Abstract: The invention relates to a method for producing a polymer, in particular a thermoplastic, window or door hollow-chamber profile (1), wherein the hollow-chamber profile (1) which comprises at least one hollow chamber (2, 2?) is produced by means of an extrusion production process (3), wherein, during this extrusion production process (3), continuous reinforcing fibres (5) are integrated into the polymer matrix (4) of the hollow-chamber profile (1), and wherein the extrusion production process (3) is intended to produce at least one continuously fibre-reinforced core profile (10) of the hollow-chamber profile (1), which core profile has at least one hollow chamber (2), and the core profile (10) is provided with a preferably extruded outer coating (12) to improve the surface quality of the hollow-chamber profile (1).

Abstract: Methods for monitoring patient parameters and blood fluid removal system parameters include identifying those system parameters that result in improved patient parameters or in worsened patient parameters. By comparing the patient's past responses to system parameters or changes in system parameters, a blood fluid removal system may be able to avoid future use of parameters that may harm the patient and may be able to learn which parameters are likely to be most effective in treating the patient in a blood fluid removal session.

Abstract: Methods for monitoring patient parameters and blood fluid removal system parameters include identifying those system parameters that result in improved patient parameters or in worsened patient parameters. By comparing the patient's past responses to system parameters or changes in system parameters, a blood fluid removal system may be able to avoid future use of parameters that may harm the patient and may be able to learn which parameters are likely to be most effective in treating the patient in a blood fluid removal session.

Abstract: Methods for monitoring patient parameters and blood fluid removal system parameters include identifying those system parameters that result in improved patient parameters or in worsened patient parameters. By comparing the patient's past responses to system parameters or changes in system parameters, a blood fluid removal system may be able to avoid future use of parameters that may harm the patient and may be able to learn which parameters are likely to be most effective in treating the patient in a blood fluid removal session.

Abstract: An flow body comprises a curved suction skin having a first perforation, a leading edge and two skin sections extending therefrom, wherein each skin section has an outer end facing away from the leading edge, an interior suction duct having a second perforation and extending through an inside of the curved suction skin in a distance from the leading edge, and two sidewall members, connected to the outer ends, wherein the sidewall members are made of a composite material. The suction skin comprises a profiled contour shape, which determines a pressure distribution over at least one of the two skin sections when air flows over the curved suction skin, wherein the pressure distribution comprises a stagnation point, a suction peak and a subsequent local pressure maximum downstream of the suction peak, wherein the first perforation extends from a stagnation point on the suction skin to the local pressure maximum.

Abstract: The present disclosure relates to a vehicle frame for a mobile crane having a frame, in particular having a middle frame part that extends in the longitudinal vehicle direction, and having at least one sliding beam box for a support apparatus that is releasably bolted to a front-face rear end of the frame, wherein the bolting between the frame and the sliding beam box comprises at least two pins extending in the longitudinal vehicle direction and at least two pins extending transversely to the vehicle direction.

Abstract: Electrode arrangements for test elements, test elements and methods of determining sample sufficiency, monitoring fill time, establishing fill directions and/or confirming electrode coverage by a sample for test elements are disclosed. The test elements have an electrode-support substrate including a spacer having an edge defining a boundary of a capillary channel. The electrode-support substrate also includes a first electrode pair and a second electrode pair, wherein the first electrode pair is positioned between the second electrode pair.

Abstract: Electrode arrangements for test elements, test elements and methods of determining sample sufficiency, monitoring fill time, establishing fill directions and/or confirming electrode coverage by a sample for test elements are disclosed. The test elements have an electrode-support substrate including a spacer having an edge defining a boundary of a capillary channel. The electrode-support substrate also includes a first electrode pair and a second electrode pair, wherein the first electrode pair is positioned between the second electrode pair.

Abstract: An interim storage device (1) for separated and oriented objects (2) includes an object inlet (3), a rotating turntable (4), a spiral-shaped object path (5), and an object outlet (6). Either the object inlet (5) or the object outlet (6) is in line with the spiral origin (7) while the other is in line with the spiral end (8). The spiral-shaped object path (5) features a fixed spiral (9) which is placed above the turntable (4) without making contact.

Abstract: Monitoring of the performance of a blood fluid removal medium of a blood fluid removal device includes monitoring of condition, such as fluid flow rate or concentration of blood waste product, downstream of the medium. Upstream monitoring of the condition may also be performed to enhance the ability to determine whether the blood fluid removal medium is performing within predetermined ranges.

Abstract: Methods include monitoring indicators of blood pH or blood electrolyte levels during a blood fluid removal session and adjusting concentrations of pH buffers or electrolytes in dialysate or replacement fluid used during the session based on the monitored indicators. Blood fluid removal systems may employ sensors that monitor blood pH or electrolyte levels to adjust the fluid parameters during a blood fluid removal session.

Abstract: An aircraft with a fuselage, wings, horizontal stabilizers and a vertical stabilizer, wherein on a front portion of the vertical stabilizer an elongated one-piece nose element is mounted which forms lateral air guide surfaces. To the front end of the nose element a perforated metal plate nose member is attached. The front end of the nose element being closed and between this closed front end and the nose member an elongated air channel is formed.

Abstract: Methods include monitoring indicators of blood pH or blood electrolyte levels during a blood fluid removal session and adjusting concentrations of pH buffers or electrolytes in dialysate or replacement fluid used during the session based on the monitored indicators. Blood fluid removal systems may employ sensors that monitor blood pH or electrolyte levels to adjust the fluid parameters during a blood fluid removal session.

Abstract: An interim storage device (1) for separated and oriented objects (2) includes an object inlet (3), a rotating turntable (4), a spiral-shaped object path (5), and an object outlet (6). Either the object inlet (5) or the object outlet (6) is in line with the spiral origin (7) while the other is in line with the spiral end (8). The spiral-shaped object path (5) features a fixed spiral (9) which is placed above the turntable (4) without making contact.

Abstract: The present disclosure relates to a vehicle frame for a mobile crane having a frame, in particular having a middle frame part that extends in the longitudinal vehicle direction, and having at least one sliding beam box for a support apparatus that is releasably bolted to a front-face rear end of the frame, wherein the bolting between the frame and the sliding beam box comprises at least two pins extending in the longitudinal vehicle direction and at least two pins extending transversely to the vehicle direction.

Abstract: Methods for monitoring patient parameters and blood fluid removal system parameters include identifying those system parameters that result in improved patient parameters or in worsened patent parameters. By comparing the patient's current parameters to past parameters in response to system parameters or changes in system parameters, a blood fluid removal system may be able to avoid future use of parameters that may harm the patient and may be able to learn which parameters are likely to be most effective in treating the patient in a blood fluid removal session.

Abstract: A method for manufacturing a shell element reinforced with support elements comprises providing a skin element that has an outer surface and an inner surface opposite the outer surface, providing a first support element that has an attaching side and a free side opposite the attaching side, attaching the first support element on the skin element such that the attaching side of the first support element faces the inner surface of the skin element. A first recess is introduced into the first support element that proceeds from the free side of the first support element and extends transversely to the first axis. A second support element is provided that has a support side and a front side opposite the support side. The second support element is inserted into the first recess of the first support element such that the support side faces the inner surface of the skin element.

Abstract: A method includes monitoring an indicator of fluid volume of a patient via a sensor device, and setting an initial fluid volume removal prescription for a blood fluid removal session based on the monitored indicator of fluid volume. The method may further include transmitting data regarding the indicator of fluid volume from the implantable sensor device to fluid removal device. The system includes a blood fluid removal device and control electronics configured to set the initial fluid removal volume and rate prescription. In some embodiments, the fluid removal device sets or calculated the initial fluid volume removal prescription based on the data received from the implantable sensor. The indicator of fluid volume may be an indicator of tissue fluid volume or an indicator of blood fluid volume.

Abstract: Methods for monitoring patient parameters and blood fluid removal system parameters include identifying those system parameters that result in improved patient parameters or in worsened patient parameters. By comparing the patient's past responses to system parameters or changes in system parameters, a blood fluid removal system may be able to avoid future use of parameters that may harm the patient and may be able to learn which parameters are likely to be most effective in treating the patient in a blood fluid removal session.

Abstract: Methods for monitoring patient parameters and blood fluid removal system parameters include identifying those system parameters that result in improved patient parameters or in worsened patient parameters. By comparing the patient's past responses to system parameters or changes in system parameters, a blood fluid removal system may be able to avoid future use of parameters that may harm the patient and may be able to learn which parameters are likely to be most effective in treating the patient in a blood fluid removal session.