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.

A compression stocking having shape memory, heat-shrinkable thermoplastic material, wherein said stocking is configured to establish, in use, a compression contact with at least one of a leg and a foot of a user upon the application of an amount of heat to the shape memory, heat-shrinkable thermoplastic material, wherein the thermoplastic material is a polymer that has a glass transition temperature below 10 C., has crystallinity with a melting temperature (Tm) between 30-50 C. and a heat of fusion of at least 10 J/g, as determined using differential scanning calorimetry (DSC) (40 C./10.0 (K/min)/100 C.) as set out by the ASTM D3418:2003.

An applicator according to one embodiment is an applicator for applying a sheet member to skin, and includes: a bottom plate facing the skin; a top plate facing the bottom plate and configured to be pressed toward the bottom plate; and a bending portion configured to apply the sheet member to the skin by bending the sheet member having advanced to the bending portion in a pressed state in which the top plate has been moved toward the bottom plate.

A wound covering device for noncontact wound protection includes a shell and a coupler. The shell, which defines an interior space, has a bottom that is open so that the shell is configured to position over a wound in skin of a user. The coupler is coupled to the shell and is configured to removably couple to the skin of the user. The coupler is configured to retain the shell over the wound to protect the wound.

A wound closure device and a method of its use are disclosed. The wound closure device comprises a wound closure strip, the wound closure strip comprising a wound-facing side and a top side, the wound-facing side comprises an adhesive applied over at least a portion of the wound facing side of the wound closure strip and a non-symmetric, two-part release liner assembly detachably adhered to the adhesive, the release liner assembly comprising a first section and a second section with the second section comprising a wound closure strip-free portion forming a tab. In an alternate embodiment, the device is multi-segmented and the wound closure strip may be coextensive with the release liner assembly.

A medical patch applicator device for easily and effectively applying medical patches on difficult to reach areas of a person's body. The medical patch applicator device includes an elongated semi-rigid patch support member for supporting a medical patch to be applied anywhere upon a user's body; and patch engagement members attached to the support member and to which the medical patch clings so that the user can effectively apply the medical patch without the medical patch bunching and crumpling up.

An adhesive bandage is provided which has at least four arms instead of standard two where two of which being of a different length than other two to resist its removal from skin by a baby. The adhesive bandage includes a first and a second bandage arms and a third and a fourth bandage arms. The first and second bandage arms are transverse to the third and fourth bandage arms. The first and second bandage arms are longer in length to the third and fourth bandage arms. The adhesive bandage further includes a medicated pad at an intersection of the first and second bandage arms and the third and fourth bandage arms. In one embodiment, the new bandage includes an adhesive strip and a clip such that the adhesive strip is looped through the clip. In another embodiment, the new bandage includes an adhesive strip and a Velcro strap such that the adhesive strip is looped through the Velcro strap.

A wound closure device and a method of its use are disclosed. The wound closure device comprises a wound closure strip, the wound closure strip comprising a wound-facing side and a top side, the wound-facing side comprises an adhesive applied over at least a portion of the wound facing side of the wound closure strip and a non-symmetric, two-part release liner assembly detachably adhered to the adhesive, the release liner assembly comprising a first section and a second section with the second section comprising a wound closure strip-free portion forming a tab. In an alternate embodiment, the device is multi-segmented and the wound closure strip may be coextensive with the release liner assembly.

A cover for protecting a tissue site may comprise a shell layer, an adhesive disposed on the shell layer, and a contact layer disposed adjacent to the adhesive. The contact layer may have an open area of about 40 percent to about 50 percent of the total area of the contact layer. A release liner may be disposed adjacent to the contact layer. Perforations through the shell layer and the contact layer can define a sacrificial segment configured to be separated from the shell layer and the contact layer. A handling bar may be coupled to the sacrificial segment.

A mechanical wound therapy (MWT) system includes a connection for a vacuum source, which is routed through an airtight covering to a porous material positioned over the wound. The porous material may be a tubing network interspaced by a netting material constructed of biologically inert or bioabsorbable material. Alternatively, the porous material may be a layered unified dressing in which layers of mesh, netting or thin perforated film are separated and fixedly attached to functional elements of the dressing (e.g., irrigation tubing) or spacers. The vacuum and irrigation systems may be completely separated. An airtight sealing layer or foldable adhesive sealing layer may seal the dressing and facilitate sealing the dressing to the wound margins. Additional modular devices such as a wound approximating system, positive pressure bladders and adjuvant therapy modules as well as enhanced monitoring technology can be added to synergistically increase the capabilities of each dressing.