Abstract: Briefly, in accordance with one embodiment, a multi-lumen shaft may be used to with an endoscopic instrument.

Abstract: Briefly, in accordance with one embodiment, a multi-lumen shaft may be used to with an endoscopic instrument.

Abstract: Briefly, in accordance with one embodiment, a multi-lumen shaft may be used to with an endoscopic instrument.

Abstract: 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.

Abstract: A system for use with an endoscopic device. The system can include a shaft having a proximal end, a distal end, and at least one output port, wherein a portion of the shaft is surrounded by a single polyurethane expandable material, wherein the polyurethane expandable material is expandable from a diameter of at least approximately 5.0 mm to a diameter of approximately 25 mm. The system can also include a manifold connected to the proximal end of the shaft, the manifold including one or more fluid coupling ports for receiving an injected fluid, wherein at least one of the one or more fluid coupling ports is in fluid communication with the at least one output port and wherein when received, the system is configured to convey the injected fluid from the manifold to the shaft resulting, at least in part, in expanding the polyurethane expandable material.

Abstract: 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.

Abstract: In various embodiments, a medical device includes an instrument head that includes two or more electrodes and a medical device tool, an impedance bridge selectively coupled to the two or more electrodes, and a processor coupled to the impedance bridge. In various embodiments, a method for controlling medical device tools comprises recording, at one or more frequencies, two or more impedance measurements, wherein each impedance measurement is associated with two or more electrodes included in an instrument head of a medical device; and determining, based on the two or more impedance measurements, a tissue type map at a location associated with the instrument head.

Abstract: A system for use with an endoscopic device. The system can include a shaft having a proximal end, a distal end, and at least one output port, wherein a portion of the shaft is surrounded by a single polyurethane expandable material, wherein the polyurethane expandable material is expandable from a diameter of at least approximately 5.0 mm to a diameter of approximately 25 mm. The system can also include a manifold connected to the proximal end of the shaft, the manifold including one or more fluid coupling ports for receiving an injected fluid, wherein at least one of the one or more fluid coupling ports is in fluid communication with the at least one output port and wherein when received, the system is configured to convey the injected fluid from the manifold to the shaft resulting, at least in part, in expanding the polyurethane expandable material.

Abstract: Briefly, in accordance with one embodiment, a tool for use with an endoscopic procedure comprises a thermoplastic polyurethane expandable vessel.

Abstract: 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.

Abstract: Briefly, in accordance with one embodiment, a tool for use with an endoscopic procedure comprises an expandable thermoplastic polyurethane vessel. The expandable vessel may be fused to a shaft and may be configured to receive a fluid from the shaft. The shaft may comprise a distal port and a proximal port configured to dispense a dye material exterior to the expandable vessel.

Abstract: Briefly, in accordance with one embodiment, a multi-lumen shaft may be used to with an endoscopic instrument.

Abstract: Briefly, in accordance with one embodiment, a tool for use with an endoscopic procedure comprises a thermoplastic polyurethane expandable vessel.

Abstract: A multi-lumen biliary catheter in which at least one of the lumens (14, 16) has a side opening port (24, 26) configured to guide a guidewire (32) out of that port at an angle to the longitudinal axis of the catheter. Radiopaque marker bands (34) having different lengths are placed on the distal end of the catheter adjacent the distal openings to facilitate fluoroscopic identification of the distal end orientation in the biliary tract.

Abstract: A biliary stent (10) is constructed of thermoplastic material with ridges (16) and valleys (18) formed along the outer surface of the stent that provide a helical, thread-like configuration. The ridges (16) and valleys (18) can be formed in a variety of configurations, depths and pitches to accommodate different delivery devices and different anatomical features of the biliary tree. The ridges (16) and valleys (18) provide additional mechanical engagement with the luminal walls of the biliary tract to prevent unwanted displacement of the implanted stent (10) from a selected implant site. The stent (10) is configured to optionally have an elongate distal end (14) to facilitate the transmission of biliary fluids through the stent (10). Optional radiopaque markers (32) are provided on one or both ends (12, 14) of the stent (10) to allow for fluoroscopic visualization of the stent (10) orientation and placement within the biliary tract.