A stent for use in the nasolacrimal duct of a patient's eye. The stent is used to maintain and improve the patency of the nasolacrimal duct The stent uses a hollow shaft to create a fluid pathway from the punctum to the inferior meatus. Either the superior or inferior punctum can be selected for insertion of the stent. An inserter is used to position the flexible stent into position. A guidewire attached to the inserter is removed from the stent and it transforms from its collapsed state to its deployed state. A first anchor stabilizes the proximal end of the stent to the punctum and ampulla. A second anchor stabilizes the proximal end of the stent near the interior meatus. The second anchor can take any of several deployed shapes, such as a pigtail or fins.

A torque device that has good manual operability and rather easily attaches to an elongated body such as a guide wire. A torque device for holding an elongated body comprises a first member and a second member in which is formed a connected space through which the elongated body can be inserted in the length direction. The first member and the second member are able to rotate with each other in a state in which the elongated body is being held, and have an opening that allows the space to communicate with the outside in the radial direction. At least one of the first member and the second member has a diameter decreasing portion that reduces the diameter of the space as a result of the first member and the second member rotating with each another.

An IV device assembly may include a lumen forming a fluidic channel within the IV device assembly. The lumen may be fluidically coupled to a vascular access device (VAD) coupler via a funnel coupler, and an IV device assembly coupler at a proximal end of the lumen. The IV device assembly may also include one or more of the following: a collapsible sleeve formed coaxially around a first portion of the lumen and mechanically coupled to the funnel coupler, a patency instrument formed along a second portion of the lumen within the collapsible sleeve and into the VAD coupler, a translation handle that translates the patency instrument out of a distal end of the VAD coupler, and a fixed grip formed around the lumen to maintain a position of the IV device assembly relative to the translation handle.

A protective assembly having a protective sheath assembly with a tubular catheter body with a proximal and distal end, and at least one connection fitting at the proximal end; and a holding device assembly with a housing, an introducer tip, a retention device. The tubular catheter body provided graduated marks or a moveable marker to identify depth of penetration. The protective assembly can deliver anesthetic to a tract, and serve as a protective sheath for medical devices.

An IV device assembly may include a lumen forming a fluidic channel within the IV device assembly. The lumen may be fluidically coupled to a vascular access device (VAD) coupler via a funnel coupler, and an IV device assembly coupler at a proximal end of the lumen. The IV device assembly may also include one or more of the following: a collapsible sleeve formed coaxially around a first portion of the lumen and mechanically coupled to the funnel coupler, a probe formed along a second portion of the lumen within the collapsible sleeve and into the VAD coupler, a translation handle that translates the probe out of a distal end of the VAD coupler, and a fixed grip formed around the lumen to maintain a position of the IV device assembly relative to the translation handle.

A guide wire safety device for preventing retained guidewire events comprises a mainbody component located between a Luer hub component for connection to a Luer hub and a locking sleeve component for connection to a catheter, wherein the main body component houses a means for gripping a guidewire.

A guide wire deployment system that can be utilized as a pre-surgical procedure without the need for radiology imaging. The clip marker would include light and sonic sensors to determine angular orientation and distance from the needle. Wireless communication between the handheld insertion device and the clip marker would provide information to guide the needle to the clip marker location. The guide wire would then be pushed from the needle and laid in a path to outside the patient.

A manipulator, including an elongated chassis containing a U-shaped channel defining a distal direction and a proximal direction. The manipulator also includes an adjuster that is configured to slide in the U-shaped channel. The adjuster includes a first wheel which on rotation translates a guidewire positioned in the adjuster along an axis of the guidewire, and a second wheel which on rotation rotates the guidewire positioned in the adjuster about the axis of the guidewire. The adjuster also includes a port, distal to the first and the second wheel, that is configured to accept a tubular balloon and the guidewire.

Disclosed is a guide wire joint, comprising: a first cover board (1), a second cover board (2), a connecting part (3) connecting the first cover board and the second cover board, and a connecting piece (4); the connecting piece (4) can connect the guide wire joint to a medical device; a side of the first cover board (1) and a side of the second cover board (2), both are away from the connecting part (3), are contacted with or separated from each other to adjust closing and opening of the guide wire joint. When the guide wire joint is closed, a guide wire passage (10) is formed between the first cover board (1) and the second cover board (2) allowing the guide wire to pass through and penetrate into a guide wire cavity of a medical device having a C-shaped groove; and when the guide wire joint is opened, the guide wire can be rapidly detached from the guide wire joint, and can be rapidly separated from the medical device.

The present teachings provide a delivery catheter with a deflectable tip and the deflection angle of the deflectable tip can be accurately controlled. Specifically, the delivery catheter includes a deflectable distal tip operably coupled to a pull wire, an elongated catheter portion, and a control mechanism. The control mechanism is configured to activate a rapid transformation of the deflectable tip from its linear profile to its curved profile. The control mechanism further includes a linear actuation mechanism. Such linear actuation mechanism converts a rotation motion of the control mechanism to a precise linear motion, which in turn accurately controls the bend angle of the deflectable tip of the delivery catheter. Such control mechanism can be used in applications that require the control of the distal deflection of the catheter, such as EP catheter, trans-septal device, and other devices.