Abstract: An implantable arrangement including an implantable electromedical device having an exterior wall and an implantable sensor and/or actuator outside of the exterior wall. The sensor and/or actuator are in signal connection with the implantable device via an electric stage and a mechanical stage arranged in series, wherein the mechanical stage sends and/or receives mechanical vibration signals through the closed exterior wall, and the electrical stage sends and/or receives the same signals in electrical form.

Abstract: A secondary header for an active implantable medical device (AIMD) incorporates a secondary header plug configured for mating insertion into an AIMD ISO DF4 or IS4 connector cavity, a secondary header ISO DF4 or IS4 connector cavity, and at least one replacement lead connector cavity. The secondary header plug has four electrical contacts which correspond to four electrical contacts of the AIMD connector cavity. The secondary header connector cavity has less than four electrical contacts conductively coupled to the secondary header plug electrical contacts. The replacement lead connector cavity has at least one electrical contact conductively coupled to at least one electrical contact of the secondary header plug. An intermediate conformal section between the secondary header plug and a housing for the secondary header connector cavity places the secondary header connector cavity housing adjacent to an exterior surface of the AIMD.

Abstract: A connection monitoring system for an implantable medical lead system includes an implantable lead, a first trial system cable, an external trial system, and a sensor. The lead has a distal end and at least one proximal end. The lead includes a plurality of terminals disposed at each proximal end. The first trial system cable has a distal end and at least one proximal end. The distal end of the first trial system cable is configured and arranged to electrically couple with the lead. The external trial system is configured and arranged to electrically couple with the first trial system cable. The sensor is electrically coupled to the external trial system. The sensor is configured and arranged for detecting a loss of electrical connectivity between the external trial system and the lead when the lead becomes electrically decoupled from the external trial system.

Abstract: A medical device includes a pulse generator, an electrode configured to contact tissue in a coronary vessel, a lead comprising a lead conductor, the lead conductor connecting the pulse generator with the electrode, and a filter circuit electrically connected in series between the lead conductor and the electrode. The filter circuit may include a band pass filter that attenuates signals having a frequency other than a natural resonance frequency (e.g. MRI device signals), and the pulse generator may transmit therapy signals to the electrode as a sinusoidal voltage wave at the natural resonance frequency. The filter circuit may include a diode that rectifies the sinusoidal voltage wave before the rectified sinusoidal voltage wave passes to the electrode. In some embodiments, therapy signals may be provided to the electrode through the band pass filter over a natural resonance frequency range.

Abstract: An electrical contact for use in the header assembly of an implantable tissue stimulator includes a metal housing having a base and a sidewall where the opening in the base is adapted to receive the terminal of a medical lead therethrough. An electrical contact support member is welded to the edge of the sidewall and affixed to the support member are a plurality of spring members that are tangent to an imaginary circle whose diameter is slightly less than the outside diameter of the lead terminal contact rings. When the contacts are axially aligned in the device header, the terminal of an electrical lead may be longitudinally inserted into the header to establish electrical contact with device feedthrough wires that are joined to the electrical contacts in the header.

Abstract: An operating room connector is used in conjunction with a multiple electrode SCS system which can easily detach and connect to an external trial stimulator (ETS). By connecting the electrode SCS system to a stylet handle, and then locking the stylet handle within a slot of the connector platform, a user is able to minimize the required steps in connecting the ETS to the implanted SCS lead system. The ETS can then be used to readjust the position of the electrode array(s) previously implanted to deliver an optimal stimulation therapy.

Abstract: An implantable medical device has a hermetically sealed housing with at least one feedthrough therein for a conductive path between an RF antenna carried by the housing, and an RF telemetry circuit contained in the housing. The feedthrough has a feedthrough housing with a capacitor element therein having first and second capacitor plate configurations, with a first of the capacitor plate configurations being connected to the RF antenna and a second of the capacitor plate configurations being connected to the RF telemetry circuit. The feedthrough functions both as a hermetic seal and as a galvanic isolation for voltage protection of the components of the RF telemetry circuit, and other circuitry in the sealed housing connected thereto.

Abstract: On aspect relates to an electrical bushing for use in a housing of an implantable medical device. The electrical bushing includes at least one electrically insulating base body and at least one electrical conducting element. The conducting element is set up to establish, through the base body, at least one electrically conductive connection between an internal space of the housing and an external space. The conducting element is hermetically sealed with respect to the base body. The at least one conducting element includes at least one cermet. The electrical bushing includes an electrical filter structure. The at least one conducting element forms at least one conducting section of an inductor of the filter structure. Moreover, one aspect relates to an implantable medical device, for example, a cardiac pacemaker or defibrillator, having at least one electrical bushing according to one embodiment.

Abstract: A connector header includes a housing formed from a plastic material having a modulus of rigidity of 100 ksi or greater. The housing defines an opening for insertion of a lead. The connector header further includes a lead receptacle having an electrically conductive element. The electrically conductive element is operably couplable to a feedthrough of the implantable medical device. The lead receptacle is in communication with the opening and is disposed within the housing such that an electrical contact of the lead is electrically couplable to the conductive element of the receptacle when the lead is inserted into the receptacle.

Abstract: An implantable medical device, such as a lead or lead extension, includes a body having a distal end portion and a proximal end portion configured to be at least partially received by an apparatus. The device further includes a conductive member at the distal end portion of the body and an electrical contact at the proximal end portion of the body. The electrical contact is electrically coupled to the conductive member and is positioned such that, when received by the apparatus, at least a portion of the apparatus is capable of electrically coupling to the electrical contact. The device further includes a reinforcement member integrated in the body.

Abstract: A stimulation system includes an implantable pulse generator having a sealed chamber and an electronic subassembly disposed in the sealed chamber. Feed through pins are coupled to the electronic subassembly and extend out of the sealed chamber. Feed through interconnects are coupled to the electronic subassembly via the feed through pins. At least one tab is disposed on at least one feed through interconnect. The tab(s) are configured and arranged to flex away from the feed through interconnect and against a side of the feed through pin. A feed through interconnect assembly includes an assembly frame; feed through interconnects extending from the assembly frame; a first contact pad and a second contact pad disposed on at least one of the feed through interconnects; and a tab formed on a first contact pad of at least one of the feed through interconnects.

Abstract: A system for therapeutically stimulating a His bundle includes an implantable pulse generator and a multi-polar medical electrical lead. The generator is configured for subcutaneous implantation and to generate a pacing stimulus. The lead includes a connector assembly, a flexible tubular body, a distal tip assembly and coil conductors. The body extends intravascularly from the generator to a location proximate the His bundle and includes a proximal end, a distal end, and a longitudinal lumen. The tip assembly includes an electrode, a fixation helix, and a shank portion. The helix extends to a location proximate the His bundle and is operable as an electrically isolated electrode. The shank portion extends within the lumen and includes a receptacle for receiving a stylet tip. The conductors extend longitudinally through the lumen and are coupled to the electrode and the helix. One or both of the conductors defines a stylet lumen.

Abstract: A connector for an electrostimulation lead includes a connector housing defining a fastener aperture, a septum disposed over the fastener aperture, and a fastener for mating with the fastener aperture to secure a received lead to the connector housing so that at least one terminal disposed on the received lead electrically couples with at least one conductor contact disposed in the connector housing. The septum includes a septum flap and an attachment cuff. The septum flap is configured and arranged for extending over the fastener aperture and for receiving a tool for folding the septum flap open to expose the fastener aperture. The attachment cuff is configured and arranged for coupling the septum flap to the connector housing. The fastener is configured and arranged to be disposed in the fastener aperture and to be tightened against the lead to hold the lead within the connector housing.

Abstract: An endoluminal treatment device and method includes introducing an endoluminal device into a lumen of a patient and engaging a wall of the lumen with an implant device. The implant device can be a drug delivery device or medical device.

Abstract: Devices and methods providing for a isolation connector for a generally cylindrical or frustro-cylindrical housing of an implantable intravascular medical device are described herein. The isolation connector has a generally annular exterior surface, a proximal end, and a distal end. The isolation connector includes a housing interface portion at the proximal end which is secured to a first end of the housing. The proximal end of the housing interface portion is constructed to be obverse to the first end of the housing and presents a perimeter of substantially similar size and shape to the perimeter of the first end of the housing. The isolation connector further includes a first insulator portion disposed adjacent to a distal end of the housing interface portion. The isolation connector may further include a feed-through channel constructed to traverse the proximal and distal ends of the isolation connector and is defined through the housing interface portion and the first insulator portion.

Abstract: A lead assembly for a small implantable medical device (a.k.a, microdevice 10) provides means to attach a remote electrode to microdevice, which means inhibit fluid ingress when microdevice is not attached to lead assembly. Microdevices may provide either or both tissue stimulation and sensing. Known microdevices include spaced apart electrodes on the outer surface of the microdevice. Lead assembly includes an insulated lead including a proximal end and a distal end, with at least one conductor therebetween; at least one electrode at the distal end of the lead and electrically connected to the at least one conductor, and a connector attached to the proximal end of the lead and adapted to be removably connectable to microdevice. Connector includes at least one contact to electrically connect at least one device electrode on microdevice to at least one conductor, thereby electrically connecting at least electrode and the at least one electrode at the distal end of lead.

Abstract: Techniques are disclosed for recharging an Implantable Medical Device (IMD). In one embodiment, a first external coil is positioned on one side of a patient's body, such as on a front side of the torso in proximity to the IMD. A second external coil is positioned on an opposite side of the patient's body, such as on the back of the torso. A recharging device generates a current in each of the coils, inductively coupling the first and the second coils to the secondary recharge coil of the IMD. According to another aspect, each of the two external coils may wrap around a portion of the patient's body, such as the torso or head, and are positioned such that the IMD lies between the coils. According to this aspect, current generated in the coils inductively couples to a second recharge coil that is angled within the patient's body.

Abstract: A lead connection assembly of an implantable medical device (IMD) may include at least two different types of electrical connectors. In some examples, the lead connection assembly may include first and second electrical connectors that have at least one of a different electrical contact arrangement, a different lead connection receptacle geometry or a different size than the first electrical connector. The first electrical connector may be electrically connected to a first therapy module that generates cardiac rhythm therapy that is delivered to a heart of a patient, and the second electrical connector may be electrically connected to a second therapy module that generates electrical stimulation that is delivered to a tissue site within the patient. The second electrical connector may be configured to be incompatible with a lead that delivers the cardiac rhythm therapy to the patient.

Abstract: A shielded three-terminal flat-through EMI/energy dissipating filter includes an active electrode plate through which a circuit current passes between a first terminal and a second terminal, a first shield plate on a first side of the active electrode plate, and a second shield plate on a second side of the active electrode plate opposite the first shield plate. The first and second shield plates are conductively coupled to a grounded third terminal. In preferred embodiments, the active electrode plate and the shield plates are at least partially disposed with a hybrid flat-through substrate that may include a flex cable section, a rigid cable section, or both.

Abstract: An electrical connection apparatus includes an electrical connection contact and an adjustment component within an interior of the electrical connection apparatus. The electrical connection contact is operatively coupled to the adjustment component so that the electrical connection contact adjusts between an insertion position and a contact position in response to rotating the adjustment component. A slider movably arranged within the interior of the electrical connection apparatus causes the electrical connection contact to move in response to rotation of the adjustment component. The electrical connection apparatus includes one or more blocks, and the adjustment component, electrical contact and slider are arranged within an interior of the one or more blocks.

Abstract: In one embodiment, an implantable pulse generator for electrically stimulating a patient comprises: a metallic housing enclosing pulse generating circuitry; a header mechanically coupled to the metallic housing, the header adapted to seal terminals of one or more stimulation leads within the header and to provide electrical connections for the terminals; the header comprising an inner compliant component for holding a plurality of electrical connectors, the plurality of electrical connectors electrically coupled to the pulse generating circuitry through feedthrough wires, wherein the plurality of electrical connectors are held in place in recesses within the compliant inner component, the header further comprising an outer shield component adapted to resist punctures, the outer shield component fitting over at least a portion of the inner compliant component.

Abstract: This application discusses, among other things, a header assembly for coupling a medical electrical lead to a medical stimulating device including a header having a capture mechanism within a bore of a lead retention device. In an example, when the lead retention device is retracted from the bore, the capture mechanism prevents the device from falling out. In another example, the header assembly has a vent disposed within the bore of the lead retention device that permits unrestricted flow of air when the lead retention device is retracted from an engagement surface.

Abstract: A catheter switch comprising a first electrical connector for connection to a first medical device, a second electrical connector for connection to a second medical device, and a third electrical connector for connection to a signal source. The catheter switch further includes an electrical switch coupled to the first, second, and third electrical connectors. The electrical switch is configured to include at least two selectable positions, a first position in which the first electrical connector is electrically coupled to the third electrical connector and a second position in which the second electrical connector is electrically coupled to the third electrical connector. A catheter switch assembly system is also provided. The catheter switch assembly system is for selectively coupling a nerve stimulator to a needle assembly or to a catheter assembly to deliver electrical pulses thereto.

Abstract: An implantable microstimulator can include a housing with a surface containing a metal region. The housing defines an exterior and an interior. At least one conductive electrode is disposed on the exterior of the housing over the metal region of the housing. Adhesive is disposed between the metal region of the housing and the conductive electrodes. An electronic subassembly is disposed in the interior of the housing and coupled to the conductive electrodes through the housing.

Abstract: In some embodiments, an apparatus includes an electrical connector having a side wall defining a lumen and an elongate opening. The lumen is configured to receive at least a conductive portion of an electronic implant. The elongate opening divides the side wall into a first portion and a second portion. The first portion of the side wall is configured to move relative to the second portion of the side wall between a first position and a second position. The first portion of the side wall is electrically conductive and includes a protrusion. The protrusion is configured to contact the conductive portion of the electronic implant such that the conductive portion of the electronic implant is electrically coupled to the first portion of the side wall when the first portion of the side wall is in the second position.

Abstract: A feedthrough assembly for use with implantable medical devices having a shield structure, the feedthrough assembly engaging with the remainder of the associated implantable medical device to form a seal with the medical device to inhibit unwanted gas, liquid, or solid exchange into or from the device. One or more feedthrough wires extend through the feedthrough assembly to facilitate transceiving of the electrical signals with one or more implantable patient leads. The feedthrough assembly is connected to a mechanical support which houses one or more filtering capacitors that are configured to filter and remove undesired frequencies from the electrical signals received via the feedthrough wires before the signals reach the electrical circuitry inside the implantable medical device.

Abstract: In an electromagnetic interference (EMI) filter terminal for an active implantable medical device (AIMD), an insulated and shielded RF telemetry pin is provided to prevent re-radiation of unwanted stray signals, including the telemetry signal itself, to adjacent sensitive circuits or lead wires. The invention provides for an EMI filter terminal assembly for an AIMD including a radio frequency (RF) telemetry pin antenna extending therethrough. The RF telemetry pin antenna includes a conductive shield extending over a portion of the RF telemetry pin antenna in non-conductive relation with the telemetry pin, and conductively connected to a ground associated with the AIMD. The assembly may also include an insulation tube between the RF telemetry pin antenna and the conductive shield covering a portion of the RF telemetry pin antenna.

Abstract: An implantable medical device is provided including a housing, an external circuit element extending outwardly from the housing, an internal circuit enclosed by the housing, a feedthrough array disposed along the housing having at least one filtered feedthrough and at least one unfiltered feedthrough, wherein the unfiltered feedthrough is adapted for connection to the outwardly extending circuit element; and including means for minimizing electromagnetic coupling between the filtered feedthrough and the unfiltered feedthrough.

Abstract: Disclosed herein is an implantable pulse generator feedthru configured to make generally planar electrical contact with an electrical component housed within a can of an implantable pulse generator. The feedthru may include a feedthru housing including a header side and a can side, a core within the feedthru housing, a generally planar electrically conductive interface adjacent the can side, and a feedthru wire extending through the core. The feedthru wire may include an interface end and a header end, wherein the header end extends from the header side and the interface end is at least one of generally flush with the generally planar interface and generally recessed relative to the generally planar interface.

Abstract: An implantable lead adaptor is disclosed that includes an encapsulated thermoplastic housing defining a proximal end portion and a distal end portion. The proximal end portion has a first receptacle configured to receive a first type of connector assembly associated with a first implantable cardiac lead, and a second receptacle configured to receive a second type of connector assembly associated with a second implantable cardiac lead. An elongated flexible lead portion extends from the distal end portion of the adaptor housing. A connector assembly is operatively associated with a distal end section of the flexible lead portion of the adaptor for connection to an implantable pulse-generating device, such as, for example, an implantable pacemaker or defibrillator. Low resistance conductor wires electrically connect the connector assembly associated with the distal end section of the lead portion with the first and second receptacles of the adaptor housing.

Abstract: A feed-through assembly is presented. The feed-through assembly includes a first end and a second end with a body therebetween. The first end comprises a substantially L-shaped end and a block. The substantially L-shaped end includes a first contact surface. The block includes a second contact surface.

Abstract: Exemplary septum assemblies include first and second housing components each defined by at least an inner surface, at least one sealing strip disposed at least partially on at least one of the inner surfaces of the housing components, and a compression member at least partially surrounding the housing components.

Abstract: Methods for ultrasonically joining portions of a medical lead are provided. One method includes providing a conductor, a fitting and a coil electrode. The conductor has a distal portion that includes an inner conductive portion and an outer insulative portion. The fitting has a first cavity and a second cavity, the first cavity being sized and configured to receive the distal portion of the conductor and the second cavity being sized and configured to receive a portion of the coil electrode. The conductor is ultrasonically welded within the first opening, providing a mechanical and electrical attachment. The coil electrode is also electrically coupled to the fitting, providing an electrical pathway from the conductor to the coil electrode. Also provided are medical leads including ultrasonic bonds and other methods of ultrasonically joining portions of a medical lead.

Abstract: A low profile electrical adapter body releasably connects to the electrodes of a pacing lead connector, such as an IS-1. Spring steel lead connector holders and the twist-tolerant cable allow continuous ECG recording while manipulating the pacing lead. The adapter body includes two lead connector holders. A grip longitudinally aligns the lead connector within the adapter body. The grip is slidably attached to a twist-tolerant cable and releasably engages the adapter to form a single adapter assembly that enlarges the device for easier digital manipulation. A twist-tolerant cable connects the low profile adapter directly or indirectly to a medical test device such as a pacemaker analyzer.

Abstract: Disclosed are various implantable medical devices adapted and configured to operation with a micro-generator comprising: an elongated housing; one or more longitudinally slidable elongated magnets; one or more coils positioned exteriorly, interiorly or integrally along at least a portion of the housing; a power wire in electrical communication with the one or more coils and with an implantable medical device; wherein the implantable micro-generator is adapted and configured to generate energy and communicate the generated energy to the implantable medical device. Additionally, methods of deploying and using the medical devices are contemplated, as well as systems, kits, and communication networks.

Abstract: A method of manufacturing a hermetic lead connector includes fixing an electrically insulating ring between an electrically conducting contact ring and an electrically conducting spacer ring to form a hermetic ring subassembly, and fixing a plurality of the hermetic ring subassemblies in axial alignment to form a hermetic lead connector. The hermetic lead connector includes an open end, an outer surface, and an inner surface defining a lead aperture. The hermetic lead connector provides a hermetic seal between the outer surface and the inner surface.

Abstract: Methods and apparatuses are provided for an electrical device that employs a feedthrough including a hermetic seal that seals an interior region of the electrical device. The electrical device includes an electrical contact disposed within the interior region of the electrical device, and a wire terminal that includes an encircled portion that is encircled by the feedthrough, and a first end that electrically connects with said electrical contact. When the electrical device is constructed, the first end of the wire terminal is coated with a conductive metal that is more resistant to oxidation than the wire terminal. The first end of the wire terminal is secured to the electrical contact using a mechanical device such as a crimping connector or a spring connector.

Abstract: A biomedical electrode connector for coupling with a biomedical electrode of the type including an electrode base and a male terminal projecting from the electrode base is provided.

Abstract: An implantable medical lead is disclosed herein. In one embodiment, the lead includes a body, at least one electrode and a lead connector end. The body includes a distal portion and a proximal portion. The at least one electrode is on the distal portion. The lead connector end is on the proximal portion and includes a pin contact and a retainer assembly. The pin contact is electrically coupled to the at least one electrode and proximally extends from the lead connector end. The retainer assembly retains the pin contact as part of the lead connector end and includes a collar and a cap. The cap is secured within the collar via an interference fit arrangement and includes a hole through which the pin contact extends.

Abstract: A structure of electrically connecting a snap electrode for medical purposes is easily attached/detached to/from various monitoring pads attached to a human body to measure electrocardiogram (ECG), electromyogram (EMG), brain wave and nervous system signals and electrically connected to medical equipment, to an electric wire using a pressing method instead of welding. The connecting structure of a snap electrode and an electric wire includes a body having a convex portion, which is formed on the top of the body and has a groove formed on the circumference thereof, in which a combining part is fitted, and the combining protrusion having a ring shape and including a predetermined number of elastic fixing pieces protruded from the inner side thereof and a pair of first pressing pieces protruded from one side thereof and combined with an electric wire. A combining protrusion of a pad is inserted into the body.

Abstract: In a medical implantable device having a hermetically sealed, radio shielded encapsulations containing an RF circuit therein and having an antenna located outside of the encapsulation, and in a method for connecting the RF circuit to the antenna, at least one hermetical feedthrough connection is provided in the form of at least one conductor passing through a wall portion of the encapsulation in a liquid-tight and gas-tight manner, with the feedthrough being electrically insulated from the encapsulation. At least one connector pin is provided on an RF circuit board, which is resiliently mounted on the RF circuit board. The RF circuit is mounted in the encapsulation so as to cause the connector pin to resiliently engage the conductor and to electrically connect the conductor with the RF circuit board.

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: An implantable lead connector configured for long term implantation and to electrically interconnect multiple medical devices and to channel electrical signals between said interconnected devices and a target organ, comprising: a first port adapted to receive a first signal suitable to stimulate a target tissue, a second port adapted to receive a second signal suitable to stimulate a target tissue, and a third port configured to connect to a target organ, wherein at least one of said first and second ports is configured to connect to a signal generator not integrated with said connector.

Abstract: Methods and apparatuses are provided for an electrical device that employs a feedthrough including a hermetic seal that seals an interior region of the electrical device. The electrical device includes an electrical contact disposed within the interior region of the electrical device, and a wire terminal that includes an encircled portion that is encircled by the feedthrough, and a first end that electrically connects with said electrical contact. When the electrical device is constructed, the first end of the wire terminal is coated with a conductive metal that is more resistant to oxidation than the wire terminal. The first end of the wire terminal is secured to the electrical contact using a mechanical device such as a crimping connector or a spring connector.

Abstract: A header for an implantable medical device such as a pacemaker which contains an advantageous molded design with encapsulated wires and conductive features. The header including a specifically formed lead lock member in which a plurality of collets residing in bores in the molded housing are used to retain and lock implantable leads in place without the use of set screws.

Abstract: In one embodiment, a pulse generator for generating electrical stimulation for delivery to a patient, comprises: a hermetically sealed housing containing pulse generating circuitry; a header coupled to the housing for receiving one or more stimulation leads, wherein feedthrough wires are provided to conduct electrical pulses from the pulse generating circuitry to the header; the header comprising a plurality of connectors for electrically connecting to each terminal of the one or more stimulation leads, wherein an inductive winding is disposed around or adjacent to each of the connector structures and is electrically connected between the respective connector structure and a corresponding feedthrough wire to limit MRI induced heating of a respective electrode of the one or more stimulation leads.

Abstract: A method for providing a header assembly for connecting an implantable medical device to at least one conductor lead terminating within a patient intended to be assisted by the medical device is provided. The implantable medical device is comprised of at least one feedthrough wire extending from the control circuitry and through a wall of the housing. The header assembly is comprised of an insulative body that is mountable on the housing of the medical device. The insulative body supports at least one conductor subassembly comprising a terminal that is directly connectable to the conductor lead, an intermediate conductor comprising a distal end connected to the terminal and a proximal end connected to a connector. Methods for making the header assembly and for connecting the header assembly to the implantable medical device are also disclosed.

Abstract: In an implantable medical device, in particular an implantable heart-stimulation device, and a method for operating an implantable heart-stimulation device and a heart-stimulation system, stimulation pulses are delivered via a number of stimulation channels to selected sites on or about a patient's heart via electrodes, and wherein coupling capacitors included in the stimulation channels are subsequently discharged through a sequence of temporally non-overlapping partial discharges of the respective coupling capacitors. By this configuration, the risk of charge neutrality of a stimulation channel not being maintained at the end of a stimulation sequence, comprising the delivery of stimulation pulses via stimulation channels, is reduced or eliminated.

Abstract: Electrode arrangement for an electrical stimulation device, having electrode line (10) with electrical connection at proximal end of electrode line and with plurality of conductive surface areas (14, 16) in region of distal end of electrode line for emitting electrical pulses to a heart or for receiving electrical signals from the heart. Electrically conductive surface areas are at least partly electrically connected with the electrical connection at the proximal end of the electrode line. Uses switch or switching means (100), arranged within the electrical connection or within the electrode line, electrically arranged between at least one connection contact of the electrical connection and at least some of the electrically conductive surface areas (14b, 16), and which has an initially electrically conductive or non-conductive component (52), configured via a permanent configuration process by an electrical switching pulse to make permanently electrically non-conductive or conductive.

Abstract: A terminal housing (14) for an electromedical implant (10) having female contacts (22.2, 22.2, 24) to receive and provide electric contact for electrode line plugs. The terminal housing has a base module (20) and a separately premanufactured cover module (40) that has a female contact (24) according to the IS-4 standard and is inserted into the base module (20) and connected thereto.