Devices and methods are described for a minimally invasive procedure offering immediate relief of brain compression and prevention of subdural hematoma re-accumulation. For example, this disclosure describes devices and methods for embolization of bleeding branch vessels of the middle meningeal artery and subdural hematoma drainage in a single endovascular intervention using multimodal catheter-based technology.

Balloon catheters that includes inner and outer elongate shafts, each of which is secured relative to an end of an inflatable member. The inner and outer elongate shafts are secured relative to one another at one more discrete connection locations. The balloon bonding locations are disposed radially inward relative to an outer dimension of the outer elongate shaft.

In some examples, a catheter comprises an inner liner, an outer jacket, and a structural support member positioned between at least a portion of the inner liner and the outer jacket. The inner liner, the outer jacket, and the structural support member define a catheter body that comprises a proximal portion having a first outer diameter, a distal portion having a second outer diameter less than the first outer diameter, the distal portion including a distal end of the catheter body, and a medial portion positioned between the proximal portion and the distal portion, the medial portion tapering from the first outer diameter to the second outer diameter.

A medical probe for guided insertion into soft tissue, such as the brain, is disclosed. The medical probe may include a flexible, elongated body having a proximal end portion and an opposed distal end portion. The elongated body has a length of at least 1 cm and an outer diameter of 80 μm or less. The distal end portion may comprise a beveled tip such that the distal end portion of the medical probe can be steered independently to a target site in the soft tissue.

Intrasaccular flow diverter including: an interior fill braid physically inverted over itself forming a proximal inverted end and an opposite free end; and a dome braid disposed distally of and secured to the interior fill braid. Subject to application of an external mechanical force, the dome braid is transitionable between an expanded state and a compressed state. The dome braid has a proximal end with an opening defined therein through which starting at the free end the interior fill braid is passable therethrough exerting a radially outward force on the dome braid. A delivery wire is releasably detachable from the proximal inverted end of the interior fill braid. The dome braid has a stiffer profile relative to that of the interior fill braid to maintain in position within the aneurysm the dome braid as the interior fill braid is advanced therein.

An implantable cranial medical device includes a first fluid flow path, a second fluid flow path, and upper flange portion, and a lower portion. The upper flange portion is configured to rest on a skull of a subject about a burr hole. The lower portion is configured to be placed within the burr hole. The first fluid flow path may extend from a first opening in the upper flange portion to a first opening in the lower portion. The second fluid flow path may extend from a second opening in the upper flange portion to a second opening in the lower portion.

A method for delivering one or more medication pellet to a subcutaneous insertion site with a round tipped obturator and blunt cannula is described. The obturator is received within the cannula. The cannula includes a tubular cannula body having a smooth anterior surface a medication slot disposed along the cannula body. The cannula body has an inner diameter that is at least 3 millimeters (mm). The cannula and obturator probe an incision into the subcutaneous tissue along an insertion path within the subcutaneous tissue. The obturator is removed from the cannula, and one or more medication pellet is placed in the medication slot. The cannula body again receives the obturator, which passes the pellet(s) through the cannula body with its anterior rounded tip so that the obturator pushes the pellet(s) through the cannula body. The pellet(s) exit the cannula body and are delivered aligned along the insertion path.

The present invention discloses a microcatheter, with tubular structure, comprising a catheter body, a sharp portion disposed at a distal end of the catheter body, the catheter body comprises: a inner layer with a hollow lumen; a tubular intermediate layer wrapped outside the inner layer, comprising a spring layer and a braid above the spring layer, the braid extending longitudinally along a part of the spring layer; and a tubular outer layer, wrapped outside the intermediate layer; the part of the spring layer which is not wrapped by the braid is bent at a certain angle along a longitudinal axis of the catheter body. The catheter body of the microcatheter of the invention is configured to have a multilayered structure, and the braid is only wrapped on spring layer near to the proximal end; the part of the spring layer not wrapped by the braid can be bent at a corresponding angle to adapt to an angle between the main branch and the branch of the coronary artery, to make sure that the microcatheter can reach the bifurcation lesions of the coronary artery.

An aortic perfusion catheter is an apparatus that is used during surgery for acute ascending aortic dissection to reduce postoperative injuries from profound hypothermia, ischemia, and reperfusion. The apparatus may include at least one main cannula, an inflation cannula, a drainage cannula, and a balloon tamponade. The at least one main cannula helps maintain blood perfusion to the body during the procedure to reduce postoperative injuries. The inflation cannula enables the selective inflation and deflation of the balloon tamponade to facilitate the insertion and removal of the balloon tamponade along with the at least one main cannula within the descending thoracic aorta. The balloon tamponade prevents blood flow into the operative area to maintain the operative area clear during the procedure. The drainage cannula enables the drainage of blood that may escape the balloon tamponade as well as other bodily fluids.

An aspiration system includes a pump and a control system in communication with the pump. The control system includes a microcontroller, an antenna configured to receive a signal, and a pump control board in communication with the microcontroller. The antenna is in communication with the microcontroller. Upon receiving the signal, the pump control board operates the pump to create negative pressure according to the signal.