993 results about "Huber needles" patented technology

A hemodialysis port comprising a flexible housing member defining one or more ports. Each port has a selectively-permeable septum member disposed thereon to permit medical devices, for example, Huber needles, sheath and / or dilators to be inserted therein. At the interface between the housing and the septum, a spring member is provided to provide an axial force on the septum which seals the puncture created by the aforementioned medical devices. In one exemplary embodiment, the hemodialysis access port of the present invention is comprised of a plurality of ports designed for multiple hemodialysis treatments over the life of the port. In other exemplary embodiments, the bottom of each port may comprise a needle stop insert formed of, for example, metal, titanium, stainless steel or ceramic.

Improved medical suturing devices, systems, and methods may hold a suture needle at a fixed location relative to a handle of the device, allowing the surgeon to grasp and manipulate the handle of the suturing device to insert the needle through tissues in a manner analogous to use of a standard needle gripper. Cycling the handle from a closed position to an open position and back to the closed position may alternate the device between gripping the needle with a first clamp (for example, along a proximal portion of the needle) to gripping the needle with a second clamp (for example, along a distal portion of the needle) and optionally back to gripping with the first clamp, with the needle often staying at a substantially fixed location relative to the suturing device body. Related single-clamp needle grasping devices can be bent plastically by a surgeon, and / or have bodies that are grasped by a hand while a portion of the hand actuates a handle.

A robotic system for steering a flexible needle during insertion into soft-tissue using imaging to determine the needle position. The control system calculates a needle tip trajectory that hits the desired target while avoiding potentially dangerous obstacles en route. Using an inverse kinematics algorithm, the maneuvers required of the needle base to cause the tip to follow this trajectory are calculated, such that the robot can perform controlled needle insertion. The insertion of a flexible needle into a deformable tissue is modeled as a linear beam supported by virtual springs, where the stiffness coefficients of the springs varies along the needle. The forward and inverse kinematics of the needle are solved analytically, enabling both path planning and correction in real-time. The needle shape is detected by image processing performed on fluoroscopic images. The stiffness properties of the tissue are calculated from the measured shape of the needle.

A safety needle device for protecting a user against inadvertent needle-stick injury. This needle device includes a needle housing having a distal housing opening. An arcuate groove extends within the needle housing terminating adjacent the distal housing opening. A needle is disposed within the arcuate groove having a distal needle portion extending away from the needle housing through the distal housing opening. An elongate sheath assembly surrounds the needle within the groove. A biasing member is disposed within the needle housing and is configured to move the sheath assembly throughout the length of the arcuate groove and through the distal housing opening. The sheath assembly then completely enclose the distal needle portion.

A surgical suturing device (10) having an axis extending between a proximal end and a distal end is operable to move a suture (32) through body tissue (34). A handle assembly (110) is coupled to an elongated shaft (14) having a hollow configuration. An actuating rod (16) is disposed to extend between the handle assembly (110) and the shaft (14). A thumb actuation assembly is coupled to a proximal end of the actuating rod (16) for moving the rod both axially and rotationally. A needle assembly (2) at the distal end of the actuating rod (16) is movable with the actuating rod (16) between an extended state and a retracted state and at various angular orientations. Bifurcated portions (24, 26) of the needle assembly (20) define a suture slot (28), the bifurcated portions having a proximate relationship when the needle assembly (20) is in the retracted state and having a separated relationship when the needle assembly (20) is in the extended state. The needle assembly (20) is biased to the retracted state and the bifurcated portions (24, 26) are biased to the separated relationship. A handle assembly (110) is operable to move the needle assembly (20) between a free suture state and a captured suture state. In an associated method of use, the needle is bifurcated to form at least one pair of arms (24, 26 or 26b, 38b) to define a suture slot (28).

An instrument for closing, by subcutaneous suturing, an orifice made in the abdominal wall of a patient. The instrument has a piston rod (5) whose end acts on a flexible support strip (8) for needles (7), thus causing them to emerge at an exterior of the lower part (4) of a cannula (3) of the instrument underneath the abdominal wall (2), so that the needle can then penetrate into a thick part of this wall. Also, a method for suturing of orifices after a surgical operation by laparoscopy.

A needle assembly 10 compromising an infusion needle 11 that includes a needle cannula 13 made of a superelastic material such as Nitinol. The needle cannula is cold-worked or heat annealed to produce a preformed bend 16 that can be straightened within passageway 21 of a coaxial outer cannula 12 for introduction into the body of a patient. Upon deployment from the outer cannula, the needle cannula substantially returns to the preformed configuration for the introduction or extraction of materials at areas lateral to the entry path of the needle assembly. The needle assembly can compromise a plurality of needle cannulae than can be variably arranged or configured for attaining a desired infusion pattern.

An automatic retraction Huber needle safety enclosure which is designed principally for a Huber needle. A Huber needle is a hypodermic needle that is in the shape of a right angle. The safety enclosure has an internal chamber which is formed between a housing and a lid with the lid being movable relative to the housing between a closed position and an open position. The Huber needle is mounted within the internal chamber. The Huber needle is movable between an extended position and a retracted position. With the Huber needle in the extended position, the Huber needle is capable of being inserted within the body of a human or animal. With the Huber needle in the retracted position, the tip of the Huber needle is to be totally confined within the internal chamber. A wing assembly is attached to the housing which functions to facilitate securement of the safety enclosure to the body of the animal or human and forming an enclosure with the wing assembly folded in abutting juxtaposition.

A needle having a shaft with a distal end defining a distal opening. The shaft has a longitudinal axis that extends through the distal opening and the distal opening has a projected area that is smaller than a cross-sectional area of a section of the shaft proximal to the distal end of the shaft. Also provided are methods of directly delivering a therapeutic agent to a target site using a Huber needle or pencil-point needle.

An access needle well-suited for percutaneous implantation in a body lumen, such as the stomach or the jejunum. In one embodiment, the access needle comprises a cannula, a needle, a retractable stopper and a spreader. The cannula is a tubular member having a proximal end, a distal end, a lumen and a pair of side windows providing access to the lumen. The needle is slidably mounted within the cannula lumen and comprises a needle stem and a needle handle, the needle stem having a proximal end, a distal end and a longitudinal lumen, the needle handle extending outwardly from the needle stem proximate to the proximal end thereof. The stopper is coupled to the needle stem for translational movement, the stopper comprising a pair of outwardly-biasing wings removably insertable through the side windows for engaging an interior surface of a patient. The spreader is mounted within the cannula and spreads the wings outwardly as the wings are inserted out the side windows.

A safety needle device for protecting a user against a needle-stick injury. This needle device includes a needle housing having a distal housing opening. A needle is disposed within the needle housing and has a distal needle portion which extends away therefrom through the distal housing opening. An elongate sheath assembly surrounds the needle within the needle housing. A trigger member retains the sheath assembly within the needle housing against a force urging the sheath assembly towards the distal housing opening. The trigger member is sized and configured to release the sheath assembly from retention to allow the sheath assembly to transition towards and out of the distal housing opening via the force. This causes the sheath assembly to enclose the distal needle portion and protect the user against the needle stick injury.

Apparatus for insufflating a body conduit or cavity includes a needle having a lumen defined by an inner surface and a sharp distal tip. An obturator, disposed within the lumen of the needle and movable axially between a proximal position and a distal position, includes an extension member which defines an insufflation channel with the inner surface of the needle. A blunt distal terminus on the extension member is disposed distally of the sharp tip of the needle when the obturator is in the distal position.

An autoinjector device for delivering a dose of medicament including a syringe including a needle wherein, prior to use of the device, the needle is substantially covered by a needle sheath (107). The autoinjector further includes a housing (112) in which said syringe is located, an outer packaging in which said housing is located, where the outer packaging comprising a front packaging (101) part and a rear packaging part. The autoinjector also includes needle sheath removing means (103) associated with said front packaging part (101), wherein, prior to use of the device, said front and rear packaging parts cooperate together to entirely enclose said housing, syringe and needle sheath, and wherein, upon axial separation of said front and rear packaging parts, said needle sheath removing means is capable of causing axial separation of said needle sheath from said needle so as to remove said needle sheath therefrom.

The present invention is a catheter device. The catheter device will include a septum that is housed within a housing. The septum is designed such that it will seal the housing. The catheter device also includes a needle shield. The needle shield is configured to retain a needle if the needle is withdrawn from the housing. The catheter device is further configured such that the septum includes a receiving portion that is designed to engage a portion of the needle shield. However, if the needle is withdrawn from the housing, the needle shield will disengage from the septum so that the needle shield may be separated from the septum.

A container is provided for storing a product, such as a fat containing liquid product, and includes a body defining a chamber for receiving the product; and a container closure including a sealing portion for sealing the product within the chamber. The container closure includes a member forming a substantially fluid-tight seal between the container closure and the body; a nipple in fluid communication with the chamber that seals the chamber with respect to the ambient atmosphere during storage of the product in the chamber and that can be opened to dispense product from the chamber therethrough; and a needle penetrable and laser resealable portion that is penetrable by the needle for aseptically filling the chamber with the product, and that is thermally resealable by the application of laser radiation thereto to seal the product within the chamber.

A needle magazine for holding a plurality of injection needles (50) is described. The needle magazine comprises a first opening adapted to receive the device fluid access portion (120) of a medical delivery device. Each needle (50) is selectively moveable from a respective storage position not aligned with said first opening into a needle mounting position aligned with said first opening. The needle magazine further comprises needle positioning means (41). configured to alter the mutual position between a needle selected from said plurality of needles (50) relative to a neighbour needle when said selected needle moves from its storage position to the needle mounting position.

The present invention is an alignment system by which a needle or other similar invasive device can be positioned for insertion so as to have a real-time, predetermined trajectory to a targeted tissue region, thereby reducing the need for repetitive needle insertion and withdrawal to move the tip of the instrument accurately to the target site.

To ensure that there is no misconnection between a needle, such as for example a spinal or epidural needle, and the appropriate medication, the needle hub the needle is formed, by molding or extrusion, to have a given configuration. An adapter is placed between the needle and a conventional fluid store, or medical line. The end of the adapter that connects to the needle assembly is formed to have a configuration that is complementary to that of the hub of the needle assembly, so that the adapter and the needle hub may be readily mated to each other. The other end of the adapter is formed to have another configuration, for example a conventional luer, that is readily connectable to a conventional fluid store, such as a syringe that has a conventional luer. The adapter is formed by inter-fitting two elements to effect an integral locking mechanism to prevent the uncoupling of the fluid store and the adapter, once they are securely coupled. By thus configuring the hub of the needle to have a given configuration that is matable only to the end of an adapter that has a complementary configuration, and further providing an adapter that prevents the removal of the fluid store connected thereto, the potential for mis-connecting the needle to a fluid store that contains a different medicament is greatly reduced, if not totally eliminated.

The invention provides a safety syringe, which has a cylinder (11), a syringe needle (21), a needle holder (31) associated to the cylinder and adapted to hold the syringe needle, and a plunger (41) associated to the cylinder (11), wherein the plunger (41) comprises a piston (42) and serves to inject a filling of the cylinder (11) via the syringe needle (21), and wherein the plunger (41) can be coupled with the needle holder (31) arranged in the region of a front hole (12) of the cylinder (11), to retract the needle holder (31) together with syringe needle (21) into the cylinder (11) by pulling the plunger (41) once coupled to the needle holder (31) is retracted into the cylinder by rotating the plunger (41) and pulling the plunger (41) aft thereby pulling the needle holder (31) into the cylinder (11). Then the aft end of the plunger (41) is broken off, and a removable cap (49) from the aft end of the plunger (41) may be placed over the opening in the forward end of the cylinder (11).

Methods and systems for spinal radio frequency neurotomy. Systems include needles capable of applying RF energy to target volumes within a patient. Such target volumes may contain target medial branch nerves along vertebrae or rami proximate the sacrum. Such procedures may be used to ablate or cauterize a portion of the targeted nerve, thus blocking the ability of the nerve to transmit signals to the central nervous system. Disclosed needles may be operable to asymmetrically, relative to a central longitudinal axis of the needle, apply RF energy. Such asymmetry facilitates procedures where a tip of the needle is placed proximate to anatomical structures for location verification. Then RF energy may be applied in a selectable direction relative to the needle tip to ablate volumes that include the targeted medial branch nerves or rami, thus denervating facet joints or the sacroiliac joint, respectively, to relieve pain in a patient.

Needle guards are disclosed for use with needle assemblies comprising a needle hub that joins a flexible trailing tube to a medical needle, the normally open front ends of the guards being closeable after a needle and hub have been pulled therein by the trailing tube. In one example (FIG. 4c), a guard (10) has a stiff upper sidewall (24a) of an inverted U-shape and a flexible lower sidewall (26b) that fits inside the upper sidewall and is resiliently biased to bring its front end (31) into contact with the front end (30) of upper sidewall (24b) so as to close the front aperture of the guard after the needle assembly (16) has been withdrawn into the guard. The lower sidewall (26b) can be locked or clipped into the upper sidewall (24b) by pressing lower sidewall passed catches (72). In this way, the needle is completely and safely enclosed after use to reduce the danger of needle-stick injury and blood-splash contamination.

To enable a user to readily determine the gauge of the needle of a needle assembly that has a base and a needle protective housing pivotably attached thereto, the needle assembly is injection molded from a color coded molding material which color was preassigned to correspond to the gauge of the needle. As a result, both the base and the protective housing of the needle assembly are the same specific color, and reflect or provide an indication of the given gauge of the needle. The needle sheath that covers the needle prior to use may be made of a plastics material that may be clear, or have the same or a different color than that of the needle assembly.

A safety enclosure which is designed for a hypodermic needle that is located in the shape of an approximate right angle (Huber needle). A safety enclosure has a needle housing within which the Huber needle is mounted. The needle housing is mounted in conjunction with a panel unit. The panel unit is composed of a series of planar panels which are edge connected together defining an enclosed area. The panel unit can be movable from a basically transverse position to an elongated position. When in the transverse position, the panel unit is to be mounted with adhesive tape onto the skin of a patient with the sharp end of the needle being inserted within the body of the patient. When the panel unit is in the elongated position, the needle is withdrawn from the body of the patient and the sharpened end of the needle is covered by the panels thereby preventing undesired needlestick injury to the medical practitioner that is installing and removing the enclosure.

A syringe includes a hollow barrel, a hollow plunger movable within the barrel and a needle assembly secured within and at a distal end of the barrel. The needle assembly includes a needle holder, a resilient member that biases the needle holder toward the proximal end opening of the barrel, and a retaining member releasably secured to the needle holder via a reduced material section. The retaining member maintains the needle holder at the distal end of the barrel against the bias of the resilient member. When the plunger is fully depressed within the barrel, the plunger engages the needle holder such that the retaining member is forced to break away and separate from the needle holder along the reduced material section to facilitate retraction of the needle holder and a needle secured to the needle holder into the retraction cavity disposed within the plunger.

A needle assembly for dispensing fluids from a fluid source and for evacuating a cavity during an endodontic procedure and a method of using the needle assembly. The needle comprises a housing and a surgical needle in fluid communication with said fluid source. The housing comprises a first pathway containing said surgical needle, and a second evacuation pathway providing evacuation means for the needle assembly. The evacuation pathway is independent and external of the surgical needle.

A medical device needle receiving port configured to stop a needle's penetration without physically engaging the needle's tip thereby reducing the likelihood of tip damage. The port preferably incorporates a particulate chamber for collecting particulates larger then a fluid outlet dimension.

The present invention relates to liquid drug medical devices for enabling the administration of liquid drugs, and also a needle shield removal device for safely removing needle shields.

The invention provides a safety syringe, which has a cylinder (11), a syringe needle (21), a needle holder (31) associated to the cylinder and adapted to hold the syringe needle, and a plunger (41) associated to the cylinder (11), wherein the plunger (41) comprises a piston (42) and serves to inject a filling of the cylinder (11) via the syringe needle (21), and wherein the plunger (41) can be coupled with the needle holder (31) arranged in the region of a front hole (12) of the cylinder (11), to retract the needle holder (31) together with syringe needle (21) into the cylinder (11) by pulling the plunger (41) once coupled to the needle holder (31) is retracted into the cylinder by rotating the plunger (41) and pulling the plunger (41) aft thereby pulling the needle holder (31) into the cylinder (11). Then the aft end of the plunger (41) is broken off, and a removable cap (49) from the aft end of the plunger (41) may be placed over the opening in the forward end of the cylinder (11).