Abstract: A device for separating and isolating components of a biological fluid comprising a container for containing the fluid to be processed, a tube cap assembly for closing the container while providing filling and extraction communication therewith, a float assembly disposed within the container for funneling and controlling biological fluid flow into an inverted domed shaped isolation chamber within the float and controlling the biological fluid flow out of the isolation chamber for effecting an encapsulation or a sealed isolation of at least one component or fraction of the biological fluid flow within the isolation chamber during a centrifugation process. The device further comprising a flexible tube for connecting an extraction passageway disposed within the float assembly and an extraction valve of the tube cap assembly for allowing extraction of at least the one component or fraction encapsulated or isolated within the chamber.

Abstract: Drug delivery device, comprising a body unit having a first opening and a second opening, a plunger arranged such that its distal end is positioned inside the body unit, wherein the plunger is moveable in the distal direction with respect to the body unit, a needle assembly, with a proximal end and a distal end comprising a needle, wherein the proximal end of the needle assembly and the distal end of the plunger are configured such that they can get into a vacuum connection.

Abstract: A syringe for the metered delivery of materials, in particular of dental materials, is described. The syringe may include a tube which accommodates material and a rotary plunger. Radially extending gripping bodies may be disposed about a longitudinal axis of the syringe are disposed on the syringe in the region of the outlet opening of the tube for applying the fingers of the hand for rotating the tube about the rotary plunger.

Abstract: The present invention relates to an injection device comprising a housing, a container containing medicament to be injected through a needle (34) attachable to said container, drive means (46) operatively acting on said container for injecting said medicament, the drive means comprising a gas spring (50), locking (57) and activating means (56) arranged to hold said gas spring in a loaded state, and when activated, releases said gas spring to inject said medicament.

Abstract: A set of instruments configured to deliver a therapy to a bone can include a cannulated syringe. The cannulated syringe can extend along a longitudinal axis between a proximal and a distal end. The cannulated syringe can have an inner tube and an outer tube that are interconnected at the distal end as a single fixed unit. A first cannulation can be formed along the longitudinal axis of the cannulated syringe within the inner tube and a second cannulation can be formed within an annular space between the inner and outer tubes. The outer tube can define an opening through a sidewall thereof. The cannulated syringe can be closed from fluid communication between the inner and outer tubes.

Abstract: Disclosed are a piston for a micro-volume syringe and a plunger. The micro-volume syringe has a syringe barrel with a space defined in it. The piston is slidable on and along a wall of the space. A leading member to be arranged on a side where the piston comes into contact with a solution filled in the space and a trailing member to be arranged on a side where a plunger rod is to be connected, the latter side being opposite to a solution side of the leading member, have been integrated with each other. The trailing member has a higher hardness than the leading member. With the micro-volume syringe in which a drug solution can be filled in a very small quantity, the piston makes it possible to perform smooth drawing and ejection of the drug solution without leakage. Even if the small piston connected to a tip of the plunger rod is operated in a direction that the piston is to be pulled out of the syringe, the plunger rod does not slip off from the piston accidentally.

Abstract: A pen injection device designed for use with dual or multi-chamber cartridges (14), is provided with an extended length plunger (24) having a non-drive portion (24?) on its forward end and the usual screw-threaded drive portion (24?) on its rearward end. This arrangement allows the plunger to be pushed forwardly whilst the dosing drive mechanism is disengaged to effect a reconstitution movement of the rearward bung (18?) in the cartridge. Thereafter the threaded portion on the plunger (24?) engages the drive mechanism to allow metered dosing.

Abstract: A cylinder/piston unit is disclosed for pre-fill, storage and release when desired of an active substance, such as a medicament. The cylinder/piston unit is provided with a cylinder and with a piston which is guided therein and which is sealed off in a sterile manner by a rubber seal, the cylinder and the piston enclosing a chamber that can be filled at least temporarily with active substance, and the cylinder having at least one discharge element at its front end. For this purpose, the piston resting in a rear position is sealed off relative to the cylinder in a sterile manner by a static front sealing element and by a static rear sealing element. Arranged spatially behind each static sealing element, there is a parking area for receiving the respective sealing element.

Abstract: The end face of a cylinder-piston unit has a press-in area, engaging around the mouth, and a press-on area, surrounding the press-in area. The press-in area comprises an inner web, delimiting the mouth, and an outer web. The webs delimit a recess, which surrounds the inner web and of which the depth measured parallel to the center axis of the cylinder-piston unit is at least a quarter of its width in a plane oriented normal thereto. The press-on area, at least during an injection, is offset counter to the injection direction relative to the end face of the press-in area. Moreover, the surface of the press-on area projected into a plane normal to the center axis is at least as large as the surface of the press-in area projected into the same plane.

Abstract: Medicament delivery device comprising: a first housing part (12) having a container holder (14) into which a medicament container (16) can be placed and wherein the container has a front opening with or for a delivery member for delivering the medicament therethrough and a movable stopper (17); a second housing part (38) arranged to be moved between a closed position and an open position in relation to said first housing part (12); a plunger rod (48) having a front end and a rear end, and wherein said plunger rod is arranged parallel beside said container holder when the second housing part is in its closed position; wherein the second housing part comprises resiliently displacement means (50, 52) wherein one of the resiliently displacement means (50) is fixedly connected to said plunger rod, such that when said second housing part (38) is moved from its closed position to its open position, the plunger rod (48) is moved by said resiliently displacement means into a position where the front end of the plunger

Abstract: An apparatus and method for delivering liquid within an orifice of an animal is disclosed. In an exemplary embodiment, the apparatus comprises a hollow syringe defining a vessel having an open end; a plunger, slidingly and sealingly disposed within the vessel; and a flexible delivery tube, having a first end sealingly coupled to the open end and a delivery end for dispensing the liquid proximate the orifice. A light source directing light to the delivery end of the flexible tube may also be included.

Abstract: An apparatus is disclosed that allows for separating and collecting a fraction of a sample. The apparatus, when used with a centrifuge, allows for the creation of at least three fractions in the apparatus. It also provides for a new method of extracting the buffy coat phase from a whole blood sample. A buoy system that may include a first buoy portion and a second buoy member operably interconnected may be used to form at least three fractions from a sample during a substantially single centrifugation process. Therefore, the separation of various fractions may be substantially quick and efficient.

Abstract: An injection device includes a multi-use drive assembly 10 and a single use disposable syringe assembly 12 releasably connected thereto. The syringe assembly includes a syringe 18 and a shield 26 mounted for telescopic movement. The drive assembly 10 is operable to extend the syringe 18 relative to the shield 26 and then to express a dose. Continued forward drive movement extends the shield 26 to re-cover the syringe needle 22 and then ejects the spent syringe assembly 12 in a safe (shrouded) condition.

Abstract: Drug delivery device, comprising a body unit having a first opening and a second opening, a plunger arranged such that its distal end is positioned inside the body unit, wherein the plunger is moveable in the distal direction with respect to the body unit, a needle assembly, with a proximal end and a distal end comprising a needle, wherein the proximal end of the needle assembly and the distal end of the plunger are configured such that they can get into an adhesion connection.

Abstract: A medicament dispensing device including a substantially rigid carpule body which has a dispensing end and an actuation end opposite the dispensing end. The carpule body is substantially tubular and thus defines a carpule bore. The device further includes a plunger operatively disposed within the carpule bore having a plunger actuator near the actuation end of the carpule body and a plunger tip opposite the plunger actuator. The plunger tip and an orifice at the dispensing end of the carpule bore define a medicament volume which may be loaded with a medicament selected to achieve specific therapeutic goals. The carpule body may also include a wound depth scale. The depth scale is typically associated with the dispensing end of the carpule body. Similarly, the medicament dispensing device may include a dosage scale. Also disclosed are methods of dispensing medicaments.

Abstract: Apparatus, e.g. a syringe, for dispensing foam includes means for ensuring that only foam of adequate quality is dispensed. In use, the syringe may be filled from a pressurised canister which generates foam e.g. for therapeutic use in treating varicose veins. An initial quantity of foam dispensed from the canister may be of inadequate quality in which case it should not be used: the syringe includes means to ensure that this initial quantity of foam is diverted to a waste port or to an internal waste chamber e.g. located in the syringe plunger. Foam dispensed after the initial quantity of poor quality foam is stored in the main barrel of the syringe ready for administration to a patient in need of treatment.

Abstract: An interface device is described which includes a body defining one or more cylindrical bores which are dimensioned to receive a standard luer lock syringe. Each bore includes a plunger movably positioned therein from a retracted position to an advanced position. The plunger and the distal end of the bore defines a first fluid reservoir and the standard syringe assembly defines a second fluid reservoir. The interface device and the syringe assembly are operable to sequentially deliver multiple fluids from the interface device to a catheter assembly.

Abstract: The invention provides a formulation designed to enhance a woman's genital health and comfort. The formulation is designed to be applied into the vaginal opening with an applicator. The formulation consists of five essential ingredients: evening primrose (Oenothera biennis) oil, shea (Butyrospermum parkii) oil, vitamin E (alpha-tocopherol), phenoxyethanol and vitamin D3 (cholecalciferol). These ingredients act synergistically to enhance the plasticity of the vaginal lining preventing and reversing dryness and discomfort. Each of these ingredients is fat soluble, and each is readily absorbed by the vaginal lining cells and synergistic action of these components occurs through creating changes in the cells, themselves, rather than merely coating the cells externally, as do vaginal lubricating gels.

Abstract: A syringe assembly includes a syringe body having an internal fluid reservoir and a fluid contained within the fluid reservoir and defining a fluid outlet adjacent the distal end thereof, a plunger at least partially disposed within the syringe body and having a plunger rod and a distal plunger head and being adapted for longitudinal movement from an initial retracted position to an actuated advanced position and a dispensing element disposed within the internal fluid reservoir of the syringe body and distal of the plunger head. The dispensing element is dimensioned and arranged to cooperate with the plunger head to permit engagement and advancing movement of the dispensing element during corresponding movement of the plunger head without effecting a coupling relationship with the plunger head whereby the plunger is movable toward the retracted position without causing corresponding movement of the dispensing element.

Abstract: Devices for delivering pharmaceutical formulations into the eye are described. The devices may be integrated to include features that allow safe and atraumatic manipulation of the devices with one hand. For example, accurate placement, including proper angulation, of the device on the eye and injection of a pharmaceutical formulation into the eye can be performed using one hand. The devices may also include improved safety features. For example, the devices may include an actuation mechanism that controls the rate and depth of injection into the eye. Some devices include a dynamic resistance component capable of adjusting the amount of pressure applied to the eye surface. Related methods and systems comprising the devices are also described.

Abstract: The present invention is an enteral syringe that can include an elongated body having a hollow cavity therein and at least one vent extending from the hollow cavity to an outside surface of the syringe body. The elongated body can have a first non-circular cross-section. The enteral syringe can also have a plunger operable to selectively travel within the hollow cavity. The plunger can additionally have a second non-circular cross-section that substantially mirrors the first non-circular cross-section. The enteral syringe can additionally have at least one support feature for hanging the syringe from a support structure.

Abstract: A medical device for the injection of a product. The device includes a body receiving an injection needle and a container containing the product to be injected; an arrangement for holding the needle in an injection position; an arrangement for holding the container in a position permitting injection; and, a piston engaged in the container. The device also includes first and second actuators which make it possible, at the end of the injection, to respectively release the arrangement for holding the needle before, or simultaneously to, the release of the arrangement for holding the container. A container support is mounted slidably on the body and is displaceable relative to the latter in order to perform the injection. The container support is held in a standby position before injection with the needle being held in the injection position.

Abstract: A fluid introduction system includes an introducer configured to create a pressure of at least 69 kPa within a spine, and an operator configured to actuate the introducer to introduce fluid into the spine according to a predetermined fluid introduction profile. The system can include a computer readable medium having code for receiving fluid introduction data indicative of a fluid introduction parameter, and for receiving response data indicative of a response of the patient at a time related to a time of the fluid introduction data. A method for introducing fluid includes positioning a first introducer in a first portion of a spine, positioning a second introducer in a second, different portion of the spine and, without removing the first and second introducers, introducing fluid into the first portion of the spine with the first introducer and introducing fluid into the second portion of the spine with the second introducer.

Abstract: An injection control device having a metered/controlled injection rate proportional to the rate of withdrawal/injection, suitable for cosmetic as well as other applications is described. For example, after the cannula is advanced into an object, the cannula is withdrawn to create a tract or tunnel within the targeted area. As the cannula is withdrawn, filler material in the injection control device is uniformly deposited into the tract or tunnel via the automatic metering system. The automatic metering system incorporates a syringe activating mechanism coupled to a system which is capable of proportioning the deposition rate to the retraction/injection rate of the cannula. Accordingly, more consistent and uniform distribution of the material injected can be achieved with less cannula passes as well as requiring less dependence on the skills of the practitioner of this device.

Abstract: An apparatus and associated method are provided for controlling the plunging action of a syringe. A plunger control device includes an attachment member adapted to fixedly engage a syringe barrel. A translating member is slideably engaged with the attachment member. The translating member includes an elongate guide member slideably engaged with the attachment member such that the translating member is slideable with respect thereto between a proximal end and a distal end of the elongate guide member. The translating member further includes a plunger attachment portion disposed about the distal end of the elongate guide member and adapted to receive a portion of a syringe plunger for coupling thereto. The translating member further includes an engagement member extending from the proximal end of the elongate guide member so as to be spaced-apart from the syringe barrel when the attachment member is engaged with the syringe barrel.

Abstract: A flow delivery system including a syringe that includes an outer plastic shell, a leur and a plunger; and a needle and/or a catheter that embodies a hub and a cannula which delivers a solution of a material. Various structures are included to provide locking engagements, torque sensitive connections, sufficient interfacing between components and visual conformation of connectors. The syringe assembly can also include an approach to a filter. Moreover, an approach to sterilization is provided.

Abstract: The present invention provides a coating system for an article including a first component having a surface in frictional engagement with a surface of a second component, wherein at least a portion of at least one surface of the component(s) is coated with a coating prepared from a composition including a first, curable organopolysiloxane comprising at least two alkenyl groups; and a second, curable organopolysiloxane comprising at least two polar groups, the second organopolysiloxane being different from the first organopolysiloxane, which can provide low breakloose force when used in syringe assemblies.

Abstract: An auto-injection syringe is provided that includes an injection assembly and a retraction assembly operatively securable to the injection assembly. The retraction assembly includes a hypodermic needle having a needle hub, an end cap having a lower seal through which a portion of the hypodermic needle can pass, a retraction spring disposed between the needle hub and the end cap and maintained in a partially compressed condition therebetween, an upper seal urged against a facially sealing surface of the retraction assembly by the force of the retraction spring on the needle hub so that a sealed area is defined between the upper and lower seals, and a vent device in fluid communication with the sealed area for pressure equalization between the sealed area and an exterior of the retraction assembly.

Abstract: A medicament delivery device (1) comprises a housing (15), a telescopic piston rod assembly (12) for driving a bung (20) of a medicament container (9), and a drive mechanism (17) for the telescopic piston rod assembly. The telescopic piston rod assembly (12) has an input drive (23) telescopically coupled to a plunger (55) for driving the bung (20) via an intermediate coupling. The intermediate coupling comprises first and second cylinders (45, 49) telescopically coupled to one another. The plunger (55) is telescopically coupled to one of the first and second cylinders (45, 49) and the input drive (23) is telescopically coupled to the other cylinder. A key (14) is provided for restraining rotation of the plunger (55) relative to the housing (15) so that as the drive mechanism (17) drives the input drive, the plunger, first and second members and input drive telescopically expand or retract with respect to one another.

Abstract: A medical device (e.g., an implantable medical device) including a sealing apparatus (sealing element, e.g., a grommet for securing a lead to the device) that includes an element (e.g., a body) having a plasma-treated surface and methods (e.g., methods of making the device).

Abstract: The invention comprises a disposable hypodermic syringe with means for passive aspiration. The syringe comprises a barrel (10) of clear synthetic plastics material and a plunger (12) comprising an elastic bung (28) slideable in the barrel (10). Pressure on the plunger elastically deforms the bung (28). If this pressure is released the bung (28) resiles to effect aspiration. This aspiration is passive, requiring no active withdrawal of the plunger by the user. After use the syringe may be disposed of as a whole, with no disassembly, using one hand only. The syringe may be made by adapting cartridges conventionally used for dental local anaesthetic.

Abstract: A self-destroying disposable syringe includes a barrel which includes a hub disposed on the front end of the barrel, a flange is disposed on the inner wall of the hub; a needle base which connects to the hub of the barrel, and includes a connecting portion, a containing portion disposed on the outer side of the connecting portion, and a self-destroying ring disposed on the back end of the needle base and connected to the connecting portion through one or more ribs; when the needle base has connected to the barrel, the connecting portion and the self-destroying ring are located in the inside of the hub of the barrel, and the self-destroying ring matches the flange each other; a plunger which is movably inserted into the barrel and includes a bar body, a pushing stem connected to the back end of the bar body, a pushing dish connected to the front end of the bar body, a cone with one end fixed to the pushing disc, and a puncturing portion fixed to the other end of the cone; and a piston which is connected to the

Abstract: A drive assembly for use in a drug delivery device is proposed, the drive assembly comprising: a housing having a proximal end and a distal end; an axis extending between the proximal end and the distal end; at least one drive member; a piston rod adapted to be driven along the axis by the drive member; an indicator adapted to provide positional information about a position of the piston rod relative to the proximal end, wherein the indicator and the piston rod are configured to convert a movement of the piston rod with respect to the housing into a rotational movement of the indicator. Additionally, a drug delivery device comprising the drive assembly is provided for.

Abstract: Described are syringe devices useful in delivering medical materials internally in patients. In certain embodiments, syringe devices of the invention include widening internal lumen to assist in effective delivery of substances therethrough, and/or curved barrel portions with curved lumens therein. In still further disclosed embodiments, syringe devices include adaptations to prevent compression of compressible carrier materials to be delivered therethrough, curved barrel portions with flexible plunger arms to track the curved barrel portions, barrel portions controllable in shape such as to introduce and remove curves, visible markings to denote the direction of deflection of syringe barrel portions, imagable markers located on the syringe barrel, a cooperating plunger apparatus, or both; or combinations of some or all of these features.

Abstract: The present invention is directed to an automatic reconstitution drug delivery device. The inventive device effects simple and automatic reconstitution of a dry drug. To effect reconstitution, a user displaces a release button which causes first and second chambers of a drug cartridge to communicate, resulting in automatic mixing of a diluent and dry drug to effect reconstitution of the dry drug. The user then simply sets the dose volume using a dose-setting mechanism, and administers the injection in a manner typical of self-injection drug delivery devices. Whole or partial automatic priming can be also achieved by the device.

Abstract: A cannula (1) for dispensing fluid products, particularly for vaginal and rectal applications, comprises: a tubular body (2) for containing a fluid product (P), having a first extremity (2a), at which a dispenser opening (3) is formed, and a second open extremity (2b), opposed to the first extremity (2a). A closing body (5) which is associable with the tubular body (2) to close the second extremity (2b). The closing body comprises a first element (6) at least partially insertable through the second extremity (2b) and suitable for acting as a sliding piston inside the tubular body (2), and a second annular body, that functions a tamper indication seal. A cover cap (4) which can be fitted on the tubular body (2) to close the dispenser opening (3) and which is made in a single body piece. Longitudinal score lines divide the cover cap into a plurality of first sections and a single second section. Fold lines extend longitudinally along the first sections.

Abstract: An angiographic injector system and a method of controllably delivering medical fluid to a patient from an angiographic injector system are disclosed. A multiple processor control system is used to actively control the injection process and to monitor sensed functions of the system. The multiple processors provide dual redundancy safety circuits for critical control functions such as syringe motor drive speed and current. A motor/servo-amplifier nested control function is also disclosed. A unique method and apparatus are disclosed for establishing injection parameter default values just prior to an injection procedure that are based on physiological values of the patient to be treated. The injector system uses an interactive display panel that presents sequenced set-up screens to the user and which enables the user to select injection procedures, parameters and other modes of operation directly through the interactive panel.

Abstract: Various embodiments of syringe assemblies include a syringe barrel and a substantially conical tip or outlet disposed on the distal end of the barrel. The substantially conical tip includes a locking mechanism that engages an extension of a plunger assembly extending from a distal end of the plunger assembly so as to retain the extension within the substantially conical tip or outlet upon full injection of the contents of the syringe to a patient. According to one embodiment, a plunger head of the plunger assembly is slidably disposed on the extension. According to another embodiment, a separate hub, which holds a needle cannula, is disposed on an outlet at the distal end of the syringe barrel, which contains the locking mechanism. According to a further embodiment, the locking mechanism includes a locking clip disposed within the substantially conical tip of the syringe assembly.

Abstract: The present invention relates to medicament delivery device comprising a generally tubular distal housing part (19); a generally tubular medicament container holder (16); a medicament container (18); a plunger rod (32); resilient force; an actuation means (34) comprising flexible locking means and an activation button; a release means (40); and a resilient means (60) characterized in that said plunger rod comprises a number of stop engagements (38) arranged on its outer circumferential surface and arranged to co-act with corresponding stop engagements (37) on the flexible locking means, such that when said activation button is proximally depressed said stop engagement (37) on said flexible locking means come out of contact from one stop engagement (38) of the plunger rod; and such that when said activation button (48) is released, said resilient means (60) forces the activation button and thereby the flexible locking means to move distally such that said stop engagements (37) on said flexible locking means co

Abstract: A syringe assembly includes a syringe barrel having an inside surface defining a chamber, an open proximal end, a distal end, and an outlet; a plunger assembly disposed at least partially within the syringe barrel, including an elongate plunger rod having a locking flange formed thereon; and a plunger head having a distal sealing surface, the plunger rod being engageable with the plunger head such that the plunger rod is adapted to move the plunger head within the chamber of the syringe barrel through an injection cycle; and a flange lock disposed at the open proximal end of the barrel. The flange lock is integral with the open proximal end of the syringe barrel. During the injection cycle, the flange lock engages the locking flange of the plunger rod so as to prevent removal of the plunger rod from the syringe barrel.

Abstract: A system in accordance with embodiments of the present invention includes a cannula interconnected to a collection vessel by a flexible conduit. The collection vessel can comprise one or more syringe bodies. The syringe bodies are provided with tissue removed from a body using the cannula by a tissue transfer channel. As a result, multiple syringe bodies can be loaded with tissue, without requiring manual handling of that tissue. Alternatively or in addition, a collection bag can be provided for receiving tissue removed from a body using a cannula. The tissue collection bag can include a filter. A collection vessel comprising a collection bag can be used in combination with a collection vessel comprising one or more syringe bodies.

Abstract: A surgical device comprises a housing, a bioprocessing module, an end effector, and a pumping device. The bioprocessing module comprises media reservoirs, fluid conduits in communication with the reservoirs, and a port through which media is expelled. The end effector is configured for insertion into a lumen and delivering a tissue repair composition into that lumen. The end effector has at least one fluid conduit extending therethrough and at least one orifice in communication with the fluid conduit. The fluid conduit in the first end effector is in fluid communication with the port on the bioprocessing module. The pumping device is operable to urge a tissue repair composition comprising at least a portion of the contents of the media reservoirs through the fluid conduit of the first end effector such that the tissue repair composition is expelled from the at least one orifice.

Abstract: An injection system applicable to off-the-shelf syringes having a microneedle hub may reduce dead space and isolate the drug fluid from the microneedle chip to avoid compatibility issues. An insert may be disposed inside a male luer fitting and extend so that it is also disposed inside the female luer fitting using an insert. A septum may isolate the drug fluid from the microneedle chip in the hub prior to activation and the septum may, after activation, seal the triangular space in the hub to prevent leakage of fluid back to the syringe.

Abstract: A drug delivery system includes an automatic injector that can deliver a small, precise amount of a therapeutic agent. The automatic injector includes a chamber for containing a liquid component and a thin porous member that carries thereon and/or therein the small, precise amount of therapeutic agent. Upon activation of the automatic injector, a flow path opens from the chamber through the porous member, enabling the liquid component to rapidly mix with the therapeutic agent before being injected.

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: An apparatus that allows for separating and collecting a fraction of a sample. The apparatus, when used with a centrifuge, allows for the creation of at least three fractions in the apparatus. It also provides for a new method of extracting the buffy coat phase from a whole blood sample. A buoy system that may include a first buoy portion and a second buoy member operably interconnected may be used to form at least three fractions from a sample during a substantially single centrifugation process. Therefore, the separation of various fractions may be substantially quick and efficient.

Abstract: An injection device including a drive unit, a delivery unit, a dosing unit, a trigger for triggering an injection, a first coupling mechanism between the drive unit and the delivery unit, and a second coupling mechanism between the dosing unit and the drive unit, wherein the drive unit is tensioned by a rotation of the dosing unit and when the drive unit is tensioned the first coupling mechanism is disengaged and the second coupling mechanism is engaged, and wherein when an injection is triggered first the first coupling mechanism is engaged and then the second coupling mechanism is disengaged. In some embodiments, the device may include a third coupling mechanism which only releases the delivery unit after the engagement and disengagement which follow a triggering.

Abstract: A braking mechanism for a retractable safety syringe is disclosed herein. In a first embodiment, the braking mechanism is disposed about the distal end of a piston. The braking mechanism may comprise a friction material about a post attached to a piston. The friction material is displaced from a seat to a landing when the piston is traversed to a fully extended position to disengage the braking mechanism. In a second embodiment, the braking mechanism is disposed at a proximal end of a syringe body. The braking mechanism has a friction member which engages an outer surface of a rigid shaft of a plunger. The friction member is selectively pivotable to disengage the braking mechanism.

Abstract: The prefilled syringe filled with a drug in advance, leaking of liquid from the cap is prevented, gas barrier properties are given to the whole of the barrel filled with the drug and the shoulder section so that degradation of the drug is prevented, permeation of microbial contaminants is prevented to a high extent, and efficiency of packing as a compact container can be increased. The prefilled syringe includes a guard-shaped extension projecting from the outer periphery of a shoulder section of the syringe barrel on the nozzle side, and a range from a part where a gasket of the plunger is positioned on the outer surface of the syringe barrel filled with the drug to the guard-shaped extension is covered with barrier packaging.

Abstract: A plunger rod assembly for use with a syringe barrel is provided and includes a plunger rod slidably disposable within the syringe barrel, wherein the plunger rod includes a hub extending distally from a distal end thereof and at least two tabs extending outwardly therefrom. The syringe further includes a plug configured for slidable disposition in the syringe barrel and configured for selective connection to the plunger rod via a bayonet-type engagement. The plug includes a base wall having at least two resilient fingers supported on a first side thereof, wherein each resilient finger is configured to snap-fit engage a respective tab of the plunger rod during connection of the plug to the plunger rod; and a plunger tip supported on a second side of the base wall, opposite the first side, and being configured to form a substantially fluid tight seal with an inner surface of the syringe barrel.