A wound/bandage protector configured as a wrap, a sock/mitten, or a bandage may be made out of stretchable material. The wrap may have one or more fastening straps as well as possibly a first catch fastening surface. The sock/mitten may have a fastening strap and a sheath. The wrap, the sock/mitten, and the bandages may have apertures and aperture covers. In addition, the wound/bandage protectors as well as the bandages may have diamond or triangular gauze configurations with the gauze pad having three or four primary corners, the primary corners of the gauze pad in most instances being oriented towards edges of the body portion or length or width tangents of the body portion, preferably mid-points or mid-sections of the length or width tangents or body portion edges.

The invention relates to a unit for hemostasis. The unit is configured to be directly applied to a bleeding wound and comprises an envelope enclosing an inner space as well as an effective amount of a hemostatic material disposed within the inner space. Furthermore, the invention relates to an arrangement of two or more such units for hemostasis, the units being coupled to each other. Moreover, the invention relates to a method for producing an arrangement of units for hemostasis. In accordance with the method, an effective amount of a hemostatic material is disposed within an interior region of a starting material, and neck regions are formed on both sides of the charge so as to form an envelope enclosing the charge.

The present disclosure is directed to a therapeutic sleeve for a medical patient. The sleeve has an interior side and an exterior side. The sleeve can include a fastener on the interior side. A wound care component such as an absorbent pad can be fastened to the interior side of the sleeve. The wound care component can be removed and replaced when it expires. The sleeve can be fabricated from stretch fabric, allowing the sleeve to conform to a patient's arm or leg.

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 system is provided comprising a columnar sleeve of stretchable fabric, the sleeve produced in various skin tone colors and configured to slip upon an individual toe or finger and an absorbent padding configured for attachment to an inside surface of the sleeve, the padding configured to cover about one half of an interior circumference of the inside surface, the padding optionally infused with at least one of pain killers, antiseptics, and soothing gels. The system also comprises wax paper covering the padding prior to use of the sleeve, an applicator shaped to facilitate slipping the sleeve upon the individual toe or finger, and convex-shaped flex bands placed lengthwise into the sleeve. The flex bands exert downward pressure on one of a toe and a finger and are placed in a U-shape, thus promoting the downward pressure.

Tattoo protector bandage and use as a tattoo protector of the type having a tubular configuration, having at least one opening for introducing a member of the human body and defining an inner side which is in contact with the skin, and an outer side; characterised in that it comprises, out of the total: 90-94% viscose, 4-6% elastane and 2-4% polyamide.

An apparatus suspends a post-amputation residuum protection device for a below the knee amputation. The suspending apparatus comprises an elongated arcuate first shell defining an open interior channel. The first shell is adapted to receive at least a portion of the residuum and the residuum protection device into the interior channel. A flexible second shell includes a circumferential wedge extending radially inwardly from a portion of an inner surface. The second shell is configured to be received within the first shell and adapted to cover the residuum adjacent to the knee. The wedge is adapted to bear against the residuum above the medial femoral condyle such that the wedge is received in the supracondylar space for suspending the residuum protection device.

An oxygen distributor (1) positionable, in use, in a wound for supplying oxygen to the wound has an oxygen delivery area (17) for, in use, receiving a supply of oxygen. At least one tube (19A) extends from the oxygen delivery area, having a tube wall with an oxygen-permeable, liquid-impermeable section. Oxygen delivered to the oxygen delivery area can flow away from the oxygen delivery area along the, or each, tube.

A wound dressing is made from a tubular inner layer and at least one outer layer disposed radially beyond the inner layer. The inner layer permits egress of fluid from weeping wounds, prevents desiccation of skin disposed beneath the inner layer, and prevents desiccation of ointment disposed between the inner layer and the skin. The at least one outer layer absorbs fluids that leak through the inner layer, protects the inner layer from outside contaminants, and prevents fluids from escaping. The at least one outer layer is affixed to the inner layer, and each of the layers is elastic in at least the radial direction. Optionally, a layer of ointment may be applied to an inner surface of the inner layer. Note that the tubular inner layer may be either pre-formed or formed at the time of application.

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.