This disclosure relates to a multi-layer wound care device having absorption and fluid transfer properties. The wound care device contains capillary force one-way pumps that are capable of transporting fluid, such as wound exudate, away from a wound site to the opposite side of the wound care device, which functions as a segregated fluid reservoir. This fluid transport mechanism generally aids in reducing wound maceration by removing excess wound fluid and the protease enzymes and infectious bacteria contained within the wound fluid. The wound care device performs this function, often times for multiple days, without the loss of the physical integrity of the wound care device. In addition to providing a uni-directional fluid transport mechanism, the wound care device provides improved absorption properties.

The present disclosure provides, inter-alia, an apparatus for wound-dressing. In particular, embodiments of the disclosure provide a wound-dressing apparatus comprising a wrapping element and a pad element, wherein the pad element is foldable and comprises at least one removable portion.

Tubular bandage, in particular a finger or toe bandage which is formed as a tube comprising an outer layer which is connected to an inner layer, and wherein the outer layer has a diameter and an elasticity such that the bandage can be clamped adhesive-free around the body part to be treated, in the particular, said finger or said toe, and wherein the inner layer is made of an elastic wound-protective material, wherein said outer layer is made of an air-permeable and water-repellent material, and wherein, at the open endings, said outer layer extends in the longitudinal direction over the inner layer over a distance of more than 0.5 mm, such that the outer layer touches the body part to be treated, in particular a finger or toe, with its endings when applied.

The present invention discloses a tubeless energy drainage device for trauma, pertaining to the field of tubeless drainage technology, especially relating to a tubeless energy drainage device for trauma. The device includes energy transmission carriers, lead wires, and a frequency electrical energy generator. The frequency energy resonance generator transmits electrical energy to the energy transmission carriers, activates metal potassium ions on the energy transmission carriers, and creates resonance through conduction of metal ions in a wound covering layer and changing frequency of a wound, thereby achieving retrograde drainage of the wound's own sinus in a drainage area. The device disclosed by the present invention is of great significance for the rapid and full drainage of intractable wounds and battlefield wounds, and the drainage, healing, and pain relief of minute wound fistulas that cannot be tubed.

In some illustrative examples, a bridge suitable for treating a tissue site may include a bridge sealing member and one or more bridge wicking layers. The bridge sealing member may extend along a length of the bridge, and may define an internal passageway in fluid communication between a receiving end of the bridge and a transmitting end of the bridge. The one or more bridge wicking layers may be disposed within the internal passageway of the bridge sealing member. Other apparatus, systems, and methods are disclosed.

A wound debridement system includes a wound dressing having an active layer and a wound interface layer. The active layer is formed from one or more transmission layers that are arranged about a central post. Activation of the transmission layers is configured to cause the movement of the wound interface layer relative to a tissue site to which the wound dressing is applied. A drive unit is operably attached to the central post. The drive unit is configured to generate and transfer a vibrational energy and/or a rotational movement to the transmission layer(s) via the central post. The resultant vibration and/or rotation of the transmission layer(s) is imparted onto the wound interface layer, thereby effectuating the desired movement of the wound interface layer relative to the tissue site, which allows for the debridement of debris that may be located at the tissue site.

The present invention includes disposable absorbent articles, such as disposable undergarment, diapers, other garments, and wound care dressings, having an elastomeric material disposed between two substrate layers and an absorbent core system that disposed on top of or between the two substrate layers. This invention may also include a disposable article having an elastomeric material disposed between two substrate layers without an absorbent core. The inclusion of an stretch adhesive in the construction of the article in various portions of the article (e.g., fastening tabs, front and/or rear sections, entire article, etc.) results in improved securement of the article to a wearer for reducing the risk of leakage and further improving comfort for the wearer. Furthermore, the inclusion of a stretch adhesive can provide a smooth contoured fit to a wearer, thereby improving appearance and self-confidence for the wearer.

The present disclosure relates to compositions, methods of use and methods of manufacturing of a transdermal delivery systems, patches, vehicles and devices used to relieve pain (i.e., analgesics) and/or inflammation that contain a pharmaceutically effective amount of a pharmaceutically acceptable and effective cannabinoid and menthol.

The present disclosure provides a magnetic dressing and a preparation method and use thereof, belonging to the technical field of pharmaceutical preparations. The magnetic dressing includes a magnetic layer, a drug-loading layer, and a protective layer that are stacked in sequence, where the magnetic layer includes polyvinyl alcohol, gluten, and iron particles. In the present disclosure, a swallowed magnetic dressing is controlled by an external magnetic field, and the magnetic dressing is moved to a pathological position by changing a direction of the external magnetic field; after the external magnetic field is removed, the magnetic dressing changes from a ring to a sheet, thereby completing attachment of an entire lesion surface to complete treatment by autonomous drug release.

A vented wound dressing barrier includes one or more membrane layers with a plurality of vents. The vents are cut along a perimeter of the vents through the one or more membrane layers. Each vent having a connection portion uncut relative to the one or more membrane layers thereby forming a hinge configured to allow the vents to open for drainage when exposed to fluid underlying the vented wound dressing barrier. The plurality of vents is each cut along the perimeter without removal of any of the membrane layer. The one or more membrane layers with the plurality of vents has a surface for covering a wound, the surface area in the absence of a fluid pressing on the vents having no openings or voids which reduce the surface area of a vented wound dressing barrier area covering a wound.