Abstract: A system for deploying an intraocular shunt can include an intraocular shunt inserter and a deflector component that is releasable attachable to a distal end portion of the inserter. The inserter can include a housing having a distal end portion and a needle extending from the distal end portion. The deflector component can have a needle guide configured to receive the needle of the inserter therein. The deflector component can be coupled to the inserter in order to permit the needle guide to bend the needle and maintain the needle in a bended configuration.

Abstract: A syringe having a dispensing element (20) and having a mounting element (2), wherein the dispensing element (20) has a dispensing sleeve (21) and a leaf spring system (3), wherein the mounting element (2) has a syringe body (17), and an injection needle (16) is formed on one end on the syringe body (17) and a detent-engagement flange (19) is formed on the other end, wherein, in the syringe body (17), there is arranged a movable stopper (18), wherein the leaf spring system (3) comprises a piston (6) and a spiral spring (5) arranged around the piston (6), wherein the piston (6) can be slid into the dispensing sleeve (21), and the spiral spring (6) is arranged between a leaf spring base (22) and a spiral spring abutment, wherein the piston (6) abuts against the stopper (18), wherein the dispensing sleeve (21) has a guide duct and the dispensing sleeve (21) comprises a first locking means (7) and a second locking means (9), wherein the detent-engagement flange (19) is movable in the guide duct and is fixable and

Abstract: An injection device includes a syringe having a body with a piston disposed therein with an open end along with a viscous fluid disposed in the body for injection by the piston. A needle assembly is provided which includes a cannula having a luer connection engageable with the syringe distal end with the luer connector including a hub. Mating engagement is provided by way of internal threads at the syringe distal end and external threads of a hub with a pitch sufficient to prevent detachment of the hub from the syringe distal end during ejection of the viscous fluid. In addition, a stepped cavity, disposed in the hub, further prevents detachment of the hub from the syringe distal end during ejection of the viscous fluid.

Abstract: A novel design of a polymer retention hub created having an innovative feature used to permanently attach a thin wall nozzle core without use of adhesives or ancillary parts to form a conjunct nozzle. Additional polymer in the correct amount is molded into a polymer retention hub in close proximity to a location where a mechanical lock must be formed to join the two components together. The inventive design of the polymer retention hub is configured to produce an enclosed cavity with the strength required for separation of a nozzle core from a standard taper.

Abstract: Devices having male connectors for preventing connection to non-compatible female connectors are described. An exemplary male connector includes an elongate tip and a collar disposed coaxially around the elongate tip including a plurality of ribs disposed on either an inside surface or an outside surface of the collar for preventing entry of a non-compatible female connector into a channel formed between the elongate tip and the collar. One or more embodiments pertain to a device with a male connector and a compatible female connector including a threaded portion for engaging a corresponding threaded portion of the male connector.

Abstract: A clam shell shaped adapter for connecting a fluid output device and a fluid input device to establish a fluid path between the fluid output and input devices has first and second shells integrally connected by a living hinge. The first shell has a connector fitting end and a catheter end connected by a tubing. The fluid output device may be a catheter that is matable to the catheter end. A retainer structure in the adapter fixedly retains the catheter when the first and second shells close upon each other. Respective latch mechanisms provided at the first and second shells lockingly couple the first and second shells to each other. The fitting end has a given configuration that prevents the fitting end from mating with a counterpart conventional luer fitting but enables the fitting end to mate with a counterpart connector fitting that has a special configuration that mirrors the given configuration.

Abstract: A catheter proximal section is preferably formed from a relatively soft part and a relatively rigid part, and includes a proximal terminal end that defines a perimeter of an opening into a lumen of the catheter. The proximal section may further include a feature for interlocking engagement with an accessory tool. An inner surface of each of the relatively soft and rigid parts may be located opposite one another, on either side of the catheter lumen. The relatively soft and rigid parts may be included in a sealing assembly that further includes an attachment feature for removable connection of the assembly to the proximal section catheter.

Abstract: The present invention relates to a delivery member attachment device (10) comprising a neck (12) having an inner space intended to accommodate a connection part of a medicament container, which neck (12) is intended to receive a delivery member (30) for creating a passage between the medicament container via the connection part and through the delivery member, that said neck (12) is arranged with threads (14) arranged to engage with corresponding threads (34) of an attachment part (32 of said delivery member (30), and wherein said neck (12) further is arranged with a number of slits (16) providing a number of tongues (18) between said slits, and wherein said tongues (18) are arranged to flex inwards, when a delivery member (30) is to be attached, to allow an axial pushing of said attachment part (32) onto, and in engagement with, said neck (12).

Abstract: A medical connector includes a body defining a lumen for fluid flow through the medical connector. The medical connector includes a luer member and an annular member disposed about the luer member. The annular member includes internal and/or external engagement structures. The medical connector may be provided on the outlet of a syringe or on a catheter. A fluid path is disclosed including a first section and a second section. The first and second sections may each include a medical connector to provide a removable connection with a syringe and a catheter, respectively. The medical connector may provide a removable connection between the first and second sections. A fluid delivery system is disclosed including an injector, a syringe operatively associated with the injector, and a fluid path connecting the syringe and a source of injection. The medical connector may provide a removable connection between the syringe and fluid path.

Abstract: A vented connector, used with male Luer tip fitting, is disclosed. The connector includes axial and bifurcating portions. The axial portion includes an exterior housing and interior post. The lumen of the post forms a continuum with an air inlet. The air inlet is furnished with a filter or membrane element, selectively allowing for the flow of air to pass therethrough while preventing an outflow of fluids therefrom. The outer diameter of the post is smaller than the inner diameter of male Luer tip fitting. This provides for a fluid flow in-between the exterior surface of the post and the interior surface of male Luer tip fitting; whereas the flow of air that is drawn into the connector from the inlet, passes via the post into the interior lumen of a receptacle, without intermingling with the concomitantly fluid flow from the receptacle.

Abstract: The illustrative embodiments described herein are directed to apparatuses, systems, and methods for managing liquid flow associated with a tissue site that involves using reduced pressure to control fluid flow. In one instance, an apparatus includes a first valve and a second valve in fluid communication with a reduced-pressure source. The valves are movable between an open position and a closed position and are operable to change flow status (open to closed or vice versa) based on a presence of reduced pressure. At least one of the first valve or the second valve is in the closed position to obstruct a flow of a liquid while the other is in the open position. The apparatus also includes a reservoir fluidly coupled to the first valve and the second valve. Other systems, methods, and apparatuses are presented.

Abstract: A syringe kit for mixing two medicinal fluids includes first and second barrels containing medicinal fluids therein. The first barrel includes a connecting tube portion at a tip portion having a male screw on an outer periphery, and a non-roughened inner tapered surface on an inner periphery. The second barrel includes a second plunger, a screw tube portion with a female screw on an inner periphery thereof freely engageable with the male screw of the connecting tube portion, and a nozzle portion situated inside the screw tube portion with a non-roughened outer tapered surface fitting to the non-roughened inner tapered surface. A surface of the male screw and the outer periphery of the connecting tube portion, or a surface of the female screw and the inner periphery of the screw tube portion are roughened to a surface roughness in a range between Ra 1.0 and Ra 2.0 micrometer.

Abstract: A needle mounting system and methods for mounting a needle assembly on a needle mount are disclosed. The needle mounting system includes a needle hub having protrusions extending radially inward. A needle mount has a plurality of slots to receive the protrusions. The slots have a first portion that defines a passageway substantially parallel to a longitudinal axis of the needle mount and a second portion substantially perpendicular to the axis. The needle hub and mount provide a method wherein a needle assembly may be mounted on an injection device without completely rotating the needle hub relative to the needle mount.

Abstract: Systems and methods involving transferrable identification tags are provided. In one embodiment, a system includes a delivery device, a container, and a tag coupled to the container and configured to store information related to contents of the container. The delivery device is engageable with the tag and at least a portion of the contents of the container are transferrable from the container to the delivery device following its engagement with the tag. The tag is removable from the container in engagement with the delivery device such that the delivery device carries the tag following its removal. In one form, a frangible member is coupled to and extends between the tag and the container, and the tag is removable from the container by the delivery device upon breakage of the frangible member. Other embodiments include unique methods, systems, kits, assemblies, equipment, and/or apparatus which involve transferrable identification tags.

Abstract: A dispenser device comprising a pistol housing, a needle direction control mechanism, a boost mechanism, a quantification control mechanism, and a combination of the pistol housing, the needle direction control mechanism, the boost mechanism, and a syringe positioning mechanism or a holding ring embodies the present invention with features and advantages shown as follows, (1) Uniform injection of agents synchronously mixed by not less than two contents; (2) Mixed agents not exposed in air; (3) Uniform injection, high air tightness, injection direction controlled by easy turning, smooth and convenient operation, high powerful operation via shifts of a push rod driven by a pressed trigger, promoted yield rate, assembly easily constructed, reduced manufacture cost, and convenient maintenance.

Abstract: A luer connector assembly is provided for enhancing the frictional engagement between medical devices such as syringes and needle assemblies. The assembly needle includes a female luer fitting having a passageway and a relatively soft, resilient member bounding the passageway. The passageway is also bounded by the body of the fitting, which is harder than the soft, resilient member. A male luer fitting inserted into the passageway engages both the soft, resilient member and the body of the female luer fitting. A method of manufacturing such a connector assembly is further provided. A first material is injected into a mold to form the body of a female luer fitting, the fitting including a passageway and a recess extending into the body. A second material is then injected such that it extends into the recess and bounds the passageway. The second material, when cool, is softer than the first material.

Abstract: The syringe is a prefillable or prefilled syringe having a syringe cylinder which is delimited to one side by a plunger and which to the other side opens into a syringe connection having a free end closed by a membrane. The syringe cylinder, the syringe connection and the closing membrane are formed as one piece as a plastic injection molded part.

Abstract: A device for retaining and dispensing a free-flowing substance includes a syringe-like retaining body (12) in which a retaining space (46) is formed. A displaceable piston (22) is axially introduced into the retaining space (46) and the retaining body (12) is provided with a dispensing nozzle (18) on its front end facing away from the piston (22). A locking pin (36) through which at least one transverse channel (44) passes, with an axial channel (42) branching off therefrom, is provided on the inside of the dispensing nozzle (18). In a closed position of the locking pin (36), a flow connection between the retaining space (46) and the transverse channel (44) is blocked. In an activation position of the locking pin (36), the transverse channel (44) is connected to the retaining space (46), so that the free-flowing substance can be dispensed from the retaining space (46) via the transverse channel (44) and the axial channel (42).

Abstract: A needle mounting system and methods for mounting a needle assembly on a needle mount are disclosed. The needle mounting system includes a needle hub having protrusions extending radially inward. A needle mount has a plurality of slots to receive the protrusions. The slots have a first portion that defines a passageway substantially parallel to a longitudinal axis of the needle mount and a second portion substantially perpendicular to the axis. The needle hub and mount provide a method wherein a needle assembly may be mounted on an injection device without completely rotating the needle hub relative to the needle mount.

Abstract: The syringe is intended for one-off use and has a syringe barrel (1), a barrel stopper (12) which can be displaced in the syringe barrel (1) by means of a plunger rod (11) and a needle unit (25) accommodated in the syringe barrel (1). The plunger rod (11) and the needle unit (25) are connected to one another by coupling means (20, 40) in order to retract the needle unit (25) into the syringe barrel (1) after the injection. As proposed by the invention, the needle unit (25) comprises a needle holder (26) made from plastic surrounding an injection needle (27) made from stainless steel along part of its length, which is closed off from an interior of the syringe barrel (1) containing an injection solution (50) by means of a seal insert (36) made from pharmaceutical rubber through the injection needle (27) extends from the rear end. As a result of this feature, an injection solution (50) contained in the syringe is in contact exclusively with permitted materials and the syringe can therefore be stored pre-filled.

Abstract: A disposable safety syringe in one embodiment includes a syringe barrel; a plunger comprising a push rod; hollow first, second, and third adapters for forming an airtight engagement with an inner surface at one end of the syringe barrel; and a needle threadedly secured to the first adapter to establish a communication with inside of the syringe barrel prior to beginning a liquid dispensing operation with respect to a subject. After injection and pulling the needle out of a subject, a pulling of the plunger can be stopped, a further pulling of the plunger can also be stopped when an annular cutting groove of the plunger is about flush with the other end of the syringe barrel with the needle being retracted into the syringe barrel, and a breaking operation along the cutting groove can break the plunger.

Abstract: A modular catheter system. The modular catheter system may include a first tubular member, a first catheter tubing, a second tubular member, a second catheter tubing and a plurality of concentric seals. The first catheter tubing may be disposed within an interior portion of the first tubular member while the second catheter tubing may be disposed within an interior portion of the second tubular member. The first tubular member and the second tubular member are removably attachable to each other. The plurality of concentric seals may encircling the first catheter tubing and the second catheter tubing, and the first catheter tubing and the second catheter tubing form a continuous path when the first tubular member and the second tubular member are removably attached to each other. The catheter system may also be formed as a dual lumen catheter.

Abstract: Syringe having a snap-fit mechanism for attaching a needle hub to a syringe barrel in a snap-fit relationship and packaged medical device comprising a syringe with a snap-fit mechanism and a needle hub are provided. An exemplary syringe includes a barrel with a collar and a rotatable arm which allows connection of a needle hub to the barrel in a snap-fit relationship. Additional features of the collar and rotatable arm may also permit disconnection of the needle hub from the barrel without the use of relative rotation of the needle hub and barrel. In a specific configuration, the syringe utilizes a torsional snap-fit element to connect the needle hub to the barrel in a snap-fit rotation. In a more specific configuration, the syringe utilizes a collar with differing interior surfaces which permit snap-fit assembly and disassembly of the needle and the barrel.

Abstract: A needle mounting assembly for mounting a pen needle in fluid communication with a medication cartridge. A collet defines an opening in which is slidably fittable the outlet end of the cartridge. The collet is shiftable relative to the cartridge outlet end. When the collet is disposed in a first axial position, a plurality of fingers of the collet extend forward of the cartridge outlet end and are disposed in a first radial arrangement in which a needle hub of the pen needle can be freely axially placed onto and freely axially removed from the plurality of fingers. When the collet is moved to a second position, the plurality of fingers are shifted by engagement with the cartridge outlet end to operationally secure the needle hub. When the collet is moved back to the first position, the plurality of fingers shift back for free axial removal of the needle hub from the mounting assembly.

Abstract: A needle assembly is disclosed, which includes a needle hub, a metal cannula and a plastic tip. The needle hub defines a fluid flow path therethrough. The metal cannula is supported on a distal end of the needle hub, where the metal cannula defines a fluid flow path into the distal end of the needle hub. The plastic tip member is connected to a distal end of the metal cannula, where the plastic tip member defines a fluid flow path into the distal end of the metal cannula. Plastic tip further includes a channel groove that runs along the length of the plastic tip to allow fluid to flow into a distal end of the metal cannula. Additionally, the plastic tip member is configured to pierce a septum of a vial.

Abstract: A braking mechanism for a retractable safety syringe is disclosed herein. In a first embodiment, the braking mechanism is disposed about the distal end of a piston. The braking mechanism may comprise a friction material about a post attached to a piston. The friction material is displaced from a seat to a landing when the piston is traversed to a fully extended position to disengage the braking mechanism. In a second embodiment, the braking mechanism is disposed at a proximal end of a syringe body. The braking mechanism has a friction member which engages an outer surface of a rigid shaft of a plunger. The friction member is selectively pivotable to disengage the braking mechanism.

Abstract: A device for retaining and dispensing a free-flowing substance includes a syringe-like retaining body (12) in which a retaining space (46) is formed. A displaceable piston (22) is axially introduced into the retaining space (46) and the retaining body (12) is provided with a dispensing nozzle (18) on its front end facing away from the piston (22). A locking pin (36) through which at least one transverse channel (44) passes, with an axial channel (42) branching off therefrom, is provided on the inside of the dispensing nozzle (18). In a closed position of the locking pin (36), a flow connection between the retaining space (46) and the transverse channel (44) is blocked. In an activation position of the locking pin (36), the transverse channel (44) is connected to the retaining space (46), so that the free-flowing substance can be dispensed from the retaining space (46) via the transverse channel (44) and the axial channel (42).

Abstract: A modular catheter system. The modular catheter system may include a first tubular member, a first catheter tubing, a second tubular member, a second catheter tubing and a plurality of concentric seals. The first catheter tubing may be disposed within an interior portion of the first tubular member while the second catheter tubing may be disposed within an interior portion of the second tubular member. The first tubular member and the second tubular member are removably attachable to each other. The plurality of concentric seals may encircling the first catheter tubing and the second catheter tubing, and the first catheter tubing and the second catheter tubing form a continuous path when the first tubular member and the second tubular member are removably attached to each other. The catheter system may also be formed as a dual lumen catheter.

Abstract: A luer connector assembly is provided for enhancing the frictional engagement between medical devices such as syringes and needle assemblies. The assembly needle includes a female luer fitting having a passageway and a relatively soft, resilient member bounding the passageway. The passageway is also bounded by the body of the fitting, which is harder than the soft, resilient member. A male luer fitting inserted into the passageway engages both the soft, resilient member and the body of the female luer fitting. A method of manufacturing such a connector assembly is further provided. A first material is injected into a mold to form the body of a female luer fitting, the fitting including a passageway and a recess extending into the body. A second material is then injected such that it extends into the recess and bounds the passageway. The second material, when cool, is softer than the first material.

Abstract: Medical devices with male luer slip fittings with either a male conical tip having a roughened outer surface or a female luer fitting with a roughened surface and methods for manufacture and use are disclosed. The outer surface of the male conical tip or a surface of the female luer fitting is roughened to increase the force required to remove the male luer fitting from the female luer fitting without causing leakage of the connection.

Abstract: A luer connector assembly is provided for enhancing the frictional engagement between medical devices such as syringes and needle assemblies. The assembly needle includes a female luer fitting having a passageway and a relatively soft, resilient member bounding the passageway. The passageway is also bounded by the body of the fitting, which is harder than the soft, resilient member. A male luer fitting inserted into the passageway engages both the soft, resilient member and the body of the female luer fitting. A method of manufacturing such a connector assembly is further provided. A first material is injected into a mold to form the body of a female luer fitting, the fitting including a passageway and a recess extending into the body. A second material is then injected such that it extends into the recess and bounds the passageway. The second material, when cool, is softer than the first material.

Abstract: A needle mounting system and methods for mounting a needle assembly on a needle mount are disclosed. The needle mounting system includes a needle hub having protrusions extending radially inward. A needle mount has a plurality of slots to receive the protrusions. The slots have a first portion that defines a passageway substantially parallel to a longitudinal axis of the needle mount and a second portion substantially perpendicular to the axis. The needle hub and mount provide a method wherein a needle assembly may be mounted on an injection device without completely rotating the needle hub relative to the needle mount.

Abstract: A medical device for use with a fluid transfer device includes a hub having an open proximal end with a frusto-conically-shaped cavity therein, a distal end and a passageway therethrough. The cavity is part of the passageway. A release element in the passageway of the hub is positioned to block fluid-tight engagement of the frusto-conically-shaped tip with the cavity of the hub. Structure is provided to release at least part of the release element, upon application of a proximally directed force on the hub, to allow the abrupt fluid-tight engagement of the tip and the cavity in the hub.

Abstract: A needle mounting system and methods for mounting a needle assembly on a needle mount are disclosed. The needle mounting system includes a needle hub having protrusions extending radially inward. A needle mount has a plurality of slots to receive the protrusions. The slots have a first portion that defines a passageway substantially parallel to a longitudinal axis of the needle mount and a second portion substantially perpendicular to the axis. The needle hub and mount provide a method wherein a needle assembly may be mounted on an injection device without completely rotating the needle hub relative to the needle mount.

Abstract: A device for administering an injectable product including a casing, an injection mechanism including an injection needle pointing in an insertion direction, and a protective cap for the injection needle wherein, in one embodiment, the administering device includes a removing device for removing the protective cap from the injection needle and, in another embodiment, the administering device includes a needle protecting sleeve shiftable generally in alignment with the casing and generally between a front position, advanced relative to the casing, for protecting the injection needle and to a rear position, retracted relative to the casing, for inserting the injection needle into a tissue. In one embodiment, the needle protecting sleeve is prevented from moving completely into the rear position by a lock when the protective cap is protecting the injection needle.

Abstract: A system for tissue augmentation using a thin-walled needle. The system includes a thin-walled needle and a syringe. The system further includes a plurality of particles for injection into a desired tissue to be augmented. The thin-walled needle has an inner diameter sufficient to allow for passage of the particles and an outer diameter designed to minimize the puncture wound in the skin when the needle is inserted. The particles may be suspended in a carrier.

Abstract: A needle assembly is disclosed, which includes a needle hub, a metal cannula and a plastic tip. The needle hub defines a fluid flow path therethrough. The metal cannula is supported on a distal end of the needle hub, where the metal cannula defines a fluid flow path into the distal end of the needle hub. The plastic tip member is connected to a distal end of the metal cannula, where the plastic tip member defines a fluid flow path into the distal end of the metal cannula. Plastic tip further includes a channel groove that runs along the length of the plastic tip to allow fluid to flow into a distal end of the metal cannula. Additionally, the plastic tip member is configured to pierce a septum of a vial.

Abstract: A needle and hub assembly for an automatic injector and a method for making the needle and hub assembly. The needle and hub assembly comprises a cap or skirt, a forward surface of which is interposed between and reinforced by first and second engaged hub portions. A needle is received in a contiguous channel formed in the two hub portions. The method for making the assembly comprises molding the first hub portion, placing the cap over the first hub portion, inserting the needle into a channel in the first hub portion, and then overmolding or otherwise forming the second hub portion on the exterior of the cap such that it is engaged with the first hub portion. An assembly created by this “two-shot” process can be used to seal a relatively large opening, and supports the needle more effectively than a conventional assembly.

Abstract: Disclosed herein are luer connectors, components thereof and fluent material delivery devices utilizing the same. The disclosed luer lock connectors can be used with syringe and needle assemblies to resist leakage through and disengagement of the syringe and needle assembly.

Abstract: Embodiments of a medical hand-grip element for injection of a substance from an ampoule, comprise a drive device for driving the ampoule and the injection needle, a delivery device for delivering the medicinal substance out of the ampoule and a coupling device for rotationally fixed coupling of the ampoule with the injection needle and for preventing a relative movement between the ampoule and the injection needle is disclosed. Embodiments of injection systems, injection units, injection needles and handling methods for them are also disclosed in which the risk of injury and contamination for the user is reduced by providing approaches for covering the ends of the cannulas of the injection needles during a number of handling steps.

Abstract: The syringe is a prefillable or prefilled syringe having a syringe cylinder which is delimited to one side by a plunger and which to the other side opens into a syringe connection having a free end closed by a membrane. The syringe cylinder, the syringe connection and the closing membrane are formed as one piece as a plastic injection molded part.

Abstract: A disposable syringe includes a tubular needle seat inserted into a barrel for fixing a needle cannula. The needle seat has an axially extending cavity with a radially yieldable catch disposed therein. A plunger is movable in the barrel, and has an engaging head defining a rearwardly facing shoulder wall which is retained by the catch when the engaging head is extended into the cavity by a pushing force applied to the plunger. The barrel defines friction diminishing regions such that when the needle seat is moved past the friction diminishing regions to be placed to a disposal position, friction between the needle seat and the barrel is diminished, thereby facilitating a subsequent pulling action of the plunger for retracting the needle cannula into the barrel.

Abstract: Cannula with protection cap for medical infusion lines and the like, comprising a hollow body provided at one end with a female luer lock connector and at the other end with an axial tubular ferrule. The hollow body and the protection cap are provided with respective formations for mutual torsional coupling acting in the direction of rotation corresponding to the unscrewing of the female luer lock connector relative to a male luer lock connector of the medical line.

Abstract: A medical device having a releasable retaining includes needle cannula connected to a hub having an open proximal end with a frusto-conically shaped cavity therein. The cavity is part of a passageway through the hub which is in fluid communication with the lumen of the needle cannula. A retaining element is releasably connected to the hub. The hub includes an aperture and at least one protuberance projecting into the aperture for engaging the frusto-conically shaped tip of a fluid delivery device. The protuberance is shaped to offer less resistance to hub movement in a direction of engagement than in a direction of disengagement with the tip. The retaining element is connected to the hub so that when the hub is engaged to the tip, the force required to disengage the retaining element from the tip is greater than the force required to disengage the retaining element from the hub.

Abstract: A safety needle-bearing device for mixing and injecting medication from a two-chambered cartridge is provided. The device includes a needle that extends through the forward end of a barrel. A two-chambered cartridge is attached to the barrel and contains components of a medication stored separately in the chambers. A plunger in the rearward end of the cartridge can be advanced into the cartridge to combine the separate components and prepare the medication. As the cartridge is advanced forwardly into the barrel, the medication is injected through the needle and into a patient. At the completion of the injection stroke, the cartridge engages a needle retainer to actuate needle retraction. The needle is subsequently retracted to shield the contaminated needle.

Abstract: A needle protection device for a vial, or capsule, has a housing hingedly or flexibly connected to a needle collar by a hinge. The collar has a main portion configured to fit about at least a portion of the body of the vial and an extension configured to fit about at least a portion of the neck of the vial. A needle hub, movable along the neck of the vial and to which a needle extends, is interposed between the body and neck of the vial. The hub has a skirt portion that could be moved along the neck of the vial for capping or overlapping the extension of the collar to thereby non-removably secure the collar to the vial. An improved syringe assembly is effected when a vial of the instant invention is placed within a vial holder applicator, such as for example a CARPUJET applicator.

Abstract: An injection needle retractable injector, comprising a barrel having a plunger inserted into a hollow formed therein, a needle base (3) fitted to the tip part of the barrel, a hub (2) fitted to a hollow in the needle base so as to be separated only to a rear end side, and an injection needle (4) having a rear end part fixed to the tip part of the hub, wherein the plunger is moved to the tip part of the barrel to engage the rear end part (11a) of the hub with the tip part (13) of the plunger so that the injection needle can be pulled into the barrel through the plunger, the hub is held in the needle base by a fitting structure formed between the tip part outer peripheral surface of the hub and the tip part hollow surface of the needle base, and the tip of the hub in the fitted state of the hub being positioned at the outermost side of the needle base is positioned near or forward of the tip of the needle base in axial direction, whereby a production can be facilitated, the effect of an external force acting on

Abstract: An injection device for injection of a medicament from a medicament cartridge 40 having a neck portion is disclosed. The injection device further comprises a main housing 4 in which the medicament cartridge 40 is releasably retained by first and second retaining means 92,94. The retaining means 92,94 are each moveable between a first position in which the neck portion is engaged thereby to retain the medicament cartridge 40 in the main housing 4 and a second position which allows the medicament cartridge 40 to be removed from the main housing 4.

Abstract: A safety syringe cylinder has a structure for attaching a syringe needle precisely. The syringe needle can be retracted into the syringe cylinder for bending. A hook seat is formed at a lower end of the needle. An annular hook groove is formed at a top end of the push rod cap. The hook seat is engaged with the annular hook groove so as to control the displacement and bending process of the syringe needle. Thereby, the processing of undesired syringe needle is safe, reliable and convenient.

Abstract: A needleless dosage transfer system for filing medicating devices such as syringes or needleless cannulas to minimize the likelihood of an unwanted needle stick and to avoid the initial cost of a needle as well as the disposal cost of the needle. A vial has a body portion 20 formed with flexibly deformable walls and defines a blind bore. An opening of the vial includes a tapered section adapted to frictionally fit over a taper of a male luer-type fitting commonly found on syringes and needleless cannulas. By deforming the walls of the vial, fluid is forced from the vial into a syringe. The opening of the vial 10 is protected with a cap and includes a scoreline which, when fractured, defines the opening. The cap to be removed from the vial prior to its use is fabricated as one piece with the vial in order to assure sterile conditions during manufacture and filling. A tab is associated with the cap which lists the ingredients within the vial. The vial also supports an area which lists the vial's contents.