Abstract: An injection device (1) for delivering a predetermined fixed dose of liquid drug, the device (1) comprising a housing (2), a first and second tubular members (7, 10). The first tubular member (7) and the housing are engaged via a first track (8) and a first protruding part (9), and the first and second tubular members (7, 10) are engaged via a second track (11) and a second protruding part (12). The first track (8) comprises a first portion (8a) which the first protruding part (9) travels during setting of the dose, and the second track (11) comprises a first portion (11a) which the second protruding part (12) travels during setting of the predetermined fixed dose. The first 10 portions (8a, 11a) of the first (8) and second (11) tracks are shaped in such a manner that the second tubular member (10) is prevented from rotating during setting 15 of a dose. The second tubular member (10) is rotationally locked to a piston rod (13), and rotation of the piston rod (13) during dose setting is thereby prevented.

Abstract: An aspect of some embodiments of the current application is a doorstop to a drug delivery apparatus that encourages a user of the apparatus to perform the proper usage steps in the proper order. For example, a user may be expected to receive an injector in a transport state, open it to an open state, insert a cartridge, and/or close the cartridge before operation. The doorstop may have an obstructing mode, optionally preventing closing of the door. The cartridge may optionally have a non-obstructing mode allowing closing of the door. Inserting the cartridge may optionally cause a doorstop to move from the obstructing mode to the non-obstructing mode. In the non-obstructing mode the doorstop may optionally prevent removal of the cartridge.

Abstract: Provided is a drug delivery device including: a reservoir for a product, having a distally projecting end-piece defining an axial passageway for the transfer of the product, with a distal portion, an adaptor having a collar engageable around said end-piece said collar being axially movable with respect to said end-piece, securing structure for limiting the axial movement of said collar with respect to said end-piece, between a most distal position and a most proximal position of said collar, and biasing element for urging said collar towards its most distal position. An adaptor for forming a drug delivery device is also provided.

Abstract: A drug delivery device comprising; a housing; a cylindrical member configured to be rotatably supported inside the housing, wherein the outer surface of the cylindrical member is provided with at least first and second tracks together forming an encoder, each track comprising conductive segments and non-conductive segments; and at least first and second groups of contacts configured to engage the first and second tracks respectively at predetermined intervals along the length of the track.

Abstract: A liquid embolic material may include a mixture of a first solution comprising between about 1.2% and about 2.5% weight per volume (w/v) carboxymethyl chitosan (CCN) in a first solvent and a second solution comprising between about 1.2% and about 2.5% w/v oxidized carboxymethyl cellulose (OCMC) in a second solvent. The liquid embolic material may be used to embolize a targeted embolization location by mixing the first solution and the second solution to form a liquid embolic material (or hydrogel precursor material), introducing the hydrogel precursor material to a targeted embolization location within a body of a patient, and allowing the CCN and the OCMC to react to form the hydrogel material and embolize the targeted embolization location.

Abstract: A drug delivery device comprising; a housing; a cylindrical member configured to be rotatably supported inside the housing, wherein the outer surface of the cylindrical member is provided with a track comprising a sequence of encoded images; and a sensor directed at the track of the cylindrical member and configured to detect features of the encoded images.

Abstract: The present invention relates to a drug delivery device for setting and dispensing a dose of a medicament, comprising: a body to accommodate a drive mechanism having a piston rod, a cartridge having a barrel sealed by a piston slidably displaced therein along an axial direction, wherein the cartridge is directly connectable with the body by way of an interface, and wherein the barrel comprises at least one radially extending portion at its outer periphery to cooperate with at least one further functional component of the device.

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 locking interface for locking a cartridge holder onto a main body of a drug delivery device comprises a locking member for locking the cartridge holder onto the main body, a user interface operable by a user, a support member, on which the locking member and the user interface are located, wherein the locking interface is configured such that a force needed for unlocking the cartridge holder and the main body is reducible by operating the user interface.

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 lock for a dosing mechanism of an injection device, the lock including at least one holding element that interacts with the dosing mechanism, or with a dosing element of the dosing mechanism, whereby an adjustment movement of the dosing mechanism or the dosing element is prevented in a starting position of the lock and is possible only after a movement or displacement of the lock or the holding element. An injection device used in conjunction with a two-chamber ampoule is encompassed, as is a method for preparing the injection device for dispensing a substance wherein the ampoule is introduced into the injection device and a lock is released when the ampoule has been introduced far enough to appropriately mix the substances in the two chambers, whereupon the mixed substances can be dispensed from the ampoule.

Abstract: An injection syringe, having a syringe cylinder, a plunger rod inserted therein and connected to a stopper by way of a coupling part, and a module that is provided in the proximal end of the syringe cylinder and having a cannula, mounted in a cannula holder received in a guided sleeve, and a sealing insert for the fluid-tight closure of the proximal end of the syringe cylinder and a protection cap for protecting the cannula, wherein the protective cap on the inner circumference has ribs extending in an axial direction, which engage in corresponding grooves of the driving part for a rotary drive thereof, and wherein in the sealing insert a hollow space is formed, which is closed on the proximal side and on the distal side transitions into an opening, by way of which a tip of the coupling part can be coupled to the hollow space.

Abstract: Embodiments of a retractable syringe assembly are provided that include a dual syringe barrel configuration. In one or more embodiments, the assemblies include a fluid barrel for retaining fluid and a retraction barrel for housing the retraction feature and the needle hub assembly. The assemblies include a trigger element that moves with the plunger rod to activate the retraction feature within the retraction mechanism.

Abstract: A prefilled syringe for injecting medicament into a patient includes a barrel constructed of a polymeric material, a cannula and a hub. The barrel has a diameter, a longitudinal axis, a proximal end and a distal end. The cannula has a proximal end and a tip opposite the proximal end. The proximal end of the cannula is fixed to the distal end of the barrel. The cannula is positioned generally coaxially with the longitudinal axis. The hub is integrally formed with the distal end. The hub includes a rib section and a cap. The rib section has a generally cruciform cross-section taken along a rib plane. The rib plane is generally perpendicular to the longitudinal axis. The cap has a generally U-shaped cross-section taken along a longitudinal plane. The longitudinal plane is generally parallel to the longitudinal axis.

Abstract: A catheter tunneling adapter including a longitudinal body having a distal end and a proximal end and a passageway extending from an entrance at the proximal end to an exit at the distal end. The passageway has a first hemisphere and a second hemisphere with the first hemisphere defining a generally unobstructed first passageway portion from the entrance to the exit. A guide ramp is positioned within the second passageway and tapers towards the first hemisphere moving from the proximal end to the distal end. The ramp defines a longitudinal notch therethrough such that a second passageway portion extends from the entrance to the exit.

Abstract: A syringe comprising a first coding feature for mechanical interaction with a second coding feature of an auto-injector device is provided. The first coding feature is designed such that the syringe is only mountable in an auto-injector device having a second coding feature mating the first coding feature. Furthermore, an auto-injector device having a housing, wherein a syringe can be mounted, and a set of at least two auto-injector devices and syringes are provided.

Abstract: The present invention relates to a medical delivery device comprising a housing (10); a medicament container (16) arranged to be placed in said housing; a stopper (18) movable within said container; a medicament dispensing means attachable to said housing and to said container through which medicament can be expelled; characterized in that the device further comprises a power unit (22) comprising a cover (24), a volute spring (26) arranged within said cover, and a pressure member (28) having a pressure pad (30) in contact with the stopper, a guide rod (34) extending into the volute spring and an annular ledge (32) in contact with the edges of the volute spring; activation means (36) mechanically connected to the cover and to the housing; and a spring locking means mechanically connected to said activation means, wherein said spring locking means (39) comprises a deformable ring-shaped member having (40) an inner diameter somewhat larger than the annular ledge, such that said ring-shaped member presents an ova

Abstract: A portable medicament dispensing device having a mechanism which is not susceptible to jamming for dispensing the medication to a user. The device employs a coupling for coupling the relative motion between reciprocating body members housing the ancillary components and a barrel plunger associated with the syringe. One embodiment provides a pivoting coupling whereas an alternate uses a rack and pinion system. The advantage of simplifying such mechanisms results in a structure which has smooth unencumbered motion with fewer parts to avoid mechanical jamming during use.

Abstract: Drug depot delivery devices and methods are provided for delivering one or more drug depots to one or more sites beneath the skin of a patient with or without repositioning the cannula. The device has a cannula capable of insertion to the site beneath the skin of the patient and one or more side port openings for delivering a drug depot. The side port openings are spaced a distance from the blunt tip, which will allow the user to implant at a set distance from a nerve. The device may also include an electronic monitor for detecting the proximity of the tip of the cannula to a nerve. In some embodiments, a method of delivering a drug depot is provided by detecting the nerve and delivering the drug depot at or near the nerve.

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: Relations between crystallinity and performance of a biodegradable resin, between weight-average molecular weight and strength thereof, and between weight-average molecular weight and performance thereof were clarified. As a result thereof, when a microneedle array was provided with microneedles containing noncrystalline polylactic acid which had a weight-average molecular weight of 40,000 to 100,000, it was possible to obtain a microneedle array which could maintain its functional performance.

Abstract: The present invention relates to a device for automatic injection of a product comprising a container, a needle and a piston. The device includes a housing receiving the container, the container being movable with respect to the housing between an initial position and an insertion position, distally spaced relative to the initial position; a safety shield coupled to the housing and movable with respect thereto between a rest position, an activation position, proximally spaced relative to the rest position, and a safety position, distally spaced with respect to the rest position; biasing feature for causing the movement of the safety shield to the safety position; triggering feature for causing the container to move from its initial position to its insertion position, the triggering feature being releasable by movement of the safety shield to the activation position; and, isolating feature for isolating the safety shield from the biasing feature when the safety shield is moved to its activation position.

Abstract: A method and device for delivering medicament such as for ameliorating pain in a patient from an injector superiorly and/or laterally and/or anteriorly towards the sphenopalatine ganglion (SPG). A device for delivering a medicament to a patient in need thereof includes (a) an injector containing a first end configured to remain outside a nasal passage of the patient and a second end configured for entry into the nasal passage of the patient; and (b) an introducer configured for engagement with a nostril of the patient and containing a passageway configured for slidably receiving the injector. The injector is moveable between a storage position preceding the engagement and an engaging position pursuant to the engagement. The device may further include a locking connection assembly that is useful in other devices.

Abstract: The invention provides a syringe or autoinjector for dispensing a drug comprising a rigid syringe body containing the drug, an oxygen absorbing material, a separating element between the drug and oxygen absorbing material to prevent the drug from contacting the oxygen absorbing material but which allows oxygen to pass from the drug to the oxygen absorbing material, and an oxygen impermeable container enclosing both the drug and the oxygen absorbing material, wherein the oxygen impermeable container partially or fully forms the rigid syringe body or is held within the rigid syringe body.

Abstract: This application covers a novel PEGylated interferon and a novel crystalline form of interferon which are useful, inter alia, for detailed structural analysis of interferon as well as treatment and prevention of viral infections and hyperproliferative diseases such as leukemia.

Abstract: A one piece molded vacuum tube holder is fitted with a one piece molded needle hub assembly. A needle protection device is further rotatably mounted to the neck of the one piece vacuum tube holder. One portion of a locking mechanism is provided at the neck of the one piece vacuum tube holder and a second portion of the locking mechanism is provided at the needle hub of the needle hub assembly, so that when the needle hub assembly is press fit to the vacuum tube holder, the two portions of the locking mechanism will coact to fixedly retain the needle hub assembly within the vacuum tube holder. The one piece vacuum tube holder is configured to have an elongate needle cover integrally extending from its neck. A finger grasp mechanism may be coupled to the needle cover.

Abstract: A syringe includes a barrel and a rotatable element on the barrel; for example at a proximal location along the length of the barrel. The rotatable element rotates at least partially around the barrel. When a handle is associated with the rotatable element, the barrel may rotate as the handle is held substantially stationary or the handle may be rotated while the barrel and any peripheral device secured thereto remain substantially stationary. When handles are associated with a rotatable element that may be removed from a barrel, a barrel that is disassembled from the rotatable element may be replaced with another barrel of the same or a different configuration. The barrel and plunger may be configured to cause the barrel to rotate as the plunger moves along the length of the barrel. Methods of using a syringe with a rotatable element on a barrel thereof are also disclosed.

Abstract: A composition for purposes of augmentation contains a plurality of substantially spherical, biocompatible semi-solid beads each having a diameter in the range of about 1 millimeter to 10 millimeters. The composition also includes a delivery solvent for sanitary lubrication of the beads. An inventive system and method are utilized to systematically administer the composition into a patient's adipose tissue for customized augmentation. The system can comprise one or more dispensing apparatus, such as in the form of one or more pre-filled syringes. The size and number of pre-filled dispensing apparatus can be selected and organized into one or more kits for use in connection with a specific treatment or group of treatments. The inventive method involves selecting an insertion site in proximity to an identified target tissue, inserting the dispensing apparatus into the tissue through the insertion site, and infiltrating the composition into the tissue in a controlled manner.

Abstract: A drug delivery device is provided. The drug delivery device includes a drug reservoir in fluid communication with a microneedle array. The drug delivery device has a sliding actuation mechanism that may be activated by a button or lever. Actuation of the drug delivery device inserts the microneedle array into the skin of a subject and causes a piston to compress the drug reservoir, thereby delivering the drug through the microneedle array to the subject.

Abstract: A dispensing device for use with a beneficial agent has a dispensing package, a dispenser disposed on an end portion of the dispensing package, and an actuator movably disposed along at least a portion of the package between a pre-dispensing state and a dispensing state. One arrangement also provides a beneficial agent dispenser having a dispensing port, an elongate portion and a plunger that is movably disposed relative to a tubular wall of the elongate portion during a dispensing stroke to partially penetrate a separable barrier and expel the beneficial agent through the dispensing port.

Abstract: A medicated module (4) for an injection system to co-deliver at least two medicaments is disclosed where a primary delivery device containing a primary medicament accepts a medicated module (4) containing a single dose of a secondary medicament (2) and where both medicaments are delivered through a single hollow needle (5). The medicated module (4) is user selectable so that it will deliver both the primary (1) and secondary medicaments (2), or only the primary medicament (1). The module (4) also contains a guard (42) that locks after dose delivery.

Abstract: A syringe assembly includes a syringe barrel defining a chamber and having a stopper disposed within the chamber, a sleeve having a first end and a second end and extending at least partially about the syringe barrel, and a cap associated with a second end of the sleeve. The syringe assembly also includes a plunger rod having a first end associated with the cap and a second end, wherein the plunger rod is transitionable from a pre-use position, in which at least a portion of the second end of the plunger rod extends along a portion of a barrel sidewall, to a ready-to-use position in which the plunger rod is aligned with the stopper. Upon proximal movement of the sleeve in a direction away from a first end of the barrel, the plunger rod is configured for lateral movement with respect to the cap into the ready-to-use position.

Abstract: An assembly for a drug delivery device is provided comprising a housing, a cartridge holder releasably connectable to the housing, a resilient member, and an interaction member which is configured to mechanically cooperate with the resilient member and with the cartridge holder. The resilient member is configured to rotationally bias the interaction member. The assembly has a locked state where the cartridge holder is connected to the housing, the cartridge holder being obstructed from movement with respect to the housing, and an unlocked state where the connection between the cartridge holder and the housing is released, the cartridge holder being freely moveable with respect to the housing.

Abstract: A drug delivery device includes a catheter having first and second ends; a flexible membrane having a rim securely connected to an inner surface of the catheter to define a first volume between the first end and the flexible membrane, and a second volume between the flexible membrane and the second end, such that the second volume is substantially the same as a desired drug volume; and a pressurizable member coupled to the catheter for operably delivering a drug. In use, a desired volume of the drug is preloaded into the second volume of the catheter that in turn is slid into a guidance device, when the guidance device is placed in a target of interest, the pressurizable member applies a pressure into the first volume to exert a force upon the flexible membrane to operably squeeze the second volume, thereby unloading the drug into the target.

Abstract: Syringe (1) including a cylinder (2) and a piston (4), in which the outlet end (6) of the cylinder (2) is integrated with a valve male luer lock connector (7).

Abstract: A drug delivery device is provided comprising a cartridge holder comprising at least one guide track, and a body comprising at least one interaction member adapted and arranged to mechanically cooperate with the at least one guide track.

Abstract: The invention relates to an injection device (1), which comprises a support housing (2), an activating sleeve (9), a cartridge (3) containing a medicine (14), a first drive unit (4), a safety device (5), a needle arrangement (6), a needle protection element (7) and a second triggerable drive unit (8), whereby the latter moves the needle protection element (7) from the non-effective position into the position covering one needle end (21) of a cannula (20). The support housing (2) is surrounded over most of its longitudinal extension between its distal and proximal end (11, 12) by the activating sleeve (9), whereby the needle protection element (7) with the second drive unit (8) cooperating therewith is arranged radially between the support housing (2) and the activating sleeve (9), as viewed in axial cross section.

Abstract: A one piece molded vacuum tube holder is fitted with a one piece molded needle hub assembly. One portion of a locking mechanism is provided at the neck of the one piece vacuum tube holder and a second portion of the locking mechanism is provided at the needle hub of the needle hub assembly. The needle hub assembly is press fit to the vacuum tube holder. The one piece vacuum tube holder is configured to have an elongate needle cover integrally extending from its neck. A tamper evident notched joint is provided at the junction where the needle cover is connected to the neck. The opening of the vacuum tube holder through which a conventional vacuum tube is inserted may be sealed for sterilization and transport of the device. A wingnut finger grasp mechanism may be coupled to the needle cover.

Abstract: Injection apparatus and methods of positioning an injection needle in an injection apparatus are described herein. The injection apparatus may include one or more axes of rotation. The injection apparatus may include an injection unit attached to a support assembly that moves between a rearward position and a forward position, with the injection unit attached to the support such that it rotates relative to the support assembly about an injection unit axis.

Abstract: Exemplary embodiments provide a syringe plunger formed of a polymeric material. The syringe plunger includes a pressurizer disposed at a proximal end, and a distal end bifurcated into a first plunger arm having a first conical surface and a second conical surface, and a second plunger arm having a first conical surface and a second conical surface. The distal end includes a first contact surface defined by the first conical surface of the first plunger arm and the first conical surface of the second plunger arm, the first contact surface configured to initially contact a firing engagement mechanism, the first contact surface disposed at a first angle of between about 40° and about 80° relative to a longitudinal axis of the syringe plunger.

Abstract: A syringe assembly having a collapsible or pivotable plunger rod with magnification properties is provided. In a pre-use or packaged state, the plunger rod is positioned substantially parallel to a barrel of the syringe assembly resulting in the syringe assembly having a reduced length and a smaller packaging footprint. The smaller packaging footprint allows for reduced storage space of the syringe assembly. Upon removal from a packaging and/or a storage space, the plunger rod can be slid or pivoted toward a proximal end of the syringe barrel and locked into place such that the syringe assembly is ready for use. The plunger rod can be shaped to provide magnification to indicia of the syringe barrel and/or contents. Alternatively, a separate magnification member can be associated with the plunger rod and/or secured about the syringe barrel.

Abstract: A clinician's hand support structure provides an ergometric grasp of a syringe housing, the support structure includes a surrounding sidewall about a longitudinal axis, the sidewall having first and second end portions, the sidewall also having an outer surface and an inner surface that defines a sidewall interior. Further, the inner surface having a portion with a frustroconical shape that is smaller adjacent to the first end portion and larger adjacent to the second end portion. Also, the sidewall has an elongated aperture therethrough, wherein the sidewall inner surface partially creates a frictional encasement of the syringe housing. Further, included is an extension element having a proximal and distal portion wherein the extension element is positioned to extend radially outward from the longitudinal axis, operationally the distal portion nests in a palm of a clinician's hand and the sidewall outer surface is grasped by a finger of the clinician.

Abstract: A syringe assembly includes a syringe barrel having an exterior surface, an inside surface defining a chamber, an open proximal end, a distal end, and an outlet disposed adjacent the distal end in fluid communication with the chamber; and a plunger assembly disposed at least partially within the syringe barrel. The plunger assembly includes an elongated plunger rod and a plunger head. The elongated plunger rod is associated with the plunger head to move the plunger head within the chamber of the syringe barrel through an injection cycle. The plunger rod is adapted to move from a collapsed position extending alongside the exterior surface of the syringe barrel to an extended position engaging the plunger head to move the plunger head through the injection cycle.

Abstract: The invention relates to an electronic sensor for detecting skin, the sensor comprising processor, an EM source, a baffle, a first EM detector and a second EM detector, the sensor arranged such that the EM source is located on a first side of the baffle and the first and second EM detectors are arranged on a second opposite side of the baffle at first and second distances from the EM source respectively, the first distance being less than the second distance, the processor configured to cause the source to emit EM radiation and to receive first and second signals from the first and second EM detectors respectively, the signals being indicative of the intensity of EM radiation detected by the sensor, the processor being further configured to process the first and second signals and thereby generate a skin signal which is indicative of whether the sensor has detected skin.

Abstract: The colorectal delivery device provides a device for rectal delivery of therapeutic compositions to the colon of a patient. The composition may be a foam application in some embodiments. The device allows medical personnel to add therapeutic drugs to the pressurized canister immediately prior to administration to the patient.

Abstract: The present invention relates to a drug delivery device comprising, a reservoir for containing a product, said reservoir having a distally projecting end-piece having a longitudinal axis A and defining a channel providing a passageway for the transfer of the product from the reservoir, an adaptor having a collar engageable with said end-piece, securing means for blocking said collar in the distal direction with respect to said end-piece once said collar is engaged around said end-piece, anti-rotation means for preventing the rotation of said collar with respect to said end-piece around said longitudinal axis A under the effect of a turning torque applied to said collar once said collar is engaged around said end-piece, deactivating means for neutralizing said anti-rotation means once said turning torque has reached a predetermined value, thereby allowing the rotation of said collar with respect to said end. The invention also relates to such an adaptor.

Abstract: An apparatus includes a simulated medicament delivery device and an electronic circuit system. The simulated medicament delivery device includes a housing, and is devoid of a medicament delivery mechanism that causes a medicament to be delivered. The electronic circuit system is coupled to the housing and includes an audible output device and a cover. The housing of the medicament delivery device and the cover of the electronic circuit system collectively define an acoustic enclosure. The audible output device is configured to be disposed within the acoustic enclosure.

Abstract: A plunger-driven delivery device for use with a feeding tube for delivering an ingestible material to a user is provided. The delivery device includes a device body having a first chamber, a second chamber and an exit orifice through which the ingestible material is delivered to the feeding tube. A first plunger is disposed in the first chamber, and a second plunger is disposed in the second chamber. The delivery device can be provided with the ingestible material disposed in the first chamber and a flushing liquid disposed in the second chamber. The delivery device is operable to provide sequential delivery first of the ingestible material and then the flushing liquid into the feeding tube. In some embodiments, a mechanical interlock is disposed between the first and second plungers to prevent use of the second plunger until the first plunger has been depressed.

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 gas-impervious container having a gas-permeable porous insert, wherein the insert contacts a flowable biomedical material, for improving access of the sterilant gas to the material.