A medical device includes a steering element defining a passage for a guide wire. A fluid injection tube defining a proximal and a distal end is also included, wherein a portion of the fluid injection tube is contoured about a portion of the steering element. A plurality of injection ports may be disposed in the portion of the fluid injection tube contoured about the steering element.

An inflation device for selectively inflating a balloon of a surgical instrument including a syringe, a connector, a mechanical pressure indicator, and a relief port. The syringe includes a plunger slidably disposed within a barrel. The connector fluidly connects an outlet of the syringe with a surgical instrument balloon to establish a closed inflation system between the syringe and an interior of the balloon. The mechanical pressure indicator is associated with the syringe and configured to transition from a non-alert state to an alert state when a pressure of the inflation system has reached a predetermined level. The relief port is associated with the mechanical pressure indicator and configured to relieve a pressure of the inflation system when the system at least reaches the predetermined level.

A system and method for controlling the inflation, ablation, and deflation of a balloon catheter. The system includes a balloon catheter, a console, a pressurized gas or liquid inflation source, and an umbilical system to deliver pressurized coolant to the balloon catheter. The system may include controller that monitors the amount of pressure and volume within the balloon catheter. During inflation, the pressure and/or volume of fluid within the balloon is maintained at a target amount in order to provide sufficient mechanized pressure against the desired target region. The system limits the inflation pressure such that a safe quantity of gas would be released should a leak occur. If the amount falls below a certain threshold level, gas or fluid egress is presumed and the inflation process is halted.

An apparatus for cutting a wall of a vessel (V), such as scoring or slicing a lesion (L) associated therewith. The device includes a cutter (10) with a single shaft (12) having a branched portion including at least two radially expandable arms. A first (16) of the expandable arms includes at least one blade (20) for slicing or scoring the lesion (L) when expanded. A second (18) of the expandable arms may also include a blade (20), or may have no blade. A sheath (S) may also be provided. The arm or arms with blades may also include a limiter (22) for limiting the cutting depth of the blade (20). An anchor may also be provided for anchoring the cutter (10) in the vessel (V).

An anchoring and non-occluding intravascular device including a guide catheter and an anchor supporting structure disposed on the guide catheter and deployable from a contracted state to an enlarged state having an enlarged outer diameter relative to that while in a contracted state. In both the contracted and in the enlarged state the anchor supporting structure is configured to allow passage of blood distally beyond the anchor supporting structure; and the anchoring is provided exclusively by the anchor supporting structure. In use, prior to capture and retrieval of a clot within a vessel, the anchor supporting structure being deployed from the contracted state to the enlarged state. While in the enlarged state, the deployed anchor supporting structure anchoring in place the guide catheter in the vessel while still allowing blood flow through the vessel distally beyond the deployed anchor supporting structure.

A system for extracting plaque from a cavity of a vasculature can include a balloon guide catheter (BGC) and an adjustable plaque displacement apparatus. The BGC can include a BGC distal end, an expandable proximal balloon, an inflation lumen extending through the BGC and including a first opening. The BGC can further include a device delivery lumen and a second opening positioned distal to the expandable proximal balloon. Also, the BGC can include an inner tube extending through the device delivery lumen. The inner tube can include a tube distal end, an expandable distal occlusion element positioned approximate the tube distal end and movable to exit the second opening. Turning to the adjustable plaque displacement apparatus, the adjustable plaque displacement apparatus can be positioned within the device delivery lumen and movable in at least one of a longitudinal and rotational direction in relation to the BGC.

The present application provides an electrode catheter system, comprising an interventional catheter for intervening to one side of an artery blood vessel and provided with an electrode element that can release an electrical signal toward an inner wall of a renal artery blood vessel; a pressure sensor for intervening to an artery blood vessel; and a data processing module, connected with the pressure sensor. The electrode element releases an electrical signal toward the inner wall of the renal artery vessel, and then the pressure sensor monitors a blood pressure change in the renal artery vessel at the other side. A data processing module processes the data monitored by the pressure sensor and determines the blood pressure change, and an activity degree of the nerve can be determined by measuring a signal such as the blood pressure of the human body, so as to screen out the patients with an overactive sympathetic nerve, and a surgical effect of a denervation surgery can also be evaluated before or after the surgery, and can be used to determine whether to perform an ultrasonic ablation again.

An ablation system for treating atrial fibrillation in a patient comprises an elongate shaft having proximal and distal ends, a lumen therebetween and a housing adjacent the distal end of the elongate shaft. An energy source is coupled to the housing and is adapted to deliver energy to a target tissue so as to create a zone of ablation in the target tissue that blocks abnormal electrical activity thereby reducing or eliminating the atrial fibrillation in the patient. A sensor is adjacent the energy source and adapted to detect relative position of the energy source to the target tissue or characteristics of the target tissue. The system also has a reflecting element operably coupled with the energy source and adapted to redirect energy emitted from the energy source in a desired direction or pattern.

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.

A cannula comprising a plastic tube having three longitudinal chambers, including a main chamber, a first lateral chamber and a second lateral chamber, and at least one reinforced section ensuring constant internal diameter, wherein the cannula is equipped from the distal side with a round end narrowing towards the end, in which there are longitudinal holes of a size enabling free venous blood flow, and a balloon. A fragment of the reinforced tube section located below the balloon is bent under an angle α of approximately 90°. From the proximal side, the tube ends with a flexible cone, sealing the cannula tightly, inside which there is a valve closing the main chamber and a port for inflating the balloon connected to the first lateral chamber.