Abstract: The wheeled support assembly for the disabled is an assembly designed to assist a disabled person to walk steadily. The assembly includes a wheeled frame having a detachable body harness. The body harness is adapted to fit around the torso of the disabled person and to provide back support therefor. The body harness includes a pair of articulated columns for removable attachment to the disabled person's legs. The lower end of each column terminates in a foot member, wherein the disabled person may insert his/her feet. When attached to the wheeled frame, the harness stabilizes the disabled person's body within the frame such that movement of the legs will propel the entire assembly. The assembly also includes rubber handles, an alarm clock and an audible emergency alert device.

Abstract: A compression belt cartridge for use with chest compression devices. The compression belt cartridge has a double-oar shaped belt and a cover plate through which the belt is threaded. The cover plate is provided with hooks and snap latches that fit into a belt drive platform. The cover plate is sized and dimensioned to fit within only selected platforms. The belt attaches to the means for tightening the belt via a spline attached to the belt. The means for tightening a belt then repetitively tightens the belt, thereby accomplishing chest compressions.

Abstract: A HFCWO apparatus includes a housing having a port, a therapy system carried by the housing and operable to deliver HFCWO therapy to a patient in accordance with a set of operating parameters, and a memory device couplable to the port for storing at least a portion of the set of operating parameters. The therapy system may be operable in accordance with the portion of the set of operating parameters stored in the memory device. The apparatus may comprise a wireless transmitter carried by the housing and operable to wirelessly transmit data relating to HFCWO therapy to a wireless device, such as a printer, PC, a PDA, and the like.

Abstract: Techniques associated with an implant system for imparting vibratory massage to tissue within a body is disclosed. Methods include placing an implant device near a surface of a colon, the implant device configured to produce and communicate a vibration to colon tissue, the implant device including a case forming a portion of an exterior of the implant device and defining an interior of the implant device, a vibration generator mounted on the case to vibrate the implant device, and a tissue engaging structure located on the exterior surface of the case to engage the colon tissue, securing the implant device to the colon, and activating the vibration generator of the implant device to cause the implant device to vibrate against the colon, wherein the vibration stimulates a nerve to induce a bowel movement.

Abstract: Techniques associated with an implant system for imparting vibratory massage to tissue within a body is disclosed. Methods include placing an implant device near tissue in a pelvic region, the implant device configured to produce and communicate a vibration to the tissue, the implant device including a case forming a portion of an exterior of the implant device and defining an interior of the implant device, a vibration generator mounted on the case to vibrate the implant device, and a tissue engaging structure located on the exterior surface of the case to engage the tissue, and activating the vibration generator of the implant device to cause the implant device to vibrate against the tissue, wherein the vibration stimulates a nerve to treat sexual dysfunction.

Abstract: The double pull body brace comprises a one-piece panel which engages around the torso and overlaps at the front. At the overlap, it is attached to itself by means of a hook-and-loop fastener so that a wide range of adjustment is possible. In the back, spaced cord guides are mounted on said panel. Each cord guide carries a plurality of cord guide lobes. An upper cord is engaged around the upper cord guide lobes, and a lower cord is engaged around the lower cord guide lobes. These cords are separately attached to pull tabs. When donned, the user pulls on the pull tabs to separately adjust upper and lower closure tension of the body brace. When in correct adjustment, the pull tabs are attached in place by hook-and-loop fasteners.

Abstract: A joint having two-axis construction having a distal member and a main member joined in co-linear pivotal relation that provides enhanced joint strength and compactness. Hydraulics further provide variable extension assist and an infinite number of flexion stops for controlled flexion flow, and two gears provide a functional gear ratio that also promotes compact construction by reducing the amount of hydraulic piston travel required for maximum joint extension. A drive gear associated with the main member is positioned between the distal end of the piston and a transfer gear partially press-fit into a cut-out in the distal member, to provide needed radial hydraulic force transfer. Although it is contemplated for joint use to be primarily in orthotic devices that assist the movement of an inadequately functioning body limb, any application for which the mechanical joint's compact configuration would provide assistance or technical advantage is considered to be within its scope.

Abstract: A finger support system comprising a wedge shaped finger support member, narrow at one end and wider at another end, with concave sides to form fit the finger support member between an injured and an adjacent finger, the finger support member being taped or otherwise removable attached between the injured and adjacent fingers with the narrow end fitting snugly at the juncture of the two fingers and the wider end separating the fingers, and extending past the middle knuckle but not to the knuckle near the finger tips so that, when the finger support member is taped in place, the hand will have greater use in basketball or other ball-handling sports.

Abstract: An apparatus for applying pressure to a body part comprising multiple interconnectable bands of compressible or noncompressible material. Optional spine to further interconnect the bands. Interconnectable pieces designed for covering specific body areas. Modular arrangement of the individual components. Customized or off-the-shelf availability of the apparatus.

Abstract: A method of treating a patient with a strap is provided. The method includes providing a strap including a retainer portion, a base portion opposing the retainer portion, a foam layer having a first surface, and a fabric layer having a second surface, the foam layer having an elasticity greater than the fabric layer, contacting a body portion of a patient with the first surface, and retaining the strap against the body portion by connecting the retainer portion to the second surface.

Abstract: Methods for promoting angiogenesis comprising administering platelet-rich plasma to a site and stimulating the site with an electromagnetic field. Platelets include platelet-rich plasma and compositions can further include stem cells such as adipose stromal cells and cells derived from bone marrow aspirate. Methods also comprise isolating platelets from a patient's blood, forming a composition including the platelets, delivering the composition to a site in need of treatment, and electrically stimulating the site.

Abstract: The invention relates to the use of a specific ligand for antibodies, preferably autoantibodies in the manufacture of a column for the treatment of thromboangiitis obliterans. The invention pertains furthermore to the apharesis column with at least one anti-IgG antibody for the treatment of thromboangiitis obliterans.

Abstract: The present invention relates to a device for extracorporeal removal of harmful agents from blood or blood components, comprising full length heparin immobilized on a solid substrate by covalent end point attachment. The present invention also relates to a method for extracorporeal removal of a harmful agent from mammalian blood or blood components. The present invention further relates to a process for covalent end point attachment of full length heparin to a solid substrate.

Abstract: A gastroplasty method involves a staple line that terminates prior to reaching the gastroesophageal junction such that the bypassed portion of the stomach does not require resection. Additionally, bougies are taught that assist a physician in following the improved staple line of the present invention.

Abstract: A method of deploying an ocular implant into Schlemm's canal of an eye. The method includes the steps of inserting a distal end of a cannula through a cornea of the eye and into an anterior chamber of the eye, the cannula having a distal opening extending from the distal end and through a side wall; placing the distal opening of the cannula into fluid communication with Schlemm's canal; advancing the ocular implant distally through the cannula with a delivery tool engaged with the ocular implant, a proximal portion of the ocular implant engaging the delivery tool proximal to a distal portion of the delivery tool; and disengaging the ocular implant and the delivery tool when the proximal portion of the ocular implant reaches the cannula distal opening. The invention also includes a system for practicing the method.

Abstract: The present disclosure is directed to alleviating the uncomfortable and unpleasant sensations that may accompany insertion and removal of personal care devices. Specifically, the present disclosure is directed to a personal care device that includes a moisture-activated composition that becomes lubricious only upon contact with moisture, such as from mucosal surfaces in the body.

Abstract: An electrosurgical method for treating foot ulcer, including diabetic foot ulcer, comprising: positioning an active electrode in close proximity to the ulcer, the active electrode being disposed on a distal end of an electrosurgical shaft; applying a high-frequency voltage potential difference across the active electrode and a return electrode in the presence of an electrically conductive fluid, the voltage potential being sufficient to generate plasma at the active electrode; and stimulating the ulcer with the active electrode to increase blood flow, remove unhealthy tissue and induce the body's natural healing response.

Abstract: An electrosurgical method for treating foot ulcer, including diabetic foot ulcer, comprising: positioning an active electrode in close proximity to the ulcer, the active electrode being disposed on a distal end of an electrosurgical shaft; applying a high-frequency voltage potential difference across the active electrode and a return electrode in the presence of an electrically conductive fluid, the voltage potential being sufficient to generate plasma at the active electrode; and stimulating the ulcer with the active electrode to increase blood flow, remove unhealthy tissue and induce the body's natural healing response.

Abstract: An electrosurgical method for treating foot ulcer, including diabetic foot ulcer, comprising: positioning an active electrode in close proximity to the ulcer, the active electrode being disposed on a distal end of an electrosurgical shaft; applying a high-frequency voltage potential difference across the active electrode and a return electrode in the presence of an electrically conductive fluid, the voltage potential being sufficient to generate plasma at the active electrode; and stimulating the ulcer with the active electrode to increase blood flow, remove unhealthy tissue and induce the body's natural healing response.

Abstract: A device (12) and method are provided for percutaneous transdermal delivery of a potent pharmacologically active agent. The agent is dissolved in water to form an aqueous coating solution having an appropriate viscosity for coating extremely tiny skin piercing elements (10). The coating solution is applied to the skin piercing elements (10) using known coating techniques and then dried. The device (12) is applied to the skin of a living animal (e.g., a human), causing the microprotrusions (10) to pierce the stratum corneum and deliver a therapeutically effect dose of the agent to the animal.

Abstract: The present invention provides a system and method for controlling resuscitation in a patient. In at least one embodiment, the invention includes a fluid rate measurer, a controller electrically coupled to the fluid rate measurer, and a pump. The controller is adapted to receive signals from a physiological monitor and controls the pump.

Abstract: A fluid management system with a detection circuit for detecting whether an attached surgical device is operational. The fluid management system changes at least one operation mode when the surgical device is detected as being operational. The fluid management system may include inflow, outflow, or inflow/outflow capabilities, and monitors at least one signal characteristic of an AC power signal provided to the surgical device.

Abstract: A method for tilling needleless injector capsules with liquid drug, whereby dissolved gas within the drug is replaced by a less soluble gas in order to reduce the inclusion of gas bubbles, or to prevent the growth of bubbles during storage and thereby prevent breakage of the capsules.

Abstract: An endoscopic device capable of autonomous locomotion through a body cavity in a pre-established direction of displacement is described. The endoscopic device comprises a tubular body that extends between a front end portion and a rear end portion and a reinforcement structure distributed along the length of the tubular body. Each end portion includes an anchoring means for temporarily and alternately attaching the end portions to a wall of the body cavity.

Abstract: A priming indicator for a fluid infusion system includes a luer cap or other component of the infusion system having an indicator surface covered by a membrane. The membrane exhibits a first visual characteristic, such as being opaque, when dry and exhibits a second characteristic, such as becoming less opaque, when wet. Once the membrane becomes wet, indicia on the surface, which may be provided on a rod at least partially covered by the membrane, becomes visible, thereby indicating an intravenous tube to which the luer cap is secured has been primed or is nearly primed. The indicator may alternately be employed at an upstream end of an infusion set, such as at the port of a medical bag providing a supply of fluid, to indicate a low level of fluid in the medical bag.

Abstract: A heating system for warming nutritional liquid fed to a neonate or preterm infant may comprise a control module and a heater. The heating system is portable so that the heating system is not connected to a syringe pump or other device used to feed the neonate. The heater of the heating system is mounted to the tube that is used to feed the neonate. The heater is positioned along the tube in close proximity to the neonate so that a temperature drop of the nutritional liquid after the nutritional liquid exits the heater and reaches the neonate is negligible. The heater raises the temperature of the nutritional liquid to a target desired temperature (e.g., body temperature of the mother and neonate or to a temperature above the temperature of the mother and neonate) so that the neonate may consume warm nutritional fluid. Once the nutritional liquid reaches the neonate, the nutritional liquid is at about the body temperature of the mother or neonate or at least above room temperature.

Abstract: Described is a system and associated materials and methods for delivering a fluid to a subject's skin, e.g., for tattoo removal. In one embodiment, the fluid is provided in a continuous flow by associating the fluid with a pump. In another embodiment, a disposable template is provided that allows for precise and ideal placement of eschar-inducing material fluid for, for example, tattoo removal.

Abstract: A needle tip of a needle tube stuck in the skin is caused to be reliably positioned in the skin upper layer part and the injected drug is caused not to leak to the outside of the body. An injection needle is provided with a needle tube having a needle tip, a hub that holds the needle tube and an adjustment unit provided around the needle tube and having a needle-protruding surface through which the needle tip of the needle tube protrudes. The needle-protruding surface of the adjustment unit is formed such that the distance S from the circumferential edge to the circumferential surface of the needle tube is in the range of 0.3-1.4 mm.

Abstract: A contrast media injection system includes detects the absolute position of the syringe ram using a non-contact sensor. A series of magnets and Hall-Effect sensors may be used or an opto-reflective system. Illuminated knobs that are connected to the drive mechanism for the syringe ram rotate with the drive and provide visual feedback on operation through the illumination. Analog Hall-Effect sensors are used to determine the presence or absence of magnets that identify the type of faceplate being used. The faceplates include control electronics, connected to the powerhead through connectors, which may be interchangeably used by the two faceplates. The faceplate electronics include detectors for automatically detecting the capacity of pre-filled syringes.

Abstract: Embodiments of the invention are directed to methods and systems associated with a disposable dispenser (100, 200) of therapeutic fluid. Preferred embodiments having a small size of less than about 75 mm in length, less than 50 mm in width and less than about 10 mm in thickness and may be releasably attached to the body (B). In one embodiments, the dispenser draws fluid from a flexible volume-conformable reservoir (4) and operates a dosing and metering pump (6, 61, 62, 63) incorporating a motor to deliver fluid through a fluid delivery tool (8, 81, 82). Disposed on the housing bottom (2B) is a peel-of-tape (22) that when removed, electrically connects a power supply (18) to power the operative components (3) of the dispenser into operation, exposes an adhesive (28) and a window (21) opened in the housing (2), and allows the fluid delivery tool (8) to extend for insertion into the skin (S).

Abstract: A dual head contrast media injection system performs a patency check or test injection, determining flow rate and/or flow volume from the programmed protocol. The tubing that connects syringes to a patient shares only a short common section near to the patient. Appropriate injection steps are taken to compensate for tubing elasticity. A wireless remote control and a touch screen control are provided, improving functionality and information delivery. The display brightness is controlled based on the ambient light, and the display panel includes a double swivel permitting re-orientation. The orientation of the display may also be controlled based on, e.g., the current step, the tilt angle of the powerhead, or a manual control. Furthermore, the display is customizable to identify the type of fluid (contrast, saline, etc.) on either side of the injector, to provide matched color coding, and to provide a folder/tab analogy for retrieving injection protocol parameters.

Abstract: The present invention relates to a device for delivering a fixed dose or an adjustable dose of liquid medicament to a patient. Characterising for the present invention is that it is equipped with a planetary gear with the purpose of increasing the power needed to deliver liquid medicament out of this type of devices. On almost all of the devices of this type appearing on the market with the purpose of delivering a fixed dose or an adjustable dose of liquid medicament, the dose volume can be set in separated steps. With assistance of a planetary gear these steps, which each represent an increase of the volume of the medicament to be delivered, get smaller, which increases the possibility to set an optimum dose volume of the medicament. In its primary field of use the invention is intended to be used together with an injection needle.

Abstract: An endoscopic instrument comprises a first flexible insertion member sized for insertion through a body lumen to a target site and a needle coupled to the insertion member for penetration of tissue, the needle including a plurality of flexibility enhancing grooves formed therein along at least a first portion of the length of the needle.

Abstract: An intravenous catheter system having a retractable needle system and a body system is disclosed. The retractable needle system includes a housing, a needle, a docking feature, and an optional anti-shearing mechanism. The body system includes a body, at least one hub, a catheter connector, at least one plug, a plug recoil mechanism, a locking mechanism, a flash chamber, and a flash window.

Abstract: A valve assembly includes a valve housing having an upper body portion and a lower body portion that define an internal chamber for accommodating a valve member. The housing has axially aligned inlet and outlet ports. The valve assembly includes a generally spherical valve member seated within the internal chamber that defines first and second bores. The first bore defines a first longitudinal axis and the second bore defines a second longitudinal axis offset relative to the first longitudinal axis. The valve member is mounted for movement between a first position and a second position. The valve assembly includes a caroming mechanism for moving the valve member between the first position and the second position, including cam surfaces formed on the exterior surface of the valve member and a cam pin formed on the interior surface of the upper body portion of the housing.

Abstract: A medical use bandage is configured to immobilize, and to facilitate the use of, a tube implanted in a body. The implanted tube defines a body exit site, and a part of the tube projects from the body. The bandage includes a base support having a lower face for application to the skin and an upper face, a first bandage fixing portion for fixing the exit site, including on the lower face of the base support an adhesive fixing part to be adhered at least partly around the exit site to the skin and to a proximal portion of the projecting part of the tube, and a second bandage fixing portion for engaging the distal portion of the projecting part of the tube in a defined shape and in a sliding manner. The second bandage fixing portion is at least partly a part of the upper face of the support.

Abstract: A medicated module (4) for an injection system to co-deliver at least two medicaments is disclosed where a primary delivery device containing a primary medicament accepts a medicated module (4) containing a single dose of a secondary medicament (2) and where both medicaments are delivered through a single hollow needle (5). The medicated module (4) is user selectable so that it will deliver both the primary (1) and secondary medicaments (2), or only the primary medicament (1). The module (4) also contains a guard (42) that locks after dose delivery.

Abstract: A single use disposable shield and supportive stand for placement on a medical tool such as a suction catheter comprises a transparent body for protecting a responder from bodily fluids of a patient during suctioning of the oral or nasal cavities of a patient. As well the device acts as a supportive stand and securing agent for multiple medical devices and tools The body has an aperture for receiving a bushing. The bushing has an aperture for receiving the medical tool or device.

Abstract: A hub assembly for a pen injection device allows a needle to be disposed in at least one of a plurality of positions prior to an injection. A hub of the hub assembly is connected to the pen injection device, and the needle is received by the hub. A shield is movably connected to the hub and allows the needle to be disposed in at least one of several positions prior to an injection, such as a position in which the needle is visible for priming and a position that prevents the needle from being visible. A tab connected to the hub is received by a channel formed in the shield to control movement of the shield.

Abstract: The present disclosure is directed to a dose setting mechanism that may be used with a drug delivery device. The dose setting mechanism may include an inner body having a helical thread along an outer cylindrical surface of the inner body, and a drive sleeve for driving a piston rod in an axial direction, the drive sleeve positioned within at least a portion of the inner body. The dose setting mechanism may further include a dose dial sleeve rotatably engaged with the helical thread of the inner body and a dial grip connected to the dose dial sleeve and releasably connected to the drive sleeve. Further when a dose is set, the dial grip is rotated so that both the dose dial sleeve and the drive sleeve rotate with respect to the inner body.

Abstract: A device and method for applying chemicals to internal tissue of living organisms, including the internal tissue of plants and animals, which organisms reside in mediums such as land, air or water. Piercing elements are engageable with a chemical reservoir in order to coat of the piercing elements with a chemical. Once coated, the piercing elements are used to pierce a living organism's tissue, such as plant tissue, to deliver the chemical.

Abstract: Embodiments described herein generally relate to improved devices, systems, kits, products and methods related to topical medicament application of measured dosages. The kits and devices can single use and/or disposable for example.

Abstract: A stocking or sock with a foot portion includes a pocket for containing the big toe that is separate from the pocket(s) for the other toes. At least one medial reinforcement, integrally attached to the foot portion, entirely or partially surrounds the big toe pocket, while the medial part of the foot portion, and the posterior part or heel of the foot portion are anchored to the posterolateral or lateral part of foot portion, coming to bear on the anterior part of said pocket, counteracting any lateral deflections, and on the medial part, corresponding to the metatarsophalangeal joint and the first metatarsal of the foot, counteracting any medial deflections.

Abstract: A wound treatment system including a treatment chamber, a source of an aqueous antibiotic, a source of an oxygen-enriched gas, and a control system adapted to alternately surround a human limb with antibiotic mist and the oxygen enriched gas, which can be used to heal lesions such as foot ulcers. A method of treating lesions such as foot ulcers is also disclosed, that includes bathing the lesion in antibiotic mist and contacting it with oxygen gas.

Abstract: An irrigation system comprising: a reservoir with an inlet for pouring liquid into the reservoir, the inlet defining a closing element for closing the inlet; an insertion member defining an insertion end for insertion into a body cavity a human being, the insertion member defining at least one opening; and a liquid tube fluidly connecting the reservoir and having with the insertion member. At least one of reservoir and the insertion member is permanently fastened to the liquid tube.

Abstract: A disposable urine bag device includes a bag having an open top; and two cuff-like supporting members formed on two sides of the open top of the bag, wherein two fingers are allowed to insert into the supporting members to position the bag and adjust size of the open top of the bag. Moreover, a zipper is provided just below the open top of the bag for sealing the bag. Hence, after use an individual may seal the bag for disposal in an environment without the provision of public toilet. Further, an opening is provided on a sidewall of the bag for urine drainage. A woman may urinate by means of the disposable urine bag device while in standing position. Furthermore, a valve is mounted on the opening so that collected urine may drain via the valve. The collected urine may be used for health examination by hospitals.

Abstract: A disposable absorbent article comprising an absorbent core having a garment surface and an opposed body surface, which surfaces meet along at least one longitudinal edge and at least one end edge; a liquid permeable topsheet positioned adjacent the body surface of the absorbent core and having a pair of opposed longitudinal edges; a liquid impermeable backsheet positioned adjacent the garment surface of the absorbent core; and a waistcap/waistband disposed adjacent to at least one projection associated with the absorbent core, wherein the waistcap/waistband is capable of absorbing moisture and subsequently deforming to fill at least a portion of space between the article and a portion of the wearer's body.

Abstract: A disposable absorbent article is claimed that comprised a backsheet and an absorbent core and a core coversheet or topsheet, that in use faces the wearer, and one or more cuffs (25, 26), comprising one or more longitudinally extending elastic laminate portion(s) (10), formed by at least an elastic material (12) attached to a supporting sheet (20) of said cuff (25, 26), said laminate portion(s) (10) comprising in at least relaxed and partially contracted state a body-facing surface with a multitude of wrinkles, and whereby said elastic laminate portion (10) has an absolute contracted length Lc and a fully stretched absolute length Ls, whereby at a partial elongation of the elastic laminate potion (10) of ?=0.5: a) said wrinkles have an average wrinkle height Hw of less than 600 micrometers; and b) said laminate portion (10) has an average wrinkle density Dw between 5 and 10 wrinkles per cm.

Abstract: An absorbent article may comprise a chassis having a front waist region, a rear waist region, a crotch region between the front waist region and the rear waist region, a pair of longitudinal edges, and a pair of side panels extending between and connecting the front waist region and the rear waist region to form a leg opening. Each side panel may comprise a uniformly colored stretch laminate. The stretch laminate may comprise a colored elastomeric member and a first substrate joined to the elastomeric material. The side panels may be joined by a mechanical bond which may form an informational indicia.

Abstract: The present invention aims to provide a wearing article improved so that various types of nonwoven fabrics can be effectively used for target nonwoven fabric without anxiety that the target nonwoven fabric once engaged with hook elements might be readily torn. As an outer sheet 8 defining a garment-facing side of a chassis 2, a commonly-used nonwoven fabric is used and this nonwoven fabric is oriented in a longitudinal direction Y. Rear waist region's side edges 14 of the chassis 2 are provided with flaps 16 attached thereto. Each of the flaps 16 has a joint region 19 along which the flap 16 is joined to the chassis 2 and first and second hook elements 21, 22. Between the joint region 19 and the first and second hook elements 21, 22 as viewed in the transverse direction X, a contractible region 23 adapted to be contractible in the transverse direction X. The contractible region 23 is provided with a plurality of flap's elastic members 24.