A61M2005/3117

Method for Reducing an Amount of Subvisible Particles in a Pharmaceutical Composition

The invention relates to a method for reducing an amount of sub visible particles in a pharmaceutical composition contained in a medical injection device comprising a container (1) including a barrel (10) lubricated with a lubricant coating (2) in contact with the pharmaceutical composition, and a stopper (14) in sliding engagement within the barrel (10), the container comprising a region (130, 121, 123) extending distally from the distal end (100) of the barrel which is not accessible to the stopper. During formation of said lubricant coating (2) on the inner wall of the barrel, the method comprises limiting lubricant from being deposited into said region (130, 121, 123) extending distally from the distal end (100) of the barrel.

Syringe assembly

A syringe assembly includes a plunger assembly, a syringe body, and a needle. The plunger assembly includes a plunger rod, a spring, a plunger base, and a plunger plug. The plunger rod includes a first end member having a first stepped part positioned in an inner wall thereof, a second end member, and a first accommodating room. The plunger base includes a plunger body, a projection, a second stepped part, a plunger member, and a locating member. The plunger body is received in the first accommodating room, and the projection abuts against the first end member. The spring is arranged around the plunger body and positioned between the first stepped part and the second stepped part. The plunger plug is mounted to the second end member, and defines a fixing groove. The syringe body includes a needle cannula, a needle base, a fixing pole, and a fixing valve. The plunger assembly is received in the needle cannula. The needle base is mounted to the needle cannula. The fixing valve is received in the needle base. The fixing pole is received in the fixing valve and protrudes out of the needle base. The needle is received in the fixing pole. The syringe assembly of the present invention is prevented from reuse and accidently damage because the needle can retract into the plunger rod using restoring force of the spring.

Attachable plunger rod and associated packaging

A syringe assembly including a plunger rod separate and detached from a syringe barrel and a packaging member, the plunger rod having a sealing member and the packaging member having a first compartment and a second compartment is disclosed. With the syringe barrel received within the first compartment and the plunger rod received within the second compartment, the sealing member of the plunger rod seals the syringe barrel and the plunger rod within the packaging member. In this manner, the syringe assembly is placed in the packaging member in a manner that allows for reduced storage space of the syringe assembly.

DISPOSABLE PROTECTIVE ASSEMBLY APPARATUS FOR A DENTAL SYRINGE

Embodiments disclose a disposable protective assembly apparatus for a dental syringe body of a dental syringe. The apparatus is a combination of a disposable syringe tip and a disposable protective sleeve, the sleeve being pre-attached to the syringe tip, and the sleeve being in a pre-folded position to be quickly and easily slid over the dental syringe prior to a dental operation.

SEALING ARRANGEMENT FOR SYRINGE

A syringe containing a high water content product and for use in a drug infusion system is provided. The syringe includes a plunger carrying front and rear o-rings made of a diene rubber compound such as chlorobutyl rubber or bromobutyl rubber to impart very low gas permeability characteristics to the o-rings. The plunger may be molded as a single part or in two parts. If molded as one part with radially-engaging mold portions, the seal glands in the plunger may include parting lines from the mold. If molded as two parts with axially-engaging mold portions, the front seal gland may include a sealing surface and under cut that has no parting line. The orings may be surface treated with a lubricant to improve sealing where the molding process gives rise to parting lines in the seal glands.

Flush Syringe With Disinfecting Feature
20190232039 · 2019-08-01 ·

Flush syringe assemblies are described herein. Such flush syringe assembly may include a barrel including a side wall defining a chamber, an open proximal end, a distal end having a distal wall with an elongate tip extending distally therefrom having a passageway therethrough in fluid communication with said chamber. A collar may be mounted on the distal wall of the barrel and surrounding the elongate tip. A disinfectant-loaded swab may be disposed in the collar. The flush syringe assembly may also include a removable cap.

Combination Plunger Device For A Dual Chamber Mixing Syringe

A combination plunger, a mixing device and a mixing syringe including the same are provided. The mixing syringe includes concentric outer and inner barrels that form an outer chamber, the inner barrel having an inner chamber. The combination plunger includes a mixing plunger and a delivery plunger and a biasing means. The mixing plunger is slidably located in the outer chamber and translated by coordinated depression of the delivery plunger to transfer a first substance from the outer chamber to mix with a second substance in the inner chamber. After the mixing stage is complete, the delivery plunger is disengaged from the mixing plunger and permitted, such as by rotation, to be further depressed in the axial direction to deliver fluid contents of the mixing syringe to a recipient. The mixing syringe needle is then retracted as result of engagement by the delivery plunger and activation of the biasing means.

DISINFECTING CAP FOR MEDICAL CONNECTORS

A disinfecting cap accepts a needleless injection site to apply an antiseptic agent. The cap includes a breakable seal located in a chamber between the proximal and distal portions so as to be spaced away from the opening. The cap body may include a compliant wall that deforms when a needleless injection site is inserted into the opening to removably hold the cap on the needleless injection site. In lieu of a compliant wall, a flexible skirt may extend from the cap body into the proximal portion, so that when a needleless injection site is inserted into the opening, the flexible skirt engages the outer diameter of the needleless injection site to removably hold the cap on the needleless injection site. A carrier strip may be used, wherein each of the plurality of disinfecting caps is removably attached at its proximal end to the carrier strip.

Cover biasing means for an apparatus

The invention relates to an Apparatus, especially a delivery device, comprising a housing (4100), a retainer (4200, 4200) for holding a cartridge (4220, 4220), a cover part (4240, 4240) for accessing the retainer (4200, 4200), the cover part (4240, 4240) being moveable relative to the housing (4100) between an open and a closed position, wherein the apparatus further comprises cover part biasing means for exerting a biasing force onto the cover part (4240, 4240) in the closed position to bias the cover part (4240, 4240) inwardly and/or distally against the housing (4100).

Sterility enhanced closure for a fluid path

A syringe assembly includes a syringe having a body with a proximal end and a distal end and a discharge outlet formed at the distal end of the syringe. The syringe assembly further includes a closure element having a body configured for removable engagement with at least a portion of the discharge outlet. The body of the closure element is porous to define a tortuous internal path through the body to allow venting of excess pressure within the syringe while preventing pathogens from entering the syringe. The discharge outlet is configured as a luer connector and the closure element has at least one engagement feature for engaging the luer connector.