A blister protector cap incorporates features such as a hemispherical/paraboloid cap dome, which goes over a blister and attaches to the skin using an adhesive compound. The blister protector cap may have air vents located at any part of its surface for ventilation purposes and aiding the skin to heal the blister. The anterior side of the blister protector cap has a cavity in order to cover the blister and protect it from any sharp or rough objects. In an embodiment, some part of the dome is flexible. In such a configuration, an accordion-like wall structure or a corrugated wall structure can be integrated to allow for some flexibility. Furthermore, this flexible part of the dome can also have vent holes or be made of a porous material to allow air and moisture to pass through but block water molecules from passing through to the inside of dome.

A compression bandage is provided that includes a zinc oxide composition and/or one or more other therapeutic agents. In use, the bandage can be compression wrapped directly contacting a subjects skin for application of the zinc oxide composition and/or other therapeutic agents.

A covering device includes an elongate wrapping member configured to be wrapped around and overlay an opening in an object in a wrapped condition, a substantially shell-shaped cover member for covering the wrapping member substantially in the wrapped condition, and a retaining arrangement for retaining the cover member and with it, the wrapping member in position relative the object in a covering condition.

Provided are a fibrous sheet having a stress relaxation rate defined by the following formula of less than or equal to 85%:

stress relaxation rate [%]=(stress S.sub.5 at extension after five minutes/stress S.sub.0 at initial extension)100

when a stress at extension immediately after extension in an in-plane first direction at 50% elongation is defined as a stress S.sub.0 (N/50 mm) at initial extension, and a stress at extension at a time of extending in the first direction at 50% elongation for five minutes is defined as a stress S.sub.5 (N/50 mm) at extension after five minutes, and a bandage including the fibrous sheet.

The present invention provides a device and method for preventing or curing pressure ulcers or chronic wounds. A multilayer dressing comprises a soft silicone jell layer of a suitable thickness which is placed in the multilayer dressing, above an absorbent layer. The matrix of the silicone jell layer is populated with a plurality of silicone beads of suitable size. The beads are connected to each other, and to the silicone jell layer. Breathing of wound and substantial supply of oxygen to the wound is duly insured for all layers of the multiple layer dressing. The beads play a pivotal role in promoting the effectiveness and performance of the multilayer dressing by acting as the plurality of effective cushions, as they absorb and uniformly redistribute a patient's body weight across the entire applied dressing area. The low adhering adhesive coating of about 5 mm in width is applied to the peripheral edges of all the layers. Unlike the multilayer dressing already available in the market, skipping the application of low adhering adhesive coatings on the entire top and bottom surfaces of the layers helps in promoting overall breathability and consequently, the efficiency of the multilayer dressing of the present invention.

A fingerstall, in particular for treatment of defects of the distal phalanx of the finger with a closed distal end, an open proximal end, and an interior. Provision is made that a chamber is formed in the fingerstall at the distal end thereof and the chamber is in liquid communication with the interior of the fingerstall.

A barrier system is provided for use in reducing infections associated with post-operative surgical incision and/or a percutaneous medical device, such as a catheter, that is disposed within the surgical incision. Such a barrier system may include: a barrier device having a skin-contacting surface and a catheter-receiving surface; and an adhesive composition configured for adhering to skin, the barrier device, and/or the catheter so as to form a barrier at or adjacent to an incision in the skin where the catheter is percutaneously inserted through the skin. A tensioning anchor and associated system of two or more tensioning anchors is provided for post-operative wound closure. A method for applying and removing the barrier device and tensioning anchors is also provided.

An umbilical cord cover includes a fluid-tight covering portion defining a cavity, a contact portion around the covering portion, and a releasable adhesive on the contact portion. The releasable adhesive and the contact portion form a fluid-tight seal around the cavity when the contact portion engages a surface.

A protective device configured in accordance with a particular embodiment includes a cover including a first region that extends over a vulnerable site on a patient and a second region that extends over an area on the patient peripheral to the vulnerable site. The first region of the cover is at least generally impermeable to liquid water. The device further includes an adhesive film and a liquid-absorbing element. The adhesive film is configured to form an adhesive bond between the second region of the cover and the patient. The bond has an inner edge portion positioned toward the vulnerable site and an outer edge portion positioned away from the vulnerable site. The liquid-absorbing element is configured to absorb liquid contamination at the outer edge portion of the bond and/or liquid contamination approaching the outer edge portion of the bond when the cover is operably positioned on the patient.

Reduced pressure wound therapy is performed on a sacral region of a patient using an adhesive dressing comprising a flexible planar layer and a non-planar fold-sealing region configured to seal to the intergluteal cleft of a patient. The fold-sealing region is located on an outer edge of the adhesive dressing and comprises a tapered configuration.