An integrated clot evacuation device having visualization for use in neurosurgical applications, particularly for the evacuation of clots formed as a result of intracranial hemorrhage (ICH). The device may further include an integrated camera and light for visualizing the interior of the brain and the clot itself. Further, the device is configured to evacuate clots through aspiration and irrigation.

A device and method is provided to gain access to interior body regions. The system includes a safety needle assembly, a stylet assembly, a blade assembly, an obturator assembly, and a dilator assembly. The safety needle assembly or stylet assembly accesses an interior body region, after which the blade assembly expands the pathway created by the safety needle assembly or stylet assembly. The obturator then further expands the pathway and delivers the dilator assembly to the desired location. The safety needle assembly, obturator assembly, and blade assembly are removed, leaving the dilator assembly in place for future procedures.

A device comprises a retractable shaft; a shaft biasing spring; and an actuator button. The retractable shaft is biased away from the actuator button by the shaft biasing spring. A magnetic attracting force is created between the retractable shaft and the actuator button upon actuation of the actuator button. Before actuation, a distance between the actuator button and the retractable shaft is great enough that the magnetic attracting force is less than a biasing force of the shaft biasing spring such that the retractable shaft is biased away from the actuator button. Upon actuation, the actuator button is depressed to make the distance between the actuator button and the retractable shaft sufficiently small such that the magnetic attracting force is greater than the biasing force of the shaft biasing spring to allow the retractable shaft to be biased towards the actuator button.

An inflow access cannula system for allowing an instrument to access a remote surgical site, wherein the instrument comprises a distal portion having a smaller diameter and a proximal portion having a larger diameter, the system comprising: an inflow access cannula comprising a distal end, a proximal end and a central lumen extending therebetween, wherein the central lumen has a diameter larger than the distal portion of the instrument and smaller than the proximal portion of the instrument; and an instrument adapter for releasable connection to the inflow access cannula, the instrument adapter comprising a lumen communicating with the central lumen of the inflow access cannula, the lumen having a diameter larger than the proximal portion of the instrument, the instrument adapter further comprising a port and a fluid passageway connecting the port with the lumen of the instrument adapter, and a spacer for spacing the proximal portion of the instrument from the distal end of the inflow access cannula, such that when an instrument is disposed in the inflow access cannula system so that the distal portion of the instrument extends within the central lumen of the inflow access cannula and the proximal portion of the instrument is disposed in the central lumen of the instrument adapter and is in engagement with the spacer, fluid can flow into the port of the instrument adapter, along the fluid passageway of the instrument adapter, into the lumen of the instrument adapter and through the lumen of the inflow access cannula.

A surgical instrument may have a handle, a support sleeve, and an inner sleeve. Illustratively, the support sleeve may be configured to actuate relative to the inner sleeve to protect the inner sleeve before and after a surgical procedure and to expose a portion of the inner sleeve during the surgical procedure. In one or more embodiments, an application of a force to a distal end of the support sleeve may be configured to retract the support sleeve relative to the inner sleeve. Illustratively, a reduction of a force applied to the distal end of the support sleeve may be configured to extend the support sleeve relative to the inner sleeve.

An implant insertion device includes: an introduction needle having a needle tip that is insertable into subcutaneous tissue; an elongated implant configured to promote tissue regeneration by attachment of cells; and a tubular implant cover that covers an outer side of the introduction needle. A space extending in an axial direction is located between the implant cover and the introduction needle, and the implant is arranged in the space.

A biosensor inserter is configured to insert a biosensor. The biosensor inserter includes a push member including a receiver, a contact member translatable relative to the push member, and a trocar holder having a sheath configured to receive a trocar assembly including a trocar therein. The trocar holder is configured to be insertable into, and removable from, the receiver. Thus, an amount of medical waste can be minimized by discarding only the removable trocar holder and trocar assembly after use. System and method embodiments are provided.

A minimally traumatic trocar apparatus for delivering one or more medication pellets to a subcutaneous insertion site is described. The minimally traumatic trocar apparatus includes a blunt cannula and an obturator. The blunt cannula includes a tubular cannula body having an anterior end with a surface that has a smooth edge. The blunt cannula also includes a medication slot disposed along the tubular cannula body and an inner diameter that is at least 3 millimeters (mm). The obturator includes an anterior rounded tip. The obturator body is inserted within the tubular cannula body so that the obturator extends through the tubular cannula body so that the anterior rounded tip of the obturator extends past the anterior end of the tubular cannula body.

A minimally traumatic trocar system is described. The trocar system includes a cannula, a plastic obturator, and hydrodissection microcannula. The cannula includes a tubular cannula body and blunt anterior surface. The obturator includes an anterior rounded tip. The hydrodissection microcannula includes an anterior rounded tip and an opening proximate to the anterior rounded tip. The cannula and plastic obturator assemble to form a minimally traumatic trocar by passing the plastic obturator through an interior passage of a tubular cannula body of the cannula. The hydrodissection microcannula probes an incision to form an insertion path while causing minimal trauma. The assembled trocar probes the incision along the insertion path to reach a delivery site within subcutaneous tissue. The plastic obturator withdraws from the cannula and at least one medication pellet is loaded within the interior passage. The plastic obturator pushes the medication pellet(s) through the interior passage to the delivery site and deposits the medication pellet(s) within the subcutaneous tissue.

A guide wire for guiding a dilator to be inserted into a living body includes: a flexible elongated shaft portion; a puncture portion at a distal end portion of the shaft portion to form a hole in biological tissue; and an elastically deformable cover portion covering the puncture portion. The cover portion includes a sparse pitch portion that has a wire member wound in a spiral shape and axially contractible, and a distal end cover located on a distal end side of the sparse pitch portion and covering at least a part of the puncture portion. The puncture portion includes a first contact portion. The distal end cover includes a second contact portion configured to contact the first contact portion from a proximal end side, so that relative axial movement of the first and second contact portions is restricted by the first contact portion contacting the second contact portion.