A dressing for treating tissue with negative pressure is provided herein comprising a composite of dressing layers, including a release film, a perforated coated polymer film, a manifold, and an adhesive cover. Additionally, a method of manufacturing the dressing may comprise applying a cross-linkable polymer to a polymer film, curing the cross-linkable polymer to a gel layer to form a coated polymer film, and perforating the coated polymer film to form fluid restrictions, such as slits and/or slots, though the coated polymer film.

An appliance is provided for negative-pressure therapy of wounds on the human or animal body in which, on the one hand, a substance is delivered to a wound bed (W) and, on the other hand, fluids, in particular an exudate and the delivered substance, are aspirated from the wound bed by negative pressure. The appliance has a suction pump housing, with a suction pump arranged therein for aspirating the fluids from the wound bed (W), and a fluid collection container for collecting the aspirated fluids. Moreover, the appliance has a first measuring device and a second measuring device. The first measuring device serves to determine the quantity of the aspirated fluids, and the second measuring device serves to determine the quantity of the substance delivered to the body.

A breast milk collection device includes a reservoir volume and an adaptor having one end to receive a woman's breast. The adaptor has a drip tube communicating with the reservoir. A source of cyclical application and relief of vacuum force is applied to the woman's breast located in the adaptor for the expression of breast milk. A one-way assembly permits breast milk to enter the reservoir and to submerge the valve element. The valve assembly includes a flexible barrier having an interior hollow chamber in fluid communication with said cyclical source of vacuum force and relief pressure, the flexible barrier fluidly isolating the source from the reservoir. The flexible barrier inflatably expands when relief pressure is applied to the interior of the flexible barrier, the flexible barrier becoming deflated when a vacuum force is applied to the hollow interior of the flexible barrier.

Embodiments of a negative pressure wound therapy systems and methods for operating the systems are disclosed. In some embodiments, a system includes a pump assembly, canister, and a wound dressing configured to be positioned over a wound. The pump assembly, canister, and the wound dressing can be fluidically connected to facilitate delivery of negative pressure to a wound. The system can be configured to efficiently deliver negative pressure in continuous and intermittent modes. The system can also be configured to gradually ramp up and down to set pressure values. The system can also be configured to detect and indicate presence of certain conditions, such as low pressure, high pressure, leak, canister full, and the like. Detection and indication of the presence of at least some of these conditions can be enabled and disabled.

A system for removing an occlusive clot from a blood vessel comprises a catheter and an apparatus for generating a pulsatile vacuum force to pulse the pressure gradient at a distal end of the catheter. The pulse generator may be integral with or separate from the vacuum pump. The pulse generator may be applied to a flexible tubing between the vacuum pump and the proximal end of the catheter.

The combination of a breast pump shield, with its ring, applied to the flange lower end of the shield, and the ring being C shaped in cross-section, having an upper flange, a lower flange, both integrally structured with a base wall. The physiological stimulator integrally formed with the lower flange of the sealing ring extends inwardly and upwardly within the shield, and therein functions as a means to place pressure upon the breast of the mother to help induce and stimulate the flow of breast milk during usage of the associated breast pump.

A method for operating a breastpump unit for expression of human breastmilk and various breast shields for use in this method allow a maximum pumping performance and a minimum pumping duration per pumping session. The breast shield has an inner chamber for receiving a nipple of the breast and also at least one outer chamber which at least partially surrounds the nipple. The inner chamber is subjected to a constant pressure and the at least one outer chamber is subjected to a pulsating pressure.

The wound therapy apparatus may include a wound interface sealingly securable to the skin surface around a wound bed to encloses the wound bed within an enclosed space that is fluid-tight. The wound interface may be sufficiently deformation resistant to distend at least a portion of the wound bed into the enclosed space when pressure p.sub.0 within the enclosed space is less than ambient pressure p.sub.amb. Fluid may be communicated with the enclosed space when the wound interface is sealingly secured to the skin surface in order to vary a pressure p.sub.0 within the enclosed space periodically over the pressure range p.sub.min≤p.sub.0≤p.sub.max. The variation of the pressure p.sub.0 may distend the wound bed into communication with a pad received within the enclosed space and decreases the wound bed contact with the pad. Related methods of use of the wound therapy apparatus are also disclosed.

A shunt for draining fluid including a first catheter, an electronic pump fluidly coupled to the first catheter, a manual pump fluidly coupled to the electronic pump, a second catheter fluidly coupled to the manual pump. During a drainage operation, the shunt arranged and configured such that a fluid is passively pressure-driven through the shunt, and the electronic pump is arranged to prevent blockages within the shunt by flowing a bolus of the fluid through the shunt. Additionally, the manual pump is arranged to prevent blockages within the shunt by flowing a bolus of the fluid through the shunt in the event that the electronic pump cannot produce a bolus of the fluid.

The present invention relates to a system and method for pulse cycle pressure modulation and negative pressure therapy in a cardio synchronous manner to improve distal limb blood flow applying negative or variable pressure to a portion of the body. The invention relates to methods and apparatus for the application of a sequential and gradient pulse wave for treating wounds that are difficult to heal or livelihood limiting claudication and/or ischemic rest pain. An integral part of the present invention includes methods to determine blood flow and effects of treatments on tissue.