3278results about "Pharmaceutical containers" patented technology

A pill container has a body, at least one lid, and at least one elastic assembly. The body comprises a first wall, a second wall, and at least one compartment. The first wall and second wall are two opposite sides of the body. The compartment is located between the first wall and the second wall. The lid is pivotably mounted on the second wall of the body. The elastic assembly is located on the second wall, and has a flexural segment and a first protruding section. The first protruding section is located on the flexural segment and contacts the second wall. The first protruding section supports a space between the flexural segment of the elastic assembly and the body.

A quick-fill pill organizer has a box, multiple retrieving covers, and a packaging cover. The box has multiple compartments. Each compartment has a retrieving opening and a packaging opening. The retrieving cover is mounted on the retrieving opening and corresponds to the compartment one-to-one such that the corresponding compartment connects to or is blocked from the outside. The packaging cover is mounted on the packaging openings such that all the compartments connect to or are blocked from the outside at the same time. When the retrieving openings are upward, the retrieving cover of the specific compartment can be opened. When the packaging openings are upward, the packaging cover can be opened or closed such that all of the compartments connect to or are blocked from outside at once.

The invention relates to the technical field of coating surface preparation, in particular to an anticoagulant coating based on novel tick-derived anticoagulant protein Qinghaenin and a preparation method of the anticoagulant coating. The functional layer of the anticoagulant coating comprises the following components: anticoagulant protein Qinghaenin or a functional peptide fragment Qinghaenin 167-192 of the anticoagulant protein Qinghaenin, wherein the amino acid sequence of the functional peptide fragment is as shown in SEQ ID NO. 2. The preparation method of the anticoagulant coating comprises the following steps: by using a polydopamine coating as a substrate layer, covalently grafting through an amido bond, immobilizing anticoagulant protein Qinghaenin capable of inhibiting FXII factor activation or a functional peptide fragment Qinghaenin 167-192 thereof on the surface of a medical polymer material, and successfully constructing a novel anticoagulant coating. Compared with an unmodified medical polymer material, the modified coating can significantly enhance the hydrophilic performance of the material and inhibit platelet adhesion and activation, finally effectively prolongs the in-vitro blood coagulation time, and shows excellent anticoagulation performance.

A container system with a recordable device having a substantially unaltered packaging profile when compared to standard commercially available prescription containers. The container includes a bottle having a cylindrical body having a length greater than its width. A cap is provided with an inclined spiral or helical land and stops to permit it to be affixed to the container. The cap is equipped with a snap fit ring or a fitting on its underside. A recording device is configured with a land or snap ring removably engageable with the snap fit ring on the underside of the cap. The cap has an aperture to accommodate a recording switch on the recording device. The cap is provided with a speaker switch aperture to permit the user to activate the message on the recording device to hear about the contents of the bottle.

The invention relates to the technical field of automatic medicine dispensing, in particular to full-automatic high-speed liquid dispensing equipment and method, and the full-automatic high-speed liquid dispensing equipment comprises a liquid dispensing table, a raw material storage device, a liquid bag transfer manipulator and at least two liquid medicine mixing devices. Specifically, the raw material storage devices are arranged on the two sides of the liquid preparation table; and the liquid bag transfer manipulator is used for transferring the liquid bags in the raw material storage device to the liquid preparation table. The two liquid medicine mixing devices are arranged on the two sides, different from the raw material storage device, of the liquid preparation table respectively and used for taking and opening ampoule bottles and penicillin bottles in the raw material storage device, mixing agents in the ampoule bottles and the penicillin bottles and then injecting the mixed agents into a liquid bag to form finished liquid medicine. The medicine liquid mixing device comprises a liquid mixing table, and a medicine bottle opening mechanism, a medicine bottle transfer manipulator, a needle cylinder frame and a suction and injection manipulator which are arranged on the liquid mixing table. The application has the effects of improving the dispensing efficiency and the equipment utilization rate and expanding the application scene of the equipment.

Pill dispenser devices, systems and methods are shown and / or described herein. Include are a method, device or system for pill delivery including disposing a pill at a known location; contacting the pill with a pick-up member; and, moving the pill from the known location by movement of the pick-up member.

This invention belongs to the field of medical syringe technology, specifically referring to a syringe connector, including a main body with an inlet end and an outlet end. The inlet end connects to the syringe. The main body has a flow channel with both ends communicating, and a sealing element is placed within the flow channel, dividing the flow channel into an inlet channel and an outlet channel. After the connector is connected to the needle, the needle passes through the sealing element and extends into the inlet channel, allowing liquid from the syringe to flow into the needle. The main body can take various shapes, as long as both ends are cylindrical. A common design is a tubular structure for the entire main body. The inlet end enables the connector to be matched with the syringe; the outlet end enables the needle to be matched with the connector. The connector acts as a carrier to connect the syringe to a mismatched needle. Furthermore, the syringe connector can prevent the waste of existing resources in the market.

The invention relates to the related technical field of medical instruments, in particular to a contrast injection device for enhancing nuclear magnetic resonance, which comprises a base, a mounting shell arranged at the upper part of the base, a first barrel arranged at the left upper part in the mounting shell, a second barrel arranged at the right upper part in the mounting shell, and a mixing barrel arranged in the middle of the upper part of the mounting shell, a first piston rod is arranged in the first barrel, a second piston rod is arranged in the second barrel, communicating pipes are respectively communicated between the first barrel and the mixing barrel and between the second barrel and the mixing barrel, a one-way water inlet pipe is arranged at the top of the barrel, and the one-way water inlet pipe is communicated with an external liquid storage tank. By rotating the adjusting screw rod, the adjusting screw rod drives the first wedge-shaped block to move to the position of the needed dosage, then the rodless air cylinder controls the extrusion plate to move upwards, and after the extrusion plate moves upwards and makes contact with the plate body, the piston rods move upwards to inject the contrast agent and normal saline of the corresponding dosage into the mixing barrel to be mixed.

A paper bottle system for pharmaceuticals is disclosed. The system includes a first frustum-shaped conical section formed of heavy-weight paper, a second frustum-shaped conical section formed of a biodegradable material, a biodegradable lid, and an aqueous coating. The conical sections are angled between 5-8 degrees from vertical, allowing for efficient nesting and stacking. The system is designed to be environmentally friendly, easily recyclable, and optimized for short-term use. When disposed of in a landfill, the paper bottle system quickly breaks down, contributing to soil health and reducing environmental impact.

An infant feeding apparatus. The bottle includes a bottle having an open connecting end, a resilient teat member connected to the open connecting end, in which the teat member has a collapsible base, the collapsible base which has two connectors. The collapsible base has a corrugated sidewall defining an inner chamber. One the connector has a first outer indent and an inner anchor receiver disposed towards the inner chamber. The other connector has second outer indent. A capsule has two ends and is sized and shaped for location in the inner chamber and has amount of powder. A cutting member is located near one capsule end and has an anchor extension to lock with the inner anchor receiver. Another cutting member is located near the other capsule end and is connected to the open connecting end of the bottle. A teat holder is located to lockingly hold the connector portion nd the cutting member. A pushing member is connected to the connector portion of the resilient teat member and is disposed to permit a pushing force to be applied against it to collapse the collapsible base portion and to cut capsule ends to release the powder into the bottle.

The utility model relates to the technical field of medical auxiliary equipment, in particular to an operation rotary table for infusion and injection and a multifunctional clamp thereof, the operation rotary table for infusion and injection and the multifunctional clamp thereof comprise a circular clamp body, and the clamp body is sequentially provided with an upper positioning groove, a limiting groove and a lower positioning groove which are communicated with one another in the axis direction; the upper positioning groove, the limiting groove and the lower positioning groove form openings in the side wall of the clamp body, the upper positioning groove and the lower positioning groove penetrate through the upper end face and the lower end face of the clamp body respectively, the width of the upper positioning groove is smaller than that of the lower positioning groove, and the width of the lower positioning groove is smaller than that of the limiting groove. According to the multifunctional clamp, after the puncture opening is clamped in, the multifunctional clamp is rotated, the opening is closed through the inner wall of the rotating disc used for installing the multifunctional clamp, and therefore the puncture opening can be fixed, and the multifunctional clamp can be suitable for installation of various puncture openings.

To provide a method for transporting thermoplastic resin vials under sterile conditions and in an exogenous pyrogen-free state, introducing the vials into a filling assembly line, and thereafter allowing the vials to stand without tipping or dropping them, the method is a method for packing vials for filling with contents such as medicaments or cells by vacuum-packing the vials, and includes the following steps:(I) inserting a plurality of vials in a tray with opening portion sides of the vials facing a bottom of the tray,(II) installing a soft film on bottom portions of the vials,(III) introducing the tray having the vials installed therein and the soft film into a gas-impermeable flexible film bag,(IV) depressurizing the inside of the flexible film bag to a prescribed vacuum pressure, and(V) sealing an opening of the flexible film bag.

A lyophilization container includes a first section having a first layer, a second layer aligned with the first layer, and a cavity defined by the alignment of the first and second layers, where at least one of the first and second layers is preformed to have a three-dimensional shape. A lyophilization fixture includes a base member and a lid member. The lid member is movable between a first position and a second position relative to the base member. The base member and lid member together define a housing that receives at least a portion of a lyophilization container.

To provide an ophthalmic product in which an ophthalmic composition is filled in a container in which a pressing deformation part is formed by using an elastic material, and although the ophthalmic composition contains chlorpheniramine, diphenhydramine or a salt thereof, adsorption of these components is suppressed.SOLUTION: An ophthalmic product comprising an ophthalmic composition and a container filled with the ophthalmic composition, wherein the container comprises a container body having a discharge port and a press-deforming part, and a cap, and the press-deforming part is formed using an elastic material, (A) one or more selected from the group consisting of chlorpheniramine, diphenhydramine, and pharmaceutically acceptable salts thereof, and (B) one or more selected from the group consisting of an amino acid and a salt thereof, glycyrrhizic acid and a salt thereof, a mucopolysaccharide and a salt thereof, trometamol and a salt thereof, ethylenediaminetetraacetic acid and a salt thereof, and a vitamin and a derivative thereof.SELECTED DRAWING: Figure 1

The invention provides pharmaceutical compositions comprising about 0.05 to 0.1% (w / v) cyclosporine dissolved in 1-perfluorobutyl-pentane for use in the topical treatment of dry eye disease and provides for dosing and treatment methods thereof. The invention further provides kits comprising such compositions.

The invention provides a one-person one-prescription traditional Chinese medicine patch preparation machine which comprises a production machine workbench, and the production machine workbench is provided with a protective film feeding frame, a stirring mechanism, a paste extruding mechanism, a pre-pressing mechanism, a uniform pressing mechanism, a cutting mechanism, a medicine patch cloth feeding and recycling assembly, a waste recycling frame, a discharging mechanism and a plurality of storage containers. The protective film feeding frame, the stirring mechanism, the paste extruding mechanism, the pre-pressing mechanism, the uniform pressing mechanism, the cutting mechanism and the discharging mechanism are sequentially arranged from left to right, the stirring mechanism and the paste extruding mechanism are provided with a stirring fast-assembling position and a paste extruding fast-assembling position respectively, the stirring fast-assembling position and the paste extruding fast-assembling position are each provided with a positioning wall, and fast-assembling clamping blocks are arranged on the positioning walls. The storage container is provided with a quick-mounting clamping hole, the protective film feeding frame is provided with a protective film, the protective film is arranged below the stirring mechanism and the paste extruding mechanism, and the patch cloth feeding and recycling assembly is provided with patch cloth. The device has the beneficial effects that a user can quickly detach and clean the storage container, and the requirements of the user are met.

A pre-filled dual-chamber medical agent delivery system assembled and configured to allow delivery of a single dose of a combined therapeutic agent (e.g., vaccine, drug, medicament, etc.) from a Blow-Fill-Seal (BFS) vial to a patient. The delivery assembly generally includes a modular design consisting of separately constructed components cooperatively arranged and coupled to one another, such as to facilitate delivery of a reconstituted lyophilized agent to a patient.

The invention relates to the field of medical dispensing automation, in particular to an ampoule bottle processing method and system for an automatic dispensing machine. The method comprises the following steps: firstly, setting a mechanical arm movement XYZ three-dimensional space coordinate system, calibrating bottle cutting and bottle knocking reference coordinates, segmentally setting a slope and an intercept calculation target value according to the diameter of a bottle body, obtaining the related size of an ampoule bottle through visual identification, calculating a compensation value, and correcting actual bottle cutting and bottle knocking in-place coordinate points. The pose parameters and the in-place coordinates of the mechanical arm are input into a control system to control the mechanical arm to work; the system comprises a visual identification module, a bottle cutting mechanism, a bottle knocking mechanism, a mechanical arm control system, a front-end clamping jaw and the like. The technical effects that the in-place coordinates of the mechanical arm can be accurately corrected according to different sizes of the ampoule bottles, the consistency of the positions and directions of bottle cutting and bottle knocking is guaranteed, and automatic uncapping operation of the ampoule bottles is achieved are achieved.

A cylindrical storage-organizer-dispenser device for solid dose medications, arranged in a 7-day by time-interval-dose matrix, specifically invented to offer a simple, user-friendly, and secure way for people who need to take multiple daily medications on a weekly basis. The device permits to visually see what medications have been already taken and implicitly indexes to the next upcoming dose; this helps to avoid missing a dose or taking dangerous double doses. Additionally the device provides secure storage for emergency medication, specific patient information and / or medication instructions, and includes a feature to securely carry it around.

A vial adapter for connecting to an injection vial comprises an adapter body comprising a top wall and a sidewall, the sidewall projecting from the top wall in a longitudinal direction to form a receptacle with a distal side of the top wall. The receptacle is configured to receive at least a portion of a barrel head of an injection vial. A movable part comprises a base part and a tipped cannula fixed to the base part. The tipped cannula extends through the top wall into the receptacle, wherein the movable part is movable relative to the adapter body in a longitudinal direction. The tipped cannula comprises an elongated fluid channel, a tipped distal end configured to penetrate a pierceable stopper of the injection vial, and a channel aperture located inside the receptacle and located proximally offset from the tipped distal end.

To provide an ophthalmic product having good reproducibility of discharge operation and reduced variation in discharge amount per drop.SOLUTION: An ophthalmic product including a liquid ophthalmic composition and a liquid dispensing container filled with the ophthalmic composition, wherein the liquid dispensing container includes a container body having a discharge port and a press-deforming portion and having a storage space for storing a liquid therein, and a cap, and the press-deforming portion is formed of an elastic material, the press deformation portion is elastically deformed between a first position at which the press deformation portion protrudes to the outside of the container body and forms a space communicating with the storage space inside the container body when the press deformation portion is not pressed and a second position at which the press deformation portion is positioned closer to the storage space than the first position when the press deformation portion is pressed, the ophthalmic composition is discharged from the discharge port by a volume change between the first position and the second position, and the ophthalmic composition contains (A) a nonionic surfactant and (B) an oily component.SELECTED DRAWING: Figure 1

This invention is method of manufacturing of child-resistant and tamper-evident packaging container, which the cap having a tamper-evident feature on the top and a press-tab on the side wall. This cap provides both tamper-evident and child safety features to warn and protect consumers as well as dispensers such as: pharmacists, hospitals, medical centers, and manufacturers that the containers have not been opened and accurately reflect the number of pills in the container. The cap's distinctive feature enables the pharmacist and medical staff or provider to securely fasten by rotating it clockwise, while the patient turns the cap counterclockwise to open it for the first time. However, this process will break off the tamper-evident feature away from the outside cap, which indicates tampering and exposes the upper surface of the inner lid, where additional marking displays, i.e., “OPENED” to warn of tampering. The cap continues function a child-resistant container thereon.

The present invention relates to a pre-assembled reconstitution and injection device, comprising an injection section having a cartridge for holding a diluent or drug product and a reconstitution section having a vial for holding a drug, whereby the injection section may only be disassembled from the reconstitution section after activation of the device has occurred. In an embodiment for use with a pen needle, the reconstitution section comprises a vial needle hub having a reconstitution needle for piercing both the vial and cartridge. In an embodiment of the invention for use with a hypodermic needle, the injection section comprises a cartridge needle hub with a cartridge needle and male luer connection having threads for securing a hypodermic needle, and the reconstitution section comprises a needle hub with a vial needle and a female luer connection for engagement with the male luer connection.

The automated modular pill dispensing device is for selectively dispensing pills of a pill regimen to a patient. The dispensing device includes a base unit having a pill dispensing chute leading to a pill receptacle area. A plurality of stackable pill trays each include a series of pill compartments. The plurality of stackable pill trays each include communication ports for communicatively interfacing with the pill tray communication interface of the base unit and adjacent stackable pill trays above and below. Each stackable pill tray includes an opening in the tray base, aligned with the pill dispensing chute of the base unit, and an actuator configured to selectively advance the series of pill compartments towards the pill hopper in response to the controller so that pills therein will be dispensed, in accordance with the pill regimen, through the pill hopper and via the pill dispensing chute to a pill receptacle positioned at the pill receptacle area.

The invention belongs to the technical field of biomedical materials, and particularly relates to a poly-4-methyl-1-pentene (PMP) gas-blood exchange membrane for an extracorporeal membrane oxygenation (ECMO) system, which realizes a long-acting antithrombotic function through a bionic interface construction technology. The invention aims to provide a bionic antithrombotic PMP gas-blood exchange membrane based on zwitter-ion gradient grafting, and through material and process innovation, the following problems existing in a traditional ECMO gas-blood exchange membrane: an antithrombotic coating is easy to fall off, and the long-term effect is insufficient; the risk of blood injury caused by dependence on heparin or anticoagulants; and the surface modification process destroys the membrane pore structure and air permeability.

A blister package is disclosed herein. The blister package includes a body, a plurality of pockets, and a top seal. The body has a top surface and a bottom surface opposite the top surface. The plurality of pockets is formed in the body. Each of the plurality of pockets extend below the top surface of the body. Each pocket of the plurality of pockets is configured to hold a pharmaceutical. The plurality of pockets is arranged in a manner that defines at least one dose. The plurality of pockets for the at least one dose includes a first pocket in parallel with a second pocket, and a third pocket perpendicular to the first pocket and the second pocket. The top seal is configured to interface with the body. The top seal is configured to hold the pharmaceutical in each respective pocket.

The invention discloses a wearable intraoperative body temperature detection and early warning device, and relates to the technical field of body temperature detection. The bracelet specifically comprises a bracelet body, a notch is formed in one end of the bracelet body, a hole is formed in one side of the notch, a clamping mechanism is arranged at the joint of the notch, a temperature sensor is fixedly installed on the inner side, close to the hole, of the bracelet body, and a pulse sensor is fixedly installed on the side, close to the temperature sensor, of the bracelet body. The bracelet comprises a bracelet body, anti-slip stickers are bonded to the inner walls of the two sides of the bracelet body, a display screen is fixedly mounted on the outer side of the center of the bracelet body, LED lamp strips are fixedly mounted on the two outer sides of the circumference of the bracelet body, a mounting cover is fixedly mounted on the side, close to the display screen, of the bracelet body, and a medicine box is fixedly mounted on the other side, close to the display screen, of the bracelet body. The temperature sensor and the pulse sensor on the inner side of the bracelet body are guaranteed to detect the temperature and pulse of a human body, and therefore the problem that an existing device of a box structure is not beneficial to surgical operation is effectively solved.

The present teachings generally include devices, systems, kits, and methods related to containers for a liquid solution intended for transport into a patient's body—e.g., via an intravenous (IV) treatment, a dialysis treatment, and the like. A container of the present teachings may be structurally configured to be relatively easy to lift and handle, transport, and / or use. Moreover, a container of the present teachings may be sized and shaped to promote grouping of multiple containers together into a predetermined group shape, which can be beneficial for packaging, handling, and / or transport. To this end, a container of the present teachings may include substantially planar sidewalls and a base featuring a connector that projects downwardly along a z-axis no further than terminal ends of sidewalls disposed adjacent to the base, where a cross-section of the container approximates a polygon to promote the grouping of multiple containers together for packaging and transport.

Provided herein are container systems for the storage of refillable pharmaceutical products. The container systems include a cap assembly configured to hold a magnetic token in place on the exterior surface. The cap assembly and container systems include design features for child resistance, case of storage, and case of refilling or dispensing contents in the systems. Also provided are refillable pharmaceutical products storage kits that include the container system and a refill pouch.