2191 results about "Bandage" patented technology

Hemostatic agents and devices are made from oxidized cellulose fiber, the oxidized cellulose having a carboxylation content increased by the action of nitrogen dioxide on virgin cellulose fiber. A composition may be incorporated into the oxidized cellulose fiber to cause a pharmacological effect on a wound to which the hemostatic agents and devices are applied. When applied, the oxidized cellulose fiber causes blood emanating from the wound to clot. The oxidized cellulose fiber can either be resorbed into the wound or removed from the wound after healing. A hemostatic bandage includes a pad of unwoven oxidized cellulose fibers mounted on a substrate. Methods of arresting a flow of blood emanating from a wound using such devices are also disclosed. Methods of fabricating oxidized cellulose are also disclosed.

Disposable bandage apparatus for use in oximetry having adhesive on at least a portion of at least one face thereof, at least one plastic receptacle mounted thereon and a radiation transparent window bounded by said receptacle.

The present invention relates to a haemostatic multilayer bandage that comprises preferably a thrombin layer between two fibrinogen layers. The dressing may contain other resorbable materials such as glycolic acid or lactic acid based polymers or copolymers. The inventive haemostatic bandage is useful for the treatment of wounded tissue.

A self-powered compression device for use in promoting circulation, said device embodying a plurality of inflatable sleeves arranged sequentially for applying compression to a body or limb and which further comprises a pump, a piping system and a bandage or boot to enclose the device in its entirety. A method for using self-generated pressure in promoting circulation in conditions including but not limited to, lymphatic and traumatic edemas, venous disorders, limb ulcers, varicose veins, muscle fatigue, sports medicine, cellulite treatment, diabetic feet, feet massage for recreation or cosmetic enhancements.

The present invention provides a device and kit and method of use thereof for wound treatment of a subject. The device may include an electrically operated patch or other means of delivery of electrical current and a connected moist surface. Optionally, the device may include a composition comprising an active substance useful in wound treatment. Preferably, the means of delivery of electrical current includes a power source and a plurality of electrodes disposed in a suitable conformation on a base substrate layer, which readily facilitates electrical contact with the body area of the subject. Preferably, the kit may include a means of delivery of electrical current and a moist surface provided as separate components. The present invention further provides a thin and flexible device for galvanic treatment to treat wounds with electrical stimulation. Preferably, the device is made using a printing technique.

A device includes a patch or bandage, applied on or adjacent to a specific external surface of a human or animal body part, which delivers light of varying wavelengths, intensity and duration for treatment of various diseases or abnormalities.

Compositions that include nanoscale structured materials or precursors thereof (e.g., self-assembling peptides) are described. The compositions can include other substances (e.g., a vasoconstrictor). Also described are methods for using the compositions to promote hemostasis, to protect the skin or wounds from contamination, to decontaminate a site upon removal of previously applied compositions that provided a protective coating, and to inhibit the movement of bodily substances other than blood. The compositions are also useful in isolating tissue, removing tissue, preserving tissue (for, e.g., subsequent transplantation or reattachment), and as bulking, stabilizing or hydrating agents. Medical devices that include the compositions (e.g., a stent or catheter), bandages or other wound dressings, sutures, and kits that include the compositions are also described.

Disclosed herein are color change laminate materials suitable for a variety of uses. The color change laminate materials include at least two layers of extensible materials having visually distinct coloration, and indicate a stretched or extended state by exposing the previously covered coloration of a lower layer. The color change laminate materials may also indicate the amount of stretching or extension is applied to the laminate. When the laminate includes elastic materials capable of stretch and recovery, the color change laminate materials may further be reversible color change laminate materials that can display color change upon extension and then recover the extension and return to the original coloration. Such color change laminate materials and reversible color change laminate materials are highly useful for use in garments or other textile type applications, in or on personal care products, protective wear products, health care and medical care products, bandages and the like.

Disclosed herein are elastic laminate materials having an elastic member and at least one fibrous nonwoven web. The elastic laminate materials have highly desirably properties of extensibility and elastic recovery, and cloth-like aesthetic properties of softness and drapability. In embodiments, the elastic laminate materials may include a second fibrous nonwoven web bonded to the opposite side of the elastic member. Also disclosed herein is a process for forming the elastic laminate materials. Such elastic laminate materials are highly useful for components in or on personal care products, protective wear garments, medical care products, bandages and the like.

The invention relates to a therapeutic device to promote the healing of a wound, comprising a porous paid which is permeable for fluids to place on the wound, a bandage to cover the wound and to provide an essentially airtight seal around the wound, a drainage line connecting the pad with a suction pump so that suction can be applied to the wound to draw the fluids away from it, whereby the line is connected to the suction pump via a canister to collect fluid sucked from the wound, a connector to connect the pad to the drainage line, means to determine a prevailing wound pressure basically comprising the wound and this surrounding skin area, as well as a control unit to control the wound pressure. In order to generally improve metrology with the goal of making possible a more reliable and more secure dressing of the wound, and also to design metrology in an especially simple and error-free way, it is proposed that the pad interconnect the suction pump solely via the drainage line.

An apertured fibrous nonwoven web with an array of apertures is made that allows for increased functionality and improved aesthetic appearance. The material is particularly well-suited for use as a topsheet or bodyside liner material for personal care absorbent articles including, but not limited to feminine hygiene products, diapers, diaper pants, training pants, adult incontinence devices, bandages and the like. The fibrous nonwoven web includes first, second and third arrays of apertures with varying characteristics that provide improved fluid handling properties for various body exudates.

A surgical bandage for treating a wound that allows various fluids or fluid-like substances including cyanoacrylate adhesives to be applied. The surgical bandage has a wound treatment portion for being placed over a wound and a place for a flowable cyanoacrylate adhesive or any other fluid or fluid-like substance to be applied to the underlying wound (laceration, surgical incision or other tissue separation). A source is used to apply the cyanoacrylate or other fluid to the wound treatment portion flowing through at least one opening of the wound treatment portion to the underlying wound and its surrounding area either by direct application or from a non-contact distance. The surgical bandage allows for direct visualization before, during and after its application. The surgical bandage allows for removal of blood or any fluid that may be present in, on or around the wound by blotting or wiping.

A modified starch material for biocompatible hemostasis, biocompatible adhesion prevention, tissue healing promotion, absorbable surgical wound sealing and tissue bonding, when applied as a biocompatible modified starch to the tissue of animals. The modified starch material produces hemostasis, reduces bleeding of the wound, extravasation of blood and tissue exudation, preserves the wound surface or the wound in relative wetness or dryness, inhibits the growth of bacteria and inflammatory response, minimizes tissue inflammation, and relieves patient pain. Any excess modified starch not involved in hemostatic activity is readily dissolved and rinsed away through saline irrigation during operation. After treatment of surgical wounds, combat wounds, trauma and emergency wounds, the modified starch hemostatic material is rapidly absorbed by the body without the complications associated with gauze and bandage removal.

The composition and method for healing tissues is a medicinal composition for facilitating the growth, protection and healing of tissues and cells in animals and humans. The composition is formulated as a either a powder, gel, paste, film, fluid injectable, rehydratable freeze-dried paste or sponge, sprayable solution, topically applied patch with adhesive and reservoir system, an intermediate for coatables such as films and bandages, a matrix for membranes, or as a matrix of flexible polymer(s), or delivered as either an orally ingestible liquid, tablet or capsule. The main ingredient of the formulated compositions is hydrolyzed collagen, which can be combined with polysulfated glycosaminoglycans, hyaluronic acid or salts thereof, or a glucosamine salt, and mixtures thereof. The composition may be formulated as an aqueous eye drop solution.

A sleeve for covering a portion of a limb at a wound site incorporates a molecular sieve material which is at least partially exposed so that blood flowing from a wound site over which the sleeve is positioned contacts the molecular sieve material to facilitate clotting. One end of the sleeve may be closed to form a stocking or a mitten. The molecular sieve material may also be incorporated into a cap or similar device for wearing on the head of a victim. A chin strap may be attached to the cap to facilitate the retaining of the cap on the victim's head. The molecular sieve material may also be incorporated into a bandage that is directly wearable on a wound.

Embodiments of the invention provide systems and methods for remote sensing and/or monitoring utilizing a sensing device, such as may be implemented in a patch that can be placed on or affixed to a subject, where the sensing device includes multiple sensors. For example, one embodiment of the present invention includes a wireless human temperature skin patch providing accurate measurement of human temperature from a sensing device applied to the skin and even in the presence of differing ambient temperature. In such an embodiment, the patch can include, for example, a flexible, breathable bandage or adhesive strip or pad to affix the sensing device to a patient. The sensing device can include multiple sensors such as two or more temperature sensors that can be used to accurately determine the patient's core body temperature from the measured temperature at the skin.

The invention relates to a modified starch material for biocompatible hemostasis, biocompatible anti-adhesion, tissue healing promotion, absorbable surgery sealing and tissue adhesion. The invention applies biocompatible modified starch to animal tissues, wherein the modified starch material has the molecular weight of more than 15,000 daltons, and the particle diameter of between 1 and 1,000 mu m. The modified starch hemostatic material has stypticity, reduces hemorrhage, blood oozing and tissue fluid oozing of wounds, maintains relative moistening or drying of wound surfaces or the wounds, inhibits bacterium growth and inflammation reaction, and contributes to locally diminish inflammation of the wounds and relieve pain of patients. Moreover, the modified starch material can wash local parts after operation is over and remove redundant modified starch which does not participate in hemostasis, and can easily remove haemostatic under the condition of debridement treatment after self-help and first-aid treatment of war wounds; and hemostatic materials with a small amount of modified starch can be absorbed by the body, so that the pain of tearing of gauzes and bandages on people is avoided.

A wound dressing or bandage that provides a galvanic current for extended periods of time before having to change the dressing or bandage is addressed in the present invention. The present invention is directed to a galvanic current wound dressing having antimicrobial properties and to a method for treating a patient with the wound dressing.

The present invention relates to a film-forming barrier composition useful for protecting the skin from body fluids, such as urine, feces, menses. The composition comprises a skin conditioning agent, a viscosity enhancing agent and an oleophilic film-forming agent. Optionally, the lotion may comprise skin care ingredients for treating or maintaining skin health. The composition may be applied to the skin by suitable delivery vehicles, such as absorbent articles or components thereof, sheet materials, pads, bandages, sponges, foam pads, pumps, sprays, depending on the viscosity of the composition.

The Breakaway Leg Sling is provided for use with a walker or crutches and suspends a single leg in a below-the-knee cast, shoe, or bandaged foot in a rearward, elevated position and assists the patient with weight avoidance on the suspended leg. The apparatus is prepared for use from a safe sitting position, and the leg is placed into its suspended position during the natural motion of standing. If needed, the apparatus includes a breakaway safety fastener that disengages at an effective, pre-determined force using the muscles of the suspended leg thereby providing the patient with immediate use of the suspended leg to regain balance and prevent a potential fall. If disengaged, the safety fastener is easily restored to operational use. The Breakaway Leg Sling is comprised of a torso harness device, a detachable foot cradle device, a load strap used to engage the torso harness to the foot cradle device, and the breakaway safety fastener incorporated into the length of the load strap. The foot cradle device may be left on the foot for extended periods of time without hampering the patient's comfort thereby leaving the foot cradle anchor in a ready-to-connect position. If desired, the foot cradle device may be removed for bathing or other purposes, and the foot cradle device will retain its custom size thus saving the patient time and effort when replacing the foot cradle device on the foot or cast.

Disclosed is a bandage, and methods for its use, which facilitates application of tissue adhesive to close and seal wounds.

The invention discloses an exoskeleton rehabilitation robot for rehabilitation of a lower limb walking function and a control system and method thereof. The robot comprises a backrest, a hip joint power source, a hip joint component, a waist component, a thigh bar component, a knee joint power source, a knee joint component, a shank bar component, an ankle joint component and a foot pedal. According to the lower limb exoskeleton rehabilitation robot, a driving scheme is designed by utilizing a bionics principle, so that the initiative degree of freedom of the ankle joint is increased; through initiatively pulling the heel tendon muscles of the patients, the rehabilitation speed of the ankle joint function is improved; the waist component, a connection rod mechanism and the foot pedal adopt a carbon fiber composite material, so that the structure weights and volumes are lightened while the strength is kept; and a non-polar adjustable function is set for the waist width, thigh length and shank length, and flexible bandages are equipped, so that the wearing comfort level requirement of the users is satisfied to the greatest extent. The robot disclosed by the invention not only can be used as a tool for riding instead of walk for the patients with walking disability, but also can help the stroke patients to obtain walking ability again through initiative training.

A device for promoting the clotting of blood comprises a clay material in particle form and a receptacle for containing the clay material. At least a portion of the receptacle is defined by a mesh. Another device comprises a gauze substrate and a clay material disposed on the gauze substrate. Another device is a bandage comprising a substrate, a mesh mounted on the substrate, and particles of a clay material retained in the mesh. A hemostatic sponge comprises a substrate, a hemostatic material disposed on a first surface of the substrate, and a release agent disposed on a second surface of the substrate. The release agent is disposed on the wound-contacting surface of the substrate. When treating a bleeding wound, application of the hemostatic sponge causes at least a portion of the hemostatic material to come into contact with blood through the release agent and through the substrate.

The invention generally relates to dextran fibers which are preferably electrospun and devices formed from such fibers. In particular, such devices may include substances of interest (such as therapeutic substances) associated with the electrospun fibers. Upon exposure to a liquid the electrospun fibers dissolve immediately and the substances of interest are released into the liquid. Exemplary devices include bandages formed from electrospun dextran fibers and associated agents that promote hemostasis, such as thrombin and fibrinogen.

The present invention relates to a bandage for use in negative-pressure wound therapy, more particularly for wounds in the abdominal region, comprising a flexible film as a wound contact layer and at least one conduit applied to the film, wherein the conduit communicates with the wound space through openings in the conduit and in the film.

An adhesive device with an ultraviolet element is disclosed. The adhesive device with an ultraviolet element can be used to provide a treatment of a surface of an object. The treatment can include cleaning, disinfection, sterilization and sanitization. The adhesive device with an ultraviolet element can also be used as a self-adhesive bandage.

Disclosed are water-dispersible fibers derived from sulfopolyesters having a Tg of at least 25° C. The fibers may contain a single sulfopolyester or a blend of a sulfopolyester with a water-dispersible or water-nondispersible polymer. Also disclosed are multicomponent fibers comprising a water dispersible sulfopolyester having a Tg of at least 57° C. and a water non-dispersible polymer. The multicomponent fibers may be used to produce microdenier fibers. Fibrous articles may be produced from the water-dispersible fibers, multicomponent fibers, and microdenier fibers. The fibrous articles include water-dispersible and microdenier nonwoven webs, fabrics, and multilayered articles such as wipes, gauze, tissue, diapers, panty liners, sanitary napkins, bandages, and surgical dressings. Also disclosed is a process for water-dispersible fibers, nonwoven fabrics, and microdenier webs. The fibers and fibrous articles have further applications in flushable personal care and cleaning products, disposable protective outerwear, and laminating binders.

The liquid, polymer-containing coating materials of this invention comprise a polymer of a polymerizable, nitrogen-containing, hydrophilic monomer, which may give thermoresponsive properties, and which is copolymerized with a hydrophobic, polymerizable siloxy-containing monomer, in a solvent system of a volatile hydrophobic (non-polar) liquid that is non-stinging to a user. The material forms a coating or bandage in the form of a film when applied to a surface or the skin of a user.

The invention provides a biodegradable polymer composition for a breathable film which comprises a biodegradable polyester such as polylactic acid, a biodegradable copolyester such as an aliphatic/aromatic copolyester, and a filler such as calcium carbonate. These compounds are melt blended and film formed and the film is then stretched in a monoaxial or biaxial direction to enhance pore formation and hence also enhance the breathability of the film. The water vapor transmission rate (WVTR) of the film is typically greater than 3,000 grams per square meter per day so that the film is suitable for use in disposable articles such as wipes, diapers, training pants, absorbent underpants, adult incontinence garments, feminine hygiene products, medical garments, bandages and the like.

A device for delivering oxygen to a wound or injury includes a bandage, which includes a base defining an opening, a cover, and a locking mechanism for releasably securing the cover to the base. An oxygen source is in fluid communication with the cover, whereby oxygen is delivered to the opening in the base.