Various embodiments of a device for splitting fluid substances and methods thereof are described. In one example, a device for splitting fluid substances among syringes includes an input port, a number of output ports, and a fluid distribution network. The fluid distribution network is formed to convey a fluid substance from the input port to the output ports. The fluid distribution network can include a number of fluid distribution channels for conveying the fluid substance from the input port to the output ports. The fluid distribution channels can be formed in a star configuration, in one example, although other configurations are possible. The device provides a more efficient way to fill smaller syringes during procedures, such as fat grafting procedures. The device can be used to fill a number of syringes concurrently, decreasing the time required to perform an operation, among other benefits.

A system for priming an infusion pump is disclosed. The system includes a priming cap including a septum and configured to matably connect with a male part comprising a needle and attached to a length of tubing for fluid, wherein when matably connected with the male part, the priming cap occludes the tubing.

A fill adapter system for an infusion pump assembly. The system includes a reusable fill adapter base, the base including a volume control mechanism to adjust an available fill volume of a reservoir of the infusion pump assembly and a pump mechanism configured to pump air into a fluid vial. The system also includes a vial adapter assembly including a first needle configured to penetrate a septum of the fluid vial for fluidly coupling the pump mechanism to the fluid vial and a second needle having a first end configured to penetrate the septum of the fluid vial and a second end configured to penetrate a septum of the reservoir of the infusion pump assembly to allow transfer of fluid from the fluid vial to the reservoir of the infusion pump assembly in response to air being pumped into the fluid vial and a needle carriage adapted to carry the first needle and the second needle, wherein the needle carriage slidably attached to the interior of the vial adapter assembly, wherein the needle carriage adapted to slide from a vial end of the vial adapter to a receptacle end of the vial adapter.

A controlled multidosing delivery device for use with a syringe includes a housing, a plunger rod and a drive shell. The housing having an axially extending chamber including openings at either end, the distal end being adapted for attachment to the syringe barrel. The plunger rod includes a contact button at the proximal end of an elongated shaft and a pusher feature at the distal end. The drive shell is disposed for axial translation within the axially extending chamber. The drive shell includes a head disposed for translation along the axis to provide dose delivery, a plurality of engagement surfaces for engagement by the pushing feature, and a retention feature that inhibits proximal movement of the drive shell when engaged. Depression of the contact button axially translates the elongated shaft and pusher feature in engagement with the at least one of the engagement surfaces to translate the drive shell in the distal direction, whereby the retention feature engages to maintain axial position of the drive shell in the housing following dose delivery, and a biasing structure translates the plunger rod in the proximal direction following translation of the drive shell.

A method of preparing a prefilled syringe is disclosed that includes obtaining a syringe barrel and a needle adaptor cap assembled on the tip of the syringe barrel, wherein the needle adaptor cap has a rubber element tightly sealing the orifice of the tip of the syringe barrel and the syringe barrel together with the needle adaptor cap assembled on the tip of the syringe barrel is sterilized by a first sterilizing. Filling a drug substance into an interior of the syringe barrel and sealing the interior of the syringe barrel. Packaging the syringe barrel with a rubber stopper sealing the interior thereof and the needle adaptor cap assembled on the tip of the syringe barrel. Providing a second external surface sterilizing of the packaged syringe barrel with the rubber stopper sealing the interior thereof and the needle adaptor cap assembled on the tip of the syringe barrel.

A delivery device for delivery of medical agent to a barrier may comprise a main body including a central region defining a receptacle, a peripheral region defined by a number of petal members, and a set of retention tabs extending into the receptacle. The delivery device may further comprise a reservoir including at least one delivery sharp, a main interior volume, and at least one septum in fluid communication with the main interior volume. The reservoir may be coupled to the main body via the retention tabs. The delivery device may further comprise an adhesive coupled to the main body. The delivery device may further comprise at least one bias member positioned within the receptacle between the reservoir and a wall of the receptacle.

A syringe for withdrawing an aspirate from a body for micro fat grafting is provided. The syringe includes a barrel having an inner wall extending therein. The inner wall has one or more apertures formed therein allowing the aspirate to contact an absorbent positioned between the inner wall and an outer wall of the barrel. A plunger moves longitudinally within the barrel along the inner wall and has a gasket attached to a proximal end forming a seal against the inner wall. The absorbent may take many forms to absorb a non-fat cell portion of the aspirate. A related method includes retracting the plunger from a first position to draw the aspirate from a harvest site of a body into the barrel, exposing the aspirate to the absorbent, and moving the plunger toward the first position so a remaining portion of the aspirate is no longer exposed to the absorbent.

An apparatus (4) for sterilizing and assembling a cartridge (8) containing a medical substance to a device (12) for dispensing said medical substance, comprising: a cartridge (8) containing the medical substance to be dispensed, the cartridge being provided with a cap (24), a device (12) for dispensing said medical substance, the device being provided with at least one needle (28) configured to pierce the cap (24) of the cartridge (8) and allow the withdrawal of the medical substance from the cartridge (8), a first interface (32) that may be sealingly joined to the cap (24) of the cartridge (8) by means of the interposition of a first gasket (36), a second interface (40) joined to the dispensing device (12) near said needle (28), wherein the second interface (40) has a seal (44) that isolates the needle (28) from the external environment in a sterile volume (48), and is provided with a second gasket (52) which may be sealingly joined to the first interface (32) in order to identify a sealed chamber (56) delimited between a portion of the cap (24) facing said needle (28) and said seal (44), the second gasket (52) being external to said sterile volume (48), and a sterilizing device (80) configured to irradiate and sterilize said sealed chamber (56).

A closed system transfer device (CSTD) includes a barrel, a plunger, and a connecting port fixed to the barrel. The barrel includes a first cavity and a second cavity, which are separated. A piston of the plunger is operably moved within the first cavity and divides the first cavity into a first region and a second region that communicates with the second cavity. The connecting port includes a first channel communicating with the first cavity and a second channel communicating with the second cavity. When the CSTD is connected to a drug-liquid container to draw liquid, the first region is enlarged to draw the liquid into the first region from the container through the first channel. Simultaneously, the second region is reduced to discharge air in the second region to the container through the second cavity and the second channel. Thus, the CSTD and the container form a closed environment.

A device for filling a reservoir. The device includes a cover portion comprising a septum window, and a bottom portion, the bottom portion configured to attach to a disposable housing assembly comprising the reservoir, wherein the cover portion and the bottom portion are rotatably attached in a locked configuration and wherein in a locked configuration, a septum is obscured through the septum window, wherein when the cover portion and the bottom portion are placed in an unlocked configuration, the cover portion rotates with respect to the bottom portion and the septum is visible through the septum window.