Embodiments are provided that enable an implantable connector, along with related apparatuses, devices, systems, methods, computing devices, computing entities, and/or the like to serve patients with neural interfaces requiring connectors with higher channel densities (>0.05 ch/mm.sup.3) or higher channel counts (>32) than is practical with conventional implant-connector technology.

Disclosed are wearable devices, such as rings and bracelets, for monitoring and diagnosing cardiovascular conditions of a wearer, along with related systems, algorithms and methods. The disclosed wearable devices can continuously monitor the wearer's cardiovascular status by measuring heart rate, motion, blood oxygenation, and/or other properties of the wearer. Disclosed wearable devices can further comprise three EKG electrodes, including a first electrode on the inner surface adapted to detect a signal from the finger/wrist, a second electrode on the outer surface adapted to detect a cardiovascular signal from a finger of the opposing hand, and a third electrode on the outer surface of the frame adapted to detect a cardiovascular signal from a EKG lead location on the wearer's chest or leg. The wearable devices can be linked wirelessly to a mobile device that the person can interact with, and can further be linked to other distributed system components and healthcare providers.

A patch for a therapeutic electrical stimulation device includes a shoe connected to the first side of the patch, the shoe including a body extending in a longitudinal direction from a first end to a second end, and having first and second surfaces, the first end of the shoe defining at least two ports, and the first surface of the shoe defining a connection member. The patch also includes at least one conductor positioned in the ports of the first end of the shoe. The shoe is configured for sliding insertion into a receptacle defined by a controller so that the conductor is connected to the controller to deliver electrical current from the controller, through the conductor, and to the electrodes, and the connection member is at least partially captured by a detent defined by the controller in the receptacle to retain the shoe within the receptacle.

Electrode lead wire connectors configured to be connected to an electrode for defibrillation and/or heart monitoring are disclosed. The electrode lead wire connector includes a one-piece electrically conductive connector contact having one end that is configured to be connected to a lead wire and an opposite end having an electrode receiving section that is configured to releasably receive a post of an electrode. The electrode receiving section includes a detent for retaining the post of the electrode within the electrode receiving section. Resilient engagement between the detent and the post provides a user of the electrode lead wire connector with tactile feedback indicating that the post of the electrode is fully engaged with the electrode receiving section of the one-piece electrically conductive connector contact.

The subject of the invention is a microprobe for selective electroporation comprising at least two metal electrodes (A) immersed in a glass rod (E), characterized in that the glass rod (E) made of a primary glass is 50 m to 2 mm in diameter, preferably 50 m to 500 m, the metal electrodes (A) made of a metal alloy are formed as rods with diameter of 1 m to 100 m, preferably 20 m to 30 m, wherein endings of those rods are exposed, wherein the primary glass and the metal alloy are matched in such manner that dilatometric softening temperature DTM of the primary glass is highly similar to the temperature of melting for the metal alloy. The invention also includes a method of manufacturing of such a microprobe.

A shield located within an implantable medical lead may be terminated in various ways at a metal connector. The shield may be terminated by various joints including butt, scarf, lap, or other joints between insulation layers surrounding the lead and an insulation extension. The shield may terminate with a physical and electrical connection to a single metal connector. The shield may terminate with a physical and electrical connection by passing between an overlapping pair of inner and outer metal connectors. The metal connectors may include features such as teeth or threads that penetrate the insulation layers of the lead. The shield may terminate with a physical and electrical connection by exiting a jacket of a lead adjacent to a metal connector and lapping onto the metal connector.

A wearable device is disclosed for managing tremors emanating from a body part of a user. The wearable device comprises a sensor that is configured to detect the tremor and transmit corresponding sensor data to at least one stimulating element, wherein the at least one stimulating element is configured to provide an electrical stimulus based on the sensor data. A dissipating portion of the wearable device is configured to increase an effective area for dissipating the electrical stimulus to the body. The dissipating portion is physically coupled with at least one stimulating element. The wearable device, when in operation, is in physical contact with body part of the user wherefrom the tremors emanate. The wearable device is stored in a docking station when not in operation. There is also disclosed a device integration application comprising software application to be executed by data processing arrangement of device.

An electrical connector, in particular for a medical device that is intended to be secured to the skin of a user, the connector comprising a base intended to be solidly connected to the device and a plug intended to be solidly connected to an electric conductor, wherein the plug comprises a connection means and the base comprises a plurality of connection means, each being adapted to engage with the connection means of the plug in order to establish a connection between the base and the plug comprising a base secured to the device and a plug configured to be secured to an electrical conductor, wherein the base includes a plurality of protuberances and the plug includes a cavity.

Implantable medical leads include a shield that is guarded at a termination by having a first portion and a second portion of the shield, where the first portion is between a termination of the shield at the second portion and an inner insulation layer that surrounds the filars. The first portion may reduce the coupling of RF energy from the termination of the shield at the second portion to the filars. The first and second portions may be part of a continuous shield, where the first and second portions are separated by an inversion of the shield. The first and second portions may instead be separate pieces. The first portion may be noninverted and reside between the termination at the second portion and the inner layers, or the first portion may be inverted to create first and second sub-portions. The shield termination at the second portion is between the first and second sub-portions.

A device for transcutaneous electrical stimulation is provided. The device comprises circuitry configured to generate transcutaneous stimulation signals. The device also comprises a first signal output component for electrically connecting to a first electrode connector to deliver generated transcutaneous stimulation signals. The first signal output component comprises a first four-pole electrical connector part. The device further comprises a second signal output component for electrically connecting to a second electrode connector to deliver generated transcutaneous stimulation signals. The second signal output component comprises a second four-pole electrical connector part. The device further comprises a controller to selectively control output of the stimulation signals to selected pairs of poles across the first and second four-pole electrical connector parts. Each selected pair of poles comprises one pole from the first four-pole electrical connector part and one pole from the second four-pole electrical connector part.