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 pressure-sensing compression bandage having a plurality of pressure sensors provided to indicate the pressures applied by and/or the pressure gradient created by, the applied bandage at various locations along its length when the bandage is applied to a limb or other extremity.

An improved abdominal hernia repair system is presented comprised of a silicone layer backed up with a knitted or woven polypropylene fabric layer, the silicone layer possessing a regular pattern of slits that permit equilibration of fluid pressure across the device. A variety of therapeutic substances can be applied to the hernia repair device to promote healing, including aloe and other medicinal preparations. A layer of water soluble or water insoluble anti-scar compound is also present, the preferred compound being Salinomycin. An improved inguinal hernia repair system is presented that is identical to the above except it does not contain the hydrophobic silicone component.

The disclosure is directed to fibrous structures finished with active pharmaceutical ingredients, as well as methods of their manufacturer and use.

A wound dressing that includes a contact layer having walls defining a plurality of perforations and a debriding matrix including a polymer and at least one debriding agent is provided herein. Systems, methods and kits using the wound dressing for debriding a tissue site are also provided herein.

This invention relates to a hemostatic member using chitosan having superior hemostatic activity, and more particularly to a chitosan-based hemostatic member for the cervix, suitable for use through insertion into an affected part upon cervical biopsy or surgery, configured to include a hemostatic pack having a projection at an upper end thereof through tying with a thread so as to form a spherical shape using chitosan nonwoven fabrics having a hemostatic function, wherein the thread contains an X-ray-sensitive material, thereby realizing effective hemostasis of the affected part upon cervical biopsy or surgery.

Provided herein are methods for making foam materials and foam material products having a polyurethane foam matrix defining a plurality of pores, a hydrophilic agent retained within at least a portion of the pores for improving an absorption of the foam material, a salt retained within at least a portion of the pores in an amount sufficient to render the foam material isotonic, a surfactant retained within at least a portion of the pores in an amount sufficient to be released upon contact with a moist surface. Also provided herein are methods for making a multilayer foam by casting a second foam layer on a first foam layer substrate and compressing the second foam layer before the second layer is fully cured to form an interface layer in situ.

A three-layered wound dressing, including: a first layer, a second layer, and a third layer. The first layer includes a blend of first hydrophilic fibers and first hydrophobic fibers, the second layer includes a blend of second hydrophilic fibers and second hydrophobic fibers, and the third layer includes hydrophobic fibers. The second layer is disposed between the first layer and the third layer. In use, the first layer contacts a wound.

An absorbent article that includes an outer covering made of two liquid-permeable cover layers that are joined together to form a pocket, and an inner layer that is initially freely movable within the pocket. The inner layer includes a mixture of particles of a superabsorbent polymer and substances that are osmotically comparatively weaker than the particles. When the absorbent article is applied to a human or animal skin surface to cover a wound, the absorbent article exerts an osmotic pressure via which endogenous wound exudate is removed from the wound. Thus, the absorbent article assists, both in a surface region and in a tissue depth, a normal interstitial hydration of the tissue by directing the wound fluids in a direction of flow to the skin surface and into the absorbent article, and by keeping the wound fluids that flow to the skin surface in the absorbent article.

The invention discloses a medical bandage, and relates to the technical field of medical supplies. One specific implementation mode of the medical bandage comprises: a bandage body and an adhesive layer provided on the surface of the bandage body; the bandage body including: a non-woven fabric base and a plurality of elastic reinforcing filaments that are sewn into the non-woven fabric base and extend in the warp direction of the non-woven fabric base; wherein the non-woven fabric base is provided with a plurality of cutting positions that are arranged at equal intervals in the warp direction; each cutting position is provided with at least one linear cutting opening that extends in the weft direction of the non-woven fabric base; and each elastic reinforcing filament punctures the non-woven fabric base up and down to form continuous coils surrounding the non-woven fabric base. The implementation mode enables easily tearing apart the bandage with bare hands in the weft direction, and has a certain strength and a certain elasticity in the warp direction.