An epistaxis clip includes a pair of wings connected to one another by a bridge portion. The pair of wings define a pair of opposing recesses or openings and a pair of absorbent pads are disposed in the respective opposing recesses or openings of the pair of wings. The epistaxis clip is designed to apply predetermined pressure on the Kiesselbach’s plexus. The pair of absorbent pads can include an absorbent foam that resists sticking to the wound and that can be replaceable.

A blood coagulant assembly includes a blood coagulant device adapted to be insertable into a nostril of a patient to stop a nose bleed. The blood coagulant device is mounted within a blood coagulant device container which has a top container section and a lower container section secured to each other in a releasable manner. The blood coagulant device is mounted in a fixed position within the blood coagulant device container prior to its removal from the blood coagulant container. The blood coagulant device has a rigid handle configured with a handle lower section and a handle upper section contoured with a channel passing through both the lower and upper handle sections. A blood coagulant mechanism is secured to an outer surface of the handle upper section and a to a ledge section of the handle member which extends radially at a joint location of the handle's lower and upper sections.

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 —CH—O— (e.g. C2H4O; C6H10O5; C6H8O6); —CH—N—O— (e.g. C8H13NO5); O—C—C— (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 present invention provides a device that can move inside a biological conduit such as an intestinal tract for sampling the content therein, and a process thereof. While moving along the intestinal tract, the device can continuously collect the content in the intestinal tract. One or more convoy belts having an adsorbent layer are configured to continuously absorb and preserve the collected intestinal content. The belt loaded with the sample may be used to establish a chemical, biochemical and microbiological spectrum along the length of the intestinal tract.

An application device for positioning an absorptive matrix (AM) element within a body cavity includes a tube, the AM element, a release element and a deflector. The AM element is disposed inside the tube in a stored state before exiting the tube towards the distal end in a released state. The release element slides inside the tube along a longitudinal axis of the tube and pushes the AM element out of the tube towards the distal end of the tube as the release element slides farther into the tube. The deflector is disposed at the distal end of the tube and bends the AM element away from the longitudinal axis of the tube as the AM element is pushed out of the tube. The deflector is an extension of the wall of the tube that protrudes from the distal end and bends inward towards the longitudinal axis of the tube.

The present invention provides a nasal cavity packing structure which comprises: a pad extending along a first direction, having a shape pressed in a second direction perpendicular to the first direction, and including a first hollow extending along the first direction inside the pad; and an elastic tube an outer circumferential surface of which is closely adhered to an inner circumferential surface of the pad.

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.

In some embodiments, a system includes a nasal packing, a delivery device releasably couplable to the nasal packing and configured to deliver the nasal packing into a nasal cavity of a subject, a reservoir configured to contain medication, and a fluid coupling configured such that the medication can flow from the reservoir to the nasal packing via the fluid coupling.

A rhinotillexis apparatus, devised for controlled insertion into a nasal cavity for collection and removal of mucus therefrom, includes a spatulate head member having a first surface and a second surface convergent at an anterior edge, a neck portion, a shield member, and a handle member for dexterous wielding in the hands of a user. The head member is tautly overlain with an absorbent layer. The shield member prevents over-insertion of the head member into the nasal cavity and shields a user's hands from contamination with mucus during use. Disposal of the apparatus after single-use decreases potential for cross-contamination.

A system includes a platform configured for insertion into a user's nostril and a catheter. The platform includes a board having first and second major surfaces and a support extending from the board. The support includes an aperture therethrough. The catheter includes an inflatable tube and a lumen having first and second ends, the first end connected to the tube and the second end connected to a pressurized fluid source for inflating the tube. The tube is configured for insertion through the aperture. A method includes inserting a platform into a user's nostril, inserting a catheter through an aperture of the platform, and inflating a tube of the catheter. Inflating the tube is accomplished by introducing a pressurized fluid through a lumen of the catheter, to thereby cause the tube to conform to a passage of the user's nasal or pharyngeal region.