912 results about "Vial" patented technology

The invention provides a medicine dispensing machine which comprises a frame, and a medicine bottle box for storing ampoule bottles and penicillin bottles, a liquid bag box for storing liquid bags and a suction and injection device hanging frame for conveying suction and injection devices are arranged in the frame. An ampoule bottle opening device for opening an ampoule bottle, a penicillin bottle cover opening device for opening a bottle cover of the penicillin bottle, a penicillin bottle liquid medicine mixing device for mixing and uniformly shaking liquid medicine injected into the ampoule bottle, and a marking device for marking a liquid bag injected with the mixed liquid medicine are arranged in the frame; the frame is internally provided with a sucking and injecting manipulator which is used for clamping a sucking and injecting device and sucking and injecting liquid medicine of an ampoule bottle into a penicillin bottle, all the devices are transferred through a transferring manipulator, full-automatic medicine dispensing is carried out, and the medicine dispensing efficiency is improved.

A tamper evident seal structure for a vial septum or other cover having a housing including a sidewall terminating in oppositely disposed open and closed ends. A retainer is fixedly disposed within the housing and structured for retaining engagement with a portion of a vial, substantially adjacent the vial cover. The housing also includes a pressure member disposed within an interior thereof in attached, relation to the closed-end. The pressure member and the retainer are cooperatively disposed and structured to respectively exert pressure on the vial cover concurrent to retaining engagement with the vial. Tamper evident capabilities are at least partially defined by a detachment of a removable sidewall section from a remainder of said sidewall.

In certain embodiments, a vial adaptor comprises a housing configured to couple the adaptor with a vial, an access channel, a regulator channel, and a regulator assembly. The access channel is configured to facilitate withdrawal of fluid from the vial when the adaptor is coupled to the vial. The regulator channel is configured to facilitate a flow of a regulating fluid from the regulator assembly to compensate for changes in volume of a medical fluid in the vial. The regulator assembly can include a valve configured to transition between a closed configuration and an opened configuration.

In certain embodiments, a vial adaptor comprises a housing configured to couple the adaptor with a vial, an access channel, a regulator channel, and a regulator assembly. The access channel is configured to facilitate withdrawal of fluid from the vial when the adaptor is coupled to the vial. The regulator channel is configured to facilitate a flow of a regulating fluid from the regulator assembly to compensate for changes in volume of a medical fluid in the vial. In some embodiments, the regulator assembly includes a flexible member configured to expand and contract in accordance with changes in the volume of the medical fluid in the vial. In some embodiments, the flexible member is substantially free to expand and contract. In some embodiments, the flexible member is not partly or completely located in a rigid enclosure.

A gripper for industrial manipulators includes a body, inside which an electric motor is housed, and a turnable portion is constrained to the body. Jaws movable toward and away from each other to hold and release a piece are present on the turnable portion. The electric motor is intended for imparting rotations to the turnable portion while the piece is held between the jaws. A pneumatic actuator, for example a piston, controls the opening of the jaws to release the piece. The electric actuator and the pneumatic actuator remain separate and do not interact while the electric actuator is on. Vice-versa, the electric actuator and the pneumatic actuator are integral while the pneumatic actuator is active. The gripper is particularly adapted for being used in inspection systems of the carousel type, for checking the quality of containers and vials in the pharmaceutical industry.

An apparatus and method for determining the presence of a disease by analyzing a specimen by providing a vial partially containing the specimen and partially containing a headspace above the specimen, injecting an inert gas into the specimen in the vial to cause bubbling of the gas throughout at least a portion of the specimen such that the gas mixes with volatile organic compounds (VOCs) present in the specimen to create a VOC / gas mixture that is released into the headspace, collecting the VOC / gas mixture from the headspace in the vial, supplying the VOC / gas mixture to a chamber within the apparatus, causing the VOC / gas mixture to pass over a sensor array in proximity to the chamber, the sensor array generating an electrical signal as a function of VOCs detected in the VOC / gas mixture, and processing the electrical signal to determine the presence of a disease in the specimen.

An apparatus for processing pharmaceutical containers, in particular vials, syringes or carpules, and a filling device for filling pharmaceutical containers. The apparatus includes a frame that can be positioned on a set-down surface and has a surface, a first side and a second side, a processing station, and a transport device arranged between the first side and the second side, with circulating holding elements for the containers which move along a transport direction on a transport segment and counter to the transport direction on a return segment. The processing station is arranged at the transport segment, and the transport segment and the return segment are arranged above the surface. The transport plane is inclined by an angle of inclination relative to a plane of the surface and / or a horizontal plane, and the transport segment is arranged above the return segment in the direction of gravity.

A refillable liquid tip or cartridge for a vaping device includes a capacitive sensor plate located in a tip liquid reservoir. The liquid refilling device provides the liquid sucked from the refilling bottle to the vapour device; the refilling device comprises a capacitance measuring circuit; a microcontroller uses data from the capacitance measurement circuit to determine whether a liquid level in the tip liquid reservoir is above or below a threshold level, if below, activates a liquid pump in the refill device to draw liquid from the refill vial, and if not, activates a liquid pump in the refill device to discharge liquid from the refill vial. And pumping the liquid through the vapour device and up into the tip liquid reservoir. The pumping is stopped once the liquid reaches the threshold level.

The present disclosure provides a method of preparing a lyophilized bispecific molecule composition comprising (a) inducing ice nucleation in a liquid protein composition having a bispecific molecule concentration of at least about 10 mg / ml in a vial exposed to a first temperature of about-18 DEG C to about-10 DEG C for about 60 minutes to about 270 minutes; (b) exposing the vial of (a) to a second temperature of about-25 DEG C to-50 DEG C for about 1 hour to about 5 hours; and (c) drying the composition of (b) at a third temperature of about-5 DEG C to about-25 DEG C for about 25 hours to about 70 hours, and (d) further drying the composition of (c) at a fourth temperature of about 25 DEG C to about 50 DEG C for about 4 hours to about 12 hours to obtain a vial comprising a lyophilized bispecific molecular composition, the composition has a percentage content of high molecular weight material (HMWS) of less than or equal to about 1.5% (mA / ). The disclosure further provides lyophilized bispecific molecule compositions prepared via the methods described herein.

A protective device for maintaining the sterilization of a self-drilling anchor inserter and prohibiting the sharp, drilling point of the inserter from puncturing sterile packaging. The device includes a cannulated tube having a proximal end and a distal end. The cannulated tube extends along a longitudinal axis and has proximal and distal portions. The proximal portion extends to the proximal end and the distal portion extends to the distal end. The cannulated tube also has an inner volume. A first slot extends into the inner volume and along the proximal portion toward the proximal end. A second slot extends partially into the cannulated tube between the proximal portion and the distal portion. A connecting portion attaches the proximal portion to the distal portion. The proximal portion is movable relative to the distal portion, between an aligned position and a bent position.

A geological analysis system, device, and method using x-ray fluorescence and spectroscopy are provided. The geological analysis system includes a sample tray which holds the geological sample materials, and sensors including an X-ray fluorescence (XRF) unit and spectrometer. The sample tray includes chambers formed in an upper surface, ports, and passages, each providing communication between an interior of a chamber and an interior of a port. The ports are configured to be attachable to vials. The system positions the sample tray with respect to the sensors for sensing one or more properties of geological sample materials in the sample tray.

A lyophilization method for lyophilizing products inside one or more vials within a lyophilization chamber is disclosed which includes humidifying a charge gas to a predetermined relative humidity, cooling shelves in the lyophilization chamber to a predetermined temperature, pressurizing the chamber with the humidified charge gas to a pressurization threshold to thereby achieving a target relative humidity level within the lyophilization chamber, and suddenly releasing pressure within the lyophilization chamber until a depressurization threshold is reached in a short time interval up to about 4 seconds, during the depressurization, product inside one or more vials nucleate.

A multi-axis robotic vial loading system designed for transporting containers. The multi-axis robotic loading system includes a conveyor belt for transporting vials to a multi-axis robotic arm. The multi-axis robotic arm includes a gripper configured to attach to one or more vials. The multi-axis robotic arm moves the vials from the conveyor belt to a storage container.

Some embodiments disclosed herein relate to a device for transferring precise amounts of fluid from at least one source container to at least one target container. In some embodiments, the fluid is first transferred from the source container (e.g., a vial) through a connector to an intermediate measuring container (e.g., a syringe). In some embodiments air can pass through an air inlet and enter the vial to compensate for the volume of fluid withdrawn from the vial. An air check valve or a bag or a filter can prevent the fluid from escaping through the air inlet. The precisely measured amount of fluid can then be transferred from the intermediate measuring container to the target container (e.g., an IV bag). In some embodiments the connector can include a source check valve and a target check valve to direct fluid first from the source container to the intermediate measuring container and then from the intermediate measuring container to the target container. Some embodiments of the device can include a motor and a controller for automatically actuating a plunger of the syringe to transfer the desired amount of fluid.

The utility model relates to an automatic array device, in particular to an automatic array device for stacking penicillin bottles, which comprises a conveyor, an operating table, a screw rod, a servo motor, a placing frame, a counting sensor and the like, the conveyor is arranged in the middle of the front side of the operating table, the counting sensor is arranged on the conveyor, the servo motor is mounted on the right side of the operating table, and the screw rod is arranged on the screw rod. A lead screw is rotationally connected to the operation table, the right end of the lead screw is connected with an output shaft of the servo motor, and a containing frame is slidably connected to the operation table and is in threaded connection with the lead screw. The penicillin bottles are sequentially conveyed into the seven spaces of the containing frame through the conveyor to be stacked in an array mode, when a contact rod makes contact with a fixing plate, an extrusion plate can be pushed to move forwards, under the blocking effect of a stop rod, the penicillin bottles can be arranged in order, people do not need to arrange the penicillin bottles manually, convenience is brought to people, and the working efficiency is improved. And the penicillin bottles are in close contact, so that the stability when the penicillin bottles are driven by the placing frame to move is improved, and the penicillin bottles are prevented from being damaged.

The present disclosure provides a keyed medication cartridge for use in a handheld oral medication dispensing device. The medication cartridge is designed with alignment features for connecting to the medication dispensing device. The cartridge includes a shell and medication vial therein. In use, alignment features on the dispensing device pass through the shell and lock against the vial, allowing a user to depress the shell and activate a pump assembly to force medication from the medication cartridge.

The utility model discloses a bottle cap assembly which is used for sealing a double-cavity clamping type bottle and comprises a top plug and a top cap. The top plug is pressed by the plug pressing assembly so as to be embedded with the double-cavity clamping type bottle, so that the double-cavity clamping type bottle is sealed; the top cover is used for fixing the top plug and sealing a bottle opening of the double-cavity clamping bottle; the plug pressing assembly comprises a press-in jig and a holding jig. According to the bottle cap assembly and the double-cavity clamping type bottle, high-precision self-plug-pressing sealing with good sealing performance can be conducted through the plug pressing assembly in a freeze dryer, meanwhile, the time cost and operation complexity needed by plug pressing and cover sealing of the double-cavity clamping type bottle in the whole freeze-drying technological process are reduced, and the freeze-drying efficiency and the freeze-drying product quality are improved.

The presently disclosed device includes a plurality of vials each bearing a unique identifier and in discrete locations in the device. An alignment assembly aligns one of the discrete locations with an access point for dispensing one of the vials. Computer executable instructions select a vial to be dispensed and store inventory information of the vials. The inventory information associates the unique identifiers with a status for each the plurality of vials indicating whether a vial is: loaded, dispensed, returned, or remaining undispensed in the device. The computer executable instructions also deactivate dispensing of the vials from the device based on at least one signal received from at least one environmental sensor configured to detect one of: location, temperature, humidity, vibration, shock, blood alcohol content (BAC), and light intrusion. A deactivation assembly deactivates dispensing of the vials based on the instructions.

A holder device for holding a plurality of vials to be moved in a processing line. The holder device includes a plate having a plurality of housing seats for housing the vials and a plurality of rigid spacer elements arranged within the housing seats and configured to maintain the vials in a suspended position with respect to a substantially horizontal operating surface of the processing line. Each housing seat includes an open base intended to face towards the operating surface.

The invention discloses a medical garbage classifying and crushing device, and relates to the technical field of garbage classifying and crushing, the medical garbage classifying and crushing device comprises a crushing and classifying auxiliary mechanism arranged in a protective cover, the crushing and classifying auxiliary mechanism is arranged, a movable puncture needle and a needle plate pair are arranged in a crushing roller, and the crushing roller is driven to move through a connecting rod; crushed glass bottle bodies, rubber plugs and aluminum caps are punctured through movable puncture of the puncture needle, the puncture needle cannot puncture the glass due to the characteristics of the glass, so that only the crushed rubber plugs and aluminum caps can be punctured, the rubber plugs and the aluminum caps are punctured on the puncture needle, follow-up classification is facilitated, and when penicillin bottles are not separated in advance, the penicillin bottles can be conveniently separated in advance. And integrated crushing is completed, classification in advance is not needed, so that the whole penicillin bottles are classified while being crushed, and the overall crushing and classification efficiency and effect are greatly improved.

The invention discloses an ethylene oxide detection and analysis method, which belongs to the technical field of detection and analysis, and comprises the following steps: weighing a sample to be detected, adding deuterated internal standard ethylene oxide-D4, and dissolving the sample with a low-temperature mixed solvent to obtain a sample solution; uniformly mixing the sample solution, adding a purifying material for purifying, uniformly mixing and centrifuging to obtain supernate; putting a part of the supernate into a small solid-phase microextraction bottle, adding sodium chloride, and uniformly mixing to obtain a solution to be detected; placing the small solid-phase microextraction bottle filled with the solution to be detected on a gas chromatograph-tandem mass spectrometer with a CTC automatic solid-phase microextraction sampling device, and extracting and detecting the prepared solution to be detected; and analyzing the data acquired by the mass spectrum by utilizing Agilent MassHunter data processing software. According to the method, volatile components in a sample are enriched, concentrated and then detected, the residual amount of ethylene oxide in the fat-soluble plant extract can be directly and quantitatively analyzed, the sensitivity is high, and the accuracy is good.

In certain embodiments, a vial adaptor comprises a housing configured to couple the adaptor with a vial, an access channel, a regulator channel, and a regulator assembly. The access channel is configured to facilitate withdrawal of fluid from the vial when the adaptor is coupled to the vial. The regulator channel is configured to facilitate a flow of a regulating fluid from the regulator assembly to compensate for changes in volume of a medical fluid in the vial. The regulator assembly can include a valve configured to transition between a closed configuration and an opened configuration.

1. The name of the product under this design: bottle (small bottle type). 2. Purpose of the product of this design: a bottle for storing liquids. 3. The design key point of this appearance design product lies in the shape. 4. The picture or photo that best illustrates the design points: three-dimensional picture.

The invention provides a radiation shielding assembly, a drug vial assembly system, a method of dispensing a drug vial assembly system, and a radiopharmaceutical infusion device. The radiation shielding assembly is used for shielding a medicine bottle assembly containing radiopharmaceuticals, and the medicine bottle assembly is provided with a puncture communication piece capable of transversely moving. The shielding body is provided with a top opening, a small bottle containing cavity and a combination port, and the medicine bottle assembly is contained in the containing cavity through the top opening. The containing cavity is provided with a circumferential matching wall, the distance between the matching wall and the vertical center line is gradually decreased from the starting end to the tail end, and a moving path is provided for assembly. The medicine bottle is guided to move along the wall, and the bottom puncture communicating piece is guided to transversely move inwards and is in butt joint with the combination port when reaching the assembly completion position. After assembly is completed, the puncture communicating piece is in butt joint with the combination port. According to the invention, only one needle puncturing the top of the medicine bottle is used as an inflow channel. Needle adjustment is not needed when medicine is nearly empty, operation is simplified, and the error rate is reduced.

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.

The invention discloses a medical waste pipe-made injection bottle treatment device and a treatment method.The medical waste pipe-made injection bottle treatment device comprises a crushing unit, a screening unit and a rubber plug and aluminum ring separation unit, the rubber plug and aluminum ring separation unit comprises a first rack, a first conveying belt device and a pressing and twisting device, and the first conveying belt device and the pressing and twisting device are both installed on the first rack; the pressing and rubbing device comprises a first gear motor and a pressing and rubbing plate, a first crank arm is installed on an output shaft of the first gear motor, a plurality of second crank arms are further rotationally installed on the first rack, a plurality of connecting sleeves are fixedly arranged on the upper side of the pressing and rubbing plate, and extending shafts at the lower ends of the first crank arm and the second crank arms are connected with the corresponding connecting sleeves in a rotating fit mode. The combination of the rubber plug and the aluminum ring is conveyed to the rubber plug and aluminum ring separation unit through the screening unit to be separated, the separation efficiency of the aluminum ring and the rubber plug is higher, and the separation effect is better.

The invention provides an apparatus and method for holding vials and other containers for use in medical and other applications wherein hands-free access to vials and other containers is desired. The apparatus includes a clamp-like vial receiving portion having a pair of opposing jaws, including a first jaw having a pair of planar surfaces arranged at an angle, and a second jaw having a pair of opposing curved surfaces each in the form of a portion of a conical frustum with the curved surfaces being arranged at an angle. The planar and curved surfaces of the opposing jaws cooperate to stably hold vials and other containers of various circumference sizes.

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.

In certain embodiments, a vial adaptor comprises a housing configured to couple the adaptor with a vial, an access channel, a regulator channel, and a regulator assembly. The access channel is configured to facilitate withdrawal of fluid from the vial when the adaptor is coupled to the vial. The regulator channel is configured to facilitate a flow of a regulating fluid from the regulator assembly to compensate for changes in volume of a medical fluid in the vial. In some embodiments, the regulator assembly includes a flexible member configured to expand and contract in accordance with changes in the volume of the medical fluid in the vial. In some embodiments, the flexible member is substantially free to expand and contract. In some embodiments, the flexible member is not partly or completely located in a rigid enclosure

In certain embodiments, a vial adaptor comprises a housing configured to couple the adaptor with a vial, an access channel, a regulator channel, and a regulator assembly. The access channel is configured to facilitate withdrawal of fluid from the vial when the adaptor is coupled to the vial. The regulator channel is configured to facilitate a flow of a regulating fluid from the regulator assembly to compensate for changes in volume of a medical fluid in the vial. In some embodiments, the regulator assembly includes a flexible member configured to expand and contract in accordance with changes in the volume of the medical fluid in the vial. In some embodiments, the flexible member is substantially free to expand and contract. In some embodiments, the flexible member is not partly or completely located in a rigid enclosure.