The present disclosure provides a coupling assembly (12) for an ostomy appliance (10) comprising a clamp arrangement (60), a first coupling and a second coupling. The clamp arrangement (60) comprises a clamp ring (61) mounted to the first and/or second coupling and a clamp locked mounted to the clamp ring (61). The clamp ring (61) comprises an inner circumference (62) adjustable between clamped and unclamped configurations. In the clamped configuration the clamp ring (61) is for maintaining the first and second couplings (20, 40) in a coupled configuration. The clamp lock (80) is adjustable into a locked configuration to lock the clamp ring (61) in the clamped configuration. The clamp lock (80) comprises a clamp actuator (81) moveable radially relative to the inner circumference (62) to unlock the clamp lock (80) from the locked configuration.

An ostomy pouch has a body side wall and a distal side wall defining a collection chamber. An opening is provided in the body side wall. A barrier is operably mounted to the body side wall over the opening. The barrier has an inlet opening. An internal collection member is mounted to the barrier. The internal collection member includes a tubular net having a first open end and a second closed end, and a ring-shaped capsule for storing the net inside the capsule in a collected manner. The ring-shaped capsule has an open central region and is mounted to the barrier with the capsule open central region and the barrier inlet opening aligned with one another to define a pouch inlet. The capsule extends into the pouch collection chamber and the first open end of the net is mounted to the capsule overlying the pouch inlet. Excretion is inlet to the pouch and is discharged into the net, paying out the net.

An ostomy pouch has a body side wall and a distal side wall defining a collection chamber. An opening is provided in the body side wall. A barrier is operably mounted to the body side wall over the opening. The barrier has an inlet opening. An internal collection member is mounted to the barrier. The internal collection member includes a tubular net having a first open end and a second closed end, and a ring-shaped capsule for storing the net inside the capsule in a collected manner. The ring-shaped capsule has an open central region and is mounted to the barrier with the capsule open central region and the barrier inlet opening aligned with one another to define a pouch inlet. The capsule extends into the pouch collection chamber and the first open end of the net is mounted to the capsule overlying the pouch inlet. Excretion is inlet to the pouch and is discharged into the net, paying out the net.

A drainable ostomy appliance including: first and second walls connected to each other at or near their peripheries, the first wall having a stoma-receiving opening; a collecting cavity defined between the first and second walls; a connection member connected to the first wall for attaching the appliance to a user or for attaching the appliance to a flange for attaching the appliance to a user; an outlet which extends away from the stoma-receiving opening, the outlet terminating at an opening; and a first stiffening member positioned immediately adjacent the opening on a wall of the outlet facing the user, in use, the first stiffening member extending across the outlet; and a second stiffening member positioned next to the first stiffening member, further away from the outlet than the first stiffening member and on the same wall as the first stiffening member, the second stiffening member also extending across the outlet.

A drainable ostomy appliance including: first and second walls connected to each other at or near their peripheries, the first wall having a stoma-receiving opening; a collecting cavity defined between the first and second walls; a connection member connected to the first wall for attaching the appliance to a user or for attaching the appliance to a flange for attaching the appliance to a user; an outlet which extends away from the stoma-receiving opening, the outlet terminating at an opening; and a first stiffening member positioned immediately adjacent the opening on a wall of the outlet facing the user, in use, the first stiffening member extending across the outlet; and a second stiffening member positioned next to the first stiffening member, further away from the outlet than the first stiffening member and on the same wall as the first stiffening member, the second stiffening member also extending across the outlet.

A skin-safe effluent containment system that may be used to contain fluid leakage from openings in the body of a patient and will adhere to skin in any condition: healthy or injured, wet or dry, smooth, scarred, or uneven. Fluid leakage can occur from natural orifices such as the anus and vagina, spontaneously formed enteric fistulas, rectovaginal fistulas, and surgical openings such as ileostomy and colostomy stomas. The system includes a vacuum-adherent pouch device, comprised of a pouch connected to a porous foam ring which has an air-permeable contact layer on its bottom surface and an air seal on its top surface. The inner and outer perimeters of the foam ring are enclosed and sealed with skin-adhesive materials. When placed on the patient, negative pressure (vacuum) is applied to the foam ring so that the foam collapses and compresses the vacuum-adherent pouch device down against the patient's skin. Negative pressure in combination with the adhesive materials on the perimeters of the foam ring forms a fluid barrier around the opening in the body of the patient so that leakage can be directed into the pouch and drawn away to a separate effluent container.

A skin-safe effluent containment system that may be used to contain fluid leakage from openings in the body of a patient and will adhere to skin in any condition: healthy or injured, wet or dry, smooth, scarred, or uneven. Fluid leakage can occur from natural orifices such as the anus and vagina, spontaneously formed enteric fistulas, rectovaginal fistulas, and surgical openings such as ileostomy and colostomy stomas. The system includes a vacuum-adherent pouch device, comprised of a pouch connected to a porous foam ring which has an air-permeable contact layer on its bottom surface and an air seal on its top surface. The inner and outer perimeters of the foam ring are enclosed and sealed with skin-adhesive materials. When placed on the patient, negative pressure (vacuum) is applied to the foam ring so that the foam collapses and compresses the vacuum-adherent pouch device down against the patient's skin. Negative pressure in combination with the adhesive materials on the perimeters of the foam ring forms a fluid barrier around the opening in the body of the patient so that leakage can be directed into the pouch and drawn away to a separate effluent container.

Provided is a device for microwave hyperthermia that may attach a flexible patch on the skin of a user based on a cross-section of a body tissue of the user, for example, a joint and muscle of a leg and an arm and may emit microwaves towards a plurality of points of the body tissue through the patch. The microwaves emitted toward the body tissue may have the same phase and maximum power. Accordingly, a maximum heat generation point may be generated in an area adjacent to the plurality of points. The device for microwave hyperthermia may move the maximum heat generation point by sequentially changing a phase and a direction of each of the microwaves. The device for microwave hyperthermia may uniformly distribute and maintain heat for treating pain and/or infection over the entire cross-section or a partial area. The device for microwave hyperthermia may be portable.

A barrier press is presented that comprises an external plate attached to a barrel tube that has a bag slot for the insertion of a body fluid bag that attaches to a stoma hole via the skin barrier, the barrel tube has a pressure ring to keep the skin barrier attached to the area around the stoma and in other embodiments an inner plate held in place by the pressure ring further reinforces the bag attachment to a body fluid bag user.

A barrier press is presented that comprises an external plate attached to a barrel tube that has a bag slot for the insertion of a body fluid bag that attaches to a stoma hole via the skin barrier, the barrel tube has a pressure ring to keep the skin barrier attached to the area around the stoma and in other embodiments an inner plate held in place by the pressure ring further reinforces the bag attachment to a body fluid bag user.