A multi-lumen implantable device configured to deliver a therapeutic agent to a selected portion of a blood vessel is disclosed. As one example, an implantable device includes a first lumen configured to flow blood from an upstream end to a downstream end of the device when implanted in a blood vessel; a second lumen fluidly separated from the first lumen and configured for introducing a therapeutic agent to a selected, first portion of a wall of the blood vessel, between the upstream end and the downstream end of the device; and at least one sealing member configured to block the therapeutic agent from entering a second portion of the wall of the blood vessel, between the upstream end and the downstream end of the device.

A hemostatic device is disclosed. The hemostatic device according to an embodiment of the present invention includes: a balloon which is expanded by a fluid supplied therein; a blood discharge pipe which includes a blood inflow hole at one end and exposes the other end to a lower side of the balloon wherein a certain section of a lower side of the blood inflow hole is surrounded by the balloon; and a fluid flow pipe communicating with the inside of the balloon for supplying or discharging the fluid and extending to a lower side of the balloon. The balloon includes a plurality of protrusions that are formed to protrude outward when the balloon is expanded by the fluid.

A catheter for isolating a region in a hollow organ of a mammal, having an elongate body designed to be inserted into a lumen of a mammal hollow organ and equipped with two balloons, the balloons being configured to be inflated to isolate an interior of the hollow organ therebetween; wherein a functional channel extending in the body has a functional opening provided in the body between the balloons; and wherein the functional channel is designed to allow a negative pressure to be produced in the isolated interior to take a biological fluid or biological gaseous medium therefrom or to allow a liquid or gaseous medium to be supplied to the isolated interior; and wherein another channel extending in the body is provided at opposite ends with an inlet and an outlet provided both in the body outside of the body part defined by the balloons.

A system for delivering a fluid to a Eustachian tube (ET) of a patient includes a guide member and a tubular member. The guide member includes a shaft having a proximal portion, a distal portion, and a bend at the distal portion. The bend is configured to provide access to an opening in the ET. The system further includes a tubular member comprising a proximal end, a distal end, and a lumen extending therebetween. The tubular member is sized to fit within the ET. One or both of the tubular member and the guide member comprises a first stop member configured to engage the other of the tubular member or the guide member. The first stop member is configured to restrict a distal advancement of the tubular member relative to the guide member.

A surgical apparatus for treating a blood clot in a vessel of a patient having an elongated member having an outer wall, a first hole at a distal portion and a second hole spaced proximally from the first hole positioned in a side wall. A first lumen is provided within the elongated member for blood flow through the second hole, through the lumen and exiting the first hole to maintain blood flow during treatment of the blood clot. An energy emitter emits energy to the blood clot or hardenings and a connector connects the energy emitter to an external energy source, wherein blood flows into the second hole positioned proximal of the blood clot and exits the first hole distal of the blood clot during activation of the energy emitter. In some instances when the apparatus is introduced from a retrograde ‘upstream” approach blood may flow through the device in the opposite direction.

A surgical apparatus for treating a vessel blockage in a vessel of a patient having an elongated member having an outer wall, a first hole at a distal portion and a second hole spaced proximally from the first hole positioned in a side wall. A first lumen is provided within the elongated member for blood flow through the second hole, through the lumen and exiting the first hole to maintain blood flow during treatment of the vessel blockage. A motor driven impeller is rotatable during blood flow through the first lumen to enhance blood flow as blood flows into the second hole positioned proximal of the vessel blockage and exits the first hole distal of the vessel blockage during injection of fluid through one or more openings to treat the vessel blockage.

In one representative embodiment, a method of perfusing organs in a patient's body is provided. The method comprises isolating the visceral arteries and the visceral veins from blood circulating through the patient's heart and perfusing the visceral arteries, the visceral veins, and the abdominal organs with a perfusion fluid that is fluidly separated from the blood circulating through the patient's heart. While the visceral arteries and the visceral veins are isolated, and the visceral arteries, the visceral veins, and the abdominal organs are being perfused, the patient's blood is allowed to continue to circulate through the heart.

A catheter devices/systems and methods therefrom are described herein for treating acute kidney in-jury, especially the contrast-induced acute kidney injury wherein the devices prevent the contrast dyes from entering into kidney and/or facilitate blood flow of kidney by said catheter system.

A balloon catheter assembly is disclosed. A balloon catheter assembly comprising a proximal part, a middle part, an inflatable balloon and a long tip located at proximal end. The distal end comprising a port for inflation and middle part is connecting member extended from the proximal part end to distal part end. The middle part comprises of three lumens which is extended up to long tip (1) the inner most lumen permit use of a guidewire, (2) a middle lumen is for inflation and deflation of inflatable balloon through proximal part and (3) an outer lumen is comprises of plurality of holes. The plurality of holes of outer lumen spacedly located before and after of the inflatable balloon. The outer lumen hole of is expandable upon starching outer lumen allow to pass blood continuously.

A method and devices for mitigating the risk of limb ischemia includes inserting a femoral arterial cannula into a femoral artery of a limb, the femoral arterial cannula having a low-profile balloon to seal the femoral artery. Once in situ in the femoral artery, the femoral arterial cannula balloon is inflated to seal said femoral artery to deliver blood flow in a retrograde direction to said limb while simultaneously delivering systemic arterial blood flow. A femoral venous cannula is also inserted into a femoral vein of said limb, the femoral venous cannula having a broad-profile balloon to seal the femoral vein. Once in situ in said femoral vein, the femoral venous cannula balloon is inflated to seal the femoral vein to drain venous blood flow from the limb while simultaneously draining systemic venous blood flow.