A fluid distribution system includes an input tube, a plurality of vessels, and a distribution hub. The input tube is configured to extend from a supply vessel. Each vessel of the plurality of vessels includes an inflow conduit. The distribution hub includes a single inlet and a plurality of outlets. The single inlet is defined in a bottom of the distribution hub and is in fluid communication with the input tube such that the distribution hub is configured to receive fluid from the input tube through the single inlet. Each outlet of the plurality of outlets is in fluid communication with the single inlet and in fluid communication with a respective inflow conduit such that the distribution hub is configured to provide an equal portion of the fluid received through the single inlet to each of the inflow conduits.

An exemplary compounding method of controlling a compounding device to prepare an admixture of at least two distinct material sources can include examining material source solutions for incompatibility of the ingredients and operating a first and a second pump to prevent one of the incompatible source solutions from entering a common flow path. The processing method can detect degradation of a fluid line by evaluating one or more of calibration error rate data, cumulative volumetric flow data, or cumulative pump operation data. The processing method can also selectively transfer a first group of source solutions using the first pump, receiving pump data from one or more sensors that sense actions of the pumps, applying fluid correction factors and calculating discrete pump movements, the pump movements being indicative of an amount of source solution displacement by a pump, and operating the pumps to selectively dispense the source solution amounts according to a preparation order.

An exemplary compounding method of controlling a compounding device to prepare an admixture of at least two distinct material sources can include examining material source solutions for incompatibility of the ingredients and operating a first and a second pump to prevent one of the incompatible source solutions from entering a common flow path. The processing method can detect degradation of a fluid line by evaluating one or more of calibration error rate data, cumulative volumetric flow data, or cumulative pump operation data. The processing method can also selectively transfer a first group of source solutions using the first pump, receiving pump data from one or more sensors that sense actions of the pumps, applying fluid correction factors and calculating discrete pump movements, the pump movements being indicative of an amount of source solution displacement by a pump, and operating the pumps to selectively dispense the source solution amounts according to a preparation order.

Medical device assemblies capable of aspirating liquid into a syringe barrel or other medical devices while evacuating any air from the syringe are described. An exemplary medical device includes a syringe barrel, plunger rod and stopper assembly having an air permeable and liquid impermeable porous portion and structure for forming a vacuum within either the stopper or the plunger rod. Described is a medical device including a syringe barrel, plunger rod and stopper assembly having an air permeable and liquid impermeable porous portion and structure for forming a vacuum within chamber between the stopper and plunger rod wherein the plunger rod includes a sealing edge and is moveable relative to the stopper. Exemplary medical devices may include a vent for allowing air that permeates through the porous portion to escape to atmosphere. Methods for aspirating a syringe barrel with a liquid are also provided.

Medical device assemblies capable of aspirating liquid into a syringe barrel or other medical devices while evacuating any air from the syringe are described. An exemplary medical device includes a syringe barrel, plunger rod and stopper assembly having an air permeable and liquid impermeable porous portion and structure for forming a vacuum within either the stopper or the plunger rod. Described is a medical device including a syringe barrel, plunger rod and stopper assembly having an air permeable and liquid impermeable porous portion and structure for forming a vacuum within chamber between the stopper and plunger rod wherein the plunger rod includes a sealing edge and is moveable relative to the stopper. Exemplary medical devices may include a vent for allowing air that permeates through the porous portion to escape to atmosphere. Methods for aspirating a syringe barrel with a liquid are also provided.

This invention relates to a fluid delivery apparatus, system and method, in particular the use of elastic bands to generate the force required to push fluid out from a container. The fluid that is delivered from the container maybe prefilled and stored prior to its actuation by the elastic band driver or it could be filled just before use. In one embodiment disclosed, a prefilled option would require the user to attach an appropriate extension tubing that acts as a flow control tube to the fluid container which in one embodiment is tubular shaped. In the application where the device is filled just before use, the fluid container that would be engaged with the actuating housing is presented with a fixed rate flow tube. The selection of a particular device configuration replaces the need for programming a flow rate into an electronic syringe pump.

This invention relates to a fluid delivery apparatus, system and method, in particular the use of elastic bands to generate the force required to push fluid out from a container. The fluid that is delivered from the container maybe prefilled and stored prior to its actuation by the elastic band driver or it could be filled just before use. In one embodiment disclosed, a prefilled option would require the user to attach an appropriate extension tubing that acts as a flow control tube to the fluid container which in one embodiment is tubular shaped. In the application where the device is filled just before use, the fluid container that would be engaged with the actuating housing is presented with a fixed rate flow tube. The selection of a particular device configuration replaces the need for programming a flow rate into an electronic syringe pump.

A conveyor and carriage assembly are synchronized to increase the speed of operation and eliminate any dwell periods to improve the rate at which a linear container filler is able to fill containers with a material. The fill rate approaches or exceeds that of prior art linear and rotary filling machines.

A conveyor and carriage assembly are synchronized to increase the speed of operation and eliminate any dwell periods to improve the rate at which a linear container filler is able to fill containers with a material. The fill rate approaches or exceeds that of prior art linear and rotary filling machines.

A cartridge handling machine for vape type cartridges is provided, which may comprise a filling module for filling of cartridge bodies with viscous consumable fluids, particularly oils extracted from hemp and cannabis and compositions thereof. The cartridge handling machine may also comprise a capping module to provide for synchronized filling of the filled cartridges and capping the cartridges with a cap, such as a mouthpiece or other cap device developed for such cartridges. The individual filling and capping modules can be operated independent of each other such that the cartridge handling machine preferably comprises both a filling module and capping module that preferably are integrated together for synchronized operation, although these modules may also be constructed and operated as separate machines for the respective filling and capping of these types of vape cartridges.