Abstract: An apparatus that includes two syringes, or a “double barrel syringe,” includes one syringe that injects or infuses while the other syringe aspirates. The double barrel syringe is a hand-held, hand-operated device with which injection and aspiration may be effected by a single action. The double barrel syringe may include a handle with two member. A first member includes one arm that pivotally couples to a plunger of a first syringe and another arm that pivotally couples to a barrel of a second syringe. A second member of the handle includes one arm that pivotally couples to a barrel of the first syringe and another arm that pivotally couples to a plunger of the second syringe. Methods for injecting or infusing simultaneously with aspirating are also disclosed.

Abstract: A method and apparatus for injecting fluid into areas having high density tissue that creates a high backpressure resistance on the injection device is disclosed. The high backpressure resistance is overcome through a mechanical advantage achieved by using a secondary reservoir having a cross-sectional area smaller than the cross-sectional area of a primary reservoir. Exemplary injection device reservoir housings may comprise a primary reservoir, a secondary reservoir, a check valve, a septum penetrating cannula, travel limits, a pen needle connecting portion, sliding seal guide ribs, a sliding seal, a pen needle assembly, a needle stop, and a patient needle.

Abstract: A syringe assembly is disclosed which includes a syringe body defining a first fluid reservoir and a fluid outlet. A plunger assembly includes a plunger rod and a plunger. The plunger is supported on a distal end of the plunger rod and defines a second fluid reservoir. The plunger is movable within the syringe body from a retracted position to an advanced position to eject fluid from the first fluid reservoir. A piercing member is supported on a distal end of the plunger rod within the second fluid reservoir. The piercing member is movable to pierce the plunger to eject fluid from the second fluid reservoir when a predetermined force is applied to the plunger in the advanced position.

Abstract: An automatic medicament injector having a compartment for a dry medicament component and a compartment for a wet medicament component. The two compartments are separated by a seal structure that has a plug that is moved from a sealing position into a mixing position when the device is activated. The seal structure includes a wiper that scrapes the interior walls in the dry component compartment to prevent the dry component from accumulating at the seal/glass interface. A tapered insert “funnels” the mixed medicament components to an attached needle assembly, but can be removed when the device is filled. A filter is provided between the medicament compartments and the needle assembly. A chamber between the filter and the needle assembly allows for better flow through the filter. An actuation assembly drives the plug into the mixing position and forces the mixed medicament through the needle and into the user.

Abstract: Certain embodiments relate to a sprayer or other medical apparatus for applying a biocompatible coating in situ. Such an apparatus may have a first conduit connected to a first exit opening and a second conduit connected to a second exit opening to deliver a first composition through the first conduit and a second composition through the second conduit to mix the first composition and the second composition outside both the first conduit and the second conduit. The first composition may be, e.g., a precursor to a material formed after the mixing of the first composition and the second composition. The first exit opening and the second exit opening may be approximately adjacent to each other and define an angle that is less than about 140 degrees.

Abstract: An automatic medicament injector having a compartment for a dry medicament component and a compartment for a wet medicament component. The two compartments are separated by a seal structure that converts from a sealing condition into a mixing condition when the device is activated. The seal structure includes a wiper that scrapes the interior walls in the dry component compartment to prevent the dry component from accumulating at the seal/glass interface. A tapered insert funnels the mixed medicament components to an attached needle assembly, but can be removed when the device is filled. A filter is provided between the medicament compartments and the needle assembly. A chamber between the filter and the needle allows for better flow through the filter. An actuation assembly drives the seal structure into the mixing condition and forces the mixed medicament through the needle and into the user.

Abstract: The invention relates to a kit for parenteral administration of drugs, particularly a kit for the infusion of those medicaments dissolved in solvents that extract toxic components from PVC, which is also suitable for the infusion of highly active medicaments, said kit ensuring a safe administration both for the patient and for healthcare staff.

Abstract: Devices and methods for simultaneous injection or delivery of two or more substances from separate syringes. The syringes are loaded into a device that has a handle and a screw driven mechanism for simultaneously depressing the plungers of the syringes. The user grasps the handle and positions the device. Thereafter, the screw mechanism is used to simultaneously advance the plungers of the syringes thereby simultaneously expelling the substances from the syringes.

Abstract: A syringe device for agitating and delivering a liquid medication to a patient is provided. The device includes an injecting member, a first syringe, a second syringe and an accumulator. The first syringe is configured to provide the liquid medication to the device. The second syringe is configured to receive the liquid medication from the first syringe. The accumulator is biased to an empty position and cooperates with the second syringe to agitate the liquid medication back and forth between the second syringe and the accumulator. The second syringe is configured to move the liquid medication to the injecting member for patient delivery.

Abstract: A syringe having two or more chambers having a needle defining two or more lumens for injecting a microparticle suspension into a desired space, the lumens being in fluid communication with respective chambers. One of the chambers has the microparticle suspension disposed therein while the other chamber is empty. The lumen in fluid communication with the empty chamber has a filter element disposed therein such that the suspension fluid may be withdrawn from the space into the empty chamber without withdrawing the microparticles.

Abstract: A delivery system is provided for mixing and dispensing a plurality of components and a method for its use. The system includes a first assembly having first and second separate chambers capable of holding first and second components respectively, a second assembly having third and fourth separate chambers capable of holding third and fourth components respectively, and a coupling device for movably coupling the first and second assemblies such that the second assembly is movable relative to the first assembly between a first position wherein the first, second, third and fourth chambers remain isolated from one another, and a second position wherein at least the first and third, and second and fourth chambers are in communication with one another via at least one conduit therebetween.

Abstract: In a device for the injection of medical preparations, into a patients body during an examination in a Computer Tomograph (CT) or in a Magnetic Resonance Tomograph (MRT) or endoscopically, including an injection needle supported by an injection-needle advancing arrangement for insertion of the injection needle into the patients body and the concurrent injection of medications with a separate dosing apparatus, a hose with a check valve for the one-way transport of the medical preparations from the dosing apparatus into the injection needle, as well as a pressure sensor for monitoring the infusion, the injection needle advancing arrangement comprises a needle holder and a linear drive for the movement of the needle holder in parallel with the injection needle and the dosing apparatus has geometric dimensions and consists of materials permitting its insertion into the CT or MRT together with the patient.

Abstract: A multichamber ampoule with a locking and dispensing mechanism to store several substances and to dispense a mixture consisting of several substances, possessing a multiple-plug closure (140) with several plugs to selectively close and open several outlet openings in the multichamber ampoule, and an adapter (130) for mixing the substances and dispensing the mixture, wherein the multiple-plug closure (140) and the adapter (130) are connected to each other in an assembly designed to be removed from the multichamber ampoule (FIG. 23).

Abstract: A separation assembly for initially keeping a first component separate from a second component includes a generally cylindrical body slidably supported within a container between the first and second components. The body includes a seal structure having an inner seal member that initially seals the first component from the second component. In response to a predetermined operating condition, the inner seal member allows the first component to flow through at least one flow path in the seal structure to mix with the second component. The body further includes a flow distributing member disposed adjacent the seal structure to evenly distribute the first component into the second component. The seal structure and the flow distributing member form a single unit.

Abstract: A system and method is provided for an injectable substance delivery pen comprising a microneedle hub assembly removably engaged with a pen device body which includes a cartridge, a plunger, and a drive mechanism. The hub assembly includes at least one microneedle for intradermal or shallow subcutaneous injection of the contents of the cartridge. The cartridge, plunger and drive mechanism components of the pen body are fabricated of non-compliant and non-compressible materials to allow effective communication of the cartridge contents via the microneedle patient interface.

Abstract: A method of fabricating an elastomeric structure, comprising: forming a first elastomeric layer on top of a first micromachined mold, the first micromachined mold having a first raised protrusion which forms a first recess extending along a bottom surface of the first elastomeric layer; forming a second elastomeric layer on top of a second micromachined mold, the second micromachined mold having a second raised protrusion which forms a second recess extending along a bottom surface of the second elastomeric layer; bonding the bottom surface of the second elastomeric layer onto a top surface of the first elastomeric layer such that a control channel forms in the second recess between the first and second elastomeric layers; and positioning the first elastomeric layer on top of a planar substrate such that a flow channel forms in the first recess between the first elastomeric layer and the planar substrate.

Abstract: A syringe cylinder 12 includes a groove 32 formed in an inner peripheral surface thereof and extending over a predetermined length from an opening end 30 thereof. Even with the intermediate sliding stopper 14 located at a position where the groove 32 is formed, the pressure inside the syringe cylinder 12 can be reduced. Thus, during vacuum tapping, the intermediate sliding stopper 14 can be held in the vicinity of the opening end 30 of the syringe cylinder 12. Consequently, the intermediate sliding stopper 14 can be inserted into the syringe cylinder 12 in a correct posture and reliably moved to a predetermined position in the syringe cylinder 12.

Abstract: Disclosed is an applicator device (10) for applying a multi-component fluid, especially a multi-component tissue glue, comprising a plurality of substantially cylindrical supply containers (12) for respectively one component of the fluid to be applied, each supply container (12) having a front end (16) with an outlet opening (18), a rear end (22) opposite to the front end (16), and a slidably displaceable piston (24) arranged within the supply container (12) and having a piston rod (26) extending out of the rear end (22) for operating the piston (24). Moreover, the applicator device includes a manifold (72) having terminal ends (50,58) with a first port for fluid connection with the front ends (16) of the supply containers (12), the manifold (72) further having internal channels (62) extending from the first ports of the terminal ends (50,58) to an outlet site.

Abstract: A dual lumen syringe includes a body having a pair of elongate cavities or lumens formed therein. A directional valve is associated with each lumen. The valve is alternated between the first position wherein the lumen is communicably connected to a fluid inlet and a second position wherein the lumen is connected with a fluid outlet. There are a pair of elongate plungers, which are fixedly interconnected by a handle. Each plunger is received and longitudinally slidable in a reciprocating manner through a respective lumen. The valves are switched to a first position wherein the lumens are interconnected with the fluid inlets and the plunger is retracted to aspirate fluids through the respective inlets and into the lumens. The valves are then switched to a second position to communicably interconnect the lumens with the outlets.

Abstract: A discharge assembly is disclosed which partitions a conventional syringe into proximal and distal chambers to provide a multi-chamber, sequentially dispensing syringe apparatus. Incorporated in the discharge assembly is a syringe stopper body and an associated valve stem which in combination form a valve. A syringe plunger communicates through fluid in the proximal chamber to force displacement of the discharge assembly. The valve is actuated by collision between a rigid member which is a part of the valve stem and the distal internal surface of the syringe. The discharge assembly may be made from two parts: (1) the stopper body (made from conventional syringe stopper material); (2) the valve (actuating) stem made from rigid material similar to material from which the syringe barrel is made.

Abstract: An injection device including an accommodating device for a substance to be delivered, e.g. a vial or ampoule holder, which is insertable into and can be displaced relative to the injection device or a part thereof; an adjusting element for adjusting a dose to be administered from the injection device, which element is inserted in the injection device; and a coupling element for coupling the accommodating device to the adjusting element so that the adjusting element is at least partially moved out from the injection device when the accommodating device is inserted. A method for preparing an injection device using a dual chamber vial or ampoule to administer a substance, wherein the method involves using an adjusting device which is released, extended or pushed out from the injection device not before or after the substance to be administered from dual chamber vial or ampoule is mixed.

Abstract: A device for dispensing a multicomponent composition composed of a mixture of different fluid components includes a first and at least a second fluid component inlet. The device also includes a mixing area located downstream from the fluid component inlets and an outlet extending from the mixing area. Each of the fluid component inlets is adapted to communicate with a source of a different fluid component. The mixing area is adapted to receive a flow of a first and at least second fluid component. Within the mixing area, the flow of the first fluid component is disrupted to allow mixing with the flow of a second fluid component to form a flow of multicomponent composition. The mixing area is further adapted to disrupt the flow of the multicomponent composition before the flow of the multicomponent composition exits through the outlet.

Abstract: A syringe is partitioned into at least proximal and distal chambers to provide a multi-chamber, sequentially dispensing syringe apparatus. The syringe includes a gas separator that prevents gas from exiting a chamber with delivered fluid.

Abstract: A dual syringe adapter for attachment to a pair of side-by-side syringes includes three interconnected portions. A first portion is configured so as to snap onto a plunger head portion of each syringe so as to connect the pair of syringes and maintain plunger movement in unison. A second portion of the adapter is configured so as to snap onto a syringe body of each syringe to help maintain the connection of the two syringes. The third interconnected portion is positioned between the first and second portions and when connected prevents relative movement of the plungers into the syringe bodies. Weakened sections allow the connecting portion to be severed from the first and second portions thereby allowing plunger movement into the syringe bodies. Once severed, the connecting portion is secured to syringe tips for dispensing a mixed composition.

Abstract: The present invention provides a syringe device including a needle, a syringe body, and a syringe adaptor between the needle and the syringe body. This syringe adaptor includes a reservoir and a plunger configured to move into and out of the reservoir in a direction perpendicular to the longitudinal direction of the needle. The position and direction of travel of the plunger in the syringe adaptor allows a user of the syringe of the present invention to safely and accurately operate the syringe with one hand.

Abstract: The invention relates to a system for dispensing two components, which comprises a syringe or cartridge, a closing cap and a mixer. The aim of the invention is to provide a system of the aforementioned kind wherein the closing cap is detachable fastened on the syringe or cartridge and the mixer is non-detachable fastened on the cartridge. For this purpose, the fastening means are configured accordingly. The inner bead on the closing cap, in the zone of transition to the cap interior, is provided with a bevelled section that rests on the retaining cams or the retaining bead of the cartridge, while the retaining means on the mixer engage behind the retaining means on the cartridge, thereby forming a non-detachable connection. The invention provides an inexpensive and yet reliable system for dispensing two components, especially for use in dental and medical technology.

Abstract: A transdermal delivery device includes a plurality of microneedles for injecting a substance such as a pharmaceutical agent into or below the stratum corneum of the skin. The device has housing formed from a top and bottom wall to define a chamber for containing a pharmaceutical agent. An inlet port is provided in the top wall of the housing for supplying the pharmaceutical agent to the chamber and directing the agent to the microneedles. The housing can have a Luer lock type fitting for coupling with a syringe having a Luer lock collar to inject the pharmaceutical agent into the housing. The housing can be divided into a plurality of chambers by an internal wall for supplying different agents simultaneously or sequentially to a patient. The microneedles have a length of about 5-250 microns and generally about 50-100 microns.

Abstract: A dual syringe assembly that allows for two liquids to be sequentially injected through the same needle. By way of example, one syringe may contain a steroid and the other syringe may hold an anesthetic. The syringes are coupled to a needle by a connector. The needle can be inserted into a hand by medical personnel and manipulated until placed in contact with a tendon sheath. The steroid can be administered by depressing a plunger of the syringe that contains the steroid. The anesthetic can then be injected into the hand by depressing the plunger of the other syringe. The needle is then pulled out of the hand. The injection of the anesthetic flushes steroid from the needle and the Y-connector so that steroid is not ejected onto surrounding tissue when the needle is removed from the hand.

Abstract: A portable system for detecting agents present in a sample is disclosed. The system comprises a sensing device, having a substrate formed with a plurality of reaction chambers and a plurality of channels interconnecting at least a portion of the plurality of reaction chambers, wherein at least a portion of the plurality of reaction chambers comprises a sensor, capable of generating a detectable signal when exposed to the agents. The system further comprises a detector, which receives signals from the sensing device and provides an image of sensors generating the optical signals. The portable system is connected to a communication network via a communication unit.

Abstract: The invention provides a lightweight, inexpensive syringe holder for substantially simultaneous multiple injections such as, but not limited to, intramuscular injections for immunizations. The syringe holder can be molded as a single unit, and can be disposable or reusable, and easily cleanable and/or sterilizable, as desired. The syringe holder can securely accommodate two or more syringes, and two or more substantially simultaneous injections can be performed easily by the administrator using only one hand. Thus, it is possible for the administrator to use two hands, and perform four or more injections that are substantially simultaneous, thus reducing pain, stress and trauma.

Abstract: In a prefilled syringe separately containing both a lidocaine solution and a hyaluronic acid solution, the viscosity of the hyaluronic acid solution is set so as to be sufficiently higher than the viscosity of the lidocaine solution. When lidocaine discharge from the tip of a hypodermic needle ends, the force f (N) required to discharge the hyaluronic acid solution from the needle tip suddenly increases, imparting sort of a jolt to the hand of the operator and creating a momentary sensation that the plunger is at rest. Letting the force f (N) required to discharge the lidocaine solution be P1 and the force f (N) required to discharge the hyaluronic acid solution be P2, the relationship therebetween is P1<P2. When (P2?P1)/P2>0.2, the operator is able to feel a sufficient jolt.

Abstract: A two-component mixing type pre-filled syringe 1 includes a nozzle member 20, a barrel 10 formed with a bypass 13 protruding outwardly in a radial direction, a tip gasket 60 sealing a tip of the barrel 10, an intermediate gasket 70 liquid-tightly partitioning an inside of the barrel 10 into a front chamber 11 and a rear chamber 12 accommodating a liquid medicine L, and a plunger gasket 80 located in a base end side relative to the intermediate gasket 70 and sealing the inside of the barrel 10, and includes a construction in which the intermediate gasket 70 has at least one seal part 71 contacting an inner wall of the barrel 10, and a bypass communication passage 72 providing communication between the front chamber 11 and the rear chamber 12 in cooperation with the bypass 13.

Abstract: A multi-chamber syringe 10 which can be manufactured at a low-cost and high-productivity is provided. The syringe 10 includes a generally cylindrical barrel 12, a push member 14 and a plug 16, both of which are disposed to fit the inner side surface 12a of the barrel 12 and slidably on the inner side surface 12a. The plug 16 has a main surface 16a provided with a projection 34 having a top 34a which is eccentric to the main surface 16a. When the push member 14 slides in the direction indicated by Arrow A, the plug 16 comes under pressure from the side on the open end 18. When the projection 34 of the projection 16 makes contact with the choked end 20, the pressure from the side on the open end 18 acts to turn the plug 16 in the direction indicated by Arrow B. This causes a bending deformation in a main body 30 and flanges 32a, 32b of the plug 16, to form a first gap 38 and a second gap 40 between the inner side surface 12a of the barrel 12 and the plug 16.

Abstract: One or more aspects of the present invention relate to syringe having an intermediate plunger that includes a one-way valve having a fluid passage define therethrough. The syringe may be utilized to sequentially inject first and second medical fluids into a patient.

Abstract: The present invention provides an injection delivery system for the injection delivery of at least two fluid doses to a small bird by penetrating the skin of the recipient bird with at least on injection needle. The present injection delivery system comprises an injection needle device and a metering device. The injection needle device can either be a stationary unit or a hand held device.

Abstract: A medical syringe employs a capsule containing multiple doses of medication within a sealed storage chamber formed between concentric inner and outer walls. The inner wall forms a cavity including a delivery chamber from which a single dose of medication is ejected. The syringe includes an ejection port, an axial moveable plunger extending into the cavity and delivery chamber, and a body with a compartment that holds the capsule. With the plunger in a first position, the capsule is closed. With the plunger in a second position, the delivery chamber is filled with a single dose of medication. With the plunger in a third position, the single dose of medication is ejected from the delivery chamber though the injection port.

Abstract: In certain embodiments, a system includes an integral manifold syringe. The integral manifold syringe may include a multi-barrel body having a first barrel and a second barrel, a manifold having first, second, third, and fourth ports, wherein the first and second ports are coupled to the first and second barrels, respectively. The integral manifold syringe also may include a flow control core disposed rotatably inside the manifold at a plurality of positions, wherein the flow control core has different flow pathway arrangements between the first, second, third, and fourth ports at the plurality of positions.

Abstract: An apparatus that includes two syringes, or a “double barrel syringe,” includes one syringe that injects or infuses while the other syringe aspirates. The double barrel syringe is a hand-held, hand-operated device with which injection and aspiration may be effected by a single action. The double barrel syringe may include a handle with two member. A first member includes one arm that pivotally couples to a plunger of a first syringe and another arm that pivotally couples to a barrel of a second syringe. A second member of the handle includes one arm that pivotally couples to a barrel of the first syringe and another arm that pivotally couples to a plunger of the second syringe. Methods for injecting or infusing simultaneously with aspirating are also disclosed.

Abstract: The present invention is a fluid dispensing device particularly suited to medicine but also having many other applications. The user manually and selectively dispenses any of one or more fluids, typically a drug, contained within the device. Generally, the device comprises a frame that holds multiple hypodermic syringes and channels the dispensed fluids through a manifold. A flushing solution, for example a saline solution, enters the manifold, flows past each of the points where the syringes input into the manifold and continues to flow out of the device to a patient where the flushing solution and dispensed fluid are delivered to a patient.

Abstract: An apparatus includes a housing and a medicament container disposed within the housing. The medicament container includes a first plunger and a second plunger, each disposed therein. The medicament container has a first configuration and a second configuration. In the first configuration, the first plunger is disposed in a first position and the second plunger is disposed in a second position spaced apart from the first position by a first distance. Accordingly, a first portion is defined between the first plunger and the second plunger. A second portion is defined between the second plunger and a distal end of the medicament container. In the second configuration, the first plunger remains in the first position and the second plunger is disposed in a third position spaced apart from the first position by a second distance, such that a volume of the second portion is greater when the medicament container is in the second configuration than when in the first configuration.

Abstract: A device and method for easily filling a syringe with one hand is disclosed. The device includes a flat hand for holding a medicine bottle, a syringe holder with a curved finger for holding a syringe, a mounted post for securing the device and a swivel arm mounted to the post which holds the flat hand, wherein the swivel arm allows the user to invert the flat hand and the medicine bottle secured therein, and easily draw medicine from the medicine bottle into the syringe with one hand.

Abstract: A mixing syringe having a first sealed chamber containing a powder (powder housing) and a second sealed chamber containing a liquid (liquid housing). When the user needs to inject a patient, he or she holds the mixing syringe approximately upright and depresses a plunger. This motion causes a piercer to pierce a foil seal separating the two chambers. The liquid then drops down into the powder housing. The liquid flows through a passage in a piston located in the powder housing, where it then comes in contact with the powder itself. As the user continues pressing the plunger downward, the piercer comes to rest within the piston and seals the passage through the piston, thereby locking the piercer and piston together. The device is then ready for an injection. As the plunger is further depressed the piston expels the powder and liquid mixture through a needle.

Abstract: A liquid dispenser (100) primarily for use in dispensing liquid drench to animals. The dispenser (100) is electronic in operation and has the ability to control the speed of its pump (5) according to environmental conditions including the viscosity of the liquid being dispensed.

Abstract: The invention relates to an ingestible, implantable or wearable medical device comprising a microarray which comprises a bioactive agent capable of interacting with a disease marker biological analyte; a reservoir which comprises at least one therapeutic agent and is capable of releasing the therapeutic agent(s) from the medical device; and a plurality of microchips comprising a microarray scanning device capable of obtaining physical parameter data of an interaction between the disease marker biological analyte with the bioactive agent; a biometric recognition device capable of comparing the physical parameter data with an analyte interaction profile; optionally a therapeutic agent releasing device capable of controlling release of the therapeutic agent from the reservoirs; an interface device capable of facilitating communications between the microarray scanning device, biometric recognition device and the therapeutic agent releasing device; and an energy source to power the medical device.

Abstract: A medical pump, comprising a reservoir having a fluid enclosing portion and a tubular element, the inside of which is arrangeable in fluid communication with the fluid enclosing portion for allowing fluid to pass into the tubular element. The fluid enclosing portion contains a volume of fluid sealed from communication with air and the fluid enclosing portion is adapted to reduce in volume essentially to the same extent as any volume of fluid transferred into the inside of the tubular element. The invention also relates to a method of delivering a medical fluid.

Abstract: A disposable or reusable spray container including a housing; at least two storage chambers in the housing, each of the storage chambers containing one or more different ingredients and an actuator on the housing, wherein activation of the actuator causes simultaneous emission of the ingredients from the storage chambers of the container.

Abstract: A device for dispensing a flowable substance includes a tubular reservoir (12) forming a reservoir chamber (14), which is closed on one end and changes into a neck section (16) with a discharge opening (18) on the end facing away from the closed end. A closure (20) is molded onto the neck section (16), which closes the discharge opening (18) and can be separated from the neck section (16) in order to activate the device. The neck section (16) is surrounded by an application device (26). The closure (20) is developed in form of a mandrel which penetrates the application device (26) in such a manner that it projects beyond the application device (26).

Abstract: A device for application of material to a surface, for example, biocompatible material to a tissue surface in a medical or clinical setting, is adapted to receive one or more biocompatible materials and one or more sources of pressurized medical gas, and to deliver these biocompatible materials via the medical gas(es) to a tissue surface or other surface. A regulation system controls flow of medical gas at a variety of pressures, and flow of biocompatible agent or agents, allowing agents to be sprayed or otherwise deployed onto a tissue surface. Switching apparatus operably connected to the regulation system directs a set of preset treatment positions allowing sequential application of biocompatible materials under various conditions in conjunction with an overall treatment protocol. The device can be used to apply a photoinitiating primer and polymeric sealant to a tissue surface, followed by light activation to form a polymer coating on the surface.

Abstract: A system of marked medical containers comprises at least two containers having different properties in at least one respect, and at least one machine-readable marking on each of the containers, each marking being designed to allow discrimination between the difference in properties. Each marking allows discrimination between the difference by having at least one area with different absorbence or reflectance when irradiated with radiation in non-visible frequency ranges. A specific container comprises a syringe cartridge type container for use with a preparation delivery device.

Abstract: The present invention provides a syringe device comprising: a first syringe comprising: a first syringe barrel including a first opening at a distal end thereof through which fluid may be forced or aspirated; and a first syringe plunger sliding within the first syringe barrel for forcing fluid through the first syringe barrel opening, the first syringe plunger including a stopper at a distal end thereof which sealingly and slidably engages the first syringe barrel; a reciprocating member which moves along a track parallel to the axial direction of the first syringe; and a reciprocating device connecting the first syringe plunger to the reciprocating member so that when one member of the group consisting of the first syringe plunger and the reciprocating member moves distally, the other member of the group is forced to move proximally.