Abstract: The invention relates to a drive system for an aircraft which is constructed for operation with a liquid fuel and a gaseous fuel, including at least one engine having a combustion chamber for operation with the liquid fuel and/or the gaseous fuel and per fuel at least one separate tank chamber which is or can be brought into connection in flow terms with the combustion chamber via a fuel line for supplying it with the corresponding fuel. A drive system which is optimized in terms of emissions and efficiency can be provided in that the drive system is constructed in such a manner that, in the event of firing at a great height, exclusively gaseous fuel is or can be used in the at least one engine during a firing operation at a great height.

Abstract: The present disclosure relates to an implantable defibrillator which comprises at least one energy source and at least one electrical component. The implantable defibrillator further comprises means for activating a coupling between the energy source and the electrical component, based at least in part on an orientation and/or a motional state of the energy source, wherein the electrical component is a capacitor.

Abstract: An electrode element (1) for an energy storage unit (200), such as a capacitor, has an electrode body (100) made of an active electrode material (E), wherein the electrode body (100) includes one or more of: at least one cavity (110) on its surface or in its interior; at least one partial volume (120) of lower density; and/or a surface coating (D) covering at least a portion of the surface of the electrode body (100), such that the surface area covered by the surface coating (D) remains unwetted when in contact with an electrolyte. Energy storage units (200) incorporating the electrode element (1) are particularly suitable for use in implantable electrotherapeutic devices.

Abstract: The invention relates to a device and method for protecting sensitive personal data held in a public storage, comprising a trusted tokenization system having at least one trusted interface to an instance that may provide, process, possess, and/or retrieve sensitive personal data, and at least one interface to a public storage not containing sensitive personal data, wherein the tokenization system is configured to replace a sensitive personal reference of the data in the public storage with a non-sensitive data element and to store an association between the sensitive personal reference and the non-sensitive data element in a secure environment, wherein the non-sensitive data element is generated in a user-specific manner such that the non-sensitive data element can be processed in an existing infrastructure of a user without adaptation of said infrastructure.

Abstract: An implantable pulse generator comprises a pulse generation device generating an output pulse, the pulse generation device comprising a control unit, shock generation circuitry and output circuitry. The shock generation circuitry comprises a first energy storage device, a second energy storage device and a switching device. The switching device is electrically connected to the first energy storage device, and is configured to connect, in a closed state, the first energy storage device with the second energy storage device, and to disconnect, in an open state, the first energy storage device from the second energy storage device. The shock generation circuitry configured to generate an output pulse by supplying energy to the output circuitry, in the open state, from the first energy storage device via a first connection line and, in the closed state, from the first energy storage device and the second energy storage device via a second connection line.

Abstract: The invention concerns a combustion chamber assembly, in particular for use in an aircraft engine, including: a peripheral wall which borders a combustion space oriented along a longitudinal axis, and at least one, preferably a plurality of fuel nozzle(s) arranged on the input side of the combustion space for the supply of liquid fuel to the combustion space. An alternative and/or combined optimised operation with fuels of different aggregate states can be achieved with comparatively low structural complexity in that the combustion chamber assembly is configured for operation with liquid and/or gaseous fuel, wherein at least one, preferably a plurality of gas supply openings arranged downstream of the fuel nozzle(s) on the peripheral wall is/are present, by means of which gaseous fuel can be introduced into the combustion space.

Abstract: Electrical component for an implantable medical device comprises an outer shell forming first and second side faces, a functional element enclosed in the outer shell, and an arrangement of connection devices arranged on the outer shell for establishing an electrical connection of the functional element to a component of the implantable medical device outside of the outer shell. A first connection device is arranged on the first side face and a second connection device is arranged on the second side face, wherein the electrical component is configurable to assume different configuration states, wherein in a first configuration state the first connection device is configured to establish said electrical connection and the second connection device is deactivated, and in a second configuration state the first connection device is deactivated and the second connection device is configured to establish said electrical connection.

Abstract: An implantable medical device for stimulating a human or animal heart. In operation, the device performs the following steps: a) sensing an atrial electric signal a the first detection unit; b) sensing an electric signal at the His bundle with a second detection unit upon termination of a first time period starting upon sensing the atrial electric signal with the first detection unit and/or starting upon applying a stimulation pulse, wherein the first time period lies in a range of from 10 ms to 100 ms; c) classifying the electric signal sensed with the second detection unit as His bundle activity signal or as ventricular activity signal.

Abstract: The disclosure relates to an implant comprising a housing, in which there are arranged an energy store and an electronics module, wherein a feedthrough to an electrode connection device is formed on the housing, wherein a first contact forms an electrical connection between the energy store and the electronics module, wherein a second contact forms an electrical connection between the electronics module and the feedthrough, and wherein the first contact and the second contact are oriented in the same contact direction. A method for assembling an implant is also disclosed.

Abstract: An implantable medical device comprises a sensing device for sensing a measurement quantity indicative of a presence of an MRI device, a processing device for controlling operation of the implantable medical device and for identifying a presence of an MRI device based on measurement values obtained from the sensing device; and a program memory. An analysis module is configured to store information concerning a multiplicity of events relating to operation of the implantable medical device. The program memory is configured to store at least two program routines for operating the implantable medical device in case of a presence of an MRI device. The processing device is configured, for controlling operation of the implantable medical device in the presence of an MRI device, to select one of said at least two program routines based on a statistical analysis of information concerning a predefined number of events of said multiplicity of events.

Abstract: An implantable leadless pacemaker configured to provide antibradycardia pacing of a human or animal heart, comprising: an electrical energy source, a sensor configured to sense intracardiac potentials of the heart, a pulse generator configured to generate electrical pacing pulses, a control unit for controlling the pulse generator, wherein the control unit is configured to inhibit generation of an electrical pacing pulse when an intracardiac potential is sensed, wherein the control unit is further configured to permanently switch off the pulse generator after passing of a predetermined timespan and/or after a pre-defined event detected by the pacemaker, an electrode pole for electrical stimulation and sensing intracardiac potentials, at least one fastening element for fastening the pacemaker to heart tissue, wherein the implantable leadless pacemaker is adapted such that a lifetime of the implantable leadless pacemaker is smaller than one year, particularly smaller than one month, particularly smaller than tw

Abstract: An active medical device, comprising a processor, a memory unit, and at least one of an accelerometer and a detection unit configured to detect a body impedance. During operation, the active medical device carries out the following steps: a) measuring a body impedance of a patient with the detection unit during a first period of time to obtain time-dependent impedance data and calculating a power spectral density of the impedance data; b) alternatively or additionally to step a), measuring an acceleration of a body of the patient with the accelerometer during the first period of time to obtain time-dependent acceleration data and calculating a power spectral density of the acceleration data; c) identifying coughing of the patient on the basis of the calculated power spectral density if at least 1% of all values of the power spectral density have a frequency of at least 1 Hz.

Abstract: A device housing for an IMD is suggested, the device housing having: a front side, a flat end face that is arranged perpendicular to the front side and connects to a straight upper edge of the front side, the front side having a maximum width (Bmax) that is measured parallel to the straight upper edge, and a maximum height (Hmax) that is measured perpendicular to the straight edge, wherein the ratio R of maximum width (Bmax) to maximum height (Hmax), i.e., Bmax/Hmax, is between 1.05 and 1.35.

Abstract: An implantable medical device for stimulating a heart, includes a stimulation electrode configured to stimulate a first cardiac region of the heart, and a detection unit configured to detect an intracardiac electrogram at a second cardiac region (ventricle) of the heart. In operation, the device: delivers a stimulation pulse to the heart; evaluates a time and at least one morphologic parameter of a responsive signal of an intracardiac electrogram, wherein the at least one morphologic parameter is chosen from: an absolute value of the signal amplitude, a width of the signal, a positive, negative and/or total area under at least a part of the signal, and a number of occurrences and/or time of occurrence of zero crossings of the signal; and identifies a dislocation of the stimulation electrode if the time of the signal is below a first threshold value and the morphologic parameter exceeds a further threshold value.

Abstract: A system for generating an alert for a systemic infection of a patient comprises an implantable medical device configured to measure at least one physiological parameter, a remote monitoring system configured to receive information from the implantable medical device, and an information system configured to communicate with said remote monitoring system. At least one of the implantable medical device, the remote monitoring system and the information system is configured to analyze information relating to said at least one physiological parameter to generate an alert signal for a systemic infection of the patient based on a state of the at least one physiological parameter, wherein at least one of the implantable medical device, the remote monitoring system and the information system is further configured to generate an alert message to be provided to a specified destination based on said alert signal.

Abstract: An implantable medical device for stimulating a human/animal heart having a stimulation unit which stimulates the His bundle and a detection unit which detects an electrical signal at the His bundle. The device performs: a) determining a first value of a parameter of a first measuring pulse measured between a first electrode pole and a housing; b) determining a second value of the same parameter of a second measuring pulse measured between the first electrode pole and a second electrode pole; c) comparing the first and second values; d) determining, based on the comparing step, whether the first or second measuring pulses enables a higher available level control range of the analog-to-digital converter; e) measuring an impedance in a unipolar manner between the first electrode pole and the housing or in a bipolar manner between the first electrode pole and the second electrode pole depending on the determining step.

Abstract: An active implantable medical device (IMD) which, in operation: repeatedly senses a body temperature of a person having the IMD implanted therein; stores the sensed body temperature values; repeatedly senses a cardiac physiologic parameter of the person; stores the sensed cardiac physiologic parameter values; determines whether one of the body temperature values exceeds a predefined body temperature threshold; if an excess is determined, the IMD: determines whether one of the cardiac physiologic parameter values exceeds a predefined cardiac physiologic parameter threshold, wherein the one cardiac physiologic parameter value is determined in the same time period as the one body temperature value exceeding the body temperature threshold; classifies an infection of the person as a local infection if the one cardiac physiologic parameter value does not exceed the threshold; or classifies an infection of the person as a systemic infection if the one cardiac physiologic parameter value exceeds the threshold.

Abstract: An implantable system for the diagnostic and/or therapeutic treatment of a human or animal patient contains a processor, a memory, a treatment unit and a remote data transmission unit. The system is characterized in that the memory includes a computer-readable program which prompts the processor to carry out the following steps when the program is being executed on the processor: a) ascertaining whether a treatment functionality of the treatment unit could jeopardize a patient in whom the system was implanted if a diagnostic and/or therapeutic treatment of the patient corresponding to the treatment functionality were to be carried out; b) deactivating the treatment functionality when a potential risk for the patient was ascertained; c) receiving reactivation data by way of the remote data transmission unit; and d) reactivating the deactivated treatment functionality based on the received reactivation data.

Abstract: An implantable medical device comprises a functional device for carrying out a therapeutic or diagnostic function, and a communication device for communicating with a remote monitoring system. The communication device, at a start of initial operation of the implantable medical device, is enabled to establish a communication with said remote monitoring system. In this way an implantable medical device is provided which allows for including the implantable medical device in a remote monitoring while reducing a risk for a patient involved with attending to the patient for activating a remote monitoring function within the implantable medical device.

Abstract: The disclosure relates to an implant comprising an electronics module and an energy store, wherein the volume of the electronics module is less than 25% of the volume of the energy store.