The invention relates to medical technology, and more particularly to a device for the conservative treatment of nasal and paranasal sinus diseases. The present device comprises obturators for the posterior and anterior nasal openings, each obturator being in the form of an expandable sheath made of a resilient material and provided with a feed tube. The distal end of the tube is in communication with the cavity below the sheath, and the proximal end is provided with an adapter having a valve mechanism. The obturator sheath for the posterior nasal opening is hermetically fastened to the distal portion of its feed tube. The obturator sheath for the anterior nasal opening is hermetically fastened to a cuff. The cuff is provided with two channels, one of which holds the feed tube of the obturator sheath for the posterior nasal opening in such a way that the cuff can move along the entire length of the feed tube. The other channel holds a catheter for evacuating a pathological secretion from the paranasal sinuses and/or for introducing solutions of medicinal preparations into same for diagnostic or therapeutic purposes. The catheter is held in said channel in such a way that the distal portion thereof can be moved into the space between the obturator sheaths. The invention is intended to provide more effective treatment of nasal and paranasal sinus disorders.

A balloon catheter which allows for faster preparation and effective purging of air. The catheter includes an elongated, flexible catheter having a tubular outer member and a tubular inner member each having a respective lumen. The inner member is at least partially disposed in the outer member lumen such that an outer surface of the inner member and an inner surface of the outer member together define an annular inflation lumen. The outer member has micropores or micro-holes configured such that when a contrast agent is injected into the inflation lumen, the micropores or micro-holes allow air to pass therethrough and thereafter become clogged by the contrast agent. The catheter also has a balloon member having its ends secured to and circumferentially around the outer member such that an inner surface of the balloon member and the outer surface of the outer member define an inflatable balloon interior.

A catheter includes: an outer tube that includes a lumen; an inner tube that is inserted into the lumen and has a base end portion joined to an intermediate position of the outer tube in an axis direction; a core wire that is inserted into the lumen and extends to a tip end of the outer tube beyond the base end portion; and a securing portion that is disposed at an intermediate position of an overlapping range in the axis direction, the inner tube and the core wire overlapping each other in the overlapping range, and secures the inner tube or the core wire to the outer tube.

An apparatus for use with an elongated medical device configured to be tacitly contacted by a user is disclosed. The apparatus includes an elongated medical-conveyance assembly defining an elongated conveyance lumen configured to receive the elongated medical device. A tactile feature is located at (in) the elongated conveyance lumen. The elongated guidewire-conveyance assembly may include biocompatible material properties suitable for sufficient performance.

A multi-lumen catheter for monitoring intramuscular pressure having an elongated body configured and dimensioned for insertion into a compartment of a patient. The catheter has a pressure sensor to determine if excessive pressure is being applied. A sensor is in communication with the lumen to continuously measure pressure to provide continuous readings of intramuscular pressure.

The embodiments disclosed herein relate to balloon catheter assemblies. The balloon catheter assemblies can include a hub, an elongated member, and an inflation balloon. The balloon catheter assemblies can also include a support wire having a proximal end that is longitudinally displaceable within a sleeve that is disposed in the catheter hub. A distal end of the support wire may be coupled to the inflation balloon at one or more positions.

The disclosure includes a balloon guiding sheath that includes an elongated sheath having a proximal end, a distal end opposite the proximal end, an inner tube extending between the proximal end and the distal end, an outer tube surrounding the inner tube and extending between the proximal end and the distal end, an access port located adjacent in the proximal end, a distal port located adjacent the distal end, and a working lumen extending through the elongated sheath between the access port and the distal port. The balloon guiding sheath also includes an inflatable balloon located on an outer surface of the elongated sheath adjacent the distal end, the inflatable balloon being fluidly coupled to an inflation lumen extending between the inflatable balloon and an inflation port located adjacent the proximal end.

The disclosure provides for an adjustable catheter system with isovolumetric suction and restoration of fluid for the removal of a thrombus and a method of use thereof. The catheter system includes an inner catheter and an outer sheath surrounding at least a portion of the inner catheter. The inner catheter may include at least three lumina extending from the proximal end to the distal end of the inner catheter, at least one infusion fenestration along the infusion segment, and a distal encapsulation balloon at the distal end. The outer sheath may include at least three lumina extending from the proximal end to the distal end of the outer sheath and a proximal encapsulation balloon at the distal end. The catheter system may further include an agitator for mechanical morcellation of the thrombus.

A catheter device for the recanalisation of an occlusion in a vessel. A proximal balloon is arranged at the distal end portion of a catheter shaft for anchoring the catheter shaft in the vessel and for opening the occlusion. A distal balloon arranged at the distal end portion for opening the occlusion.

A method of forming a three-dimensional object is carried out by providing a carrier and an optically transparent member having a build surface, the carrier and the build surface defining a build region therebetween; filling the build region with a polymerizable liquid; irradiating the build region through the optically transparent member to form a solid polymer from the polymerizable liquid and advancing the carrier away from the build surface to form the three-dimensional object from the solid polymer, while also concurrently with the irradiating and/or advancing steps: (i) continuously maintaining a dead zone of polymerizable liquid in contact with the build surface, and (ii) continuously maintaining a gradient of polymerization zone between the dead zone and the solid polymer and in contact with each thereof. The gradient of polymerization zone comprises the polymerizable liquid in partially cured form (e.g., so that the formation of fault or cleavage lines between layers of solid polymer in the three-dimensional object is reduced). Apparatus for carrying out the method is also described.