A non-adhesive absorbent wound dressing (10) is suitable for application about a jointed limb. The wound dressing (10) has a first portion (20) adapted to conform to and wrap around an upper part of the limb, a second portion (30) adapted to conform to and wrap around a lower part of the limb, and a hinge portion (40) between said first portion (20) and said second portion (30), said hinge portion (40) in use lying adjacent to the joint of the limb. The wound dressing (10) also comprises a porous wound contact sheet (80) and a substantially liquid-impermeable backing sheet (90), the wound contact sheet (80) and the backing sheet (90) being bounded (50) together at their periphery and along lines that define a plurality of pockets (60) in both the first portion (20) and the second portion (30), the pockets (60) containing absorbent material (70).

A medical compression garment for applying compression to a patient's body part comprises a first material (3) adapted to be wrapped around the body part, and a second material fixated on a section of the first material (3), wherein the second material (4) collapses the first material (3) such that the first material (3) forms wrinkles (5) along the section.

A medical compression garment for applying compression to a patient's body part comprises a first material (3) adapted to be wrapped around the body part, and a second material fixated on a section of the first material (3), wherein the second material (4) collapses the first material (3) such that the first material (3) forms wrinkles (5) along the section.

A dressing includes a first manifold layer, a second manifold layer, a first barrier layer coupled to the first manifold layer, a second barrier layer coupled to the second manifold layer, a first fenestrated film layer coupled to the first manifold layer, and a second fenestrated film layer coupled to the second manifold layer. The first manifold layer and the second manifold layer are positioned between the first barrier layer and the second barrier layer. The first fenestrated film layer and the second fenestrated film layer are positioned between the first manifold layer and the second manifold layer.

A dressing includes a barrier film layer, a wound contact layer coupled to the barrier film layer, and a plurality of felted foam strips positioned between the barrier film layer and the wound contact layer. Each strip provides a manifolding pathway. The barrier film layer and the wound contact layer include a central region and a plurality of peninsular projections extending therefrom in the shape of a hand.

In a method for producing bandages such as support bandages for knee and elbow joints, an elastic fabric material layer is provided on which reinforcement elements are placed and an uncured elastomer is applied to the fabric material in several layers or sprayed onto the fabric material layer so as to completely cover and embed the reinforcement elements which are firmly engaged thereby with the fabric material layer and form three-dimensional stabilizing structures projecting from the surface of the fabric material layer.

Medical articles comprising a conformable wound dressing and delivery system. The wound dressing generally comprises a backing having a first major surface and a second major surface, an adhesive on the second major surface of the backing, and an absorbent pad proximate the second major surface of the backing. The backing extends beyond the perimeter of the absorbent pad, typically beyond the entire perimeter of the pad. The perimeter of the wound dressing has a concave feature that exhibits a local minimum. An axis extends from the local minimum to the perimeter of the wound dressing opposite the local minimum. The carrier overlies at least a portion of the backing on each side of the axis but does not overlie the backing along the axis. The wound dressing is especially designed for use on round or irregular shaped body parts, such as an elbow or heel.

In the configuration of a supporter that at least partially includes a tubular cover portion which covers a part of a human body and which elastically expands and contracts, a load addition pattern portion that is adhered to at least a part of a half or more circumference in a circumferential direction on the front surface of the tubular cover portion and that can apply a load of a predetermined magnitude to the part of the human body when the part of the human body to which the tubular cover portion is fitted is moved is continuously formed of an elastic rubber material. Preferably, as the elastic rubber material, a silicone rubber material is used, and a part or the whole of the area of the load addition pattern portion is formed with a mesh-shaped portion and preferably a honeycomb shape.

A novel ultrasonic oscillation-induced sericin extraction method produces a high-molecular-weight sericin solution from silk cocoon threads at room temperature. In one embodiment, unique pH variation-resistant alkaline ionic water is produced from a novel strongly-alkaline ionic water generator device, wherein the unique pH variation-resistant alkaline ionic water is subsequently utilized as a beneficial solvent that contributes to the feasibility of the novel ultrasonic oscillation-induced sericin extraction method at room temperature. The high-molecular-weight sericin solution produced and coated in a glove provides a high coating adhesion for economical manufacturing of sericin-coated gloves, while also providing superb skin moisturizing and protection properties. Furthermore, once coated in a glove, the high molecular weight of sericin beneficially resists a rapid skin seepage of sericin to human skin layers, thereby acting as natural moisturizing factor (NMF) simulants on top of the human skin layers when the glove is worn.

Disclosed is a medical dressing having a pad and a border portion. The pad can have a rim and the border portion extends along said rim. The medical dressing can be arranged in a first substantially planar configuration and be folded along a first line, and a second portion of said medical dressing is formed and a second substantially cup-shaped configuration. The first portion can be facing and contacting said second portion. Said first substantially planar configuration the first and second portions can be connected by means of a fixed connection along a second line, which defines a second line segment having a first and a second end-point. The first and second line segments are connected at their respective first end-points such that an angle between 90 and 175 degrees is formed between the first and second line segments when the medical dressing is in the first substantially planar configuration.