Systems and methods are provided for filling syringes, e.g., for use during pneumatic retinopexy or other medical procedures. In one embodiment, the system includes a housing carrying a gas canister including an outlet communicating with a fluid path extending from the outlet to a syringe cavity. A syringe includes a barrel receivable in the syringe cavity such that a port of the barrel communicates with the fluid path. An actuator is provided on the housing for selectively opening the outlet of the gas canister to deliver gas therein along the fluid path into the interior of the barrel, thereby causing the plunger to move from a distal position to a proximal position.

Disclosed herein are otic product kits for administration of a sterilized formulation. In some embodiments, the otic product kit comprises: an aseptic container containing the sterilized formulation; a syringe; and an administration needle connectable to the syringe, wherein the sterilized formulation comprising: from about 5.5 wt % to about 6.5 wt % multiparticulate ciprofloxacin; from about 15 wt % to about 17 wt % poloxamer 407; and water. Also disclosed herein are methods of preparing and administrating the sterilized formulation. In some embodiments, the method comprising (1) transferring the sterilized otic formulation from an aseptic container to a syringe through a preparation needle; (2) replacing the preparation needle with an administration needle; and (3) injecting the sterilized otic formulation from the syringe through the administration needle into the ear of a patient.

A closed-system grinding syringe (10, 110) is provided for liquefying and delivering a solid dosage form (20), including a barrel (22), a fluid port (30) disposed on a bottom wall (28) of the barrel (22), and a plunger (32). A head (36) of the plunger (32) is insertable into and moveable within the barrel (22) such that (a) a portion of the barrel (22) defines a closed-system syringe chamber (46) between the bottom barrel wall (28) and a lower surface (64) of the plunger head (36), and (b) a plunger-head annular seal (42) forms a fluid-tight seal between an outer surface (44) of the plunger head (36) and a cylindrical inner surface (26) of the barrel (22). A solid-dosage-form support disc (60, 360) is disposed below a bottom plunger wall (38) so as to define a grinding compartment (62) between the lower surface (64) of the bottom plunger wall (38) and an upper surface (66) of the solid-dosage-form support disc (60, 360), and is shaped so as to define a plurality of holes (68, 368) through the solid-dosage-form support disc (60, 360).

An apparatus for filling a syringe with a verified dose of radiant fluid has a container holder that holds a container of the radiant fluid wherein a syringe oriented at a septum of the container can penetrate the septum. The syringe holder is configured to continuously grip the syringe, to drive the syringe to the container holder and penetrate the septum, to fill the syringe with a dose of the radiant fluid from the container, to drive the syringe to a transfer post, to drive the syringe to a metering zone of a metering station in order to verify that measured radiation is compatible with the dose, and to release the continuous grip.

[Problem] To provide an economic suction adaptor that is capable of suctioning a highly viscous enteral nutrient to a gastric fistula catheter syringe without the intake of air.

[Solution] The number of people having meals of highly viscous enteral nutrients such as blended diets through a gastric fistula catheter is increasing among pediatric patients who need long-term intubation nutrients, and among elderly people who have trouble with oral intake. Suctioning a blended diet on a dish with a syringe alone is undesirable because air is introduced. The suction adaptor of the present invention is used by being connected to the syringe, wherein a suction tube having, on an upper portion thereof, a connection part connected to a nozzle of the syringe is formed in the middle of a bowl-shaped suction pad which is an elastic body.

A prefilled syringe includes a tubular containment body extending along an axis between a front end element and a rear end element, a fixed plug and two sliding plugs. A bypass channel in the initial position of the syringe is between the first two plugs which form, together with a third plug at the end of the syringe plunger, a first containment chamber containing a first liquid substance and a second containment chamber containing a second solid or liquid substance. The fixed plug is in contact with the front end element and is provided with a non-through cavity offset with respect to the axis and facing towards the front end element.

A syringe rack securable to a surface of a fixture and configured for facilitating a sterile transfer of fluid from a non-sterile environment to a sterile environment. The syringe rack includes a securing portion and a syringe-receiving station. The syringe-receiving portion is coupled to the securing portion and configured to receive the syringe in a selectively releasable coupling arrangement where the syringe is oriented such that an opening in a barrel of a syringe projects away from the fixture when the syringe is received by the syringe-receiving station and when the securing portion is secured to the surface of the fixture.

Provided is a micro-jet drug injection device comprising: a pressure chamber having a pressure driving liquid hermetically filled therein; a drug chamber having a micro nozzle defined in a wall; an elastic membrane elastically expandable and restorable and to separate the pressure chamber from the drug chamber; an energy-focusing unit concentrating energy on the pressure driving liquid in the pressure chamber; and the storage unit supplying the drug solution therein into the drug chamber through a drug supply channel. The drug chamber has a partial inner space defined therein. The partial inner space is in fluid communication with the drug supply channel and is partially defined by the membrane. A nozzle closure is disposed inside or outside the drug chamber. The nozzle closure blocks inflow of air outside the micro-nozzle into the partial inner space after the elastic membrane has expanded and before elastic recovery of the membrane is completed.

A dual-needle syringe capable of preventing infection, including: an infusion needle shaft (3) configured to aspirate a liquid from a drug container (30); an injection needle shaft (5) having a sharp point of one end inserted into a body, and the other end connected to the syringe (10), through which the liquid filled in the syringe (10) is injected into a body; a hub barrel (7) engaged to a barrel (15) of the syringe (10) to infuse the liquid, which is aspirated from the drug container (30) through the infusion needle shaft (3), into the syringe (10) through the injection needle shaft (5), the hub barrel having an infusion needle shaft hub (21) and an injection needle shaft hub (23) which can be separated from each other before the liquid is injected; and a filter (9) configured to filter foreign substances contained in the liquid.

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.