Abstract: A syringe assembly includes a syringe barrel having a first end, a second end, and a sidewall extending between the first end and the second end. The syringe assembly further includes a stopper disposed within a chamber of the syringe barrel, a plunger adapter engaged with the stopper, and a plunger rod having first and second ends. The first end of the plunger rod is pivotally secured to the plunger adapter. The plunger rod has a pre-use position where the second end of the plunger rod is positioned adjacent to the syringe barrel, and a use position where the plunger rod is configured to displace the stopper relative to the syringe barrel. A recessed portion of the plunger adapter receives a portion of the first end of the plunger rod when the plunger rod is in the pre-use position and the use position.

Abstract: A system effectively narrows a patulous Eustachian tube (ET) of a patient with a guide catheter, instrument, and insert. The guide catheter includes a shaft, a lumen and a distal end configured to provide access the ET when the guide catheter is inserted into a head of the patient. The instrument comprises a shaft. The insert comprises a body configured to radially expand and retract between a non-expanded state and an expanded state. The insert is sized and shaped to be received within the first lumen when in the non-expanded state and is operable to expand to the expanded state to substantially reduce an effective diameter of the ET.

Abstract: An apparatus and method for mixing and dispensing bone cement is provided. The apparatus includes a mixing vessel for mixing bone cement attached to a syringe body. The syringe body having a lumen that is connected to the mixing vessel by a passageway between the mixing vessel and the lumen of the syringe body. A separator is provided between the mixing vessel and the syringe body and includes an orifice therein so that when the opening in the separator is misaligned with the lumen the passageway is blocked and when aligned the passageway is continuous with the lumen so that bone cement can pass into the syringe body. A plunger is provided and is slideably movable along the longitudinal axis of the syringe body so as to advance the bone cement out of the distal end of the syringe.

Abstract: A syringe assembly includes a syringe barrel having a first end, a second end, and a sidewall extending between the first end and the second end. The syringe assembly further includes a stopper disposed within a chamber of the syringe barrel, a plunger adapter engaged with the stopper, and a plunger rod having first and second ends. The first end of the plunger rod is pivotally secured to the plunger adapter. The plunger rod has a pre-use position where the second end of the plunger rod is positioned adjacent to the syringe barrel, and a use position where the plunger rod is configured to displace the stopper relative to the syringe barrel. A recessed portion of the plunger adapter receives a portion of the first end of the plunger rod when the plunger rod is in the pre-use position and the use position.

Abstract: A syringe assembly includes a syringe barrel having a first end, a second end, and a sidewall extending between the first end and the second end. The syringe assembly further includes a stopper disposed within a chamber of the syringe barrel, a plunger adapter engaged with the stopper and defining a recessed portion therein, and first and second plunger arms each having a first end pivotally secured to the plunger adapter. The first and second plunger arms each have a pre-use position where the plunger arms are spaced from each other, and a use position where the plunger arms are positioned adjacent to each other and configured to displace the stopper relative to the syringe barrel. The recessed portion of the plunger adapter receives a portion of a first end of a plunger rod when the first and second plunger arms are in the pre-use position and the use position.

Abstract: An apparatus and method for mixing and dispensing bone cement is provided. The apparatus includes a mixing vessel for mixing bone cement attached to a syringe body. The syringe body having a lumen that is connected to the mixing vessel by a passageway between the mixing vessel and the lumen of the syringe body. A separator is provided between the mixing vessel and the syringe body and includes an orifice therein so that when the opening in the separator is misaligned with the lumen the passageway is blocked and when aligned the passageway is continuous with the lumen so that bone cement can pass into the syringe body. A plunger is provided and is slideably movable along the longitudinal axis of the syringe body so as to advance the bone cement out of the distal end of the syringe.

Abstract: A dispensing device which disperses medicate through a needle across a zone within a body with zero pressure differential. The device includes a needle which is, during use, becomes encapsulated within a tubular needle-receiving member, a therapeutic agent reservoir in fluid communication with the needle, positioned within said housing, and in communication with the needle, a second reservoir, a reservoir-connecting conduit in communication with the therapeutic agent reservoir, a fluid drive in communication with the fluid in the second reservoir and in communication with said reservoir-connecting conduit, and a linear drive attached to said needle or to said needle-receiving member.

Abstract: In a background-art medical gripping device, when a wall surface of an in vivo tissue has a large tear, a side portion of the tear can be gripped by the gripping device, but the other side portion opposed to the side portion cannot be gripped simultaneously. Therefore, to close the tear, complicated operation is required to be performed using plural gripping devices. A medical gripping device according to the present invention includes a fixed clip, a pair of movable clips made from an elastic material and provided to face the fixed clip, the movable clips having lower ends fixed to the fixed clip and the other ends opened, and a control mechanism which shifts from each other a timing at which a gripping target is gripped between one of the movable clips and the fixed clip and a timing at which the target is gripped between the other movable clip and the fixed clip.

Abstract: A Luer securement device comprising a Luer adapter having a septum and a catheter hood, the Luer adapter further having a wedge seal for receiving a base portion of a catheter. The Luer securement device further includes an inserter body in which is slidably housed a catheter threader having a probe which is configured to advance a base portion of a catheter through the septum thereby seating the base portion of the catheter into the wedge seal of the Luer adapter as a tip portion of the catheter is inserted into a patient. The catheter threader further includes a needle adapter having a needle which is threaded through the probe and the catheter to assist in inserting the catheter into the patient. Following insertion of the catheter, the catheter threader is retracted within the inserter body thereby withdrawing the needle from the catheter and shielding a sharpened tip of the needle within at least one of the inserter body and the catheter threader.

Abstract: According to the invention, an injection device (D) comprises a pre-filled syringe and a safety device. The pre-filled syringe comprises a barrel with an inner cavity in fluid communication with a hypodermic needle attached to a distal end of the pre-filled syringe and a piston fluid-tightly sealing a proximal end of the inner cavity. The safety device comprises a support body for retaining the pre-filled syringe therein, an outer body operably connected to the piston, a needle shield and a releasable retaining means (R). The retaining means comprises a radial projection and a longitudinal recess adapted to receive the radial projection. The radial projection is connected to or integral part of one of the support body or the outer body and a longitudinal recess formed into the other of the support body or the outer body. The needle shield, the support body and the outer body are telescopable relative to each other.

Abstract: A steroid delivery system including a mixing syringe having a first chamber and a second chamber and at least one hypodermic needle is provided. The first chamber of the mixing syringe contains a pre-measured volume of a local anesthetic and the second chamber contains a pre-measured volume of a corticosteroid. An improved mixing syringe and a method for treating pain using the steroid delivery system of the present invention is also provided herein. The improved syringe achieves mixing without the introduction or elimination of air and without puncturing or rupturing of a membrane, diaphragm or other material. The kit concept improves the speed of the procedure, sterility, accuracy of dosing, and immediate availability of disparate items to implement the procedure in a variety of medical practice settings.

Abstract: The invention pertains to an applicator (1) for inserting an implant, in particular a rod-like implant (2) containing an active substance, under the skin of a human or animal, comprising a housing (3), a cannula (6) extending from the housing (3), and a handle (15) for grasping and maneuvering the applicator (1) and the cannula (6) during insertion of an implant (2). In accordance with the invention, the handle (15) extends above at least part of the length of the cannula (6). Such a handle facilitates insertion of the cannula and/or accurate positioning of the implant.

Abstract: A syringe including a barrel, a needle subassembly holder positioned in the barrel, and a needle subassembly positioned in the holder. The needle subassembly includes a needle hub releasably connected to the holder and a needle connected to the hub. Further, the syringe includes a piston slidably received by the barrel. The piston includes a piston body and a piston head having a releasable portion temporarily covering a hatchway. The piston also includes a valve positioned proximal of the hatchway and movable between blocking and passing positions. A user may push the piston distally beyond an injected position in which the piston head contacts the holder causing the holder to move distally and the hub to contact the barrel, causing the barrel to bow, thereby storing potential energy.

Abstract: A flexible endoscopic device including an elongate flexible member having opposite ends, an effector assembly mounted on one of the opposite ends of the flexible member, and a handle mounted on the end of the flexible member opposite the effector assembly. The handle includes a fastener for receiving a portion of the flexible member spaced from the end of the member opposite the effector assembly. The device also includes an actuator assembly extending through the flexible member and operatively connected to the effector assembly for actuating the effector.

Abstract: A safety device for a medicine cartridge comprising a body for receiving a cartridge, a guard for covering a used needle, a plunger to dispense medicine from the cartridge and a spring for activation of the guard. The trigger fingers of the guard are spaced to avoid or minimize contact with the spring flange during assembly to avoid trigger finger unseating. An elongated trigger finger head enables the device to activate for all known syringe and syringe plunger tolerances. The spring end coils have larger diameter than the inner coils to reduce the likelihood of the spring end coil end interfering with the cartridge subassembly. Syringe capture features are configured to retain a syringe having a small round or conventional cut flange in place during use and reduce the stress on the syringe flange during insertion while maintaining the ability to hold the syringe in place during use.

Abstract: A safety device having a tubular support for a needle mount end and a protective shield slidably mounted on the support from a set position, a retracted position and then to a locked position to covers the needle. A locking member mounted on the support, within the shield and a cam follower is engaged with a cam profile on the locking member. Forward axial movement of the support relative to the locking member causes the locking member to rotate relative to the support. The shield has a guide defining a shoulder towards its rearward end and an abutment on the locking member is receivable behind the shoulder when the shield is in its locked position. A spring acts such that when the locking member is turned to engage its abutment with the shoulder of the shield when the latter is in its locked position, so preventing subsequent rearward movement thereof.

Abstract: A medical injector is provided herein which includes first and second body portions each having a longitudinal axis and configured to couple at a coupling. The first and second body portions are complementarily formed so as to be movable about the coupling. The medical injector also includes an axially-displaceable plunger; biasing element for advancing the plunger a predetermined distance; and, a releasable retainer for releasably retaining the plunger in a first state against the force of the biasing element. In an initial state, the axes of the first and second body portions are not aligned and the plunger is in the first state. In a coupled state, the axes of the first and second body portions are axially aligned, and the releasable retainer releases the plunger, thereby allowing the biasing element to advance the plunger the predetermined distance.

Abstract: A device for administering an injectable product, including a housing, a displaceably mounted product container accommodated by the housing, a plunger in the container so that it can be displaced in a forward-drive direction in order to dispense the product, a plunger rod acting on the plunger in the forward-drive direction and having a releasable retained position, and a spring acting on the plunger rod in the forward-drive direction, the plunger rod releasably held in the retained position in a retaining engagement against the force of the spring, wherein the spring projects into the container in the retained position.

Abstract: The present invention concerns a prefilled injection device having a container and a dose setting mechanism encapsulated inside the housing. The housing is made from two parts which are locked together by a bayonet coupling: In addition to the bayonet coupling, the two parts are also provided with irreversible locking means locking the two parts permanently together.

Abstract: A fluid syringe of the type used with fluid infusion devices is presented here. The fluid syringe generally includes a barrel, a piston, and a check valve seal. The barrel has an interior wall and a sealed main fluid chamber. The piston is slidably coupled within the barrel, and the piston has a piston seal forming an interference fluid seal against the interior wall. The check valve seal is coupled to the piston, and it is located between the piston seal and the main fluid chamber. The check valve seal forms an interference fluid seal against the interior wall when the piston is unloaded, and it disengages the interior wall to allow gas flow from the main fluid chamber toward the piston seal when the piston is loaded.

Abstract: A safety IV catheter includes a unitary, resilient needle guard received in a catheter hub. The needle guard includes a proximal arm or wall that includes an opening through which a needle passes for axial movement. When the needle is retracted from the catheter, it releases the force that had previously prevented movement of the needle guard within the catheter hub. This in turn causes the needle guard to snap into a position in which it is clamped onto the needle shaft and in which its distal wall blocks access to the needle tip. In this condition, the spring needle guard and needle can be removed from the catheter hub. A slot or crimp may be formed in the needle shaft that engages with the needle guard after the protected needle and needle guard are removed from the catheter hub, thereby to prevent removal of the protected needle from the needle guard.

Abstract: A rapid exchange balloon dilation catheter includes a catheter shaft with a proximal tubular member defining a proximal inflation/deflation lumen for conveying fluids therethrough with a distal portion of the bore of proximal tubular member filled with a fluid-impervious barrier, a distal body extending from the fluid-impervious barrier to the distal end of the shaft, a plurality of distal tubular members defining distal inflation/deflation lumens in fluid communication with the proximal inflation/deflation lumen and extending through the fluid-impervious barrier and the distal body to the distal end of the shaft distal portion, a guidewire tubular member having a bore extending from a side aperture formed in the distal body through the distal body alongside the distal tubular members in a multi-lumen arrangement, and a plurality of stiffening members extending from within the fluid-impervious barrier into the distal body to a point within the shaft distal portion.

Abstract: A system for perfusion management that monitors, maintains, diagnoses, or treats perfusion deficiencies.

Abstract: A system for perfusion management that monitors, maintains, diagnoses, or treats perfusion deficiencies.

Abstract: A system for perfusion management that monitors, maintains, diagnoses, or treats perfusion deficiencies.

Abstract: An expandable medical balloon for use in combination with a catheter assembly, the balloon having a torque in a first and second unexpanded state, and to methods of making and using the same.

Abstract: A syringe for administering medicament from a cartridge. The syringe includes a sleeve having an interior for receiving the cartridge extending between a distal hub and a proximal opening. The syringe has a cap selectively covering the proximal opening for retaining the cartridge in the interior of the sleeve. The cap includes a finger grip extending outward from the sleeve for engaging fingers of a user. The syringe also has a plunger rod movably connected to the cap. The plunger rod has a distal connector for selectively connecting the rod to the cartridge plunger when the cartridge is received in the interior of the sleeve to push medicament from the cartridge reservoir as the plunger rod moves with respect to the cap.

Abstract: A needle containing medical device having a retractable needle [90], the device comprising an outer body [93], an inner member [97] which can slide within the outer body, a releasable needle holder [91] in a front portion of the outer body, a needle attached to the needle holder, the inner member being provided with a series of spaced needle holder engaging means [108], and the needle holder being provided with a series of spaced inner member engaging means [108] thereby enabling the inner member to be attached to the needle holder at at least one of the series of engaging means.

Abstract: The invention concerns a device for ocular application of an active principle (1) comprising a main electrode (2) including an insulating layer, an adhesive layer designed to bind the insulating layer to a conductive layer, characterized in that the main electrode comprises a zone (21, 22) designed to be urged into contact with an eyelid.

Abstract: A needle safety device is provided having a housing, a needle assembly movably mounted within the housing and a spring for biasing the needle assembly within the housing. The needle assembly is movable along a first axis and the spring is movable along the second axis different from the first. There is also provided a lens for enhancing visualization of the flow of fluid through the needle safety device. There is further provided a safety sheath for covering a needle of the needle assembly and restraining the needle assembly against movement due to the bias of the spring.

Abstract: A cover for a syringe includes an elongated flexible envelope and an absorbent material. The elongated flexible envelope includes a body portion and a needle-receiving portion. The body portion has a first end that defines an opening and an opposite second end. The needle-receiving portion extends from the second end of the body portion and terminates in a distal end. The body portion and the needle-receiving portion define a cavity of sufficient size to allow the syringe to be placed therein. The cavity is in communication with the opening. The envelope is made of a material that is impervious to liquid. The absorbent material is disposed in the distal end of the needle-receiving portion.

Abstract: Medical dilatation balloons comprise a polymer that has the attribute of memory, and/or is crosslinked to impart memory. Such balloons exhibit a reduced tendency to overinflate at high inflation pressures. Furthermore, such balloons when shrunk radially by the application of heat while restraining axial shrinkage, exhibit customizable linear or non-linear compliance curves and lower crosslinking profile relative to the same balloon when unshrunk. Also disclosed is an expansive element within a tube whose outer diameter is equal to the outer diameter of the tube from which it was made. In addition, disclosed are (a) processes for preparing crosslinkable polymers, (b) joining crosslinked balloons to catheter systems, (c) forming shrunk balloon elements, and (d) forming an expansive element within a tube whose outer diameter is equal to the outer diameter of the tube from which it was made.

Abstract: A safety syringe has a barrel, an inner needle hub, an outer needle hub, a plunger. The barrel has a distal end and a spout. The spout is formed axially on and protrudes the distal end. The plunger is mounted in the barrel and has a mounting protrusion being formed axially on the distal end of the plunger. The outer needle hub is mounted on the spout of the barrel and has a mounting chamber formed in the outer needle hub. The inner needle hub is mounted in the mounting chamber of the outer needle hub and has multiple resilient wing sections that are mounted in the mounting protrusion. Therefore, the inner needle hub may be withdrawn without touching the needle or outer needle hub and disposed of safely.

Abstract: A safety arrangement for a medical needle (15) has a support (14) for carrying the mount end of the needle, and a sleeve (16) slidably mounted on the support (14) for movement from an initial position to a retracted position and then back to a protecting position where the sleeve (16) covers the tip (21) of the needle (15). A spring (32) urges the sleeve toward its protecting position and a blocking member (23) projects forwardly from the support (14) and is movable between non-blocking and blocking positions. In the non-blocking position the sleeve (16) is free to slide from its initial position to its retracted position. On movement of the sleeve to its protecting position, the blocking member (23) moves to lie between the support (14) and sleeve (16) to prevent subsequent movement of the sleeve away from its protecting position.

Abstract: A manually-powered injection device that self-administers a painless injection. The injection device provides a method for substantially painless injections of vaccine and other medication into a patient that does not require the use of an anesthetic, that does not require the medical personnel to spend a substantial amount of time performing the injection procedure, that is relatively simple and inexpensive to perform and operate, and that provides a relatively high degree of safety for both the medical personnel and for the patient. The injection needle can have an outside diameter greater than 0.10 mm and less than about 0.38 mm. The vaccine or other medicament can be injected painlessly through the needle and into the patient at a substantially constant volumetric flow rate of about 0.05 ?L/s to about 50 ?L/s, typically over a 3- to 5-minute period of time.

Abstract: A medical device, such as a Huber-type device, includes a structure that enhances operator safety by reducing the likelihood that a needle will accidentally injure an operator. In one embodiment, the device includes a collapsible structure that can move from a use position to a non-use position. The device includes first and second wing portions and a channel for covering the needle as it is extracted from the patient. The structure enables the operator to leverage applied pressure for a smooth removal of the needle into the device for safe disposal.

Abstract: A device for injecting fluid from a pre-filled cartridge is provided. The device includes a needle for piercing a patient. After an injection, the needle can be retracted to prevent inadvertent contact with the contaminated needle. A needle retainer releasably retains the needle in the retracted position. The needle can subsequently be re-extended to administer a subsequent injection. After the cartridge is emptied, the cartridge can be removed, if desired, and replaced with another cartridge for additional injections. Alternatively, the needle can be substantially permanently retracted into the device and safely disposed of in a sharps container.

Abstract: An infusion medium delivery system, device and method for delivering an infusion medium to a patient-user, includes a needle inserter device and method for inserting a needle and/or cannula into a patient-user to convey the infusion medium to the patient-user. The needle inserter device and method operate to insert a needle and cannula into a patient-user's skin and automatically withdraw the needle from the patient-user, leaving the cannula in place and in fluid flow communication with a reservoir. The delivery device may include a base portion and a durable portion connectable to the base portion, and wherein the base portion can be separated from the durable portion and disposed of after one or more specified number of uses. The base portion supports the reservoir and the needle inserter device, while the durable portion supports a drive device for selectively driving the infusion medium out of the reservoir and into the needle and/or cannula.

Abstract: A balloon catheter and a method of making the balloon catheter, having a balloon which is bonded to an elongated shaft, and which has a first layer and a second layer and an improved bond between the balloon and the shaft. One aspect of the invention is directed to a balloon in which the balloon first layer includes eUHMWPE and has at least a section that has been oxidized with a chromic acid solution to provide improved bondability.

Abstract: A safety hypodermic syringe includes a barrel, which has a tapered hollow connector disposed at the front side and holds a needle assembly, a hollow plunger inserted into the barrel, and a retainer, which is fastened to the front side of the hollow plunger to keep the hollow plunger in a vacuum status and forced into engagement with the tapered hollow connector after the service of the safety hypodermic syringe for enabling the needle assembly and the retainer to be sucked into the inside of the hollow plunger after breaking of the tapered hollow connector from the barrel.

Abstract: An injection device including a sterile injection needle, the injection device including a container for an injectable product including an outlet for the product at a front end sealed by a membrane, the injection needle, which has a front needle portion facing away from the container for injecting into tissue and a rear needle portion which, in an initial state of the injection device lies opposite and faces the membrane and which is injected through the membrane into the container for an injection, a needle support which holds the injection needle in a central needle portion, and a casing which supports the needle support and the container and movably guides them relative to each other for piercing the membrane, wherein, in the initial state of the injection device, the needle support forms a sterile chamber for the rear needle portion, the chamber sealed by a sealing element on a rear side of the chamber facing the outlet of the container, and wherein the front end of the container for piercing the membran

Abstract: The invention provide a cylindrical pushrod for the syringe needle-retracting safety injector, comprising an outer cylinder, an inner cylinder, a push pole, an underpinned piece and a seal gasket; the push pole is set at the front end of chamber of outer cylinder, its front end appears as a tubular shape or projects partially in the longitudinal direction, the back end of push pole is supported on the underpinned piece; the underpinned piece is set at the front end of the chamber of outer cylinder and supports the push pole; the cylinder wall of the inner cylinder supports the underpinned piece; a clamping structure is set at the tail of this cylindrical pushrod. With the safety injector with the cylindrical pushrod according to the invention, the medical personnel can control the time of the needle retraction as desired, and is not necessary to change their habitual injection practice, and thereby the safety injector is easy to operate.

Abstract: Methods are provided for producing non-glycosylated, single-chain and two-chain pro-urokinase (pro-UK) mutants. The methods include cultivating a specific E. coli type B strain that has been transformed with specific plasmids carrying a cDNA sequence that encodes pro-UK mutants and carries specific promoter sequences. Products produced by the methods have medical use for thrombolysis performed while sparing hemostatic clots, e.g., for particular applications such as after a stroke or heart attack.

Abstract: A method for withdrawing a fluid sample from a patient is disclosed comprising the steps of: a) providing a sampling device (10) having a housing (20) and a needle (40) having a sharpened tip for piercing the skin of the patient; b) withdrawing fluid from the patient into the housing; c) retracting the needle so that the sharpened tip of the needle is enclosed within the housing; and d) expelling the fluid from the housing after the needle is retracted.

Abstract: A hypodermic syringe includes a barrel, the barrel having two stop portions in the rear side, a radially compressible constraint member mounted in the barrel and stopped between the stop portions of the barrel, and a plunger holding a rubber stopper and axially movably inserted through the constraint member into the inside of the barrel, the plunger having a breaking portion, and front stop flange, which is stopped against the constraint member upon back stroke of the plunger after use of the syringe for enabling the user to break the breaking portion.

Abstract: The syringe (10) for self-injecting an extemporaneous mixture comprises: a body (60) containing at least two substances (36, 38) initially separated by an intermediate piston (32), which body (60) has two relatively movable portions (64, 66) that are movable between an initial position in which the two substances (36, 38) are separate and a final position in which the two substances (36, 38) are mixed together to form an extemporaneous mixture; automatic means (70, 72) for injecting the extemporaneous mixture out from the body (60) in order to proceed with injection; and latch means (73) for preventing triggering of the automatic injection means (70, 72). The syringe includes locking means (154, 109) for locking the latch means (73) so as to prevent the automatic injection means (70, 72) being triggered until the two substances have finished being mixed together.

Abstract: A method for hemostasis of an artery having a puncture after arterial catheterization, the catheterization using an introducer sheath, the method including the steps of inserting into an artery a catheter introducer having a forward end and a balloon adjacent the forward end prior to arterial catheterization, following arterial catheterization and removal of a catheter from the catheter introducer, retracting the catheter introducer such that the forward end thereof lies exterior of the artery adjacent a puncture in the wall of the artery, inflating the balloon, thereby causing inward collapse of the forward end of the catheter introducer, thereby defining an enhanced surface area surrounded by the balloon adjacent the puncture for hemostasis, and following hemostasis, deflating the balloon and removing the catheter introducer from the patient. An introducer sheath suitable for use in the method is also described and claimed.

Abstract: A plastic needle guard is mounted on a hub in which a needle is secured. In order to cover the end of the needle, the needle guard is slid manually off the hub and over the end of the needle to position the needle end within the guard. A washer that is loosely mounted within the guard and through which the needle passes drops off the end of the needle to block any return movement of the needle out of the guard. Other embodiments use lock-type washers to prevent a return movement of the needle.

Abstract: A device for injecting fluid from a pre-filled cartridge is provided. The device includes a needle for piercing a patient. After an injection, the needle can be retracted to prevent inadvertent contact with the contaminated needle. A needle retainer releasably retains the needle in the retracted position. The needle can subsequently be re-extended to administer a subsequent injection. After the cartridge is emptied, the cartridge can be removed, if desired, and replaced with another cartridge for additional injections. Alternatively, the needle can be substantially permanently retracted into the device and safely disposed of in a sharps container.

Abstract: The present invention generally relates to a medical device and procedure for accurately positioning a catheter across a desired region within a patient's vasculature. In particular, the present invention provides a hub assembly unit that allows a physician to precisely position a stent within a vessel utilizing a stent delivery catheter. The hub assembly unit includes a fine adjustment mechanism. The fine adjustment mechanism extends or contracts the length of the hub assembly unit in controlled incremental units. These controlled fine displacements are then translated directly to the stent delivery or balloon dilation catheter.