The invention relates to a flat wound care article having an essentially polygonal or ellipsoid base surface and at least one recess arranged on one side.

A device used for applying an antiseptic preparation to a surgical site of a patient prior to surgery outside of an operating theater. A loose-fitting bag is provided which encloses the surgical site by securing the open end(s) to the patient by closing means. A high friction scrub surface is provided in the bag. A method and apparatus are also provided for releasing antiseptic into the interior of the bag. The method provides that the surgical site can be scrubbed within the bag so as to properly prepare the skin for surgery. A temperature indicator for the antiseptic preparation is also provided.

A device used for applying an antiseptic preparation to a surgical site of a patient prior to surgery outside of an operating theater. A loose-fitting bag is provided which encloses the surgical site by securing the open end(s) to the patient by closing means. A high friction scrub surface is provided in the bag. A method and apparatus are also provided for releasing antiseptic into the interior of the bag. The method provides that the surgical site can be scrubbed within the bag so as to properly prepare the skin for surgery. A temperature indicator for the antiseptic preparation is also provided.

Disclosed is a medical dressing having a pad and a border portion. The pad can have a rim and the border portion extends along said rim. The medical dressing can be arranged in a first substantially planar configuration and be folded along a first line, and a second portion of said medical dressing is formed and a second substantially cup-shaped configuration. The first portion can be facing and contacting said second portion. Said first substantially planar configuration the first and second portions can be connected by means of a fixed connection along a second line, which defines a second line segment having a first and a second end-point. The first and second line segments are connected at their respective first end-points such that an angle between 90 and 175 degrees is formed between the first and second line segments when the medical dressing is in the first substantially planar configuration.

A cannulated tube protector comprising a main body, a first pair of securing members extending from the main body, a second pair of securing members extending from the main body, and a splinting member comprising a viewing door. The viewing door is structured to open thereby exposing a viewing aperture, defined as a doorway. The doorway extends from a first surface of the main body to an opposing second surface of the main body.

A fingertip protector having a flexible cover with a top contacting surface and a bottom gripping surface. A lip is attached to the flexible cover so as to define the contacting surface and a strap is attached on both of its ends to the flexible cover. The contacting surface is sized and shaped to fit on a tip of a finger and the strap is configured to wrap around a finger to assist in securing the contacting surface on the tip of the finger. The flexible cover is comprised of a heat-resistant elastomer. The contacting surface contacts the tip of a finger while the lip engages that tip to assist maintaining the finger and thumb tip protector in place.

A compressive brace for intraarticular needle procedures that provides constant radial compression. One embodiment comprises a non-pneumatic releasable compressive planar device or tubular sleeve, a method to apply tension to the device or sleeve comprising a non-stretchable material or stretchable elastomeric material with fasteners or external compression straps or both resulting in fluid displacement and increased intraarticular fluid pressure, a design that displaces fluid within the joint to low pressure areas to be readily accessible by needle or catheter via specific anatomic portals so that the joint can be completely aspirated, tension and pressure can be released so that fluid can be easily removed or injected into the joint, and integration of the device into arthrocentesis, surgical, diagnostic, and joint therapy kits. Some embodiments define a window or aperture to allow pooling of fluid and to introduce needles and catheters. Some embodiments dilate the patellofemoral joint and may displace the patella-making introduction of the needle more successful.

A surgical kit for the repair of a nail bed includes implantable nail plate guides adapted to guide the regrowth of a fingernail over a nail bed, drapes, a suture needle with absorbable suture, a suture needle with non-absorbable suture, wound dressings, and all instruments required to perform the procedure. The instruments preferably include an elevator, a needle driver, a clamp, a tweezers, and a scissors. The kit also includes anesthesia, a syringe, and needles for loading and then administering the anesthesia to the finger. The kit may include a tourniquet, antiseptic, and an antiinfective. Therefore, the kit assembles together several nail plate guides, the instruments for implanting a selected one of the nail plate guides onto the nail bed over a patient, the pre-implantation surgical preparation materials, and the post-implantation wound care materials.

A surgical kit for the repair of a nail bed includes implantable nail plate guides adapted to guide the regrowth of a fingernail over a nail bed, drapes, a suture needle with absorbable suture, a suture needle with non-absorbable suture, wound dressings, and all instruments required to perform the procedure. The instruments preferably include an elevator, a needle driver, a clamp, a tweezers, and a scissors. The kit also includes anesthesia, a syringe, and needles for loading and then administering the anesthesia to the finger. The kit may include a tourniquet, antiseptic, and an antiinfective. Therefore, the kit assembles together several nail plate guides, the instruments for implanting a selected one of the nail plate guides onto the nail bed over a patient, the pre-implantation surgical preparation materials, and the post-implantation wound care materials.

A protective liner for use with a blood pressure measuring cuff includes three layers of material configured to protect a person's skin, wick moisture away from the person's skin, and provide a moisture permeable, microporous barrier to microbes. The protective liner is porous and sufficiently thin so that the protective liner will not substantially interfere with blood pressure monitoring through the protective liner. The three layers of material are configured to wick moisture therethrough away from the person's skin, while substantially preventing passage of microbes therethrough.