Abstract: The invention consists of a tube syringe holding device for blood collection and for producing vacuum into the tube which target is to enable the collection of blood, that can be manufactured in a light material where two bodies, one of them cylindrical and the other semi-cylindrical, both hollow and of the same length, form one structure. Its bottom ends are opened. The top end of the cylindrical body is continued by a conduit with a male luer adapter, and the top end of the semi-cylindrical one is continued by two conduits with threads.

Abstract: A locking mechanism 10 for a medical sharp device such as a syringe assembly 62 includes a retainer part 12 for retaining a hypodermic needle 22, and a connector part 14. The retainer part includes lugs 46 for engagement with a recess 82 formed in a neck 70 of the syringe assembly. When a plunger 72 of the syringe assembly is pushed fully forwards, the lugs 56 of the retainer part 12 engage behind a ledge 54 of the connector part 14 and the lugs 46 disengage from the recess 82. The plunger 72 may then be retracted, pulling the needle 22 into the barrel 64 of the assembly. The neck portion may be eccentrically mounted on the barrel and means 116,118 may be provided for preventing rotation of the plunger 72 in the barrel 64.

Abstract: A syringe device includes a core member received in the plunger and the core member is fixedly connected to a base member to which a needle cannula is connected. When the plunger is pulled, the base member is pulled into the barrel. Two flexible protrusions extend from the plunger and which expand wide when the plunger is pulled to a desired position. The expanded flexible protrusions limit the plunger from being pushed into the barrel again.

Abstract: An animal identification and medication syringe includes a barrel, a plunger piston which moves longitudinally within the barrel in response to air pressure within the barrel, and a syringe needle for penetrating the hide of an animal and for introducing medication into the animal. A valve mechanism or plug assembly enables the syringe to selectively deliver medication into the animal. The plunger piston evacuates the medication chamber within the barrel, and also acts as the force by which the syringe is ultimately ejected from the animal after medication has been delivered. A marking disk may be mounted on the distal end of the syringe to disinfect the needle and/or to mark the animal upon impact of the syringe with the animal. A rapid refill device is also provided to refill the syringe numerous times without having to disassemble or otherwise manipulate the syringe.

Abstract: A medication injection or delivery system is provided for injecting fluids such as insulin within body tissue. The device includes a housing, a flexible shaft movably mounted within the housing, and a dose setting mechanism for controlling the movement of the shaft with respect to a fluid-containing cartridge removably positioned within or mounted to the housing. The flexible shaft, according to exemplary embodiments, includes a plunger and a flexible cable connected to the dose setting mechanism. The plunger and dose setting mechanism are connected together by the flexible shaft. The dose setting mechanism, in one aspect of the invention, includes a screw, a locking mechanism, and a nut assembly connected to the flexible shaft. The dose setting mechanism is used to set the dosage and prime the catheter. The plunger retracts into a recess to permit a new cartridge to be installed quickly.

Abstract: The implant syringe has a spacer which limits the advance movement of the plunger into the syringe needle in such a way that a distance equivalent to the length of the strand-shaped preparation to be discharged remains between the outlet orifice of the syringe needle and the head end of the plunger. The syringe needle is connected to a grip member that can be retracted over a distance coinciding with the length of the preparation. An insertion channel is initially made with the implant syringe in the body of a patient. Subsequently, the preparation to be discharged is pushed forward to the tip of the needle by advancing the plunger, whereupon the syringe needle is retracted to such an extent that the head end of the plunger reaches or projects beyond the tip of the needle.

Abstract: An improved safety syringe device includes a shield from which a vacuum needle extends and retracts, a vial that is telescopically received within a cavity of the shield and that attaches to the vacuum needle at its distal end, and a ring rotatably connected around a portion of the vial near its distal end. The vial includes a protrusion that engages with a tab on the ring to move the tab within a channel defined on the interior surface of the shield cavity. The safety syringe device further includes a temporary locking feature to maintain the vial at a generally fixed position within the shield during use of the syringe.

Abstract: Fibrin sealant applicator systems are provided for dispensing a first and a second protein solution to form a biological adhesive which overcome the disadvantages of the prior art. The fibril sealant applicator system according to the present disclosure includes two piston-type sub-assemblies coupled to two vials storing a fibrinogen and a thrombin via a coupling unit. The piston-type sub-assemblies store sterilized water within reservoirs which are in fluid communication with the vials via the coupling unit. The water is forced into the vials to form a fibrinogen and a thrombin solution. The solutions are then drawn into the reservoirs and a Y-coupler is attached to the distal end of the piston-type sub-assemblies. The Y-coupler provides fluid communication between the reservoirs and a nozzle body for dispensing the solutions when distal pressure is created within the reservoirs to force the solutions towards the nozzle body.

Abstract: A medication injection or delivery system is provided for injecting fluids such as insulin within body tissue. The device includes a housing, a flexible shaft movably mounted within the housing, and a dose setting mechanism for controlling the movement of the shaft with respect to a fluid-containing cartridge removably positioned within or mounted to the housing. The flexible shaft, according to exemplary embodiments, includes a plunger and a flexible cable connected to the dose setting mechanism. The plunger and dose setting mechanism are connected together by the flexible shaft. The dose setting mechanism, in one aspect of the invention, includes a screw, a locking mechanism, and a nut assembly connected to the flexible shaft. The dose setting mechanism is used to set the dosage and prime the catheter. The plunger retracts into a recess to permit a new cartridge to be installed quickly.

Abstract: A dental syringe system having a syringe body containing a needle assembly wherein the syringe body serves as a protective shield after medication is injected. A reusable plunger assembly pushes a slidable seal of a carpule and the needle out for medication delivery and then pulls the needle back within the syringe body after the medication is delivered. The needle assembly, syringe body, carpule carrier and carpule are disposable and the plunger is reusable.

Abstract: A hypodermic syringe comprises a barrel having at least one catching piece disposed at the end; an outer sleeve fitted rotatably with the barrel to turn to locate at the first position and the second position and provided at least one escape hole; a needle holder having a cylinder cooperating portion disposed slidably in the receiving hole of the barrel, a retaining circular groove disposed in the outer periphery of the needle holder for retaining the catching piece of the barrel; a plunger having a rod body capable of pulling back the needle holder. As the outer sleeve is turned to the first position, each catching piece of the barrel retains the retaining tooth of the barrel. The needle holder is unable to displace. As the outer sleeve is turned to the second position, the escape hole is corresponding to the catching piece of the barrel to eject outward. The needle holder is not confined so as to be pulled back by the plunger.

Abstract: A prefilled syringe of cartridge barrel having a tamper evident closure. Tamper evidence is provided by: a frangible tip seal which is integral with the tapered tip of the barrel; a frangible tip cap covering the tip, the tip seal and a portion of the distal end of the barrel; and an overwrap covering the frangible tip cap and the distal end of the barrel sealed to the distal end of the barrel by a tamper evident seal. The tapered tip is optionally equipped with a luer collar to receive an external luer connector. Alternatively, the tapered tip can be provided with a bore therethrough which can be closed with an elastomeric plug and the external connector can be a tubing conduit.

Abstract: A disposable hypodermic syringe comprises an outer barrel, an inner barrel slidingly disposable in the outer barrel, a hypodermic needle disposed axially at the front end of the outer barrel so as penetrate its front end wall and being held, at its rear end, by the front end wall of the inner barrel, and a plunger which is slidingly disposable in the inner barrel. The outer barrel includes elements for interlocking with the inner barrel when the inner barrel is in a fully inserted position. The plunger includes release elements for releasing the inner barrel from the outer barrel while interlocking with the inner barrel so as to allow the inner barrel and the plunger to be withdrawn in combination with the hypodermic needle for a distance sufficient to displace the needle into a space formed between the outer barrel and the inner barrel.

Abstract: An improved assembly of a syringe and a nozzle tip and method of use. The syringe includes nozzle tip having a sleeve portion that fits on the free end of the syringe barrel and a curved nozzle end. The nozzle tip may include a filter screen of preselected mesh size. In use, a preselected amount of marrow blood may be aspirated through the curved aspirating nozzle end and filter screen into the syringe barrel where it mixes with bone regeneration material therein to form a viscous fluid mixture. The nozzle tip is removed from the syringe and the mixture is expelled from the syringe and applied to a surgical site by depressing the syringe plunger.

Abstract: The present invention relates to a biodegradable disposable syringe and more particularly, to the biodegradable disposable syringe by using a novel polyester resin composition under a specific injection molding condition, thus being able to be disposed of without causing environmental contamination.

Abstract: An ejection device for ejecting a liquid or a liquid containing solid particles at high pressure, comprising a head unit; a pressure chamber (11) which opens into a distal ejection opening and is delimited by a working piston which, upon application of an elastic impact on its end facing away from the pressure chamber, is capable of transmitting a compression wave which may displace the pressure chamber-facing end of the working piston into the pressure chamber so that the volume thereof is reduced, with the reduction in volume of the pressure chamber being significantly smaller than the original volume of the pressure chamber; and a drive unit having a drive member which is accelerated across an acceleration portion formed within the drive unit so that it generates the elastic impact to be transmitted to the working piston. The pressure chamber is at least partially formed by a pressure cavity formed in the head unit.

Abstract: A disposable syringe comprises a syringe body (1), a plunger (40) mounted on a stem (50) slidable inside the syringe body (1), and an injection needle (10) integral with a needle-carrier (11) engageable with the fore end (2) of the syringe body (1) or the plunger, retaining means (20, 23, 24) able to retain spring means (30) under compression being provided integrally with the syringe body (1) and engagement means (59) able to cooperate with the retaining means (23) to release the spring means (30), when the plunger (40) has reached the end of its stroke, being provided integrally with said stem (50), so that the spring means (30) can act on the stem (50) to cause retraction thereof into the retracted position.

Abstract: The invention relates to a device for administering an injectable product, comprising:

Abstract: A safety syringe in which the needle holder has a mounting unit fixedly fastened to the front end of the barrel, a body holding a needle cannula outside the barrel, a breakable slotted connecting portion connected between the mounting unit and the body, and a rear engagement block, and the plunger has a front tubular retaining member adapted to engage the rear engagement block for enabling the needle cannula with the body of the needle holder to be separated from the mounting unit and moved backwards with the plunger to the inside of the barrel after the service of the safety syringe.

Abstract: A medical syringe 2 includes a cylindrical syringe body 3 and a plunger 4 fitted in the syringe body 3 for injecting a liquid agent filled in the syringe body 3 from the syringe body 3 into the vascular system of the human body by advancing the plunger 4 relative to the syringe body 3. The plunger 4 comprising a plunger body 5 and an elastic cover 9 fitted over the plunger body 5 from the front. The plunger body 5 is provided with a backplate 62 at a rear end thereof, the backplate 62 having an annular groove 68 forwardly opened and formed in a front surface outer peripheral portion thereof. The portion of the elastic cover 9 to be rearwardly stretched by the advance of the plunger 4 is allowed to ingress into the annular groove 68 for escape.

Abstract: A medication delivery device comprising a container containing a fluid medicament. The medicament is expelled from the container by moving forward an elastomeric piston inside the cartridge. The piston is moved forward by a telescopic piston rod, which can either be centrally located in the container or eccentric located. One end of the telescopic piston rod abuts the elastomeric piston either by itself or through an additional plate. The abutment having a friction large enough to prevent a lower part of the telescopic rod from rotating. In order to prevent the elastomeric piston from rotating inside the container a second telescopic piston rod is provided parallel with the first telescopic piston rod.

Abstract: A manually operated hydraulic syringe includes a syringe barrel having an interior surface. The interior surface bounds a first chamber having a first transverse cross-sectional area and a second chamber having a second transverse cross-sectional area. The first chamber is in fluid communication with the second chamber and the transverse cross-sectional area thereof is smaller than the transverse cross-sectional area of the second chamber. A first plunger has a distal end slidably disposed within the first chamber. A second plunger is slidably enclosed within the second chamber. Sealed in substantial isolation within the syringe barrel between the first and second plungers is a hydraulic fluid, such as water or oil. Rotatably coupled to the distal end of the syringe body is a nozzle or cartridge in which a dispensing material, such as a high viscosity fluid, can be selectively disposed.

Abstract: This device comprises: a syringe body equipped with an access which may be connected in succession to a filling member, such as a needle, and to an infusion line fitted with a non-return valve to allow liquid to pass from the syringe into the line; a housing mounted so that it can slide in leaktight fashion inside the body so as to vary the volume of a chamber which it delimits with the body of the syringe; an element which, forming a piston, mounted on the housing and in contact with the chamber, is able, according to its position, to create a raised pressure or reduced pressure in the chamber; means for moving the piston-forming element back and forth.

Abstract: Multi-sectioned fluid delivery devices with sensor membranes for use in detection of target molecules in gas or liquid samples are provided.

Abstract: A safety syringe for intravenous injection includes: a syringe cylinder having a plurality of sleeve ribs formed in a sleeve portion eccentrically formed on the syringe cylinder, a needle device having a needle detachably coupled on an shank portion which is provided with a plurality of shank ribs on the shank portion to be engaged with the sleeve ribs in the sleeve portion, with the needle device retractable in and automatically biased in the syringe cylinder to prevent outward protruding of used needle; whereby upon external connecting and rotative coupling of the needle on the shank portion, the shank portion will be locked without being rotatable, thereby enhancing a smooth coupling of the needle on the shank portion of the needle device. The syringe cylinder is also formed with an annular extension for limiting a rearward releasing of the plunger once inserted in the cylinder.

Abstract: An electrically-driven dental injector used in orally injecting such an injection liquid as an anesthetic in dental treatment. Electrically-driven dental injectors includes one having a mechanism for disengaging a pinion (82) from a rack (48) in order to retract a plunger rod (44) upon completion of injection; however, it has heretofore been necessary to manually operate the operating part from outside each time. The inventive electrically-driven dental injector is so arranged that the plunger rod can be manually pushed back directly oupon completion of injection without reqiring manual operation, and, to this end, the injector comprises a latch mechanism (84) for engaging/disengaging the ring gear (70) of a planetary reduction gear (50) with/from a casing (52), and an operating rod (94) extending through a support member (20) and functionally cooperating with the latch mechanism (84).

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: A syringe is provided for delivering compositions having a hollow elongated barrel engaged by a plunger with a unique plunger tip. The plunger tip extends from a round and hollow sidewall of the stem of the plunger by bifurcating into an inset branch and a spring lever. The inset branch and the spring lever define a radial tensioning groove. The lower portion of the spring lever is flat while the upper portion of the spring lever flares outward at an angle with respect to the lower portion and then terminates at a rounded distal contact end. As a result, the diameter of the spring lever at the rounded distal contact end is slightly greater than the diameter of the inside of the barrel before the plunger is inserted into the barrel. The spring lever is sufficiently flexible that upon insertion of the plunger into the chamber of the barrel, the radial tensioning groove compresses due to the spring lever flexing toward the inset branch.

Abstract: An improved syringe that allows one-handed operation, without requiring the user to reposition her hands during any portion of the injection process. The syringe comprises a housing having a plunger disposed therein that expels medication through a needle when the plunger is pressed toward the opposing end wall. Instead of having the needle in the same axis as the plunger, the needle port is carried by the wall of the syringe housing at an acute angle with respect to the longitudinal axis of the housing. With this configuration, the housing can be gripped between a finger and thumb, with the one of the fingers on the handle and the other finger on the end wall of the housing. A pair of rings are positioned at opposing ends of the housing receive the user's fingers so that relative movement of the finger and thumb creates both suction as well as pressure for injection of medication from the housing's chamber.

Abstract: A fibrin glue applicator system (10) is provided for dispensing a first and a second protein solution which form a biological adhesive when intermixed on an application site. The fibrin glue applicator system (10) includes a coupler interface (16), a disposable loading unit (DLU) (14), and a housing (12) having a handle portion (20) which includes a trigger (22) operatively associated with a slide bar (36) for dispensing the solutions from the DLU (14). Each piercer (66) is fluid communication with one of the two cylinders (46) of the DLU (14) via a respective conduit (64) connected to a respective main conduit (60). A first one-way valve (68) is included within each conduit (64) to open, and close a path leading from the piercer (66) to the main conduit (60). A second one-way valve (70) is fixed within each main conduit (60) in proximity to each dispensing orifice to open, and close a path leading from each cylinder (46) to its corresponding dispensing orifice.

Abstract: A drug delivery system for administering preset doses of a substance such as a drug, vaccine or the like is provided. The drug delivery system includes a holder and a pre-filled drug container such as a syringe which is securely retained in the holder. The drug container includes a barrel for containing the substance, a movable stopper situated within the barrel, and a blunt end having an opening through which the substance within the barrel can be expelled. The holder includes a distal portion and a proximal portion, each configured to accommodate the drug container, with the distal portion being able to be assembled to the proximal portion, which acts as a plunger rod during activation of the delivery system.

Abstract: Ampoule for dispensing a substance comprising: a container having a chamber therein for storing a substance to be dispensed; a piston arranged in the chamber so as to be displaceably in longitudinal correction of the chamber; an outlet means which can be connected to the container such that a fluid communication is established between an inlet portion of a discharge passage of the outlet means and an outlet opening of the chamber; and a plug closure means being insertable in a fluid-tight manner into the outlet opening of the chamber and, when it has been fluid-tightly inserted into the outlet opening, being displaceable by the outlet means connected to the container in direction towards the interior of the chamber from a closed position into an open position in which a fluid communication is provided between the interior of the chamber and the inlet portion of the discharge passage of the outlet means via the outlet opening of the chamber, the plug closure means having retaining means retaining the plug clos

Abstract: A kneading device adapted for preparing calcium phosphate-based cement and for applying the cement directly to a required site which comprises a cylinder 1 which includes a hollow cylindrical body portion 11 and a nozzle 12 formed at the distal end of the cylindrical body portion; a plug 2 having an axial through-hole 21 slidably disposed within the proximal end of the cylindrical body portion; a piston assembly 3 which includes a shaft 31 extending through the through-hole 21 of the plug 2 for axial and rotatable movement, a kneading element 32 at the distal end of the shaft 31 within the cylindrical body portion, and a handle 34 formed at the proximal end of the shaft 31 external of the cylindrical body portion; a cover member 4 attached to and forming a closure for the nozzle 12; and a stop member 5 for locating the plug 2 in position at the proximal end of the cylindrical body portion.

Abstract: A retracting needle assembly for use with a syringe barrel having a cylindrical collar and a plunger having a release element with a sharp distal end includes an outer hub having a passageway therethrough and an inner hub having a proximal end, a distal end and a conduit therethrough. The proximal end of the inner hub has an inner portion and a dissociable outer portion connected to the inner portion. The dissociable outer portion is further connected to the outer hub. The distal end of the inner hub is smaller than the passageway of the outer hub at the distal end of the outer hub and projects distally outwardly therefrom. A needle cannula having a distal end, a proximal end, and a lumen therethrough is connected to the inner hub so that the lumen is in fluid communication with the conduit. An energized spring is contained between the inner and outer hub. Structure is provided for connecting the outer hub to the collar of the syringe barrel.

Abstract: A disposable syringe plunger immobilizing device includes first and second hollow members, a means for connecting the first and second hollow members to one another, and a means for holding the first and second hollow members in contact with one another. When in contact with one another, the first and second hollow members contact a syringe plunger and the main body of the syringe to hold the syringe plunger in place in a bore of the main body of the syringe, so that movement of the syringe plunger relative to the main body of the syringe is inhibited. In this fashion, the syringe may be preloaded with a medicament and then safely transported without loss of the medicament within the syringe until the syringe is used. The disposable syringe plunger immobilizing device may be manufactured in different sizes to accommodate various syringe sizes and volumes of medicament to be injected and colors to assist in identification of the various sizes of the device.

Abstract: A syringe has a slide member slideably mounted on the barrel of the syringe, and the slide member is interconnected to a plunger that is slideably mounted in the barrel so that movement of the slide member effects simultaneous and corresponding movement of the plunger. This allows a syringe operator to perform aspiration and injection in sequence with one-handed operation of the syringe. The slide member is mounted near the leading end of the barrel in trailing relation to the leading end of the plunger so that the operator can see the leading end of the plunger and control its instantaneous position by sliding the slide member with a thumb or finger. The hand position of the syringe operator does not change, assuring that precise needle positioning can be made and maintained even during procedures such as sclerotherapy where needle positioning is critical.

Abstract: A power injector and a removable replacement faceplate therefor are provided along with a method of front loading syringes, particularly prefilled syringes, which have outwardly extending structure such as flanges which have been typically breech loaded or side loaded into injectors or operated in a hand held fashion. The holder or faceplate of or for the injector is provided with a set of jaws spaced around a syringe receiving opening into which a syringe is loaded, rearward end first, with the jaws in a retracted position, until the flange or other outwardly extending structure on the syringe is rearward of the syringe is beyond a locking position of the jaws. The jaws are then actuated, either by operating an actuator on the faceplate or injector or by twisting the syringe in the opening, so that the jaws move radially inward and close in iris-like fashion about the syringe.

Abstract: A syringe comprises a barrel (1) having a plunger (7) in slidable and sealing engagement therewith. In order to provide an autodestruct system, so that the syringe can be used once only, being rendered disabled after one normal use, the barrel (1) has means interrupting the cylindrical surface of its inner wall in the form of grooves (10, 11) or a projection (29), and the plunger (7) has a locking means (17, 20) which operates on engagement with a groove (10, 11) or projection (29) on withdrawal of the plunger (7) to prevent further withdrawal movement. The locking means (17, 20) is provided on the head of the plunger (7) adjacent an elastomeric sealing cap (15). The locking means may comprise a pair of flukes (17) or a cross-shaped disc (20).

Abstract: A syringe with replaceable needle assembly (10), having a syringe barrel (18) with a proximal end (14), a distal end (16), and an outer surface (87). The syringe barrel (18) surrounds an internal bore (20). A plunger assembly (60) is inserted into the syringe barrel internal bore (20). A needle assembly (80) has a sealing portion (72), which is configured to be removably insertable into the internal bore (20). The sealing portion (72) forms a fluid-tight seal with the internal bore (20). The needle assembly (80) further includes a releasable locking mechanism (79), which includes a collar (76) having a locking flange (86). Also disclosed is a replaceable needle assembly (80), which releasably locks onto the outer surface (87) of the proximal end (14) of a syringe barrel (18).

Abstract: A syringe assembly comprises a syringe barrel having an elongated body defining a chamber for retaining fluid, an open proximal end, a distal end and a frusto-conically shaped tip extending from the distal end and having a passageway therethrough in fluid communication with the chamber. The chamber has an inside diameter of at least 13.5 mm. A stopper is in fluid-tight engagement inside the barrel. An elongated plunger rod extends proximally from the stopper through the open proximal end of the barrel. A flange is positioned at the proximal end of the plunger rod. The flange is shaped and positioned to limit the distal motion of the plunger rod in the barrel by contacting the proximal end of the barrel. A tip cap is releasably connected to the tip for sealing the passageway and the chamber contains injectable liquid.

Abstract: A syringe includes a barrel having a fluid chamber, a proximal end, a distal end and an elongated tip extending from the distal end and having a passageway therethrough in fluid communication with the chamber. A collar surrounds the tip and includes at least one deflectable locking tab projecting radially inwardly from the collar. The locking tab is adapted to engage the hub of a needle assembly to prevent removal of a needle assembly away from the tip. The locking tab is configured to allow the assembly of the needle assembly to the barrel through axial motion of the hub toward the barrel. A plunger is provided for drawing fluid into and out of the barrel. The plunger includes an elongated plunger rod having a proximal portion and a distal portion connected by a breakable connection. The breakable connection is strong enough to hold the proximal portion and distal portion together during normal use of the syringe and breakable upon application of additional force to the proximal portion.

Abstract: The invention relates to a plunger stopper for syringe barrels, the plunger stopper having one or more constrictions and a first and a second end, wherein at least the first end of the plunger stopper is of tapered design. In a first particular embodiment, at least the first end is of conically tapered design. In a further particular embodiment, at least one end is provided with a bore. However, both ends can also be of conically tapered design and can be provided with a bore.

Abstract: A multiple-dose syringe including a barrel with a closed end and an open end, the closed end having an injection port adapted to receive a needle. A plunger is slidably disposed through the open end of the barrel. A container is connected to an end of the plunger to move with the plunger. The container has a deformable shell with an opening at a forward end thereof and a predetermined quantity of fluid sealed therein by a closure member disposed over the opening. The container is slidably disposed in the barrel and includes a seal proximal to the forward end to form a first cavity in the barrel with a volume that is adjustable by moving the container in the barrel with the plunger so that fluid can be selectively drawn into and expelled from the first cavity. After at least a substantial portion of the fluid is expelled from the first cavity, the shell is configured to be collapsed by further pressure applied by the plunger to expel the predetermined quantity of fluid contained therein.

Abstract: The invention refers to a device for administering an injectable product in doses, comprising a casing, itself comprising: a reservoir for the product; a piston which forces product out of the reservoir when moved in a feed direction towards a reservoir outlet; a drive member (6); a driven member which is slaved by the drive member (6) when the drive member (6) is moved in the feed direction, so moving the piston in the feed direction; and a dosing member (15) which may be rotated about the sliding axis (V) of the drive member (6), to set the product dosage to be administered. The drive member (6) and the dosing member (15) abut each other via at least one dosage stopper (14, 18) each, one of which is provided on the drive member (6) and the other on the dosing member (15). At least one of these dosage stoppers (14, 18) at least partially encircles the sliding axis (V) of the drive member (6) in the form of a spiral.

Abstract: A safety syringe includes a barrel, a needle-carrier and a plunger. The plunger and the needle-carrier each have a coupling system which connects them by a simple axial push of the plunger. The distal part of the barrel has an internal annular stop. The central part of the needle-carrier has an external diameter corresponding to the internal diameter of the annular stop while the proximal extremity of this part of the needle-carrier has a diameter corresponding to the internal diameter of the distal part of the barrel. Elements are provided to prevent temporarily the needle-carrier from being pushed inside the barrel through axial pressure against the distal tip of the needle-carrier.

Abstract: An ampule having a body portion and a sealed end portion and a sealed delivery portion adapted for use in a delivery syringe system for controllably dispensing a low viscosity material, such as a liquid, gel, or paste. An ampule having sealed rear portions adapted to mate with a plunger of a syringe so as to facilitate controlled dispensing of a low viscosity material. The syringe has a breach positioned to provide controlled flow of the dispensed low viscosity material and facility easy removal from the syringe. Low viscosity materials, such as liquids and gels, are controllably dispensed in a measured unit dose quantity. The present invention has many applications, but is particularly applicable to dispensing low viscosity materials such as used in coatings and not injected parenterally, and is particularly applicable to dental applications.

Abstract: A drug delivery device comprising a housing (1) with a drug container (2) being provided with delivering means comprising a piston (5) for expelling a drug (4) from the drug container (2). The housing (1) further comprising a displaceable piston rod (6) abutting the piston (5) of the drug container (2) and rotating means being in engagement with the piston rod (6), said rotating means being provided with a one-way mechanism. The one-way mechanism comprises a helical spring (12) wound tightly around an axle (11), one end of said helical spring (12) being fixed in relation to the housing (1), the other end of the helical spring (12) being in a free state.

Abstract: Three collar groups 6A through 6C, each group comprising collars 5a through 5b, 5c through 5e and 5f through 5h which are thin walled and close to each other are provided in a spaced manner in a piston sliding direction. A first group 6A which is provided at the front most end of the piston head 5 comprises two collars 5a and 5b. The front collar 5a which is in contact with the liquid drug has a larger diameter than that of the rear collar 5b. First and third collar groups 6B and 6C which are at the rear of the first collar group 6A comprise three collars 5c to 5e and 5f to 5h, respectively. The intermediate collars 5d and 5g have larger diameters than those of the front and rear collars 5c and 5e; and 5f and 5h, respectively. A support collar 5i is provided at the rear of the collar groups 6B and 6C in such a manner that it is spaced therefrom. The support collar 5i has a thick walled portion x at its base excepting the peripheral edge thereof.

Abstract: A multi-chamber ampoule comprises a container having at least one movable partition therein, the movable partition being adapted to sealingly isolate at least two substances to be mixed with each other, a seal or plunger movably disposed in the container, a holder connected to the container, and a screw actuator engageable with the seal or plunger for displacing the same in the container. The screw actuator has a male thread, and the holder includes a female thread engageable with the screw actuator male thread. The screw actuator is provided with a bore therethrough for slidably receiving a dispensing rod.

Abstract: A drug is administered to a patient through a beveled needle by rotating the needle as it is advanced into tissues. The rotation of the needle insures that the needle is not deflected as it is advanced. In this manner, the amount of pain felt by the patient may be reduced, and the drug is delivered to accurately to the selected site.