A carrying box is releasably attachable to a portion of a piece of clothing. The carrying box has a top section connectable to a bottom section in a sealing manner. The bottom section has a curved bottom face with a curve radius substantially corresponding with the curve shape of a body part of a human being to be covered by the portion of piece of clothing. The carrying box further is arranged for releasable interconnection with said portion of piece of clothing by at least one attachment means, wherein at least one of a curved inward top face of the top section and the curved bottom face of the bottom section is arranged to carry a compress element.

A hemostatic device for treatment of a gunshot wound includes a barrel, which has a first end that is open, and a plunger. The barrel is arcuate adjacent to a second end to define a tip section. A clotting medium and a gauze are positioned in the barrel proximate to the tip section and between the clotting medium and the first end, respectively. A plurality of slits that is positioned in the tip section defines a plurality of petals, which comprise plastic and are resiliently deformable. The plunger, which has a head that is sealably positioned in the barrel adjacent to the first end, is configured to be pushed into the barrel to apply pressure to the gauze and the clotting medium so that the petals separate. The clotting medium and the gauze are sequentially expelled from the barrel into a wound to induce clotting and to pack the wound.

A first aid medical treatment apparatus, wherein the apparatus' case and duct tape allow for efficient and easy use and creation of different bandages without necessitating every type of bandage being part of the first aid kit.

The invention relates to a bandage (10) comprising a flat material web (12) having a first (14) and a second (16) side and a first (18) and a second (20) end spaced apart in the longitudinal direction of the bandage (10), a wound pad (22) on the first side of the flat material web (12), a pressure application means (32) on the second side (16) of the flat material web (12) opposite the wound pad (22), a securing element (24) on the second end (20) of the flat material web (12) for securing the second end (20) of the flat material web (12) on or to itself for a bandage (10) positioned on a carrier.

Items that can adhere to the skin for medical or paramedical use are described. Also described, is a skin-adhesive item.

A medical bandage is provided, capable of being rapidly, adjustably, intuitively and universally fitted on a head, limb, stump, finger or other body part, such as to conceal and protect a wound. The medical bandage is cap-shaped and deformable, is formed of several layers, and comprises at least one port for obtaining quick access to a wound concealed by the medical bandage. When open, a port can stabilize a drainage tube, or provide a passage through which to easily and rapidly apply a medicine. The medical bandage can be directly fit on the head or other body part, providing an all-in-one dressing, wrap and treatment, and eliminating the need for cumbersome and difficult to manage gauze roll and multiple bandages of various sizes, shapes, and uses. The medical bandage can include one or more sensors for measuring or monitoring body parameters or functions.

A medical bandaging and tourniquet system for use in dressing puncture wounds is provided. The medical bandaging and tourniquet system includes a primary dressing, a secondary dressing, a band, a tightening buckle, a retaining clip, and a tightening rod. The primary dressing serves as a main wrapping bandage that mounts the secondary dressing and tourniquet components together. The secondary dressing removably attaches to the primary dressing and serves as a bandage that can be installed onto minor wounds. The band connects to the primary dressing, serving as an elastic tourniquet band. The tightening buckle and the retaining clip are connected to the primary dressing. The tightening rod is positioned between the tightening buckle and the retaining clip. The primary dressing straps tightly along a wound though the tightening buckle. The strap is further compressed by turning the tightening rod. The tightening rod can then be secured to the retaining clip.

A hemostatic device for treatment of a gunshot wound includes a barrel, which has a first end that is open, and a plunger. The barrel is arcuate adjacent to a second end to define a tip section. A clotting medium and a gauze are positioned in the barrel proximate to the tip section and between the clotting medium and the first end, respectively. A plurality of slits that is positioned in the tip section defines a plurality of petals, which comprise plastic and are resiliently deformable. The plunger, which has a head that is sealably positioned in the barrel adjacent to the first end, is configured to be pushed into the barrel to apply pressure to the gauze and the clotting medium so that the petals separate. The clotting medium and the gauze are sequentially expelled from the barrel into a wound to induce clotting and to pack the wound.

Fibrin Sealant products are used for topical hemostasis and tissue adherence. They are composed of two main reagents, fibrinogen and thrombin. When mixed in solution fibrinogen is converted to fibrin upon the addition of activated thrombin. Therefore typically these two components are stored separately in a lyophilized or liquid state, and mixed, upon or immediately before, application to a patient. While effective, these products require significant preparation that must take place immediately before application, thus delaying treatment and limiting the use of these haemostatic products to the treatment of mild forms of low pressure and low volume bleeding. Attempts to eliminate this delay and expand the usefulness and effectiveness of these products have resulted in products produced by processes that require the separation of these components and their deposition in distinct layers within the product. The processes described herein permit the mixing of fibrinogen and thrombin during product manufacture, without excessive fibrin formation. The resulting pre-mixed fibrin sealant material can then be stored in either a frozen or dried state, or suspended in a non-aqueous environment. Activation of the material to form therapeutic fibrin sealant is accomplished by permitting the product to thaw (if frozen) or by the addition of water or other aqueous fluid, including blood, or other bodily fluids, if dried or suspended in a non-aqueous environment. The resulting material can be used to make a product in which a pre-mixed form of activatable fibrin sealant is a desired component.

An emergency trauma stretch bandage cap shaped as a skull cap with roll able edges capable of holding hot or cold packs, which is placed on the cranium to cover the crown, forehead, back of the head, ears, sides of the head around the ears, and the temples of an injured patient with minimal movement of the neck and spine made of two or more layers of a stretchable warp knit fabric cut and sewn to form a form-fitting head bandage shape to apply sufficient pressure to suppress bleeding.