Abstract: A nozzle assembly group for a combustion chamber of an engine, with multiple nozzles for introducing fuel into the combustion chamber that are arranged next to each other, wherein each nozzle has a nozzle outlet opening and a fuel channel for conveying fuel in the direction of the nozzle outlet opening. According to the invention, it is provided that at least two different types of nozzles are provided, wherein the nozzles of different types have nozzle outlet openings with an identical cross section, and for predetermining different flow rates of fuel through the fuel channels of the nozzles of different types, a cross section of a fuel channel of one type of nozzle is different from a cross section of a fuel channel of another type of nozzle.

Abstract: A test apparatus for an implantable electrode line and also for an electrode line and an implantable device, including a directional coupler or a circulator for coupling an electrical test symbol into at least one electrical conductor of the electrode line and for decoupling the reflected test signal from the electrical conductor of the electrode line. Such a directional coupler makes it possible to couple a test signal, e.g., a steep voltage pulse, into an electrical conductor of the electrode line and to decouple again the returning reflected voltage pulse (namely, the reflected test signal) from the electrical conductor by means of the directional coupler or circulator. A method for testing an electrical conductor of an implantable electrode line including: 1) coupling a test signal into the electrical conductor; 2) decoupling the test signal reflected in the electrical conductor from the electrical conductor; and 3) evaluating the reflected test signal.

Abstract: The invention relates to a swirl generator of a fuel nozzle 6 of a gas turbine, with an inner 22 and an outer 21 ring element, wherein the ring elements 21, 22 are arranged so as to be concentric with respect to each other, and an outer annular channel 18a is formed between the inner ring element 22 and the outer ring element 21, having a radial height of h in its axially central area, characterized in that the outer annular channel 18a has a radial height of H at its inflow area 23 and is provided with air guiding elements 11 in the inflow area 23, wherein H>h applies, wherein an inner annular channel (18b) is formed at the radially inner side of the inner ring element (22), with its inflow area (23), which is provided with air guiding elements (11), having a larger radial height than a central area of the inner annular channel (18b), wherein the outer annular channel (18a) has an effective flow surface (A) in the area of the guide elements (11) that is larger than the effective flow surface in the axiall

Abstract: An electrical implant or implant system includes an energy supply unit or is connected to an energy supply unit and includes at least one fixing device for permanently fixing the electrical implant or implant system to bodily tissue, or is connected to the fixing device. At least two implant components are releasably mechanically connected to one another. A first of the implant components includes at least parts of the fixing device. A second of the implant components includes an electromechanical component which, as a result of current drain or current feed, can swell in such a way that it causes a swelling at an outer contour of the electromechanical component at least at one point. The electromechanical component is disposed in such a way that a swelling of the electromechanical component results in a separation of the mechanical connection between the first and second implant components.

Abstract: A gas turbine combustion chamber includes first admixing air holes having first inner and outer center points, and second admixing air holes having second inner and outer center points. The first and second inner center points respectively lie on a side of the first and second admixing air holes oriented towards the combustion chamber. The first and second outer center points lie on a side of the first and second admixing air holes facing away from the combustion chamber. An equation L=D2/D1*(D2?D1)/C2 is fulfilled, with L being a distance between the first and second inner center points and/or the first and second outer center points; D1 and D2 being flow diameters of the first and second admixing air holes respectively at an entry and/or exit side to the combustion chamber and C being an average flow rate coefficient of the first and second admixing holes.

Abstract: An implantable cardiac system that includes an implantable cardiac pacemaker or leadless pacemaker (iLP) and a second device such as a subcutaneous implantable cardioverter-defibrillator (S-ICD). The pacemaker includes an R-spike amplifier that amplifies stimulated ventricle excitations or R-waves to increase R-wave to T-wave signal to noise ratio and to improve indirect detection of ventricular rhythm classification by the S-ICD. The S-ICD includes an electrode line for defibrillation, a sensing unit and a stimulation detection unit. The S-ICD records a subcutaneous electrocardiogram between shock electrode poles and provides potentially life-saving therapy based thereon. The system significantly increases the specificity and sensitivity of an S-ICD in combination with an implanted cardiac pacemaker or iLP having an R-spike amplifier.

Abstract: Embodiments include an implantable device configured to be used in an MRI device, including a control unit, a memory unit, an MRI sensor and a statistics unit. The memory unit includes program information including control programs and/or control parameters that control the function of the control unit, and current state parameters. The MRI sensor is connected to the control unit and responds to a positioning of the implant and/or a patient within or in the immediate vicinity of the MRI device. The statistics unit is connected to the control unit and detects current state parameters present prior to a respective response of the MRI sensor. The control unit selects a control program or control parameters indicated by the state parameters and maintains the control program or control parameters until the MRI sensor indicates a positioning of the implantable device within or in the immediate vicinity of the MRI device.

Abstract: A medical implant including an implant body for insertion into a human and/or animal body. The implant body includes at least one first and at least one second contact portion, wherein the at least one first and the at least one second contact portions contact two tissue regions performing a relative movement with respect to one another. The at least one first and the at least one second contact portions are movable relative to one another, wherein a relative movement of the contact portions may be converted into an electrical signal.

Abstract: Embodiments include a medical implant for insertion into the human and/or animal body. The medical implant includes a helical fixing device to fix the implant at a site of implantation, wherein the helical fixing device is one or more of coupled to a locking device on the fixing device and coupled to an implant surface. One or more of the locking device and the implant surface impedes an autonomous detachment of the fixing device.

Abstract: Embodiments include a medical implant including a fixing device with at least one fixing element to fix the implant at a site of implantation. The implant includes a belt drive that rotates an actuation device, wherein the actuation device is coupled to the fixing device and converts the rotary movement into a longitudinal movement of the fixing device. Embodiments include an insertion device to insert the medical implant.

Abstract: Embodiments include an implantable electronic device with at least one electromagnetic field detection unit and at least one antenna, wherein the at least one electromagnetic field detection unit is connected to the at least one antenna. The at least one electromagnetic field detection unit responds to electromagnetic fields that occur or are present in an environment surrounding a patient outside an environment of an MRI device and electromagnetic fields that are shielded in the environment of the MRI device. The at least one electromagnetic field detection unit indicates an absence of the electromagnetic fields that typically occur in the environment surrounding a patient outside an MRI device and that are shielded in the environment of an MRI device.

Abstract: An implantable cardiac therapy device having a heart assist pump, a stimulation unit, and a control unit. The heart assist pump is designed to be connected to a ventricle of a heart and an associated artery, and is designed to pump blood from a particular ventricle into an associated artery, thereby supporting the particular ventricle. The stimulation unit is designed to electrically stimulate a heart contraction, and the control unit is designed to control the heart assist pump and the stimulation unit in such a way that the stimulation unit induces synchronized motions of cardiac contraction while the heart assist pump operates in a ventricle-supporting manner.

Abstract: A combustion chamber of a gas turbine, including an external combustion chamber wall as well as an internal combustion chamber wall, wherein the internal combustion chamber wall, at its frontal end area as it appears with respect to the flow direction of the combustion chamber, is supported in a longitudinally slidable manner inside a groove of a base plate that is arranged in the area of a combustion chamber head, and is fixedly attached at the external combustion chamber wall at its back end area.

Abstract: Embodiments include a method of determining an oxygen content in a bodily tissue or in blood of a human or animal body, wherein a variable representative of oxygen content in the bodily tissue or in the blood is detected at least over one cardiac cycle and is correlated with a contraction state of a heart. Embodiments include a device configured to be inserted into the human or animal body, wherein the device includes at least one sensor unit that detects a signal representative of an oxygen content along a measurement path. Embodiments include a reflector provided on the device, wherein the reflector is arranged in the measurement path between a transmitter and a receiver of the at least one sensor unit to reflect the signal.

Abstract: Embodiments of the invention include an implant having an energy converter, wherein the converter is designed to convert applied energy to heat. In embodiments of the invention, the energy converter is situated in such a way that heat generated from the energy conversion is active at an outer surface of the implant.

Abstract: An implantable medical device including at least one electrode line having an electrode pole, an electrode feed line, a counter electrode to the at least one electrode line, and an insulation sleeve. The insulation sleeve surrounds the electrode feed line and provides insulation between the electrode feed line and an electrolyte formed by bodily fluid. The electrode feed line and the electrode pole(s) include different materials, wherein the materials are different based on electrochemical series. The implantable medical device includes an insulation test unit having a DC voltage detector arranged between the electrode pole and the counter electrode, in order to detect an electrochemical voltage produced in the event of an insulation fault of the insulation sleeve due to defective contact between the electrolyte and the electrode feed line.

Abstract: Embodiments include an active implantable medical therapy and/or monitoring system that includes at least one implant. The at least one implant includes at least one ultrasonic transducer directly or indirectly connected to a control and evaluation unit in order to emit and receive ultrasonic signals. The control and evaluation unit prompts an emission of ultrasonic signals by the at least one ultrasonic transducer cyclically or in a triggered manner and evaluates received ultrasonic signals such that the control and evaluation unit identifies an actual position or change in position of one or more of the at least one implant and an electrode line.

Abstract: An implantable electrostimulation assembly, including an electrostimulation device and an electrode lead that is connected to the electrostimulation device when in use, wherein the electrode lead has an optically readable electrode identification and a cable adapter is provided for the temporary insertion between the electrostimulation device and the electrode lead, the adapter comprising an optical pick up device for reading the electrode identification and an electrode identification transmission stage for transmitting the same to the electrostimulation device and/or to an assembly-external receiver.

Abstract: A device (110) for insertion into a human or animal body has a surface (610) which at least partially bears a surface structure (140, 140?), wherein the coefficient of static friction between the surface structure (140, 140?) and an interface within the body is anisotropic.

Abstract: An implantable cardioverter-defibrillator system that includes at least one or more stimulation units, one or more detection units, one or more control units, two or more electrode poles and one or more high voltage capacitors. The at least one control unit is connected with the at least one stimulation unit, and the at least one control unit is connected with at the least one detection unit. The two or more electrode poles are in contact with body tissue, and the one or more high voltage capacitors are charged by at least one charging unit, wherein the at least one charging unit is connected to the at least one control unit.