Abstract: The present disclosure is directed to a stent manufacturing assembly including an inner shield, a patterned metal sheet, and an outer shield. The patterned metal sheet may include a polymer coating with an embedded therapeutic agent. The inner shield, patterned metal sheet, and outer shield are arranged in a layered configuration and placed in a stent rolling mechanism with a mandrel. In particular, the patterned metal sheet is disposed on the outer shield and the inner shield is disposed on the patterned metal sheet in the layered configuration. In the layered configuration, the stent manufacturing assembly is rolled by the rolling mechanism into a tubular shape and welded to form a tubular stent.

Abstract: The present disclosure is directed to a stent manufacturing assembly including an inner shield, a patterned metal sheet, and an outer shield. The patterned metal sheet may include a polymer coating with an embedded therapeutic agent. The inner shield, patterned metal sheet, and outer shield are arranged in a layered configuration and placed in a stent rolling mechanism with a mandrel. In particular, the patterned metal sheet is disposed on the outer shield and the inner shield is disposed on the patterned metal sheet in the layered configuration. In the layered configuration, the stent manufacturing assembly is rolled by the rolling mechanism into a tubular shape and welded to form a tubular stent.

Abstract: A connection device for use in the negative pressure therapy of wounds includes a flexible conduit which can be impinged with negative pressure and/or fluid media, the conduit having at least two lumens, a coupling body formed by an elastomeric flexible material which is non-detachably injection molded to a wound-side end section of the conduit, and being constructed for placement on a negative pressure bandage which covers and seals the wound negative pressure tight against the atmosphere, the conduit communicating through at least one opening in the coupling body with the wound space, and an end cap attached and preferably non-detachably fastened to the injection molded-on material of the coupling body, thereby sealing the coupling body tight against the outside.

Abstract: A method for producing a connection device for use in the negative pressure therapy of wounds, includes introducing a flexible conduit into an injection mold, the conduit being constructed for impingement with negative pressure and/or fluid media, and comprising at least two lumens, forming a coupling body at an end section of the conduit by injection molding an elastomeric material to the end section of the conduit, said coupling body being constructed for attachment to a negative pressure bandage which covers the wound and seals the wound tight against the environment, said the conduit being constructed for communication with the wound space through at least one opening, and attaching and fastening an end cap to the coupling body, thereby sealing the coupling body tight to the outside.

Abstract: A connection device for use in the negative pressure therapy of wounds includes a flexible conduit which can be impinged with negative pressure and/or fluid media, the conduit having at least two lumens, a coupling body formed by an elastomeric flexible material which is non-detachably injection molded to a wound-side end section of the conduit, and being constructed for placement on a negative pressure bandage which covers and seals the wound negative pressure tight against the atmosphere, the conduit communicating through at least one opening in the coupling body with the wound space, and an end cap attached and preferably non-detachably fastened to the injection molded-on material of the coupling body, thereby sealing the coupling body tight against the outside.

Abstract: A stent manufacturing assembly for assisting in the manufacturing of a medical stent and a process for manufacturing a medical stent are disclosed. A patterned sheet of metal can be wrapped around the manufacturing assembly's outer surface. The assembly includes a mandrel and a sleeve. The mandrel includes a rigid and substantially cylindrical external surface, and the sleeve surrounds the mandrel and has a variable inner diameter. The sleeve adheres to the inner surface of the stent formed around the sleeve to allow the sleeve to remain in place. After the mandrel is slidably removed from the sleeve, the sleeve radially collapses and contracts, thereby causing minimal shear stress on the stent's inner surface and preventing or minimizing friction and pressure between the mandrel and the stent.

Abstract: Compositions that comprise a polymer entrapping an oxidizing agent are disclosed. The disclosed compositions are used in the treatment of skin ailments such as human papilloma virus infections.