Abstract: This document discusses, among other things, a lead assembly including a porous polyethylene cover. In an example, the cover includes sections that have differing pore sizes. In an example, a section of the cover near a distal end portion of a lead assembly includes pores that are large enough to allow tissue ingrowth. In another example, a lead assembly includes two or more polyethylene covers having different porosities.

Abstract: A conductor assembly for an implantable medical device includes a first conductive coil and a second conductive coil co-radial with and electrically isolated from the first conductive coil. The first and second conductive coils each including a plurality of turns. Two or more adjacently wound consecutive turns of the first conductive coil alternate with two or more adjacently wound consecutive turns of the second conductive coil.

Abstract: A method of determining cleanliness of a manufacturing area is disclosed. The method of determining cleanliness of a manufacturing area comprising swabbing at least one target area within the manufacturing area, placing the swab in a testing apparatus, analyzing for the presence of the at least one substance with the testing apparatus and determining in real time the cleanliness of the manufacturing area.

Abstract: A lead assembly for an implantable medical device includes a lead body having a first portion and a second portion. The first portion adapted for coupling to a pulse generator and the second portion is adapted for implantation. First and second conductive coils are positioned within the lead body and electrically isolated from each other. The first and second conductive coils each including a plurality of turns. Two or more adjacently wound consecutive turns of the first conductive coil alternate with two or more adjacently wound consecutive turns of the second conductive coil.

Abstract: The present invention is an apparatus and method for making a polymer patterned electrode for cardiac pacing and sensing. The electrode surface includes a polymer overlayed on an electrode. The polymer layer is patterned to form an electrode surface consisting of a polymer and a conductive metal surface. The electrode can be made of a high or low impedance electrode by changing the conductivity of the polymer. Furthermore, the electrode surface texture can be optimized with a micro pattern that may enhance the biocompatibility. The polymer may be conductive or insulative.

Abstract: A lead assembly for an implantable medical device includes a lead body having a first portion and a second portion. The first portion adapted for coupling to a pulse generator and the second portion is adapted for implantation. First and second co-radial conductive coils are positioned within the lead body and electrically isolated from each other. The first and second conductive coils each including a plurality of turns. Two or more adjacently wound consecutive turns of the first conductive coil alternate with two or more adjacently wound consecutive turns of the second conductive coil.

Abstract: A lead assembly for an implantable medical device includes a lead body having a first portion adapted for coupling to a pulse generator and a second portion adapted for implantation. First and second co-radial conductive coils are electrically isolated from each other and include a first and second number of coil turns. The first and second number of coil turns include a number of matched turns and a number of unmatched turns, and the number of unmatched turns is less than approximately 2.0% of the total number of unmatched and matched turns. First and second electrodes located at the second portion are respectively coupled to the first and second conductive coils. At least one capacitor element is connected in parallel with one or both of the first and second conductive coils and/or between the first and second conductive coils.

Abstract: A lead assembly for an implantable medical device includes a lead body having a first portion adapted for coupling to a pulse generator and a second portion adapted for implantation. First and second co-radial conductive coils are electrically isolated from each other and include a first and second number of coil turns. The first and second number of coil turns include a number of matched turns and a number of unmatched turns, and the number of unmatched turns is less than approximately 2.0% of the total number of unmatched and matched turns. First and second electrodes located at the second portion are respectively coupled to the first and second conductive coils. At least one capacitor element is connected in parallel with one or both of the first and second conductive coils and/or between the first and second conductive coils.

Abstract: A lead assembly for an implantable medical device. The lead assembly comprises a lead body having a first portion and a second portion. The first portion is adapted for coupling to a pulse generator and the second portion is adapted for implantation in or near a heart. First and second co-radial conductive coils are positioned within the lead body and electrically isolated from each other. The first and second conductive coils include a first and second number of coil turns and the first number is substantially equivalent to the second number. A ring electrode is located at the second portion and a tip electrode is located distal to the ring electrode and coupled to the second conductive coil.

Abstract: A lead assembly for an implantable medical device. The lead assembly comprises a lead body having a first portion and a second portion. The first portion is adapted for coupling to a pulse generator and the second portion is adapted for implantation in or near a heart. First and second co-radial conductive coils are positioned within the lead body and electrically isolated from each other. The first and second conductive coils include a first and second number of coil turns and the first number is substantially equivalent to the second number. A ring electrode is located at the second portion and a tip electrode is located distal to the ring electrode and coupled to the second conductive coil.

Abstract: Embodiments of the invention are related to medical devices filled with a liquid composition, amongst other things. In an embodiment, the invention includes a hermetically sealed housing defining an interior volume, a component module disposed within the interior volume, the component module comprising a circuit board, the component module displacing a portion of the interior volume. A liquid composition can be disposed within the housing, the liquid composition filling at least 80% of the interior volume not displaced by the component module. Other embodiments are also included herein.

Abstract: A lead assembly for an implantable medical device. The lead assembly comprises a lead body having a first portion and a second portion. The first portion is adapted for coupling to a pulse generator and the second portion is adapted for implantation in or near a heart. First and second co-radial conductive coils are positioned within the lead body and electrically isolated from each other. The first and second conductive coils include a first and second number of coil turns and the first number is substantially equivalent to the second number. A ring electrode is located at the second portion and a tip electrode is located distal to the ring electrode and coupled to the second conductive coil. The first conductive coil extends past the ring electrode and transitions to a non-coiled region, which extends back to and couples to the ring electrode.

Abstract: A lead assembly for an implantable medical device. The lead assembly comprises a lead body having a first portion and a second portion. The first portion is adapted for coupling to a pulse generator and the second portion is adapted for implantation in or near a heart. First and second co-radial conductive coils are positioned within the lead body and electrically isolated from each other. The first and second conductive coils include a first and second number of coil turns and the first number is substantially equivalent to the second number. A ring electrode is located at the second portion and a tip electrode is located distal to the ring electrode and coupled to the second conductive coil. The first conductive coil extends past the ring electrode and transitions to a non-coiled region, which extends back to and couples to the ring electrode.

Abstract: The present invention is an apparatus and method for making a polymer patterned electrode for cardiac pacing and sensing. The electrode surface includes a polymer overlayed on an electrode. The polymer layer is patterned to form an electrode surface consisting of a polymer and a conductive metal surface. The electrode can be made of a high or low impedance electrode by changing the conductivity of the polymer. Furthermore, the electrode surface texture can be optimized with a micro pattern that may enhance the biocompatibility. The polymer may be conductive or insulative.

Abstract: An improved method of weldbonding utilizing inclusion bodies, placed directly between materials to be bonded or included in a weldbonding adhesive. The inclusion bodies maintain a gap between the materials to be welded which provides a gas releasing egress route to disperse the gas and gaseous byproducts produced during welding. This egress route substantially prevents the gases and gaseous byproducts from being expelled through the weld pool and the resultant degradation of the quality of the weld pool, particularly with coated materials, partial penetration welds, and such materials as 6000 series aluminum. The method further comprises an optional step of including a crack-reducing additive, applied either directly to the materials to be welded or included in the adhesive. A laser weldbonding embodiment may use a plurality of phased heat cycles to reduce weld imperfections, and enhance the effects of the adhesive and optional crack-reducing additive.

Abstract: An improved method of weldbonding utilizing inclusion bodies, placed directly between materials to be bonded or included in a weldbonding adhesive. The inclusion bodies maintain a gap between the materials to be welded which provides a gas releasing egress route to disperse the gas and gaseous byproducts produced during welding. This egress route substantially prevents the gases and gaseous byproducts from being expelled through the weld pool and the resultant degradation of the quality of the weld pool, particularly with coated materials, partial penetration welds, and such materials as 6000 series aluminum. The method further comprises an optional step of including a crack-reducing additive, applied either directly to the materials to be welded or included in the adhesive. A laser weldbonding embodiment may use a plurality of phased heat cycles to reduce weld imperfections, and enhance the effects of the adhesive and optional crack-reducing additive.