Abstract: An arterial blood collection device is provided having a one-piece plunger rod for use with a blood collection syringe. The plunger rod is hollow, with a closed front end. A self-sealing filter is provided within the closed front end of the plunger rod. Vents are spaced radially about the front end of the plunger rod for fluid communication into the hollow interior thereof. The plunger rod is intended for use in slidable communication within a syringe barrel. In use, the plunger can be retracted within the syringe barrel to form a cavity therein. Upon arterial blood contact, the cavity fills with blood and air can be expelled from the cavity through the vents and the filter and out to ambient air. The plunger rod is a one-piece assembly, eliminating the need for a separate rubber plunger seal.

Abstract: A safety syringe device includes a pusher rod, a connecting sleeve, a syringe tube, a needle base, and a needle cap. The connecting sleeve is sleeved onto the front end of the pusher rod so as to allow insertion of the needle base. After being syringed, the needle base and the acute needle tip is withdrawn together with the pusher rod to be accommodated in the syringe tube, and the emerged main body of the pusher rod is broken so as to insert the needle cover backwardly to the end opening of the syringe tube thereby to avoid exposing the needle tip. The safety syringe device constructed as such is able to avoid hurting any person with the used needle.

Abstract: An I.V. flush syringe assembly includes a barrel having an inside surface defining a chamber for retaining fluid, an open proximal end and a distal end including a distal wall with an elongate tip extending distally therefrom having a passageway therethrough in fluid communication with the chamber. A plunger having an elongate body portion and a stopper slidably positioned in fluid-tight engagement with the inside surface of the barrel is provided. Anti-reflux structure for controlling stopper deflection when fluid has been delivered from the chamber and the stopper is in contact with the distal wall is provided.

Abstract: A syringe for dispensing liquid materials to a substrate. In one embodiment, the syringe includes a barrel having a first end, a second end, and an interior reservoir. A piston is slidably disposed within the reservoir and is movable to increase or decrease a volume of the interior reservoir near the first end of the barrel. A first end of the piston has a hemispherically-shaped surface profile, with an elongated apex extending therefrom, to dispense liquid from the first end of the barrel when the piston is moved in a direction toward the first end.

Abstract: A reloadable medicine injector and methods are described in which a barrel with a receiving cavity is adapted to slidably receive a syringe subassembly for axial movement therein. Upon removal of a safety and release of a syringe driver, the syringe driver moves forward and injects the syringe needle. A plurality of penetration controls are shown for controlling injection needle penetration depth. The penetration controls have an abutment and various lengths to provide different needle penetration depth positions. In one form of penetration control a sleeve is used against which the syringe or related parts contact. In another form the front return spring is used as a penetration control. A cushioning ring may be used to reduce syringe breakage. A load distribution and guide ring may be used to distribute loading applied to the syringe and help guide the moving syringe.

Abstract: A plunger cover for use with a syringe includes a sealing portion adapted to form a seal with the syringe and a central portion adapted to contact fluid within the syringe. The central portion can, for example, be more rigid than the sealing portion. The sealing portion and the central portion are connected in an overmolding process. The sealing portion can, for example, be formed from a thermoplastic elastomer or a thermoplastic polyurethane. The central portion can, for example, be formed from polypropylene, acrylonitrile butadiene styrene, polycarbonate or copolymers thereof.

Abstract: A disposable syringe includes a barrel, a needle assembly in fluid communication with the barrel, and a plunger movable in an accommodation chamber of the barrel. The needle assembly includes a needle seat sleeved on a small-diameter wall portion of the barrel, and a tubular insert extending axially into a duct of the needle seat and defining a fluid channel, and a needle cannula in fluid communication with the fluid channel. A space minimizing member is disposed to be in a fluid-tight engagement with an inner surface of the small-diameter wall portion, and has a tubular grip surface which defines a passageway fluidly communicated with the duct such that the insert is in a fluid-tight engagement with the grip surface to thereby communicate the channel with the chamber. Thus, the amount of residual medication fluid in the barrel after completion of an injection operation can be minimized.

Abstract: A flexible piston rod includes a piston and a row of elements, each having top, bottom, and lateral surfaces, the top surface of one element being connected to the bottom surface of an adjacent element by a hinge that allows the two adjacent elements to pivot from a first position, where a portion of the top surface of one element abuts a corresponding portion of the bottom surface of the adjacent element and corresponding to a rectilinear, relatively stiff configuration of the piston rod, to a second position wherein the top surface of one element is spaced from the bottom surface of the adjacent element and corresponding to a curved configuration of the piston rod. The lateral surface of each element has first and second mutually-opposed cylindrical surface portions incorporating a thread for meshing with a corresponding thread of an actuator for displacing the piston rod longitudinally.

Abstract: Valve syringes of the invention include a syringe barrel and an applicator valve adapted to rotate relative to the barrel between closed and open positions. In the open position, one or more slots in the applicator valve align with one or more holes in a discharge end of the syringe barrel in order to allow fluid material to flow therethrough. In a closed position, the contact surface of the applicator valve occludes the holes in the barrel in order to seal them and prevent flow of fluid material therethrough. The valve syringe may include structure that increases the sealing engagement between the syringe barrel and applicator valve when rotated toward at least one of the open or closed positions. The applicator valve may include an applicator tip that is either integrally or detachably connected to the applicator valve. The valve syringe may also include a plunger adapted to expel fluid material contained in the syringe barrel through the discharge end and into the applicator valve.

Abstract: The invention provides a syringe barrel formed by injection moulding of a polypropylene composition, characterised in that said polypropylene composition contains a polyethylene wax. The invention further provides a syringe having a barrel formed by injection moulding of a polypropylene composition, characterised in that said polypropylene composition contains a polyethylene wax and a polypropylene composition suitable for such moulding.

Abstract: An apparatus that allows for separating and collecting a concentrated fraction of a fluid, such as a whole blood sample, adipose tissue, or a bone marrow sample. The apparatus, when used with a centrifuge, allows for the creation of at least three fractions in the apparatus. It also provides for a new method of extracting the buffy coat phase from a whole blood sample. The apparatus includes a container to be placed to a centrifuge after being filled with a whole blood sample. A buoy or fraction separator, which has a density less than that of red blood cells of a whole blood sample, is disposed in the container. During the centrifuge process the buoy separates the red blood cells from another fraction of the whole blood. After the centrifuge process is finished a plunger is used to produce at least two other fractions, including a plasma fraction and a buffy coat. Then, the buffy coat may be removed from the container without commingling the fractions of the sample.

Abstract: A system for breast augmentation includes a plurality of microballoons. An injector can be provided for injecting microballoons into a breast through an incision in the breast. The microballoons can have a first dimension when in the injector and a second, larger dimension when in the breast. An injector and tissue dissector are also disclosed. A method for performing breast augmentation surgery and microballoons for use in the method are also disclosed.

Abstract: The invention relates to a receptacle with a plunger, which is displaceably arranged therein. The plunger comprises a plunger body with a flat face, whereby at least two encircling sealing lips are shaped onto the plunger body. Each sealing lip has slot-shaped notches at at least one location that, as soon as the plunger is inserted into the receptacle, permit a gas exchange between the inside of the receptacle and the outside atmosphere. The invention also relates to the use of the receptacle and of the plunger for storing and discharging, in particular, dental materials.

Abstract: An adaptor for retrofit attachment to a syringe has a slide slideably mounted on the barrel of the syringe, a housing for releasably engaging a flange formed on the trailing end of the syringe plunger, an elongate connector for interconnecting the slide and the plunger housing, and a guide that releasably engages a flange formed at the trailing end of the barrel. Movement of the slide 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 is adjacent the leading end of the plunger so that the operator can see the leading end of the plunger. The user's fingers support the syringe from below. The flange housing permanently engages the flange in a second embodiment. In a third embodiment, the elongate connector and plunger are formed integrally at their respective trailing ends.

Abstract: An end-of-content arrangement for preventing a dose setting member of an injection device to be set to a dose larger that the medicament remaining in the injection device. The arrangement is particular suitable for injection devices operating with non-equistant dose volumes. The arrangement comprises an indentation provided on the housing or on the dose setting and injection member which indentation arrest a stop member when less than one dose unit is left in the cartridge. The stop member is coupled to the dose setting member such that the interaction between the indentation and the stop member prevents a dose larger that the remaining medication in being set.

Abstract: An applicator for delivering pharmaceutical products or the like to a bodily cavity includes a barrel member having a distal end which is equipped with an opening. The applicator also includes a plurality of petals extending outwardly from the distal end in a generally axial direction. The petals cooperate with the opening so as to form a receptacle for releasably receiving a pharmaceutical product in the distal end of the barrel member. Each of the petals has a truncated flexible tip sized and shaped so as to engage a substantially central portion of the pharmaceutical product such that a large section of the pharmaceutical product extends outwardly beyond the petals so as to facilitate the release of the pharmaceutical product from the receptacle. The device also includes a plunger member for releasing the pharmaceutical product from the receptacle. In accordance with the present invention, the device can be packaged in a package together with the pharmaceutical product received in the receptacle.

Abstract: An auto-disable safety syringe including a needle, a needle seat, a plunger, and a barrel. A cover of a needle seat chamber formed in the needle seat is provided with a splined hole having teeth and grooves. The needle seat has a ring block and an outer wall with splined teeth capable of passing through the grooves. A locking groove is formed in an inner cavity of the ring block and a locking head is formed on a connecting head to form a locking mechanism. Spiral grooves on the inner cavity engage with protrusions on the connecting head. When the locking head and the locking groove are interlocked and the plunger is retracted, the needle seat and the needle are retracted inside the barrel together. The syringe protects both patient and medical staff, is simple in structure, convenient to use and destructible.

Abstract: A device suitable for use as an intra vaginal device or as a bolus where, after initiation, a member (usually a plunger) moves with a known movement characteristic and is involved in the stagger release of multiple materials. That moving member is used to time the discharge of one or more material from its reservoir in the device (there being separate powering of the timed discharge) or is used to both time and indirectly power the discharge of one or more material from its reservoir, such discharges preferably being in a staggered manner. Optionally the moving member as a plunger may itself also directly discharge a material from a reservoir.

Abstract: A syringe (and a prefilled syringe) of a structure with ventilation means allowing a pusher to be easily pushed or pulled in use, providing an excellent operability of discharging (injecting) chemicals, making it hard for foreign matter such as dirt and dust to enter into a syringe outer tube when not in use during storage or transporation, capable of assuring, by itself, the sanitation of the syringe outer tube when not in use, and allowed to be shipped without individually packaging the syringe with packaging material, wherein, as more desirable embodiments, the aseptic condition in the outer tube can be surely maintained even if the push and pull operations of the pusher are performed and, even if the pusher is pushed when not in use, a gasket does not move in tip direction and the arrangement of the pusher at the time of shipping can be stably maintained.

Abstract: Disclosed is a medical device used to prevent the cross-contamination of patients or injectors in which various components placed on the injector minimize or eliminate back splash contamination of the injector.

Abstract: A dispenser assembly for liquid products comprising an elongated, generally cylindrical barrel of a predetermined internal cross-sectional diameter having a discharge opening at one end and open at its opposite end, an elongated, generally cylindrical hollow plunger having an outer diameter less than the barrel internal diameter and a circumferentially extending axially directed sealing lip adjacent the tip portion having an outer diameter greater than the internal diameter of the barrel in the relaxed state to thereby flex the lip inwardly against its bias and providing the sole sliding contact between the plunger and barrel when the plunger and barrel are actuated axially relative to one another.

Abstract: A suction piece for a device for administering an injectable product, the suction piece including a suction chamber having a chamber opening rim via which the suction piece may be placed on a tissue, a connection part in order to produce a mechanical connection to the device, a first passage extending through the connection part into the suction chamber in order to produce a fluid connection between the suction chamber and a product reservoir of the device, wherein the pressure in the suction chamber may be reduced when the chamber opening rim is placed on the tissue in order to apply suction to the tissue.

Abstract: The invention concerns a syringe for administering medication to an animal. The syringe includes a handle that may be manually actuated to dispense medication to the animal. The syringe also includes a valve that controls the flow of medication both into and out of the syringe. A sensor device on the syringe monitors when the medication has been administered in order to inform any attached pump that the syringe may be refilled. An LED informs the user when the syringe has been filled with medication and is ready for the administration of medication to the animal.

Abstract: A syringe, on which a needle member is mounted, includes a barrel, a plunger and a stopper. The barrel has a chamber, a stop portion adjacent to the needle member, a lock portion on a wall of the chamber and a needle mount. The plunger has a lock device and an operation portion for operation. A stopper has a stopper body to be squeezed into the chamber of the barrel for movement, a lock flange on the stopper body to be elastically deformed and to be locked with the lock portion of the barrel. The lock device is provided to the stopper body to be connected to the lock device of the plunger that connects the stopper to the plunger to move together. While the plunger is drawn, the lock device of the plunger or the stopper is broken and the stopper is restricted in the barrel.

Abstract: A drug delivery system for administering preset doses of a substance such as a drug, vaccine or the like. The drug delivery system includes a holder and a pre-filled drug container such as a syringe which is 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. A plurality of slots are provided on the holder that permit multiple equal doses of the substance to be administered to each nostril of the patient.

Abstract: A hand-held power syringe. The power syringe includes a handle with pivotally connected first and second members. The first member is also pivotally connectable to a syringe barrel, while the second member is pivotally connectable to a syringe plunger. These three pivotal connections provide leverage for forcing high viscosity fluids into and out of a receptacle of the syringe barrel. One or both of the first and second members of the handle may be bent to facilitate a user's gripping and movement of the first and second handle members. The power syringe may be used in any suitable injection, infusion, or sample-obtaining application, including angiography and angioplasty.

Abstract: The invention relates to a continuous liquid infusion device which can be easily prepared for operation with small force, and can infuse liquid at constant infusion rate and amount over a long time. It comprises a liquid syringe section and a driving pump section mounted on the liquid syringe section, wherein sliding the pressing arm of the driving pump section upward leads to axially slides the piston in the negative pressure chamber to produce a negative pressure therein; and using returning force of the piston under the negative pressure, the liquid pushout plunger barrel is biased toward the upper edge of a pressing member through a locking member engaged with the piston so as to push out liquid in the liquid syringe from the liquid infusion port. Further, only the liquid syringe is disposable while the vacuum pump barrel on the driving side is good for repeated use (reusable).

Abstract: The present invention concerns a medication pump, a cartridge for use in a medication pump, a pump cap for use with a medication pump, components of the cartridge and methods of use of these devices. A cartridge includes a plunger having a tab that projects from an interior wall of the plunger. The tab can be used to lock the plunger into engagement with a drive rod of the pump. The drive rod defines a channel for receiving the tab of the plunger, where the channel includes an axial portion disposed parallel to an axis of the drive rod and a locking portion disposed in a circumferential direction around an outer surface of the drive rod. A similar channel structure can be provided on a removable fill rod used while filling the cartridge. The cartridge axially inserted into a cartridge chamber and then is rotated into engagement with the drive rod. The cartridge may also include axial guides at one end that interface with a guides on pump cap.

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 retracted into the device and safely disposed of in a sharps container.

Abstract: A syringe loading/filling device (or “syringe loader”) includes a syringe mounting mechanism adapted to cooperate with an attachment mechanism of a syringe to attach the syringe to the syringe loader and a drive member adapted to impart motion to the syringe plunger. The syringes for use with the syringe loader include a syringe plunger slidably disposed therein and an attachment mechanism for attachment of the syringe to an injector. Such injectors include a mounting mechanism adapted to cooperate with the attachment mechanism on the syringe to mount the syringe on the injector.

Abstract: Injection devices are known for the self administration of medicament by patients. The medicament is typically contained within a cartridge located within the injection device. It is a problem that injection devices should be small enough to fit into a jacket pocket or a hand bag without difficulty. Also, the injection device must be of a size that enables a piston or similar used to drive the Cartridge bung within the cartridge to be moved both to a maximum dispense position within the cartridge and to be fully withdrawn from the cartridge to allow for replacement of the cartridge. A drive mechanism for an injecting device is disclosed in which the drive mechanism comprises a displaceable dosing spindle 6, a dial dose means 8, a transmission means 10, and a cable means 12, a piston comprising a plurality of nested piston members 30, 32, 34, displacement of the transmission means 10 causing the cable means 12 to move at least one of one of the nested piston members to drive a cartridge bung 18.

Abstract: A single use syringe assembly is provided as well as a locking element for such an assembly. The single use syringe assembly includes a barrel, a plunger rod assembly and a locking element positioned within the barrel. The locking element includes one or more barbs for engaging the inside surface of the barrel. The barbs prevent the locking element from moving proximally within the barrel, but allow its distal movement therein with the plunger rod assembly. A spring member may be provided for urging the barbs towards the inside surface of the barrel. Structure provided for holding the proximal end and the distal end of the plunger rod assembly together during normal use of the syringe is breakable upon application of an additional force applied to the proximal end of the plunger rod.

Abstract: A device for administering an injectable product in doses including a dosage reservoir from which a product dosage is administered, a storage reservoir for storing the product, a transfer conveyor for conveying the product dosage from the storage reservoir into the dosage reservoir, an evacuator for evacuating the dosage reservoir, and a dosing and activating mechanism for performing a dosing movement for selecting the product dosage, a conveying movement for activating the transfer conveyor and an evacuating movement for activating the evacuator.

Abstract: The plunger systems for use in an injector-actuated syringe of the present invention include a dynamic wedge seal which improves the sealing engagement between the plunger cover and syringe barrel, and flexible capture members extending from the rear surface of the plunger which permit the engagement and disengagement of the plunger from the injector drive means at any plunger position within the syringe. Further, the plunger systems include a contrast saving tip which expells the injection liquid from the syringe tip.

Abstract: A liquid dispensing device for the selective oral administration of a liquid medicine simultaneously with a liquid beverage. The device includes a cup for holding a beverage and a lid sealably connectable onto the open upper end of the cup. The cup includes an elongated cylindrical medicine cavity having an open lower end and a narrowing upper discharge tip. The medicine cavity is formed into the outer perimeter surface of the cup for concealment. A medicine plunger is sealingly movable within the medicine cavity for discharging liquid medicine from the discharge tip. The lid has a tapered upwardly extending drinking spout with preferably two spaced ports and a second port positioned between the first ports whereby liquid beverage in the cup may be dispensed from the first ports by gravity feed and liquid medicine in said medicine cavity may be independently selectively dispensed from the second port by movement of the medicine plunger.

Abstract: A safety syringe has a hollow barrel, a plunger, a connector, a plug and a needle hub. The plunger has a protrusion extended from the plunger and along a longitudinal axis of the plunger. The connector is mounted around the protrusion of the plunger. Multiple limit stubs and multiple curved limit channels communicating with a corresponding notch with an inclined side-wall are respectively formed on the connector and a connecting chamber in a connecting tube of the needle hub. When the plunger is being pushed towards the needle hub, the multiple limit stubs respectively pass through the corresponding curved limit channel and are contained in the corresponding notch. The inclined side-wall of the notch will stably connect the limit stub so the plunger can stably retract the needle hub in the hollow barrel.

Abstract: Syringes of the invention include a barrel having a tapered outlet portion and a plunger that is conformingly tapered to enter the tapered portion of the barrel and to expel the fluid material contained within the tapered portion of the barrel. To help expel the material from the barrel, the syringes of the invention include sealing means that are configured to seal the stem of the plunger to the barrel. The sealing means may include one or more rings that circumferentially protrude away from the stem and slidably engage the inner surface of the barrel. In certain embodiments, the syringes also include applicator valves that are disposed at the outlet end of the barrel and that can be rotated between open and closed positions to control the flow of the fluid material out of the barrel.

Abstract: A syringe for use with an injector includes a body comprising a distal discharge end, a plunger movably disposed within the body, and an agitation element disposed within the body between the plunger and the distal discharge end. A movement mechanism is operably associated with the injector to move the syringe in such a way that the at least one agitation element agitates a fluid contained in the syringe. Preferably, the syringe contains an ultrasound contrast agent that is agitated by the agitation element. An injector system and a method for agitating the contents of a syringe are also provided.

Abstract: A disposable device for inserting one or more implants, the device including a tublar cannula (10) having a tip (11), the cannula also serving as a container for the implants, a plunger (20) and a handle (30) having a first end (31) directed towards the cannula, and a second end (32) directed away from the cannula. The plunger and handle are attached or attachable to each other in fixed manner, and the cannula is arranged to be movable in the longitudinal direction, so that the plunger is placed within. The cannula can, after inserting the implant or implants, be drawn on top of the plunger (20) so far that tip (11) becomes covered by handle (30) or by a piece connected to handle (30), and/or cannula (10) is, when drawn to its extreme position, towards second end (32) of handle (30), arranged to be irretrievably locked in relation to plunger (20).

Abstract: A metering receptacle has an elongate hollow body which at one end has a closable exit opening, and which at the other end is closable by way of a plastic plunger stopper. The plunger stopper is at the same time longitudinally displaceable in the hollow body by way of a plunger rod. The metering receptacle is configured such that the plunger stopper is formed of two parts, with a sealing stopper part of plastic which is rigidly positionable in the elongate hollow body and has a centric bore for the passage of the plunger rod, and with a longitudinally displaceable plunger part of lubricious plastic which is connected to the plunger rod.

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: An injection device having an incremental clicking mechanism providing the user with an indication of the number of doses being set. For handling different types of medicaments having different dose volumes in the same type of injection device it is beneficial to provide an additional clicking mechanism which is easy changeable. The clicking mechanism is preferably a curved track provided between the dose setting member and a non-rotatable clicker element.

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: An elongated syringe for administering a substance to a patient includes an elongated syringe chamber that may be inserted into a duct of a patient without unwantingly injuring the patient, a needle extending from the distal end of the syringe chamber, and a plunger rod extending from the proximal end of the syringe chamber. The syringe chamber may be flexible to accommodate curvatures of the duct of the patient. The syringe chamber includes a plurality of chamber compartments that will contain a fluid. At least one of the chamber compartments contains a fluid that is administered to a patient. The syringe chamber may include a driving piston located between two or more chamber compartments. The needle of the syringe may be a component of a transition-bore needle apparatus to facilitate delivery of a relatively viscous fluid from the syringe. The needle may also be flared at its proximal end so that the diameter of the proximal end of the needle is greater than the diameter of the distal end of the needle.

Abstract: A sealant applicator suitable for dispensing a coagulable sealant, for example a two-component fibrin sealant mixed in the applicator, employs impulse clearing to remove residual coagulated or coagulating material from the dispensing pathway and mixing chamber, if present. Impulses may be generated by manual application of a clearing member such as a plunger which can enter into the dispensing pathway to engage, dislodge and discharge residuals or can generate a gas impulse to impact the residuals to similar effect. A clearing valve having a clearing port can be operated by movement of the clearing member to provide access to the dispensing pathway.

Abstract: A disposable needleless injection device includes an integral unit that is dimensioned and arranged to be grasped in the hand of a user. The system is spring-loaded and is manufactured and shipped with the spring in a pre-cocked condition. An integral ampule is fillable by manipulation of a thrust rod/shaft which extends longitudinally through the device and is able to be grasped by a user. Once the unit is filled with a selected medication, it is held proximate the skin in order to inject the selected dosage. The unit is constructed from a maximum of eight component parts and is assembled in a matter of moments by unskilled personnel.

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 capsule for dental restoration material capable of administering, immediately after mixing, a mixture substantially free of air bubbles to a patient site to be restored is disclosed. The capsule comprises a dental restoration material comprising two components of definite amounts of previously weighed powder component and liquid component accommodated in a cylindrical mixing compartment in an isolated state from each other, and an air-permeable filter that does not allow the powder component to exit the mixing compartment, but can ventilate air within the mixing compartment into the outside of the mixing compartment.

Abstract: An implant syringe including a guide sleeve which has seated therein a syringe needle arrangement composed of a syringe needle, a needle holder, a grip member and a preparation receiving member. The syringe needle arrangement is blocked in an initial state by two spring arms that are cut out from the guide sleeve and obliquely project inwards such that they rest on a rear wall of the syringe needle arrangement. When the plunger of the implant syringe is pushed forwards to advance the preparation up to the head end of the syringe, a sleeve which is connected to the plunger abuts on the spring arms and bends them outwards, whereby the syringe needle arrangement can be retracted. The two operations are carried out without changing the position of the hand, thereby simplifying the handling of the implant syringe.

Abstract: An improved pump, reservoir and reservoir piston are provided for controlled delivery of fluids. A motor is operably coupled to a drive member, such as a drive screw, which is adapted to advance a plunger slide in response to operation of the motor. The plunger slide is removably coupled to the piston. The piston comprises a first member and a second member. The first member has an external proximate side and an external distal side. The external proximate side is adapted to contact the fluid and is made of a material having a first stiffness. The second member has a first side and a second side and is at least partially disposed within the first member. The first side of the second member is adjacent to the external proximate side of the first member and is made of a material having a stiffness which is greater than the first stiffness.