Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
  • A61M1/14—Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis
  • A61M1/16—Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis with membranes
  • A61M1/1654—Dialysates therefor
  • A61M1/1656—Apparatus for preparing dialysates
  • A61M1/1668—Details of containers
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
  • A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
  • A61J1/14—Details; Accessories therefor
  • A61J1/1406—Septums, pierceable membranes
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
  • A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
  • A61J1/14—Details; Accessories therefor
  • A61J1/1462—Containers with provisions for hanging, e.g. integral adaptations of the container
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
  • A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
  • A61J1/14—Details; Accessories therefor
  • A61J1/1475—Inlet or outlet ports
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
  • A61M1/14—Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis
  • A61M1/16—Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis with membranes
  • A61M1/1654—Dialysates therefor
  • A61M1/1656—Apparatus for preparing dialysates
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
  • A61M1/14—Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis
  • A61M1/16—Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis with membranes
  • A61M1/1654—Dialysates therefor
  • A61M1/1656—Apparatus for preparing dialysates
  • A61M1/1666—Apparatus for preparing dialysates by dissolving solids
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
  • A61M1/14—Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis
  • A61M1/16—Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis with membranes
  • A61M1/1654—Dialysates therefor
  • A61M1/1656—Apparatus for preparing dialysates
  • A61M1/1668—Details of containers
  • A61M1/167—Flexible packaging for solid concentrates
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
  • A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
  • A61J1/05—Containers specially adapted for medical or pharmaceutical purposes for collecting, storing or administering blood, plasma or medical fluids ; Infusion or perfusion containers
  • A61J1/10—Bag-type containers
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M39/00—Tubes, tube connectors, tube couplings, valves, access sites or the like, specially adapted for medical use
  • A61M39/22—Valves or arrangement of valves
  • A61M39/26—Valves closing automatically on disconnecting the line and opening on reconnection thereof

Definitions

• the present invention refers to a system and a method for connecting a concentrate container with a blood treatment device and / or a fluid dosing unit. Further aspects of the present invention refer to a container and a fluid dosing unit / blood treatment de vice, preferably a dialysis machine for renal replacement therapy, configured to be used in a method according to the present invention.
• the present invention refers to a container comprising a connection portion allowing for an easy, efficient and more hygienic connection of the container to a fluid dosing unit of a blood treatment device.
• the fluid dosing unit comprises a valve that fluidically closes the fluid dosing unit if no con tainer is connected to the fluid dosing unit and that opens the fluid dosing unit upon connection of a container to the fluid dosing unit.
• dry powder concentrate is generally provided in a container that is fluidically coupled to the blood treatment device so that water can be dispensed into the container by the blood treatment device for dissolving the dry concentrate. Simul taneously the basic liquid concentrate / the bicarbonate solution generated in this way is withdrawn by the blood treatment device from the concentrate container.
• a conventional concentrate container is known from e.g. EP1344550.
• the concentrate con tainer cannot be connected to the hydraulic system/fluidics system of the blood treat ment device during disinfection/rinsing of the blood treatment device.
• the blood treatment machine and the correspond ing concentrate container are configured in such a way that a connection element of the container is inserted into a connection element of the machine in a downward movement, so that gravity assists the movement of the connection element of the con tainer into / over the connection element of the machine.
• this configuration has the disadvantage that because of the opening of the connection element of the container being opened in a downward direction (so that it can be coupled with a corresponding connection element of the blood treatment device by moving the connection element of the container from above in a downwards move ment of the connection element of the blood treatment device) after a treatment has ended and the concentrate container is removed from the blood treatment device, liq uid concentrate can drip from the connection element of the container.
• liquid concen trate can spill, leak or drop from a withdrawal line of the blood treatment device config ured to withdraw concentrate from the container upon disconnection of the container from the blood treatment device. Since the liquid concentrate contains solutes, crystal lization may occur as an additional disadvantage to these spillages generally not being hygienic.
• This liquid concentrate can then collect in the connection element of the blood treat ment device causing undesired crystallization and thus potential clogging of the con nection element of the blood treatment device.
• the present invention uses the container to collect any drops dripping from the connection elements of the blood treatment de vice and / or prevents such drops / spillages / leakages in the first place.
• the opening element(s) of a container according to the present invention are preferably opened in an upward direction so that the connection element(s) of the blood treatment device can be inserted into the opening element(s) of the container from above in a downward motion or the container can be moved in an upward motion so that the hat the connection element(s) of the blood treatment device can be inserted into the opening element(s) of the container.
• a valve is provided at the fluid dosing unit / blood treatment device that fluidically closes the fluid dosing unit / blood treatment device if no container is connected to the fluid dosing unit / blood treatment device so that no liquid drops from the fluid dosing unit / blood treatment device in the absence of a container.
• the container can be attached to the blood treatment device at an arbitrary point of time so that the blood treatment device is set up correctly for the subsequent connection to the container when desired.
• the present invention provides a container that is easier and cheaper to manufacture as fluid flows along connection elements in the form of linear channels through a connection portion of the container from the blood treatment device into the container.
• the structure of the connection portion of the container can be simplified in comparison to the prior art in which the fact that the connection portion generally is connected to the blood treatment device via a downward movement dic tates a design in which the openings are opened at a lower surface of the connection portion.
• fluid flow through the connection portion of the container is not strictly linear / unidirectional but the fluid is diverted in multiple direc tions which requires a more complex design and more material.
• the structure of a container according to the present invention and especially the structure of the connection portion thereof allows filters to be mounted more easily into the openings of a fluid inlet and / or outlet of the container.
• a container for concentrate comprises a main body for containing concentrate, at least one attachment element configured to revers ibly attach the container to at least one corresponding attachment element present on a blood treatment device, and at least one connection element, configured to interact with at least one corresponding connection element present on a blood treatment de vice to fluidically couple the container with the blood treatment device, wherein the at least one attachment element projects in a first direction and the at least one connec tion element projects in a second direction that is oriented essentially at right angles to the first direction.
• the first direction in that the at least one attach ment element projects is oriented essentially at right angles to the longitudinal axis of the main body of the container.
• the attachment element of the blood device is inserted into the attachment element of the container preferably along the first direction. If the attachment element of the container is hook-shaped, an attachment element of the blood treatment device that is inserted into the hook-shaped attachment element of the container preferably projects along the first direction.
• the second direction in that the at least one connection element projects is oriented essentially in parallel to the longitudinal axis of the main body of the container and the at least one connection element has the form of a hollow cylinder opened at an end surface of the container opposite to the main body of the container and configured to receive a corresponding connection element, e.g. a spout, of the blood treatment device.
• the at least one connection element of the container preferably has an opening at the flat (top) end surface of the container facing away from the main body of the container.
• the at least one connection element of the container that can serve as an inlet for conducting fluid into the container or as an outlet for removing fluid from the container projects in a straight line through a connection portion of the container from a flat (top) end surface of the container facing away from the main body of the container to an end surface of the connection portion facing the main body of the container.
• the container has two connection elements serving as an inlet and an outlet each and each projecting in a straight line through a connection portion of the container from a flat (top) end surface of the container facing away from the main body of the container to an end surface of the connection portion facing the main body of the con tainer.
• a fluid permeable actor in the outlet and / or the inlet a fluid permeable actor can be arranged to open a valve in a corresponding connection element of a fluid dosing unit, e.g. a fluid dosing unit of a blood treatment device, upon connection of the container to the fluid dosing unit.
• a fluid dosing unit e.g. a fluid dosing unit of a blood treatment device
• the container comprises two attachment elements each formed as a hook configured to be hooked over a corre sponding attachment element present on a blood treatment device that is preferably formed as stud, preferably comprising a circumferential groove, for receiving the hook of the container, thereby to reversibly attach the container to the blood treatment de vice.
• the container comprises two attachment elements each formed as a hollow cylinder configured to receive a corre sponding attachment element present on a blood treatment device formed as a stud to be inserted into the hollow cylinder of the container, thereby to reversibly attach the container to the blood treatment device.
• the container comprises two connection elements in the form of hollow cylinders opened at an end surface of the container opposite to / facing away from the main body of the container and configured to receive a corresponding connection element, e.g. spout, of the blood treatment device, wherein the spout of the blood treatment device is inserted into each hollow cylinder in a direction projecting from the end surface of the container opposite to the main body of the container towards the main body of the container.
• a connection element e.g. spout
• the at least connection element is advantageously sealed by a lid, preferably in the form of a flexible film, that is removably attached to an end surface of the container opposite to / facing away from the main body of the container.
• the lid can be glued or welded to the end surface of the container oppo site to the main body of the container.
• the end surface comprising the opening of the at least one connection element of the container preferably is facing the at least one connection element of the blood treatment device and forms a top end surface of the container.
• the flexible film forming the lid preferably comprises a surface configured to be easily peeled from the end surface of the con tainer.
• the surface of the flexible film is surface-treated to allow a user to easily peel the flexible film from the end surface of the container thereby to expose the at least one connection element of the container and for example a central opening of the container through that the container can be filled with dry concentrate.
• the container can be configured to attach to the blood treatment device according to a lock- and-key-configuration.
• the container can comprise two attachment elements that are formed in different sizes and / or geometrical configurations to allow attachment of the container to a blood treatment device in only one defined mounting position.
• the blood treatment device in this embodiment preferably comprises two cor responding attachment elements in different sizes and / or geometrical configurations.
• the container or the blood treatment device can comprise two connection elements that are formed in different sizes and / or geometrical config urations to allow fluidic coupling of the container to a blood treatment device in only one defined mounting position.
• the blood treatment device or the container in this em bodiment preferably comprises two corresponding connection elements.
• the number of attachment elements and / or connection elements present on the con tainer and / or the blood treatment device is arbitrary and can be varied according to specific applications.
• a fluid permeable actor in a connection element of the container a fluid permeable actor is arranged that opens a valve in a corresponding connection element of a fluid dosing unit, for example a fluid dosing unit of a blood treatment device, upon connection of the container to the fluid dosing unit.
• the fluid permeable actor comprises a spike that removes a valve body from a valve seat upon connection of the container to the fluid dosing unit.
• the fluid permeable actor preferably comprises at least one lumen to conduct fluid.
• Another aspect of the invention refers to a blood treatment device and / or a fluid dosing unit, preferably a blood treatment device comprising a fluid dosing unit, configured to be used with a container according to the present invention.
• Such a blood treatment device comprises a main body, at least one attachment ele ment to that a corresponding attachment element of a container for concentrate can be attached, wherein the at least one attachment element is movable relative to the main body in a direction projecting essentially at right angles from a side surface of the main body, and at least one connection element configured to fluidically couple the blood treatment device to a container for concentrate.
• the main body of the blood treatment device comprises a top surface, a bottom surface and four side surfaces. Depending on the direction of view from a user, a side surface of the blood treatment device can also be referred to as a front surface.
• the at least one attachment element of the blood treatment device has the form of a pin or stud projecting outward from a side surface of the main body and the at least one connection element has the form of a spout projecting in a direction essentially parallel to the side surface of the main body.
• the blood treatment device further comprises a movable and / or motorized guiding element in that preferably a cavity is formed and the at least one attachment element is mounted onto the movable and preferably motorized guid ing element.
• the guiding element can be moved / is movable into a first position, in that the at least one connection element of the blood treatment device, preferably a spout for fluidically connecting the blood treatment device to a container, is received in the cavity present on the guiding element thereby allowing the blood treatment de vice to be rinsed.
• the cavity in the guiding element short-circuits and / or closes the internal fluidic circuits of the blood treatment device to form a closed circuit so that rinsing liquid can be circulated in the blood treatment device.
• the guiding element can also be moved / is movable into a second position in that the spout is fluidically connected to a container attached to the at least one attachment element of the blood treatment device.
• the guiding element is preferably movable in the horizontal and / or vertical direction.
• the guiding element In the second position, the guiding element preferably positions the container attached to the at least one attachment element mounted on the guiding element, especially the at least one connection element of the container, relative to the at least one connection element of the blood treatment device so that the container is fluidically coupled to the blood treatment device.
• the guiding element can be moved by a motor of the blood treatment device. In this case, movement of the guiding element is preferably automatic. Alternatively, the guid ing element may be manually moved. In this case the blood treatment device prefera bly has a lever or similar structure that allows a user to manually move the guiding element.
• the at least one connection element of the blood treatment device is movable in a vertical direction essentially parallel to a side sur face of the main body of the blood treatment device.
• the at least one connection element of the blood treatment device is movable in a downward direction towards a bottom surface of the main body of the blood treatment device. Additionally or alternatively, the at least one connection element of the blood treatment device is movable in an upward direction towards a top surface of the main body of the blood treatment device. For example, the at least one connection element of the blood treatment device can be first moved upwards to allow a container attached to the attachment elements to be moved by the guiding element into a position in that the at least one connection ele ment of the blood treatment device and the at least one connection element of the container align in a vertical direction.
• the at least one connection element of the blood treatment device can be moved downwards towards the guiding element to fluidically couple the container to the blood treatment device, for example, by inserting the at least one connection element of the blood treatment device into the at least one connection element of the container.
• the at least one connection element of the blood treatment device can be retracted upwards again to withdraw the at least one connection element of the blood treatment device from the at least one connection element of the container to thereby fluidically separate / decouple the container and the blood treatment device from each other.
• the blood treatment device preferably further comprises a projection portion present on a side surface of the main body.
• the guiding element is preferably movable relative to the projection portion in the fashion of a drawer. In other words, the guiding element can be slidably moved relative to the projection portion in a direction essentially at right angles to the side surface of the blood treatment device, i.e. in a horizontal direction.
• the at least one connection element of the blood treatment device is mounted to the projection portion and can be moved in a direction essentially parallel to the side surface of the blood treatment device to project (preferably in a vertical direction downwards towards the bottom surface of the blood treatment device) out from the projection portion. Further preferably, the at least one connection element of the blood treatment device can be retracted / moved into the projection portion in a vertical direction essentially parallel to the side surface of the blood treatment device. The movement of the guiding element and / or the at least one connection element of the blood treatment device can be performed automatically or non-automatically, mo torized and / or manually.
• the blood treatment device comprises two attachment elements each formed as a pin / stud, preferably comprising a circum ferential groove, for receiving a corresponding attachment element of the container, preferably formed as a hook, thereby to reversibly attach the container to the blood treatment device.
• the hook can be inserted into the circumferential groove to prevent slipping.
• the blood treatment device preferably comprises two at tachment elements that are formed in different sizes and / or geometrical configura tions to allow attachment of a container to the blood treatment device in only one de fined mounting position.
• the blood treatment device can comprise two connection elements that are formed in different sizes and / or geometrical configurations to allow fluidic coupling of a container to the blood treatment device in only one defined mount ing position.
• connection element can be quipped with a valve that closes the connection element if no container is attached to the connection element and opens the connection element if a container is connected to the connection element to fluidically couple the connection element with the con tainer.
• connection element is a fluid line, for example a supply line or withdrawal line, of a fluid dosing unit, preferably a fluid dosing unit of a blood treatment device.
• the connection element is a withdrawal line of a fluid dosing unit.
• a blood treatment device comprising a fluid dosing unit that can be connected to a container comprising dry concentrate to dispense fluid into the container and to withdraw fluid from the container.
• the present invention is not limited to blood treatment devices but can be applied to any fluid dosing unit.
• the fluid dosing unit comprises a valve in the connection element / fluid line (preferably in a withdrawal line), wherein the valve comprises a valve body that can be moved in an axial direction between a closed position (valve body is in contact with a valve seat) and an open position (valve body is removed from the valve seat). In the open position, fluid can flow from the connection element / fluid line through the valve into the container.
• the valve is biased into the closed position, for example by means of a spring.
• the valve is opened by means of a fluid permeable actor arranged in an connection element of the container wherein the connection element serves as an inlet or outlet for fluid into or out of the container.
• a fluid permeable actor arranged in an outlet of the container, because this fluid path contains concen trate (instead of water being dispensed into the container through the inlet) that causes crystallization if the concentrate drips from the connection element / fluid line of the fluid dosing unit.
• the fluid line is the withdrawal line through which liquid concentrate (e.g. a bicarbonate solution) flows, crystallization due to spillages is a problem.
• Another aspect of the present invention refers to a system comprising at least one container according to the present invention and at least one blood treatment device according to the present invention.
• the container is reversibly attached to the blood treatment device by means of the at least one attachment element present on the container interacting with the at least one attachment element present on the blood treatment device.
• the at least one connection element of the blood treatment device is fluidically coupled to the at least one connection element of the container.
• a further aspect of the present invention refers to a method for connecting a container for concentrate, preferably a container according to the present invention, to a blood treatment device, preferably a blood treatment device according to the present inven tion, comprising the steps:
• the method may comprise an additional step in that the container is used to capture any liquid drops or spills originating from the at least one connection element of the blood treatment device.
• Such additional steps can be, for example:
• the container after disconnecting the container from the blood treatment device, the container is not immediately removed but remains for a while vertically below the con nection element of the blood treatment device, e.g. a spout, to capture any drops drip ping downwards from the connection element.
• the con nection element of the blood treatment device e.g. a spout
• the method can comprise a rinsing step in that the blood treatment device is rinsed prior to connecting a container to the blood treatment device or after discon necting the container from the blood treatment device.
• the blood treatment device preferably comprises a movable and / or motorized guiding element comprising the at least one attachment element of the blood treatment device and further comprising a cavity configured to receive the at least one connection element of the blood treatment device.
• the method further com prises the step:
• connection element of the blood treatment device instead of inserting the connection element of the blood treatment de vice into the connection element of the container to, for example, dispense water into the container to dissolve concentrate powder to form a liquid concentrate, in the rinsing position, the connection element of the blood treatment device is inserted into the cav ity of the guiding element.
• the internal fluidic circuit of the blood treatment device is closed and rinsing fluid can be circulated in the blood treatment device.
• all method steps apart from the step of reversibly attaching the container to the blood treatment device by means of the at least one attachment element present on the container and the at least one attachment element present on the blood treat ment device are performed by the blood treatment device.
• the container can be attached to the blood treatment device at an arbitrary and convenient time (e.g. during regular working hours) and the blood treatment device establishes a fluid connection between the con tainer and the blood treatment device as needed (on demand) at a specific time point (e.g. during night time) determined for example by a treatment regime.
• An aspect of the invention refers to a container for concentrate, comprising: a main body for containing concentrate, a connection portion having a flat end surface facing away from the main body and an opening through that the main body can be filled with concentrate, an inlet through that fluid can be supplied to the main body and an outlet through that fluid can be withdrawn from the main body, wherein at least in the outlet a fluid permeable actor is arranged that is configured to open a valve in a fluid line of a fluid dosing unit when the container is connected to the fluid dosing unit to fluidically couple the container to the fluid dosing unit.
• the fluid permeable actor comprises a spike configured to open the valve and at least one lumen to conduct fluid.
• the outlet and the inlet each project along a straight line traversing the con nection portion from the flat end surface facing away from the main body to a flat end surface facing the main body.
• the container comprises two attachment elements arranged at two opposing sides of the connection portion and configured to reversibly attach the container to two corresponding attachment elements present on a blood treatment device, wherein the two attachment elements project in a first direc tion and the outlet and inlet project in a second direction that is oriented essentially at right angles to the first direction.
• connection portion is formed handleless and comprises concave grip ping portions.
• a fluid dosing unit preferably a fluid dosing unit of a blood treatment device, wherein at least in a fluid line (also referred to as a “withdrawal line”) of the fluid dosing device configured to withdraw fluid from a con tainer connected to the fluid dosing unit, a valve is arranged that is configured to flui- dically close the fluid line if no container is connected to the fluid dosing unit and further configured to be openable upon connection of a container to the fluid dosing unit to allow fluid to be withdrawn from the container through the valve.
• a fluid line also referred to as a “withdrawal line”
• a valve is arranged that is configured to flui- dically close the fluid line if no container is connected to the fluid dosing unit and further configured to be openable upon connection of a container to the fluid dosing unit to allow fluid to be withdrawn from the container through the valve.
• the fluid dosing unit can be part of a blood treatment device, e.g. a dialysis machine for renal replacement therapy.
• the fluid line is a withdrawal line of the fluid dosing unit.
• the invention could also be applied to a supply line or other fluid line of the fluid dosing unit.
• the valve comprises an axially movable valve body that is removable from a valve seat upon connection of a container to the fluid dosing unit to allow fluid to be withdrawn from the container and through the valve.
• Another aspect of the invention refers to a system comprising at least one container according to the present invention and at least one fluid dosing unit / blood treatment device according to the present invention, wherein preferably the container is reversi bly attached to the fluid dosing unit / blood treatment device.
• a further aspect of the invention refers to a method for connecting a container for con centrate, preferably a container according to the present invention, to a fluid dosing unit, preferably a fluid dosing unit according to the present invention, comprising the steps:
• the container and / or the withdrawal line of the fluid dosing unit are preferably moved relative to each other so that the fluid permeable actor is inserted into the withdrawal line to move an axially movable valve body away from a valve seat to fluidically couple the container to the fluid dosing unit.
• Fig. 1 shows an embodiment of a container according to the present invention
• Fig. 2 shows another embodiment of a container according to the present invention that comprises a peelable, flexible film to seal the connection elements of the container;
• Fig. 3 shows how a user can peel the flexible film from the end surface of the container
• Fig. 4 shows a state in which the user has almost completely removed the flexible film from the top end surface of the container
• Fig. 5 shows a connection portion of a concentrate container according to the prior art
• Fig. 6 shows a connection portion of a container according to an embodiment of the present invention
• Fig. 7 shows a side view of the connection portion of figure 5;
• Fig. 8 shows a side view of the connection portion of figure 6
• Fig. 9 shows a sectional view of the connection portion of figure 7;
• Fig. 10 shows a sectional view of the connection portion of figure 8.
• Fig. 11 shows a top view of the connection portion of figure 5;
• Fig. 12 shows another side view of the connection portion shown in figure 5;
• Fig. 13 shows a top view of the connection portion of figure 6
• Fig. 14 shows a different side view of the connection portion of figure 6;
• Fig. 15 shows a perspective top view of the connection portion of figure 6
• Fig. 16 shows a detailed view of the connection portion of figure 6 that is sealed by a flexible film
• Fig. 17 shows a blood treatment device according to the present invention comprising two attachment elements
• Fig. 18 shows how a container is attached to the attachment elements of the blood treatment device of figure 17;
• Fig. 19 shows the blood treatment device of figure 17 with a container attached thereto;
• Fig. 20 shows the detailed view of the blood treatment device of figure 17 in which the guiding element is positioned relative to the projection portion in a closed, rinsing po sition;
• Fig. 21 shows a side view of the blood treatment machine of figure 17, in which the guiding element is positioned relative to the projection portion in the closed, rinsing position;
• Fig. 22 shows the blood treatment device of figure 21 , wherein a container is attached to the attachment elements of the blood treatment device;
• Fig. 23 shows a sectional view illustrating the rinsing position of the guiding element relative to the projection portion
• Fig. 24 shows a perspective view of the container that is attached to the attachment elements of the blood treatment device in the closed rinsing position
• Fig. 25 shows the container connected to the blood treatment device in a position, in which the container is fluidically coupled to the blood treatment device;
• Fig. 26 shows a sectional view of the arrangement of figure 25
• Fig. 27 shows a blood treatment device, to which a container is fluidically coupled;
• Fig 28 shows the blood treatment device of Fig. 27 in the rinsing position.
• Fig. 29 shows the guiding element and the projection portion of the blood treatment device in the closed rinsing position
• Fig. 30 shows the arrangement of figure 29, to which a container has been attached
• Fig. 31 shows the position, in that the container is fluidically coupled to the blood treat ment device
• Fig. 32 shows how the container is attached to the attachment elements of the blood treatment device
• Fig. 33 illustrates how the guide element moves inwards toward the side surface of the main body of the blood treatment device to position the container in a position that it can be fluidically coupled with the connection elements of the blood treatment device;
• Fig. 34 shows a position in that the connection elements of the blood treatment device and the connection elements of the container are aligned in a vertical direction;
• Fig. 35 demonstrates how the container is moved upwards to insert the connection elements of the blood treatment device into the connection elements of the container;
• Fig. 36 illustrates the position of the container fluidically connected with the blood treat ment device during blood treatment
• Fig. 37 demonstrates how the container is moved downwards after the treatment has ended, to fluidically decouple the connection elements of the container from the con nection elements of the blood treatment device;
• Fig. 38 shows how the container is held in a position, in that the connection elements of the blood treatment device and the container are fluidically coupled but aligned in a vertical direction;
• Fig. 39 illustrates how droplets dripping from the connection elements of the blood treatment device are captured by the concentrate bag;
• Fig. 40 demonstrates how after completion of the treatment the container is removed from the blood treatment device by moving the container away from a side surface of the blood treatment device;
• Fig. 41 how after completion of the treatment the container is detached from the blood treatment device
• Fig. 42 demonstrates how the guiding element is then moved into the rinsing position by aligning the cavity present on the guiding element in a vertical direction with the connection elements of the blood treatment device;
• Fig. 43 illustrates the guiding element in the rinsing position in that the connection ele ments are inserted into the rinsing cavity present in the guiding element.
• Fig. 44 shows an embodiment in which the guiding element can be manually moved using a lever 21 .
• Fig. 45 shows a sectional view of an embodiment in that the fluid dosing unit of a blood treatment device is equipped with an integrated valve to prevent fluid from dripping from the fluid dosing if no container is connected to the fluid dosing unit.
• Figs. 46 and 47 show sectional views of the embodiment auf Fig. 45 in a state in that a container is connected to the fluid dosing unit and the valve is open.
• Fig. 48 shows sectional views of the embodiment auf Fig. 45 in a state in that no con tainer is connected to the fluid dosing unit and the valve is closed.
• Fig. 49 shows a detailed view of a fluid permeable actor that can be provided at a container according to the present invention to open the valve of the fluid dosing unit shown in Fig. 45.
• Fig. 50 shows a sectional view of the fluid permeable actor of Fig. 49.
• a container 1 comprises a main body 2 configured to contain a dry and/or liquid concentrate. Furthermore, the container 1 comprises two attachment elements 3 having the form of hooks that are arranged at opposite sides of an attach ment portion 4 of the container 1 .
• the container 1 comprises connection elements 5 that are opened to wards a top end surface 6 of the connection portion 4 of the container 1 that is opposite to / facing away from the main body 2.
• the container also com prises a handle 22 allowing a user to grip the container 1 .
• the top end surface 6 is sealed by a flexible film 7 that covers the connection elements 5 as well as the central opening 8 of the connection portion 4.
• Figure 2 shows another container 1 according to the present invention.
• the flexible film seals the connection element 5 but does not completely cover the central opening 8.
• the attachment elements 3 take the form of hollow cylinders configured to receive corresponding studs / pins of a blood treatment device.
• Figure 3 shows a user peeling off the flexible film 7 from the top end surface 6 of the container 1 .
• components denoted by the same reference numerals are the same or similar components.
• connection portion 4 of a concentrate container known from the prior art.
• Such conventional connection portions of containers known from the prior art generally comprise connection elements 5 that are opened downwards so that liquid can drip from these connection portions into connection elements present on the blood treatment device that are configured to be inserted into the connection elements 5.
• the connection portion further comprises a handle 22 allowing a user to grip the connection portion.
• connection portion 4 of the container according to the present inven tion.
• This connection portion comprises attachment elements 3 formed as hollow cyl inders and configured to receive corresponding connection elements, especially in the form of studs, pins or cylinders, present on the blood treatment device.
• connection portion 4 further comprises connection elements 5 that are opened upwards towards a top end surface 6 of the connection portion.
• connection portion 4 furthermore comprises grip ping portions 8 at opposing sides of the connection portion 4 that replace the handle 22 present in the conventional connection portion shown in figure 5.
• connection portion 4 shows the connection portion 4 according to the prior art in a side view, show ing the connection elements 5 as well as the handle 22.
• connection portion 4 of the container according to the present invention shown in Fig. 8 comprises attachment elements 3 arranged at opposing sides of the connection por tion 4 and formed as hollow cylinders. The openings of the connection portions cannot be seen in this view.
• Figure 9 shows a sectional view of the connection portion 4 of figure 7 in that the handle 22 is clearly visible.
• the gripping portions 9 are clearly visible as well as the attachment elements 3 and the connection elements 5 that are opened towards a top end surface 6 of the connection portion 4.
• the connection elements 5 of the connection portion 4 according to the prior art also function as attachment elements, because the connec tion elements 5 in the form of hollow cylinders are arranged over corresponding spouts of the blood treatment device.
• connection elements of the blood treatment device i.e. connection elements of a blood treat ment device according to the prior art are inserted into the connection elements 5 of the connection portion 4 in an essentially vertical position/direction in Figure 12, thereby allowing liquid from the connection elements 5 to drip out of the connection elements 5 of the connection portion 4 of a container 1 .
• the attachment elements 3 and the connection elements 5 are separate from each other. From Figure 13 it can also be easily seen, that the attachment elements 3 and the connection elements 5 are arranged relative to each other in that they project along directions that are essen tially arranged at right angles to each other, preferably horizontally and vertically re spectively.
• connection elements 5 are openings projecting or extending in the direction into and out of the paper plane.
• Figure 14 provides another clear view of the gripping portion 9, that can substitute the handle 22 present in connection portions 4 known from the prior art.
• Figure 15 further illustrates how the direction of extension of the attachment elements 3 is arranged essentially at right angles to the direction of extension of the connection elements/openings 5.
• connection elements 5 are preferentially sealed off by the flexible strip 7 that is preferentially welded to the top end surface 6 of the con nection portion 4 to close the connection elements 5.
• the flexible film 7 comprises a gripping section 10 that allows the user to grip the flexible film 7 to remove the flexible film 7 from the top end surface 6 of the connection portion 4 of container 1 .
• a blood treatment device 11 includes a main body 12 that has a bottom surface 13 and a attachment assembly 14 configured for attaching to and connecting to the container 1 .
• the attachment assembly 14 comprises a guiding element 15 to which two attachment elements 16 are mounted that in this embodiment have the form of protruding cylinders / studs / pins each having a circumferential groove into which the hooks or hook shaped attachment elements 3 of a container 1 can be inserted.
• the attachment assembly 14 furthermore comprises a projection portion 17.
• a front surface 18 of the projection portion 17 and front surface 19 of the guiding element 15 are aligned with each other to form a con tinuous front surface of the attachment assembly 14. This corresponds to the rinsing position.
• a bag 1 can be attached by means of hook shaped at tachment elements 3 onto the stud-shaped attachment elements 16 mounted onto the guiding element 15.
• Figure 19 shows the blood treatment device 11 with a container 1 attached to the at tachment elements 16 of the guiding element 15.
• the container 1 is in a position in which it is fluidically coupled to the blood treatment device.
• Figure 20 shows the attachment assembly 14 of a blood treatment device 11 in that the guiding element 15 is arranged relative to the projection portion 17 in a closed position used for rinsing the blood treatment device.
• a front surface 18 of the projection portion 17 and a front surface 19 of the guiding element 15 form a continuous front surface.
• the rinsing position of the guiding element 15 relative to the projection portion 17 is further illustrated in a side view of the blood treatment device 11 shown in Figure 21 . From this figure it becomes especially clear, that in the closed position/rinsing position of the guiding element rel ative to the projection portion 17, the front end surface 18 of the projection portion 17 and the front end surface 19 of the guiding element 19 form a continuous front end surface.
• Figure 22 shows the blood treatment device of Figure 21 , with a container 1 being attached via its attachment elements 3 to the attachment elements 16 of the blood treatment device. This position is adopted when the blood treatment device is rinsed/disinfected by internal circulation but already prepared for the next blood treat ment by the provision of the container 1 . Prior to commencing the next blood treatment, the container 1 will be fluidically connected to the blood treatment device 11 .
• Figure 23 illustrates in more detail the structural configuration of the attachment as sembly 14 of the blood treatment device by providing a sectional view of the attachment assembly 14 in the closed/rinsing position illustrated in Figures 21 and 22.
• the front end surfaces 18 and 19 of the projection portion 17 and the guiding element 15 provide a continuous front surface.
• connection element 20 of the blood treatment device that in the embodiment of figure 23 has the form of a spout used for dispensing water into the container 1 is inserted in a cavity 18 present in the guiding element 15.
• the internal fluidic system of the blood treatment device is closed off from the outside and rinsing fluid can be circulated within the blood treatment device without fluid leak ing from the spout 17 to the outside of the blood treatment device 11 .
• Figure 24 shows a close-up view of the connection assembly 14 of the blood treatment device 11 to that a container 1 has been attached via the attachment elements 3 and 16.
• the connection assembly 14 is in the closed position/rinsing position.
• the guiding element 15 is subsequently moved inwards towards the side surface of the blood treatment device 11 , as shown in Figure 25.
• the container 1 attached to the attachment element 16 of the blood treatment device 11 is thus moved towards the side surface of the blood treatment device 11 until it is ar ranged under the projection portion 17 and the connection elements 5 of the bag 1 are horizontally aligned with the connection elements 20 of the blood treatment device.
• the guiding element 15 and thus the container 1 attached to the attachment elements 16 mounted onto the guiding element 15 are moved up wards to connect the connection elements 5 of the container 1 with the connection element 20 of the blood treatment device.
• the container 1 can be held stationary by the guiding element 15 and the connection elements 20 of the blood treatment device are moved downwards to be inserted into the connection elements 5 of the container 1 to thereby fluidically couple the container 1 to the blood treatment device 11 .
• Figure 27 shows a side view of the blood treatment device with a container 1 fluidically coupled to the blood treatment device 11 in that position/relative positioning shown in figure 26.
• Fig. 28 shows a side view of the blood treatment device 11 with the attachment as sembly 24 being in the position shown in Fig. 24.
• Figure 29 shows another view of the connection assembly 14 of the blood treatment device in the closed rinsing position.
• Figure 30 shows the attachment assembly 14 of figure 29, wherein a container 1 has been attached via its attachment elements 3 (hook-shaped) and the attachment ele ments 16 (stud-shaped) of the blood treatment device. In this depiction, the attachment assembly 14 is still in the closed rinsing position.
• Figure 31 shows the attachment assembly 14, wherein the container 1 has been moved inwards under the projection portion 17 and has been fluidically coupled to the blood treatment machine by inserting the connection elements of the blood treatment device into the connection elements of the container 1 , by either moving the container 1 upwards towards the projection portion 17 or by moving the connection elements 20 of the blood treatment device downwards into the connection elements 5 of the con tainer 1 .
• the attachment elements 16 of the blood treatment device are inserted into the attachment elements 3 of the container 1 .
• the attachment elements 16 of the blood treatment device and the attachment ele ment 3 of the container are configured asymmetrically to allow mounting of the con tainer to the blood treatment device only in one correct mounting position.
• Figure 33 shows the container 1 connected to the attachment elements 16 of the blood treatment device via the attachment elements 3 of the container.
• the guiding element 15 then moves inwards in a horizontal direction toward a side surface of the blood treatment device 11 to draw the container 1 under the projection portion 17, as illus trated in Figure 34.
• connection elements 20 of the blood treat ment device and the connection elements 5 are in this position aligned in a vertical direction so that the connection elements 20 can be inserted into the connection ele ments 5 of the container 1 by movement along the vertical axis.
• connection elements 20 of the blood treatment device can be / are inserted into the connection elements 5 of the container 1 by moving the guid ing element 15 and thus the container 1 upwards towards the projection portion 17.
• the connection elements 20 of the blood treatment device can be moved downwards to be inserted into the connection elements 5 of the container 1.
• treatment can be carried out by the blood treatment machine that generates the liquid concentrate from the powder concentrate contained within the main body 2 of the container 1 .
• the guiding element 15 and thus the container 1 attached thereto is moved downwards, as illustrated in Figure 37.
• the downward movement of the container 1 is continued until the connection elements 20 of the blood treatment device are removed from the connection elements 5 of the container 1 , as illustrated in Figure 38.
• the guiding element 15 and thus the container 1 attached thereto is then subsequently moved outwards in a horizontal direction similar to a drawer from the side surface of the blood treatment device 11 .
• the movement of the container 1 can be paused in a position in which the container 1 is vertically aligned with the connection elements 20 of the blood treatment device, so that any droplets dripping from the connection elements 20 of the blood treatment device are caught by the container 1 , preferably the connection elements 5 of the container 1 .
• the container 1 is then moved by means of moving the guiding element 15 relative to the projection portion 17 until the container 1 is positioned further out / away from the side surface of the blood treatment device 11 than the front edge of the projection portion 17. This allows a user to easily grab the container 1 .
• the container 1 can easily be disconnected from the attachment elements 16 of the blood treatment device by pulling the container 1 away from the blood treatment device 11 .
• the blood treatment machine can then move the guiding element 15 upwards and/ or inwards towards the side surface of the blood treatment device 11 until the connection elements 20 of the blood treatment device are aligned in a vertical direction with the cavity 18 of the guiding element 15, as shown in Fig. 42. In this position, the blood treatment device can enter the closed/rinsing position. As shown in Figure 43, the guiding element 15 is moved further upwards or the connection elements 20 of the blood treatment device 11 are further moved downwards, to insert the connection elements 20 into the cavity 18 of the guiding element 15 to enter the closed rinsing position.
• the blood treatment machine can now be rinsed and a new concentrate bag can be attached during rinsing to the guiding element 15 by use of attachment elements 16 to commence a new treatment.
• an attachment assembly 14 of a blood treat ment device can comprise a lever 21 as shown in Fig. 44 or a similar structure allowing a user to manually move the guiding element relative to the projection portion 17.
• Fig. 45 shows a sectional view of an embodiment in that the fluid dosing unit of a blood treatment device is equipped with an integrated valve 23 to prevent fluid from dripping from the fluid dosing unit / the connection element 20 of the fluid dosing unit if no container 1 is connected to the fluid dosing unit.
• the fluid dosing unit in this example corresponds to an attachment assembly 14 dis cussed above.
• the term fluid dosing unit refers to any unit that serves to connect to a container and to dispense fluid into the container and withdraw fluid from the con tainer in a controlled manner.
• the valve comprises a valve body 24 and a valve seat 25.
• the valve 23 is biased in the closed position by means of a biasing element, in this embodiment by a spring 26.
• a container 1 is attached and fluidically coupled to the fluid dosing unit, so that the valve 23 is open.
• Figs. 46 and 47 show sectional views of the embodiment auf Fig. 45 in a state in that a container is connected to the fluid dosing unit and the valve is open.
• a fluid permeable actor 27 comprising a spike 28 holds the valve 23 in the open position, so that fluid can flow through an inner lumen 29 of the fluid permeable actor 27, through the open valve 23 and through the connection element 20 of the fluid dosing unit.
• the connection element 20 in this embodiment corresponds to a fluid line of the fluid dosing unit.
• the flow path of fluid in this state is indicated by a line in Fig. 47.
• the valve body 24 can comprise a recess 30 for receiving the spike 28.
• Fig. 48 shows sectional views of the embodiment auf Fig. 45 in a state in that no con tainer is connected to the fluid dosing unit and the valve 23 is closed. In this state, the spring 26 is expanded and presses the valve body 24 against the valve seat 25.
• Fig. 49 shows a detailed view of a fluid permeable actor 27 that can be provided at a container 1 according to the present invention to open the valve 23 of the fluid dosing unit shown in Fig. 45.
• the fluid permeable actor 27 comprises a spike 28 and in this embodiment four Lumina 29 for conducting fluid.
• the fluid permeable actor 27 com prises an outer bush / hollow cylinder 31 that defines the outer circumference of the fluid permeable actor 27.
• the spike 28 can be mounted onto a platform 32 that is ar ranged concentrically with the outer bush / hollow cylinder 31 and connected to the outer bush / hollow cylinder 31 via ribs 33.
• the fluid permeable actor 27 is arranged in a connection element 5 of the container.
• the connection element 5 can be an inlet or an outlet of the container.
• Fig. 50 shows a sectional view of the fluid permeable actor 27 of Fig. 49.

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• 2020
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