Abstract:
A catheter for changing insertion direction of a guide wire according to an exemplary embodiment of the present invention may be inserted in a body along the guide wire inserted in the body through a puncture region, and may change the insertion direction of the guide wire. The catheter may include: a hollow hub having an entrance at one end thereof, the guide wire being inserted in the entrance; a tubular member connected to the other end of the hub, extending in a length direction thereof, and having an exit at the other end thereof, the guide wire coming out through the exit; and a direction changing hole formed at the tubular member, the guide wire coming out through the direction changing hole so as to change the insertion direction of the guide wire.
Abstract:
A clam shell shaped adapter for retaining a catheter to establish a fluid path between the catheter and a fluid device or line has two shells integrally connected by a living hinge. A first shell has a luer end and a catheter end wherein a catheter is insertable through its aperture. A flexible tube at the inner surface of the first shell connects the luer end to the catheter end. The catheter is inserted through the catheter end to extend along the flexible tubing. A retainer structure is provided at the inner surface of the second shell so that when the first and second shells close upon each other, the retainer structure presses against the flexible tubing to fixedly retain the catheter in a fluidly sealing manner. Respective latch mechanisms provided at the shells lockingly couple the two shells to each other. The latch mechanisms are located remotely from the outer surfaces and peripheries of the shells to prevent inadvertent uncoupling of the shells. The shells may be uncoupled by inserting a pointed object through a notch to the interior of the device to disengage the latch mechanisms.
Abstract:
A proximally trimmable catheter is disclosed. In one embodiment, the catheter includes a multi-lumen catheter tube, one or more extension tubes, and a hub for fluidly connecting the two. In a first unlocked state, the hub is axially slidable along the catheter tube. The hub includes tube pins that are in fluid communication with the extension tubes. A cutting member is positioned to longitudinally cut the catheter tube during axial sliding of the hub along the catheter tube such that distal portions of the tube pins remain disposed within the lumens of the catheter tube. When positioned as desired, the hub is locked into a second locked state and is no longer axially slidable along the catheter tube. The tube pins are fluidly sealed within the lumens of the catheter tube as to establish fluid communication between the extension tubes and the lumens via the tube pins.
Abstract:
A system for delivering an antimicrobial agent into the lumen of a trans-dermal catheter. In an embodiment, the system comprises an elongate member configured for insertion into a lumen of a catheter; an expandable portion of the elongate member, said expandable portion configured to increase in diameter upon exposure to an aqueous fluid; and an antimicrobial composition positioned to be delivered into the catheter. In another embodiment, the system comprises an elongate member configured for insertion into a lumen of a trans-dermal catheter, said elongate member comprising a hydrogel; and an antimicrobial composition positioned to be delivered into the catheter; wherein the elongate member defines a volume of liquid that is at least substantially contained within the lumen of the trans-dermal catheter.
Abstract:
When a main stent-graft is placed in a vessel of a patient and a branch vessel is blocked by the main stent-graft, a RF plasma catheter is used to cut out a portion of the graft cloth of the main-stent graft adjacent to an ostium of the branch vessel to be perfused. To ameliorate possible adverse effects associated with the use of the RF plasma catheter, e.g., creation of coagulum, (desiccated, coagulated blood) or perhaps a cut stent strut, a special process using saline flushing, a novel RF plasma catheter with an insulated tip, or a combination of the two is used.
Abstract:
An in-dwelling port for providing repeated entry to a body during and/or after an operation is described. The port may include an external portion secured to a body outside an incision and a collapsible insertion portion that is inserted through the incision. The collapsible portion collapses when no instrument or lumen is present to permits the body to return to substantially a normal profile around the incision.
Abstract:
A medical device (20) includes a device housing (24), which contains a lumen (26) having first and second ends and is configured to be implanted in a bone (34) of a subject so that the first end opens into a body cavity (30) in proximity to the bone and the second end opens into a medulla (32) of the bone. A valve (28) is contained in the device housing and is configured to control a flow of a body fluid from the body cavity into the medulla. The device may include an evacuation mechanism (37) coupled to the device housing for evacuating particulate matter from the lumen.
Abstract:
A method for producing a catheter (100) having a plurality of axially spaced apart electrodes (5) towards a distal end (4) of the catheter (100) comprises forming the electrodes (5) from a single sheet (110) of electrically conductive foil material by forming spaced apart slots (111) in the sheet material to define a plurality of spaced apart electrically conductive elements (114) extending transversely between spaced apart elongated connecting portion (112,113). The electrically conductive elements (114) subsequently form the electrodes (5), and are retained spaced apart by the connecting portions (112,113) until bonded to the catheter (100). Electrically conductive wires (10) electrically coupled to the electrically conductive elements (114) extend through an elongated slot (105) into and along an axial communicating bore (9) to a proximal end (3) of the catheter (100). Two pieces of double-sided adhesive tape (118) bonded to the electrically conductive elements (114) in turn bond the electrically conductive elements (114) to the catheter (100). After entering the wires (10) into the axial communicating bore (9) the electrically conductive elements (114) with the double-sided tape (118) are wrapped around the catheter (100) and are severed from the connecting portions (112,113). Free ends (115) of the electrically conductive elements (114) abut each other to form the electrodes (5) as band electrodes.
Abstract:
A medical device may include a vascular access device having a body and a membrane of the body. The membrane communicates with a pathogenic environment and discourages adhesion of a pathogen to the membrane. A method of discouraging a pathogen from residing on the membrane of a vascular access device includes providing a vascular access device with a body having a membrane and discouraging a pathogen from residing on the membrane.
Abstract:
This invention relates to flexible medical device. The flexible medical device may comprise interlocking portions formed of a continuous channel. When formed of a continuous channel, the medical device comprises interconnected interlocking portions, rather than independent interlocking portions. The flexible medical device may also be designed so that different portions of the device have different flexibility characteristics.