A drug mixing system including at least one receptacle port adaptor adapted to be inserted into a port of a fluid receptacle, at least one syringe adaptor adapted to be attached to a syringe and to the at least one receptacle port adaptor and at least one vial adaptor adapted for connection to a vial containing a drug and adapted for connection to the at least one syringe adaptor, the system being characterized in that at least one of the receptacle port adaptor, the at least one syringe adaptor and the at least one vial adaptor being vented to the atmosphere in a manner which prevents release to the atmosphere of possibly harmful contents of the vial in a liquid, solid or gaseous form.

This document relates to methods and materials for improving the removal of gas from cryogenic freezing bags. For example, this document describes methods and devices for restricting air paths within the cryogenic freezing bag.

The present invention relates to a bag (1) for the production of baby food, specifically baby milk or baby puree, comprising a first chamber (3) and a second chamber (5), which are separated from one another other by a separating region (7), wherein the first chamber (3) is which is designed to receive a baby food concentrate, wherein the second chamber (5) is designed to receive a fluid, wherein the first and second chamber (3, 5) are arranged along the longitudinal direction (L) of the bag (1); wherein the separating region (7) can be at least partially opened by the applying force to the bag (1) in order to be able to mix the components contained in the first and second chamber (3, 5) to form baby food, wherein the bag (1) has a first opening (11) at a first end (9) located adjacent to the first chamber (3) and a second opening (15) at a second end (13) located adjacent to the second chamber (5), and wherein the first opening (11) can be closed by means of a first closure and the second opening (15) can be closed by means of a second closure.

Furthermore, the invention relates to a device for tempering baby food and a process for producing baby food.

This document relates to methods and materials for improving the removal of gas from cryogenic freezing bags. For example, this document describes methods and devices for restricting air paths within the cryogenic freezing bag.

This document relates to methods and materials for improving the removal of gas from cryogenic freezing bags. For example, this document describes methods and devices for restricting air paths within the cryogenic freezing bag.

A drug mixing system including at least one receptacle port adaptor adapted to be inserted into a port of a fluid receptacle, at least one syringe adaptor adapted to be attached to a syringe and to the at least one receptacle port adaptor and at least one vial adaptor adapted for connection to a vial containing a drug and adapted for connection to the at least one syringe adaptor, the system being characterized in that at least one of the receptacle port adaptor, the at least one syringe adaptor and the at least one vial adaptor being vented to the atmosphere in a manner which prevents release to the atmosphere of possibly harmful contents of the vial in a liquid, solid or gaseous form.

A lyophilization bag is provided herein for containing a solution in a lyophilizer during lyophilization. The lyophilization bag includes a body having a flexible base member, and a flexible top member. The base member and the top member, collectively, at least partially encompass an interior volume of the body. A first portion of the interior volume is defined between at least portions of the base member and a reference plane located spaced from the at least portions of the base member, the first portion of the interior volume defining a volume corresponding to the initial volume of the solution. A second portion of the interior volume is defined between the reference plane and at least portions of the top member. At least one port defining an opening is in communication with the second portion of the interior volume.

A drug mixing system including at least one receptacle port adaptor adapted to be inserted into a port of a fluid receptacle, at least one syringe adaptor adapted to be attached to a syringe and to the at least one receptacle port adaptor and at least one vial adaptor adapted for connection to a vial containing a drug and adapted for connection to the at least one syringe adaptor, the system being characterized in that at least one of the receptacle port adaptor, the at least one syringe adaptor and the at least one vial adaptor being vented to the atmosphere in a manner which prevents release to the atmosphere of possibly harmful contents of the vial in a liquid, solid or gaseous form.

A fluid transfer assembly, drug container, and method for enabling fluid transfer in an infusion system is taught. The assembly includes a fluid container containing an infusion fluid, and a drug container. The fluid container has at least one inlet port for receiving a medical substance from the drug container. The assembly further includes at least one fluid barrier controlling fluid passage between the drug container and the fluid container. The inlet port exhibits a first luer-lock connector, and the drug a container is sealed by a cap exhibiting a second luer-lock connector for attachment to the first luer-lock connector. The fluid barrier is designed and arranged to be ruptured by an external force to allow the fluid passage.

Bag for providing patient-specific, in particular oncological drugs, with an interior divided into a plurality of, preferably four, separate chambers interior, wherein in at least one, preferably three chambers an infusion solution can be provided and patient-specific active substances can be added.