482results about "Pharmaceutical packaging" patented technology

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 a tablet container that allows consumers to easily and quickly refill the tablets themselves. [Solution] The case comprises a case body 1, a discharge cap 2 rotatably held via a shaft portion 14a provided at one end of the case body, and a bottom cover 3 rotatably held via a shaft portion 14b provided at the other end of the case body 1. The case body 1 has a receiving portion 11 for arranging tablets and a cover portion 13 rotatably connected to the receiving portion 11 via a hinge 12. The shaft portions 14a and 14b are connected to the end of the cover portion 13 and have cantilever engaging pieces 15a and 15b that abut the discharge cap 2 and bottom cover 3 against their respective inner wall surfaces, preventing the cover portion 13 from rotating relative to the receiving portion 11. The discharge cap 2 and bottom cover 3 are provided with notches 26 and 35 that release the contact between the cantilever engaging pieces 15a and 15b and their respective inner wall surfaces, allowing the cover portion 13 to rotate.

[Problem] The purpose of the present invention is to provide a portable anticancer agent container for preventing exposure and infection to the human body caused by chemical solution leakage that arises during a removal operation of a coupling connector at the time of system cleaning using a cleaning solution. [Solution] Provided is a pressurization-type drug injector having a drug exposure preventive function and having a system cleaning function, the pressurization-type drug injector comprising: a reservoir that has a chemical solution filling opening and a chemical solution discharging opening; a pressurization deformation means that undergoes pressurization and deformation by the injection of a chemical solution and that pushes out the chemical solution by a force caused by restoration of the pressurization and deformation; a flow rate control means that adjusts the flow rate of the chemical solution by resistance; a system cleaning port that includes a cleaning solution injection opening, a chemical solution filling opening, and a liquid discharging opening; and a case that contains therein said reservoir, said pressurization deformation means, and said system cleaning port. The case has openings respectively in the vicinity of the chemical solution filling opening, the system cleaning injection opening, and the chemical solution discharging opening. The chemical solution being filled is filled into the pressurization deformation means from the chemical solution filling opening of the reservoir, and moves from the chemical solution discharging opening of the reservoir to the exterior of the container via the flow rate control means. A cleaning solution is injected from the injection opening of the cleaning port arranged downstream from the flow rate control means, and moves to the exterior of the container. The pressurization-type drug injector having a drug exposure preventive function is characterized in that the periphery of the cleaning port is completely covered by a sterile seal, and thus, the cleaning port injection opening is kept clean until use.

Provided is a connection device capable of preventing two housings from being separated due to a force generated at a ratchet when the housings are screwed. The connection device includes a frame (30) including a first housing (36) and a second housing (37); a connection member (40) configured as a cylinder that internally forms a flow path (L1), provided to the frame (30) so as to be rotatable about an axis, and forming a threaded portion (42) for screwing a syringe (1); a flow path member (80) provided to the connection member (40); and a ratchet (50) including a gear (51) provided to the connection member (40) and having a plurality of teeth (51a) in a circumferential direction, and a pawl (52) provided to the frame (30) and engaged with a restriction surface (51b) of the gear (51) that rotates in a screwing direction of the syringe (1) in a direction intersecting a protruding direction in which a protruding portion (36b) of the first housing (36) protrudes from a first end surface (36a), so as to restrict rotation of the gear (51).

To obtain a water-soluble film that is excellent in cold water solubility and is useful as a chemical agent package, provided is a water-soluble film, which is a polyvinyl alcohol water-soluble film including a carboxylic acid-modified polyvinyl alcohol resin (A) as a main component, wherein a lactonization rate of a carboxylic acid modifying group in the carboxylic acid-modified polyvinyl alcohol resin (A) is from 20% to 70%.

The blood treatment system includes durable hardware components and disposable fluid flow circuits. The hardware components include a control unit configured to perform procedures for separating and collecting red blood cells from whole blood. An additive solution can first be provided in the red blood cell collection container of the fluid flow circuit, and the control unit operates the pump system of the hardware components to convey the additive solution from the red blood cell collection container to the additive solution container of the fluid flow circuit. After the red blood cells are separated from the blood and conveyed to the red blood cell collection container (along with at least a portion of the additive solution from the additive solution container), the red blood cells and the additive solution in the red blood cell collection container are conveyed to the whole blood container for collection and storage.

The cleaner assembly is configured for cleaning an automated dispensing device is described herein. The cleaner assembly includes a pallet; a plurality of side walls enclosing an inner chamber; a blower configured to propel contaminants into said inner chamber; and at least one roller operably supported by and projecting above at least one of said side walls, said at least one roller being configured to scrape contaminants off of a base plate of the automated dispensing device and towards said blower.

The present disclosure relates to a visual aid for assisting a user in the preparation of a plurality of syringes, the visual aid comprising a plurality of images, wherein each image: is visually representative of a respective syringe of the plurality of syringes; and comprises a respective first visual feature that is representative of a respective first visual feature of the respective syringe and a respective second visual feature that is representative of a respective second visual feature of the respective syringe, the visual features arranged such that they indicate a respective volume of a medicament to be drawn into the respective syringe. The present disclosure also relates to a system comprising a visual aid and a plurality of syringes. The present disclosure also relates to a method of using a visual aid.

The present invention relates to a package for storing a sterile pharmaceutical composition, comprising at least an inner layer of polypropylene having a thickness of 200 to 800 μm and an outer layer made of polyethylene, the outer layer being in contact with the environment and having a thickness of 300 to 1000 μm. The present invention also relates to a method for the sterile storage of a pharmaceutical composition using such a package.

Described herein is a home stock management system (1) for packaged items comprising a stationary data collection module (10) configured to wirelessly collect data from one or more packaged items (11) and to transmit the collected data to a processing module (12) wherein the packaged item(s) (11) include(s) a wireless tag (15), a processing module (12) for receiving, storing and processing the collected data from the collection module (10), and a notification means (13), wherein, the data collection module (10) is configured to collect data from the one or more packaged items (11) present in the home without user intervention. The processing module (12) is configured to process the collected data to determine status information and the notification means (13) is configured to communicate to one or more authorized users the status information. The home stock management system (1) can be used for the monitoring of consumable packaged items in the house or for monitoring and managing the stock and use of medication in a patient home or residence.

An apparatus for reconstitution, withdrawal and administration of drugs or nutrients obtained from active substances in powder, liquid or gel form contained in vials or other containers with hermetic closure, comprises a sealed flexible bag (2) and a hooking and piercing device (19) which is hookable to the closure plug (23) of a vial (22) containing an active substance (52) in powder, liquid o gel form for simultaneous piercing of said plug (23). The bag (2) is divided into two bag portions (3, 5). A first bag portion (3) has a first internal space (4) fillable with a sterile liquid sterile (51) and a second bag portion (5) having a second internal space (6) communicating with said hooking and piercing device (19). The two bag portions (3, 5) are separated by a hermetic transversal welding (7) which prevents communication between the first internal and second internal spaces (4, 6) and is openable by lateral compression of said first bag portion (3). There is provided at least a divarication tube (16) which keeps spaced the walls of said second bag portion (5).

An improved wearable device delivers a fluid medicament to the subcutaneous tissue of a user. The device is better suited for patients with Parkinson's Disease and other central nervous system disorders, than conventional infusion devices. The device can include a reusable part including a drive component (e.g., motor) and control electronics and a disposable part including one or two medicament reservoirs. Medicament can be evacuated from the medicament reservoir(s) by a plunger assembly that includes a plunger head attached to a lead screw that is linearly moved by a nut rotating in a bushing, all within the disposable part. The device can be fluidically coupled with the tissue via a flexible cannula.

A deformable container for dispensing a medical substance comprising a body defining an internal volume configured to receive a fluid substance, said body comprising a filling access configured to receive the fluid substance, a dispensing outlet configured to dispense the fluid substance, a valve arranged at the filling access movable between an open configuration and a closed configuration. The body comprises an elastically deformable wall delimiting the internal volume. The disclosure further relates to a connecting accessory comprising a first coupling portion, configured to fluidly connect to the filling access of the deformable container, and a second coupling portion configured to fluidly connect to an internal compartment of a vial. The container and the connecting accessory are configurable in a coupled configuration wherein the connecting accessory is coupled to the filling access of the container, and the valve of the container is in the open configuration.

Pharmaceutical compositions having enhanced active component permeation properties are described.

This invention relates to a catheter with a photo-initiated in-situ self-polymerized silver zwitterionic hydrogel coating that enhances antibacterial and antithrombotic functions. The catheter comprises a hydrogel matrix loaded / coated / attached to the catheter surface. This hydrogel matrix is ​​subjected to self-polymerization of SBMA monomers under ultraviolet light irradiation using MBA as a crosslinking agent, forming a three-dimensional crosslinked network while simultaneously embedding Ag NPs within the hydrogel matrix. This catheter exhibits both antibacterial and antithrombotic functions.

To provide immunogenic compositions capable of providing appropriate protection against Streptococcus pneumoniae serotypes not found in conventional vaccines.SOLUTION: The present invention provides new immunogenic compositions comprising conjugated Streptococcus pneumoniae capsular saccharide antigens (glycoconjugates) and uses thereof. Immunogenic compositions of the present invention typically comprise at least one glycoconjugate from a S. pneumoniae serotype not found in PREVNAR, SYNFLORIX and / or PREVNAR 13. The invention also relates to vaccination of human subjects, in particular infants and elderly, against pneumoccocal infections using the novel immunogenic compositions.SELECTED DRAWING: Figure 1

The present invention relates to a multi-part closure device for coupling to a medical active substance container with a suitable collar, the multi-part closure device comprising a sealing plug, a plug fastening device and a protective cover, the sealing plug being fastened to the active substance container with the plug fastening device, thereby sealing the opening in the bottle neck of the active substance container and allowing airtight removal of the liquid active substance. The plug fastening device comprises a fastening cage made of thermoplastic with a central ring, a central opening and side walls, one or more latching elements, in particular a plurality of integrally formed undercut webs, extending from the inner surface of the side walls and projecting away in the direction of the longitudinal axis, a plug engaging edge formed on the fastening cage engaging in a cage recess on the sealing plug, and the protective cover being removably attached to the plug fastening device.

This invention relates to a device for separating blood components (e.g., plasma or serum) in a whole blood sample. The device comprises a tube that holds 0.1-50 mL liquid volume; one or more pieces of membrane reversibly fixed inside the tube, wherein the membrane has a pore size at least 8 micrometers in diameter, and the membrane comprises an anti-red blood antibody; wherein the tube is a centrifuge or a tube adaptable to fit a centrifuge. The invention also relates to a method for separating plasma from a blood sample using the device in a low speed (300G-1000G or 300-600G) and a short time (< 3 minutes). The present device and method collect plasma from a whole blood sample in a larger volume and in a shorter time, which are useful in critical care or in emergency care.

The present application relates to the technical field of stent preparation, and particularly relates to an anticoagulant and anti-cell proliferation multifunctional coating, a preparation method thereof and a stent, and provides an anticoagulant and anti-cell proliferation multifunctional coating, which comprises a stent inner layer coating and a stent outer layer coating; the stent inner layer coating is Mirococept, polycaprolactone, heparin, an emulsifying agent, and the rest is an azidobenzoyl chitosan solution; the stent outer layer coating is astragaloside IV, everolimus, puerarin-6''-O-xyloside, an emulsifying agent, and the rest is an azidobenzoyl chitosan solution. Experimental data provided by the present application fully verify the significant advantages of the coating in terms of antithrombosis, inhibition of cell over-proliferation, regulation of inflammatory response and long-term safety, and the coating has a good application prospect.

This invention relates to the field of intelligent medical device technology, and more particularly to a portable intelligent medicine box with an emergency alarm function. The medicine box includes a main body, a medicine compartment assembly, a display and operation module, an emergency unit, a control system, and a power module. The main body comprises a lower shell and an upper cover, the upper cover being hinged to the lower shell for opening and closing, and positioned by a locking structure when closed. The upper cover is equipped with a portable grip component. The medicine compartment assembly is arranged in a 2x3 matrix within the lower shell, containing six independent medicine compartment units. Each medicine compartment unit is equipped with an openable and closable unit cover and a drug-related identifier. The display and operation module is correspondingly adapted to the medicine compartment assembly. The emergency unit is independently located within the lower shell. The control system and power module are electrically connected to the medicine compartment assembly, the display and operation module, and the emergency unit, respectively. This invention improves safety management and rapid response to emergencies through multi-sensor reminders, QR code binding, anti-accidental touch emergency alarms, and modular low-power design.

A method and medical device (200, 500, 600, 700, 800, 900) for mixing a medicament (106) contained within a medicament vial (210), the medical device comprising a track (220) configured to support the medicament vial, wherein the track comprises an inclined first track section (241) arranged such that, in use, the medicament vial can roll along the track to mix the medicament contained within the medicament vial.

Provided herein are devices and methods for mixing and delivering a multi-component fluid capable of decreasing post-surgical adhesions. The devices are configured to impart shear stress on the multi-component fluid and increase yield stress of a resulting gel. In some cases, the devices can be airless. In some cases, the devices can use gases to impart additional shear stress on the fluids in the devices. Mixers for imparting sheet stress can include mixer stages, vortex inducers, spacers, or any combination thereof.

This utility model discloses a pharmaceutical packaging film bag, including a film bag body and an anti-drip coating nozzle. The anti-drip coating nozzle consists of a nozzle sleeve, a leakage tube, a first retaining ring, a spring, a sealing plug, a protective cap, and a tube sleeve. The nozzle sleeve is integrally formed from a cylindrical section and a disc section. The opening of the leakage tube is heat-fused and sealed to the cylindrical section of the nozzle sleeve. The sealing plug is fixedly embedded in the inner end of the cylindrical section, and the tube sleeve is fixedly sleeved on the outer end of the leakage tube. This pharmaceutical packaging film bag allows for direct application of compound calamine lotion to the affected area without the need for other tools, offering the advantage of ease of use. Compared to plastic or glass bottles, the film bag has lower operating costs and can be squeezed to accelerate the flow rate of compound calamine lotion, improving application efficiency.

The application discloses a medicine precise dosing device and relates to the technical field of medicine dosing.The medicine precise dosing device comprises a medicine box, a solid medicine storage cavity and a liquid medicine storage cavity are arranged in the medicine box, a first cover and a second cover corresponding to the solid medicine storage cavity and the liquid medicine storage cavity are arranged on the upper side of the medicine box, stirring assemblies and cutting and crushing assemblies are arranged in the solid medicine storage cavity and the liquid medicine storage cavity respectively, a control panel and an identification camera are arranged on one side of the medicine box, and an intelligent dosing system connected with a metering pump and a sub-packaging device is arranged in the control panel.The intelligent dosing system arranged in the control panel can accurately calculate the required medicine dose according to the age, weight, illness condition and other factors of children, comprehensively analyzes the received data, uses a built-in professional algorithm and a big data model, and obtains the most suitable medicine dose for the children, so that the safety risk of medicine use is remarkably improved.

A valve is provided for use with a container for mixing biological fluids to facilitate homogeneous mixing and sampling. [Solution] The device comprises a body 14 having a first section 26 and a second section, an expansion flange disposed on the body 14, an elongated bore penetrating the body and having a proximal end and a distal end, a longitudinally displaceable plunger 62 disposed within the bore and extending along the bore, a diaphragm seal 60 that seals the bore, a gland seal 51 that seals the bore at a position midway between the diaphragm seal 60 and the distal end of the bore, the plunger 62 penetrating the gland seal 51 and being sealed and fixed to the gland seal 51, and a fluid transfer opening in the bore between the diaphragm seal 60 and the gland seal 51, wherein the longitudinal displacement of the plunger 62 moves the diaphragm seal 60 and opens the bore.