Abstract: A food arrangement with at least one receptacle which is filled with a liquid, sterile food is described. The food arrangement has a connector, which is introduced into the receptacle and has a pierced membrane arranged in a filler neck. The food arrangement also has a tamper-evident seal, which is connected to the connector and closes the filler neck. Therefore, a sterile food arrangement is made available without the need for final autoclaving of the entire filled receptacle.

Abstract: A sealing cap for a container for holding a medical liquid includes a cap body and a connection device having a sealing element arranged on the cap body. The sealing element is arranged at the opening and is retained in the cap body in a clamped manner by a, preferably annular, flanged rim. The connection device has a break-off piece, which is firmly connected to the cap body and covers an outer face of the sealing element in the outward direction. The break-off piece is integral with the cap body, is connected to the cap body by a predetermined breaking point where the break-off piece can be detached from the cap body. The sealing element outer face is substantially flat and is accessible for wiping to provide a sealing cap having a sealing element arranged that can be simply and reliably disinfected.

Abstract: An infusion bag can be filled with a medical liquid. The infusion bag includes a connector having at least one port and a head piece as a lower part, and a connection region as an upper part. A sealing element is clamped between the upper part and the lower part. The lower part has a welded portion via which the lower part is connected to at least a first chamber of the infusion bag. Between the welded portion and the upper part, the lower part has a flexible region that can be clamped to form a body having shoulders and a neck. Between the sealing element and the flexible region is a pierceable membrane.

Abstract: A connector for a medical container is described. The connector includes a connector element defining an inner lumen extending axially from a first end of the connector element to a second end of the connector element that is opposite the first end. The connector element includes a fastening section at the first end of the connector element that is secured to the medical container, a pinch-off section extending from the fastening section towards the second end of the connector element, a head section extending from the pinch-off section towards the second end of the connector element, and a deflection element extending from the head section towards the first end of the connector element.

Abstract: A medical package is made from a multi-layer film and is filled with a medical liquid for infusion and/or for parenteral nutrition. The medical package has at least one weld seam and at least one inner layer of a matrix-phase polymer system, an intermediate layer of a matrix-phase polymer system, and an outer layer of a matrix-phase polymer system.

Abstract: Disclosed is a method and a system for producing an ampoule filled with a medical liquid. A preform is produced by plastic injection moulding that is then inhomogeneously heated and blown to form an ampoule body. Further disclosed is an ampoule produced by means of stretching and blowing, which comprises a connector with a break-off part in which the predetermined breaking point is aligned with the septum of the connector.

Abstract: A sealing cap for a container for holding a medical liquid comprises a cap body and a connection device having a sealing element arranged on the cap body. The sealing element is arranged at the opening and is retained in the cap body in a clamped manner by a, preferably annular, flanged rim. The connection device has a break-off piece, which is firmly connected to the cap body and covers an outer face of the sealing element in the outward direction. The break-off piece is integral with the cap body, is connected to the cap body by a predetermined breaking point where the break-off piece can be detached from the cap body. The sealing element outer face is substantially flat and is accessible for wiping to provide a sealing cap having a sealing element arranged that can be simply and reliably disinfected.

Abstract: Disclosed is a method and a system for producing an ampoule filled with a medical liquid. A preform is produced by plastic injection moulding that is then inhomogeneously heated and blown to form an ampoule body. Further disclosed is an ampoule produced by means of stretching and blowing, which comprises a connector with a break-off part in which the predetermined breaking point is aligned with the septum of the connector.

Abstract: The invention relates to a medical package designed as an infusion bag, which medical package is made from multi-layer films that are welded to one another and is filled with a medical liquid for infusion and/or for parenteral nutrition. The invention is described by a medical package designed as an infusion bag, which is made up of a film comprising multiple layers welded to one another and has at least one weld seam, preferably longitudinal and transverse weld seams, and is filled with a medical liquid. The multi-layer film has at least one inner layer of a matrix-phase polymer system, an intermediate layer of a matrix-phase polymer system, and an outer layer of a matrix-phase polymer system.

Abstract: A sealing element is received between a connector and an attachment member. The sealing element includes a foot section received by a recess of the connector, a shoulder engaging an inner surface of the attachment member, and a flange engaging a support surface of the connector. The sealing element also includes a cylindrical body extending from the shoulder to the flange along an insertion direction and, where the cylindrical body deforms to create a flow path through the sealing element, and a sealing head defines an opening that transitions from a closed state to an open state when the cylindrical body deforms.

Abstract: A sealing element is received between a connector and an attachment member. The sealing element includes a foot section received by a recess of the connector, a shoulder engaging an inner surface of the attachment member, and a flange engaging a support surface of the connector. The sealing element also includes a cylindrical body extending from the shoulder to the flange along an insertion direction and, where the cylindrical body deforms to create a flow path through the sealing element, and a sealing head defines an opening that transitions from a closed state to an open state when the cylindrical body deforms.

Abstract: A connector for a medical container is described. The connector includes a connector element defining an inner lumen extending axially from a first end of the connector element to a second end of the connector element that is opposite the first end. The connector element includes a fastening section at the first end of the connector element that is secured to the medical container, a pinch-off section extending from the fastening section towards the second end of the connector element, a head section extending from the pinch-off section towards the second end of the connector element, and a deflection element extending from the head section towards the first end of the connector element.

Abstract: The invention relates to a piston stopper (10) for a medical syringe (1) wherein the piston stopper (10) has an end wall (11), a lateral wall (12) and an internal thread (16) for securing a piston rod (7). The piston stopper (10) comprises a main body (10a) which made of a cycloolefin, in particular a cycloloefin copolymer or a cycloolefin polymer. A plurality of sealing rings (13a-13d) that are made from a plastic material extend around the main body of the piston (10) and are materially bonded to the main body of the piston (10a). The invention furthermore relates to a medical syringe (1) and to a method for the production thereof.

Abstract: A prefilled syringe and a method of filling a syringe with a pegfilgrastim solution to provide a target extracted volume of pegfilgrastim solution from the syringe are described. A method includes selecting the target extracted volume of pegfilgrastim solution, determining an estimated drug transfer loss, determining an estimated syringe dead volume, filling the syringe with a volume of pegfilgrastim solution comprising at least the target extracted volume plus the estimated drug transfer loss plus the estimated syringe dead volume.

Abstract: The invention relates to a syringe body having a nozzle and a threaded connection. The syringe body consists of an inner part and an outer part, the inner part comprising, at least in regions, a cycloolefin, in particular a cycloolefin copolymer or a cycloolefin polymer, as a first material. The first material forms an inner wall of the syringe body. The threaded connection of the outer part comprises, at least in regions, a material different from the cycloolefin as a second material. The invention further relates to a syringe having the syringe body.

Abstract: The invention relates to a piston stopper for a medical syringe. The piston stopper has an end wall, a side wall and an internal thread for securing a plunger rod, wherein the piston stopper is made of a butyl rubber. The end wall is conical in the distal direction both on the outside and on the inside. The end wall merges towards the side wall into a first sealing ring which extends around the circumference of the side wall. The side wall has at least three further sealing rings. Further, the invention relates to a medical syringe provided with the plunger stopper.

Abstract: The disclosure relates to a syringe, comprising a syringe body with a nozzle and a threaded connection. The syringe body comprises a side wall and a front wall, wherein the syringe body comprises a cycloolefin as a first material, at least in portions. The first material forms an internal wall of the syringe body. The threaded connection comprises, at least in portions, as a second material a material other than the cycloolefin, wherein the first and the second material are integrally bonded to one another. The second material extends in the region of the front wall at least in portions over the first material, so that the front wall comprises, at least in portions, a two-layer region. The first and the second material in the two-layer region have a mutually engaging structure.

Abstract: The invention relates to a connector for a medical packaging. The connector comprises an attachment part with a sealing element, the sealing element having a sealing head with at least one slit. The sealing head sits in an inner sleeve of the attachment part, the sealing head being adjoined by at least one trunk portion, which has a larger outer diameter than the sealing head. A gap is present between the at least one trunk portion and an opposite inner wall of the attachment part. An interior of the sealing element is free from a body with a tip that is intended to assist the opening of the sealing head. The attachment part has an outer sleeve which surrounds the inner sleeve and which has an internal thread.

Abstract: The invention relates to a packaging in the form of an infusion bag, having a connector for a vial, said connector having a spike for piercing the septum of the vial to establish a fluid connection to the inner volume of the infusion bag. The spike is designed to be rotatable. When the vial is rotated, the spike is rotated and the fluid connection between the vial and the inner volume of the infusion bag is opened.

Abstract: The invention relates to a connector for a medical package containing a liquid. The connector comprises a lower section which has a connecting piece for a container of said medical package and a passageway which is closed by a septum, as well as an upper section which is provided with a cap that covers the septum and can be broken off, said septum having, on a top side, a plurality of connections in the form of elevations, for a spike and/or for a needle.