Abstract: A syringe mixing system is provided for housing and mixing contents between at least two syringes. In some embodiments, a syringe coupler is provided that receives first and second syringes and includes a valve member that is convertible between a closed position and an open position. Retention systems for preventing or inhibiting removal of at least one syringe after use are also provided.

Abstract: In some illustrative examples, a conduit interface may include a mounting surface and an exterior-facing surface positioned across from the mounting surface, an internal cavity, an inlet port, a vent, and a temporary plug. The internal cavity may include an opening positioned proximate to the mounting surface. The inlet port may be in in fluid communication with the internal cavity through the exterior-facing surface. The vent may be in fluid communication with the internal cavity through the exterior-facing surface. The temporary plug may be configured to temporarily preclude fluid communication through the vent. The conduit interface may be suitable for providing fluid communication with a dressing at a tissue site. Also provided are other examples, apparatus, systems, and methods.

Abstract: A pharmaceutical container for drug delivery includes a barrel configured to slidably receive a stopper. The stopper has a proximal end suitable for contacting a plunger rod and a distal end suitable for contacting a pharmaceutical composition. The stopper has a circumferential surface partially contacting an inner surface of the barrel. A surface roughness of the inner surface of the barrel declines from the stopper's start position to its end position by at least 3% of at least one of Ra roughness or Rms roughness.

Abstract: A system for delivering an injection of a fluid into a void within a subject is disclosed. A barrel extends from a first end to a second end and forms a lumen extending from the first end to the second end. A plug and a floating seal are arranged within the lumen. A hollow needle includes a distal end with an opening for fluid to flow from the lumen. The plug, the barrel and the floating seal include material and dimensions selected based on a threshold flowrate for a fluid arranged within the lumen to: overcome a force opposed to a force being applied to the fluid in the lumen to move the floating seal and the hollow needle into a tissue of the subject, and succumb to the opposing force to displace the fluid through the opening into the void.

Abstract: The disclosure relates to a drug delivery device comprising: a case adapted to hold a medicament container, a plunger disposed within the case and slidable from a proximal position into a distal position for delivering a medicament from the medicament container, at least one feedback mechanism that is in operative connection with the plunger, the feedback mechanism comprising a collar, a control spring biasing the collar in a distal direction, a needle shroud, operatively axially abutting the collar in a first coupled state and prevented from axially decoupling the collar by the plunger in its proximal position, wherein the plunger, when approaching the distal position during movement from the proximal position towards the distal position, is adapted to allow axial decoupling of the needle shroud from the collar, thus allowing for a limited axial movement of the collar relative to the needle shroud until the collar axially abuts the needle shroud in a second coupled state.

Abstract: The present disclosure relates to an operation aid for a medication delivery device, which is configured to alleviate the operation of an actuator of the medication delivery device. Furthermore, a system comprising a medication delivery device and an operation aid is disclosed.

Abstract: A sealing article for use with a fluid conveyance device comprises an elastomeric body including a first end defining a disk-shaped annular protrusion, and an annular recess formed in a sidewall thereof directly adjacent the first end of the body in an axial direction of the body. The recess is sized to receive at least a portion of the annular protrusion in response to the sealing article being inserted into an interior cavity of the fluid conveyance device. A barrier material is attached to or formed on a first end of the body and extends over the radial protrusion.

Abstract: Rectal suppositories are used to administer a predetermined drug dosage to treat a variety of diseases and symptoms in a variety of patient populations. Certain medical conditions, such as digestive disorders, may be more effectively treated when the suppository is placed in a particular location of the patient's anal canal or rectum. An apparatus for inserting a suppository can include an applicator having a barrel, such as a hollow cylindrical body, and a plunger, such as a substantially cylindrical elongated body. The apparatus can include features to ensure that beneficial gas flow paths associated with the plunger or the barrel are maintained or that the apparatus can accommodate suppositories of different sizes. Embodiments may include features to facilitate gripping and manipulation of the apparatus for use by patients with limited dexterity. These benefits may encourage patients to maintain a course of treatment, thereby potentially avoiding additional complications, hospitalization, and costs.

Abstract: The invention relates to a drug delivery device, comprising: a case for retaining drug container, the drug container defining a cavity for containing a drug, wherein a stopper is slidably disposed within the container so as to displace the drug through a discharge nozzle on translation in a distal direction, an inner magnet disposable within the drug container for abutting the stopper, at least one outer magnet disposed within the case coaxially with the container and slidable in an axial direction, a trigger arrangement for advancing the outer magnet in a distal direction on actuation, wherein the outer magnet and inner magnet are arranged for magnetically interacting through the drug container wall such the outer magnet advances the inner magnet on trigger actuation.

Abstract: An elastomeric stopper that can be partially inserted in a rear opening of a glass carpule and that also serves, when fully inserted in the carpule, as a plunger for forcing fluid inside the carpule out through a front opening thereof. The stopper has a thin central portion at its front end that can be readily pierced by a pointed hollow rod of a syringe. When the hollow rod is removed, the elastomeric material of the thin central portion will “seal itself” around the puncture hole. The stopper also has a retractable lip at its rear end that allows the entirety of the stopper to be pushed down and into a fluid-containing glass carpule, thereby acting as a plunger and ejecting fluid from the front opening of the carpule.

Abstract: A thermoplastic elastomer stopper that meets the desired material properties of a stopper for a syringe assembly is disclosed. The compression set of the thermoplastic elastomer stopper of the present disclosure is ?50% when measured at 25% compression for 22 hrs at 70 degree C. The hardness of the thermoplastic elastomer stopper of the present disclosure is 40-70 Shore A. The viscosity of a thermoplastic elastomer stopper of the present disclosure is ?70 Pa·s at 1,000 s?1 shear rate, ?12.0 Pa·s at 10,000 s?1 shear rate, and ?3.0 Pa·s at 50,000 s?1 shear rate when measured using a capillary rheometer at 205 degree C. (Die: Roundhole 20 mm length/1 mm diameter/180 degree inlet, Piston: d=15 mm, and melting time=7 min). The present non-lubricated stopper exhibits the required functional performance of a lubricated stopper.

Abstract: A medication cartridge plunger including a sealing member, which is formed of a resilient material, and a force distributing member, which is attached to sealing member and formed of a material more rigid than the resilient material. The force distributing member is shaped complementary with the sealing member to distribute to the sealing member a medication expelling force that may be applied to the force distributing member by an external drive element to drive the plunger forward. The force distributing member includes a radial periphery fit within a hollow of the sealing member. The radial periphery has a plurality of apex regions connected by spanning regions, which apex regions are disposed along a common circle centered on an axial center of the medication cartridge plunger. The spanning regions are disposed within the common circle, and each apex region, relative to the common circle, is not in diametric alignment with any of the other apex regions.

Abstract: The present invention provides for an injection device including a syringe with a proximal end, a distal end, a needle extending from the distal end, and a plunger inserted into the proximal end. A guard is slidable on the syringe, has a proximal end, a distal end, and is biased from a first position wherein the needle is exposed towards a second position wherein the guard covers the needle. The injection device includes first and second sets of cooperating detents for retaining the guard and syringe in the first and second positions, respectively. A latch member extends proximally from the guard that is engageable by the plunger as the plunger is depressed to release the first set of cooperating detents. Upon release, a spring element biases the guard towards the second position until the second set of cooperating detents engage and secure the guard in the second position.

Abstract: An injection device has a dispensing chamber housing, a plunger, and a temperature control device. The dispensing chamber housing has a first part and a second part. The first part is thermally coupled to a needle. The second part is thermally coupled to the first part. The second part has an inner surface and an outer surface. The inner surface partially defines a dispensing chamber for holding a quantity of a substance. The plunger is engaged with an inner surface of the dispensing chamber housing, is capable of sliding in the dispensing chamber housing, and is fluidly sealed to the inner surface of the dispensing chamber housing. The temperature control device at least partially surrounds the dispensing chamber housing and is capable of altering a temperature of the substance in the dispensing chamber. The second part has a greater thermal coefficient than the first part.

Abstract: Describe is an auto-injector comprising a syringe carrier arranged to retain a syringe, a plunger arranged to displace a stopper within the syringe, a feedback component retainable in a first position and biased towards a second position, a pin disposed on the feedback component, and an exterior component having a bore. The feedback component moves from the first position to the second position when the plunger during displacement of the stopper reaches a predetermined position. The pin enters the bore when the feedback component is in the second position.

Abstract: A finger grip extension for a syringe is configured to increase the leverage the hand of an operator on the plunger of a syringe during injection of medical fluid into, or withdrawal of medical fluid from a body site. The finger grip extension for a syringe is used with a syringe having a barrel portion having an open proximal end and a distal end for mounting a medical fluid conduit thereon. The open proximal end of the syringe barrel terminates in a rim or flange. The syringe also includes a plunger having a proximal end and a distal end for insertion into the open proximal end of a syringe. The extension grip includes an upwardly extending portion located inside or outside of a syringe barrel. The upwardly extending portion includes a finger support at the uppermost portion thereof.

Abstract: A medical appliance including a slidable coating layer moves in contact with an inner surface of a medical member or that of a lumen. The medical appliance has the slidable coating layer formed at a part thereof which contacts the medical member or the lumen. The slidable coating layer is formed of a composition containing a solventless-type hardening silicone-based resin.

Abstract: A medical appliance having a slidable coating layer that moves in contact with an inner surface of a medical member or that of a lumen and has the slidable coating layer formed at a part thereof which contacts the medical member or the lumen. The slidable coating layer is formed of a composition which does not contain solid fine particles and contains a silicone-based resin which is a product of an addition reaction between silicone having a vinyl group and silicone having a hydrogen group bonded to a silicon atom.

Abstract: The invention relates to an injection device comprising a housing, a container holder arranged within said housing, the container holder being configured for accommodating a medicament container having a needle attached to one end thereof and a stopper sealingly and slidable arranged inside the medicament container at the other end thereof, a plunger rod being arranged with a proximal end thereof contactable with said stopper, a first and a second energy accumulating member arranged in the interior of the housing of the injection device and adapted to accumulate and store energy, plunger drive means being slidable arranged in relation to the plunger rod, being rotationally locked to the plunger rod and being rotatable in relation to the housing, the plunger drive means being operationally associated with the first energy accumulating member, a container driver arranged for being connectable to the container holder and threadedly connected to the plunger rod, the container driver being operationally associated

Abstract: The present invention relates to a medicament container holder arrangement comprising a medicament container holder 16 and a medicament container 18 wherein the medicament container holder 16 is provided with distally arranged support surfaces 25 for flanges 24 arranged on a distal part of the medicament container 18 to be placed in said medicament container holder 16, which medicament container 18 is arranged with a needle shield 20 to the proximal end thereof, wherein said needle shield 20 has a diameter generally equal or larger than the diameter of said medicament container 18, wherein said medicament container holder arrangement further comprises holders arranged on the container holder for holding said medicament container 18 around a proximal shoulder portion 22 thereof and a resilient support element 23 arranged between the flanges 24 and the support surfaces 25 whereby the holders and the resilient support element 23 absorb and spread forces between the medicament container and the container holder.

Abstract: A medical appliance including a slidable coating layer moves in contact with an inner surface of a medical member or that of a lumen. The medical appliance has the slidable coating layer formed at a part thereof which contacts the medical member or the lumen. The slidable coating layer is formed of a composition containing a solventless-type hardening silicone-based resin.

Abstract: A fluid syringe of the type used with fluid infusion devices is presented here. The fluid syringe generally includes a barrel, a piston, and a check valve seal. The barrel has an interior wall and a sealed main fluid chamber. The piston is slidably coupled within the barrel, and the piston has a piston seal forming an interference fluid seal against the interior wall. The check valve seal is coupled to the piston, and it is located between the piston seal and the main fluid chamber. The check valve seal forms an interference fluid seal against the interior wall when the piston is unloaded, and it disengages the interior wall to allow gas flow from the main fluid chamber toward the piston seal when the piston is loaded.

Abstract: An extendible plunger rod for use with a syringe is provided. Example plunger rods may include an outer plunger rod with a proximal end and a distal end, the outer plunger rod having an inner cavity; an inner plunger rod, housed at least partially within the inner cavity of the outer plunger rod; a compression spring disposed within the inner cavity of the outer plunger rod and between the proximal end of the outer plunger rod, and the inner plunger rod, the compression spring configured to exert force tending to push the inner plunger rod in a direction distal to the outer plunger rod; and a locking mechanism, the locking mechanism configured to prevent movement of the inner plunger rod relative to the outer plunger rod while both the inner and outer plunger rods are depressed into a syringe body, until the outer plunger rod has been depressed at least a first predetermined distance into the syringe body.

Abstract: Described generally herein are tissue therapy devices, which may comprise a sealant layer and a suction apparatus. The sealant layer functions so as to create a sealed enclosure between it and the surface of a patient by forming, preferably, an airtight seal around an area of tissue that requires negative pressure therapy. The tissue therapy device may comprise a suction apparatus. The suction apparatus is typically in fluid communication with the sealant layer and functions so as to reduce the amount of pressure present underneath the sealant layer. The reduced pressure is self-created by the suction apparatus. Together the sealant layer and the suction apparatus preferably create a closed reduced pressure therapy system. Preferably, the pressure under the sealant layer is reduced by expanding the volume of the enclosure space and thereby decreasing the density of the air molecules under the sealant layer.

Abstract: An object of the present invention is to provide a syringe for prefilled syringe in which the adsorption of a low-molecular medical agent or a protein for a long term is precluded. In accordance with the present invention, the above-described object is achieved by a syringe for prefilled syringe including: a plunger in which a gasket is attached to a top; and a syringe barrel in which the plunger is slidably accommodated, wherein the surface of the gasket and the inner wall of the syringe barrel are subjected to surface modification with a polymer containing zwitterion.

Abstract: A medical article is provided including a chamber formed from a cyclic polyolefin having an inner surface in sliding engagement with an exterior surface of a sealing member, the inner surface of the chamber being coated with a composition including a first mixture of organopolysiloxanes having different molecular weights and a viscosity ranging from about 5,000 centistokes to about 100,000 centistokes; and a sealing member having an exterior surface coated with a second mixture of organopolysiloxanes having different molecular weights and having a viscosity ranging from about 10,000 centistokes to about 500,000 centistokes, the coatings being adhered to the surfaces by crosslinking induced by irradiation with an isotope, electron beam, or ultraviolet radiation.

Abstract: The invention refers to an arrangement for coupling a plunger (9) to either a syringe (3) or a stopper (6) arranged in the syringe (3), the arrangement comprising a syringe holder (22) which is slidably arranged in a housing (2), wherein the syringe holder (22) is provided with at least one resilient syringe holder arm (23) arranged distally, the syringe holder arm (23) having an inclined surface for bearing against a shoulder (24), which is arranged at the plunger (9), wherein the syringe holder arm (23) is supportable by an inner surface of the housing (2) in order to prevent it from being flexed outward in a first position and wherein a widened portion (2.1) is provided in the housing (2) for allowing the syringe holder arm (23) to flex outwards and disconnect from the plunger (9) when in a more proximal position so as to switch load of the plunger (9) from the syringe (3) to the stopper (6).

Abstract: Some embodiments of an infusion pump system may be configured to provide air pressure equilibrium between the ambient air pressure external to the infusion pump system and the internal air pressure inside the infusion pump system. In particular embodiments, the infusion pump system can be equipped with an air-transmissible, liquid-tight seal along an interface between a pump body and a cap device configured to attach to the pump body.

Abstract: An ergonomic syringe includes a slide member, wherein force exerted on the slide member causes movement of a syringe plunger within a hollow or partially hollow syringe barrel, for withdrawing fluid from a source into the syringe, and also includes a reusable adaptor for use with existing conventional syringes, which has a ring that wholly or partially encircles the barrel and indirectly attaches to a plunger flange.

Abstract: A syringe comprising a cylinder and a plunger arranged in the latter has a sealing element which, with a contact region, abuts an inner wall of the cylinder and seals an annular gap between the plunger and an inner wall of the cylinder. The contact region has a front section which, in the rest state, abuts the inner wall of the cylinder with an abutment pressure. The plunger is connected to the sealing element in such a way that the sealing element does not follow an initial movement of the plunger out of the rest state and such that the sealing element follows a continued movement of the plunger. The abutment pressure between the sealing element and the inner wall in the front section of the contact region decreases during the initial movement. With the syringe, less force is required in order to overcome the static friction between the sealing element and the inner wall of the cylinder.

Abstract: A syringe containing a high water content product and for use in a drug infusion system is provided. The syringe includes a plunger carrying front and rear o-rings made of a diene rubber compound such as chlorobutyl rubber or bromobutyl rubber to impart very low gas permeability characteristics to the o-rings. The plunger may be molded as a single part or in two parts. If molded as one part with radially-engaging mold portions, the seal glands in the plunger may include parting lines from the mold. If molded as two parts with axially-engaging mold portions, the front seal gland may include a sealing surface and under cut that has no parting line. The o-rings may be surface treated with a lubricant to improve sealing where the molding process gives rise to parting lines in the seal glands.

Abstract: A medication delivery device (100) comprises a container (101) for holding a medication (104) and a piston (102) which is at least partly arranged within the container (101) and which is axially displaceable with respect to the container (101). The piston (102) is at least partly arranged at a distance from an inner surface (112) of the container (101), thereby providing a channel (116) between the piston (102) and the container (101). The device (100) further comprises a seal (103), the seal (103) being arranged to limit the channel (116) proximally.

Abstract: A medical appliance having a slidable coating layer that moves in contact with an inner surface of a medical member or that of a lumen and has the slidable coating layer formed at a part thereof which contacts the medical member or the lumen. The slidable coating layer is formed of a composition which does not contain solid fine particles and contains a silicone-based resin which is a product of an addition reaction between silicone having a vinyl group and silicone having a hydrogen group bonded to a silicon atom.

Abstract: A container for collecting, storing and dispensing fluid, as in enteral feeding and/or medication deliver to neonatal infants. The container includes a hollow tube with a body, a first end, a second end, and an outer diameter. The hollow tube is configured to receive a movable plunger that advances and retracts therein to define a variable contained volume. The container also includes a sealing head assembly removably mounted at an end of the hollow tube. The sealing head assembly has a diameter or outside dimension that is substantially similar or identical to a corresponding outside diameter or dimension of the hollow tube, so that the container lies flat within the receiver of an enteral feeding pump.

Abstract: A system to minimize fluid turbulence inside a tissue cavity during endoscopic procedures. A body tissue cavity of a subject is distended by continuous flow irrigation using a solenoid operated pump on the inflow side and a positive displacement pump, such as a peristaltic pump, on the outflow side, such that the amplitude of the pressure pulsations created by the outflow positive displacement pump inside the said tissue cavity is substantially dampened to almost negligible levels. The present invention also provides a method for accurately determining the rate of fluid loss into the subject's body system during any endoscopic procedure without utilizing any deficit weight or fluid volume calculation, the same being accomplished by using two fluid flow rate sensors. The present invention also provides a system of creating and maintaining any desired pressure in a body tissue cavity for any desired cavity outflow rate.

Abstract: An embodiment in accordance with the present invention provides an integrated syringe-device which can store a volume of fluid for infusion, can connect via an air-tight connector to another device (such as a luer connector), can flush fluid through the connector into the other device, and can deliver a cap that forms an air-tight closure to the device connector.

Abstract: A medical vacuum aspiration apparatus (100) includes: a vacuum cylinder (110) closed at a first end by a valve (140), and closed at a second end by a plunger (120) moveable along the cylinder (110), the valve (140) being formed from a flexible nozzle (130) and a releasable nozzle clamp (142), the nozzle (130) having also an aperture (136) in fluid communication with a vacuum chamber formed by the cylinder (110), characterised in that the aperture (136) is stepped in diameter or tapered in size to accept cannulae (10) of different sizes in use. Disclosed also is a plunger locking mechanism which requires the twisting of a plunger handle (124).

Abstract: A precision syringe (10) can comprise an annular fluid pathway (16) and annular plunger (12) sealing received within the annular fluid pathway. Various precision pumps (50, 200, 300, 400, 500, 600, 700, 800, 900, 1000, 1100, 1200, 1300, 1400, 1500, 1600, 1700) are configured for discrete displacement of precise volumes of fluid. The precision pumps can operate by reciprocating movement to expand and contract a cavity (204, 304, 404, 504, 604, 704, 804, 904, 1040, 1104, 1204, 1304, 1404, 1504, 1604, 1704). Fluid can be introduced by movement along an axis or rotation about an axis of one or members forming, in whole or in part, the cavity. Associated methods are also disclosed.

Abstract: The present invention provides for an injection device including a syringe with a proximal end, a distal end, a needle extending from the distal end, and a plunger inserted into the proximal end. A guard is slidable on the syringe, has a proximal end, a distal end, and is biased from a first position wherein the needle is exposed towards a second position wherein the guard covers the needle. The injection device includes first and second sets of cooperating detents for retaining the guard and syringe in the first and second positions, respectively. A latch member extends proximally from the guard that is engageable by the plunger as the plunger is depressed to release the first set of cooperating detents. Upon release, a spring element biases the guard towards the second position until the second set of cooperating detents engage and secure the guard in the second position.

Abstract: A syringe including a barrel and a plunger slidably disposed within the barrel is disclosed. A distal end of the barrel defines a roof, and an elongate tip, in fluid communication with the barrel, extends from the roof. A protrusion forming a ridge may be disposed on one of the roof of the barrel and the plunger head. When the plunger head contacts the roof, the protrusion forms a channel between the plunger head and the roof. The channel isolates fluid within the channel from the elongate tip, which in turn reduces the spray of fluid through the distal end of the syringe. In another embodiment to reduce the spray of fluid through the distal end of the syringe, an impulse reduction system may be used to reduce or prevent the proximal portion from applying a distally directed impulse to the distal portion after the breakable connection is broken.

Abstract: A syringe assembly for connecting to an intravenous (“IV”) line includes: a syringe barrel having an actuation end and a discharge end; a syringe plunger moveable within the syringe barrel, the syringe plunger including a plunger head connected to a plunger arm; a seal between the plunger arm and the syringe barrel, the seal residing on an actuation end side of the syringe plunger; and a tube in fluid communication with the syringe barrel at a location between the seal and the plunger head, the tube having a distal end configured to be connected to the IV line.

Abstract: A medical device having a barrel, a retractable needle, a needle retraction assembly and a plunger, the needle retraction assembly including and being held inside the barrel prior to retraction at least in part by a retainer member contacting the barrel, the plunger comprising a plunger seal with an body having at least a portion that is rearwardly moveable relative to the plunger and an elastomeric web that seals a retraction cavity inside the plunger prior to retraction of the needle, the retainer member and the plunger seal each cooperating with an inside wall of the barrel to provide a sealed liquid containment chamber inside the device.

Abstract: A hypodermic needle assembly configured such that the movement of a needle shield into position to block the needle tip occurs as a direct consequence of a longitudinal force applied by insertion of a syringe plunger is provided. The hypodermic needle assembly according to the present invention comprises a needle, a needle hub, and a safety spring clip assembly, the safety spring clip assembly being configured to automatically launch from the needle hub and slide along the needle until the spring clip meets a needle stop at the needle tip, thus preventing the guard from being removed from the needle shaft. A method of using the hypodermic needle assembly according to the present invention is also provided, which includes the method of launching the spring clip with a syringe having multiple advancing mechanisms.

Abstract: A liquid medication dispenser includes a housing that has open top and bottom. The housing includes a central channel and a plurality of internal compartments disposed around the central channel. Each internal compartment is configured to hold liquid medication. The central channel is provided with symmetrically disposed bottom apertures configured to open into respective internal compartments. A shaft is configured to rotate and advance within the central channel. The shaft has a bottom hollow portion and at least one lateral aperture thereon configured to align with each one of the bottom channel apertures. The lateral shaft aperture aligns with a respective bottom channel aperture to allow transfer of liquid medication under gravity from the corresponding internal compartment into the bottom hollow portion of the shaft. The bottom hollow portion is apertured at one end to allow for transferred liquid medication to drip out of the dispenser in a controlled fashion.

Abstract: To provide a syringe barrel and a syringe capable of allowing an operator to feel the amount of injected medical solution or the inserting distance of a piston by a difference in sliding resistance when an injection operation is performed. A syringe 1 includes a syringe barrel 11 which has an inner surface provided with a structure in which a sliding resistance F is changed step by step upon sliding a piston 32. The syringe barrel 11 includes steps which are formed at one or two or more positions of the inner surface in the axial direction so as to face from the rear end to the front end or from the front end to the rear end, and which include edges formed along the circumferential direction.

Abstract: Syringes and methods of using are described which protect the syringe barrel cavity from contaminants. A syringe is formed with an end cap contaminant shield having an extension wall that is mated with the rearward end opening of the syringe barrel cavity. Alternatively, the end cap contaminant shield can be provided with a flat design without the extending wall and is bonded or molded to the rearward end terminus of the syringe barrel. The end cap contaminant shield designs are provided with an opening defining the shape of the cross-section of the plunger shaft.

Abstract: The present invention provides for an injection device including a syringe with a proximal end, a distal end, a needle extending from the distal end, and a plunger inserted into the proximal end. A guard is slidable on the syringe, has a proximal end, a distal end, and is biased from a first position wherein the needle is exposed towards a second position wherein the guard covers the needle. The injection device includes first and second sets of cooperating detents for retaining the guard and syringe in the first and second positions, respectively. A latch member extends proximally from the guard that is engageable by the plunger as the plunger is depressed to release the first set of cooperating detents. Upon release, a spring element biases the guard towards the second position until the second set of cooperating detents engage and secure the guard in the second position.

Abstract: A container or vial (1) for a fluid, the container (1) comprising a casing defining an interior for storage of the fluid and a closure member (2). The closure member (2) comprises a body and at least one resilient projection (7) to seal in a storage condition an outlet of the casing, wherein upon an increase in the pressure of the interior of the container (1) the at least one resilient projection (7) is deflected to accommodate outflow of fluid through the outlet. The pressure in the interior of the container (1) may be increased by displacing the closure member (2) into the container (1) or by displacing some other element such as a bung (61, 82) into the container (1). The container (1) and closure member (2) may be used in a dispenser (90) and the closure element may be used in a valve (110).

Abstract: The invention relates to an attachment (1) or a cartridge comprising a sealing element (5) having an opening (9) for a medium located in the syringe or cartridge or to be introduced into the syringe (3) or cartridge. The attachment (1) is characterized by an actuating device (11) which, in a first functional position, exerts a force on the wall of the opening (9) in such a way that the opening (9) is closed, and leaves the opening (9) open in a second functional position.

Abstract: A casing may be configured to envelop at least a portion of a plunger arm attached to a plunger head located in a reservoir. A plunger head moveable in a reservoir may have a front portion comprising a first material compatible with fluidic media in an interior volume of the reservoir. A seal member having a first end and a second end that taper to a mid-portion may be positioned between a reservoir and a plunger head. A bias member may be configured to force a plunger arm operatively connected to a plunger head against a drive member to operatively engage the plunger arm to the drive member. A plunger head moveable in a reservoir may have a first ridge, a second ridge, a seal member adjacent at least one of the ridges, and protrusions arranged around at least one of the ridges.