A deformable nose plug, comprising a deformable core material and an outer coating provided on said deformable core material, wherein said said outer coating comprises a hemostatic compound. The nose plug has a tapered distal end for insertion into a nostril and a proximal end whereby the nose plug is inserted into the nostril. The deformable core material may comprise a multi-phasic core material wherein a first phase of the multi-phasic core material is characterized by a solid or a semi-solid structure at a temperature of 35 C. or less, and wherein a second phase of the multi-phasic core material is characterized by liquifaction at a temperature of 37 C. or greater. Alternatively, the deformable core material may comprise a porous resiliently compressible substrate. Alternatively, the deformable porous resiliently compressible core material may be one of polymeric sponges, naturally occurring sponges, fluffy cellulosic materials, cotton, rolled gauze, and mixtures thereof.

A facial bandage assembly for absorbing nasal drainage includes a dressing is configured to be positioned on a face such that the dressing extends laterally beneath a nose. The dressing is comprised of a fluid absorbent material to absorb fluid draining from the nose. A strip is positioned within the dressing and the strip is comprised of a resiliently bendable material. The strip is manipulated to shape the dressing into a selected shape to conform to contours of the face. A pair of straps is provided and each of the straps is coupled to the dressing. Each of the straps is extended over a selected one of a pair of ears thereby retaining the dressing beneath the nose.

The invention relates to porous absorbent Composite Material, which may be used e.g. in the form of a plug or tampon, for instance for controlling bleeding, wound closure, prevent tissue adhesion and/or support tissue regeneration. The invention provides a hydrophilic Self-Dispersive, fragmentable and Bio-Absorbable Porous Composite foams, suitable for packing antrum or other cavities of the body, comprising of composite of polymers, which polymer preferably comprises C(O)O; NH2/3+; OH; CH2OCH2C(O)O groups as functional or CHO (e.g. C2H4O; C6H10O5; C6H8O6); CHNO (e.g. C8H13NO5); OCC (e.g. O-CH2-CH2); C(O)N groups in the backbone of the polymers e.g. gelatin, chitosan, collagen, alginate, polyvinyl alcohol, polyethylene glycol, keratin, cellulose.

The invention relates to porous absorbent Composite Material, which may be used e.g. in the form of a plug or tampon, for instance for controlling bleeding, wound closure, prevent tissue adhesion and/or support tissue regeneration. The invention provides a hydrophilic Self-Dispersive, fragmentable and Bio-Absorbable Porous Composite foams, suitable for packing antrum or other cavities of the body, comprising of composite of polymers, which polymer preferably comprises C(O)O; NH2/3+; OH; CH2OCH2C(O)O groups as functional or CHO (e.g. C2H4O; C6H10O5; C6H8O6); CHNO (e.g. C8H13NO5); OCC (e.g. OCH2-CH2); C(O)N groups in the backbone of the polymers e.g. gelatin, chitosan, collagen, alginate, polyvinyl alcohol, polyethylene glycol, keratin, cellulose.

A penile condom catheter facilitates urine collection and egress of urinary fluids away from the body torso. A circumferential anchoring structure includes a web of flexible strands sized and arranged to at least partially contact a portion of the penis. The anchoring structure provides a flexible yet secure hold against the penis when flaccid and provides an increase in the hold when a longitudinal force is exerted upon the anchoring structure. An annularly circumferential penile skin covering material is affixed to the anchoring structure and sized to fit over at least a portion of the penis. A seal is affixed to at least a portion of a covering material, a covering material orifice, or an anchoring structure. A conduit is affixed to at least one of a covering material, a covering material orifice, a seal and an anchoring structure created to permit the flow of urinary fluid away.

A device for treating nosebleeds includes a mouth insert comprising a horizontally extending elongated portion and a center portion extending downward from a bottom surface of the elongated portion. The center portion comprises a narrower width than the horizontally extending elongated portion and the elongated portion is shaped and dimensioned to be inserted into a buccal cavity of a user's mouth and to fit behind the user's upper lip and in front of the user's upper gums. The center portion is shaped and dimensioned to be positioned only in front of the user's upper front teeth. The center portion comprises a push-structure formed at a bottom end of the center portion and the push-structure comprises a push-surface used for placing a user's tongue or finger and pushing the device upward in order to provide pressure to the user's nose.

Effective treatments of pain and/or inflammation are provided. Through the administration of a porous biodegradable drug depot film, patch, strip or sponge being implantable within a nasal or sinus cavity and having pores sized to prevent the depot from functioning as a scaffold for tissue growth, one can reduce, prevent or treat pain and/or inflammation and prevent cells from infiltrating the drug depot and laying down scaffolding cells.

A medical packing device for use within a body cavity of a subject is provided. The medical packing device comprises an absorbent member having at least a first major side surface and at least one depression that is formed in the first major side surface and has a predetermined shape and volume. The at least one depression is defined by a continuous perimeter wall that is formed in the first major side surface and forms a reservoir capable of receiving and retaining a volume of a medicament therein.

A device for treating nosebleeds includes a mouth insert having a horizontally extending elongated portion, a center portion extending downward from a bottom surface of the elongated portion and a bite tab extending backward from the center portion. The elongated portion is shaped and dimensioned to be inserted into a buccal cavity of a user's mouth and to fit behind the user's upper lip and in front of the user's upper gums. The center portion is shaped and dimensioned to be positioned in front of the user's upper front teeth and the bite tab is shaped and dimensioned to provide a biting surface for the user's front teeth. Biting down onto the bite tab pushes the elongated portion upward and applies pressure upward to the user's buccal cavity and towards an anterior portion of the user's nose.

An exemplary medical apparatus includes a heated nasal insert, where the nasal insert is configured to heat tissue to be treated to a temperature in the range of substantially 46 C. to substantially 52 C. in use. An exemplary medical method for inducing hemostasis in tissue of a patient includes possessing a nasal insert; apposing the nasal insert to tissue of a patent; heating said nasal insert to a temperature that causes tissue of a patient to be heated to a temperature in the range of substantially 46 C. to substantially 52 C.; and maintaining the tissue of a patent treaded by said nasal insert within a temperature range of substantially 46 C. to substantially 52 C.