Abstract: A closure container that can house a preset drug applicator in an easily accessible manner with tamper evidencing means. The closure container contains a plurality of dosing ribs and a retainer to retain the syringe in a preset dosage amount and preferably has a window to view the barrel of the syringe.

Abstract: Disclosed is a functional drug injection module including: an injection unit including a body that is elongated, keeps a functional drug therein, has an outlet formed at a front end thereof, and is open at a rear end thereof, and a piston that is inserted in the body through the rear end of the body and discharges the functional drug by longitudinally sliding; a cover unit at least partially formed like a projection, inserted in the outlet, and adjust opening/closing of the outlet by selectively separating; and a sealing unit surrounding the injection unit and the cover unit, having a first crease formed in a longitudinal direction of the injection unit, and separating from the injection unit together with the cover unit by being divided along the first crease by external force.

Abstract: A needle shield assembly for use with a needle assembly is disclosed. The needle shield assembly includes an elongate needle shield comprising a shield portion, a hub connection portion and a bridge portion including a living hinge having a thickness. The bridge portion joins the hub connection portion and the shield portion. The hub connection portion includes a partially circular receiving ring having a diameter sized to frictionally receive a flange of a hub of the needle assembly. The shield portion includes two longitudinal walls defining a cavity and a needle assembling receiving cavity between the two longitudinal walls defining a recess. The shield portion is configured to pivot from an open position in which a needle cannula is exposed, to a closed needle protecting position in which a distal end of the needle cannula is within the longitudinal opening of the shield.

Abstract: A closure container that can house a preset drug applicator in an easily accessible manner with tamper evidencing means. The closure container contains a plurality of dosing ribs and a retainer to retain the syringe in a preset dosage amount and preferably has a window to view the barrel of the syringe.

Abstract: Provided is a syringe cap including a projection extending in the circumferential direction of a cap body, wherein the projection includes an apex located radially outward of the cap body from the outer circumferential surface of the cap body, a first inclined surface having a starting end located at the apex and having a terminal end located at a position on the side closer to the proximal end of the cap body than the starting end is, and a second inclined surface having a starting end located at the apex and on the outer circumferential surface of the cap body having a terminal end located at a position on the side closer to the distal end of the cap body than the starting end is, on the outer circumferential surface of the cap body, and the shortest distance from the starting end to the terminal end of the first inclined surface is smaller than the shortest distance from the starting end to the terminal end of the second inclined surface.

Abstract: A storage device (30) for storing a pen needle assembly (10) includes a housing (30) having first wells (44) with a dimension for receiving the pen needle assembly and second wells (46) for receiving an inner shield (24) of the pen needle assembly. The second wells (46) have a diameter less than a diameter of the first wells (44). An ejector (40) in the housing (34) can be actuated to eject the used needle hub (16) and outer covers (22) from the first well (44) and the inner shield (24) from the second well (46) for disposal. A method of coupling a pen needle delivery device to a needle hub positions a needle hub assembly (18) in the first well (44) and inserts the coupling end of the delivery device (10) into the first well (44) and is coupled to the needle hub. The needle hub is pulled from the outer cover (22). The inner shield (24) is inserted into the second well (46) to remove the inner shield from the needle hub.

Abstract: A functional medical package is disclosed having a disposable package and a sterile container removably received inside the disposable package. A subsystem is received in the sterile container and is configured to be at least partially inserted into a host. The sterile container has an insertion exit opening for the subsystem and a liner closes the insertion exit opening. The liner is attached to the disposable package and automatically peels off the insertion exit opening when the sterile container is removed from the disposable package. Also disclosed are a method of manufacturing the medical package and a method of using the medical package with an inserter.

Abstract: A syringe packaging system that includes a tube and a cap for enclosing a pre-filled syringe is disclosed. The tube includes a proximal end, a closed distal end, and a sidewall extending between the proximal and closed distal ends. The sidewall includes an injection molding gate. In one embodiment, a film is securable to a portion of the tube and a portion of the cap to connect the tube and the cap with the pre-filled syringe enclosed within the cap and the tube.

Abstract: A method for removing or controlling or quantifying the presence of aldehydes, in particular acetaldehyde, is described. Such a method is useful in prolonging the shelf life of a pharmaceutical product.

Abstract: An injection analgesia system advantageously numbs a patient's skin around an injection site. An injection window guides a caregiver's injection placement to a relatively small area while allowing standard injection procedures to be followed, such as stretching the skin and puncturing the site with a jabbing motion. The injection analgesia system has a needle shield and an analgesia, which are layered together and applied to a skin surface. A needle shield window and a analgesia window align to form the injection window. Advantageously, the needle shield may fold and/or wrap around the injection needle for sharp object protection during and after needle disposal.

Abstract: An apparatus for the safe removal and replacement of hypodermic needle caps, interchanging of needles, and storage during tasks is disclosed, including a heavy base with space hollowed out to allow for cap gripping mechanism and tunnel for capped needle removal, wherein the base may be slanted slightly towards the user. The friction or mechanical needle cap gripping mechanism may be comprised of rubber, soft plastic, or the like, with a top to secure the cap gripping mechanism in the base. A ramped cone shaped opening is provided in the top to allow for the cap of a capped needle to pass through and be captured by the cap gripping mechanism, and an extended tunnel shaped opening is provided to allow for the re-capped needle to be removed and needles to be interchanged.

Abstract: A multi-chamber injection device includes multiple syringes. The multiple syringes may be arrayed in a circular, linear, or other format. In some implementations, a needle, port, or similar may be shared by all the syringes in configuration that allows only one syringe to deliver contents at a time while blocking the other syringes from delivering their respective contents. In some implementations, the syringes may be all stored in the same container. One or more of the chambers of a multi-chamber injection device may be preloaded with medication. Different medications may be loaded into different chambers. The medications may be selected to treat the same medical condition.

Abstract: Fluid collection/injection device comprises a body having a front end, a back end, and a main hollow section arranged between the front and back ends and a needle hub securing section arranged on the front end and being structured and arranged to receive therein a needle member. The fluid collection/injection device is structured and arranged to utilize at least an operational mode, an operational mode, and a post-use mode. In the installation mode, the needle member is coupled to the body via the needle hub securing section. In the operational mode, fluid passes through the needle member and into or out of a receptacle inserted into the main hollow section.

Abstract: Packaging for safety needle devices are described herein. Such packaging can include hard packaging for safety needle devices. Such packaging can include a cavity or recess in a compartment of the packaging to house an activation element of a safety needle device to prevent accidental activation of the safety needle device prior to use by the user. Such packaging can include a cavity or recess in a safety needle device to house an activation element located on the inside surface of the compartment of the packaging to prevent accidental activation of the safety needle device prior to use by the user.

Abstract: An integrated structure of a preparation syringe includes a stretchable piston, a barrel, a needle, an exposed rubber plug, a sealing sheet, a built-in rubber plug, a sealing rubber plug and an engaging rubber plug. One end of the barrel is provided with the stretchable piston, and another end of the barrel is provided with a clamping column. The exposed rubber plug is provided on a side of the stretchable piston away from the barrel. The built-in rubber plug is provided within the barrel. A Scale mark is provided on a circumferential surface of the barrel. The sealing rubber plug is inlaid and sleeved on the clamping column. The sealing sheet is provided on a side of exposed tuber plug away from the barrel. A blunt end is provided at an end of the needle away form a needle tip. The engaging rubber plug is provided outside the blunt end.

Abstract: An injection device including a needle protection system, said injection device including a delivery needle (10) that is provided with a delivery orifice (11), said protection system comprising a removable needle guard (20) that, in a non-dispensing position, is adapted to be arranged on said needle (10) so as to protect and isolate said delivery orifice (11) of said needle (10), said needle guard (20) including an isolator portion (21) made of flexible material, said delivery orifice (11) of the needle (10) being poked into said isolator portion (21) in the non-dispensing position, said needle guard (10) including at least one outwardly-radial projection (25), said protection system further comprising an outer cap (30) that is provided with grip means (35, 35?, 36; 38; 300) that are adapted to co-operate with said at least one radial projection (25) of said needle guard (20), such that moving said outer cap (30) in the longitudinal direction of said needle (10), away from said delivery orifice (11), removes

Abstract: A tray for a soft tissue cutting device includes a housing slot for removably housing the soft tissue cutting device prior to use and a priming slot for receiving the soft tissue cutting device during a priming procedure. The priming slot allows connection of the soft tissue cutting device to a priming syringe for priming the soft tissue cutting device. The tray also includes a safety slot for testing whether the soft tissue cutting device is primed for use and a sterile cover connectable to the tray. The sterile cover substantially encloses the tray when it is connected thereto.

Abstract: Provided is an apparatus, system, and method for a nested syringe assembly. The nested syringe assembly (100) includes a first syringe (104) having a cylindrical body defining an inner diameter and a second syringe (102) having a cylindrical body defining an outer diameter. The outer diameter of the second syringe is less than the inner diameter of the first syringe. At least a portion of the cylindrical body of the second syringe is disposed within the cylindrical body of the first syringe.

Abstract: A magazine assembly (1) that stores a plurality of needles (56) configured to engage a medication pen (2) via an adapter (4) for medication delivery, the magazine assembly (1) comprising a magazine housing (20) enclosing a plurality of hub chambers (22) each enclosing one of a plurality of needle hubs (50), a connector (28) in each of the plurality of hub chambers (22), each connector (28) engages one of the plurality of needle hubs (50), and a plurality of enclosures (30) each sealing the plurality of hub chambers (22), wherein a selected enclosure of the plurality of enclosures (30) is removed to expose a selected needle hub (52) of the plurality of needle hubs (50), the adapter (4) attaches to the medication pen (2) to engage the selected needle hub (52) while disengaging the selected needle hub (52) from the hub chamber (22), and the selected needle hub (52) is removed from the magazine housing (20) to prepare the medication pen (2) for medication delivery.

Abstract: The invention relates to a wound care product, comprising a wound care article located in a sterilized sealed chamber defining a sterile environment. The wound care product also comprises an openable and reclosable container which has at least one outer surface portion in said sterile environment. The invention further relates to a method for using such a wound care product.

Abstract: The invention provides devices and methods for adjusting particle size in nanoemulsions of fluorocarbons and perfluorocarbons (e.g., perfluoropentane and perfluorohexane) via sonication (e.g., ultrasonication).

Abstract: Packages comprising a syringe and a blister package are described. The blister package incorporates elements that allow one-handed opening. Also described are methods of removing a syringe from a package using only one hand.

Abstract: A self-injection device (100, 200), including a pen body (108, 208) connectable to a pen needle (10), and a cap (104, 204) selectively connectable to the pen body (108, 208) in a first orientation with respect to the pen body (108, 208) to minimize the length or volume of the self injection device (100, 200), and in a second orientation to provide sufficient length or volume in an interior of the cap (104, 204) to house a pen needle (10) connected to the pen body (108, 208).

Abstract: A removal device (121, 221) for removing and disposing of a pen needle (113, 213) connectable to a drug delivery device (111, 211) includes a body (123, 223) having a cavity (141, 241) for receiving the pen needle of the drug delivery device such that a patient end (116, 216) of a needle (115, 215) of the pen needle is covered by the body. An ejector (151, 251) is movably connected to the body (123, 223) for engaging the received pen needle (113, 213) and selectively ejecting the engaged pen needle from the body. The pen needle (113, 213) is securely retained within the removal device (121, 221) without exposing the needle (115, 215) of the pen needle until the pen needle (113, 213) can be properly disposed of, such as in a sharps container, thereby substantially preventing an accidental needle stick.

Abstract: A method of treating pain, e.g., acute post-operative pain, by intravenously administering to a human patient(s) a dose of tramadol of about 45 mg to about 80 mg, based on tramadol hydrochloride, together with an intravenous dose of a therapeutically effective amount of ketorolac about every 6 hours.

Abstract: A compact drying rack is disclosed having a portable carry case which is opened to reveal various sized pegs to accommodate a variety of different types of bottles and bottle brushes.

Abstract: A medical device packaging assembly includes a cover (10), a medical packaging paper (20), a medical device (50), and an adhesive dressing (30). The cover has a pocket (14) and a perimeter (12) extending from the perimeter of the pocket. The medical packaging paper forms a hermetically tight seal between the medical packaging paper and the perimeter of the cover around the pocket. The medical device is contained in the hermetically sealed pocket along with the adhesive dressing. The adhesive dressing is removably adhered to the medical packaging paper.

Abstract: The invention relates to a boot remover (10) for removing a protective needle boot (11) from a drug delivery device (1), wherein the boot remover (10) is arranged to engage the protective needle boot (11) when attached to the drug delivery device (1), wherein the boot remover (10) comprises a tab (10.2) extending in a distal direction (D), wherein the tab (10.2) is engageable to a packaging (13) of the drug delivery device (1). Furthermore, the invention relates to a drug delivery arrangement comprising a drug delivery device (1), a packaging (13) and the boot remover (10).

Abstract: In accordance with one embodiment, a method of capturing biomatter includes placing a device comprising the biomatter within an extension tube, the extension tube being coupled to a tray. A fold is created in the extension tube sealing the extension tube and the biomatter contained therein. The extension tube is secured to the tray to maintain the fold. The assembly is discarded, e.g., into a bio-waste disposal bag in a bio-waste container. The fold is a smooth fold, in contrast to a sharp tip, thus minimizing the possibility of puncture of the bio-waste disposal bag.

Abstract: A method of treating pain, e.g., acute post-operative pain, by intravenously administering to a human patient(s) a dose of tramadol of about 45 mg to about 80 mg, based on tramadol hydrochloride, together with an intravenous dose of acetaminophen in an amount from about 500 mg to about 1000 mg, about every 6 hours.

Abstract: The invention relates to a sampling assembly (1), in particular for relatively small quantities of bodily fluids. The said sample assembly (1) comprises a sample container (2) and a support assembly (15). The sample container (2) has an open end (4), an end (5) closed by a bottom (6) as well as a side wall (7). The support assembly (15) protrudes axially over the sample container (2) in the area of the closed end (5) thereof, and comprises at least two container extension pieces (16). The container extension pieces (16) are each integrally connected with the sample container (2) via a hinge assembly (17) and are pivotable from a production position aligned at an angle (18) to the longitudinal axis (8) to a use position which is aligned approximately parallel to the longitudinal axis (8).

Abstract: Use of the peritoneal space provides a more direct tracking of blood glucose, capturing faster glucose kinetics, avoiding membrane/encapsulation effects, having less lag time and lag time variability, and eliminating the effect of variations in skin temperature, cardiac output, and body position during sleep. A peritoneal sensor system may be implanted within the peritoneal space and may generally include a sensor/sampler portion, which is implanted in the peritoneal space, and a control portion/controller, which may be implanted elsewhere, such as subcutaneously, or may be external to the patient.

Abstract: A packaging body is configured to house a prefilled syringe that comprises an outer cylinder fillable with a liquid and a plunger movable with respect to the outer cylinder. The packaging body includes a container comprising a housing portion configured to house the prefilled syringe. The housing portion is configured to house the prefilled syringes with various protrusion lengths of the plungers from the outer cylinders, and comprises a first regulating portion that regulates movement of the plunger in a distal end direction in a housed state in which the prefilled syringe is housed in the housing portion.

Abstract: A package for a medical cannula with a hub, such as a pen needle, is disclosed. The package includes a cover for receiving a medical cannula and for engaging a hub of the medical cannula. The cover has open ends that are in communication through the cover. The packaging also includes a sterility barrier for the cover.

Abstract: The disclosed embodiment relates to an injection device that is a single patient use, disposable device containing a needle and a cartridge containing a drug, pharmaceutical product or other injectable agent. The device is initially provided in a pre-armed state in a first engagement configuration wherein the needle is separated from the septum of a cartridge. To arm the injection device, the professional urges the device from the first engagement or pre-armed configuration to a second engagement or armed configuration wherein the needle pierces the septum and provides a sterile fluid path to the drug, pharmaceutical product or other injectable agent contained within the cartridge. The disclosed embodiment is particularly adaptable to dental anesthetic applications, as well as other medical and veterinary applications.

Abstract: A prefilled syringe includes a syringe body filled with a medical fluid, which has a nozzle at a front side, the nozzle being closed with a cap, and which is closed at a rear side with a displaceable plunger; and a plunger rod that can be inserted into the syringe body via the rear side. The plunger rod has a connecting portion at a front side, via which the plunger rod can be connected to the plunger. At least three annular elements, which extend at least in some sections about a longitudinal axis of the rod, are arranged on a rear side of the connecting portion on the plunger rod in such a manner that they are located in the syringe body when the plunger rod is fully connected to the plunger. The three annular elements support a coaxial connection of the rod to the plunger positioned in the syringe.

Abstract: The present invention refers to a pen cap, being capable of covering a distal end of a drug delivery device comprising at least one protruding element located inside the pen cap which prevents that the rim of an outer needle cap, while being a protective casing for the needle at the distal end of the drug delivery device, can get stuck within a part of the pen cap if the user puts the pen cap on the drug delivery device. The inner diameter of the pen cap is reduced by means of the at least one protruding element, such that the inner diameter of the pen cap is smaller than the largest outer diameter of the outer needle cap. Furthermore, the invention relates to a drug delivery device comprising a pen cap with the described protruding elements.

Abstract: Medicant mixing/administration systems are provided that can include: a medicant vial; a syringe assembly comprising a barrel and a piston; a protective material supporting the syringe assembly and medicant vial; and a member within the system, the member separating the piston of the syringe assembly from the medicant vial. Systems are provided that can include: a syringe assembly comprising a barrel and a piston; having a forward end and an opposing back end; a protective material supporting the syringe assembly; and a needle housing coupled to the protective material. Medicant mixing/administration methods are also provided that can include, within a package, sufficiently clearing a restraining member from between a medicant vial and syringe plunger to pierce the medicant vial with a piercing structure coupled to the syringe plunger, the piercing providing medicant from the vial to the syringe assembly.

Abstract: The invention refers to a needle cap remover (7) for a needle cap (5.1) of a drug delivery device (2). The needle cap remover (7) comprises a body (8) having a material which differs from the material of the needle cap (5.1) or of a rigid needle shield (5) encasing the needle cap (5.1) in at least one parameter, wherein a body portion (8.1), which covers the needle cap (5.1) or the rigid needle shield (5) encasing the needle cap (5.1), is adapted to capture the needle cap (5.1) or the rigid needle shield (5) encasing the needle cap (5.1) by a positive and/or non-positive connections before or during removing of the needle cap (5.1) and is adapted to shrunk when a pulling force is applied.

Abstract: A system for storing instruments is provided. The system includes a tray including at least one tray end. At least one slot is formed in the at least one tray end. The system also includes a cover constructed and arranged to be positioned on the tray. The cover includes at least one cover end. The system also includes a latch positioned within the at least one cover end. The latch includes an actuating member and a locking member. The locking member includes at least one locking flange constructed and arranged to be received in the at least one slot. The at least one locking flange includes an angled lower edge constructed and arranged to engage the at least one tray end when the cover is positioned on the tray so that the latch is actuated into an open position to enable the at least one locking flange to be received within the at least one slot.

Abstract: A blood collection assembly includes a hub with a distal end, a proximal end, a hub outer surface and an internal opening extending therethrough. The assembly also includes a holder housing defining a receiving chamber and having a rearward end adapted to receive a sample collection tube within the chamber and a forward end including a receiving port extending into the chamber, where the receiving port receives a portion of the proximal end of the hub therein. An internal opening of the hub accommodates a puncturing element at the proximal end thereof for providing passage of a fluid therethrough, and the puncturing element contacts the sample collection tube. The hub and the holder housing include an interengaging structure extending substantially perimetrically therearound for axially locking the hub with the holder housing.

Abstract: An injection aid for use with an injection device, such as a safety syringe, for example, is disclosed. The injection aid employs a flexible clip-based design to compensate for manufacturing tolerances associated with the injection device. The injection aid includes a body and a lever mounted to the body, the lever being configured to rotate about the body. The injection aid may further include gears rotate with rotation of the lever, and which function to remove a needle shield from the injection device. The body positions the injection device so as to ensure consistent injection depth.

Abstract: A syringe assembly including a plunger rod separate and detached from a syringe barrel and a packaging member, the plunger rod having a sealing member and the packaging member having a first compartment and a second compartment is disclosed. With the syringe barrel received within the first compartment and the plunger rod received within the second compartment, the sealing member of the plunger rod seals the syringe barrel and the plunger rod within the packaging member. In this manner, the syringe assembly is placed in the packaging member in a manner that allows for reduced storage space of the syringe assembly.

Abstract: A closure container that can house a preset drug applicator in an easily accessible manner with tamper evidencing means. The closure container contains a plurality of dosing ribs and a retainer to retain the syringe in a preset dosage amount and preferably has a window to view the barrel of the syringe.

Abstract: A fold open face seal package is provided. The package may comprise a one or two-piece thermoformed blister adhered to a backing card. In the one piece embodiment upper and lower portions of the blister are connected by one or more hinges. In the two-piece embodiment the blister is cut into upper and lower pieces which are adhered to the backing card. The package may be opened by folding the backing card back along a bend line and then reclosed for later use.

Abstract: The invention relates to the use of an inhibitor of the dihydrofolate reductase enzyme selected from the group that consists of methotrexate, trimetrexate and pemetrexed; or a pharmaceutically acceptable salt thereof, for the preparation of a drug for the treatment or prevention of recurrences of a disease selected from the group that consists of cancer, psoriasis, psoriatic arthritis, juvenile polyarticular arthritis, rheumatoid arthritis, Crohn's disease, polymyositis, dermatomyositis and sarcoidosis, wherein said treatment or prevention includes administering to a patient, simultaneously, separately or sequentially, a lipophilic statin and the inhibitor of the dihydrofolate reductase enzyme. The invention also relates to a pharmaceutical composition which includes the inhibitor of the dihydrofolate reductase enzyme and the lipophilic statin together with pharmaceutically acceptable carriers and/or vehicles.

Abstract: Packaging (4) for an injection device (6, 92), the packaging comprising: a compartment (32) forming a recess configured to house the injection device therein, the compartment extending in a longitudinal direction, a depth direction, and having a variable lateral width to accommodate the injection device; a first sidewall (54) extending in the depth direction and longitudinal direction contiguous a portion of the compartment; and a lip (56) adjoining the sidewall and said portion of the compartment, wherein the first sidewall is arranged within a field of width of the compartment, the lip arranged at a height (h) from a base of said portion of the compartment, such that the lip and first sidewall prevent user gripping of a housed injection device at said portion of the compartment.

Abstract: An injection needle assembly is presented having an injection needle where the distal pointed end is arranged to penetrate a membrane arranged at the proximal end of a medicament container; a tubular needle holder having a distal engagement means and proximal engagement means; a tubular cap having a proximal outer engagement means and proximal inner engagement means; a tubular needle cover comprising first engagement means arranged to cooperate with the proximal engagement means, and second engagement means arranged to cooperate with the proximal outer engagement means of the cap. The needle cover is arranged to be displaced from a first position wherein the second engagement means and the proximal outer engagement means prevents the needle cover and the needle holder to be axially displaced by a linear displacement, to a second position wherein the needle cover and the needle holder are distally displaced.

Abstract: Apparatuses and systems are provided which include one or more receptacles for receiving drugs and further include one or more stored supplies of one or more absorbent materials comprising crosslinkers, wherein the apparatus and systems are adapted to release the absorbent materials comprising crosslinkers into the one or more receptacles. A method is provided which includes depositing a drug into a predetermined amount of fluid and adding to the drug containing fluid a absorbent material comprising crosslinkers which is capable of encapsulating the drug containing fluid and possibly killing infectious materials within the fluid and/or denaturing the drug within the fluid.

Abstract: A flip-open multi-pack assembly which contains a plurality of new pen needles via a rectangular or tube-shaped, hinged shell housing, wherein new pen needles are stored in a plurality of user accessible openings each having a sterility barrier formed by covers that cover the non-patient end of the openings where the new pen needles are contained. Used pen needles are returned and stored in openings accessible by rotatably opening the shell housing. One or more of the openings within first and second opposite ends of the housing shell include a slidable internal holder configured to releasably secure the inner shield of the new pen needle, and subsequently be pulled forward when the new pen needle is removed and locked at a forward position, to create an interior space, accessible from an opposite end when the hinged housing is opened, for a used pen needle to be inserted and stored.