An intravenous (IV) fluid delivery system include first and second IV bags and a fluid delivery device. The IV bags are made of many fluidic channels that keep the fluid distributed across the bags such that the bags may be easily and comfortably wrapped around the arm and shoulder of a person. The fluid delivery device includes a processor controlled electromechanical delivery mechanism that controls a positive displacement pump. The pump moves the fluid into a tube and a needle that is connected to a person's vein. The processor repeatedly turns the pump on or off to gradually transfer the fluid from the IV bags into the person's vein. The processor controls the granularity of the fluid delivery, where the fluid may be administered in a fluid delivery period, the fluid delivery may then be stopped in a subsequent fluid stoppage period, followed by other fluid delivery periods.

An intravenous (IV) fluid delivery system include first and second IV bags and a fluid delivery device. The IV bags are made of many fluidic channels that keep the fluid distributed across the bags such that the bags may be easily and comfortably wrapped around the arm and shoulder of a person. The fluid delivery device includes a processor controlled electromechanical delivery mechanism that controls a positive displacement pump. The pump moves the fluid into a tube and a needle that is connected to a person's vein. The processor repeatedly turns the pump on or off to gradually transfer the fluid from the IV bags into the person's vein. The processor controls the granularity of the fluid delivery, where the fluid may be administered in a fluid delivery period, the fluid delivery may then be stopped in a subsequent fluid stoppage period, followed by other fluid delivery periods.

The assembly comprises: a stand for hanging a container of a main liquid, a spike, to be introduced into the container of main liquid, a multi-inlet connector with inlet tubings, to be connected to containers of additional liquids and to the container of main liquid through the spike, and an outlet tubing to be connected to a luer syringe to be introduced into a patient. The length of the spike inlet tubing of the connector has a length determined for, during use of the assembly with a container of main liquid, keeping the connector hung up on the stand through the spike and the container of main liquid. Thanks to the invention, the problem of the tubing traffic is solved.

The assembly comprises: a stand for hanging a container of a main liquid, a spike, to be introduced into the container of main liquid, a multi-inlet connector with inlet tubings, to be connected to containers of additional liquids and to the container of main liquid through the spike, and an outlet tubing to be connected to a luer syringe to be introduced into a patient. The length of the spike inlet tubing of the connector has a length determined for, during use of the assembly with a container of main liquid, keeping the connector hung up on the stand through the spike and the container of main liquid. Thanks to the invention, the problem of the tubing traffic is solved.

A user-initiated fluid pathway connection includes: a connection hub, a piercing member, a sterile sleeve, and a drug container having a cap, a pierceable seal, a barrel, and a plunger seal, wherein the piercing member is initially retained within the sterile sleeve between the connection hub and the pierceable seal of the drug container. The connection hub may include an internal aperture within the connection hub which functions as a flow restrictor and wherein a piercing member is connected to one end of the internal aperture and a fluid conduit is connected to another end of the internal aperture. A drug delivery pump with integrated sterility maintenance features includes a housing, upon which an activation mechanism, an insertion mechanism, a fluid pathway connection as described above, a power and control system, and a drive mechanism connected to a drug container are mounted. Methods of assembly and operation are also provided.

A user-initiated fluid pathway connection includes: a connection hub, a piercing member, a sterile sleeve, and a drug container having a cap, a pierceable seal, a barrel, and a plunger seal, wherein the piercing member is initially retained within the sterile sleeve between the connection hub and the pierceable seal of the drug container. The connection hub may include an internal aperture within the connection hub which functions as a flow restrictor and wherein a piercing member is connected to one end of the internal aperture and a fluid conduit is connected to another end of the internal aperture. A drug delivery pump with integrated sterility maintenance features includes a housing, upon which an activation mechanism, an insertion mechanism, a fluid pathway connection as described above, a power and control system, and a drive mechanism connected to a drug container are mounted. Methods of assembly and operation are also provided.

Drug delivery devices and related methods of assembly are disclosed. The drug delivery device may include a container including a wall with an interior surface and a seal member with an end surface. The interior surface of the wall and the end surface of the seal member may define a reservoir filled with a drug. A fluid pathway assembly may be connected to the container and include an overmold member that covers a length of a container access needle and which defines an enclosed space with the seal member. The overmold member may be moveable relative to the seal member to carry the container access needle between a storage position, where a point of the container access needle is disposed exterior to the reservoir, and a delivery position, where the point extends through the end surface of the seal member into the reservoir.

Drug delivery devices and related methods of assembly are disclosed. The drug delivery device may include a container including a wall with an interior surface and a seal member with an end surface. The interior surface of the wall and the end surface of the seal member may define a reservoir filled with a drug. A fluid pathway assembly may be connected to the container and include an overmold member that covers a length of a container access needle and which defines an enclosed space with the seal member. The overmold member may be moveable relative to the seal member to carry the container access needle between a storage position, where a point of the container access needle is disposed exterior to the reservoir, and a delivery position, where the point extends through the end surface of the seal member into the reservoir.

There is provided a medicinal liquid injection port to be implanted subcutaneously. A housing main body is provided with a medicinal liquid storage portion therein, an opening portion that opens the medicinal liquid storage portion, and a discharge hole that communicates with the medicinal liquid storage portion and configured to be connected with a tube. A septum attached to the opening portion of the housing main body and provided with a puncturable region that can be punctured with a puncture needle. A contrast portion is disposed in the septum over a thickness direction of the septum so as to detect the puncturable region of the septum with the ultrasonic wave. The contrast portion is provided in the septum within a thickness region of the septum and all of the contrast portion is positioned at an inner side of the septum in the thickness direction of the septum.

There is provided a medicinal liquid injection port to be implanted subcutaneously. A housing main body is provided with a medicinal liquid storage portion therein, an opening portion that opens the medicinal liquid storage portion, and a discharge hole that communicates with the medicinal liquid storage portion and configured to be connected with a tube. A septum attached to the opening portion of the housing main body and provided with a puncturable region that can be punctured with a puncture needle. A contrast portion is disposed in the septum over a thickness direction of the septum so as to detect the puncturable region of the septum with the ultrasonic wave. The contrast portion is provided in the septum within a thickness region of the septum and all of the contrast portion is positioned at an inner side of the septum in the thickness direction of the septum.