A scaffold for tissue repair or wound dressing comprising: a material layer; a polymer fibre layer; and an adhesive component between the material layer and the polymer fibre layer, wherein the adhesive component comprises material having a lower melting temperature (Tm) than the material layer and the polymer fibre layer.

Disclosed embodiments relate to apparatuses and methods for wound treatment. In some embodiments, a wound dressing apparatus can comprise a wound contact layer, a spacer layer, an absorbent layer positioned on the spacer layer, an electronics unit comprising a negative pressure source and/or electronic components, wherein the absorbent layer comprises a recess configured to receive the electronics unit and the absorbent layer is configured to be in fluid communication with the electronics unit, and a cover layer configured to cover and form a seal over the wound contact layer, the spacer layer, the absorbent layer, and the electronics unit.

According to certain embodiments, an apparatus for applying negative pressure to a wound can include a negative pressure source, a sensor, and a controller. The negative pressure source can be configured to couple via a fluid flow path to a wound dressing and provide negative pressure to the wound dressing. The sensor can be configured to monitor a magnitude or frequency of pressure in the fluid flow path generated by the negative pressure source. The controller can be configured to determine an activity classification, such as breathing, changing positions while lying, sitting, walking, standing, jumping, traversing stairs, leg extending, leg bending, and performing chair squats, based on a change in the magnitude of pressure over time while the negative pressure source maintains the magnitude of pressure in the fluid flow path below a negative pressure threshold. The controller can output an indication of the activity classification.

A medical bandaging and tourniquet system for use in dressing puncture wounds is provided. The medical bandaging and tourniquet system includes a primary dressing, a secondary dressing, a band, a tightening buckle, a retaining clip, and a tightening rod. The primary dressing serves as a main wrapping bandage that mounts the secondary dressing and tourniquet components together. The secondary dressing removably attaches to the primary dressing and serves as a bandage that can be installed onto minor wounds. The band connects to the primary dressing, serving as an elastic tourniquet band. The tightening buckle and the retaining clip are connected to the primary dressing. The tightening rod is positioned between the tightening buckle and the retaining clip. The primary dressing straps tightly along a wound though the tightening buckle. The strap is further compressed by turning the tightening rod. The tightening rod can then be secured to the retaining clip.

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.

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 wound dressing is selectively configurable for use in a pressure gradient wound therapy system and for use without a pressure gradient wound therapy system. The wound dressing can include a covering layer, an aperture and a base plate. the base plate can be configured to sealingly receive a connector part.

A wound dressing is selectively configurable for use in a pressure gradient wound therapy system and for use without a pressure gradient wound therapy system. The wound dressing can include a covering layer, an aperture and a microbial barrier. The microbial barrier can be arranged to cover the aperture.

A packaged kit of parts is provided for use with a selectively configurable wound dressing. The kit includes a piercing tool configured to pierce a covering layer of the wound dressing to produce an aperture therein and thereby configure the wound dressing for use in a pressure gradient wound therapy system. The kit may also include a) packaging indicating that the piercing tool is configured to pierce a covering layer of a wound dressing; (b) instructions instructing a user as to how to use the piecing tool; (c) one or more selectively configurable wound dressings; (d) a source of non-atmospheric pressure; (e) a port to connect the wound dressing to a source of non-atmospheric pressure; or (f) tubing for connection between a wound dressing and a source of non-atmospheric pressure. The kit is arranged within a sealed package.

The present disclosure relates to a dressing (100) comprising a backing layer (101), an adhesive skin contact layer (102) and a first release liner (103), wherein the adhesive skin contact layer (102) comprises a central portion (102a) and an edge portion (102b) surrounding the central portion (102a). The first release liner (103) is configured to be releasably attached to at least the central portion (102a) of the adhesive skin contact layer (102). The dressing (100) comprises a second release liner (104) arranged between the first release liner (103) and at least part of the edge portion (102b) of the adhesive skin contact layer (102).