Abstract: A method of manufacturing a syringe for use in enteral feeding includes providing a premolded syringe body having a plunger end and an outlet end, loading the premolded syringe body into a mold having a core pin extending into the outlet end of the premolded syringe body, closing the mold to thereby retain the premolded syringe therein and to close a mold cavity around the outlet end of the syringe body, injection molding by injecting plastic molding material into the mold cavity and cooling to thereby form a tip at the outlet end of the premolded syringe body, and opening the mold and extracting the syringe body and the tip.

Abstract: A method of manufacturing a syringe for use in enteral feeding includes providing a premolded syringe body having a plunger end and an outlet end, loading the premolded syringe body into a mold having a core pin extending into the outlet end of the premolded syringe body, closing the mold to thereby retain the premolded syringe therein and to close a mold cavity around the outlet end of the syringe body, injection molding by injecting plastic molding material into the mold cavity and cooling to thereby form a tip at the outlet end of the premolded syringe body, and opening the mold and extracting the syringe body and the tip.

Abstract: A safety needle device for percutaneous drug delivery to a patient includes a housing that is slidably mounted on a second portion of a substantially L-shaped, hollow needle for drug delivery. The housing includes a chamber provided between a sleeve portion and a passage. A forward end of the needle, which includes a tip, must deflect in order to pass through the passage into the chamber. The forward end of the needle is restricted from exiting the chamber through the sleeve portion and through the passage.

Abstract: A method of manufacturing a syringe for use in enteral feeding includes providing a premolded syringe body having a plunger end and an outlet end, loading the premolded syringe body into a mold having a core pin extending into the outlet end of the premolded syringe body, closing the mold to thereby retain the premolded syringe therein and to close a mold cavity around the outlet end of the syringe body, injection molding by injecting plastic molding material into the mold cavity and cooling to thereby form a tip at the outlet end of the premolded syringe body, and opening the mold and extracting the syringe body and the tip.

Abstract: An enteral connector includes a body defining a passageway therethrough. The body has an inlet segment defining an inlet opening of the passageway, suitable for connection of an enteral feeder such as an enteral feeding extension set or an enteral-only syringe. The body also has an outlet segment including a stem projecting from the inlet segment and a frustoconical tip defining an outlet opening of the passageway, for connecting to an enteral feeding tube or a tube of an enteral feeding extension set. The enteral connector also includes a cap having an external cover for covering the outside of the inlet segment and a plug integral with and extending from the external cover for inserting into the inlet opening. The cap is connected to and integral with the body by an intermediate flexible neck.

Abstract: A safety needle device for percutaneous drug delivery to a patient includes a housing that is slidably mounted on a second portion of a substantially L-shaped, hollow needle for drug delivery. The housing includes a chamber provided between a sleeve portion and a passage. A forward end of the needle, which includes a tip, must deflect in order to pass through the passage into the chamber. The forward end of the needle is restricted from exiting the chamber through the sleeve portion and through the passage.

Abstract: There is provided a needle device for percutaneous drug delivery to a patient. The device comprises a substantially L-shaped, hollow needle for drug delivery therethrough and a body. The needle includes a needle end and the body is secured to the needle and longitudinally spaced from the needle end. The body includes an integral pair of flexible handles adapted to be grasped for insertion of the needle device into and removal of the device from the patient.

Abstract: A medical intravenous injection site is provided having a single piece elastomeric septum and valve combination element. The septum has a slit therein, through which a blunt cannula or a male luer slip or male luer taper can be inserted. A valve element is suspended below the septum by straps extending between the septum and valve element, and formed integrally with them as a single, one-piece elastomeric septum, valve, and strap structure. When the blunt cannula is inserted through the slit in the septum, the valve portion will be displaced away from the septum portion, and away from a valve seat formed in the interior of a substantially rigid housing in which the septum and valve structure is mounted. Fluid communication, in either direction past the valve seat, may therefore be established. Because the septum is mounted across the end of the rigid housing, it is wipeable.