A biosignal measurement system comprises an adapter for a biosignal measurement device, and an external support structure separate from the adapter. The adapter comprises tool-less connectors, which are repeatedly connectable to and disconnectable from their counter connectors of the external support structure, and a device connector, which has an electrical connection with the tool-less connectors and which has a connection with the biosignal measurement device that the adapter carries. The external support structure comprises an electrode support structure with electrodes and tool-less counter connectors, the electrodes and the tool-less counter connectors having an electrical connection therebetween. The electrodes form an electrical contact with skin for receiving the biosignal. The counter connectors are in electrical contact with the connectors of the adapter for transferring the biosignal to the biosignal measurement device through the adapter.

A magnetic connector has a plug core disposed around a plug contact set and a receptacle core disposed around a receptacle contact set. The plug core defines a generally elongated circular plug core edge. The receptacle core defines a generally elongated concentric-circular receptacle core edge. The receptacle core edge defines an air gap and the plug core defines an anchor configured to insert into the air gap. A coil is disposed around the receptacle core, and the coil, the plug core and the air gap define a magnetic circuit. The coil is electrically energized so as to form a magnetic field within an air gap, lock the anchor within the air gap and lock the plug contact set to the receptacle contact set accordingly.

Provided is a connector assembly for use in an implantable medical device. The connector assembly for use in an implantable medical device includes an insulating sealed housing and at least one conductive element. The sealed housing defines at least one connecting hole along an axial direction of the sealed housing, a hole wall of each of the at least one connecting hole defines at least one circumferential mounting groove, and the at least one circumferential mounting groove is arranged along an axial direction of the at least one connecting hole. The at least one conductive element is disposed in a corresponding one of the at least one circumferential mounting groove and is drawn out to an outside of the sealed housing through a respective electrical contact element.

A surgical stapling instrument includes a body portion and a tool assembly extending from the body portion. The tool assembly includes a jaw member, and a first connector assembly disposed within the jaw member. The first connector assembly includes a first connector housing and first and second connector members extending from the first connector housing. The surgical stapling instrument further includes a cartridge assembly selective receivable within the jaw member. The cartridge assembly includes a second connector assembly configured for electrical connection with the first connector assembly. The second connector assembly includes a second connector housing and first and second contact members disposed within the second connector housing. The first and second connector members of the first connector assembly are configured to engage the respective first and second contact members of the second connector housing when the cartridge assembly is received within the jaw member of the tool assembly.

A biocompatible electrical connection includes: a substrate; a ferrule having a concentric flange at a first end of the ferrule; a first adhesive; and a second adhesive. The substrate includes a hole having a diameter that is a specified amount larger than an outside diameter of the ferrule forming an annular space between the hole and the ferrule, the first adhesive adheres a first surface of the concentric flange of the ferrule to a first surface of the substrate, and the second adhesive fills the annular space between the hole and the ferrule.

A surgical instrument includes a body assembly, a shaft assembly extending distally from the body assembly along a shaft axis, and an end effector at a distal end of the shaft assembly. The shaft assembly includes an outer tube configured to rotate relative to the body assembly about the shaft axis. The surgical instrument further includes a slip ring assembly configured to enable electrical communication between the shaft assembly and the body assembly while permitting relative rotation therebetween. The slip ring assembly includes a first electrical contact supported by the outer tube, and a second electrical contact electrically coupled with the first electrical contact and positioned radially outward of the outer tube. The first electrical contact is configured to rotate with the outer tube about the shaft axis relative to the second electrical contact while the first and second electrical contacts remain electrically coupled.

The present disclosure relates to implantable neuromodulation devices and methods of fabrication, and in particular to a separable high density connectors for implantable neuromodulation devices. Particularly, aspects of the present disclosure are directed to a medical device comprising an electronics module and a header for connecting the electronics module to a lead assembly. The header includes: a housing that includes (i) a cavity having a central axis or plane and an internal surface, and (ii) an opening aligned with the central axis or plane of the cavity, an array of retractable contacts extending from the internal surface towards the central axis or plane of the cavity, and an array of connection terminals on the housing, where each connection terminal of the array of connection terminals is: (i) electrically connected to the electronics module, and (ii) electrically connectable to a retractable contact of the array of retractable contacts.

Seals used within lead passageways of implantable medical devices for creating a seal to implantable medical leads inserted into the lead passageways include a body defining a lead passageway with an axial dimension. The body further defines a first circumferential protrusion extending radially a first distance into the lead passageway, and the body further defines a second circumferential protrusion separated from the first circumferential protrusion along the axial dimension. The second circumferential protrusion extends radially a second distance into the lead passageway, the second distance being less than the first distance. The body further defines a first circumferential depression immediately adjacent the first circumferential protrusion and between the first circumferential protrusion and the second circumferential protrusion.

A system for electrically and mechanically connecting an electrical cord and a medical device includes: a cord-side connector including a cord connecting surface, a cord-side conductive portion, and at least one protrusion extending from an intermediate surface; and a device-side connector including a device connecting surface, a device-side conductive portion, and a recess configured to slidably receive the cord-side connector in a sliding direction, the recess including at least one slot configured to slidably receive the at least one protrusion to guide the cord-side connector in the recess in the sliding direction, where the at least one protrusion and slot are configured to form a mechanical connection through an interference fit upon slidable receipt of the at least one protrusion into the at least one slot, and the cord-side conductive portion and the device-side conductive portion are configured to contact each other upon formation of the interference fit.

A diagnostic imaging catheter is disclosed, which is capable of preventing a solution from an internal space of a hub from flowing into a portion communicating with the internal space of the hub and to which the signal lines such as the optical fiber and the electric signal cable are electrically or optically connected. The optical diagnostic catheter includes a rotatable drive shaft, an elongated sheath configured to be inserted into a biological lumen, a hub that includes a port connected to the sheath for supplying the solution, a connector portion that includes an optical connector accommodated in an internal space of the hub and optically connected to an external optical connector, a first seal portion that prevents the solution from the port from flowing into a first connection portion, and a second seal portion that prevents the solution from the port from flowing into a second connection portion.