A negative pressure wound therapy device, kit, and method are provided for improved treatment of wounds on complex three-dimensional anatomies. The device includes a conformable manifold made of a porous and permeable material with a pattern of cuts designed to transform the manifold from a relaxed, planar state to a pliable three-dimensional state when extended along the lateral axis. The kit further may include a wound interface layer, an adhesive, breathable drape, and a pneumatic connection to a negative pressure wound therapy device. Finally, a method for treating wounds using reduced pressure and the presently disclosed kit is provided.

A dressing includes an application site covering and an oxygen scavenger provided with or positioned with respect to the application site covering so as to remove oxygen from a volume beneath the application site covering and around an application site covered by the application site covering. The application site covering and the oxygen scavenger are configured to maintain gas pressure beneath the application site covering around the application site that is above a therapeutic negative pressure while the oxygen scavenger is consuming oxygen beneath the application site covering.

A more robust packaging structure for maintaining the integrity of compressible biologically active materials during storage and especially during transportation is provided. These containers protect the materials from shock, vibration, deformation, or separation from agitation. The compressible materials may be in the form of synthetic fibers, and may include a composite of fibers and beads or granules. Suitable materials that may benefit from such a robust packaging structure include synthetic materials that comprise a biologically active ceramic or glass.

The present disclosure relates to apparatus for covering a burn or other wound in ways that prevent or limit touching the wound. The present disclosure describes Burn Bandages that may include domes or structures that bridge over a wide range of a burn or wound size. In certain instances these structures may expand in one or more directions as they are adjusted to fit to a particular burn or wound size. Such bridging structures may include airways, openings, or voids that promote air/oxygen flow to the wound as the Burn Bandage sits upon surfaces or pads that contact healthy surrounding tissue while they cover a wound site. The apparatus may be any shape including, yet not limited to, a circle, a rectangle, a square, a hexagon, an octagon, an oval, a cone, a cylinder, have a semi-cylindrical shape, or that have any another geometric shape.

A more robust packaging structure for maintaining the integrity of compressible biologically active materials during storage and especially during transportation is provided. These containers protect the materials from shock, vibration, deformation, or separation from agitation. The compressible materials may be in the form of synthetic fibers, and may include a composite of fibers and beads or granules. Suitable materials that may benefit from such a robust packaging structure include synthetic materials that comprise a biologically active ceramic or glass.

The present disclosure relates to apparatus for covering a burn or other wound in ways that prevent or limit touching the wound. The present disclosure describes Burn Bandages that may include domes or structures that bridge over a wide range of a burn or wound size. In certain instances these structures may expand in one or more directions as they are adjusted to fit to a particular burn or wound size. Such bridging structures may include airways, openings, or voids that promote air/oxygen flow to the wound as the Burn Bandage sits upon surfaces or pads that contact healthy surrounding tissue while they cover a wound site. The apparatus may be any shape including, yet not limited to, a circle, a rectangle, a square, a hexagon, an octagon, an oval, a cone, a cylinder, have a semi-cylindrical shape, or that have any another geometric shape.

A system for providing a protective covering for a human or non-human animal comprising a supply of dispensable plastic stretch film pre-wound onto a spool and a dispenser-applicator for dispensing the film and applying the film to the human or non-human animal, wherein the surface of the side of film applied to the human or non-human animal is coated with a mixture of manuka honey, activated charcoal, and tea tree oil.

A method of preparing an occlusive wound dressing involves preparing a slurry of an occlusive composition with a hydrophobic compound and a bacteriostatic agent, applying the occlusive composition on a fabric to produce a coated fabric, disposing the coated fabric in packaging, adding water onto at least one of the coated fabric and the packaging, sealing the packaging containing the coated fabric, and irradiating the sealed package to sterilize and produce the occlusive wound dressing. The occlusive wound dressing has from about 60 wt % to about 75 wt % hydrophobic compound, from about 2 wt % to about 5 wt % bacteriostatic agent, from about 2 wt % to about 5 wt % water, and from about 5 wt % to about 36 wt % fabric.

The present invention provides a novel packaging material for sterilization which has processing suitability as a packaging material, is compatible with all sterilization processing methods such as those performed under high-temperature conditions, has small variation in shapes and dimensions, and is capable of maintaining an internal sterilized condition. This packaging material for sterilization is configured from at least two layers of laminated non-woven fabrics comprising a non-woven fabric layer (I) formed of continuous long fibers having an average fiber diameter of 5-30 μm and a non-woven fabric layer (II) formed of ultra-fine fibers having an average fiber diameter of 0.1-4 μm.

A surgical drain device includes an adhesion matrix of biodegradable polymer material and a plurality of drain tubes attached to the matrix. The device is implanted within a surgical wound to treat the presence of seromas, for example, and is used to promote drainage, tissue adhesion, and wound closure. The drain tubes converge into a common collection tube that leads wound fluid outside the body under gravity feed or negative pressure applied to the collection tube. The matrix contains an array of apertures that allow tissue contact across the device. The device also can include a coating of surgical adhesive and a tissue anchoring system of hooks or barbs. The device can be used with a negative pressure system to further improve the drainage band can also be used with a wound dressing. The device and systems containing the device are particularly useful to promote the healing of surgical wounds from abdominal surgery.