A system and method for coating an expandable member of a medical device comprising a support structure to support the expandable member and a dispenser positioned with at least one outlet proximate a surface of an expandable member. A drive assembly establishes relative movement between the at least one outlet and the surface of the expandable member to apply fluid on the surface of the expandable member along a coating path. A guide maintains a substantially fixed distance between the at least one outlet and the surface of the expandable member during relative movement therebetween by displacing the expandable member relative to the at least one outlet.

A parison for being blow molded into a medical balloon for a catheter includes a first tubular layer having a functional modification and a second tubular layer adapted for bonding with the first tubular layer to form the blow molded balloon. Related methods are disclosed.

A catheter (10) for introduction into a body vessel includes a shaft, a balloon (12) positioned at the distal end of the shaft, and at least one scoring wire (30) to score a vascular lesion. A distal end portion of the scoring wire is detachably connected to the catheter, such as by way of magnetic coupling (30a), thereby allowing for selective use of the catheter in a scoring or non-scoring configuration. The balloon expands when fluid is delivered to the balloon through an inflation lumen. This expansion pushes the scoring wire against the vascular lesion.

A balloon in which a rupture in a circumferential direction can be prevented from occurring, and a method of manufacturing the same is disclosed. The balloon is configured to be arranged on a medical catheter, and includes a dilatable cylindrical portion formed with a birefringent polymer material. A ratio of the number of orientation distributions, calculated by dividing the number of orientation distributions of the cylindrical portion in a circumferential direction by the number of orientation distributions of the cylindrical portion in an axial direction, is less than 2.

The invention relates to a coated balloon catheter with a catheter substrate and a coating on the catheter substrate. The coating comprises a pharmaceutically active ingredient embedded in a binder matrix. The binder matrix consists of a polyethylene glycol-polyvinyl alcohol copolymer (PEG-PVA copolymer) and optionally shellac or a shellac derivative and additional pharmaceutically acceptable additives. A composition for coating the balloon catheter comprises the pharmaceutically active ingredient and a binder consisting of a PEG-PVA copolymer and optionally shellac or a shellac derivative. The active ingredient and the binder are dissolved in a solvent consisting of water, DMSO and at least one additional organic solvent indefinitely miscible with water.

In some examples, a medical device includes a balloon inflatable to an inflated configuration. The balloon includes an outer layer coextruded on an inner layer. The outer layer has a maximum radial ratio that is lower than that of the inner layer.

An expandable medical balloon, comprising a balloon, the balloon comprising a cone portion, a waist portion and a body portion and a fiber braid disposed along the cone portion, the waist portion and the body portion of the balloon, the fiber braid comprising a first fiber and a second fiber that is different than the first fiber, the first fiber comprising a polymer material having a first melting temperature and the second fiber is a non-melting fiber.

Textile balloon catheters, textile sleeves useful in balloon catheters, and methods of making balloon catheters are described. An example catheter includes an elongate shaft and a balloon movable between uninflated and inflated configurations, and a textile sleeve secured to the balloon. The textile sleeve has a plurality of warp threads and at least one weft thread extending circumferentially around the balloon. Circumferential loops in the portion of the textile sleeve that is secured to the body of the balloon are larger in diameter than circumferential loops in the portion of the textile sleeve that is secured to one or more of the proximal neck, distal neck, proximal cone and distal cone portions of the balloon.

A medical assembly includes a balloon expandable endoprosthesis comprising a plurality of ringed stent elements flexibly connected to each other via at least one flexible connector, the endoprosthesis being deployable from an undeployed state with an undeployed diameter to a deployed state with a deployed diameter. The medical assembly further includes a catheter assembly comprising a balloon, and a cover along the balloon. The endoprosthesis is coaxially located about the balloon and the cover. One or more portions of the balloon and the cover reach an intermediate diameter between the undeployed diameter and the deployed diameter in which the portions of the balloon and the cover are inflated by increasing an inflation pressure within the balloon and approximately maintained at about the intermediate diameter until the inflation pressure increases by at least 1 atmosphere to overcome a yield strength of the cover.

Described here are systems and methods for delivering an active agent to target tissues of the ear, nose, or throat using an expandable member having drug crystals layered thereon, and methods for manufacturing such systems. The expandable member can be delivered to the target tissues in a low-profile configuration and expanded to contact and/or dilate surrounding tissue. Expansion of the expandable member transfers the drug crystals to the target tissues, which then act as an in situ depot that enables maintenance of a therapeutic level of an active agent for a desired time period after removal of the expandable member. Multiple expansions of a single expandable member can be employed during treatment. For example, the systems and methods can be useful when it is desired to treat multiple paranasal sinuses with a single expandable member.