Abstract: The disclosed medical dressing includes a dressing body with an overlying carrier system that is releasably secured to the dressing body. The carrier has a perimeter carrier portion overlying the perimeter of the dressing body and a central carrier portion overlying some, but not all, of a central area of the dressing body. This carrier construction allows for better handling of the medical dressing during application by giving both stability in some areas and stretching and flexibly in areas without the carrier.

Abstract: Medical dressings including stiffening systems fixedly attached to backing layers are described herein along with methods of using the medical dressings. The stiffening system is fixedly secured to the backing to limit flexing and stretching of the backing layer. Typically, the medical dressing and stiffening system is applied over a medical device that is secured to skin. The stiffening system covers some of the medical device and also extends beyond the medical device. The stiffening system stabilizes the medical device over the skin.

Abstract: Compression sleeve (1) for application circumferentially around a human limb (10) to exert therapeutic pressure on the limb. The compression sleeve has a fabric (80), which comprises viscoelastic strands (90) for providing the fabric with viscoelastic properties.

Abstract: A compression system for applying compression to a body part of a user. The compression system has a sleeve for substantially covering a portion of the body part of a user. The sleeve has two lateral side edges. In the transverse direction from the first lateral side edge to the second lateral side edge the sleeve has a first lateral side region, a central region and a second lateral side region. At least the central region of the sleeve has a material with elasticity in the transverse direction and longitudinal direction of the sleeve. The compression system has a releasable closure system. Upon closure of the closure system the sleeve is restrained and tightened about the body part of the user.

Abstract: Disclosed is a compression device for applying compression to a body part of a user. The compression devices comprises a sleeve for substantially covering a portion of the body part of a user, wherein the sleeve has an outer surface, an inner surface, an upper edge, a lower edge and two lateral side edges. In the transverse direction from the first lateral side edge to the second lateral side edge the sleeve comprises a first lateral side region, a central region and a second lateral side region. At least the central region of the sleeve comprises a main material having elasticity in at least the transverse direction of the sleeve. A maximum elongation in the transverse direction is from 5% up to and including 30% under a load of 10 N per cm width and a difference quotient of tension in transverse direction from 20% elongation to 25% elongation equal to or greater that 0.6 N per cm width per percent elongation.

Abstract: A medical article and methods of using same. The medical article can include a machine direction (MD) and a cross-machine direction (CMD); a support layer; and a viscoelastic layer. The viscoelastic layer can be coupled to the support layer, and the viscoelastic layer can be discontinuous in the MD and/or the CMD. The viscoelastic layer can recover at least 70% of its deformation after 48 hours at room temperature after being strained to 50% elongation, such that the medical article has a first tensile stiffness T1 at a first strain rate S1, and a second tensile stiffness T1 at a second strain rate S1. The ratio of S1/S2 can be at least 100, and the ratio of T1/T2 can be at least 1.5. The method can include wrapping the medical article around a body part; applying the first strain rate S1; and applying the second strain rate S2.

Abstract: A compression bandage for a human calf having a) a first engagement zone on a first major surface, comprising mechanical engagement means, b) a second engagement zone on the first major surface, comprising mechanical engagement means, c) a soft section between the first and the second engagement zone, having a reduced modulus of elasticity in length direction, and d) a stiff section having an elevated modulus of elasticity in length direction, and having a length greater than the length of the soft section. The stiff section comprises a third engagement zone on the second major surface, comprising mechanical engagement means, for engagement with the first and with the second engagement zone. When wrapping the bandage around the calf, the third engagement zone can engage, in a subsequent turn, with the first engagement zone, and with the second engagement zone, so that the stiff section bridges the soft section.

Abstract: Compression device (1) for application circumferentially around a patient's limb (10), comprising a) a first band portion (20a) and a second band portion (20b), both band portions (20) being arrangeable along at least a part of the circumference of the limb for creating radial pressure on the limb, b) a spine element (30), extending in axial direction (100) when the compression device is applied around the limb, and comprising a first and a second guide opening (40a, 40b) for guiding the first and the second band portions, respectively. The guide openings (40a, 40b) are arranged offset in axial direction with respect to each other such that, when the first band portion is arranged along at least a part of the circumference of the limb and guided through the first guide opening, and the second band portion is arranged along at least a part of the circumference of the limb, parallel to the first band portion, and guided through the second guide opening, the band portions overlap in an axial direction.

Abstract: Compression sleeve (1) for application circumferentially around a human limb (10) to exert therapeutic pressure on the limb. The compression sleeve has a fabric (80), which comprises viscoelastic strands (90) for providing the fabric with viscoelastic properties.

Abstract: Compression bandage for use as the only bandage in a single-bandage system for compression therapy, comprising an elastic compression layer and an elastic comfort layer, of which at least 50% is permanently attached to the compression layer. The compression bandage has a full-stretch elongation (FSE) of between 25% and 60% beyond its unstretched length. Full-stretch elongation is defined as the elongation at which the second derivative (130) of a curve (110) showing tensioning force over longitudinal elongation has its global maximum (140).

Abstract: A compression device for applying compression to a body part of a user. The compression device comprises a sleeve for substantially covering a portion of the body part of a user. The sleeve has an upper edge, a lower edge and an opening extending from its upper edge to its lower edge, said opening having two side edges. The first side edge is provided with one half of a zipper and the second side edge is provided with a complementary half of said zipper. The sleeve includes at least one expandable gusset provided with a releasable closure system extending along the length of said gusset, said gusset and releasable closure system being configured and arranged, such that when said releasable closure system is closed said gusset is prevented from expansion and when said releasable closure system is opened said gusset is allowed to expand.

Abstract: Disclosed is a compression device for applying compression to a body part of a user. The compression devices comprises a sleeve for substantially covering a portion of the body part of a user, wherein the sleeve has an outer surface, an inner surface, an upper edge, a lower edge and two lateral side edges. hi the transverse direction from the first lateral side edge to the second lateral side edge the sleeve comprises a first lateral side region, a central region and a second lateral side region. At least the central region of the sleeve comprises a main material having elasticity in at least the transverse direction of the sleeve. A maximum elongation in the transverse direction is from 5% up to and including 30% under a load of 10 N per cm width and a difference quotient of tension in transverse direction from 20% elongation to 25% elongation equal to or greater that 0.6 N per cm width per percent elongation.

Abstract: Provided are reactive compositions for making a polyurethane-based rain-erosion protective coating for rotor blades, the reactive composition comprising an isocyanate-reactive component and an isocyanate-functional component and wherein the isocyanate-reactive component comprises a first component i) being a short chain hydroxyl-functional compound having two terminal (?-?) hydroxyl groups, a molecular weight of less than 250 g/mole and containing at least 2 carbon atoms and a second component ii) comprising a high molecular weight hydroxyl-functional compound having two terminal (?-?) hydroxyl groups and a molecular weight of at least 250 g/mol and comprising one or more units selected from oxyalkylene units and polyoxyalkylene units and wherein the isocyanate-functional component is an isocyanate prepolymer of the general formula NCO—Z—NCO, wherein Z is a linking group comprising at least two urethane (—NH—CO—O—) units and additionally one or more units selected from alkylenes, oxyalkylenes, polyoxyalkylen

Abstract: A compression device for applying compression to a body part of a user. The compression device has a sleeve with two lateral side regions and a central region in-between. The central region of the sleeve comprises a main material having elasticity in at least a transverse direction. A maximum elongation in the transverse direction is from 5% up to and including 30% under a load of 10 N per cm width and a difference quotient of tension in the transverse direction from 20% elongation to 25% elongation equal to or greater that 0.6 N per cm width per percent elongation. The device further includes a releasable closure system configured and arranged relative to the sleeve, such that, in use, upon closure of the closure system the sleeve is restrained and tightened about the body part of the user.

Abstract: Compression device (1) for application circumferentially around a patient's limb (10), comprising a) a first band portion (20a) and a second band portion (20b), both band portions (20) being arrangeable along at least a part of the circumference of the limb for creating radial pressure on the limb, b) a spine element (30), extending in axial direction (100) when the compression device is applied around the limb, and comprising a first and a second guide opening (40a, 40b) for guiding the first and the second band portions, respectively. The guide openings (40a, 40b) are arranged offset in axial direction with respect to each other such that, when the first band portion is arranged along at least a part of the circumference of the limb and guided through the first guide opening, and the second band portion is arranged along at least a part of the circumference of the limb, parallel to the first band portion, and guided through the second guide opening, the band portions overlap in an axial direction.

Abstract: Disclosed is a monitoring system for determining the efficacy of at least one compression device for use in compression therapy. The monitoring system comprises at least one pressure sensor for measuring a pressure exerted onto a body part of a user by the compression device and at least one evaluation unit which is connectable to the pressure sensor. The evaluation unit is adapted to acquire at least one resting pressure prest with the user being in a resting position.

Abstract: Provided are reactive compositions for making a polyurethane-based rain-erosion protective coating for rotor blades, the reactive composition comprising an isocyanate-reactive component and an isocyanate-functional component and wherein the isocyanate-reactive component comprises a first component i) being a short chain hydroxyl-functional compound having two terminal (???) hydroxyl groups, a molecular weight of less than 250 g/mole and containing at least 2 carbon atoms and a second component ii) comprising a high molecular weight hydroxyl-functional compound having two terminal (???) hydroxyl groups and a molecular weight of at least 250 g/mol and comprising one or more units selected from oxyalkylene units and polyoxyalkylene units and wherein the isocyanate-functional component is an isocyanate prepolymer of the general formula NCO—Z—NCO, wherein Z is a linking group comprising at least two urethane (—NH—CO—O—) units and additionally one or more units selected from alkylenes, oxyalkylenes, polyoxyalkyl