The medical device may comprise an elongate body having a proximal portion, a distal portion, and defining a lumen therethrough. Also, the medical device may include an expandable element coupled to the distal portion of the elongate body and in fluid communication with the lumen. The expandable element may define a first end and a second end, the second end being proximal to the first end. The medical device may further include a cannula surrounding at least a portion of the elongate body and the cannula may define a proximal end and a distal end. The distal end of the cannula may be disposed proximal and adjacent to the second end of the expandable element. An outer dimctcr diameter of the cannula may be substantially equal to or lesser than an outer diameter of the expandable element when inflated. The medical device may be maneuvered through a patient's body.

A double-balloon catheter device for gastrointestinal anastomosis. The double-balloon catheter device for gastrointestinal anastomosis includes a liquid injection assembly, a double-balloon assembly, and a supporting device (15) connecting the liquid injection assembly and the double-balloon assembly. The liquid injection assembly includes a first balloon liquid injection connection port (2), a guide wire connection port (3), and a second balloon liquid injection connection port (4). The double-balloon assembly includes a double-balloon catheter device (5), and includes a first balloon (6) and a second balloon (7) that can expand-and that are respectively disposed on the two ends of the double-balloon catheter device (5). The double-balloon catheter device (5) is provided with a first balloon liquid injection channel (51), a guide wire channel (52), and a second balloon liquid injection channel (53).

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.

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.

Balloon/infusion catheters comprise internal corewires within a single lumen structure in which the corewire can slide relative to the catheter tube within limits, and the balloon is attached to the catheter tube on one end and to the sliding corewire on the other end. The lumen provides fluid to inflate the balloon and to infuse fluid into the vessel proximal to the balloon. The infusion ports can have a polymer valve to limit infusion to lumen pressures at which the balloon is appropriately inflated. The balloon/infusion catheter can have an integral flow meter near its proximal end. Corresponding methods for use of the balloon/infusion catheter are described, such as for the delivery of hydraulic forces when used in conjunction with an aspiration catheter.

A medical catheter includes a multi-lumen tube including a first lumen and a second lumen; an extension tube fixed to an end surface in a longitudinal direction of the multi-lumen tube, extending from the end surface along the longitudinal direction, and including a third lumen communicating with the first lumen; and an outer wall portion extending from the multi-lumen tube along the extension tube and configured to cover a part of an outer surface of the extension tube, the outer wall portion including a pipeline formed to communicate with the second lumen and having a part of the outer surface in an inner surface of the pipeline.

An example connector for a balloon catheter assembly according to an example of the present disclosure includes, among other possible things, an inlet branch, a first outlet branch in fluid communication with the inlet branch and configured to be connected to a first balloon, a second outlet branch in fluid communication with the inlet branch and configured to be connected to a second balloon, and a valve integrated the first outlet branch. The valve has a first position and a second position. The valve is configured to limit fluid flow through the valve when in the first position. Another example connector for a balloon catheter assembly and a method of inflating a balloon catheter assembly are also disclosed.

An interventional ostium occlusion catheter includes a catheter tube with at least one port at a first end, a tip at a second end, and a central lumen, with a positioning component and an occlusion component on the surface of the catheter tube close to the tip. A method of coronary intervention using the catheter includes maneuvering the catheter to an ostium; inserting the catheter into a coronary vessel; activating the positioning component and the occlusion component; and delivering an infusion via the lumen. An interventional system for improving management of ischemic cardiac tissue during acute coronary syndromes includes the catheter; a blood infusion device that delivers controlled reperfusate; and a ventricular unloading device that manipulates myocardial oxygen demand in a coronary chamber. The operator can mitigate reperfusion-related and oxygen-related tissue injury by precisely modulating oxygen re-exposure when re-establishing flow and when using a ventricular unloading device.

A balloon catheter includes a catheter (1) and a balloon body (2) sleeved on the catheter (1). The balloon body (2) includes an inner layer balloon (21) and an outer layer balloon (22). The inner layer balloon (21) and the outer layer balloon (22) are both directly wrapped and fixed on the catheter (1). The inner layer balloon (21) is located inside the outer layer balloon (22). A medium channel (23) is formed between the inner layer balloon (21) and the outer layer balloon (22). An outer layer medium inlet hole (11) and a medium backflow hole (12) both in communication with the medium channel (23) are provided in the catheter (1). In the balloon catheter, the double-layer balloon body (2) is provided, so that a medium can flow in the medium channel (23) between the inner layer balloon (21) and the outer layer balloon (22), the medium flows into the medium channel (23) through the outer layer medium inlet hole (11), and then the medium in the medium channel (23) flows out through the medium backflow hole (12) to implement circulation. In this way, more medium can exchange heat on the inner surface of the outer layer balloon (22) and the flow rate distribution is relatively uniform, to increase the flowing quality of the medium on the surface of the balloon body, thereby improving the heat exchange efficiency.

The disclosure provides for a device and method for dilation. The dilation device may include a catheter body having a proximal portion and a distal portion, a dilation expandable body in fluid communication with a first opening on the distal portion of the catheter body, and an occlusion anchor expandable body in fluid communication with a second opening on the distal portion of the catheter body. The method for dilating a stricture site may include inserting the dilation device into a stricture site of a patient, expanding the occlusion anchor expandable body at the stricture site, and expanding the dilation expandable body at the stricture site.