A medical dressing is described that includes: a porous layer having a first side and a second side; a first coating extending along at least a portion of the surface area of said first side of said porous layer; a second coating extending along said first side of said porous layer, said second coating comprising a pattern of through openings; wherein said first coating extends along at least those portions of the surface area of said first side of said porous layer that coincide with the through openings of said second coating and wherein said first surface of said second coating extends in a plane (B) that is farther away, in the vertical direction, from the first side of said porous layer, than the corresponding plane (A) defined by the first surface of said first coating.

A protective dressing includes an outer dressing and an adhesive layer. The outer dressing includes an opening and a cavity sized to receive a phase-change material (PCM) insert inserted through the opening. The adhesive layer is configured to adhere to a patient's skin surrounding an anatomic site. When adhered to the patient's skin, the PCM insert modifies the patient's skin at the anatomic site. The PCM insert may be removed and replaced with another PCM insert. For example, a warm PCM insert may be replaced with a refrigerated PCM insert. The opening of the outer dressing may be self-sealing. The opening of the outer dressing may be sealed with an upper layer dressing coupled to the PCM cooling insert.

A controlled oxygen dressing includes a flexible drape that is selectively permeable to air and is adhere to skin to define a first volume around a tissue site. A cover layer, impermeable to air, is sealed to the drape to thereby define a second volume between the cover layer the drape. An oxygen scavenger is arranged in the second volume and consumes oxygen in the second volume, which produces an oxygen concentration differential between the first and second volumes, This differential causes oxygen to diffuse through a covered portion of the drape, from the first volume to the second volume, thus decreasing the amount of oxygen in the first volume. Oxygen entering into the first volume from the surrounding environment diffuses through a non-covered portion of the drape. Therefore, an area of the cover layer can be selected to produce a desired level of oxygen in the first volume.

A bandage includes a top film, an absorbent layer and a perforated adhesive lower layer positioned under the absorbent layer for adhering the bandage to a user's skin. The absorbent layer includes at least one incision that improves the flexibility of the bandage.

The disclosed adhesive medical article has a backing layer having a first major surface and a second major surface opposite to the first major surface. The backing layer has a central portion and an outer circumferential portion. The article further has a pressure sensitive adhesive pattern coating applied onto at least part of the first major surface of the backing layer in such a way as to form a plurality of adhesive coated and adhesive uncoated areas of the backing layer. The adhesive uncoated areas comprise a central collection portion and at least one longitudinal extension radiating from the central collection portion towards the outer circumferential portion of the backing layer.

According to one aspect, a medical device may be configured to couple to a body. The medical device may comprise a material layer; a plurality of adhesive layers coupled to the material layer and configured to couple to a user's skin, wherein each adhesive layer of the plurality of adhesive layers includes a plurality of micro passages; a channel extending between two adjacent adhesive layers of the plurality of adhesive layers; and a superhydrophobic coating covering at least a portion of each of the two adjacent adhesive layers and the material layer forming the channel.

Multi-layer contact patches, as well as related apparatus, kits, systems, and methods, enable improved allergen testing and diagnosis. Multi-layer contact patches include a shield layer releasably coupled to an adhesive layer. The adhesive layer at least partially defines and is fixably coupled to an allergen complex layer. The allergen complex layer defines a plurality of allergen complex cavities. At least a subset of the allergen complex cavities include an allergen complex positioned therein, each allergen complex comprising an absorbent matrix and an allergen.

A device for application onto wounds with a liquid rapidly polymerizable adhesive for forming skin closure systems, comprising a thin flexible flat porous tape, preferably a mesh, elongated along a longitudinal axis and having a lower side or wound-facing side and an opposing upper side, a periphery, and central portion in immediate vicinity of the axis; said tape coated or impregnated with an initiator or accelerator of polymerization; said tape having a plurality of elongated traces of soluble pressure sensitive adhesive (PSA) disposed on the wound-facing side; said traces covering from about 3% to about 50% of area of said tape and extending from the periphery to the central portion of said tape.

The disclosed securement tape strip comprises a tape having a midsection, a stabilizing section, and a wrapping strip. The tape strip has an adhesive along the midsection to adhere the tape strip to a substrate. The wrapping strip can include an adhesive for wrapping the wrapping strip around a device to hold the device securely in place on the substrate. The tape strip can include a perforation set along the midsection. The perforation set can be useful in removal of the tape.

A dressing for a wound includes a drape, an absorbent core, and a wicking member. The drape can be configured to sealingly couple with a patient's skin surrounding the wound. The drape may enclose an inner volume of the dressing. The absorbent core layer may be positioned within the inner volume of the dressing. The wicking member is positioned within the inner volume, wherein the wicking member extends from an underside of the absorbent core layer to the drape. The indicator may be configured to fluidly couple with the wicking member through the drape and receive fluid from the wicking member. The indicator may be configured to provide a visual wound status indication in response to receiving fluid from the wound through the wicking member.