Abstract: A drug delivery device for administering a drug is presented having a body adapted to retain a cartridge containing a drug, at least one electrical unit and a port for electrically contacting the electrical unit, an adapter for attaching an injection needle to the drug delivery device, a safety mechanism arranged to prevent access to the port while an injection needle is in fluid communication with the cartridge and arranged to prevent establishing a fluid communication between an injection needle and the cartridge while the port is accessible.

Abstract: Apparatus for supporting implements such as hypodermic syringes. The structure is made so as to protect operators against inadvertent sticking and the possible consequences thereof.

Abstract: A cap is configured to provide antimicrobial protection to a female luer port of an intravenous device. The cap distributes an antimicrobial solution within the intraluminal surfaces of the port when the cap is connected to the port. A cap may also be designed to distribute an antimicrobial solution around the exterior surfaces of the port. Once connected to a port, the cap can form a seal that minimizes the evaporation of the antimicrobial solution from within the lumen of a port. The cap can therefore provide antimicrobial protection against another device that is connected to the port once the cap is removed.

Abstract: A method for assembling an assembly for a syringe that includes a cylindrical outer barrel; a puncture needle; and a cylindrical cap. The method includes forming a closed space in a receiving hole of the cap by inserting the puncture needle and a barrel tip at least partially into the receiving hole before a tip end of the puncture needle is inserted into a bottom wall of the cap; discharging gas in the closed space; and sealing a tip end of the needle hole by further inserting the barrel tip into the receiving hole to insert the tip end of the puncture needle into the bottom wall.

Abstract: A medical injector includes an injector housing defining a reservoir, a plunger rod, and a stopper engaged with a portion of the plunger rod. The stopper being slidably disposed within the reservoir and sized relative to an interior of the injector housing to provide sealing engagement with a sidewall of the injector housing. The medical injector further includes a needle having a sharpened first end and a second end in communication with the reservoir, a first cap covering the sharpened first end of the needle, and a second cap covering at least a part of the first cap. The second cap includes a body having a proximal end, a distal end, and a flange provided adjacent the distal end. The second cap is engaged with the first cap such that removal of the second cap simultaneously removes the first cap from the first end of the needle.

Abstract: A safety support device for a syringe comprises a support sheath for the body of the syringe and an inner sheath suitable for sliding relative to the support sheath between a waiting, retracted position and the extended position for protecting the needle of the syringe. The device has means for holding the syringe body relative to the support sheath and retaining means suitable for being activated to retain g the inner sheath in the waiting, retracted position inside the support sheath and for being deactivated by the piston of the syringe to allow the inner sheath to extend into its protective, extended position.

Abstract: A drug delivery device for administering a drug is presented having a body, at least one electrical unit and a port for electrically contacting the electrical unit, an adapter for attaching an injection needle to the drug delivery device, a safety mechanism arranged to prevent contacting the electrical unit whilst an injection needle is in fluid communication with the drug delivery device and arranged to prevent establishing a fluid communication while the electrical unit is contactable.

Abstract: A conventional syringe defines a longitudinal axis and includes a syringe barrel having a syringe barrel flange laterally extending from an open proximal end of the syringe barrel and a plunger advanceable into the syringe barrel. A rotatable finger flange for such a syringe includes identical first and second flange components, each having an attachment member configured to releasably engage the syringe barrel flange and/or the other flange component, and a flange member laterally extending therefrom. The first and second flange component are engageable and rotatable relative to one another about the longitudinal axis between a non-use position, wherein the first flange member overlies the second flange member to reduce the finger flange footprint, and a use position, wherein the first flange member and the second flange member are angularly spaced apart from one another to provide a finger flange having a greater lateral extent than the syringe barrel flange.

Abstract: A vial holder is provided to protect a user's hand from needle sticks. The holder includes a handle and a shield attached to a distal end of the handle. An opening is formed in the distal end of the handle to receive a vial. The vial is placed through the opening and into a passageway of the handle with the upper end of the vial exposed. A user grasps the handle which holds the vial in a stabilized manner. A needle may then safely approach the vial in which inadvertent slippage or movement of the needle results in contact with the needle against the shield and not contact with the user's hand.

Abstract: Embodiments of the shield assemblies include a shield that is pivotably secured to a needle hub. A ball-and-socket hinge secures the shield and the hub to one another. The assembly includes a reversible shield lock to hold the shield in the needle-protected position. The assembly further includes at least one stop piece to stop the shield from over-rotating.

Abstract: A training device for training a user on the operation of an auto-injector that dispenses a medicament. A needle guard is slidable from a first extended position relative to a housing prior to operation of the training device, to a retracted position during operation of the training device, and to a second extended position after operation of the training device. An actuation assembly controls the movement of the needle guard from the retracted position to the second extended position. A lock locks the needle guard in the second extended position. A safety is proximate a proximal end of the housing and prevents movement of the needle guard from the first extended position to the retracted position in a storage position. The needle guard is moveable into the retracted position with the safety in an armed position. The safety resets the lock upon returning the safety to the storage position.

Abstract: A connection between a guard tube and a needle holder for a syringe for injecting medication into an IV bag, the guard tube having a needle holder receiving end having an aperture for the needle holder to be inserted from the outside, the aperture terminating at an inner end face, the needle holder having an aperture-penetrating portion having a rim wider than the aperture, or than a step in the aperture, that can be pushed through the aperture to snap fit over the end face or over the step and resist retraction therefrom by a force F which is greater than forces normally experienced by the aperture penetrating portion after it has effected a snap fit.

Abstract: A medical device having a frontal attachment and a connector housing having at least a body part of an associated medical apparatus, the frontal attachment slidably engaging the connector housing and having a forwardly projecting, rearwardly biased needle and a needle retraction assembly, and the connector housing having a needle retraction cavity laterally offset from the needle in a first position, the needle retraction cavity being selectively movable relative to the frontal attachment following use to reposition the needle retraction cavity into alignment with the needle to permit retraction.

Abstract: An apparatus includes a microneedle that defines a lumen therethrough. The microneedle has a proximal end portion a distal end portion and a hub portion between the proximal end portion and the distal end portion. The proximal end portion is configured to be coupled to a medicament container, such as, for example a syringe. The portion of the lumen within the proximal end portion has a first diameter. The distal end portion is configured to pierce a target tissue. The portion of the lumen within the distal end portion has a second diameter smaller than the first diameter. The hub portion includes a surface configured to contact the target tissue when the distal end portion is disposed with the target tissue.

Abstract: A syringe (1) for mixing and ejecting an active pharmaceutical ingredient is disclosed. The syringe (1) comprises a syringe body (2) defining a first lumen (8), a first plunger (4) arranged movably in said first lumen (8), said first plunger (4) being hollow, thereby defining a second lumen (9) being separated from the first lumen (8), and a second plunger (5) arranged movably in said second lumen (9). A liquid diluent is contained in one of the first lumen (8) and the second lumen (9), and an active pharmaceutical ingredient is contained in the other of the first lumen (8) and the second lumen (9). The second plunger (5) is movable in such a manner that the active pharmaceutical ingredient and the liquid diluent are brought together, e.g.

Abstract: In one aspect, a safety pen needle assembly is provided which includes a hub having an open proximal end, a needle fixed to the hub having a distal end, and a shield moveably mounted to the hub so as to be movable relative to the hub to selectively cover the distal end of the needle. An interface is defined between the shield and the hub which is sufficiently sealed so as to define a sterility barrier which prevents ingress of contaminants through the interface. At least one sterility barrier is mounted directly to, and across, an open proximal end of the hub and an open distal end of the shield.

Abstract: The present invention relates to a device for removing delivery member shields which are intended to cover and protect delivery members, said device comprising a remover body arranged to accommodate a delivery member in its interior. The invention is characterized in that the remover body comprises at least two sets of gripping members extending into its interior and wherein each set of gripping members is configured for gripping a certain type of delivery member shield.

Abstract: A microneedle array includes a microneedle unit that includes microneedles; and a microneedle unit support member that includes an opening, guides both ends of the microneedle unit through inclined grooves, and arranges tips of the microneedles so as to project through the opening in an inclined manner.

Abstract: A connector mountable to a syringe barrel has a proximal barrel-engaging portion, a distal luer fitment portion, and a fluid aperture therethrough. The barrel-engaging portion of the connector includes an axial ledge configured to abut the axial distal edge of a glass syringe barrel. The connector facilitates mounting a luer assembly to the barrel. The luer assembly may be a tip cap, a luer needle assembly, or a luer needle-less assembly, having a complementary luer fitment for connection to the luer fitment portion of the connector. The connector and syringe may further include an immobile, compressible needle seal. The needle seal is adjacent to or engageable with the barrel-engaging portion of the connector.

Abstract: A liquid administration tool includes a structure including a tubular body in which liquid is fillable, the tubular body having a bottom portion at a distal end and, an opening portion at a proximal end, and a needle tube positioned at a distal portion of the tubular body, the needle tube having a needle tip at a distal end thereof, and the needle tube being communicable at a proximal end thereof with an inside of the tubular body; an operation member having a pusher; a cover member; a biasing member configured to bias the cover member in the distal direction; a locking unit configured to restrict the movement of the cover member; and a movement amount restriction unit configured to restrict the movement amount of the cover member.

Abstract: A fluid management system for transferring fluid, the system including a connector component comprising a first end and an opposite second end, a first syringe with a distal end that is removably attachable to the first end of the connector component, and a second syringe with a distal end that is removably attachable to the second end of the connector component.

Abstract: The syringe systems disclosed herein provide in part devices for allowing patients with compromised joint strength to more easily administer medicine. Certain exemplary syringe embodiments include a handle forming a handgrip, a syringe barrel that magnifies the dosage marks located on an inner barrel, and a tip cap slidably engageable with the syringe barrel for shielding a needle.

Abstract: Provided is a cassette unit suitable for use with an auto-injector having an electrically powered drive unit. The cassette unit has a housing defining a cassette unit housing cavity and a needle projection aperture. The housing cavity is arranged for receipt of a syringe for injected delivery of a drug to a patient. The cassette unit includes a removable cap that in a capping position fits over and thereby acts to close off the needle projection aperture; and connecting to the removable cap, a needle cover defining a needle sheath for sheathing the needle tip of the syringe. The removable cap is provided with one or more first engagement features arranged for selectively engaging one or more second engagement features of the cassette unit housing when the removable cap is in the capping position to thereby restrict/prevent rotation of the removable cap and needle cover relative to the housing.

Abstract: In some examples, a mixing syringe includes a fluid housing defining an internal housing chamber for storing a medical agent, and a fluid outlet. An outer plunger is disposed within the internal housing chamber of the fluid housing. The outer plunger includes an outer barrel defining a barrel cavity and an outer plunger head connected to the outer barrel. The outer plunger is adapted for longitudinal movement within the internal housing chamber of the fluid housing. The outer plunger head defines a flow passage whereby, upon movement of the outer plunger the medical agent passes from the internal housing chamber through the flow passage into the barrel cavity of the outer plunger. An inner plunger is adapted for longitudinal movement relative to the outer plunger to force the medical agent through the flow passage of the outer plunger head for disposition through the fluid outlet of the fluid housing.

Abstract: There is provided a cassette unit that is suitable for use with an auto-injector having an electrically powered drive unit. The cassette unit has a housing defining a cassette unit housing cavity and a needle projection aperture. The cassette unit housing cavity is arranged for receipt of a syringe that is suitable for use in the injected delivery of drug to a patient. The cassette unit includes a removable cap that in a capping position fits over and thereby, acts such as to close off, the needle projection aperture. The cassette unit includes a cap lock feature movable from a first cap locking position in which it prevents removal of the removable cap from the capping position with the cassette unit to a second cap non-locking position in which it no longer prevents such cap removal.

Abstract: A catheter assembly includes: an inner needle; an inner needle hub connected to the inner needle; a catheter through which the inner needle is inserted; a catheter hub connected to a proximal end portion of the catheter; and a protector that covers at least the tip of the inner needle when the inner needle is withdrawn. The protector includes: an inner tube, and an outer tube. The inner tube includes at least one arm that releasably engages with a proximal end of the catheter hub. The catheter assembly is configured such that, when the inner needle is withdrawn, after the tip of the inner needle has been stored in the protector, the outer tube is retracted with respect to the inner tube thereby allowing the at least one arm to be displaced outwardly, whereby engagement between the at least one arm and the catheter hub is released.

Abstract: A cartridge holder for retaining a cartridge comprising a distal end and a proximal end being spaced apart from one another in the direction of an axis, an interior which is suitable to receive and retain a cartridge in a cartridge retaining section of the interior, and a main part and at least one protrusion which is moveably connected to the main part. The protrusion is arranged to define the radial extension of a subsection of the interior, wherein the subsection is arranged at an axial position which is further away from the distal end than the cartridge retaining section. Furthermore, the protrusion is arranged to vary the radial extension of the subsection when the protrusion is moved with respect to the main part. Moreover, a method for securing a cartridge in a cartridge holder is proposed.

Abstract: A shieldable needle device including a shield assembly having a first shield member extending from a first side of a hub and a second shield member extending from a second side of the hub, the second side being substantially opposite the first side is disclosed. The shield assembly is pivotable between an open position in which a needle cannula is exposed and the first shield member is spaced apart from the second shield member and a shield position in which the first shield member contacts the second shield member and at least a portion of the first shield member and the second shield member are disposed over the distal end of the needle cannula. In one embodiment, the hub, the first shield member, and the second shield member form an integral component.

Abstract: An apparatus for accessing the lumen of a vessel. The apparatus includes a handheld device and a cartridge. The handheld device includes an imaging device attachment utilized to secure an image capturing instrument, an arm coupled to the imaging device attachment. The cartridge includes a sheath, needle or guidewire coupled to the cartridge. The sheath or needle extends to the insertion depth when fully advanced, thereby allowing the sheath, needle, or guidewire to access the lumen of a vessel.

Abstract: The present invention is directed to a safety needle assembly having the high safety and high operability, comprising: a hub; a cannula; a collar; a protector; and a sheath. The sheath includes an opening of housing the cannula; a cannula fixing part of locking the cannula housed in the opening; an attachment part of rotatably supporting the sheath attached to the hub or the collar; and a protrusive stopper which a user pushes by a finger to pivot the sheath thereby to house the cannula in the opening of the sheath. Herein, the stopper is arranged at a vicinity of a central portion of the sheath in a longitudinal direction at the opposite side of the aperture of the opening, or arranged at a portion closer to a distal end side than the central portion of the sheath.

Abstract: A spring clip needle tip shielding device for arrangement in a catheter hub of an intravenous catheter assembly is provided. The spring clip needle tip shielding device comprises a base plate with a hole extending therethrough and at least one resilient arm extending at an attachment point at said base plate. The at least one resilient arm has a resting state, from which it may be urged to yield free passage through said hole in an axial direction of said base plate in a tension state, said at least one resilient arm being adapted for clamping a needle tip of a needle extending through said hole when said resilient arm is in said resting state. Any straight imaginary line extending longitudinally through said hole in the axial direction of said base plate coincides with said at least one resilient arm when said resilient arm is in said resting state of said body. The spring clip needle tip shielding device is of a rigid material, and at least a part thereof is coated with a solid lubricant.

Abstract: A delivery adapter which may be used as an interface between a syringe and a catheter hub is described.

Abstract: A catheter and introducer needle assembly, including a flexible catheter and a catheter hub having an uninterrupted outer surface portion, a Luer-connecting feature, and a disabling feature. The assembly includes an introducer needle disposed in the catheter, a needle shield having a resilient clip adapted to flex between first and second positions in a plane perpendicular to the introducer needle. The resilient clip includes a cantilevered arm with a pawl. In the resilient clip's first position, the cantilevered arm is flexed so that the pawl frictionally contacts the catheter hub's uninterrupted outer surface portion and frictionally retains the needle shield with the catheter hub, and the pawl is axially aligned with and spaced apart from the disabling feature. In the second position, the pawl no longer frictionally contacts the hub's uninterrupted outer surface, thereby permitting needle shield displacement relative to the catheter hub.

Abstract: There are disclosed devices and methods for protecting a user from a sharp tip of a medical needle. In an embodiment, a device includes a central body portion, a medical needle having a sharp tip, a pair of wings in attachment to the central body portion, and a hook-and-loop fastening system disposed on at least one of the wings, and configured to selectively attach the wings together with the medical needle positioned between the wings so as to protect a user from the sharp tip of the medical needle. In another embodiment, a method includes withdrawing a sharp tip of a medical needle from a patient, closing a pair of wings with the medical needle positioned between the wings, and fastening the wings together with the medical needle positioned between the wings so as to protect a user from the sharp tip of the medical needle.

Abstract: There is provided a cassette unit that is suitable for use with an auto-injector having an electrically powered drive unit. The cassette unit has a housing defining a cassette unit housing cavity and a needle projection aperture. The cassette unit housing cavity is arranged for receipt of a syringe that is suitable for use in the injected delivery of drug to a patient. The cassette unit includes a removable cap that fits over and thereby, acts such as to close off, the needle projection aperture; and connecting to the removable cap, a needle cover defining a needle sheath for sheathing of the needle tip of the syringe. The removable cap is provided with a finger-grip feature that is sized and shaped for gripping by the finger of a user to allow for removal of the removable cap and needle cover from the cassette unit housing.

Abstract: According to the invention, an injection device (D) comprises a pre-filled syringe and a safety device. The pre-filled syringe comprises a barrel with an inner cavity in fluid communication with a hypodermic needle attached to a distal end of the pre-filled syringe and a piston fluid-tightly sealing a proximal end of the inner cavity. The safety device comprises a support body for retaining the pre-filled syringe therein, an outer body operably connected to the piston, a needle shield and a releasable retaining means (R). The retaining means comprises a radial projection and a longitudinal recess adapted to receive the radial projection. The radial projection is connected to or integral part of one of the support body or the outer body and a longitudinal recess formed into the other of the support body or the outer body. The needle shield, the support body and the outer body are telescopable relative to each other.

Abstract: Described is a needle shield assembly comprising an inner body adapted to receive a needle and an outer body coupled to the inner body. The inner body comprises a proximal portion having a first outer diameter (D4) and a distal portion having a second outer diameter. The first outer diameter is larger than the second outer diameter. The outer body has a third outer diameter (D3) substantially equal to or less than the first outer diameter.

Abstract: A lock mechanism includes a hood (20) that is arranged so as to surround the periphery of a male member (10) and is for insertion of a female connector (100), and a single lock lever (30) having a cantilever support structure capable of elastic displacement. The lock lever (30) includes a claw (34) for engaging with the female connector (100), and an operation portion (35) for elastically displacing the lock lever (30) in a direction of separation from the male member (10). The claw (34) and the operation portion (35) are provided on the free end side of the lock lever (30).

Abstract: Needle assembly having the following modes of operation; a first mode wherein the safety shield can move to a first retracted position allowing injection of the piercing portion of needle from a position at least partially covering the piercing portion of the needle and a second mode wherein the safety shield moves to a position protecting the piercing portion of the needle after the first mode and is prevented from moving back to a position exposing the piercing portion of the needle.

Abstract: A cap is configured to provide antimicrobial protection to a female luer port of an intravenous device. The cap distributes an antimicrobial solution within the intraluminal surfaces of the port when the cap is connected to the port. A cap may also be designed to distribute an antimicrobial solution around the exterior surfaces of the port. Once connected to a port, the cap can form a seal that minimizes the evaporation of the antimicrobial solution from within the lumen of a port. The cap can therefore provide antimicrobial protection against another device that is connected to the port once the cap is removed.

Abstract: An injection device (110) comprises a housing (112) having a syringe (114) with a discharge nozzle (118). The syringe is movable between a retracted position in which the discharge nozzle is contained within the housing and an extended position in which the discharge nozzle extends from the housing. There is syringe cap (180) for enclosing the discharge nozzle. The syringe cap is removable from the syringe by rotation to the syringes. A syringe carrier (150) in the housing is adapted to restrain rotation of the syringe relative to the housing as the cap is removed.

Abstract: The invention relates to a dispense interface for use with a drug delivery device with an inner body and with a lockout element, wherein the lockout element is coupled to the inner body, wherein the lockout element is movable from a receptive condition to a locked condition, wherein in the receptive condition the dispense interface is attachable to the drug delivery device, wherein in the locked condition the dispense interface is not-attachable to the drug delivery device and wherein the lockout element is configured to move from the receptive condition to the locked condition when said dispense interface is attached to and detached from said drug delivery device. The invention solves the technical problem of reducing the risk of reuse of a dispense interface, after it has already been used with a drug delivery device.

Abstract: A urinary incontinence device for insertion in a urethra of a user. The device includes a non-absorbent body having an outer surface, the body having a leading end and a trailing end; a removal mechanism having a first end attached to the body and a portion of the removal mechanism located outside the user; a portion of the body having a generally bulbous shape for positioning within the urethra and providing a seal within the urethra preventing urinary leakage from the urethra; and a coating applied to the outer surface of the body for engaging a wall of the urethra and securing the device within the urethra of the user. Another embodiment relates to a method of controlling urinary incontinence comprising: engaging an applicator with the body of the device and introducing into the urethra the device wherein the device is positioned in the user's bulbar urethra.

Abstract: A dispensing mechanism for dispensing measurement strips is presented having a strip cartridge with an enclosure for retaining a plurality of measurement strips and a dispensing slot for dispensing one measurement strip at a time, a spring rotatably arranged with respect to the strip cartridge, the spring comprising at least one engagement section adapted to engage one of the measurement strips at a time and move it out of the dispensing slot when the spring is rotated, and a guide slot arranged in the strip cartridge for guiding the engagement section of the spring as the spring is rotated.

Abstract: A segmented safety cover may include: a) a proximal segment combined with a needle hub; b) a needle cannula that extends from the proximal needle hub to a distal sharpened end; c) a distal end cap with a hollow bore through which the cannula shaft passes; d) a centrally mounted toggle locking mechanism, separating the proximal needle hub from the distal end cap; e) the toggle locking mechanism is torsion spring assisted; f) a proximal cover segment is connected to the hub via a proximal hinge and a distal cover segment is connected to the end cap via a distal hinge; g) said proximal cover segment and said distal cover segment of said toggle locking mechanism being configured with abutting faces when the segmented safety cover is in a safety mode; and h) wherein the proximal hinge, abutting faces and distal hinge are in line in the safe mode.

Abstract: Apparatuses, kits and methods useful in the storage and delivery of nutritional compositions and other fluids are described. In a general embodiment, an integrated storage and delivery system for nutritional compositions comprises a container defining a chamber, a finish, and a penetrable seal. The finish defines an opening and the penetrable seal separating the chamber from an external environment. A spike assembly is attached to the container. The spike assembly including a cap and a spike. The cap is engaged with the finish of the container and the spike defines a projection having a distal end defining a second opening. The projection is moveable between a first position in which the distal end is adjacent a first side of the penetrable seal and a second position in which the distal end is adjacent a second side of the penetrable seal.

Abstract: A container having a barrier layer is provided. The container may be of thermoplastic and the barrier may inhibit materials from leaching from the thermoplastic material or from extraction of compounds from medicants by the thermoplastic. A process is also described that allows for molding thin barrier layers as container lines and for forming thermoplastic containers with barrier liners.

Abstract: A dedicated needle assembly (300) that can be attached only to a dedicated drug delivery device (400) is disclosed. The dedicated needle assembly (300) comprises a connecting body (320) extending from a distal end to a proximal end. A dedicated mechanical coupling (310) is configured at the proximal end of the connecting body (320). The dedicated mechanical coupling (310) forms a releasable connection to a distal end of the dedicated drug delivery device (400). The dedicated needle assembly (300) may comprise a medicated module or, alternatively, a non-medicated module. In one arrangement, the dedicated mechanical coupling (310) is integral with the dedicated needle assembly (300).

Abstract: A needle shield assembly for enclosing a needle cannula includes a needle cannula having a needle hub at a proximal end thereof and a sharp distal end. A needle shield adapter is mounted to the needle hub and a needle shield is connected to the adapter. The needle shield is moveable between a first position enclosing the needle cannula and a second position exposing the needle cannula for use.

Abstract: A needle cover assembly includes a manually operable member; a rigid needle shield (RNS) provided with an internally arranged resilient cap, in turn arranged to house and protect an injection needle; and a RNS remover assembly including a tubular shaped member surrounding the RNS, in which the tubular shaped member is arranged with at least one grip member capable of gripping the RNS in order to remove the RNS. The RNS remover assembly further includes a spinning attachment member having a distal end fixedly attached to the tubular shaped member and a proximal end rotatably attached to the manually operable member such that the manually operable member can be freely turned in relation to the RNS remover assembly but is locked in an axial direction.