64 results about "Cannula tip" patented technology

Method for carrying out the recovery of an intact volume of tissue wherein a delivery cannula tip is positioned in confronting adjacency with the volume of tissue to be recovered. The electrosurgical generator employed to form an arc at a capture component extending from the tip is configured having a resistance-power profile which permits recovery of the specimen without excessive thermal artifact while providing sufficient power to sustain a cutting arc. For the recovery procedure, a local anesthetic employing a diluent which exhibits a higher resistivity is utilized and the method for deploying the capture component involves an intermittent formation of a cutting arc with capture component actuation interspersed with pauses of duration effective to evacuate any accumulation or pockets of local anesthetic solution encountered by the cutting electrodes.

Method for carrying out the recovery of an intact volume of tissue wherein a delivery cannula tip is positioned in confronting adjacency with the volume of tissue to be recovered. The electrosurgical generator employed to form an arc at a capture component extending from the tip is configured having a resistance-power profile which permits recovery of the specimen without excessive thermal artifact while providing sufficient power to sustain a cutting arc. For the recovery procedure, a local anesthetic employing a diluent which exhibits a higher resistivity is utilized and the method for deploying the capture component involves an intermittent formation of a cutting arc with capture component actuation interspersed with pauses of duration effective to evacuate any accumulation or pockets of local anesthetic solution encountered by the cutting electrodes.

A device is described which allows simultaneous application of suction or vacuum for evacuation of fat with application of energy to the fat inside an opening in a cannula. A pair of electrodes is situated within the cavity of the cannula just under the surface of cannula tip opening(s) or as part of the walls of such openings. The electrodes are spaced to allow coagulation of fat entering the cannula. Irrigation may be applied in a continuous or discontinuous or intermittent stream within the cannula to cool the tip and facilitate removal of suctioned tissue and prevent buildup of debris on electrodes. A method for using the cannula to remove adipose tissue or fat destroyed by the energy application through the use of suction with mechanical motion of the cannula, with energy application and optionally with the use of irrigation is also disclosed.

The invention relates to a needle guidance system provided by a needle with a steerable tip. The needle has a cannula and a stylet. The stylet adjacent to its tip has a naturally curved portion The stylet is movable in two degrees of freedom with respect to the cannula-axial translation and axial rotation with respect to the cannula axis. When extended, the stylet curves off-axis and provides cannula tip steering. Driving and / or steering systems may be provided to the orientation and relatively move the stylet.

A bi-directional cannula feature capture mechanism is described herein. Generally, the capture mechanism comprises an inner housing, an outer housing, and a cannula. The inner housing comprises a proximal and a distal cannula feature mating component. The outer housing is adapted to slidably receive the inner housing in a proximal direction. Additionally, the cannula extends through the inner housing and the cannula's feature has a proximal engagement and a distal engagement. The proximal and distal engagements are respectively configured to irreversibly engage the proximal and distal cannula feature mating components when the cannula tip is moved into a shielded position.

A bi-directional cannula feature capture mechanism is described herein. Generally, the capture mechanism comprises an inner housing, an outer housing, and a cannula. The inner housing comprises a proximal and a distal cannula feature mating component. The outer housing is adapted to slidably receive the inner housing in a proximal direction. Additionally, the cannula extends through the inner housing and the cannula's feature has a proximal engagement and a distal engagement. The proximal and distal engagements are respectively configured to irreversibly engage the proximal and distal cannula feature mating components when the cannula tip is moved into a shielded position.

The present invention is directed toward fluid transfer devices including a vial adapter having a top wall and a cannula with a cannula tip, and an elastic O-ring like sealing element sealingly encircling the cannula and initially disposed towards the cannula tip and spaced apart from the top wall, the sealing element being brought into initial contact with the vial stopper subsequent to the cannula tip contacting the vial stopper at a puncture site and thereafter being slidingly urged towards the top wall and continuously sealing the puncture site during snap fit mounting the vial adapter on the vial.

A bi-directional cannula feature capture mechanism is described herein. Generally, the capture mechanism comprises an inner housing, an outer housing, and a cannula. The inner housing comprises a proximal and a distal cannula feature mating component. The outer housing is adapted to slidably receive the inner housing in a proximal direction. Additionally, the cannula extends through the inner housing and the cannula's feature has a proximal engagement and a distal engagement. The proximal and distal engagements are respectively configured to irreversibly engage the proximal and distal cannula feature mating components when the cannula tip is moved into a shielded position.

The invention relates to a needle guidance system provided by a needle with a steerable tip. The needle has a cannula and a stylet. The stylet adjacent to its tip has a naturally curved portion. The stylet is movable in two degrees of freedom with respect to the cannula—axial translation and axial rotation with respect to the cannula axis. When extended, the stylet curves off-axis and provides cannula tip steering. Driving and / or steering systems may be provided to the orientation and relatively move the stylet.

A cannula for transferring fluid relative to a vial or intravenous port having an elastomeric membrane includes: a cannula body having first and second opposite ends; the first end terminating in a tip for penetrating the elastomeric membrane; the body having a passage opening through the second end and extending within the cannula body towards the first end, the passage opening through at least one horizontal-oriented port through a side surface of the cannula body thereby to enable flow of fluid along the passage and between the opening through the second end and the side port. An axial width of the port is smaller than a thickness dimension of a vial through which the cannula tip is to be inserted. A related method is also described.

The present invention is directed toward fluid transfer devices including a vial adapter having a top wall and a cannula with a cannula tip, and an elastic O-ring like sealing element sealingly encircling the cannula and initially disposed towards the cannula tip and spaced apart from the top wall, the sealing element being brought into initial contact with the vial stopper subsequent to the cannula tip contacting the vial stopper at a puncture site and thereafter being slidingly urged towards the top wall and continuously sealing the puncture site during snap fit mounting the vial adapter on the vial.

Methods for forming a rib on a cannula for cooperation with a safety cover which securably and reliably locks the tip of a cannula in an interior chamber within the safety cover. The cover comprises an elongate body having the interior chamber and an axial through hole which extends along the entire length of the body, through the interior chamber and through which the cannula is slidably received. Displacing elements are positioned within the interior chamber, each of which includes a hole for receiving the cannula therethrough, and which displaces upon retraction of the tip of the cannula, thereby preventing subsequent advancement of the cannula tip. The cannula includes a thickened rib adjacent to the tip, and the safety cover should correspondingly include an annular section in the rear portion thereof. The through hole extending through the rear portion has a diameter which is smaller than the thickened rib of the cannula whereby the cannula tip may not be retracted from the safety cover. The rib is formed by a thermal method in which a sleeve is heated to expand its inside diameter to allow the sleeve to be slid onto the cannula. The sleeve is then cooled to room temperature so that the inside diameter contracts to attach the sleeve to the cannula. In another method, a sleeve is placed on the cannula and crimped at the desired location.

Methods and apparatus for performing a medical procedure which involves penetrating a bone structure are disclosed. According to one aspect of the present invention, a method for performing a surgical procedure includes introducing an assembly that includes a threaded cannula and a stylet into a bone structure. The threads have a shape that allows the cannula tip to be pushed into the bone body yet prevent the tip from being pulled out of the bone body. In one embodiment, the threads have a buttress shape. The method may also include applying a rotational motion, as for example a torque, to the threaded cannula to adjust the depth of insertion with respect to the implantation site when it is determined that the depth of insertion is to be adjusted.

A surgical cannula system. The surgical cannula system includes a cannula having a proximal end, a distal end, and a lumen extending therebetween. A tissue attachment ring, being configured to be coupled to a biological tissue, includes a lumen extending therethrough. A locking mechanism has a first locking state, in which the cannula is configured to move with respect to the tissue attachment ring, and a second locking state, in which movement of the cannula with respect to the tissue attachment ring is resisted.

A breathing gas delivery system and method provides a flow of breathing gas to a patient. The gas flow is purposely interrupted for the patient's exhale phase in order to minimize irritation and injury to nasal tissues due to constant, uninterrupted flows. Embodiments include an oscillating ball valve that interrupts oxygen supply during the patient's exhale phase, cannula tips that are shaped to minimize trauma, and a sleep apnea treatment system that interrupts breathing gas supply during the patient's exhale phase.

A bi-directional cannula feature capture mechanism is described herein. Generally, the capture mechanism comprises an inner housing, an outer housing, and a cannula. The inner housing comprises a proximal and a distal cannula feature mating component. The outer housing is adapted to slidably receive the inner housing in a proximal direction. Additionally, the cannula extends through the inner housing and the cannula's feature has a proximal engagement and a distal engagement. The proximal and distal engagements are respectively configured to irreversibly engage the proximal and distal cannula feature mating components when the cannula tip is moved into a shielded position.

A delivery device delivery system and a method for delivering substances into blood vessels. The delivery device includes a body having a first end, a second end, and an outer surface. A first substance reservoir is disposed within the body and at least one cannula extends from the first end of the body. The cannula includes a cannula tip having a cannula opening therethrough and a cannula sheathing defining an interior passage in fluid communication with the first substance reservoir. A means is provided for delivering the first substance from the first substance reservoir through one of the at least one cannula, and a means is provided for delivering the second substance through one of the at least one cannula.

A surgical cannula system. The surgical cannula system includes a cannula having a proximal end, a distal end, and a lumen extending therebetween. A tissue attachment ring, being configured to be coupled to a biological tissue, includes a lumen extending therethrough. A locking mechanism has a first locking state, in which the cannula is configured to move with respect to the tissue attachment ring, and a second locking state, in which movement of the cannula with respect to the tissue attachment ring is resisted.

A needle tip shielding mechanism is described herein. The shielding mechanism comprises an outer housing, an inner housing, and a needle having a needle feature. Generally, the outer housing comprises at least one adapter-interlock feature. Moreover, the inner housing comprises a needle-feature capture mechanism, such as a washer feature, and a needle-tip capture mechanism, such as duckbilled tip barrier. In some cases, the inner housing is slidably moveable within the outer housing. In such cases, the inner housing is movable between a first position that biases the adapter-interlock feature into an engaged position and a second position that allows the adapter-interlock feature to move to an unengaged position. This ability to bias the interlock feature in the engaged position and to allow the interlock feature to move to the unengaged position allows the shielding mechanism to be selectively coupled to and released from an interlock-feature mating component within a catheter adapter.

An infusion assembly comprises a cannula subassembly and a source subassembly. The cannula subassembly includes a substantially planar base, a cannula projecting from the base so as to be beneath the patient's skin when the subassembly is deployed, and a generally cylindrical docking structure having a center axis substantially perpendicular to the base. A liquid medicament is dispensed from the cannula. The source subassembly is arranged to dock with the docking structure and includes a supply of liquid medicament that couples to the cannula upon the source subassembly docking with the cannula subassembly. The source subassembly also includes a primer that automatically primes the insulin fluid path to the cannula tip when the subassemblies are joined.

A needle shield and needle shield assembly are provided for preventing accidental needle sticks. The needle shield includes opposing sidewalls and is pivotable between an open position that allows use of the needle cannula and a closed position that covers at least the tip of the needle cannula. A locking member extends from one of the sidewalls of the needle shield and includes a relatively rigid base portion and a relatively flexible end portion. The needle cannula engages the relatively flexible end portion when entering the needle shield cavity, deflecting it with respect to the base portion. Upon any attempt to move the needle shield from the closed position to the open position, the needle cannula is directed by the locking member towards the relatively rigid base portion, thereby making it very difficult to reuse the needle cannula.

The present invention involves an eye drop dispenser attachment having a cannula tip that can provide a consistent dose of medication. The attachment includes a base portion, a neck portion, and a tip portion. The base portion can contain threads for removable attachment to a bottle. The attachment can also include a protective covering for surrounding the tip to prevent injury to a user. The attachment can further include a cap that can be removably attached to either the base portion or the neck portion. The attachment can be incorporated into a bottle assembly or it can be screwed onto an existing bottle. The tip preferably has dimensions consistent with current ophthalmic cannula technology in the range of 20-40 gauge depending on the size of drop desired. An alternate embodiment of the attachment can be slidably disposed on the end of a traditional bulb-type eye dropper.

A method and apparatus for inserting and monitoring the placement of a cannula tip within a peripheral vein of a human body where the cannula includes a sensor located at predetermined location and mounted on the cannula for sensing the biological material of the body to guide the insertion of the cannula tip into the vein and alerts to the withdrawal of the cannula tip from the vein in the body.

A transition device for placement at the opening of the tip of a cannula body for the purpose of controlling the shape of the cannula tip opening under various loads such as might be encountered during device placement.

In one embodiment of the present invention, a cannula for use with a blood circulation device may include the cannula having a longitudinal axis and proximal and distal directions along the longitudinal axis. The cannula may also include a proximal portion having a wall extending around the longitudinal axis and having outer and inner faces, the inner face may define a bore, the proximal portion may have dimensions transverse to the longitudinal axis, and the dimensions may be constant in the proximal and distal directions. Also, the cannula may have a distal portion having an outer face, continuous with the outer face of the proximal portion. The outer face of the distal portion may extend around and along the longitudinal axis, and the outer face of the distal portion may taper distally toward the longitudinal axis. The distal portion may include at least two openings extending from the outer face of the distal portion, which may merge with one another within the distal portion. Then, the openings may communicate with the bore of the proximal portion. One type of blood circulation device may be a ventricular assist device.

A method and apparatus for inserting and monitoring the placement of a cannula tip within a peripheral vein of a human body where the cannula includes a sensor located at predetermined location and mounted on the cannula for sensing the biological material of the body to guide the insertion of the cannula tip into the vein and alerts to the withdrawal of the cannula tip from the vein in the body.

The present invention provides an inflow cannula tip that is shaped to prevent suction with the ventricular wall and adapted to prevent platelet adhesion. In particular, the inlet portion of the cannula tip comprises two projections extending from the cylindrical body of the cannula tip with gaps between the projections. The projections may have beveled edges. The inlet portion of the cannula tip can accept blood flow from either the gaps in the side or from the bottom of the tip. Even if the edge of the cannula tip is close to or even touching ventricle wall, a suction condition will not result, as blood is allowed to flow through the gaps between the projections.

In one embodiment of the present invention, a cannula for use with a blood circulation device may include the cannula having a longitudinal axis and proximal and distal directions along the longitudinal axis. The cannula may also include a proximal portion having a wall extending around the longitudinal axis and having outer and inner faces, the inner face may define a bore, the proximal portion may have dimensions transverse to the longitudinal axis, and the dimensions may be constant in the proximal and distal directions. Also, the cannula may have a distal portion having an outer face, continuous with the outer face of the proximal portion. The outer face of the distal portion may extend around and along the longitudinal axis, and the outer face of the distal portion may taper distally toward the longitudinal axis. The distal portion may include at least two openings extending from the outer face of the distal portion, which may merge with one another within the distal portion. Then, the openings may communicate with the bore of the proximal portion. One type of blood circulation device may be a ventricular assist device.

The present invention involves an eye drop dispenser attachment having a cannula tip that can provide a consistent dose of medication. The attachment includes a base portion, a neck portion, and a tip portion. The base portion can contain threads for removable attachment to a bottle. The attachment can also include a protective covering for surrounding the tip to prevent injury to a user. The attachment can further include a cap that can be removably attached to either the base portion or the neck portion. The attachment can be incorporated into a bottle assembly or it can be screwed onto an existing bottle. The tip preferably has dimensions consistent with current ophthalmic cannula technology in the range of 20-40 gauge depending on the size of drop desired. An alternate embodiment of the attachment can be slidably disposed on the end of a traditional bulb-type eye dropper.

A bi-directional cannula feature capture mechanism (30) is described herein. Generally, the capture mechanism comprises an inner housing (80), an outer housing (100), and a cannula (40). The inner housing comprises a proximal and a distal cannula feature mating component. The outer housing is adapted to slidably receive the inner housing in a proximal direction. Additionally, the cannula extends through the inner housing and the cannula's feature has a proximal engagement and a distal engagement. The proximal and distal engagements are respectively configured to irreversibly engage the proximal and distal cannula feature mating components when the cannula tip is moved into a shielded position.