascade is activated over the entire wound surface.

Abstract: A system for wound treatment using a serum, comprising a device for recovering serum from whole blood, comprising: a blood bag for the reception and coagulation of whole blood, which has an outlet for discharging the serum-containing fluid from the blood bag and a barrier in the region of the outlet for retaining the coagulum, a filter module which is fluidically connected to the blood bag and comprises a housing and an interior, in which a semi-permeable membrane is arranged, said membrane dividing the interior into a retentate space and a permeate space and separating the fluid discharged from the blood bag into a permeate comprising the serum and into a retentate in which any particulate components contained in the fluid remain. The system for wound treatment further comprises a wound care system with a capillary membrane system for dispensing the serum to a wound.

Abstract: A lace tension-controlled compression sock that can be easily donned and removed and delivers the necessary amount of pressure to mitigate the effects of chronic venous disorders (CVDs) comprises easily read, graphic pressure indicators for use by the wearer when adjusting the degree of compression.

Abstract: Methods and apparatuses for treating webs are disclosed. In one embodiment, an apparatus for treating at least one web passing through the apparatus may comprise a first roller comprising a pair of spaced apart ends, a length extending between the ends, a circumference, and at least two bearer rings connected to the first roller between the pair of spaced apart ends of the first roller, a first pressure applicator coupled to the first roller and operatively connected to a load source for selectively applying a force to the first roller, and a second roller positioned adjacent the first roller to define a nip for receiving the at least one web.

Abstract: A machine for making absorbent sanitary articles which includes an absorbent pad in turn including one or more absorbent materials; the machine includes a line for feeding at least one continuous web of impermeable material and at least one unit for forming and applying a succession of absorbent pads along the continuous web of impermeable material and a device for detecting at least one between the weight, density profile (or weight profile) parameters of at least one of the absorbent materials defining the absorbent pad the detecting device including at least one microwave resonator.

Abstract: An absorbent article has a longitudinal direction, a transverse direction and a thickness direction, and includes a fluid permeable topsheet, a fluid impermeable backsheet and an absorbent core enclosed between the topsheet and the backsheet having, in the longitudinal direction, a front section, a rear section and a crotch section between the front section and the rear section. The absorbent core has two longitudinally extending side regions and a longitudinally extending central region between said side regions. The central region and the side regions are spaced apart in the transversal direction by longitudinally extending channel regions. Furthermore, the width of the central region in the transversal direction is less than the width of each of the side regions in the transversal direction, at least in the front section and the rear section, and the channel regions are of less basis weight than the side regions and the central region.

Abstract: A disposable pant-type absorbent article adapted for a male user. The disposable pant-type absorbent article includes a chassis having a front section and a back section, an absorbent core, a front region configured for receiving the genitals of a male user, in which the front section at least partly is made of an elastic material comprising at least one elastic element. The absorbent core within a front region, under the influence of side elastic elements and elastic web material is adapted to bulge outwardly during use of the article to form a bowl shaped portion for receiving the genitals of a male user.

Abstract: An absorbent article with a liquid-permeable topsheet, an absorbent core and a liquid-impermeable backsheet is provided with a liquid-redirecting layer. The liquid-redirecting layer may be a water-repellent layer and is located underneath of the absorbent core. A method of manufacturing of an absorbent article having a water-repellent layer underneath of the absorbent core is described.

Abstract: Provided are a water absorption treatment material with excellent water disintegrability and a method for manufacturing the water absorption treatment material. A water absorption treatment material is a water absorption treatment material that absorbs a liquid, and includes a granule. The granule contains a foaming agent. Upon the water absorption treatment material absorbing a liquid, gas bubbles are produced in the granule as a result of a reaction of the foaming agent, and the granule collapses.

Abstract: The present invention provides a water absorption treatment material that has a structure suitable for obtaining a high level of water disintegrability. A water absorption treatment material is a water absorption treatment material that absorbs a liquid, and includes a granular core portion and a coating layer portion. The granular core portion has a granular shape. The granular core portion contains a first water-absorbent polymer. The coating layer portion covers the granular core portion. The coating layer portion contains a second water-absorbent polymer. The second water-absorbent polymer has a mean particle size smaller than the mean particle size of the first water-absorbent polymer.

Abstract: A patient handling apparatus includes a frame, a base, and a lift assembly supporting the frame relative to the base, the lift assembly configured to extend or contract to raise or lower the base or the frame with respect to the other of the base and the frame. The patient handling apparatus further includes a control system, which comprises at least one hydraulic cylinder to extend or contract the lift assembly, a hydraulic circuit to direct the flow of hydraulic fluid to and from the hydraulic cylinder, and a controller operable to control the hydraulic circuit. Based on an input signal, for example, an input signal that is indicative of a status or condition of the patient handling apparatus, the controller is configured to open, optionally automatically, fluid communication between the rod end chamber and the cap end chamber to redirect a portion of the fluid output from the rod end chamber to the cap end chamber when the rod is extending to thereby increase the extension speed of the rod.

Abstract: A bed with movable frame; comprising a support base (1); —a movable headboard (3) and a movable footboard (2) with ability for vertical displacement and coupled to operational drive elements (32, 22); —a frame (4) provided with side rails (41) and end crosspieces (42); —a first mechanism (5) for attachment of the frame (4) to the movable footboard (2) with ability for displacement in the longitudinal direction; for rotation relative to a longitudinal axis X and rotation relative to a transverse axis Y; and —a second mechanism (6) for attachment of the frame (4) to the movable headboard (3) with ability for rotation relative to a longitudinal axis X? and with ability for rotation relative to a transverse axis Y?.

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: Methods and systems for lift monitoring are described. In one embodiment, a first operation signal may be received from a first relay coupled to an electro-mechanical patient lift when the electro-mechanical patient lift is being operated in a first position. A second operation signal may be received from a second relay coupled to the electro-mechanical patient lift when the electro-mechanical patient lift is being operated in a second position. A determination of whether a lift qualification threshold is met may be based on the receiving of the first operation signal and the second operation signal. An occurrence of a lift may be recorded when a determination is made that the lift qualification threshold is met. Additional methods and systems are disclosed.

Abstract: An emergency cot includes a litter frame, a base, and a lift assembly supporting the litter frame relative to the base. The lift assembly includes load bearing members pivotally coupled to the litter frame by head-end upper pivot connections and foot-end upper pivot connections and to the base by head-end lower pivot connections and foot-end lower pivot connections for raising or lowering the base or the litter frame with respect to the other. The foot-end upper pivot connections or head-end upper pivot connections are movable toward or away from the longitudinal axis of the litter frame to allow one end of the litter frame to be tilted upwardly.

Abstract: A patient repositioning apparatus doubles as a repositioning sheet and a sling. The repositioning apparatus includes a sheet with an upper surface and an opposing lower surface and defines an outer periphery that has opposing side edges. The upper surface of the sheet has an upper surface material, and the lower surface of the sheet has a lower surface material that is formed from a relatively low-friction material as compared to the upper surface material. The handles are disposed along the opposing side edges of the sheet, and the strap members are attached to the sheet and distributed across both opposing side edges. Each of the strap members includes a strap portion that forms a bight in the strap member.

Abstract: A patient isolator includes a base and a cover which is arranged to seal with the base. The cover is formed from a rigid material and has two access ports on an end face. The two access ports are angled in a width direction relative to a plane which extends parallel to the width direction of the patient isolator. The two access ports are angled relative to each other. A method of isolating a patient from an environment is also disclosed.

Abstract: A system for positioning a patient before, during or after a medical procedure can include an arm assembly having a proximal end, an opposing distal end, and at least one joint therebetween. The joint can be configured to permit the distal end of the arm assembly to move with respect to the proximal end of the arm assembly. The proximal end of the arm assembly can be configured to be fixed with respect to a surgical table. The system can also include a ball joint mechanism attached to the distal end of the arm assembly and to a head support configured to support a patient's head. The ball joint mechanism can include a ball joint and a motor. Activation of the motor can permit or prevent movement of the ball joint.

Abstract: A system for positioning a patient before, during or after a medical procedure can include an arm assembly and a surgical drape for use with the arm assembly. The surgical drape can be configured to be placed around a surgical site where an operative procedure is to be conducted. The surgical drape includes a transparent viewing window, multiple handle covers, and an expandable opening on the top side of the surgical drape. Additionally, the surgical drape may also include adhesive components on the bottom side of the drape that may be independently removed in order to affix the drape around a surgical site.

Abstract: The disclosed apparatus, system and method may include at least an adjustable platform for a surgical footpedal, such as may be associated with a phacoemulsification surgical console. The adjustable platform for a surgical footpedal may include a bearing arm having a mount; a pedal, having associated therewith one or more sensors indicative of at least one surgical setting; and a platform at a first end of the bearing arm distal from the mount, comprising a mating surface for receiving the pedal.

Abstract: A method of performing rehabilitation includes moving a first limb of a patient and displaying, for viewing by the patient in virtual reality, the movement of the first limb of the patient as the first limb of the patient is being moved.

Abstract: A rehabilitation mechanism rehabilitates the joints, muscles, and tendons of the legs of a bedridden patient in an automated manner according to a plan. A knee module can be operatively connected to the knee joint of the patient. A control module controls rehabilitation movements by way of the knee module. The knee module is a module to be arranged above the patient and the mattress, which module is supported directly or indirectly on a bed or the mattress frame, and includes a knee prosthesis which receives a knee joint of the patient, a connection element connected to the knee prosthesis, an extension arm to which the connection element is secured, and a mechanism to be actuated by the control module and which introduces a defined force into the knee prosthesis via the extension arm and the connection element to carry out rehabilitation movements according to a plan.

Abstract: A gait training system has a motor connected to a first linkage system by an actuator. The first linkage system has multiple linkage members connected to multiple joints and an endpoint that is configured to produce a cyclic gait motion when the motor is activated. First and second linkage members have an adjustable length. A method of customizing a gait pattern on a gait training system is also described.

Abstract: This disclosure includes manipulating apparatuses and related methods. Some manipulating apparatuses include an actuator having a semi-rigid first segment, a semi-rigid second segment, and one or more flexible cells disposed between the first segment and the second segment, where the actuator is configured to be coupled to a fluid source such that the fluid source can communicate fluid to vary internal pressures of the one or more cells, and where each cell is configured such that adjustments of an internal pressure of the cell causes angular displacement of the second segment relative to the first segment.

Abstract: An interface system in an exoskeleton includes a base support, a strap assembly, and posterior strut. The posterior strut has a vertical member defining a lower end connecting to the base support, and an upper end connecting to first and second transverse members extending in opposed directions from the vertical member. The first and second transverse members connect to the strap assembly. The interface system is adapted to receive and support an assistive device adapted to augment a user's performance and mitigate repetitive strain injuries.

Abstract: Provided is a method and apparatus for setting a torque of a walking assistance apparatus. A rotation angle and a rotation angular velocity of the walking assistance apparatus may be measured to set the torque. An amount of torque to be set may be calculated based on the rotation angle and the rotation angular velocity of the walking assistance apparatus.

Abstract: A system for coupling a user to a support apparatus includes a harness for the user, a hoist, and frame. The harness and the hoist have co-operable attachment means for releasably coupling the harness to the hoist. The frame is configured to receive the user, where the harness and the frame have co-operable attachment means for releasably coupling the harness to the frame.

Abstract: A method for providing information to a user, preferably including: determining environmental information; determining a set of features based on the information; determining output parameters based on the features; and controlling a sensory output system to generate outputs based on the output parameters. A sensory output device, preferably including a plurality of sensory output actuators. A system for providing information to a user, preferably including one or more: sensory output devices, sensors, and computing systems.

Abstract: Shoe-shaped, foot-operated massage device, in particular a shoe-shaped, foot-operated masturbator for men, comprising a footbed (1), an upper (2), a shoe opening (3) between the upper (2) and the footbed (1) for accommodating a foot or to be temporarily connected to a foot, a sole (4), and a base (5) between the footbed (1) and the sole (4), an open masturbator position being provided in order for a penis to be accommodated therein.

Abstract: A therapeutic apparel article is configured with a supple wearable fabric article that can be configured over limb or nub of an amputated limb. The therapeutic apparel article is configured with a plurality of nodes for detachably attaching vibrating devices thereto. In addition, a control unit having a power source may be detachably attached to the wearable fabric article. A conductive network may extend from the control unit and/or the power source to provide electrical power to the nodes and the vibrating devices attached. A user may attach vibrating devices to various nodes of the wearable fabric article as desired. In addition, the vibrating devices and the control unit can be detached from the wearable fabric article to enable the wearable fabric article to be washed.

Abstract: An automated chest compression device has a housing for supporting a patient and a motor within the housing. A conical drive spool is operatively connected to the motor and a cable, is operatively connected to the conical drive spool. The cable is adapted to extend at least partially around the chest of the patient. A controller is operable to control the motor to compress the chest to variable thresholds.

Abstract: A chest compression device with a chest compression belt assembly including guards and sensors operable with a control system to control operation of the system depending on detection of proper installation of the guards.

Abstract: A scraping plate is provided. The scraping plate includes a main body, a storage chamber for storing a liquid medicine and an electric heater for heating the liquid medicine. One end of the main body is provided with a scraping blade, and the other end opposite to the scraping blade is provided with a grip portion. Both the storage chamber and the electric heater are provided inside the main body. A surface of the scraping blade is provided with at least one liquid medicine outlet, wherein each liquid medicine outlet is communicated with the storage chamber.

Abstract: Coated pharmaceutical packages are disclosed. The coated pharmaceutical packages may Include a glass body formed from borosilicate glass that meets Type 1 criteria according to USP <660> or alkali aluminosilicate glass having a Class HGA 1 hydrolytic resistance when tested according to the ISO 720-1985 testing standard. A low-friction coating comprising a polymer may be positioned on a portion of the exterior surface. A coefficient of friction of an abraded area of the portion of the exterior surface with the low-friction coating may be less than 0.7 after exposure to a temperature of 260° C. for 30 minutes and abrasion under a load of at least 10 N and does not have observable damage. A retained strength of the coated glass article in horizontal compression does not decrease by more than 20% after the temperature exposure and the abrasion.

Abstract: The present invention provides a secure pharmaceutical container. The secure container includes a plurality of compartments for storing pills, tablets, solutions, pastes, creams, ointments, gels, emulsions, or any other pharmaceutical product. The compartments each include a locking mechanism that is operably connected to a biometric system, such as a fingerprint scanner. The compartments become unlocked upon the fingerprint scanner reading an approved fingerprint, ensuring that only individuals approved to have access to the container are granted access.

Abstract: A drug-filled synthetic resin ampule has an ampule body capable of standing by itself and a drug accommodated inside the ampule body. The ampule body has a tip part positioned at an upper part thereof when the ampule body stands by itself, a hollow part having a drug accommodation portion, and a breakable part provided between a lower portion of the tip part and an upper portion of the hollow part. The tip part has pressing portions, for guiding a pressing force applied thereto respectively in a predetermined direction when an operation of breaking the breakable part is performed. The hollow part has a bottom surface part for allowing the ampule body to stand by itself. The bottom surface part has extension portions extended in predetermined directions (X-direction, Y-direction) in which the pressing force applied to the pressing portions respectively is guided when the operation of pressing the pressing portion is performed to break the breakable part.

Abstract: The present invention relates to a container comprising at least a dry concentrate, wherein the dry concentrate is designed such that it forms at least one acid liquid concentrate, or a part of an acid liquid concentrate, which is suitable for manufacturing at least on dialysis solution, on its dissolving in a liquid, preferably in water.

Abstract: A label includes (a) a base segment, (b) a first lobe segment comprising at least one protruding member and a pull tab, (c) a second lobe segment comprising at least one protruding member, (d) a first cutout segment, (e) a second cutout segment, (f) a first perforation forming a boundary between the base and first lobe segments, (g) a second perforation forming a boundary between the base and second lobe segments, and (h) a third perforation forming a boundary between the first lobe segment and its at least one protruding member. The first and second lobe segments are connected to the base segment and opposed to one another. The first and second cutout segments separate the at least one protruding member of the first and second lobe segments, respectively, from the base segment. The label comprises at least (A) a facesheet layer and (B) an adhesive layer.

Abstract: A container containing a concentrate for dialysis includes a pouch or cartridge containing a solid concentrate of constituents for the dialysis solution, the pouch or cartridge being closed by a connector having a filling channel extending completely through the connector, which is for filling the pouch or cartridge with the solid concentrate, means for introducing a solution-forming liquid into the pouch or cartridge and for extracting the solution obtained, these introduction and extraction means having at least one connecting portion for connecting them to a corresponding port of the dialysis machine. The filling channel is closed by a stopper which has a reservoir containing a second constituent or group of constituents for the dialysis solution, and means for producing an outlet opening in the reservoir contacting the inside of the reservoir with the side of the stopper located in the container.

Abstract: The present invention relates to a syringe, and more particularly, to an apparatus obtained by improving an conventional syringe formed with an injection flow passage including an injection needle, so as to share a portion of the injection flow passage except the injection needle or to form a suction flow passage completely independent of the injection flow passage, thereby further smoothing suction of a liquid medicine. The syringe is configured such that the separate suction flow passage bypassing the injection needle is formed in an conventional syringe to more smoothly perform the suction of the liquid medicine, thereby maximizing user's convenience and marketability of the product.

Abstract: A first image pickup unit picks up a first image including a conveyed object. A printing unit performs printing on the object based on the first image. A second image pickup unit picks up a second image including the object on which printing has been performed. A check unit checks a print state of the object in the second image. A first acquisition unit acquires feature data from one of the first image and the second image, as registration data. A second acquisition unit acquires feature data from the other image of the first image and the second image, as collation data. A verification unit compares the registration data and the collation data and verifies that reliability of the registration data is equal to or greater than a predetermined criterion value. A storage stores the registration data as data for determining an identity of the object.

Abstract: A tamperproof dosage form article comprising: a core, wherein the core comprises a first end and a second end; a first shell on at least a portion of the first end of the core; a second shell on at least a portion of the second end of the core; wherein the first and second shells comprise one or more locking protrusions extending along at least a portion of the circumference and inner surface of the shells, and the core comprises one or more locking recesses, and wherein at least a portion of the shells proximal to the locking protrusions is elastically deformable and arranged such that each one locking protrusion is snapped into each one of the locking recesses once inserted over a predetermined portion of the core to provide a locking force between the core and the shells.

Abstract: A tamperproof dosage form for oral administration comprising: a caplet comprising first and second ends, a middle region extending between said first and second ends, parallel and oppositely disposed top and bottom faces, and a land interposed between the top and bottom faces and extending along a perimeter of the caplet on a plane parallel to a caplet length axis; and first and second shells, each comprising an open end and a closed dome-shaped end, each fitted over at least a portion of the caplet, the portion comprising at least the first and/or second ends of the caplet and at least part of the middle region. An adhesive substance being arranged between the caplet and the shells at least over a portion of the top and/or bottom faces proximal to the first and second ends of the caplet and a corresponding portion of an inner surface of the closed dome-shaped end of the shells to fixedly join the shells to the caplet.

Abstract: In an apparatus for dispensing, a dispenser includes a housing, a reservoir housed within the housing, a chute in fluid communication with the reservoir, wherein the chute is adjacent to the reservoir, a user input device, a power source housed within the housing, a logic housed within the housing, wherein the power source powers the logic, a motor housed within the housing, wherein the power source powers the motor, wherein the logic controls the motor, a gear train housed within the housing, wherein the motor drives the gear train, a first platform defining an opening, wherein a portion of the first platform abuts a bottom portion of the chute when the dispenser is in a non-dispensing state, and a second platform including a well, wherein the gear train is configured to rotate the second platform relative to the housing, and wherein when the logic sets the dispenser to a dispensing state a position of the well is adjustable relative to the housing via the user input device, such that the well substantially

Abstract: A pill dispenser system; the device is lockable and able to hold and dispense premanufactured roll(s) of medication with pouches linked together in a continuous strip. The premanufactured roll of medication pouches is manufactured according to a prescribed dosage schedule. The pill dispenser system includes a combination of dispenser assembly including a housing having a first-member, and a second-member, computer components, a premanufactured roll of medication, an adjustable holder, a roll advancing mechanism, a separator, a securer, a power source, a user-interface, at least one locking mechanism, at least one sensor, and a code reader providing a safe and convenient way for patients and caregivers to manage medication-dosing schedules.

Abstract: A fluid delivery device and system is operable to fluidly couple a pair of fluid delivery conduits. One embodiment includes a fluid delivery device sized to meet ANSI/AAMI ID54:1996(R) 2005 and not mate with ANSI/HIMA MD70.1 or ISO 594/1 and ISO 594/2 standards for intravenous ports and connectors to prevent accidental intravenous delivery of fluids intended for enteral delivery. The system includes at least one of a locking tab and a stop flange configured to not mate with matching connectors not configured to satisfy the enteral feeding standards and not specifically configured to mate with the fluid delivery device.

Abstract: Provided is a curable composition including a polymerizable monomer component (A), a spherical filler (B) having an average particle size within the range of 230-1000 nm, and a polymerization initiator (C), wherein the curable composition is characterized by having a value (V) of less than 5 and a chroma (C) of 0.05 or higher in colorimetric values according to the Munsell Color System in colored light on a black background, and a value (V) of 6 or higher and a chroma (C) of less than 2 in colorimetric values according to the Munsell Color System in colored light on a white background, each of the values (V) and chroma (C) being measured using a color difference meter in a state in which a 1-mm-thick cured article has been formed.