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.

A method of promoting hemostasis in the mouth or oral cavity utilizes a non-absorbent, low surface energy and highly conformable non-disruptive hemostasis material. Traditional wound packing material is highly absorbent and has large open surfaces that allow clot forming materials, such as the platelet plug to adhere to the packing material and whereupon removal, the clot is disrupted. A non-disruptive highly conformable hemostasis material does not have large open pores and therefore does not adhere to forming clots. A non-disruptive hemostasis material may consist of expanded polytetrafluoroethylene that has a pore size of no more than about 10 microns. A non-disruptive hemostasis material may comprise a thin film of material over a portion of the outside surface that is non-absorbent and thin to allow for conforming into an oral cavity, such as from a tooth extraction. A thin film may cover porous material, such as a foam, that may be elastomeric.

An elongate strap support system for anatomical support, pain reduction, or therapeutic treatment includes a package containing a first elongate strap support and at least one additional elongate strap support. In one example, the first elongate strap support includes a woven fabric support layer including synthetic fibers. The woven fabric is shaped so as to form an elongated strap with rounded portions. The woven fabric is substantially resistant to stretching in one direction under such test conditions as those specified in ASTM D3759. The first elongate strap support additionally includes an adhesive layer on the support layer for adhesive attachment of the woven fabric support layer to an outer skin surface of a body and a removable cover layer on the adhesive layer.

An elongate strap support system for anatomical support, pain reduction, or therapeutic treatment includes a package containing a first elongate strap support and at least one additional elongate strap support. In one example, the first elongate strap support includes a woven fabric support layer including synthetic fibers. The woven fabric is shaped so as to form an elongated strap with rounded portions. The woven fabric is substantially resistant to stretching in one direction under such test conditions as those specified in ASTM D3759. The first elongate strap support additionally includes an adhesive layer on the support layer for adhesive attachment of the woven fabric support layer to an outer skin surface of a body and a removable cover layer on the adhesive layer.

The Barrier Band for an area on a human body, involving a vascular device access area. The present invention relates to an apparatus that provides a barrier between a person's skin, and any vascular access device, and its components, to prevent compromising skin, and to provide comfort to a person.

The barrier band is offered in many sizes, and is made with a stretchable material, to accommodate every patient, and any body part being serviced. It is offered in both a washable and disposable version. Its design and stitching may vary, and it may or may not have an adjustable apparatus, or any other suitable component to tighten or loosen the band.

A wound dressing for a burn or open wound is formed of a foam material body with an open center area. The thickness of the foam body creates a zone for air circulation and prevents contact with the wound. This may have a mesh, gauze or other air permeable cover over the open center area.

The present invention provides a scalp protector for use following a hair transplant procedure conducted on a subject including: a cover having a central region and elongated portions extending from the central region for covering the surface of the scalp of the subject, each of the elongated portions provides at least one set of a first part of a snap fasteners closure; a band configured to extend around the periphery of the scalp of the subject, the band includes anchoring regions deployed on the band so as to align with the elongated portions of the cover, each of the anchoring regions providing at least one set of a complementary part of a snap fasteners closure for fastening to the elongated portions.

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.

Disclosed herein are devices for preventing or treating an injury to an individual. Also provided are devices and methods for alleviating pain or discomfort caused by equipment or other padding or articles of clothing or uniform. The device can include a disposable padded tape having a plurality of force absorbing zones. It can also include an adhesive layer for attaching the device to a body contacting surface.

A wound care accessory device providing pre-cut tape and an infection control barrier includes a sheet that comprises a first section and a second section. The sheet is substantially rectangularly shaped. A plurality of tape strips is disposed on and peelable from the second section of the sheet. The sheet is configured for placement proximate to a wound that requires care. The sheet provides a barrier to control infection. The first section is configured for placement of accessories used in caring for the wound. The tape strips are positioned on the second section of the sheet. The strips are configured for peeling by the user from the sheet to be used in caring for the wound.