Described is a novel epicutaneous test plaster useful for the application of test substances for direct and continuous contact with the skin of a human patient. The plaster comprises a support lattice with a flexible carrier lattice adhered thereto, the combination forming a series of test chambers capable of receiving test substances for application to the skin.

A wound care bandage for treating a wound is provided. The bandage includes an SIS layer to be placed on the wound surface and a cover to be placed over the wound. The bandage further includes a structure to provide a vacuum space. A method for promoting wound healing is further provided. The method includes applying the above-mentioned wound care bandage to the wound and creating a vacuum in the vacuum space to draw blood controllably from the wound into the SIS layer.

A vacuum bandage is provided for use with a wound having a wound surface. The bandage is connectable to a vacuum source and includes a wound dressing member having a wound contacting surface, a top surface, and a port configured for communication with the vacuum source. The wound dressing member further includes holes in the wound contacting surface configured for communication with the wound surface of the wound and a passageway between the port and each hole. The vacuum bandage further includes a pack adjacent to the top surface of the member. The pack may include an aperture positioned about the port.

The invention relates to a wound dressing comprising a carrier layer and an absorbent wound contact layer fixed to the carrier layer, which has wound contact surfaces spaced from one another by interstices in which the wound contact layer is not in contact with the wound, the wound contact layer being designed to be absorbent overall and in that the wound contact surfaces are connected to each other by connection regions of the wound contact layer.

A wound dressing assembly includes a wound cover and a carrier. The wound cover has a length and width substantially greater than a height (or thickness), a first major surface, and a second major surface, opposite the first. The first major surface has disposed thereon a wound cover pressure sensitive adhesive comprising a colloidal absorbent, and it is arranged and configured to adhere to mammalian skin during use. The carrier has a length and width substantially greater than a height (or thickness), a first major surface, and a second major surface, opposite the first. The first major surface of the carrier is disposed in facing relation and is removably attached to the second major surface of the wound cover, and it has disposed thereon at least one pressure sensitive adhesive. After application of the wound cover to skin for use, the carrier is removable from the wound cover to leave the wound cover adhered to the skin.

The present disclosure, when used by a live actor, may allow users to safely simulate hemorrhaging in some of the most challenging blood vessels in the most challenging anatomical locations such as the carotid artery, the axillary artery, and the femoral artery. The present disclosure may further provide the ability for users to safely perform hemorrhage control procedures, such as compression and ligation. The simulated wound of the present disclosure may be compressed to control hemorrhage. The simulated wound receptacle of the present disclosure may be packed with hemostatic or simple gauze to control hemorrhage. The simulated blood vessel of the device may be ligated with hemostats or other ligating instruments or material and bandaged with pressure dressings to control hemorrhage.

Carefully coordinated patches having camouflaging and/or benefit properties can be formed for application to a desired region of human skin. The patches include a flexible film having a first, adhesive, outwardly facing major surface and a second outwardly facing surface which is textured to correspond to skin covered by the patch during use; wherein the flexible film further comprises at least one pigmented region and at least one region adapted to modify one or more optical properties selected from the group consisting of light transmission, light reflection, and light absorption. Methods of custom use of such patches may include 3D printing processes.

A dressing includes a drape, a pressure-sensitive acrylic-based adhesive disposed on a skin-facing surface of the drape, an island of absorbent material including non-woven superabsorbent fibers, and a wound contact layer. The drape is a thin film capable of maintaining a negative pressure underneath the drape upon application of a vacuum. The island of absorbent material has a smaller area than the drape and is connected with and disposed beneath the sin-facing surface of the drape so as to leave a first margin of adhesive-coated drape around the island of absorbent material. The island of absorbent material further includes interruptions to reduce or eliminate tension or compression in the island of absorbent material as the dressing bends. The wound-contact layer is disposed on a skin-facing side of the island of absorbent material. The wound contact layer is configured not to stick to a wound.

The present disclosure provides a wound dressing in the form of a bandage having a seal strength that is sufficient to allow it to be used in medical applications, and a low trauma, peel-off releasability for the convenience and comfort of the patient. An adhesive for use with such a bandage is also provided. The adhesive comprises a polyurethane adhesive including a mixture of: (a) a polyol mixture, (b) an isocyanate, and (c) a catalyst mix. The adhesive may have a thickness in the range of about 50 to about 525 pm and may have an adhesion value of less than about 150 g/cm against a metal plate.

Occlusive tissue dressings and methods including an elastomeric drape and a liquid component, at least partially cross-linked at least after one of drying and curing, suitable for application at a dressing-to-skin interface in order to create a substantially air-tight seal. The same or a different liquid component may be applied by a user at a tube-to-dressing interface in order to create a similar air-tight seal around the tube, if not occlusively sealed during its manufacture.