311results about "Automatic syringes" patented technology

The present disclosure relates to a medicament delivery device comprising a housing having a proximal end and contains a container of medicament positioned within the housing in a medicament container holder. The medicament container can be dual chambered, for example a pre-filled medicament container having a needle, a dose of medicament and one or more sliding stoppers. The medicament container holder can be configured with a recess or pocket to accommodate the loading of a dual chambered container and interact with an inside surface of the housing to rotationally fix the container holder relative to the housing and the medicament container. A tubular activation member, e.g., a needle cover, is slidably positioned within a housing of the delivery device to move from a first position to a second position, and then to a final locked position. A plunger rod can only move proximally relative to the needle cover when the needle cover is in the second position.

A device may receive, by an intelligence analytics module of an intelligent dosing platform at least one applicable governance standard from a governance library. A device may determine, by the intelligence analytics module based on the at least one applicable governance standard, at least one analysis type to be performed regarding the request. A device may execute, by an artificial intelligence module of the intelligent dosing platform, the at least one analysis type with respect to the request according to the at least one applicable governance standard. A device may generate, based on a result of the at least one analysis type, a determination regarding whether to permit the requested dosage administration or the requested device control decision, wherein the determination accounts for compliance with the at least one applicable governance standard.

An insertion device includes an upper casing (10), an insertion module (30) and a lower casing (20). The insertion module (30) includes a main body assembly (300), insertion and retraction seats (33, 35), and first and second elastic members (34, 37). When the upper casing (10) is depressed, the insertion seat (33) is driven by the first elastic member (34) to perform an automatic-insertion operation, such that limiting structure between the insertion and retraction seats (33, 35) collapses upon the collapse of another limiting structure between the insertion seat (33) and the main body assembly (300), and that the retraction seat (35) is driven by the second elastic member (37) to perform an automatic-retraction operation.

The techniques described herein relate to computerized methods and apparatus for determining a dose injected into a user by one or more medication delivery devices. Data is accessed that is indicative of an injection event group that includes one or more injection events associated with one or more medication delivery devices. The injection event group is processed to determine the dose injected into the user based on one or more of whether the injection event is associated with a medication delivery device change, a dose size of one or more of the injection events, a position of one or more of the injection events in the injection event group, and / or a time period between one or more injection events to a next injection event in the injection event group.

An auxiliary device is configured to couple to an injection device, the auxiliary device comprising a sensor assembly and a processor assembly, wherein the processor assembly is configured to cause the auxiliary device to use the sensor assembly to sense an identifying feature of the injection device and determine a type of the injection device based on the sensed identifying feature.

Providing an electrode array for electroporation, as well as related systems and methods. [Solution] An electrode array for use with an electroporation device includes a support member having an upper surface and a bottom surface, defining a plurality of injection channels extending from the upper surface to the bottom surface. The plurality of needle electrodes are coupled to the support member such that the distal ends of the plurality of needle electrodes extend to a needle depth below the bottom surface. The plurality of needle electrodes are arranged in a matrix pattern having rows and columns of needle electrodes arranged along the support member. The plurality of injection channels are dispersed within the matrix pattern.

Inhaler for administering a pharmaceutical with a) a reservoir (1) for storing the pharmaceutical, wherein the reservoir (1) has a dispensing opening (2), b) a triggering device (3) for triggering an application of a pharmaceutical product, wherein the pharmaceutical product is dispensed through the dispensing opening (2), c) an information storage medium (4) for storing application data, d) a conversion device (5) for converting analog application data into digital application data, e) a wireless information transmission device (6) for transmitting the application data to an external display and / or storage medium and f) a power generation unit (7) for providing electrical energy to the conversion unit (5), the information storage medium (4) and the information transmission unit (6) characterized by the fact that the energy generation device (7) is designed as an inductive element, or as a vibrationally excited element (13) in an outlet opening of the inhaler (3), which is excited to vibrate by the outflowing pharmaceutical, wherein the inductive element comprises a coil (9) arranged on the reservoir (1) and magnets (8) arranged on a base body and cooperating with the coil (9) and a movement of the reservoir (1) both induces an electronic current and opens the path for the pharmaceutical through the dispensing opening (2). will and that during the application, the required electrical energy can be generated and provided by the energy generation device (7) instead of a long-term energy storage device.

In one instance, disclosed herein is a system for assembling an auto-injector including a housing and a shroud, the housing including an opening, and the shroud including a coupling mechanism, the system comprising: a holder configured to control a movement the housing along a first direction; a brace configured to control a movement of the shroud along the first direction; and a pin extending from the brace, wherein in a first configuration, the pin is spaced apart from the housing and the shroud, and in a second configuration, the pin extends through both of the housing and the shroud, the pin configured to maintain the housing and the shroud in contact with one another until the coupling mechanism extends through the opening to couple the housing and the shroud.

Disclosed is an audible indicator, preferably for a drug delivery device, comprising:At least two wing shaped sections,A plastically deformed bend arranged between the at least two wing shaped sections,wherein the audible indicator comprises an elastically deformed bend or is configured to be deflected to form an elastically deformed bend,wherein the elastically deformed bend is arranged oblique to the plastically deformed bend, andAt least two lateral tabs extending from outer edges of the two wing shaped sections respectively,wherein the lateral tabs are configured to position the audible indicator within a device.

Plunger drive systems used with injectors to expel a fluid drug for injection into a patient include a housing and a plunger rod that extends from the housing. The plunger rod includes a first leg and a second leg individually coupled with separate rollers over one portion of the first leg and second leg and engaged together over another portion of the first leg and second leg to form a column. The legs may include a reinforcement member. The first leg and second leg meet at a location between the rollers and are engaged with one another through complementary registration surfaces. When the rollers are rotated, typically through action of an electric motor, the rollers rotate in opposite directions to increase a length of the column. The column may be operatively coupled to a plunger of a syringe to dispense a fluid drug as the column increases in length.

The application discloses a handheld injector and relates to the technical field of medical devices.The handheld injector comprises a handheld gun body, an injector clamping assembly, an injector injection assembly and an injection injection trigger assembly.The handheld gun body comprises an upper gun body and a lower gun body which are designed in a split mode, and the injector is located between the upper gun body and the lower gun body.The injector clamping assembly is slidably arranged in the lower gun body, and is used for clamping the injector to slide forward and backward in the handheld gun body, so that the needle body of the injector can be extended into and out of the handheld gun body.The injection injection assembly is arranged at the tail of the lower gun body and is in a locked state in a natural state.The injection injection trigger assembly is arranged in the lower gun body and is synchronously retreated to the lock with the injector clamping assembly.The handheld injector does not need to switch the hand posture between the needle puncture and the drug injection, can ensure the stability of the position of the injector during the puncture process, avoids the deviation of the needle tip from the preset puncture path, and ensures that the drug can be relatively accurately injected into the target area.

A syringe comprising a barrel and a needle at an end thereof, a syringe plunger configured to move within the barrel to cause a medicament within the barrel to be expelled from the needle; and an electrically erasable programmable read-only memory (EEPROM) configured to store information related to the syringe.

Method and system for controllably administering and / or withdrawing fluid from a patient. In one embodiment, the system may include a needle assembly, an ultrasound imager, a fluid supply storage unit, a waste storage unit, a fluid pump, and a foot pedal assembly. A syringe may serve as the fluid supply storage unit and the waste storage unit. The pump may include a bi-directional motor and a gear coupled to the motor. The gear may be engageable with a rack on the syringe plunger to drive the plunger either for fluid aspiration or infusion. Depression of one portion of the foot pedal assembly causes the motor to drive the gear in one direction, and depression of another portion of the foot pedal assembly causes the motor to drive the gear the other direction. The system may include a control device to keep pressure in the fluid path from exceeding a limit.

An automatic constant pressure and constant flow liquid injection device, comprising a voltage stabilizing power supply, an electric gas injection mechanism, a gas tank, a liquid medicine tank, an outer shell, an electromagnetic valve, a flow meter, a manual valve, a power switch, further comprising a speed regulating circuit, a control circuit, a prompt circuit, the electric gas injection mechanism, the gas tank, the liquid medicine tank, the electromagnetic valve, the flow meter and the manual valve are installed in the outer shell, the voltage stabilizing power supply, the power switch, the speed regulating circuit, the control circuit and the prompt circuit are installed in a component box and electrically connected with the electric gas injection mechanism, the electromagnetic valve and the flow meter. The present application does not need human to inject liquid, ensures that the liquid medicine entering the human body tissue is in constant pressure and flow rate. Medical staff can also select and set different liquid injection pressure according to the different tolerance of different patients, which brings convenience to medical staff, improves work efficiency and ensures good liquid injection effect. Therefore, the present application has good application prospect.

An intelligent dosing platform system for device lifecycle management and predictive maintenance comprising intelligent injection devices with sensors configured to detect operational parameters, device monitoring modules tracking sensor calibration state, battery life metrics, and device performance data. A predictive analytics module analyzes device operational data to forecast maintenance timing, sensor calibration requirements, and device replacement needs. The system includes maintenance scheduling modules that generate automated maintenance alerts based on predicted device performance degradation. A lifecycle documentation module maintains comprehensive device history records including deployment dates, calibration events, maintenance activities, and retirement tracking. The system optimizes device fleet performance through proactive maintenance scheduling, minimizes device downtime through predictive failure prevention, ensures patient safety through continuous device integrity monitoring, and maintains regulatory compliance through comprehensive lifecycle documentation and firmware management capabilities.

A therapeutic agent delivery system includes a therapeutic agent delivery assembly carried by a housing. The therapeutic agent delivery assembly includes a chamber having a first passageway, a therapeutic agent transported in the first passageway, and a needle in communication with the first passageway. The therapeutic agent delivery assembly is translatable relative to the housing from a stowed configuration to a deployed configuration. The therapeutic agent delivery assembly is also translatable relative to the housing from the deployed configuration to a retracted configuration. The system also includes a user input device actuatable to translate the therapeutic agent delivery assembly from the stowed configuration to the deployed configuration. The system also includes a retraction mechanism actuatable to translate the therapeutic agent delivery assembly from the deployed configuration to the retracted configuration.

The present disclosure relates to a medicament delivery device comprising a housing, a chamber for receiving medicament from a container of medicament, and a drive mechanism. The medicament delivery device further comprises a plunger within the housing and configured such that, in use, the plunger is moveable relative to the housing in a first direction from a first position to an second position to draw medicament into the chamber from the container and is moveable relative to the housing in a second direction from the second position to a primed position to expel a priming volume of the medicament from the chamber. The drive mechanism is configured such that, in use, the drive mechanism is operable to move the plunger from the primed position in the second direction to expel a dosage volume of the medicament from the chamber for delivery to a user. The present disclosure also relates to a medicament delivery system and to a method of preparing a medicament delivery system.

An auto injector comprises a housing 2 and a syringe assembly 4 that carries a needle 6. A drive spring 8 is configured to urge a driver 10 to rotate, which controls delivery of a drug. Biasing means 60 are configured to retract the syringe assembly 4 and the driver 10 relative to the housing 2 when drug delivery is complete. During retraction, the drive spring 8 continues to act on the driver 10 and urges a latching element 94 of the driver 10 to bear against a fixed, longitudinal guide element 90. At the end of retraction, the latching element 94 reaches the end of the guide element 90 and snaps behind a ledge 92, whereby the driver 10 and the syringe assembly 4 are prevented from advancing again.

Syringe drivers and injector devices are provided. The driver includes a housing including a port communicating with a gas chamber therein and connectable to an external air source, and a cavity that receives a syringe containing an agent. A drive piston within the housing includes a first end disposed adjacent the gas chamber and a second end including a plunger connectable to the syringe. A damping mechanism is provided within that housing that is coupled to the drive piston that includes a damper piston within a damping fluid chamber such that, when the drive piston is advanced by gas delivered into the gas chamber from the external source to deliver the agent from the syringe, damping fluid within the damping fluid chamber flows through an orifice or valve from a first region to the second region, thereby limiting movement of the drive piston.

The present disclosure relates to a medicament delivery device comprising a housing, a plunger, and an actuator moveable relative to the housing to urge the plunger to move in a first direction relative to the housing. The device comprises a drive mechanism configured such that, in use, the drive mechanism is operable to move the plunger in a second direction to expel medicament from the device. The device comprises a trigger configured such that, prior to movement of the actuator relative to the housing the trigger is prevented from being actuated to operate the drive mechanism, and such that once the actuator has been moved relative to the housing the trigger is permitted to be actuated by a user to operate the drive mechanism. The present disclosure also relates to a medicament delivery system and to a method of preparing a medicament delivery system.

This utility model discloses a portable syringe plunger auxiliary device, comprising: a base and a power supply module. A syringe holder and an electric plunger are mounted on the base; the syringe holder is configured to engage an injection syringe; the electric plunger is positioned such that its output shaft extends toward the syringe holder, and the electric plunger pushes the piston handle of the injection syringe engaged in the syringe holder toward the needle tip of the injection syringe; the power supply module is installed within the base and electrically connected to the electric plunger through a first power supply circuit, and the power supply module supplies power to the electric plunger. This utility model helps nursing personnel achieve a stable and uniform injection operation over a long period during subcutaneous injections.

The utility model relates to pen formula injection device technical field, concretely is a kind of dose setting and correction structure and injection device, dose setting and correction structure include: shell and dose setting ring, the double-direction ratchet wheel engagement tooth slot of being provided on the inner wall of shell one end, multiple curved arms are provided on dose setting ring, double-direction ratchet wheel tooth is provided on curved arm;Double-direction ratchet wheel tooth and double-direction ratchet wheel engagement tooth slot engage;When dose setting ring rotates one unit cell in time, double-direction ratchet wheel tooth is separated from current double-direction ratchet wheel engagement tooth slot, enters next double-direction ratchet wheel engagement tooth slot and is engaged, completes the setting of one unit cell dose;When dose setting ring rotates one unit cell in reverse, double-direction ratchet wheel tooth is separated from current double-direction ratchet wheel engagement tooth slot, retreats to last double-direction ratchet wheel engagement tooth slot and is engaged, completes the correction of one unit cell dose.The utility model can realize correction under dose setting error condition, improve injection accuracy, improve the use friendliness of injection device.

An assembly for a drug delivery device comprising a cap, having a first mark located on the outer surface of the cap, and a device body, having a second mark located on the outer surface of the device body, wherein the first and the second mark form a continuous marking, which extends form the device body to the cap, wherein the cap has first axial position relative to the device body, wherein the cap, when not in the first axial position relative to the device body, can be brought in the first axial position relative to the device body only when the first mark and the second mark form the continuous marking.

A drug delivery device may include a housing defining a longitudinal axis and having an opening and a drug storage container including a delivery member having an insertion end configured to extend at least partially through the opening during a delivery state. The device may also include plunger moveable toward the distal end of the drug storage container to expel a drug from the drug storage container through the delivery member, the plunger including a body portion having an inner wall defining an axial chamber and an outer wall cooperating with the inner wall to define a body thickness. The device may further include a plunger biasing member disposed at least partially within the axial chamber, the plunger biasing member configured to urge the plunger toward the distal end of the drug storage container.

The present disclosure provides a reading device adapted to read-out infrared readable data provided by a covered part of a movable component of a drug delivery device, wherein the reading device comprises at least one electromagnetic radiation source configured to emit infrared radiation and adapted to illuminate the infrared readable data on the covered part; at least one optical sensor unit configured to detect infrared radiation reflected from the covered part of the movable component; and at least one processing unit configured to determine a data value of the infrared readable data as a function of the detected reflected infrared radiation. The disclosure further provides a drug delivery device and a drug delivery device in combination with the reading device.