Abstract: A medical device may include an extravascular system, a vascular access device attached to the system, and at least one access port attached to the device capable of displacing stagnant fluid within the extravascular system. A method for eliminating stagnant fluid within an extravascular system may include providing an extravascular system, providing a vascular access device having an access port, attaching the device to the system via the access port, accessing the access port with a separate vascular access device, and displacing stagnant fluid within the extravascular system.

Abstract: A valved sheath introducer for venous cannulation, including a valve, sheath, handle and cap. The valve is configured to permit safe introduction and removal of medical instruments through the sheath introducer. The valve may have one or more anchoring members and a thickened central portion through which a slit is formed. The central portion may have one or more concave surfaces and the slit can be angled with respect to the top surface of the valve. The cap is attached to the handle, compressing a portion of the valve therebetween.

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

Abstract: A drug injection needle comprises a puncturing needle part that has a puncturing part that is capable of puncturing a body, a drug introducing needle part that is capable of communicating with the inside of the drug container, and a housing that supports the puncturing needle part and the drug introducing needle part in such a way as to allow the liquid drug to flow between the needle parts. The outer diameter of the puncturing part is not more than 0.254 mm. The outer diameter of the drug introducing needle part is larger than at least that of the vicinity of the distal end of the puncturing part of the puncturing needle part, and a cutting edge is formed at the end of the drug introducing needle part for penetrating through an elastic member that is provided to seal the drug injection port of the drug container.

Abstract: A method of administering liquid medicine such as epinephrine to a patient includes administering a first dose followed by administering an optional second dose is described herein. Also described herein are devices useful for carrying out the methods described and kits containing these devices.

Abstract: Injectors are provided that may be pre-filled aseptically with an active biological agent into a sterile cavity and sealed in such a manner that the injectate may be readily expelled into the body. The injectors are particularly useful for injecting precisely measured small volumes of sterile agents.

Abstract: A medication and needle module (20) for an injection device. The module (20) includes a housing (22) including a first portion (39) and a second portion (38) detachably connected together, the second housing portion having a periphery complementarily shaped with a cavity (154) in the injection device (150) to be loadable therein, a primary container (120) within the first housing portion and including a medication filled reservoir (124), a secondary container (70) within the second housing portion and including a medication tillable reservoir, a needle cassette (60) rotatably mounted within the second housing portion and including a plurality of delivery needles (64), and a transfer needle assembly (100) within the housing. The detachability of the second housing portion from the first housing portion permits the second housing portion with the secondary container and the needle cassette to be loaded as a unit independently of the first housing portion into the injection device cavity for use.

Abstract: The present invention relates to a device and method for a chemical applicator used applying chemicals to Irving organism's internal tissue, including the internal tissue of plants and animals, for organisms which reside in mediums such as land, air or water. The device of the present invention is predicated, in part, on the piercing elements being engageable with the chemical reservoir in order to effect the coating of the piercing elements with the chemical. Once coated, these piercing elements are then used to pierce the living organism's tissue such as plant tissue to deliver the chemical.

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: Kits and methods for closed-system sampling blood in patients are disclosed. The kit includes a four-port stopcock adapted to allow communication at least between two ports. The stopcock has a first port adapted to receive a syringe, a second port for communicating with an infusion solution reservoir, a third port for receiving a flush solution, and a fourth port for communication with a patient. The kit also includes at least one sampling site adapted to fluidically communicate with the fourth port and to be positioned between the four-port stopcock and the patient. At least one of the sampling sites is adapted to allow extraction of a fluid being communicated between the stopcock and the patient.

Abstract: The application includes an improved syringe (100) for use with a receptacle of the type having a self-contained movable piercing member. The syringe includes a barrel (114) having a distal end (114d) and a proximal end (114p). At least one finger member (150) is provided proximate to the distal end (114d) of the barrel (114). The finger member (150) is non-slidably attached to the barrel (114) and configured to permit application of a substantial force by one or more fingers of a person's hand such that the syringe (100) is urged in a distal direction.

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: A syringe includes in one embodiment a fluid cartridge including a rear sliding member; a syringe barrel; a hypodermic needle assembly releasably secured to the syringe barrel; a nut member releasably secured to the syringe barrel; and a plunger including a rear handle, a front member disposed through the nut member to urge against a rear end of the sliding member, and an arm interconnected the handle and the front member. In response to dispensing fluid disengage the syringe barrel with the hypodermic needle assembly so as to separate the syringe into first and second portions, and wherein the first portion consists of the hypodermic needle assembly and the fluid cartridge and is adapted to discard, and the second portion consists of the nut, the plunger, and the syringe barrel and is adapted to sterilize for a next use.

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 microfluidic system, particularly a microfluidic chip, with at least one operational channel, in which a fluid and/or the constituents contained therein are moveable in the direction of the operational channel by a driving force, particularly by using pressure, acoustic energy, or an electrical and/or a magnetic field. At least one measurement sensor used to measure a measurable value assigned to the fluid and derivable in the region of the fluid and at least one regulator is provided to regulate the driving force and/or a parameter that may be influenced by it, wherein the regulator is coupled with a measurement sensor and a device used to alter the driving force and/or the parameter that may be influenced by it. The microfluidic system further relates to a procedure to transport and guide a fluid and/or the constituents contained therein within a microfluidic system of the type described above.

Abstract: A pants-type disposable wearing article includes a liquid-pervious topsheet, a liquid-impervious backsheet, a liquid-absorbent panel interposed between these sheets and a liquid-impervious outer sheet lying on the outer side of the backsheet, and having a waist-hole and leg-holes. This article has a first folding guide formed in left half of the crotch region, a second folding guide formed in right half of the crotch region and third folding guides transversely extending between the first and second folding guides so that first and second regions of the crotch region are folded along the first and second folding guides so as to be tucked toward inner sides of the respective leg-holes and the third region of the crotch region is folded along the third folding guides so as to be tucked toward the waist-hole.

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: Provided is a micro fluidic device that can control a flow time of micro fluid by using a capillary phenomenon. The micro fluidic device includes: a flow channel for flowing fluid, the flow channel being formed between a top substrate and a bottom substrate or between a top substrate, a bottom substrate, and a middle substrate; a flow blocking surface for stopping a flow of the fluid in the flow channel temporarily; and a hump for delaying the flow formed in the line of continuity with the flow blocking surface. The micro fluidic device of the present research can control the flow time in a simple manner.

Abstract: The delivery of a fluid cutaneously is effected by generating a suction force on a surface of a housing. A surface of a cutaneous layer is received under the suction force about which the proximal end of a needle thereby to pierce the cutaneous surface and to effect an injection of fluid. There is generated a suction force to operate the movement of a needle in the housing. The needle is moved under the suction force from the housing thereby to permit piercing a cutaneous layer. The bladder for containing fluid is emptied under the suction into the distal end of the needle and thereby permit the expulsion of fluid through the proximal end of the needle for injection below the cutaneous layer.

Abstract: The injection syringe has at least one syringe body (12) provided with a needle (22) and a pusher (14) mounted so as to be able to move in the body (12). The syringe has a movable guard (36) for protecting the injection end (22A) of the needle. The guard (36) is able to move with respect to the body (12) between a position retracted in the body (12) and an active protection position. The guard (36) and the body (12) have associated projecting and recessed reliefs for holding the guard in a retracted position. It has a retractable member (70) for positive holding of the engagement of the said associated reliefs, when the guard (36) is in a retracted position. The pusher (14) and the said holding member (70) are adapted for a retraction of the said holding member (70) under the action of the pushing in of the pusher (14) into the body, at the end of injection, providing a release of the positive holding of the engagement of the associated reliefs.

Abstract: A drug injection needle comprises a puncturing needle part having a puncturing part capable of puncturing a body, a drug introducing needle part capable of communicating with the inside of the drug container, and a housing supporting the puncturing needle part and the drug introducing needle part to allow the liquid drug to flow between the needle parts. The outer diameter of the puncturing part is not more than 0.254 mm. The outer diameter of the drug introducing needle part is larger than at least that of the vicinity of the distal end of the puncturing part of the puncturing needle part, and a cutting edge is formed at the end of the drug introducing needle part for penetrating through an elastic member that is provided to seal the drug injection port of the drug container.

Abstract: A needle assembly for use with an injection device including a pair of housing members slidably coupled with one another. A needle is structurally attached to one of the housing members such that it is positioned within the two housing members. A first membrane is disposed on an opening of one housing member and a second membrane is disposed on an opening of the other housing member such that the needle is concealed from the view and access of a user thereof. The needle assembly may be contracted by sliding one housing member relative to the other causing the needle to penetrate one of the membranes and administer an injection into or below the skin of the user. Additionally, one or more locking mechanisms may be incorporated to prevent inadvertent needle sticks.

Abstract: A syringe, for injecting anesthetic contained in a medicine vial. The syringe includes a housing having a needle end and a plunger end, connected by a body; to which housing is attached a plunger assembly having a plunger at the plunger end. There is a vial slot in the housing, cooperatively sized for receiving a medicine vial. A needle assembly slot is in the body, at the needle end, for receiving a needle assembly from a side of the body. A seat at the needle end of the housing receives and locates a corresponding seat portion of the needle assembly within the housing. Depressing the plunger housingward impales the vial onto a penetrator of the needle assembly and seats the assembly firmly.

Abstract: The invention provides a safety syringe for extracting blood, with retractable or removable needle that can be retracted into the syringe body or removed after use and safety locks that lock the retractable needle in an extended position during use and in a retracted position after use to ensure that the syringe is not reused or that the needle is not inadvertently extended. When retracted, the needle assembly is cocked at an angle identifying the syringe as used and adding further protection to prevent the needle from being inadvertently extended and exposed from the tube. These safety features work in conjunction to enhance the usability and increase the safety of the syringe. Thereby protecting medical workers from being injured by an exposed needle or contaminated by disease or infection from contact with the patient's blood present on a used needle.

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

Abstract: A needle assisted jet injector and method for jet injecting medicament are disclosed. In one embodiment of the injector, the needle is retractably located within an injector nozzle assembly. Upon activation of the force generating source, a portion of the needle extends past the nozzle assembly and penetrates the outer layer of skin to deliver the medicament via jet injection to a deeper region. After activation, the needle retracts back into the nozzle assembly. In another embodiment, the needle is fixed to the end of the nozzle assembly. In both embodiments, the length of the portion of the needle that penetrates the skin is less than 5 mm.

Abstract: A sequential delivery syringe which has an internal chamber located within a body with the internal chamber being substantially closed at one end except for a discharge opening and totally open at the opposite end. A luer is connected to the discharge opening with the luer including a piercing member. A mid-piston is movably mounted within the internal chamber of the syringe with there also being a separate stopper piston which is connected to plunger. Between the stopper piston and the mid-piston is mounted a collapsible structure within which is an internal chamber. A liquid is to be contained within this internal chamber of the collapsible structure.

Abstract: A new and improved anesthetic delivery tool and method of using the tool in transmucosal absorption applications of a gel topical anesthetic agent and in subdermal injections of a liquid anesthetic agent is disclosed. The anesthetic delivery tool comprises a housing unit having a hollow central cavity with a slip plate containing a plurality of needles directed towards the front end of the housing unit. The slip plate and the front portion of the hollow central cavity defining a front-end cavity for affixing a therapeutically effective aliquot of gel topical anesthetic agent. The anesthetic delivery tool also comprises a thin membrane positioned directly behind the slip plane and a push plate positioned at the rear end of the housing unit. The push plate, the thin membrane and the rear portion of the hollow central cavity defining a rear-end cavity for affixing a therapeutically effective amount of liquid anesthetic agent.

Abstract: A needleless injector cartridge has an adaptor for introducing fluid from a filling device into an orifice of the cartridge. The adaptor has a frangible connection which is broken to allow removal of the filling device after the cartridge is filled with the fluid.

Abstract: A medical sequential syringe apparatus has two or more fluids of predetermined volume dispensed therefrom. The apparatus includes a tubular cartridge containing fluid is sealed at one end by a membrane with a hollow tubular spike mounted at one end of the body facing inwardly into the tubular body. A plunger mounted within the tubular body moves the cartridge toward the spike to puncture the membrane and allow the fluid to flow from the cartridge through the hollow of the spike out of the tubular body.

Abstract: The invention provides a safety syringe for extracting blood, with retractable or removable needle that can be retracted into the syringe body or removed after use and safety locks that lock the retractable needle in an extended position during use and in a retracted position after use to ensure that the syringe is not reused or that the needle is not inadvertently extended. When retracted, the needle assembly is cocked at an angle identifying the syringe as used and adding further protection to prevent the needle from being inadvertently extended and exposed from the tube. These safety features work in conjunction to enhance the usability and increase the safety of the syringe. Thereby protecting medical workers from being injured by an exposed needle or contaminated by disease or infection from contact with the patient's blood present on a used needle.

Abstract: A system is provided for providing syringes filled with pharmaceuticals whose components must be stored separately, using a liquid such as water in a pharmaceutical vial, an active ingredient in a protosyringe such as a bottomless vial or a cartridge, and a combiner assembly which enables the content of the pharmaceutical vial to be transferred into the protosyringe and converts it into a ready-to-use syringe on activation. The combined assembly includes a tubular body having recesses at opposite ends for receiving capped ends of the vial and the protosyringe, and a hub and needle assembly between penetrable sheaths or shields which acts on activation of the assembly to enable the transfer and conversion referred to above. Components of the system may also be used to convert protosyringes and pharmaceutical vials containing pharmaceuticals into delivery systems.

Abstract: The present invention relates to an adapter for the transport of fluids with a microneedle device. The adapter can receive a syringe, for example, that is used to transport a fluid through the adapter for injection into a patient using the microneedle device. The adapter can include a seal through which a syringe needle is inserted to deliver fluid from the syringe into a fluid cavity in the adapter.

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

Abstract: A syringe device includes a barrel in which a stopper connected to a plunger is movably received, and an engaging section extends from an end of the barrel. A base member is disengagably received in an engaging section of the barrel and a needle cannula is connected to the base member. The stopper has a protrusion which is engaged with a recess in the base member when the stopper is moved to a extreme position when pushing the plunger. The base member is disengaged from the engaging section and moved into the barrel together with the stopper when the plunger is pulled backward. A pushing device is located between the base member and the stopper to tilt the base member in the barrel.

Abstract: A pre-slit injection site (34) includes a housing (40) with a flow path therethrough. A first end (42) of the housing (40) carries a pre-slit septum (52). One form of a blunt cannula (98), usable with the injection site (34), carries a locking member (100). When the pre-slit injection site (34) slidably receives the blunt cannula (98), the locking member (100) latches to the injection site (34) and creates a mechanically coupled unit. Another form of the cannula (280) includes a tube having a tapered distal end region (298) and having elongate discharge slots (294) for reducing contact surface area and for directing the flow laterally out of the cannula. The cannula may also include a rounded lead post (330), an annular barb (394), and axially oriented grooves (268).

Abstract: A needle-bearing device for injecting medicinal fluid from a pre-filled vial is provided. After use, the needle is retracted into the body of the device to prevent inadvertent contact with the sharpened end of the needle. In one embodiment, the invention provides a manually actuable button that effectuates retraction of the needle after use. In another embodiment, retraction is effectuated automatically after the injection is complete.

Abstract: The invention relates to methods and devices for delivering medicament by jet injection to an injection site in a patient. The method includes inserting a needle into an insertion point, wherein the needle has a length of less than 5 mm and is operatively associated with an orifice in a nozzle assembly in fluid communication with an ampule chamber containing the medicament. The needle extends less than about 5 mm from the nozzle assembly orifice when the medicament is expelled. Next, a force generating mechanism is activated, and a pressure wall member that is operatively associated with the force generating member moves in response to the activation of the force generating mechanism at a speed sufficient to jet inject the medicament from the ampule chamber through the orifice and needle under a pressure of less than about 4000 psi to deliver a substantial portion of the medicament through the needle and past the insertion point to the injection site.

Abstract: A needle assisted jet injector and method for jet injecting medicament are disclosed. In one embodiment of the injector, the needle is retractably located within an injector nozzle assembly. Upon activation of the energy source, a portion of the needle extends past the nozzle assembly and penetrates the outer layer of skin to deliver the medicament via jet injection to a deeper region. After activation, the needle retracts back into the nozzle assembly. In another embodiment, the needle is fixed to the end of the nozzle assembly. In both embodiments, the length of the portion of the needle that penetrates the skin is less than 5 mm.

Abstract: This invention relates to a protection device for a syringe needle comprising an elastic needle cap of general longitudinal direction presenting a closed distal end and an open proximal end, said cap being formed by a lateral wall defining an inner housing intended to receive the distal part of the body of a needle syringe, and by an end wall capable of being pierced through a part of its thickness by the free end of said needle. Said housing comprises, from said proximal end, an opening, a first portion, a second portion intended to house the distal part of the syringe body which bears said needle, and a third portion which narrows from said second portion in the direction of the back of said housing.

Abstract: An automatic mixing and injecting apparatus comprises a syringe assembly within a housing. The syringe assembly has a chamber for holding a liquid, which can be a liquid medicine or a solvent. A second chamber may hold a dry medicine. The second chamber is releasably sealed with respect to the first chamber. A spring-operated plunger forces liquid from the first chamber and causes the releasable seal to disengage when the needle has entered the recipient. At this time, the liquid flows through the second chamber and dissolves any dry medicine in that chamber. A releasable coupling disengages the plunger from the driver spring and allows the plunger, syringe, and needle to retract under the urging of a return spring.

Abstract: This design relates to a disposable syringe assembly with possibly small-sized finger grip, while any part of the syringe is applicable for injection and medicaments are pre-filled for quick use.

Abstract: There is provided a syringe comprising a barrel having inner walls defining a compartment in the barrel, a closable nozzle at the base of the barrel and a plunger movable longitudinally within the barrel compartment. The plunger has inner walls defining a chamber suitable to receive a vial. A hollow needle extends through the plunger to enable fluid communication between the plunger chamber and barrel compartment. A compressible and puncturable sealing element within the plunger chamber provides a sterile seal for the needle and barrel compartment.

Abstract: A fluid delivery device for infusing medicinal fluids at a precisely controlled rate which includes adapter sleeve means for insuring that only a proper medicament can be used to fill the fluid reservoir of the apparatus. More particularly, the apparatus includes a unique polarity adapter that will mate only with a particular delivery device and positively prevent filling the reservoir of the device with a medicament that is incompatible with the delivery profile of the device. In one form of the invention, the polarity adapter includes a novel double-ended cannula that is carried within the polarity adapter and controls filling of the fluid reservoir.

Abstract: A pre-slit injection site (34) includes a housing (40) with a flow path therethrough. A first end (42) of the housing (40) carries a pre-slit septum (52). One form of a blunt cannula (98), usable with the injection site (34), carries a locking member (100). When the pre-slit injection site (34) slidably receives the blunt cannula (98), the locking member (100) latches to the injection site (34) and creates a mechanically coupled unit. Another form of the cannula (280) includes a tube having a tapered distal end region (298) and having elongate discharge slots (294) for reducing contact surface area and for directing the flow laterally out of the cannula. The cannula may also include a rounded lead post (330), an annular barb (394), and axially oriented grooves (268).

Abstract: A luer connector which facilitates connection of a hypodermic syringe to the vial, comprising a luer connectable to a syringe and which extends to a sharpened end capable of being driven through a puncturable vial closure to thereby puncture the closure; a luer support, mountable on a vial, and which initially supports the luer in a first position in which the sharpened end of the conduit is pointed toward the closure; a luer driver such that movement of the driver relative to the support causes the luer to be driven so that the sharpened end punctures the closure and enters the vial.

Abstract: The present invention relates to an automatic injector having a drive assembly with an actuator extending from the rearward end portion of the housing and a removal resistant cover for preventing unintended operation of the actuator. The present invention also relates to a sealing arrangement wherein the needle is sealed within a sterilized needle chamber by at least three sealing members which cooperate to form the chamber. Also, the present invention relates to an injector in which the cartridge is mounted to a tubular cartridge mounting portion of the needle carrier with an annular sealing member disposed therebetween. The cartridge mounting portion has at least one generally axially extending groove which allows air to escape from the cartridge mounting portion as the cartridge is being moved forwardly to a medicament supplying position.

Abstract: A pre-slit injection site (34) includes a housing (40) with a flow path therethrough. A first end (42) of the housing (40) carries a pre-slit septum (52). One form of a blunt cannula (98), usable with the injection site (34), carries a locking member (100). When the pre-slit injection site (34) slidably receives the blunt cannula (98), the locking member (100) latches to the injection site (34) and creates a mechanically coupled unit. Another form of the cannula (280) includes a tube having a tapered distal end region (298) and having elongate discharge slots (294) for reducing contact surface area and for directing the flow laterally out of the cannula. The cannula may also include a rounded lead post (330), an annular barb (394), and axially oriented grooves (268).

Abstract: A needleless injector cartridge has an adaptor for introducing fluid from a filling device into an orifice of the cartridge. The adaptor has a frangible connection which is broken to allow removal of the filling device after the cartridge is filled with the fluid.

Abstract: A self-sealing needle injection hub has two resilient, elastomeric sealing members mounted adjacent one another in a housing, both having pierced passages through which a needle can be inserted. The outer member is thick and relatively rigid; the inner member is thinner and flexible. Both members are radially compressed by the housing, the inner member bowing away from the outer member at its center. The action of withdrawing a needle from the hub, combined with the pressure of blood on the inner member, maintains the inner member flat against the outer member, thereby further compressing the passage through the inner member.