Koska Family Limited

Star Syringe Limited

Other

Marc Andrew Koska

Jay S Walker

Chelsea Carter

Graham John Madin

Jeff Price

Hanjin In

A fluid delivery manifold system assembled and configured to allow delivery of a single dose of a 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 manifold design consisting of separately constructed components cooperatively arranged and coupled to one another. The modular manifold construction allows for rapid manufacturing reconfigurations of one or more components with minimal costs to create new delivery manifold configurations that meet specific needs (i.e., different modes of delivery depending on agent to be delivered, such as subcutaneous, intramuscular, intradermal, intravenous injection, spray, or droplet delivery).

Systems and methods for fluid delivery manifolds

Sealed fluid container

The invention provides for a delivery system including a delivery assembly configured to allow delivery of a single dose of a therapeutic agent (e.g., vaccine, drug, medicament, etc.) from a Blow-Fill-Seal (BFS) vial to a patient.

Systems and methods for fluid delivery

The invention is a single use delivery device configured to enable reconstitution of a lyophilized agent (e.g., vaccine, drug, medicament, etc.) stored within for subsequent delivery of the reconstituted fluid agent to a patient in a controlled manner and without requiring specialized skill in reconstituting the agent or administering delivery of such agent. The delivery device is prefilled with an individual dose of a lyophilized agent and configured to be filled on-site and in the field with a dose of diluent for reconstitution of the lyophilized agent, while remaining sterile and preventing the potential for contamination during the filling process. The delivery device is further configured to be rendered incapable of reuse followings its intended use of delivering the fluid agent to a patient, thereby preventing reuse of the device and reducing the risk of the spreading blood-borne diseases through reuse.

Single use delivery device

The invention provides for a delivery system including a delivery assembly configured to allow delivery of a single dose of a 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. The modular construction allows for rapid manufacturing reconfigurations of one or more components with minimal costs to create new delivery assembly configurations that meet specific needs (i.e., different modes of delivery depending on agent to be delivered, such as subcutaneous, intramuscular, intradermal, intravenous injection, spray, or droplet delivery). The delivery assembly is generally configured to be filled on-site and in the field and is further capable of delivery of the agent in a controlled manner and without requiring specialized skill in administering delivery of such agent.

Single use delivery device prefilled with a reconstitutable agent

A needlestick prevention device for an injection device having a hollow needle comprises a sheath for attachment to the injection device. The sheath has three positions. In a first, inoperative position the sheath sealingly encloses the needle. In a second operative position a first part of the sheath is removed, a second part remains attached to the injection device and a third part is pivoted about a hinge to expose the needle. In a third, cover position the third part is pivoted about the hinge to cover at least the tip of the needle and is retained in position by a retaining device acting between the second part and the third part. The needlestick prevention device is simple to manufacture and use.

Needlestick prevention device

A syringe comprises a barrel with a plunger in slidable and sealing engagement therein, and a needle attached to one end of the barrel. The barrel has an aspiration device in the form of manually-operable resilient portions, which can be operated to cause a pressure differential in the barrel, the pressure differential then being used to perform aspiration. The resilient portions are preferably formed by localized reductions of wall thickness in the external surface of the barrel.

Syringe having a resilient part in order to facilitate an initial aspiration

A syringe comprises a barrel ( ) having a plunger ( ) in slidable and sealing engagement therewith. In order to provide an autodestruct system, so that the syringe can be used once only, being rendered disabled after one normal use, the barrel ( ) has means interrupting the cylindrical surface of its inner wall in the form of grooves ( ) or a projection ( ), and the plunger ( ) has a locking means ( ) which operates on engagement with a groove ( ) or projection ( ) on withdrawal of the plunger ( ) to prevent further withdrawal movement. The locking means ( ) is provided on the head of the plunger ( ) adjacent an elastomeric sealing cap ( ). The locking means may comprise a pair of flukes ( ) or a cross-shaped disc ( ).

Growing community of inventors

East Sussex, United Kingdom

Marc Andrew Koska