An endoscopic peripheral includes a first end of a flexible cable including at least a camera and one or more lights enclosed by a tip at the first end. The tip is tapered for insertion of a portion of the first end into a body of a patient. The endoscopic peripheral includes one or more controls interconnected with and controlling the camera and the one or more lights. A second end of the flexible cable terminates in a plug configured to physically connect the endoscopic peripheral to an electronic device. The electronic device powers the camera and the one or more lights and displays content captured by the camera. The endoscopic peripheral is plug and play when connected to the electronic device. The diameter of the diameter of the endoscopic peripheral between the first end and the second end is approximately the same.

This patent document discloses guide extension catheters for use with a predefined length guide catheter and related methods for treating blood vessel lesions and abnormalities. A guide extension catheter can include a push member, an elongate tube member, and a balloon radially surrounding a portion of the elongate tube member. The balloon can include an inflatable tube coupled to an elongate shaft having a lumen for receiving inflation fluid, and the inflatable tube can be coiled in a helical manner around the elongate tube member. A bioactive layer can coat an outer surface portion of the balloon and, when the balloon is inflated, one or more drugs of the bioactive layer can be received by the blood vessel. Inflation of the balloon can engage the elongate tube member with an inner surface of the blood vessel and/or an inner surface of the guide catheter.

A drug delivery balloon apparatus is disclosed herein, comprising: (a) at least two lumens, comprising a first lumen and a second lumen, (b) a balloon inflation port in fluid communication with the first lumen, (c) a drug delivery port in fluid communication with the second lumen, (d) a guidewire port in fluid communication with the second lumen, wherein the second lumen is configured to receive both a guidewire and a drug solution, (e) an occlusion balloon, (f) a drug delivery balloon, where the occlusion balloon and the drug delivery balloon are in fluid communication with the first lumen, (g) one or more drug delivery channels extending the length of the second lumen, and (h) one or more drug delivery ducts extending from the one or more drug delivery channels to an exterior surface of the second lumen.

In one embodiment, the present application discloses, in part, a balloon catheter assembly comprising: a) a balloon catheter comprising a proximal end, a distal end; and b) a connecting line comprising a proximal end and a distal end, wherein the proximal end comprises a first terminal magnetic connector for forming a water tight connection with the magnetic click connector on the port panel.

A medical instrument includes a shaft, a distal-end assembly and a puller-wire. The shaft is configured for insertion into a body of a patient. The distal-end assembly, which is coupled to the shaft, includes a telescopic assembly, configured to elongate so as to collapse the distal-end assembly, and to compress so as to expand the distal-end assembly. The distal-end assembly further includes an elastic element, coupled to self-elongate and thus elongate the telescopic assembly. The distal-end assembly also includes an inflatable balloon, which is coupled to the telescopic assembly and is configured to collapse by the telescopic assembly elongating, and to expand by the telescopic assembly compressing. The puller-wire runs through the shaft and is connected to a distal end of the telescopic assembly, and is configured, when pulled, to compress the telescopic assembly.

A dilation catheter system includes a body, a guidewire, and a dilation catheter having an elongate shaft. The dilation catheter system may include a locking mechanism to prevent the guidewire from moving relative to the elongate shaft or to lock the guidewire to the dilation catheter to form a fixed wire unit. The dilation catheter system may include a stabilizing tube extending from an actuator, to provide rigidity to the guidewire. The dilation catheter may include a grip element having a plurality of grip features disposed thereon. The dilation catheter may include a cap biased toward a first longitudinal position and movable to a second longitudinal position. A guide catheter secured to the cap is prevented from changing angular orientation in the first longitudinal position and is free to change angular orientation in the second longitudinal position.

This patent document discloses guide extension catheters for use with a predefined length guide catheter and related methods for treating blood vessel lesions and abnormalities. A guide extension catheter can include a push member, an elongate tube member, and a balloon radially surrounding a portion of the elongate tube member. The balloon can include an inflatable tube coupled to an elongate shaft having a lumen for receiving inflation fluid, and the inflatable tube can be coiled in a helical manner around the elongate tube member. A bioactive layer can coat an outer surface portion of the balloon and, when the balloon is inflated, one or more drugs of the bioactive layer can be received by the blood vessel. Inflation of the balloon can engage the elongate tube member with an inner surface of the blood vessel and/or an inner surface of the guide catheter.

A purpose is to enable partial replacement of an indwelling urethral catheter. A unit for a balloon catheter according to the present invention includes a urethral catheter tube (13) provided with a first urethral catheterization passage (14), a branch tube (11) provided with a first passage (12) adapted to allow passage of a liquid used to inflate or deflate a balloon (54), and a connecting tube (30) configured to be connected at one end to the first urethral catheterization passage (14) or the first passage (12).

A functionally integratable catheter system comprising functional units that can be assembled to produce different configurations. The functional units include: one or more FICS support catheters; one or more FICS dilators: one or more FICS PTA catheters; and one or more FICS lock-grip handles. Functional units can be provided in a pre-assembled form by the manufacturer, optionally pre-packaged as a device tray, for assembly into different configurations by clinical operators. The configurational adaptability of the FICS platform enables physicians to efficiently address multiple procedural aspects of treatment processes, including lesion access, lesion penetration, guide-wire negotiation, lesion recanalization, and dilation, by providing in situ treatment options, including intraluminal and/or extraluminal recanalization, and enables multi-stage, patient-customized treatments of complex lesions in vivo, including lesion-length-selective, multi-stage angioplasty treatment.

The present invention provides a stretchable material suitable for use in an inflatable medical device. The stretchable material has at least one reinforcing polymer layer with a top and bottom side forming a porous matrix which is imbibed with a sealing material to infiltrate and substantially seal spaces of the porous matrix and extend beyond the reinforcing polymer layer to form a surface coating.