Waterproof apparatus for cables and cable interfaces are provided herein. An exemplary apparatus includes a coupler body that includes a first end configured to releaseably couple with a connector bulkhead and a second end having an opening that is sized to receive a sealing gland, a cavity for receiving the sealing gland, the sealing gland comprising an outer peripheral surface configured to sealingly engage with an inner surface of the cavity, the sealing gland comprising an aperture that is configured to receive a cable.

An implantable medical lead has a torsional stiffness and is rotationally coupled to a stylet. Applying rotation directly to the lead in turn causes rotation of the stylet. Where the stylet has a bent tip for purposes of steering the lead, the rotation applied to the lead rotates the bent tip so that the lead can be steered by rotating the lead rather than rotating a hub of the stylet. The rotational coupling may be achieved through one or more features provided for the lead and/or the stylet, such as a feature within a lumen of the lead that mates to a feature along the stylet or a feature of the stylet hub that engages the proximal end of the lead. The torsional stillness of the lead may be provided by adding a feature within the lead body, such as a braided metal wire or an overlapping foil.

A method of assembling an electrical connector includes inserting an electric terminal with an attached wire to an initially inserted position in a wire opening defined by a connector body. The electric terminal is moved through the wire opening in an insertion direction relative to the connector body. The electric terminal is attached to the connector body in a seated position, wherein the wire is coaxial with the wire opening.

Waterproof apparatus for cables and cable interfaces are provided herein. An exemplary apparatus includes a coupler body that includes a first end configured to releaseably couple with a connector bulkhead and a second end having an opening that is sized to receive a sealing gland, a cavity for receiving the sealing gland, the sealing gland comprising an outer peripheral surface configured to sealingly engage with an inner surface of the cavity, the sealing gland comprising an aperture that is configured to receive a cable.

A shield located within an implantable medical lead may be terminated in various ways. The shield may be terminated by butt, scarf, lap, or other joints between insulation layers surrounding the lead and an insulation extension. For lap joints, a portion of an outer insulation layer may be removed and a replacement outer insulation layer is positioned in place of the removed outer insulation layer, where the replacement layer extends beyond an inner insulation layer and the shield. The replacement layer may also lap onto a portion of the insulation extension. Barbs may be located between the replacement layer and the inner insulation layer or the insulation extension. The shield wires have ends at the termination point that may be folded over individually or may be capped with a ring located within one of the insulation layers of the jacket.

Electrical terminals and methods of manufacturing the same are disclosed. An example method of making an electrical terminal is disclosed that includes forming a base portion of a housing for the electrical terminal, forming a top portion of the housing, the top portion having an opening defining an entry point for a wire to be terminated, extending a connector pin out through a bottom surface of the base portion of the housing to enable electrical connection with a printed circuit board, and sealingly mating the top portion to the base portion to enclose a first wire clamp within the housing, the first wire clamp to secure the wire in electrical contact with the connector pin when the wire is extending into the housing through the opening, the base portion and the top portion being immovably affixed, wherein the first wire clamp is actuated by a screw.

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 shield located within an implantable medical lead may be terminated in various ways. The shield may be terminated by butt, scarf, lap, or other joints between insulation layers surrounding the lead and an insulation extension. For lap joints, a portion of an outer insulation layer may be removed and a replacement outer insulation layer is positioned in place of the removed outer insulation layer, where the replacement layer extends beyond an inner insulation layer and the shield. The replacement layer may also lap onto a portion of the insulation extension. Barbs may be located between the replacement layer and the inner insulation layer or the insulation extension. The shield wires have ends at the termination point that may be folded over individually or may be capped with a ring located within one of the insulation layers of the jacket.

Implantable medical leads and implantable lead extensions include a shield. The implantable medical lead is coupled to the implantable lead extension. Stimulation electrodes of the implantable medical lead contact stimulation connectors within a housing of the implantable extension to establish a conductive pathway for stimulation signals from filars of the implantable extension to filars of the implantable medical lead. Continuity is established between the shield of the implantable medical lead and the implantable extension by providing a radio frequency conductive pathway within the housing. The radio frequency conductive pathway extends from a shield of the implantable extension to a shield connector that contacts a shield electrode of the implantable medical lead. The radio frequency conductive pathway may have various forms such as a jumper wire or an extension of the shield within the implantable extension.

Radiopaque markers represent that a lead is suitable for a particular medical procedure such as a magnetic resonance image scan and are added to the lead or related device. The markers may be added after implantation of the lead in various ways including suturing, gluing, crimping, or clamping a radiopaque tag to the lead or to the device. The markers may be added by placing a radiopaque coil about the lead, and the radiopaque coil may radially contract against the lead to obtain a fixed position. The markers may be added by placing a polymer structure onto the lead where the polymer structure includes a radiopaque marker within it. The polymer structure may include a cylindrical aperture that contracts against the lead to fix the position of the polymer structure. The polymer structure may form a lead anchor that includes suture wings that can be sutured to the lead.