Abstract: A method of forming an ostomy pouch comprising: providing a film to form a first cavity wall and a second cavity wall; providing a comfort material to form a comfort layer; wherein the comfort material is a woven fabric material with a hot melt adhesive coating thereon; joining the first cavity wall to the second cavity wall at a first temperature and a first pressure for a first time period; and subsequently joining a comfort layer to at least one of the first and second cavity walls at a second temperature and a second pressure for a second time period.

Abstract: The invention relates to a wetting mechanism 20 for wetting a tube 12 of a catheter 10. The wetting mechanism 20 includes a housing 16 to be positioned at or proximal to the tip end 13 of the catheter tube 12, where the housing 16 comprises a holding chamber 22 and a wetting chamber 23. The wetting mechanism 20 comprises a fluid release control component 26 for controlling release of fluid within the holding chamber 22 into the wetting chamber 23. At least a portion of the catheter tube 12 is then able to be introduced and be moved through the wetting chamber 23 to wet the catheter tube 12, in use.

Abstract: Fluid collection apparatuses and methods of use in negative pressure therapies are provided.

Abstract: An intermittent catheter, preferably a female intermittent catheter, is provided in an assembly. The assembly may include a cap which may be attachable to the base of the assembly in use, and/or a seal which misaligns with sealing surfaces of a chamber wall and a moveable insert in use. It may have a two-step deployment, and/or a sheath that pulls out a storage chamber. Internal and external housing may define the storage chamber. The housing may have a filling aperture and/or the storage chamber may comprise an insert configured to move axially in response to rotation.

Abstract: An intermittent catheter, preferably a female intermittent catheter, is provided in an assembly. The assembly may include a cap which may be attachable to the base of the assembly in use, and/or a seal which misaligns with sealing surfaces of a chamber wall and a moveable insert in use. It may have a two-step deployment, and/or a sheath that pulls out a storage chamber. Internal and external housing may define the storage chamber. The housing may have a filling aperture and/or the storage chamber may comprise an insert configured to move axially in response to rotation.

Abstract: 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.

Abstract: Described is a catheter arrangement in which a sealed container of wetting agent is provided in a housing cap. The sealed container is pierced with a piercing member such that the wetting agent is directed towards the catheter. The wetting agent may bypass a handling surface of the catheter whilst being directed to the catheter tube.

Abstract: Wound sampling devices for detecting infection status may be used for point-of-care devices that can be placed at a wound site and detect an infection marker, infection status, or wound healing status by displaying a visible signal such as a color change.

Abstract: A wound dressing according to certain embodiments includes an adhesive layer for adhering the wound dressing adjacent to a wound, a wound contact layer for contacting the wound, a backing layer comprising a port, a tube having a first end connected with the port and an opposite second end, a first fitting connected to the second end of the tube, the first fitting configured for connection with a second fitting of the negative pressure wound therapy system to apply a negative pressure via the port, and a filter disposed within the first fitting. In certain embodiments, the filter is formed of polyethersulfone (PESU) and has an average pore size of at least 2 microns.

Abstract: Provided herein are fabric materials and debridement devices comprising gel-forming hydrofibres for disrupting a biofilm, loosening, or sequestering unwanted materials from wounds, and uses thereof. In particular, debridement and detection devices for selective and atraumatic removal of unwanted tissues and for detection of a wound infection are provided.

Abstract: The present invention relates to a catheter 10. The catheter 10 includes a catheter tube 12 having a tip end 13 and a distal end 14, with the distal end 14 being coupled to or forming at least part of a funnel 16 for discharging fluid from within the catheter tube 12. A sleeve 18 is provided about the catheter tube 12 which is coupled at an end thereof to the funnel 16 and extends towards the tip end 13 of the catheter tube 12. The catheter 10 additionally includes a wetting mechanism 20 which is integrally formed with the funnel 16 and includes a holding chamber 22 and a fluid outlet 26 operable to allow fluid 24 from within the holding chamber 22 to be released within the sleeve 18 for wetting an outer surface of the catheter tube 12.

Abstract: The invention relates to a wetting mechanism 20 for wetting a tube 12 of a catheter 10. The wetting mechanism 20 includes a housing 16 positioned initially at or proximal to the tip end 13 of the catheter tube 12. The housing 16 comprises a wetting chamber 23 into which at least a portion of the catheter tube 12 is able to be introduced and be moved therethrough to wet the catheter tube 12 in use. The wetting mechanism 20 includes a wetting applicator 40 positioned within the wetting chamber 23 configured to hold fluid therein and release said fluid to wet the catheter tube 12 upon movement of the tube 12 through the wetting chamber 23.

Abstract: A coupling assembly according to certain embodiments is configured for use with an ostomy appliance, and generally includes a first coupling, a second coupling, and a clamp arrangement. The second coupling is mounted to the first coupling and surrounds at least a portion of the first coupling. The clamp arrangement is mounted to the second coupling and surrounds at least a portion of the second coupling. The clamp arrangement generally includes a clamp ring and a clamp lock. The clamp ring includes a first end portion, a second end portion, and a continuous body extending between the first end portion and the second end portion. The clamp lock is operable to selectively couple the first end portion with the second end portion to thereby discourage separation of the first coupling from the second coupling.

Abstract: The invention relates to a wetting mechanism 20 for wetting a tube 12 of a catheter 10. The wetting mechanism 20 includes a housing 16 positioned initially at or proximal to the tip end 13 of the catheter tube 12. The housing 16 comprises a wetting chamber 23 into which at least a portion of the catheter tube 12 is able to be introduced and be moved therethrough to wet the catheter tube 12 in use. The wetting mechanism 20 includes a stopper 26 which is moveable between a first and second positions to prevent or allow the tip end 13 of the catheter tube 12 to be moved through the wetting chamber 23.

Abstract: A wetting device for wetting a catheter. The wetting device has an enclosure bounding the wetting device and enclosing a chamber, the enclosure having at least two wetting device apertures in a surface of the enclosure though which a catheter tube passes. The wetting device also has a port disposed through the enclosure thereof for loading wetting agent into the chamber.

Abstract: The present invention relates to packaging 10 for housing a medical device 100. The packaging 10 includes first and second sides 12, 14 sealed or otherwise secured around the periphery thereof to define a plurality of edges. An interaction region 24 is provided and defines a first point of contact for a user of the packaging 100. The packaging 10 also includes a tear-away region 28 which may be at least partially separated from the remainder of the packaging to form an open upper end of the packaging 10, in use. The tear-away region 28 includes an interaction point defining a second point of contact for a user of the packaging 10. A sealing arrangement including first and second sealing members 42, 44 provides a user-sealable seal between the first and second sides 12, 14 of the packaging 10.

Abstract: Disclosed herein are catheter assemblies (100) with a locator tip (134) proximal to the distal tip (112) of a catheter tube (110). The locator tip is sized to remain outside a female urethra and configured to allow the catheter tube to pass there through. As an example, the locator tip allows a woman using a urinary catheter to target her urethra without exposing the catheter tube to tissue until the urethra is located and insertion is initiated. This avoids infecting the urethra with a catheter tube that has been contaminated by bacteria around the urethra.

Abstract: An ostomy appliance having an appliance wall of flexible sheet material forming a cavity for containing a stomal output. The wall has a stomal inlet for receiving the stomal output and a gas vent for allowing the stomal gas to migrate out of the cavity. A filter arrangement is mounted to the appliance wall and has a filter channel extending from a filter channel inlet to a filter channel outlet. The filter channel inlet is located in the cavity for receiving the stomal output from the cavity and the filter channel outlet is mounted in communication with the gas vent for allowing stomal gas to migrate out of the filter channel to the gas vent. A separation element extends along the filter channel for maintaining the filter channel in an open configuration along part of the filter channel for allowing stomal gas to pass therethough.

Abstract: A wound dressing for pressure gradient wound therapy. The wound dressing includes a dressing body and an adhesive layer. The adhesive layer provides an adhesive region for providing a seal between the wound dressing and the periphery of a wound site, in use. Sensors are provided associated with the adhesive region, the sensors being configured to monitor one or more conditions indicative of a hermeticity of the seal between the wound dressing and the periphery of the wound site.

Abstract: A pressure gradient wound therapy apparatus (50) including a pump assembly (10). The pump assembly (10) includes a diaphragm (12) comprising a magnetic material (16), an electromagnetic actuator (18) switchable between two or more operational states and a valve arrangement (24) including an inlet valve (26) and an outlet valve (28) for the introduction and/or removal of fluid into a fluid chamber (30) of the pump assembly (10). The actuator (18) is configured to move the diaphragm (12) with respect to the actuator (18) between a first position corresponding to a first operational state of the actuator (18) and a second position corresponding to the second operational state of the actuator (18).