Abstract: Disposable absorbent articles comprising a liquid pervious topsheet, a liquid impervious backsheet that is at least partially joined to the topsheet, an absorbent core disposed at least partially between the topsheet and the backsheet, and a wetness indicator printed onto a surface of the backsheet wherein the wetness indicator comprises a graphic that further comprises at least one responsive color composition and a varnish coating disposed adjacent to the responsive color composition; wherein upon wetting, the graphic becomes visible to the unaided eye.

Abstract: The Holistic Breast Patch is the first known, non-pharmaceutical, effective device available which inhibits prolactin production safely and aids the relief of discomfort from breast engorgement pain by drying breast milk after pregnancy. The benefits of treatment of prolactin dependent diseases remain to be fully disclosed. It works transdermally and is comprised of a unique, approximately 1½ inch by ¾ inch natural and organic carbonyl disc housed within cotton gauze and nonstick adhesive Telfa®. It meets the Federal Drug Administration's definition of a non-significant risk device (21 CFR 812). Its use will aid in the treatment of prolactin dependent diseases and conditions and eliminate the serious risks of health complications and fatalities that have been documented by the use of prescription drugs, hormones and pharmaceuticals lacking FDA approval for this use by women. Wearing the Patch device is both easy and convenient.

Abstract: A reduced-pressure treatment system for treating a tissue site on a patient includes a gasket releasably attached around a perimeter of the tissue site that may remain in place for an extended time and allows an over-drape to be attached to it. The system and method further may include a manifold sized and configured to be placed in contact with the tissue site the over-drape positioned over the manifold and sealed to the gasket to create a sealed space between the over-drape and the tissue site; and a reduced-pressure source fluidly coupled to the sealed space to deliver reduced pressure to the tissue site. A method is also presented.

Abstract: A wound cover connecting device for the sealing connection of a drainage tube and a wound cover covering a wound has a base body for the sealing contact on an outside of the cover. According to the invention, the device comprises at least one penetration element for producing a through-passage in the cover. The device enables a simple, fast, and tight connection between the cover and the tube. In addition, it enables a treatment of the wound that is as uniform and has as large a surface as possible.

Abstract: A dialysis system includes a source of dialysis fluid; at least one pump for pumping dialysate to or from a patient or dialyzer; and a drain container configured to receive effluent dialysis fluid from the patient or dialyzer through a drain tube, the drain container including an at least semi-rigid body, the body including a handle, a drain tube receiving portion, a spout, and wherein at least a portion of the body is non-opaque such that effluent dialysis fluid inside the at least semi-rigid body can be viewed.

Abstract: The drainage pump unit according to the invention for aspirating body fluids by means of a suction pump comprises a drainage pump device with a pump housing (4) for receiving the suction pump, and a fluid collection container (5) that can be secured releasably on the pump housing (4). The drainage pump unit also comprises a pump-side attachment part (2) which has a connection element for connection to a patient-side drainage tube (10). The attachment part (2) is held releasably on the pump housing (4), and it has a connector piece (20) onto which an attachment opening (54) of the fluid collection container (5) can be fitted. Alternatively, the attachment part (2) can have an attachment opening into which a connector piece of the fluid collection container (5) can be inserted. The connection element and the connector piece (20) or attachment opening are connected to each other via a drainage channel (24) extending through the attachment part (2).

Abstract: A controller is operable to selectively supply gas to, and evacuate gas from, regions of a hyperbaric wound treatment chamber. The controller operates to inflate a passage or rib of the device to provide that the device is made sufficiently rigid for inserting a limb therethrough, and inflate an inflatable cuff to create a seal against the limb. The controller also operates to evacuate ambient air trapped within the chamber, and optionally partially evacuate the passage or rib, after the seal is created by the inflatable cuff, and then introduce oxygen into the chamber, and optionally inflate the passage or rib. The cuff, when inflated and creating a seal against a limb, optionally is at least partially within the chamber, and the treatment gas is supplied to the chamber to maintain the seal of the cuff against the limb.

Abstract: The drainage pump unit according to the invention for aspirating body fluids by means of a suction pump comprises a drainage pump device with a pump housing (4) for receiving the suction pump, and a fluid collection container (5) that can be secured releasably on the pump housing (4). The drainage pump unit also comprises a pump-side attachment part (2) which has a connection element for connection to a patient-side drainage tube (10). The attachment part (2) is held releasably on the pump housing (4). This drainage pump unit allows the fluid collection container to be replaced without removing the drainage tube and, therefore, without disturbing the patient.

Abstract: A percutaneous catheter includes a longitudinal catheter shaft having a distal end, a proximal end, a hollow portion, and a wall portion, a wire embedded within said wall portion at said distal end wherein said wire forms a pigtail curve when in a relaxed state, and a stylet capable of entering said hollow portion of said longitudinal catheter at said proximal end wherein said stylet substantially straightens said longitudinal catheter at said distal end.

Abstract: An external catheter device is disclosed which prevents infection arising from bacterial and/or yeast growth within the external catheter. To achieve such result, the external catheter device is coated with an antiseptic agent that is able to effectively kill and prevent the growth of bacteria and yeast. Additionally, the external catheter device may have an adhesive agent coating on its inner surface to prevent the condom from shifting while on the patient's penis.

Abstract: A device for extracting and collecting blood from a delivered placenta comprising a compartment to contain and support a delivered placenta and umbilical cord. The compartment includes a flexible membrane which can be displaced (preferably under the influence of a fluid (preferably gas) pressure differential between the compartment side and non compartment side of the membrane) to impart onto the placenta a pressure to encourage the displacement of fluid carried by the placenta towards the umbilical cord. The compartment includes at least one outlet opening via which the umbilical cord can extend (preferably in a sealed manner) to allow the flexible membrane pressure induced flow of fluid carried by the placenta to displace from the compartment for external to the compartment collection of the fluid.

Abstract: Reduced-pressure treatment systems and methods are disclosed that employ debridement mechanisms to remove unwanted tissue. In one instance, a reduced-pressure treatment system for treating a tissue site on a patient includes a manifold member for distributing reduced pressure to the tissue site, a support member for disposing proximate the tissue site and the manifold, and a debridement mechanism coupled to the support member. The debridement mechanism is for debriding the tissue site. The system further includes a sealing drape for placing over the tissue site and manifold member. The sealing drape is operable to form a fluid seal over the tissue site and manifold member. The system also includes a reduced-pressure subsystem for delivering a reduced pressure to the sealing drape. The system may further include a chemical-debridement subsystem. Other systems, manifolds, and methods are disclosed.

Abstract: Devices and methods useful for storing and retrieving information related to a medical device such as an implantable valve or an implantable sensor are disclosed. An implantable valve can include a valve housing adapted to receive fluid flow therethrough between a valve inlet and a valve outlet. A valve assembly can be disposed within the valve housing and adapted to control a rate of fluid flowing through the valve housing. The implantable valve can also include a radio frequency identification (RFID) tag associated with the valve housing, adapted to store data, and including an antenna for communicating stored data to an external reading device. The RFID tag can store data related to, for example, a patient, a pressure setting of the valve assembly, and/or pressure sensor disposed within the valve. The RFID tag can also store an identifier that identifies the implantable valve, a pressure sensor disposed in the valve housing, a patient associated with the implantable valve, and/or patient clinical history.

Abstract: [Subject] To obtain a body fluid absorbent article with the perfect protection against the body fluid leakage. [Means for Solving Problem] In the body fluid absorbent, the body fluid retainable absorbent member 53A is disposed under the face sheet 51. Then, the body fluid permeable absorbent member 52, which include the assembly of fibers in tows, is disposed between the face sheet 51 and the body fluid retainable absorbent member 53A.

Abstract: There is disclosed a catheter assembly comprising a catheter and a receptacle. The receptacle has an elongate pocket, for accommodating at least an insertable end of said catheter, a urine collection bag, having a width extension wider than a greatest width of said elongate pocket, and at least two tab areas on at least one tab are arranged at the periphery of the urine collection bag on opposite sides of said bag. Further, in a storage state, said elongate pocket is folded over said urine collection bag, and lateral parts of said urine collection bag extending outside said elongate pocket are folded towards each other over said elongate pocket, said lateral parts being dimensioned to overlap each other in the folded disposition, and wherein said tab areas are arranged on said lateral parts and are attached to each other, in at least one point of attachment, to releasably maintain said catheter assembly in a folded disposition during storage.

Abstract: A fluid dispenser device comprising a body provided with a dispenser orifice, a reservoir containing at least one dose of fluid being disposed statically in said body, said reservoir being closed in sealed manner by two stoppers, a first stopper and a second stopper the fluid being disposed in a fluid chamber, said device further comprising opener means for opening said first stopper, said opener means being disposed statically in said body, actuator means being connected to said second stopper, the actuation of said second stopper creating pressure in the fluid chamber; said pressure displacing and/or deforming said first stopper towards said opener means, and then fluid is expelled through said open first stopper towards said dispenser orifice, a spray profile being provided downstream from said dispenser orifice, the device further comprising precompression means.

Abstract: Surgical drains and methods for using the same for draining a body cavity are provided. Aspects of the surgical drains of the invention include an elongated structure having a proximal end and a distal end and a lumen configured to drain a substance from the body cavity. The distal end is configured to be placed in a body cavity and change in diameter when present in the body cavity from a first diameter to a second diameter that is smaller than the first diameter, where the change in diameter is mediated by a diameter-varying element. Aspects of the invention further include sheaths configured to be disposed around surgical drains, such as surgical drains of the invention, and methods of using the surgical drains and sheaths. The devices and methods of the invention find use in a variety of applications.

Abstract: The present invention relates to a system suitable for monitoring multiple leakage events such as wetting of a diaper or alike sanitary product. The system includes two or more than two electrodes that are supported in a spaced apart relationship and a liquid permeable substrate between the electrodes that lacks or has a low capacity for holding or storing liquid. In the event of liquid leakage, an electrical bridge connecting the electrodes can be formed by the liquid, and before the product becomes saturated liquid can freely drain from the permeable substrate and disconnect the electrodes. Upon further liquid leakage, electrical connection between the electrodes can be reformed indicating multiple liquid leakage events. In the situation where the sanitary product becomes saturated and liquid is prevented from draining from the permeable substrate, the electrical connection will continue, indicating that the sanitary product requires changing.

Abstract: A disposable urine collection device may include an absorbent pad disposed proximate to the inner surface of a shell. The device may be contoured to be positioned against and enclose the urinary area of a user such that the absorbent pad may absorb a quantity of urine associated with a complete urinary discharge from the user. The absorbent pad may be formed from one or more commercially available diapers. One or more elastic cuffs may be provided to conform to the user's urinary area and to help contain the flow of urine as it is discharged from the user. An invertible bag may be attached to the bottom of the shell so that the user may conveniently enclose the absorbent pad after use and dispose of the device in a sanitary manner.

Abstract: A low-profile reduced pressure treatment apparatus and system are provided. The apparatus includes a moldable conduit holder, a conduit through the conduit holder, and a flexible base. The conduit holder has first and second bulkhead surfaces, a convex top surface, and a bottom surface adapted to conform to a tissue contact region adjacent to a tissue site. An end of the conduit is substantially flush with the first bulkhead surface and a longitudinal axis of the conduit is substantially perpendicular to the first and second bulkhead surfaces. The base is connected on a first side to the bottom surface of the conduit holder, and extends beyond the first bulkhead surface to form an overlay zone adjacent the first bulkhead surface. An adhesive is disposed on a second side of the flexible base to secure the flexible base to the tissue contact region.