Patent classifications
A61F13/00017
REDUCED-PRESSURE DRESSING ASSEMBLIES FOR USE IN APPLYING A CLOSING FORCE
A closing dressing bolster and assembly for use with a system for treating a linear wound on a patient includes a bolster body formed from a flexible closing bolster material having closing members that are operable to develop an inward closing force when the closing dressing bolster is placed under reduced pressure. In one aspect, when the closing dressing bolster is under reduced pressure, the system, dressing, or assembly develops an inward force realized at the linear wound and a compression force. A wicking-material holder and wicking material may be used as well. The member components may all be see-through to allow visual inspection of the wound without requiring removal of the dressing.
COMPRESSION BANDAGE
The invention relates to a compression bandage comprising a first non-woven laser (1) and at least one second non-woven layer (2) connected in a planar manner to the first non-woven layer (1), wherein superabsorbent fibers are provided in the first non-woven laser.
Method of oral hemostasis using a conformable non-disruptive hemostasis material
A method of promoting hemostasis in the mouth or oral cavity utilizes a non-absorbent, low surface energy and highly conformable non-disruptive hemostasis material. Traditional wound packing material is highly absorbent and has large open surfaces that allow clot forming materials, such as the platelet plug to adhere to the packing material and whereupon removal, the clot is disrupted. A non-disruptive highly conformable hemostasis material does not have large open pores and therefore does not adhere to forming clots. A non-disruptive hemostasis material may consist of expanded polytetrafluoroethylene that has a pore size of no more than about 10 microns. A non-disruptive hemostasis material may comprise a thin film of material over a portion of the outside surface that is non-absorbent and thin to allow for conforming into an oral cavity, such as from a tooth extraction. A thin film may cover porous material, such as a foam, that may be elastomeric.
Medical device containing a multi-ply knit fabric
A medical device comprising a device that covers at least a portion of a patient's skin and has an inner surface designed to be in contact with the patient's skin. It contains a multi-ply knit fabric that contains a first knit ply and a second knit ply. The first knit ply contains a plurality of first yarns and forms the upper surface of the fabric. The second knit ply contains a plurality of polytetrafluoroethylene (PTFE) yarns which forms the lower surface of the fabric. The first and second ply are integrated through combined portions formed by interlacing first yarns among the PTFE yarns, interlacing PTFE yarns among the first yarns, and interlacing a plurality of third yarns among the first and the PTFE yarns. The multi-ply knit fabric also contains a composition comprising at least one silver ion-containing compound on at least the upper surface of the multi-ply knit fabric.
Polymer compositions, fibers and threads with petrolatum and/or oleic acid-containing oils
This invention relates to a polymer composition containing at least one polymer and at least one agent, formed bodies having such a polymer composition, the use of the formed bodies and polymer compositions, and corresponding threads, nonwoven materials, clothing articles, and medical aids.
WOUND DRESSING MATERIAL AND METHODS OF MAKING AND USING THE SAME
A wound dressing material comprises first and second wound-contact scrims, and an antimicrobial layer disposed therebetween. The wound-contact scrims comprise water-sensitive fibers comprising a copolymer comprising divalent hydroxyethylene monomer units and divalent dihydroxybutylene monomer units. The wound dressing material may be contacted with an exposed surface of a wound. A method of making the wound dressing material is also disclosed.
BIOMIMETIC WOUND DRESSING WITH ARTICULATING MICROPATTERN
A surface is covered with microstructures that extend from the surface, and are made of a resilient material that allows the microstructures to bend or articulate. The microstructures are generally columnar and can have fingers on their distal or top end that is opposite the base from which the microstructures extend. In addition to the ordinary roughness presented by the microstructures, the articulation further discourages biofouling and bioadherence. The articulation of the microstructures can be oriented, and the orientations can be mixed or varied among the microstructures so that adjacent ones of the microstructures have different orientations of articulation.
Medical multi-layer product comprising nanofibrillar cellulose and method for preparing thereof
The present application provides a medical multi-layer product comprising a layer comprising nanofibrillar cellulose, and a layer of gauze. The present application also provides a medical product comprising the medical multi-layer product, and a cosmetic product comprising the medical multi-layer product. The present application also provides a method for preparing a medical multi-layer product, the method comprising providing a filter, providing a dispersion comprising nanofibrillar cellulose, providing a gauze, applying the dispersion onto the filter, applying the gauze onto the dispersion, and dewatering the structure through the filter to obtain the medical multi-layer product.
Absorbent article
(Object) To prevent a high compression portion from being defectively formed and also a top sheet from being torn. (Means of Achieving the Object) A sanitary napkin (1) in which a low compression portion (15) and a high compression portion (16, 17, 18) are formed on a bottom surface of a compressed groove (10) that is recessed from a skin contact surface side. The high compression portion includes regularly-arranged high compression portions (16) that are regularly arranged in a longitudinal direction of the compressed groove (10), a large-area high compression portion (17) that is irregularly arranged in the compressed groove (10) and has an area larger than an area of each of the regularly-arranged high compression portions (16), and an auxiliary high compression portion (18) that is arranged at one side, in a longitudinal direction of the napkin, of the large-area high compression portion (17) through the low compression portion (15) so as to surround the one side, in the longitudinal direction of the napkin, of the large-area high compression portion (17).
Wound dressing system
A wound dressing containing a multi-ply knit fabric, where the fabric contains a first and a second knit ply. The first knit ply contains a plurality of first yarns and forms the upper surface of the fabric. The second knit ply contains a plurality of polytetrafluoroethylene (PTFE) yarns, where the PTFE yarns have a transmission in the IR region of 8-10 μm at least about 40%, and a thermal conductivity of at least about 0.2 W/(m.Math.K) forms the lower surface of the fabric. The first ply and the second ply are integrated through combined portions formed by interlacing first yarns among the PTFE yarns of the second knit ply, interlacing PTFE yarns among the first yarns of the first knit ply, or interlacing a plurality of third yarns among the first yarns and the PTFE. The multi-ply knit fabric also contains a composition containing at least one silver ion-containing compound.