The present disclosure is directed to a flexible cap for a medical fitting, such as a luer-lock fitting. The flexible cap includes a cap component defining a top surface, a cylindrical wall extending opposite from the top surface of the cap component, and an inner sealing surface. The cylindrical wall defines a hollow interior configured to receive an internal tapered sealing wall of a male connector of the medical fitting so as to form a seal with an outer surface of the tapered sealing wall. Further, the inner sealing surface of the flexible cap is configured within the hollow interior. Thus, when the tapered sealing wall of the male connector of the medical fitting is received within the hollow interior of the cylindrical wall, the inner sealing surface of the flexible cap seals the fluid passageway of the tapered sealing wall.

An applicator syringe (1) is disclosed containing a sterile solution having a medical active substance, in particular for introducing the solution containing the active substance via a urinary tract and/or bladder catheter into the bladder of a patient. The applicator syringe (1) includes a cylindrical jacket (2), which is closed by a syringe cover (3), which is integrally formed with the jacket (2) and includes an outlet opening (5) and is formed from a cycloolefin copolymer (COC). The applicator syringe (1) furthermore comprises a plunger tip made of an isobutene-isoprene rubber, which is halogenated in particular. The sterile solution containing the medical active substance is arranged in a cavity (6) delimited by the cylindrical jacket (2) having syringe cover (3) and the plunger tip.

A package includes a tray having a plurality of openings and a plurality of barrel covers. Each of the plurality of barrel covers extend through one of the plurality of openings. A tub can receive the tray. A plurality of tamper evident devices can be attached to the plurality of barrel covers. Each tamper evident device includes a collar, a tamper evident cap, and a frangible connection between the collar and the tamper evident cap. A method of packaging a plurality of syringe bodies includes inserting the plurality of syringe bodies into a plurality of barrel covers positioned in a tray, and inserting the tray into a tub.

A syringe assembly and methods of producing the syringe assembly are described. The syringe assembly may include a syringe body, a plunger rod, a barrel cover, and a tamper evident device. The syringe body has a chamber configured to receive a material. The plunger rod moves within the chamber to dispense the material. The barrel cover covers the syringe body. The backstop is attached to the barrel cover to prevent a portion of the plunger rod from moving proximally through the backstop. The tamper evident device includes a tamper evident cap covering a distal portion of the syringe body, a collar attached to the barrel cover, and a frangible connection between the tamper evident cap and the collar.

An assembly for a drug delivery device comprises a housing, a dose member which is displaceable in a proximal direction with respect to the housing for setting of a dose of a drug, a clutch member which is displaced in the proximal direction with respect to the housing when setting the dose, and a stop member configured to define a clutch stop position. The clutch member and the dose member are configured to mechanically cooperate with one another when the clutch member is in the clutch stop position, thereby preventing further displacement of the dose member in the proximal direction with respect to the housing during setting of the dose.

A cartridge for use with a beneficial agent delivery device having a fillable reservoir. The cartridge includes a reconstitution, unit dose package having first and second compartments and a fitment. The first compartment contains at least a first constituent of the beneficial agent. The second compartment contains at least a second constituent of the beneficial agent. The fitment is disposed on the package for interfacing the package to the fillable reservoir.

A syringe assembly including: (1) a syringe barrel defining a chamber; (2) a plunger mounted in the chamber and moveable with respect to the barrel; and (3) a cap holder assembly containing a cap and an absorbent material removably attached to the syringe.

The invention provides a syringe for use in an ophthalmic injection. The syringe comprises a body, a stopper and a plunger. The body comprises an outlet at an outlet end and the stopper is arranged within the body such that a front surface of the stopper and the body define a variable volume chamber from which a fluid can be expelled though the outlet. The plunger comprises a plunger contact surface at a first end and a rod extends between the plunger contact surface and a rear portion. The plunger contact surface is arranged to contact the stopper but not couple thereto, such that the plunger can be used to force the stopper towards the outlet end of the body, reducing the volume of the variable volume chamber, but not to move the stopper away from the outlet end.

Flush syringe assemblies are described herein. Such flush syringe assembly may include a barrel including a side wall defining a chamber, a collar mounted on a distal wall of the barrel and surrounding an elongate tip. A cap may be attached to the collar via a hinge. The flush syringe assembly may also include a cap attached to the collar via a hinge. A ring may be disposed around the collar with a locking element that engages with a corresponding mating locking projection on the cap. The cap may include a slanted surface. The slanted surface of the cap may include one or more ribs made of an elastomeric material.

A connection structure of a medical container includes a liquid medicine containing part that contains a liquid medicine and a liquid medicine discharge part that discharges the liquid medicine includes: a sealing member including a mounting part to be mounted to cover the outside of the liquid medicine discharge part, an opening formed in the mounting part in an extending direction of the liquid medicine discharge part, and an elastic sealing body disposed in a space between the opening and the liquid medicine discharge part and sealing the liquid medicine discharge part; and a connector including a connection needle that punctures the elastic sealing body, and a needle hub that holds the connection needle, in which the connector has a push-in structure that compresses the elastic sealing body when the connection needle punctures the elastic sealing body.