An implantable medical lead may include an electrode at a distal portion of the lead that is configured to monitor or provide therapy to a target site. The lead may include a visible indicator that is visible to the naked eye of a clinician at a medial portion of the lead that is configured to indicate when the electrodes of the lead are longitudinally and radially aligned properly to monitor or treat the target site. A clinician may insert the lead into the patient using an introducer sheath inserted to a predetermined depth into the patient and subsequently aligning the distal portion of the lead by orienting the indicator at an entry port of the introducer sheath.

A splittable sheath for an implantable medical device can include a jacket having an outer diameter and an inner diameter. A lumen can be defined by the inner diameter and extended from a proximal end to a distal end of the jacket. An electrode can be located at the distal end of the jacket. A signal wire can be disposed within the jacket and can be electrically coupled to the electrode. A rail can be configured to shield the signal wire from a cut path of a sheath splitter. In some examples, the sheath can further include a second rail. For instance, the signal wire can be located between a first rail and a second rail along the length of the sheath. The cut path can be located between the first rail and the second rail on a radially opposing side of the sheath from the signal wire.

A delivery system for an intracorporeal device includes a sheath defining one or more lumens shaped to receive a delivery catheter or shaft and a guidewire. The system may include a delivery shaft having a distal coupling feature adapted to releasably couple with a proximal coupling feature of the intracorporeal device. The delivery system may further include a hub through which the delivery shaft and guidewire are passed. The delivery shaft may be coupled to a feature, such as a knob, that enables manipulation of the delivery shaft to decouple the distal fixation feature from the proximal fixation feature of the intracorporeal device in order to deploy the intracorporeal device within a patient.

In one embodiment, a catheter introducer for compressing a distal end assembly of a catheter for insertion into a sheath includes a compression conduit having a truncated conical-form cavity, and including a distal and proximal opening, the proximal opening being configured to receive the distal end assembly, the cavity tapering from the proximal to the distal opening so that successive portions of the distal end assembly are compressed as the catheter is advanced distally, a distal connector connected to the distal opening, and configured to be reversibly coupled to the sheath and provide passage for the compressed portions of the distal end assembly into the sheath, and a proximal retainer disposed adjacent to the proximal opening and including opposing surfaces to at least partially prevent compression of portions of the distal end assembly while more distally disposed portions of the distal end assembly are compressed in the compression conduit.

A system for treating and/or monitoring a medical condition of a patient comprises: an implant configured to be inserted into a body space of the patient, such as the left atrial appendage. The implant comprises a frame or ring configured to engage tissue of the patient proximate the body space. Methods of treating and/or monitoring a medical condition of a patient are also provided.

A medical device system may include a structure including a first elongate member, a line including a plurality of flexible members, and an actuator coupled to the line to selectively transmit force to at least the first elongate member. The structure may include a delivery configuration in which at least a portion of the structure is arranged to be percutaneously delivered to a bodily cavity. Respective portions of the flexible members may be intertwined together to form a braided portion of the line, and the line may include an unbraided portion secured at least to the first elongate member. The braided portion of the line may be located between the actuator and the first elongate member.

A catheter device for placing a sensor device comprises a shaft and a coupling device, arranged at the shaft, for coupling the catheter device to the sensor device comprising at least one bracket element. The coupling device comprises a coupling element and a locking element adjustable with respect to the coupling element, wherein the coupling element comprises at least one engagement section with which the at least one bracket element of the sensor device can be brought in engagement, wherein the locking element is designed, in a coupled position, to block the at least one bracket element at the at least one engagement section, and is adjustable with respect to the coupling element so as to release the at least one bracket element for detachment from the at least one engagement section.

A septal closure device includes a frame comprising one or more tissue anchor features, an occluding membrane, and a pressure sensor device attached to the occluding membrane.

The implanting system (1) for implanting a totally implantable device (2) in a human or animal body comprises an introducing device (3) equipped with at least one operative channel (4a, 4b) and a transparent cover element (11) detachably attached to a distal end (6) of said introducing device (3), the cover element (11) has a rounded configuration that is outwardly convex and facilitates the sliding of said introducing device (3).

Disclosed embodiments include apparatuses, systems, and methods for providing a sheath tip with an angled distal face to conform the sheath to a surface of tissue toward which the sheath is being extended to potentially help reduce or avoid tissue damage upon extending a sheath to convey an elongated instrument for sampling or treatment. In an illustrative embodiment, an apparatus includes a sheath tip positionable at an end of a sheath configured to convey an elongated medical instrument to a location adjacent a detection range of a detecting device. The sheath tip includes a distal member that extends a finite distance beyond the end of the sheath. The distal member is detectable by the detecting device when the end of the sheath is within the finite distance of the detection range of the detecting device.