An example debriding pad includes a support layer, a first region, and a second region. The first region includes a first material defining a plurality of first loop piles arranged on the support material. The second region includes a second material defining a plurality of second loop piles arranged on the support material. The second material is stiffer than the first material to provide more aggressive debridement of a wound.

The present invention belongs to the field of medical accessories, more precisely to the field of accessories for protection against outer conditions such as impacts, high or low temperature and similar conditions that can harm a human being. The invention relates to a personalized accessory for protection of a body part, which comprises a protective element, which fits to the shape of the excrescence, a scar or a wound, and an adjustable part to which the protective part is attached, glued, sewed or inserted, wherein the adjustable part can be stretched or in any other way adjusted to the particular body part, which has to be protected. The said accessory is manufactured in the following way: first the body part with the injury is scanned or measured in order to obtain a 3D model of the scanned or measured body part. Then the protective element is made using a 3D printer or thermoforming with an adjustable mould, wherein the finished protective element is then attached to the adjustable part.

A composite material is described, which is of particular use in wound treatment, and to a method for producing said composite material is also described. The composite material has a first foam layer having a first hydrophilic polyurethane foam material, and, in immediate contact therewith, a second foam layer having a second hydrophilic polyurethane foam material, which second hydrophilic foam material is different from the first hydrophilic foam material.

Proposed is an improved cast used for covering an affected area of a patient having a fracture or dislocation or diabetic patient to keep the continuity of the affected area and the unaffected area, and to protect the affected area from external shock.

Provided by this disclosure is a method and system for the preparation of a blood clot-based wound dressing whereby a fluid, typically gas such as air is propelled through one conduit into a sealed, blood-containing test tube, and at the same time blood s permitted to flow out of the test through a second conduit and thereby transferred into a blot clot molding space where the blood is permitted to coagulate forming a clot of a shape defined by the molding space. The propelling fluid is typically air that is propelled to flow in the first conduit by a syringe. Provide by this disclosure is also a coupling device useful in said method and system; as well as a kit of parts comprising elements needed for carrying out the method of this disclosure.

A therapeutic device includes a generally rigid but elastically deformable sheet body including a bridge portion, first and second support portions extending outwardly from the bridge portion in opposite directions along a longitudinal dimension, and adhesive or an adhesion member on a first surface along the bridge portion that is adapted for adhesion to skin of a user above a target site. The therapeutic device also includes first and second projections on the first surface proximate to lateral edges of the sheet body. The sheet body is configured to assume a neutral configuration in which the first and second projections space the bridge portion and the adhesive or the adhesion member apart from the target site by an air gap, a depressed position during affixation of the first surface to the target site, and an adhesion configuration after affixation of the first surface to the target site.

A wound dressing includes a patient interface layer, a wicking layer, an absorbent layer, and a cover layer. The patient interface layer is configured to engage a wound bed and has a first side and a second side, the second side configured to face the wound bed. The wicking layer, absorbent layer, and cover layer all also have a first side and a second side. A perimeter of the first side of the wicking layer is adhered to the second side of the cover layer, forming an adhesive border surrounding the wicking layer and the absorbent layer, and the wicking layer is configured to peripherally wick perspiration from underneath the adhesive border towards the center of the wicking layer and upwards towards the absorbent layer.

Devices and methods for encapsulating a portion of a wound dressing with biocompatible coating are disclosed. In some embodiments, a method includes coating a first side of a flexible wound contact layer of the wound dressing with a hydrophobic coating. The first side of the wound contact layer can support a plurality of electronic components. The method can further include coating a second side of the wound contact layer opposite the first side with the hydrophobic coating. The wound contact layer can be formed at least partially from hydrophilic material.

A therapeutic medical garment including a knitted welt proximate one end thereof with a surface adapted for residing against the wearer's skin. The garment includes a ground yarn and a plurality of raised, skin-engaging stabilizer elements, such as elongate bars extending in spaced-apart relation around an inner surface of the welt and along a longitudinal axis of the garment to reduce a tendency of the welt to roll over on itself.

A wound dressing, a method of manufacturing a wound dressing, and a method of treating a patient are disclosed. The wound dressing may include an absorbent layer for absorbing wound exudate; and an obscuring element for at least partially obscuring a view of wound exudate absorbed by the absorbent layer in use.