Disclosed are introducer components, assemblies, and methods. For example, an introducer assembly can include a fluidly connected syringe and needle. The needle can include a needle shaft and a needle hub over a proximal portion of the needle shaft. The needle hub can include a port and a valve disposed in the port. The port can be in a side of the needle hub proximal of a proximal end of the needle shaft. The valve can be configured to form a fluid-tight seal around an elongate medical device such as an access guidewire when passed through the port and into a needle-hub lumen of the needle hub. Such an access guidewire can be disposed in the introducer assembly just proximal of a needle tip of the needle. In this way, the access guidewire can be immediately advanced into a blood-vessel lumen upon establishing a needle tract thereto with the needle.

A torque device useable in some embodiments in an endovascular procedure. The torque device is connectable to catheter end to provide an interlocked torque-device/catheter that can be mounted to, and slid over, a guidewire as a unit. A spring arm extends from a main body section of the torque device and can be depressed into the main body section so that the spring arm and main body section can be secured in position with respect to each other. In one embodiment, the depressed spring arm and main body section are mountable to an end of a catheter to secure them in position and to the catheter. Alternatively, the torque device can be mounted to a guide wire by depressing the spring arm, and releasing the spring arm can cause torque device to grip the guide wire and allow the operator to turn or move the torque device and gripped guide wire. Some embodiments provide a torque device through which material may be injected into a catheter to which the torque device is connected.

An access device may be provided that includes a hub configured to improve the flow of blood within a lumen, in order to prevent, e.g., thrombus formation, while also avoiding hemolysis. The hub may have a removably attachable second arm, protrusions/depressions with the lumens of the hub or system, and/or plugs or plug analogs may be used to prevent flow from entering certain regions of the lumens within the hub. These hubs may be used, e.g., as part of an access device, which may have a modular configuration.

An access port can be connected to a catheter and includes a port body including a liquid storage portion and a diaphragm body covering the liquid storage portion. The port body includes a connection passage connected to the liquid storage portion and allows the liquid storage portion to communicate with the inside of the catheter. In the cross-section along the axial direction of the connection passage at the connection position where the connection passage is connected to the liquid storage portion, the length in the direction perpendicular to the axial direction between the surface of the diaphragm body on the side opposite to the liquid storage portion and the inner surface of the liquid storage portion gradually decreases as it proceeds away from the connection position in the inclined region exceeding half of the liquid storage portion along the axial direction.

A hemostasis seal member for a medical device, the seal member comprises a cylindrical main body portion having a proximal face, a distal face, and a peripheral surface face extending between the proximal and distal faces, the main body portion having a first diameter, and a radial sealing feature extending radially inward or outward from the peripheral surface and configured to sealingly engage an inner cylindrical surface of a hemostasis valve housing. The radial sealing feature comprises a radial projection extending radially outward from the peripheral surface, or a concave recess extending radially inward from the peripheral surface.

An elongated medical catheter body, which may constitute an introducer sheath includes: a catheter body; a hub fixed to a proximal portion of the catheter body; and a support member connected to the hub and configured to cover of the proximal portion of the catheter body. The catheter body includes a groove on the outer surface of the catheter body, and the support member is disposed so as to partially cover the groove. The support member includes a drug part having a drug solution, and a partition wall portion is located between the drug part and the groove, and the partition wall portion is configured to make the drug part communicate with the groove portion upon being broken by pressure or by causing damage.

The disclosure relates to a subcutaneously implanted port device for establishing access to the vascular system of a patient requiring multiple blood treatments over an extended period of time. The systems, devices and methods disclosed herein may reduce miscannulation, promote intra-session hemostasis, and decrease the incidence of bacteremia and sepsis among other improvements and advantages. The devices include a port with a tapered seat for receiving an access tube, the first tapered seat having a proximal portion, a distal portion, and a conical section extending between the proximal portion and the distal portion; and an interface surface configured to engage a blood vessel or a vascular access catheter. The proximal portion of the tapered seat is configured to receive the access tube therethrough, and the tapered seat creates a mismatch fit with a diameter of the access tube when in use for an increase in flow during treatment.

An instrument advancement device may include a housing, which may include a distal end and a proximal end. An instrument, such as a vascular access instrument configured to enter vasculature of a patient, may be disposed within the housing. The instrument advancement device may include an advancement element. In response to movement of the advancement element with respect to the housing, the instrument may be configured to advance distal to the distal end of the housing. The housing or a distal end of the housing may include a compressible portion proximate a chamber configured to hold blood. In response to compression of the compressible portion, the housing may be configured to dispense blood distally from the chamber through the distal end of the housing.

A system for facilitating instrument delivery through a peripheral intravenous catheter may include a catheter adapter having a proximal end, a distal end, and a lumen extending there through. The catheter adapter may include a side port. The system may include an extension tube extending from the side port. The system may include a blood control valve disposed in the lumen of the catheter adapter. The system may include a peripheral intravenous catheter extending distally from the catheter adapter.

A medical device may include an outer assembly having a first shaft, a first lumen extending through the first shaft, and an atraumatic first tip removably coupled to a distal end of the first shaft; an inner assembly configured to extend through the first lumen of the outer assembly, the inner assembly including a second shaft, a second lumen extending through the second shaft, and a second tip removably coupled to a distal end of the second shaft, the second tip being configured to pierce tissue; and a plug assembly configured to extend through the second lumen of the inner assembly, the plug assembly including a third shaft and a plug removably coupled to a distal end of the third shaft.