A61M2025/0031

DOUBLE-LUMEN CATHETER
20220233809 · 2022-07-28 ·

A double lumen catheter includes: a circumferential wall 101 forming a lumen extending from a proximal end to a distal end; and a partition 102 dividing the lumen into a first passage 110 and a second passage 120 extending in a longitudinal direction. Distal ends of the first passage 110 and the second passage 120 of the circumferential wall 101 are aligned with each other. The partition 102 includes a projection 103 projecting beyond the distal end of the circumferential wall 101, and having a U-shaped plane. The first passage 110 has, at the distal end, a first passage slit 111 formed by cutting out a part of the circumferential wall 101 around a circumferential center of the circumferential wall 101.

Dual Lumen Cannula with Adjustable Length Infusion Tube
20210402138 · 2021-12-30 ·

A dual lumen coaxial cannula assembly including a first infusion tube having a proximal end, a distal end, and a sidewall extending circumferentially therebetween, as well as a second drainage tube co-axially aligned with the first infusion tube, the second drainage tube having a proximal end, a distal end, and a sidewall extending circumferentially therebetween. The assembly also includes a connector assembly, which has an inlet portion through which a portion of the first infusion tube is configured to extend and an outlet portion through which a portion of the second drainage tube is configured to extend. The connector assembly is configured to enable selective axial displacement of the first infusion tube through the second drainage tube.

Method and device for infusion of pharmacologic agents and thrombus aspiration in artery

A catheter device and method for treating an artery with thrombus, the catheter comprising an inflatable member. A carrier catheter has a proximal end and a distal end adapted to be inserted percutaneously into an artery, the carrier catheter having a tubular body adjacent to a rear end of the inflatable member. An inflating tube passes through the tubular body and having an open front end in fluid communication with the inflatable member to inflate same. An infusion tube is adapted to infuse pharmacologic agents, the infusion tube passing through the tubular body and having an open front end extending beyond the inflatable member. An aspiration tube is adapted to aspire the thrombus, the aspiration tube passing through the tubular body and having an open front end between the carrier catheter and the inflatable member.

HYDRAULIC DISPLACEMENT AND REMOVAL OF THROMBUS CLOTS, AND CATHETERS FOR PERFORMING HYDRAULIC DISPLACEMENT
20210386440 · 2021-12-16 ·

Clot removal from a patient's vessel, such as an artery, are described using aspiration and hydraulic forces supporting the removal process. Hydraulic forces can be generated by occluding the vessel distal to the clot and delivering liquid between the clot and the occlusive device. The aspiration catheter is positioned proximal to the clot. Catheters designed to facilitate the delivery of hydraulic forces can be based on single lumen designs or dual lumen designs. The catheters may have a fixed internal wire, or in some embodiments the catheters can ride over a wire with a valve/seal positioned to restrict flow into or out from the guide lumen such that the guide lumen can further function for balloon inflation and/or for infusion of liquid.

Gas sampling catheters, systems and methods

Embodiments herein include gas sampling catheters, systems and related methods. In an embodiment, a gas sampling catheter is included. The catheter can include a catheter shaft having a proximal end and a distal end, the catheter shaft defining a lumen therein. The catheter can include a gas sampling port providing fluid communication between the exterior of the catheter shaft adjacent the distal end of the lumen of the catheter shaft. The catheter can further include a sensor element disposed in fluid communication with the lumen, the sensor element configured to detect a component of a gaseous sample. The sensor element can include a first measurement zone comprising a plurality of discrete binding detectors. Other embodiments are also included herein.

RADIOEMBOLIZATION DELIVERY DEVICE

A delivery assembly includes a console including a vial containment region and a vial engagement mechanism extending from the console within the vial containment region. The engagement mechanism is configured to engage a vial assembly. The delivery assembly further includes a sled assembly removably coupled to the console at the vial containment region and a safety shield removably coupled to the console over the vial containment region such that the vial engagement mechanism and the sled assembly are encapsulated within the safety shield when the safety shield is coupled thereto. The sled assembly, the vial assembly, and the safety shield are configured to inhibit radioactive emissions from within the vial containment region.

STABILIZER FOR AN INSERTED CATHETER AND METHOD FOR INSTALLING THE STABILIZER
20220193374 · 2022-06-23 ·

A catheter stabilizer and a method for installing the stabilizer are especially suited to retaining a catheter in its position of insertion into the body of a patient. The stabilizer is a laminate of clear film atop double-backed adhesive preferably atop peel-off release paper. The double-backed adhesive defines a viewing window through the stabilizer. The stabilizer and method reduce preparation-of-materials steps, eliminate performance of arbitrary, awkward or inconsistently-performable installation steps, result in predictably effective catheter-to-patient connections, mitigate against the likelihoods of migration of the catheter out of the incision or expansion of the length of the incision during and after installation, create a sterile environment to the area surrounding the point of penetration of the catheter into the anatomy, extend the effective life of the installation, reduce the risks of complications and costs associated with replacement of a catheter and enable a rapid and sound installation.

Double-Lumen Percutaneous Femoral Cannula for Extracorporeal Membrane Oxygenation
20220168488 · 2022-06-02 ·

A double-lumen percutaneous femoral cannula for extracorporeal membrane oxygenation (ECMO) is an apparatus that is used to perform an ECMO procedure in non-ideal conditions. The apparatus may include at least one first cannula and at least one second cannula of different sizes that are arranged to form a single structure. By providing a single structure instead of several separate components, the apparatus makes the insertion of the apparatus easier and reduces the risk of the apparatus dislodging while the patient is being transported. The at least one first cannula and the at least one second cannula are preferably elongated tubular structures designed to prevent the recirculation of oxygenated blood. The at least one first cannula is designed to enable the aspiration of deoxygenated blood, while the at least one second cannula is designed to enable the pumping of oxygenated blood back into the body.

Split-tip catheter including lateral distal openings

A split-tip catheter for placement within the vasculature of a patient and for use in hemodialysis or other suitable procedures, and methods of use. The split-tip catheter can include a catheter body defining a first lumen and a second lumen, and a split distal region extending from a distal end of the catheter body. The split distal region can include an arterial segment defined by an outer wall enclosing an arterial segment lumen, the arterial segment lumen in fluid communication with the catheter body first lumen, and a venous segment defined by an outer wall enclosing a venous segment lumen, the venous segment lumen in fluid communication with the catheter body second lumen, the venous segment outer wall extending from the catheter body distal end to a distal nose portion. The distal nose portion can taper from a first outer perimeter to a second smaller outer perimeter.

Infusion site for improved mixing of fluids
11738132 · 2023-08-29 · ·

The present disclosure relates to a blood line (108) comprising an infusion site (145) intended to inject into the line a solution comprising: —a first main channel (200) having a first passage section, —a second main channel (220) having a second passage section, —means for the formation (210) of a turbulence area located downstream from the first main channel, located upstream from the second main channel, these formation means comprising a first fluid passage means (224) defining a reduction (225) in the passage section and whose smallest passage section is smaller than the first passage section and smaller than the second fluid passage section, —a secondary channel (230) comprising an inlet (231) for letting in the solution and an outlet (232) in fluid communication with the first main channel or the means for the formation of a turbulence area or the second main channel.