A pouch for transporting and/or processing a biopharmaceutical fluid, the pouch comprising a flexible wall, the flexible wall comprising a shape memory material being adapted to change shape when induced by an external stimulus, so that the pouch can be alternately in a collapsed state and in an unfolded state, the wall of the pouch in the unfolded state delimiting a closed internal cavity adapted to contain the biopharmaceutical fluid.

A teething device can include a base having a handle, and a coupling on an opposite end. The base and coupling can be formed from a first material having a first hardness. A reservoir may be configured to contain a liquid therein. The reservoir may be coupled and sealed to the base coupling and configured to provide a watertight seal. The reservoir can have at least one self-sealing aperture. The self-sealing aperture can have a default position wherein the self-sealing aperture is configured to be substantially closed to essentially prevent the liquid from flowing therethrough, and a flexed position wherein the self-sealing aperture is configured to be opened to allow the liquid to flow therethrough. In addition, the reservoir can be formed from a second material having a second hardness that is softer than the first hardness.

The present application provides a unique way for storing cigars, and medicines in a portable environmental storage container system. The portable environmental storage container system can comprise a lid, an inner compartment, an outer container, electronics, and a bottom enclosure. An inner compartment can slide in and out of an outer container and seal shut with a seal keeping the inside of the container air tight with the humidity kept in when sealed, or the humidity out if none is desired. After the contents have been stored within the portable environmental storage container the user can monitor the contents inside the container with a portable computing device in real time.

An actively heated or cooled portable container has a body with a chamber that receives and holds a liquid, and one or more heating or cooling elements in thermal communication with at least a portion of the chamber. An outer surface of the body has one or more electrical contacts. A module is removably coupled to a portion of the body. The module has one or more electrical contacts on an outer surface of the module that contact the one or more electrical contacts on the outer surface of the body, control circuitry, and one or more power storage elements that provide power to the control circuitry and/or the one or more heating or cooling elements. The control circuitry wirelessly communicates with a mobile electronic device to wirelessly transmit information to the mobile electronic device associated with the operation of the module and/or wirelessly receive instructions from a user via the mobile electronic device.

A medical fluid storage and transportation enclosure can include a housing, a chamber, an exhaust duct, an inlet duct, and a valve. The housing can include walls defining a cavity, where the cavity can be configured to receive a medical product therein. The chamber can be adjacent to the cavity and can be configured to exchange heat with the cavity. The valve can be located in the inlet duct, where the valve can be movable in response to an air.

An improved baby bottle apparatus having a baby bottle adapted to be filled with a liquid and any chosen additives and then releasably attached to a base member with the base member adapted to releasably connect with the bottle member and heat a liquid to a desired temperature and stir the liquid to mix any chosen additives added to the liquid before a baby sucks on the nipple and drinks the liquid.

The baby bottle with mixer is an infant feeding bottle with an integral, controllable internal mixer. The baby bottle with a mixer includes a conventional bottle having an open upper end and a closed lower end, and a conventional cap for releasably covering and sealing the open upper end of the bottle. An internal wall is mounted within the bottle such that a fluid-tight chamber is defined between a lower surface of the internal wall and the closed lower end of the bottle. An agitator is rotatably mounted on an upper surface of the internal wall, and the agitator is selectively driven by a motor, which is housed within the fluid-tight chamber. A speaker is mounted on the closed lower end of the bottle for playing music, soothing sounds or the like while the baby is being fed. A controller is in communication with the speaker and the motor.

An apparatus, comprising an environmental control element configured to control at least one environmental condition of a substance contained within a chamber, the environmental control element includes a thermal insulator configured to provide a thermal shield to the substance and a phase change material (PCM) configured to thermally regulate at least one environmental condition. The environmental control element is configured to control the environmental condition without use of an external power source, and the PCM is configured to return to its solid phase without user intervention.

An apparatus for heating beverages is disclosed. The apparatus includes a base and a container for holding liquids. The base has a heater plate that is heated by one or more heater elements attached to the heater plate. A power source in the base provides electricity to the heater elements. The base is removably attachable to the container. The container has an inner cup that sits inside a chassis. The inner cup is made of metal and has an open top for receiving liquid, a circumferential wall, and a closed bottom. The chassis has an open top for receiving a liquid, a circumferential wall, and an open bottom. When the container is attached to the base, the closed bottom of the inner cup is configured to contact the heater plate and receive heat from the heater plate.

A method of storing and warming a sterile corticotropin composition by storing the sterile corticotropin composition in a multiple-dose vial comprising 80 USP units/mL of the sterile corticotropin composition, wherein the vial comprises a rubber stopper coated with cross-linked silicones, at a temperature of 2? to 8? C.; and warming the vial to a temperature of 18? to 26? C., wherein the corticotropin comprises amino acids 1-39 of SEQ ID NO: 1, or wherein the sterile corticotropin composition has not more than 0.05 USP Vasopressin Units/USP Corticotropin Units.