A leadless pacemaker, and method for storing event data therein, comprising a central processing unit, a first logic circuit configured to generate event data based on a first event occurring during operation of the leadless pacemaker, a first hardware event counter configured to be incremented if specific event data are generated by said first logic circuit, a first memory unit comprising a first bit configured to be set if said first hardware event counter is incremented to a first maximum number of counts, a second memory unit communicating with said first memory unit, wherein said central processing unit is configured to transfer said first bit to said second memory unit, a first RAM event counter in a random access memory of said leadless pacemaker, wherein said central processing unit is configured to increment said first RAM event counter if said first bit is transferred to the second memory unit.

A piezoelectric energy harvesting device is provided. The piezoelectric energy harvesting device includes a piezoelectric material, which includes an inner surface having a concave shape, and an outer surface having a bottom surface. The piezoelectric energy harvesting device further includes a ball positioned on the inner surface. The bottom surface acts as a ground, the inner surface acts as a positive node, and the inner surface, the outer surface, and the ball are configured so that movement of the ball causes mechanical stress to the piezoelectric material, producing an electrical current.

An implantable medical electrical lead connectable to an electrical header of an implantable medical device includes a lead body extending from a proximal end to a distal end, a lead terminal disposed at the proximal end of the lead body and configured to couple the lead to the electrical header, and a lead boot disposed at the lead terminal. The lead boot includes a strain relief portion and a seal portion. The strain relief portion is formed of a first elastic polymer and the seal portion is formed of a second elastic polymer. The first elastic polymer is different from the second elastic polymer.

This disclosure relates to a communication amplification device for an implantable capsule, in particular for an autonomous cardiac stimulation capsule. The amplification device comprises a first holding element and a second element configured to hold the implantable capsule. The first holding element is configured to receive the distal end of the capsule and the second holding element is configured to receive the proximal end of the capsule. The first holding element comprises a communication amplification antenna configured to couple to a distal electrode of the capsule.

The disclosure describes a medical lead system that includes a first lead portion and a second lead portion. The first lead portion includes a first elongate body extending along a longitudinal axis from a distal end to a proximal end and defining a coupling recess. The second lead portion includes a second elongate body extending along the longitudinal axis from a distal end to a proximal end and a connector defining a channel configured to receive the proximal end of the first lead portion. The connector includes a coupling member configured to, when the first lead portion is inserted into the channel, mechanically engage the coupling recess to secure the first lead portion to the second lead portion at least in an axial direction relative to the longitudinal axis.

A bio electrode and a method of forming the same are provided. The bio electrode comprises a first core-shell nanowire/polymer composite comprising a first core-shell nanowire and a first polymer. The method of forming a bio electrode comprises a step of forming a core-shell nanowire by carrying out epitaxial growth of a biocompatible metal on a surface of a core comprising a conductive metal.

The module comprises a pendular unit with an elastically deformable piezoelectric beam having a clamped end and an opposite, free end, coupled to an inertial mass. The beam produces an oscillating electrical signal collected by electrodes, which is rectified and regulated to output a voltage for charging a battery. The number and configuration of the electrodes (T1, T2, B1, B2, N) carried by the piezoelectric beam define a plurality of pairs of electrodes between which a corresponding plurality of said oscillating signals can be simultaneously collected. A switching matrix, as a function of an input command, selectively switches the plurality of pairs of electrodes between each other according to a plurality of different series (S), parallel (P) and/or series-parallel (SP) configurations, the selected configuration being that which maximizes the power sent to the battery as a function of the voltage level (VBAT) present at the terminals of the latter.

An electrode assembly for the positioning of an electrode of an implantable medical lead includes a housing and an electrode subassembly. The housing includes a proximal end for connecting to the lead and a distal end. The housing defines a housing lumen extending between the proximal end and the distal end. The housing lumen includes internal screw threads extending along at least a portion of the housing lumen. The electrode subassembly is disposed at least partially within the housing lumen. The electrode subassembly includes a needle electrode and a coupler. The needle electrode is disposed coaxially with the longitudinal axis of the housing lumen. The coupler is disposed at a proximal end of the needle electrode. The coupler includes external screw threads engaged with the internal screw threads of the housing lumen such that rotation of the coupler moves the needle electrode along the longitudinal axis of the housing lumen.

Various aspects of the present disclosure are directed toward apparatuses, systems and methods for connecting a lead to an implantable medical device. The apparatuses, systems and methods may include a clamp arranged within a connector port configured to secure the lead with a header in response to frictional engagement between a portion of the implantable lead and the clamp.

Provided herein are systems for providing therapy to the heart of a patient. The systems include an implantable device for implantation proximate the heart of the patient. The implantable device includes: an anchoring element for maintaining the position of the implantable device after implantation in the patient, at least one sensing electrode for sensing the electrical activity of the heart, at least three pacing electrodes for delivering electrical energy to the tissue of the heart, and a controller including an algorithm for determining when the patient requires therapy. The systems further include an external device having a transceiver for transmitting energy to the implantable device.