Hemostasis valves and methods for making and using hemostasis valves are disclosed. An example hemostasis valve may include a main body having a proximal end region. A cartridge may be at least partially disposed within the proximal end region. The cartridge may include a seal member. The seal member may be designed to shift between an open configuration and a sealed configuration. A plunger, having an inner tubular region and a distal end, may be coupled to the proximal end region of the main body. The distal end of the inner tubular region may be spaced a clearance distance from a proximal end of the seal member so that when the seal member is in the sealed configuration and exposed to pressures of 80-250 pounds per square inch, the seal member deflects into contact with the distal end of the inner tubular region and remains in the sealed configuration.

Medical devices and methods for controlling the flow of fluid from wounds are disclosed herein. The medical device can have an adhesive pad defining a catheter-receiving opening, a flexible elongate tensioner, and a tensioner retainer. The tensioner retainer is configured to hold the flexible elongate tensioner such that the adhesive pad applies sufficient pressure to a subject's skin to press the subject's tissue toward a catheter when the catheter is positioned in the catheter-receiving opening and the adhesive pad is adhered to the subject's skin.

In a sheath device for inserting a catheter into a patient's body, comprising a first sheath (10, 11, 13, 21, 21, 21, 41, 43) having a proximal end and a distal end, wherein when used as intended the distal end of the first sheath is provided for arrangement in the patient's body and the proximal end of the first sheath is provided for arrangement outside the patient's body, and wherein the first sheath comprises a tubular section (11, 21, 21, 21, 41) and a sheath housing (13, 43), which is disposed at the proximal end of the section and comprises a receiving channel (46) for a catheter, according to the invention the tubular section (11, 21, 21, 21, 41) is detachably held in a clamping element (45, 48, 50, 62, 63, 64) of the sheath housing in a non-positive manner so as to be able to easily shorten the tubular section.

A trocar assembly includes a trocar that includes a trocar housing and a cannula that extends distally from the trocar housing, and an integral seal system positioned within a central passageway extending axially through the trocar and engageable against a surgical tool shaft extended therethrough. The integral seal system includes an asymmetric seal and a duckbill seal arranged distal to the asymmetric seal, and the asymmetric seal defines a diaphragm that complements insertion and extraction drag forces generated by the duckbill seal against the surgical tool shaft such that total insertion and extraction drag forces generated by the integral seal system are equalized.

A valve actuator that moves in a catheter assembly between a first position where a valve is closed and a second position where the valve is open, the valve actuator including a shaft portion at a distal end of the valve actuator that is configured to pierce the valve, a mating portion at a proximal end of the valve actuator that is configured to engage a Luer device, a diameter reduction region that connects the shaft portion and the mating portion, and a plurality of windows that extend through the valve actuator for flushing fluid, the plurality of windows being disposed in the diameter reduction region, wherein each of the plurality of windows does not extend a full length of the diameter reduction region.

A hemostasis valve includes a housing having a central bore therethrough, a compression tube positioned within the central bore, a soft annular elastomeric seal positioned within the central bore distal to the compression tube, and at least one actuator coupled to the housing. Movement of the actuator relative to the housing may move the compression tube towards or away from the annular elastomeric seal to increase adjust the inner diameter of the annular elastic seal. The large-bore hemostatic valves described herein may be particularly well suited for use with controllably adjusting the seal pressure around a medical device (e.g., catheter) inserted through the valve and may maintain a tight seal at high pressure and with large diameter medical devices.

The fluid delivery devices, systems and methods described herein include a subcutaneous port, a catheter, and a connection assembly configured to fluidly couple the port and catheter.

Deflectable catheters, hemostasis valves, and materials for the same are disclosed. The deflectable catheters and hemostasis valves can be made at least partially, if not entirely, from a fluoroelastomer and ePTFE combination. A deflectable region of the catheters can be articulated to form simple and/or complex curves.

The present disclosure provides at least one hemostasis valve, an introducer, and a retrieval device. The hemostasis valve may include a sealing member, a pressing assembly and a rotary motion assembly. The sealing member may be configured to define a sealing cavity which is transversely contractible. The pressing assembly is disposed at an outer periphery of the sealing member. The pressing assembly is configured for linear motion in a transverse direction of the sealing cavity to change a dimension of the sealing cavity. The rotary motion assembly is coupled to the pressing assembly, and the rotary motion assembly may be configured to convert rotary motion into the linear motion of the pressing assembly through the coupling. The hemostasis valve of the present disclosure can perform active hemostasis sealing for one or more medical devices and is convenient to use.

A catheter is provided with a collection chamber located between a seal and a cap. The seal is located distal from the collection chamber, and the cap is located proximal from the collection chamber. The seal may be opened and closed to alternately allow the passage of material into the collection chamber and prevent fluid from escaping from the shaft lumen. The cap may be opened and closed to allow the removal of a mass from the collection chamber and to prevent fluid from escaping during collection of the mass.