Abstract: A component is suitable for protecting skin around an opening in the skin or around a stoma. The component can be formed from a carrier (2; 2?) that is enclosed between layers of soft and skin-compatible adhesive (3; 3?), and the adhesive has a softness of 8-22 mm. The adherence of the adhesive to dry skin can be 0.2-3 N/25 mm.

Abstract: Provided is a protection gown having a front part, a back part joined to the front part and two sleeves. The back part has two portions connected to each other in a neckline region of the gown. The two portions of the back part of the protection gown are connected to each other by a strip of material. The connection between the two portions of the back part of the protection gown can be released by manually breaking the strip of material or its attachment to one of the two portions of the back part of the protection gown. At least a portion of the neckline of the gown is resiliently stretchable.

Abstract: An article (1) of a medical and technical nature intended to be affixed to skin, or a component for affixing a medical article or part thereof to skin, which article or component comprises a layer of carrier material (2) that has a layer (3) of a soft skin-friendly adhesive on one side, and a protection layer (4) that protects the adhesive layer before use of the article or component and is affixed to the adhesive layer in such a way that it is releasable. According to the invention, the protection layer (4) is provided with a pattern of projections (6) on the side facing towards the adhesive layer (3) and a reinforcing layer (5) is arranged on the layer of carrier material (2), on the opposite side to the side that has the layer of soft skin-friendly adhesive, in such a way that it can be removed.

Abstract: A wound dressing with a wound pad and a layer of vapor-permeable material arranged on top of the wound pad and extending peripherally outside the wound pad is described, wherein at least that part of the vapor-permeable layer extending peripherally outside the wound pad is coated with adhesive, and wherein the wound pad includes a liquid-retaining and liquid-transporting layer, and an upper distributing layer and lower distributing layer which bear against the top and underside, respectively, of the liquid-retaining and liquid-transporting layer.

Abstract: The present invention relates to a wound dressing including a first wound pad and a first cover layer covering the first wound pad and extending beyond the first wound pad around the circumference thereof. According to the invention a second wound pad is disposed outside the first cover layer and enclosed in a second cover layer. Furthermore, the first and second wound pads are connected to each other by liquid transferring means.

Abstract: The present invention relates to a film dressing comprising a thin plastic film (2) coated with an adhesive (3). In accordance with the invention, the adhesive (3) has a softness of 10-22 mm, and the adhesive coating has a weight per unit area of 50 g/m2 or more.

Abstract: A surgical tape (1) includes a carrier (2, 3), on one side coated with an adhesive (4) and including a layer of non-woven (3). A layer of plastic film (2) is laminated to the layer of non-woven and the surgical tape (1) is tearable in a cross direction relative its longitudinal direction and liquid impermeable.

Abstract: Provided is a wound dressing including a wound pad of absorbent material having a first side and a second side opposite thereto, a backing layer covering the wound pad on the first side thereof an adhesive layer for attaching the dressing to skin. The backing layer has at least one conductive region and consists of plastic film.

Abstract: Provided is a fixation device for retaining a skin penetrating medical device, such as a cannula, on the skin of a patient. The fixation device includes a retaining component including a support layer having an adhesive coating, and a landing zone component, including a support layer having an adhesive coating, the landing zone component being adapted to be adhesively attached to the skin around the point of penetration. The retaining component acts as a skin-contacting component and is adapted to be applied on top of the landing zone component, and at least partially cover the medical device, such that the adhesive coating of the retaining component is applied to the support layer of the landing zone component. The adhesive coating of the retaining component includes a first adhesive, and the adhesive coating of the landing zone component includes a second adhesive, the first adhesive being different from the second adhesive.

Abstract: A device for treatment of wounds using reduced pressure is provided. The device includes a pump, a reservoir connected to said pump for collecting exudate from a wound, an inlet to the reservoir for connecting the reservoir with the wound so as to allow the pump to expose the wound to the reduced pressure, a wound pad to be arranged in the wound cavity, and a sealing covering the wound and the wound pad. The wound pad consists of an open-cell polyurethane foam which is fully impregnated with a soft hydrophobic silicone gel, and the foam has a hardness of 1.0-6.0 kPa measured according to ISO 3386-1 at at 40% compression The wound pad can be used with an absorbent member. A method is also provided for manufacturing the wound pad.

Abstract: The present invention relates to a component (1) making it easier to fasten a stoma bandage (6) to skin. According to the invention, the component comprises a plastic film (2) coated with a layer (3) of a soft and skin-compatible silicone elastomer which adheres to skin. The component also has a through-opening (4) intended to be applied around a stoma.

Abstract: The present invention pertains to antimicrobial compositions comprising inter alia at least one alkenyl-and/or alkynyl-substituted polysiloxane, at least one polysiloxane comprising silicon-bonded hydrogen atoms, and at least one hydrosilylation catalyst, as well as antimicrobial silicone gels, wound dressings, and methods of preparing the above.

Abstract: Provided is a body attachment wafer for attaching an ostomy device to a wearer. The body attachment wafer includes a plastic film having an opening therein, a layer of adhesive coated onto one side of the plastic film, and a stiffening layer releasably attached to the plastic film on the side thereof opposite to the side coated with adhesive. The layer of adhesive comprises a region surrounding the opening in the plastic film in which the thickness of the layer of adhesive is decreasing in a direction towards the circumference of the plastic film, the layer of adhesive having its largest thickness adjacent to the opening in the plastic film. The adhesive consists of a silicone gel adhesive having a softness exceeding 8 mm.

Abstract: A body attachment wafer for an ostomy device is provided, which body attachment wafer has a stoma opening, and an adhesive layer. The adhesive layer is covered by a release layer, having an opening which corresponds to the stoma opening. The release layer is divided along at least one dividing line from the stoma opening to the periphery of the body attachment wafer, and the release sheet includes a first grip tab extending from the release sheet in the area of the at least one dividing line. The first grip tab is arranged to overlap the release sheet on the other side of the dividing line.

Abstract: Provided is a device for treatment of wounds using reduced pressure, which includes a pump, a gas barrier cover, a first compressible material which expands after compression, and a second material capable of absorbing wound fluids several times its own weight. The first and second materials are arranged inside the cover and form a reservoir connected to the pump. The device also includes an inlet for connecting the reservoir with a wound, a wound pad to be arranged in the wound cavity, and a sealing covering the wound and the wound pad. A third material with high liquid spreading capability is arranged around at least a major part of the first material, and the second material is in the form of at least one layer arranged outside the third material and separated from the first material by the third material.

Abstract: A surgical garment (1) has a front portion (2) and a back portion (3) and two sleeves (4). Each sleeve (4) has at least one adhesive region (6) for affixing a donned surgical glove (11) thereto, each such region (6) being covered by a strip (7) of release material being removable from the associated adhesive region (6) in a sterile manner after donning of the surgical glove (11).

Abstract: An ostomy device is provided including an ostomy pouch having an entrance opening, a body attachment wafer having a through-going opening and a coupling layer, which couples the pouch to the body attachment wafer and has a central opening therein. The body attachment wafer includes a plastic film, which is coated with a layer of skin friendly adhesive on the side thereof distal to the ostomy pouch. The coupling layer is affixed to the body attachment wafer along an attachment line extending around the central opening in the coupling layer, the attachment line being distanced from the central opening in the coupling layer. The region around the entrance opening of the pouch is affixed to the coupling layer in a landing zone located between the attachment line and the opening in the body attachment wafer.

Abstract: A surgical drape (1) has a first absorbent region (4) on the upper side thereof. According to the invention, the first absorbent region (4) extends along at least one edge of the drape (1), the first region having a dispersion of liquid on an inclined plane better than in a region (3) or regions adjacent to the first absorbent region.

Abstract: A method of producing a hydrophilic polyurethane foam structure containing a silver salt, chosen from the group of silver sulphate, silver citrate, silver acetate, silver carbonate, silver lactate and silver phosphate, or a mixture of these salts includes the steps of (a) providing a water phase containing a surfactant, and at least one silver salt, wherein the at least one silver salt is dispersed in the water phase; (b) providing a isocyanate-terminated polyether having functionality of more than (2); (c) mixing the water phase and the isocyanate-terminated polyether, immediately transferring the resulting mixture to a mould whereby a foam structure is obtained; and (d) drying the foam structure until it has a moisture content of at most 10% (wt). The hydrophilic polyurethane foam structure produced by the method and a wound dressing containing the foam structure are also described.

Abstract: Provided are articles for use in wound treatment. The article is colored in a chosen color. The chosen color is green, and has in dry state the following mean values: a lightness factor L* along the black-white axis of between 20-55 according to Test Method T-397, a chromatic coordinate a* along the red-green axis of between ?45 to ?20 according to Test Method T-397, and a chromatic coordinate b* along the yellow-blue axis of between ?4.0 to ?1.0 according to Test Method T-397. The article can be used as a wound filler in an apparatus for treating a wound with negative pressure.