A port is provided for use with a wound dressing. The port has piercing means to change the configuration of wound dressing for use in a pressure gradient wound therapy apparatus or for use without a pressure gradient wound therapy apparatus. The port is for connecting a non-atmospheric pressure source to a wound dressing. It comprises a first aperture configured to connect to the non-atmospheric pressure source; and a wound dressing contact surface. The wound dressing contact surface includes a second aperture in fluid communication with the first aperture and configured to allow fluid communication with the wound dressing. The piercing means is configured to pierce the wound dressing as the wound dressing contact surface of the port is applied to the wound dressing.

A wound dressing for use in the application of negative pressure to a wound, comprising a support member and a cover member positionable over the wound in use. The support member can have a first support element having a first portion aligned with a first axis and a body portion coupled with and extending away from the first portion, and a second support element having a first portion aligned with the first axis and a body portion coupled with and extending away from the first portion of the second support element. At least the body portion of each of the first support element and the second support element can be independently rotatable about the first axis. The support member can support at least a middle portion of the cover member above a surface of the wound so as to define a space between the wound cover and the wound.

A waterproof protector for a body member and a method for fabricating the waterproof protector. The waterproof protector comprises a body comprising a fabric layer comprising polyester; a water repellent applied to a first surface of the fabric layer; an antimicrobial substance applied to an opposite surface of the fabric layer and located on an inner surface of the body. The body comprises a main seam formed by a junction of the fabric layer, the junction being sewn by an ultrasound to form a main seam which is further sealed with an additional layer of a waterproof material positioned on the inner surface of the body and sealed to the inner surface by heat. The waterproof protector further comprises a stretchable strap attached to an end of the body and having several hook-and-loop fastener portions for leakless securing of the protector to the body member.

A bandage configured to be administered from a continuous roll, comprising: (I) a first layer of flexible webbed material, the first layer including a self-adhesive disposed on a top surface; and (II) a second layer of flexible padded material adhered to the first layer along a longitudinal axis by the self-adhesive, the second layer having a width less than a width of the first layer so that a portion of the self-adhesive is exposed on each longitudinal side of the second layer; wherein the self-adhesive may releasably adhere to a bottom surface of the first layer in a rolled form so that, when unrolled, an adhesive bond is broken free of damaging the first layer; and wherein, when the self-adhesive is bonded to itself and opposing adhesive portions, the resulting peel strength is greater than a peel strength when the self-adhesive is bonded to skin.

The present invention relates to a method and system for aseptically filling of flexible packages containing dry cloth. Such a method may include a first stage that is performed in a non-sterile environment. The first stage may include cutting a first substantially dry cloth to a predetermined size; inserting the first cloth into a flexible package; sealing a first end of the flexible package; and sterilizing the flexible package. The method may also include a second stage performed in a sterile environment. The second stage may include filling the flexible package with a medical solution such that the substantially dry cloth absorbs at least a portion of the medical solution; and sealing the open end of the flexible package.

A casting tape package system is provided comprising an outer package defining a first interior portion enclosing a casting tape substrate including curable casting formulation and a second interior portion enclosing a curing agent. In certain embodiments, the curing agent is separated from the casting tape substrate by a barrier which is breakable to release the curing agent to activate the curable casting formulation.

A sexual assault evidence collection kit that may be used by the victim or other non-professionals. The kit may be simplified compared to kits for professional use, and may be usable with no specialized training. Victims may therefore be able to collect evidence themselves after an assault, instead of searching for a facility with personnel trained in forensic evidence collection, and enduring a long, intrusive examination. Embodiments may include a package (for example a clear bag) and the following components inside the package: gloves, swabs, swab containers, water, evidence collection bags, evidence bag sealing tape, evidence collection tape, a permanent marker, and instructions on how to identify, collect, seal, document, and store evidence.

Polyurethane material for indicating pH at a locus, preferably as indication of presence of microbes, comprising a polyurethane network having immobilised therein one or more hydrophilic copolymers, the or each said copolymer comprising: hydrophilic monomer; and indicating monomer, which provides an indication in response to a change in hydrophilic state of said hydrophilic monomer and/or copolymer; characterised in that the or each copolymer further comprises one or a plurality of ionisable groups or moieties or polymerisable monomers having one or more characteristic pKa values in the range 5 to 10 and which are responsive to pH at the locus in the range pH 5 to pH 10 and in that hydrophilic state of hydrophilic copolymer is dependent on ionisation of said ionisable groups, moieties or monomers; kit and device comprising the material and process for preparation thereof; and use in detecting or sensing microbes or pH.

A disposable dressing forms a compartment around and above a wound site and a volatile antimicrobial compound is allowed to sublimate/evaporate into the compartment. A heating element is included in the dressing, with heat stimulating wound healing and simultaneously accelerating sublimation/evaporation of the antimicrobial compound.

The invention relates to a unit for hemostasis. The unit is configured to be directly applied to a bleeding wound and comprises an envelope enclosing an inner space as well as an effective amount of a hemostatic material disposed within the inner space. Furthermore, the invention relates to an arrangement of two or more such units for hemostasis, the units being coupled to each other. Moreover, the invention relates to a method for producing an arrangement of units for hemostasis. In accordance with the method, an effective amount of a hemostatic material is disposed within an interior region of a starting material, and neck regions are formed on both sides of the charge so as to form an envelope enclosing the charge.