Abstract: A method for manufacturing an implant and an implant, in particular an intraluminal endoprosthesis, including a body having a coating on at least a portion of the surface thereof, and the degradation of which can be influenced from the outside in a targeted manner, the method having the following steps: a) providing an implant body, and b) applying a coating to the surface of the implant body, wherein the coating comprises unfilled cavities, preferably in the form of microbubbles (2).

Abstract: A method for manufacturing an implant and an implant, in particular an intraluminal endoprosthesis, including a body having a coating on at least a portion of the surface thereof, and the degradation of which can be influenced from the outside in a targeted manner, the method having the following steps: a) providing an implant body, and b) applying a coating to the surface of the implant body, wherein the coating comprises unfilled cavities, preferably in the form of microbubbles (2).

Abstract: An active medical implantable device with at least two diagnostic and/or therapeutic functions is constructed from separate active implant modules (2 to 7) which are adapted to the respective desired functions and can be coupled to each other.

Abstract: Housing for medical implant, such as cardiac pacemaker, defibrillator, cardioverter, etc. Housing including hollow housing and terminal body attached to hollow housing, which has electrical terminal(s), situated in an externally accessible cavity of the terminal body, for connecting an electrode line, and terminal body including a base body made of electrically insulating plastic, connected to hollow housing and carries electrical supply lines and electrical contacts, which are electrically connected thereto, for the electrical terminal so that the contacts are connected via the electrical supply lines to electrical components in the interior of the hollow housing, electrical supply lines being welded to the electrical contacts and the electrical supply lines and electrical contacts, which are welded to one another, being embedded in the base body and thus fixed in their final position, and the base body being glued to the hollow housing using an adhesive between hollow housing and terminal body.

Abstract: An intravascular electrode arrangement 10 includes a first and a second electrode line 12, 14 adapted for placement in blood vessels such as veins or arteries, each having at least one stimulation and/or sensing electrode in the region of the distal end of the respective electrode line, wherein there are longitudinal guides 18, 18?, 18?, 18?? provided externally on the first electrode line 12, 12?, 12?, 12?? for the second electrode line 14.

Abstract: Housing for medical implant, such as cardiac pacemaker, defibrillator, cardioverter, etc. Housing including hollow housing and terminal body attached to hollow housing, which has electrical terminal(s), situated in an externally accessible cavity of the terminal body, for connecting an electrode line, and terminal body including a base body made of electrically insulating plastic, connected to hollow housing and carries electrical supply lines and electrical contacts, which are electrically connected thereto, for the electrical terminal so that the contacts are connected via the electrical supply lines to electrical components in the interior of the hollow housing, electrical supply lines being welded to the electrical contacts and the electrical supply lines and electrical contacts, which are welded to one another, being embedded in the base body and thus fixed in their final position, and the base body being glued to the hollow housing an adhesive between hollow housing and terminal body.

Abstract: A biatrial triple-chamber cardiac pacemaker has at least one sensing unit for sense events of a first atrium and a ventricle of a heart and at least one stimulation unit which is adapted to produce stimulation pulses to a second atrium and the ventricle, and a control which is connected to the sensing unit and the stimulation unit and is adapted to evaluate at least the atrial sense events (AR-Sense) associated with the first atrium and the ventricular sense events (V-Sense) associated with the ventricle, for actuation of the stimulation unit, which is actuated so that the delivery of a left-atrial stimulation pulse is suppressed if previously a ventricular sense event occurs in a crosstalk window which adjoins a postatrial ventricular blanking time and at the same time the distance in respect of time to the last ventricular event ascertained outside a crosstalk window, to the next possible ventricular stimulation event, is greater than a predetermined maximum value.

Abstract: A personal health monitoring and care system includes at least one diagnostic device (2) implanted in a person (1), a data communication device (4) associated to the diagnostic device (2) for communicating relevant personal health data collected by the diagnostic device (2) to an external data information retrieval device (5), which processes and presents said relevant personal health data to the person (1) via information output means (6), wherein the person (1) according to the relevant personal health data perceived from the information output means (6) is able to start a health relevant action.

Abstract: A housing for a medical implant, such as a cardiac pacemaker, defibrillator, cardioverter, or the like, the housing having a hollow housing and a terminal body attached to the hollow housing, which has at least one electrical terminal, situated in an externally accessible cavity of the terminal body, for connecting an electrode line, and the terminal body comprising a base body made of electrically insulating plastic, which is connected to the hollow housing and carries electrical supply lines and electrical contacts, which are electrically connected thereto, for the electrical terminal in such a way that the contacts are to be connected via the electrical supply lines to electrical components in the interior of the hollow housing, electrical supply lines being welded to the electrical contacts and the electrical supply lines and electrical contacts, which are welded to one another, being embedded in the base body and thus fixed in their final position, and the base body being glued to the hollow housing an a

Abstract: An active medical implantable device with at least two diagnostic and/or therapeutic functions is constructed from separate active implant modules (2 to 7) which are adapted to the respective desired functions and can be coupled to each other.

Abstract: Apparatus for treating fibrillation of at least one chamber of a heart comprising a fibrillation detector for detecting a fibrillation, a defibrillator for defibrillating the chamber of the heart, wherein the defibrillator is connected to the fibrillation detector and is adapted to effect defibrillation subsequently to a time interval after detection of the fibrillation, a warning device which is connected to the fibrillation detector and which is adapted to delivery a warning signal when a fibrillation has been detected, and a control circuit having a control input actuable by a patient, wherein the control circuit is connected to the defibrillator and is adapted to delay the time of a defibrillation if the control circuit receives a corresponding signal by way of the control input, wherein the apparatus includes a condition detector which is adapted to detect a hemodynamic condition of the heart, and the control circuit is connected to the condition detector and is adapted to prevent a delay in the time of

Abstract: A stimulation apparatus, in particular for a human heart, has a stimulation unit, a signal detector and a control unit. The stimulation unit is adapted to deliver a stimulation pulse having a pulse duration, a pulse strength and a stimulation intensity. The signal detector is adapted to detect stimulation success on the basis of a picked-up signal. The control unit is connected to the stimulation unit and to the signal detector. It is designed such that the stimulation intensity varies depending upon the picked-up signal. A time-determining unit is provided that is at least indirectly connected to the control unit and with which a time difference between the delivery of a stimulation pulse and the pick-up of the picked-up signal or a signal feature of the picked-up signal can be detected.

Abstract: This invention relates to an electrically active implant with a plurality of energy-consuming components and an activation device designed to activate the implant. The electrically active implant is characterized by a deactivation device designed to deactivate the energy-consuming components of the implant, where the energy-consuming components of the implant can be deactivated during the implant's storage by means of the deactivation device, and, furthermore, characterized by a device for permanent storage of the implant-specific data.

Abstract: A method of applying a marker element (6; 6?; 6?; 25; 25?; 26; 28) to an implant (1; 1?; 1?; 1??; 20; 20?), in particular a stent, intended for implantation in the human or animal body, comprising a main body and an opening (3; 3?; 3?; 3??; 21; 21?) provided in said main body (2; 2?; 2?; 2??; 22; 22?) for receiving the marker element (6; 6?; 6?; 25; 25?; 26; 28), wherein to form at least a part of the marker element (6; 6?; 6?; 25; 25?; 26; 28) a hardenable material or material mix is introduced into the opening and hardened therein.

Abstract: A medical therapy system has logic and/or signal processing stages between sensors on the input side and therapy applicators on the output side. A signal parameter is determined from the input signals using the logic/processing stages, and/or an indicator signal is determined from the input signals using a logic/processing module consisting of several logic/processing stages. The indicator signal is a measure of the probability of a future event requiring therapy, or a measure of the success of the therapy.

Abstract: The invention concerns an electromedical implant for intracardial coronary therapy comprising an implant housing in which functional component parts of the implant, namely a circuit, a battery and the like, are disposed. It is characterized in that the battery (10) has a flat side (10.2), an underside (10.3) and a peripherally extending narrow side (10.1) and the battery (10) is arranged with its underside (10.3) on an internal base surface (18.1) of the implant housing (18) and the circuit (22) is arranged in adjacent relationship with a flat side (10.2) of the battery (10).

Abstract: A stent has a surface with an irregular coating formed on that surface. The irregular coating provides coating islands, especially coating islands that are substantially round. In some embodiments, the coating islands are arranged at a greater spacing in regions involving a greater degree of local stretching of the stent surface upon stretching of the stent than in regions involving a lesser degree of local stretching of the stent surface. In other embodiments, the coating islands are smaller in regions involving a greater degree of local stretching of the stent surface upon stretching of the stent than in regions involving a lesser degree of local stretching of the stent surface.

Abstract: A stent, in particular a coronary stent, for expansion from a first condition into an expanded second condition in which it holds a vessel in an expanded state, comprising a tubular body whose peripheral surface (1) is formed by a number of annular support portions (2, 2.1, 2.2, 2.3) comprising bar elements (3, 3.1, 3.2, 3.3) which are connected in the longitudinal direction of the stent by way of connecting bars (4, 4.1, 4.2), wherein the bar elements (3.1) of at least a first support portion (2.1) and a second support portion (2.2) in adjacent relationship in a first direction (6.1) extend in a meander configuration in the peripheral direction of the stent and the connecting bars (4, 4.1, 4.2) to the second support portion (2.2) engage in the region of the turning points (5, 5.2, 5.3) of the first support portion (2.1), which turning points face in the first direction (6.1), wherein at least two adjacent connecting bars (4.1, 4.2) engage respectively in the region of a turning point (5.

Abstract: An arrangement for determining the heart rate (fRR) or the refractory time of the cardiac tissue, particularly for detecting tachycardia or fibrillation, has an electrode (E) for sensing heart action signals (SIG), an input stage, connected to the electrode, for processing the heart action signals, a refractory member for ascertaining a refractory time value of the arrangement, in each case after a predetermined segment of a heart action signal, and a processing device, connected to the output of the input stage or of the refractory member, for determining the rate of the heart action signals, processed with blanking of the component that occurs during the refractory time, or for determining the refractory time value of the cardiac tissue.

Abstract: A method of storing signals having a course over time in an implantable medical device, and/or transmitting the signals out of the device and out of the patient's body, with the course over time being detected in the device, particularly at predetermined time intervals with a constant sampling interval, and a sequence of signal samples being obtained therefrom, of which a partial quantity is stored and/or transmitted as the result of a selection made with a predetermined selection criterion, with the selection criterion being the first derivation of the course over time of the signals according to time, and with the selection being made such that the first derivation of the straight-line connection between an nth and the (n?1)th signal sample is determined and compared to the first derivation of the straight-line connection between the (n?1)th nth signal sample and the last-stored and/or last-transmitted signal sample, and the nth (n?1)th signal sample is then stored and/or transmitted as the new last signal