Abstract: A thrombectomy system includes an inner catheter, an outer catheter, an adjustable basket, and at least one debulking element. The outer catheter defines an outer catheter lumen. The inner catheter is slidably received within the outer catheter lumen such that the inner catheter is slidable relative to the outer catheter. The adjustable basket has a fenestrated structure extending between a proximal collar and a distal collar. The proximal collar is attached to a distal end of the outer catheter and the distal collar is attached to a distal end of the inner catheter. The at least one debulking element is positioned on the outer catheter proximal to the adjustable basket. The fenestrated structure is radially expanded by sliding the inner catheter in a first direction relative to the outer catheter and is radially collapsed by sliding the inner catheter in a second direction opposite the first direction.

Abstract: A thrombectomy guidewire system includes a thrombectomy guidewire having a wire shaft with a proximal portion and a distal portion, the wire shaft is sized for receiving and delivering guidewire deliverable intravascular thrombectomy devices. The thrombectomy guidewire includes a self-expanding basket positioned at the distal portion of the wire shaft and configured to self-expand from a collapsed configuration to an expanded configuration. A exchange sheath includes a first lumen configured to slidably receive the wire shaft and a second lumen aligned with the central lumen. The exchange sheath is slidable in a distal direction over the wire shaft from the proximal portion of the wire shaft at least until the self-expanding basket is sheathed within the central lumen and collapsed into the collapsed configuration.

Abstract: A thrombectomy assembly includes a sheath catheter having a sheath lumen and a trumpet catheter including a trumpet lumen. The trumpet catheter is received in the sheath lumen. A manipulation controller is coupled with the trumpet catheter and the sheath catheter. The manipulation controller includes a sheath actuator coupled with the sheath catheter and a catheter lock. The catheter lock includes a deformable collet having a collet passage configured to receive a capture catheter therein. The sheath actuator is configured to move the sheath catheter between a deployed configuration with the sheath actuator retracted from a deployable trumpet of the trumpet catheter and a stored configuration with the sheath actuator covering the deployable trumpet. The deformable collet is configured to transition between a locked configuration with the deformable collet compressed around the capture catheter and an unlocked configuration with the deformable collet expanded around the capture catheter.

Abstract: Catheters and methods for supporting a guidewire or delivering a radiopaque, diagnostic or therapeutic agent through a vessel stenosis or other tortuous anatomy are disclosed. A catheter can comprise an elongate shaft body and a tip member disposed at a distal end of the shaft body. The shaft body can extend from a proximal end to the distal end and can define an inner lumen. The shaft body can include a liner, a braid member surrounding the liner, a multi-layer coil surrounding the braid member, and a polymer cover surrounding the multi-layer coil. An outer surface portion of the polymer cover can include one or more helical threads, which can be enveloped in an outer wrapper. The tip member can be made from a metal or a polymer. Polymer tip members can include a hard or semi-hard distal tip.

Abstract: Catheters and methods for supporting a guidewire or delivering a radiopaque, diagnostic or therapeutic agent through a vessel stenosis or other tortuous anatomy are disclosed. A catheter can comprise an elongate shaft body and a tip member disposed at a distal end of the shaft body. The shaft body can extend from a proximal end to the distal end and can define an inner lumen. The shaft body can include a liner, a braid member surrounding the liner, a multi-layer coil surrounding the braid member, and a polymer cover surrounding the multi-layer coil. An outer surface portion of the polymer cover can include one or more helical threads, which can be enveloped in an outer wrapper. The tip member can be made from a metal or a polymer. Polymer tip members can include a hard or semi-hard distal tip.

Abstract: Catheters and methods for supporting a guidewire or delivering a radiopaque, diagnostic or therapeutic agent through a vessel stenosis or other tortuous anatomy are disclosed. A catheter can comprise an elongate shaft body and a tip member disposed at a distal end of the shaft body. The shaft body can extend from a proximal end to the distal end and can define an inner lumen. The shaft body can include a liner, a braid member surrounding the liner, a multi-layer coil surrounding the braid member, and a polymer cover surrounding the multi-layer coil. An outer surface portion of the polymer cover can include one or more helical threads, which can be enveloped in an outer wrapper. The tip member can be made from a metal or a polymer. Polymer tip members can include a hard or semi-hard distal tip.

Abstract: Catheters and methods for supporting a guidewire or delivering a radiopaque, diagnostic or therapeutic agent through a vessel stenosis or other tortuous anatomy are disclosed. A catheter can comprise an elongate shaft body and a tip member disposed at a distal end of the shaft body. The shaft body can extend from a proximal end to the distal end and can define an inner lumen. The shaft body can include a liner, a braid member surrounding the liner, a multi-layer coil surrounding the braid member, and a polymer cover surrounding the multi-layer coil. An outer surface portion of the polymer cover can include one or more helical threads, which can be enveloped in an outer wrapper. The tip member can be made from a metal or a polymer. Polymer tip members can include a hard or semi-hard distal tip.

Abstract: Described herein is a process and apparatus for the production of an article made of moulded plastic material including a first component formed in a first step of injection and possible compression, and at least one second component overmoulded on said first component in a second step of injection and possible compression step. The two steps of injection and possible compression are carried out within the same moulding cavity defined between a mould and a countermould in a single station, without any need for displacing the countermould into a second station.