A surgical system comprising a catheter comprising an irrigation tube, a suction tube, an occlusion balloon disposed about the irrigation tube and suction tube, and a console in operative communication with the irrigation tube and the suction tube. The surgical system also comprising a remote operations unit in communication with the console via a connector, wherein an input to the remote operations unit is communicated to the console, which in turn acts to operate the irrigation tube and suction tube in a manner corresponding to the input.

A catheter having a multilumenal tube surrounded by a slotted hypotube is provided. The catheter has a tube holder that houses the multilumenal tubing and slidably engages the hypotube, and has internal passages configured to receive one of more tubes from the multilumenal tube. The multilumenal tubing separates into one or more tubings, each comprising a lumen, such that the tubings exit the tube holder at different locations. The slotted hypotube slidably engages a key in the tube holder that prevents the multilumenal tubing from rotating relative to the tube holder and the one of more tubings that separate from the multilumenal tubing. Advantages provided by the slotted hypotube/tube holder assembly are described.

A diagnostic imaging catheter is disclosed, which is capable of preventing a solution from an internal space of a hub from flowing into a portion communicating with the internal space of the hub and to which the signal lines such as the optical fiber and the electric signal cable are electrically or optically connected. The optical diagnostic catheter includes a rotatable drive shaft, an elongated sheath configured to be inserted into a biological lumen, a hub that includes a port connected to the sheath for supplying the solution, a connector portion that includes an optical connector accommodated in an internal space of the hub and optically connected to an external optical connector, a first seal portion that prevents the solution from the port from flowing into a first connection portion, and a second seal portion that prevents the solution from the port from flowing into a second connection portion.

A medical liquid injection device including a catheter shaft having a first lumen, and a connector being connected to a proximal end portion of the catheter shaft and including a second lumen communicating with the first lumen. The connector is formed with a weak portion extending from an outer peripheral surface of the connector to an inner peripheral surface of the connector and being weaker than another portion of the connector.

A delivery device may comprise a sheath configured to be inserted into a body lumen of a patient. The sheath may have a proximal end, a distal end, a first channel extending within the sheath from the proximal end to the distal end, and a second channel extending within the sheath from the proximal end to the distal end. A collective cross-sectional area of the first channel and the second channel may be more than 50% of a total cross sectional area of the sheath. The device may also be comprised of a handle at the proximal end of the sheath, wherein the handle is configured to provide fluid communication between a first port and the first channel and a second port and the second channel.

A guidewire management device, a method of manufacturing the guidewire management device and a method for guidewire management are disclosed. The guidewire management device includes a housing through which a lumen of a catheter passes; and a locking mechanism mounted within the housing; wherein the locking mechanism is configured to lock the housing if a guidewire is present in the lumen and to unlock the housing if the guidewire is absent from the lumen. In one embodiment, the locking mechanism comprises a lever structure comprising a first arm connected to a second arm, wherein the first arm is configured to abut the lumen such that it becomes displaceable from a first position to a second position and actuates the second arm to engage a latch member to lock the housing if the guidewire is inserted through the lumen. Conversely, the housing unlocks if the guidewire is removed from the lumen.

A catheter system may include a catheter assembly. The catheter assembly may include the catheter adapter, which may include a distal end, a proximal end, an inner surface forming a lumen, the lumen extending through the distal end and the proximal end, and a side port disposed between the distal end and the proximal end. The catheter assembly may include an annular valve, which may be disposed within the lumen and aligned with the side port. The annular valve may seal a fluid pathway from the side port to the lumen. The catheter assembly may include a retainer ring or a bump disposed proximal and/or proximate the annular valve within the lumen. The catheter assembly may include a catheter extending distally from the distal end of the catheter adapter.

A catheter assembly includes a shaft with two non-communicating lumens for simultaneous inflow and outflow of fluids from a vein. A return lumen extends to an outlet assembly at the tip. A draw lumen includes an inlet assembly, proximally of the outlet assembly, with multiple openings to avoid blockage causing pressure elevation due to suction. The draw lumen has a larger crescent-shape profile while the return lumen has a smaller, circular profile within the arms of the crescent shape.

The present invention relates to a cannula comprising a catheter assembly, a body member, an elongated tubular member, a needle hub, and a safety device fixedly connected to a distal end of the elongated tubular member and releasably connected to the body member. The body member includes an annular groove, and the safety device comprises locking elements. When the needle is retracted from the catheter assembly after puncturing the vein of a patient, the body member is disengaged by disengaging the locking elements from the annular groove, thereby separating the safety device from the body member after the needle has been arrested within safety device. The locking elements are solid spherical elements of stainless steel material.

An infusion coupling allows administration of IV drugs to a patient through an IV fluid line, and ensures that successive courses of medication are fully passed or flushed from the line to prevent mixing of incompatible drugs in the IV line. The infusion coupling includes a vessel body, and a plurality of branch inlets to receive medication through IV tubing connected to the inlets. The vessel body has a generally cylindrical shape such that each of the branch inlets is in fluidic communication with the interior volume for receiving the IV fluids for transport. The inlets are angled on the body of the infusion coupling. A transverse bar or obstruction extends across an interior diameter of the infusion coupling for disrupting a circular flow that can result in a vortex. Formation of a vortex can retain the infused medication in the infusion coupling and result in mixing with successive medication courses.