Abstract: A hydrant has a riser pipe and a shut-off element which can be brought from at least one open position into at least one closed position and vice versa. The shut-off element in the closed position seals the interior of the riser pipe from a hydrant inlet. The hydrant comprises at least one first passage, by which the interior can be fluidically connected to the outside of the hydrant, and one second passage, by which the pressurized hydrant inlet can be fluidically connected to the outside of the hydrant, wherein the first passage and the second passage can be brought into operative connection with each other. The operative connection produces a vacuum by water flowing through the second passage such that water in the interior of the riser pipe is led away via the first passage and the riser pipe is thereby drained.

Abstract: Systems and methods for enabling gaze-based virtual content control may include (1) displaying an artificial scene with one or more virtual elements to a user wearing a head-mounted display system, (2) identifying the user's eye gaze based on gazing data collected by one or more sensors in the head-mounted display system, (3) determining that the user's eye gaze is focused on a specific virtual element, and (4) in response to determining that the user's eye gaze is focused on the specific virtual element, increasing the specific virtual element's visibility to the user. Various other methods, systems, and computer-readable media are also disclosed.

Abstract: The disclosed computer-implemented method may include: identifying, using an eye-tracking system, an object within a scene viewed by a user; identifying, within a database of object interaction commands, a subset of commands that apply to the object viewed by the user; and presenting, to the user, the subset of commands that apply to the object. Various other methods, systems, devices, and computer-readable media are also disclosed.

Abstract: The disclosed computer-implemented method may include (i) determining, using an eye-tracking system, an orientation of at least one eye of a user, (ii) identifying, based at least in part on the orientation of the user's eye, a point of interest within a field of view of the user, (iii) determining that the point of interest is a candidate for tagging, and (iv) performing, in response to determining that the point of interest is the candidate for tagging, a tagging action that facilitates tagging of the point of interest. Various other methods, systems, and computer-readable media are also disclosed.

Abstract: A method for lyophilizing a substance is provided which may include placing at least one vial containing the substance in a lyophilization chamber, the at least one vial having an opening in which a stopper is inserted in a closed state not allowing gas exchange between the interior and exterior of the vial; providing mechanical means external to the stopper and arranged at the opening for restricting an upward movement of the stopper; lowering the temperature within the lyophilization chamber to a predefined value below the freezing temperature of the substance and reducing the pressure within the lyophilization chamber to a predefined pressure at a predefined temperature, the predefined pressure being chosen such that the force exerted by it on the stopper lifts the stopper from the closed state to an exchange state in which the stopper is only partly inserted in the opening of the vial allowing gas exchange between the interior and exterior of the vial, wherein the lowering of the temperature within the ly

Abstract: A medical system comprising a display is presented. In response to the reception of triggering information, a subset of data is selected from a displayed or non-displayed dataset according to a data priority scheme and the displayed dataset is replaced by the display of the selected subset of data. The display of the selected subset of data uses a variety of rendering options. The triggering information is provided by the user or provided by one or more sensors. The data priority scheme is predefined or computed. It is static or dynamic. The data priority scheme can comprise a threshold which is applied for the selection or determination of the subset of data. Examples of priorities associated with data for diabetes care are provided. A range of displays can be used and combined.

Abstract: A conveyor and metering device having a continuous conveyor belt or conveyor band, sub-regions of this conveyor belt or conveyor band being mounted on weighing devices for determining the mass of the conveyed material, which are connected to an electronic evaluation device, the weighing devices generating a signal proportional to the load of the conveyor belt or conveyor band and transmitting it to the evaluation device, weighing devices are provided, each of which includes a bearing bracket, which is used to receive an attachment in a form-filling manner from the outside, preferably from above, through an opening in the frame of the conveyor and metering device during the operation of the conveyor.

Abstract: A conveying and metering device with an endless apron belt that is movable by rollers on guide rails, wherein sections of the guide rail that are opposite one another are separated from the adjacent sections and, for determining the mass of the conveyed material, are supported on weighing devices that are connected to an electronic analysis device. Provision is made that the sections of the guide rail to be weighed, together with longitudinal members and transverse struts that are perpendicular to the longitudinal members, form a weighing frame, and this weighing frame is supported at each of its four corners on a separate weighing device, wherein an adjustable centering device is provided between the weighing frame and each of the weighing devices.

Abstract: A hydrant has a riser pipe and a shut-off element which can be brought from at least one open position into at least one closed position and vice versa. The shut-off element in the closed position seals the interior of the riser pipe from a hydrant inlet. The hydrant comprises at least one first passage, by which the interior can be fluidically connected to the outside of the hydrant, and one second passage, by which the pressurized hydrant inlet can be fluidically connected to the outside of the hydrant, wherein the first passage and the second passage can be brought into operative connection with each other. The operative connection produces a vacuum by water flowing through the second passage such that water in the interior of the riser pipe is led away via the first passage and the riser pipe is thereby drained.

Abstract: A method for lyophilizing a substance is provided which may include placing at least one vial containing the substance in a lyophilization chamber, the at least one vial having an opening in which a stopper is inserted in a closed state not allowing gas exchange between the interior and exterior of the vial; providing mechanical means external to the stopper and arranged at the opening for restricting an upward movement of the stopper; lowering the temperature within the lyophilization chamber to a predefined value below the freezing temperature of the substance and reducing the pressure within the lyophilization chamber to a predefined pressure at a predefined temperature, the predefined pressure being chosen such that the force exerted by it on the stopper lifts the stopper from the closed state to an exchange state in which the stopper is only partly inserted in the opening of the vial allowing gas exchange between the interior and exterior of the vial, wherein the lowering of the temperature within the ly

Abstract: The present invention is directed to an improved lyophilization process wherein a plurality of vials is not in contact with the shelf of the lyophilization device. The present invention is further directed to lyophilization cake and intermediate cake obtainable according to the process of the invention.

Abstract: A power-measuring device serves to measure the power of a three-phase system. It comprises a measuring unit for measuring a power of a first phase of the three-phase system, a display unit for displaying measured results and an operating unit for the operation of the power-measuring device by a user. Furthermore, it comprises a communications unit by means of which it can communicate with one or more further power-measuring devices. In this context, the power-measuring device is embodied, jointly with the one or more further power-measuring devices, to measure a power of several phases of the three-phase system.

Abstract: The present invention relates to dried reconstituted vesicle (DRV) compositions and water based formulations thereof, which contain one or more therapeutic agents (e.g. hydrophilic protein). More particularly, it relates to DRVs comprising at least one lipid and a fusion promoting agent which after reconstitution form large multilamellar liposomes encapsulating an active agent in an aqueous phase.

Abstract: A device for sealing a vessel, in particular a cartridge (7) or a test-tube for accommodating a freeze-dried pharmaceutical product (S), wherein the vessel (1) comprises at its opening end (3) an opening edge (4) and an adjoining longitudinal portion (5) with an evenly formed inner cross section, including a front plunger (2) to be positioned inside the vessel (1) at the longitudinal portion (5), is characterized in that the front plunger (2) is configured to be positioned in the vessel (1) in a sealing state, in which the front plunger (2) is fully inserted in the vessel (1), or in an exchange state, in which the front plunger (2) is inserted partly in the vessel (1) and partly protrudes over the opening edge (4) of the vessel (1), wherein the front plunger (2) comprises sealing means that are configured to seal the inside of the vessel (1) against the outside when the front plunger (2) is positioned in the sealing state, and one or more communicating grooves (2i) that are configured to place the inside and

Abstract: A device for accommodating a freeze-dried pharmaceutical product (S) for reconstitution, comprising: a vessel (1) having at its opening end (3) an opening edge (4) and an adjoining longitudinal portion (5) with an evenly formed inner cross section, a front plunger (2) to be positioned inside the vessel (1) at the longitudinal portion (5), wherein the front plunger (2) is configured to be positioned inside the vessel (1) in a sealing state, in which the front plunger (2) is fully inserted in the vessel (1), or in an exchange state, in which the front plunger (2) is inserted partly in the vessel (1) and partly protrudes over the opening edge (4) of the vessel (1), and wherein the front plunger (2) comprises sealing means that are configured to seal the inside of the vessel (1) against the outside when the front plunger (2) is positioned in the sealing state, and one or more communicating grooves (2i) that are configured to place the inside and outside of the vessel (1) in communication with each other when the

Abstract: The invention provides a polymer based material comprising a water binding agent present in an amount sufficient to chemically and/or physically absorb and/or adsorb water to prevent degradation of the polymer. The invention also provides a polymer based material comprising a plasticizer or organic solvent as well as a multi-component material or composite including materials encompassing a second polymer and/or an active agent. The invention further provides a pharmaceutical composition comprising the aforesaid polymer based material, which can be used for treatment of bone, cartilage and/or periodontal defects.

Abstract: A device for sealing a vessel, in particular a cartridge (7) or a test-tube for accommodating a freeze-dried pharmaceutical product (S), wherein the vessel (1) comprises at its opening end (3) an opening edge (4) and an adjoining longitudinal portion (5) with an evenly formed inner cross section, including a front plunger (2) to be positioned inside the vessel (1) at the longitudinal portion (5), is characterized in that the front plunger (2) is configured to be positioned in the vessel (1) in a sealing state, in which the front plunger (2) is fully inserted in the vessel (1), or in an exchange state, in which the front plunger (2) is inserted partly in the vessel (1) and partly protrudes over the opening edge (4) of the vessel (1), wherein the front plunger (2) comprises sealing means that are configured to seal the inside of the vessel (1) against the outside when the front plunger (2) is positioned in the sealing state, and one or more communicating grooves (2i) that are configured to place the inside and

Abstract: A medical system comprising a display is presented. In response to the reception of triggering information, a subset of data is selected from a displayed or non-displayed dataset according to a data priority scheme and the displayed dataset is replaced by the display of the selected subset of data. The display of the selected subset of data uses a variety of rendering options. The triggering information is provided by the user or provided by one or more sensors. The data priority scheme is predefined or computed. It is static or dynamic. The data priority scheme can comprise a threshold which is applied for the selection or determination of the subset of data. Examples of priorities associated with data for diabetes care are provided. A range of displays can be used and combined.

Abstract: The present invention relates to a polymer based material comprising a water binding agent, whereas the water binding agent is present in an amount sufficient to chemically and/or physically absorb and/or adsorb water to prevent degradation of the polymer. It also relates to a polymer based material which comprises a plasticizer or organic solvent as well as a multi-component material or composite including materials encompassing a second polymer and/or an active agent. Furthermore it relates to a method for manufacturing the polymer comprising material and use of the material for the preparation of a pharmaceutical composition to be used for treatment of bone, cartilage and/or periodontal defects. The invention also encompasses a kit using the polymeric material.

Abstract: The present invention relates to a material having osteoinductive and osteoconductive properties in vivo comprising a ceramic carrier, preferably containing calcium phosphate, and an active agent, preferably an osteoinductive protein/peptide or a drug, and a polymer, wherein the active agent is homogeneously coated on the carrier and within the polymer, which is preferably a degradable polymer. Said polymer modulates the release kinetic of the active agent and protects same from degradation to prolong the half-life in vivo. Moreover, the present invention relates to a method for the production of a material having osteoinductive and osteoconductive properties in vivo.