Abstract: There is provided an apparatus for extracorporeal blood treatment, comprising: a treatment unit (10), a blood circuit coupled to the treatment unit (10), a blood pump (22) configured to be coupled to a pump section of the blood circuit, at least two fluid lines (40, 60, 70, 70b, 70c) connected to respective containers (48, 68, 78, 88) and to the blood circuit and/or to the treatment unit (10). The apparatus further comprises a fluid dispatcher (300) having a common zone (310), wherein said at least two fluid lines (40, 60, 70, 70b, 70c) are connected one to the other at said common zone (310) upstream the blood circuit, for selectively allowing fluid flow between said at least two fluid lines (40, 60, 70, 70b, 70c) through said common zone (310).

Abstract: Absorbent articles comprising elastic waist members and methods of manufactured are disclosed. In an embodiment, an absorbent article may comprise a chassis including an absorbent body and a body facing surface. The article may further comprise a first adhesive disposed on the body facing surface of the chassis and an elasticated waist member coupled to the body facing surface of the chassis by the first adhesive. The article may still further comprise a second adhesive disposed on the elasticated waist member and a waist region covering material coupled to the elasticated waist member by the second adhesive.

Abstract: A vial adapter includes a body having a component connection interface, a piercing member having a first end connected to the body and a second end positioned opposite the first end, with the piercing member and the body defining a fluid passageway in fluid communication with the component connection interface, and a vial securing member extending from the body. The vial securing member is configured to secure the body to a vial. The vial securing member is moveable between a first position where the vial securing member defines a first length and a first width and a second position where the vial securing member has a second length and a second width, where the first length is larger than the first width, the first length is larger than the second length, and the second width is larger than the first width.

Abstract: A multi-vial adapter includes an adapter body including at least two body parts, which are connected to each other at a certain angle, a head part, which protrudes upward from a connection portion between the body parts, and at least two spike parts, which extend downward from the body parts, respectively, at positions spaced a certain distance from the connection portion, and at least two adapter caps which are physically fastened and fixed to the body parts, respectively, and through which the spike parts respectively pass. The adapter body is formed by an injection molding process such that the head part, the body parts, and the spike parts are integrated with each other, and a liquid drug flow path that guides the movement of a liquid drug from the respective spike parts to the head part via the respective body parts may be formed inside the adapter body.

Abstract: A garment-like absorbent article can have a front region, a back region, and a central region extending between and connecting the front region and the back region. The front region and the back region of the absorbent article can be formed from a combination of elastic materials. The combination of the elastic materials can be asymmetrically configured about the absorbent article to provide an improved fit of the absorbent article to the body of the wearer as well as to provide the wearer with an absorbent article that resembles traditional woven underwear.

Abstract: The present invention relates to multi-layered non-woven structures being useful as components of disposable absorbent articles and garments comprising super absorbent particles and thereby acts as a core. The invention thereby ensures that the body fluids can penetrate from a first layer, which acts as an acquisition layer, up to a third layer comprising SAP particles, the second non-woven layer serving to decrease the fluid volume per surface unit, as a conventional dispersion layer. However the second layer of the invention additionally acts like a non-return valve, preventing, or at least strongly limiting, any fluid transfer from the third layer to the first layer. Channels free of SAP can additionally be design to improve the inlet and rewet properties of the multilayer acquisition and distribution sheet non-woven material.

Abstract: A wound therapy system having a wound dressing for treating a wound includes a sensor that measures a pH level at a wound area. The sensor has a circuit that includes a first electrode and one or more second electrodes. The first electrode has a changeable conductivity that changes according to a hydrogen ion concentration level. The one or more second electrodes are configured with a fixed conductivity that does not change with the hydrogen ion concentration level. The first electrode is coated with a porous protective membrane formed from a sulfonated and/or carboxylated copolymer.

Abstract: An interventional catheter is adapted for treating a blood vessel. In an embodiment, the catheter includes an elongate shaft sized for insertion in a blood vessel and a stent positioned on a distal region of the elongate shaft. An expandable dilation member is coupled to a distal region of the elongate shaft. The expandable dilation member is adapted to expand outward. A stent containment member is positioned over the elongate shaft and the stent to contain the stent in a collapsed state.

Abstract: Systems and methods for delivering to and/or receiving fluids or other materials, such as blood or interstitial fluid, from subjects, e.g., from the skin. Beading disruptors and/or capillaries may be used for facilitating the transport of fluids from a subject into a device. Beading disruptors may disrupt the “pooling” of bodily fluids such as blood on the surface of the skin and help influence flow in a desired way. A capillary may conduct flow of fluid in the device, e.g., to an inlet of a channel or other flow path that leads to a storage chamber. A vacuum (reduced pressure relative to ambient) may be used to receive fluid into the device, e.g., by using relatively low pressure to draw fluid into the inlet of a channel leading to a storage chamber. The vacuum source may be part of the device and have a volume that is larger than a recess of the fluid transporter that receives fluid from a surface.

Abstract: An extracorporeal blood treatment apparatus includes an extracorporeal circuit, a dialysis fluid circuit, and a dialyzer. A blood side and a dialysis fluid side of the dialyzer are separated by a membrane. A control unit automatically empties the dialyzer by setting a reduced pressure or negative pressure in the dialysis fluid circuit and by a passage of fluid from the blood side to the dialysis fluid side via the membrane. Once fluid has passed from the blood side to the dialysis fluid side and the blood side has been emptied, the control unit brings about a passage of air from the blood side to the dialysis fluid side via the membrane, and a displacement of the fluid out of the dialysis fluid side toward a dialysis fluid outflow by continued setting of the reduced pressure or negative pressure in the dialysis fluid circuit.

Abstract: A vascular constricting device for constricting vascular lumens to regulate blood flow in a vascular system includes a cuff having an inflatable body and a frame adapted for wrapping round a vascular lumen, such as a native blood vessel or non-native graft, and a pump having an internal reservoir for doling a fluid and a fluid circuit for controlling the flow of fluid between the reservoir and the inflatable body for selectively inflating and deflating the inflatable body. In a hemodialysis treatment, the vascular constricting device is actuated to inflate the inflatable body to restrict blood flow and lower blood flow rate during off-treatment periods, and is actuated to deflate the inflatable body to permit an unrestricted blood flow and a higher blood flow rate during on-treatment periods.

Abstract: Examples relate to systems, devices, and methods for removing fluid from a fluid collection device using a portable vacuum source operably coupled thereto. The fluid collection devices include urine collection devices shaped to complement the female or male anatomy near the respective urethras and the vacuum source is operably coupled to the fluid collection device via one or more sections of conduit.

Abstract: An absorbent article for absorption of body fluids, including an absorbent member that includes at least one plant protein based absorbent material obtainable by a method including the steps of i. providing a mixture or suspension including a liquid and a plant protein, wherein the plant protein is insoluble in the liquid, ii. acylating the plant protein by adding an acylating agent thereto, and iii. obtaining the plant protein based absorbent material.

Abstract: In some examples, an auxiliary port assembly may be configured to be coupled to a cover for providing a sealed space at a tissue site. The auxiliary port assembly may include an access portal and an adhesive. The access portal may include an exterior side and a mounting side opposite the exterior side. The mounting side may be configured to face the cover. The access portal may be configurable between an open state and a closed state, and may provide a passage through the cover in the open state. The adhesive may be configured to couple the mounting side of the access portal to the cover. Other systems, dressings, apparatuses, and methods are disclosed.

Abstract: Various systems and methods for the pressure-regulated transfer of medical fluids are disclosed. The system can include an adapter assembly that connects with a medical container and with a syringe assembly. The syringe assembly can include a first reservoir and a second reservoir. In various embodiments, when the adapter assembly and the syringe assembly are coupled, the first reservoir and the container can exchange regulating fluid and the second reservoir and the container can exchange medical liquid from the medical container.

Abstract: A transdermal drug delivery device includes a reservoir, a transdermal membrane, a piston, a control rod, a spring, and a rotational cam. The reservoir is configured to hold a formulation. The transdermal membrane is configured to allow the formulation from the reservoir to pass therethrough. The piston is configured to move into the reservoir. The control rod is attached to the piston and includes a plurality of teeth thereon. The spring is configured to apply force to the control rod in the direction of the reservoir. The rotational cam has a first camming surface and a second camming surface that are configured to engage with the plurality of teeth. The rotational cam, when rotated, is configured to disengage the first camming surface from a first tooth of the plurality of teeth, thereby allowing the spring to advance the piston into the reservoir to expel the formulation onto the transdermal membrane.

Abstract: The present disclosure relates generally to the field of medical devices and establishing fluid communication between body lumens. In particular, the present disclosure relates to devices and methods for establishing a controlled flow or access passage between body lumens.

Abstract: A medical appliance for use in extracorporeal blood treatment. The appliance includes a housing component, a cover and a pivot bearing arrangement by which the cover is mounted on the housing component. The cover is pivotable between a covering position, in which the housing component is covered, and a exposure position, in which the housing component is exposed. The pivot bearing arrangement has pivot bearings, each having a bearing element and a bearing element receptacle. The cover can move linearly relative to the housing component between a dismounting position, in which at least one of the bearing elements is disengaged from a bearing element receptacle, and a bearing position, in which both bearing elements engage the bearing element receptacles. The cover is mounted resiliently and elastically preloaded relative to the housing component by a spring arrangement.

Abstract: A negative pressure wound therapy system includes a wound dressing, at least one pump fluidly coupled to the fluid interface, a pressure sensor fluidly coupled to the wound dressing, a control housing, and an electrical coupler. The wound dressing includes a sealing layer, an absorbent layer adjacent to the sealing layer, and a fluid interface attached to at least one of the sealing layer or the absorbent layer. The at least one pump is configured to apply negative pressure to the fluid interface to draw fluid from the wound dressing via the fluid interface. The pressure sensor is configured to detect a fluid pressure of the wound dressing. The control housing is remote from the wound dressing. The electrical coupler is configured to removably connect the control housing to the at least one pump.

Abstract: A device for detecting a state of a diaper includes a sensor unit with a conducting unit including at least two electrodes. The electrodes are configured to detect electrical parameters of their environment. A coupling portion is disposed on at least one end side of the conducting unit and is connectable to a measuring device. The conducting unit is attached to a carrier layer. The measuring device comprises an input portion being connectable to the sensor unit, and a processor configured to receive signals corresponding to values of the electrical parameters detected by the sensor unit and to process said signals. A power control means is configured to control electrical power supplied from a power supply, and a determination means is configured to determine whether a state of a diaper has changed. A transmitting means is configured to transmit information regarding the determined state change to a receiving means.