DEVICE AND SYSTEM FOR DISPENSING A FLUID UNDER ASEPTIC CONDITIONS

Abstract

A device (1) for dispensing a fluid, in particular under aseptic conditions, preferably to a patient. The device comprises a conveying device (2) for conveying the fluid to a dispensing opening (3). The device (1) also comprises a coupling element (4) for coupling a syringe (5). The fluid can be conveyed from the syringe (5) to the dispensing opening (3) via the coupling element (4) and the conveying device (2) exclusively by the effect of the conveying device (2). The invention further relates to a system for dispensing a fluid under aseptic conditions, comprising such a device (1) and to a syringe (5) that can be coupled to the coupling element (4).

Claims

1-14. (canceled)

15. A device for dispensing a fluid, comprising: a delivery device for delivering the fluid to a dispensing opening, wherein the device further comprises a coupling element for coupling a syringe, and the fluid is delivered from the syringe to the dispensing opening via the coupling element and the delivery device exclusively by an effect of the delivery device.

16. The device according to claim 15, wherein the coupling element comprises a septum that is pierceable by a syringe needle or a cannula.

17. The device according to claim 16, wherein the coupling element is configured as a needle receiver into which the septum is fitted.

18. The device according to claim 17, wherein the needle receiver is configured as a conduit section.

19. The device according to claim 17, wherein the needle receiver is formed as one piece with a housing of the device.

20. The device according to claim 17, wherein the needle receiver is in fluidic communication with a conduit element, and the conduit element is embedded in a wall of the needle receiver or is connected to the needle receiver via a sealing element.

21. The device according to claim 15, further comprising a holder into which the syringe is insertable, and the syringe, when inserted into the holder, is coupled to the device via the coupling element.

22. The device according to claim 21, wherein the holder is configured as a drawer unit which can be pushed into a drawer region of the device.

23. The device according to claim 22, wherein the drawer unit has a pull-off element with which a protective cap of a syringe, inserted into the drawer unit, can be pulled off.

24. A system for dispensing a fluid under aseptic conditions, said system comprising the device according to claim 15 and a syringe that is coupled to the coupling element.

25. The system according to claim 24, wherein the syringe is configured without a plunger rod.

26. The system according to claim 24, wherein the syringe has a hollow needle or a cannula mounted on the syringe body.

27. The system according to claim 26, wherein the device comprises a syringe holder which is configured in such a way that the syringe needle or a cannula of a syringe inserted therein is shielded.

Description

[0022] Further advantages and individual features of the invention will become clear from the following description of an illustrative embodiment and from the schematic drawings, in which:

[0023] FIG. 1 shows a perspective view of the top of a device according to the invention;

[0024] FIG. 2 shows a perspective view of the underside of the device according to FIG. 1;

[0025] FIG. 3 shows a perspective view of the device according to FIGS. 1 and 2, but with the holder shown separately and configured as a drawer unit into which a syringe in inserted;

[0026] FIGS. 4 to 7 show perspective views of a sequence of steps involving the insertion of a syringe into the drawer unit of a device according to FIGS. 1 to 3 and the pulling-off of the protective cap of the syringe.

[0027] FIG. 1 shows a device 1 according to the invention, wherein the upper part of a housing 10 has been omitted in order to provide greater clarity. Moreover, individual parts of the device 1, for example a delivery drive or control electronics, are not shown. In the device shown, a holder for the syringe 5 is configured as a drawer unit 13, which is here pushed into the device 1. The syringe 5 has a plunger 17 on which, in contrast to customary syringes, no plunger rod is mounted. Moreover, the syringe 5 has a fixedly mounted syringe needle 6. It will be seen that the syringe needle 6 protrudes into a coupling element 4 which, in the present example, is configured as a needle receiver 8. The region of the needle receiver 8 directed toward the syringe 5 has a funnel-shaped configuration in order to guide the syringe needle 6 in the direction of a septum 7. The septum 7 is embedded in a peripheral groove 9 of a wall 12 of the needle receiver 8. The needle receiver 8 is configured as a curved conduit section which is formed in one piece with the housing 10 of the device 1. The needle receiver 8 is connected to the delivery device 2 via a conduit element 11, which is here configured as a steel cannula. The fluidic attachment of the conduit element 11 to the needle receiver 8 is via a septum 7, which is likewise embedded in a peripheral groove 9 inside the wall 12 of the needle receiver 8. Besides the delivery device 2, the device 1 has an injection device 18, and these are both actuated or controlled via a barrel cam 19 driven by a delivery drive (not shown).

[0028] FIG. 2 shows an underside of the device 1. It will be seen that the housing 10 there has a contact face 20 via which the device 1 is to be placed onto the body of a patient, in particular via an adhesive film. In the illustrative embodiment of the device 1 shown, a dispensing opening 3 is configured as a combination of puncture cannula and indwelling cannula 21, which are applied through the opening 22 in the housing 10 via an applicator mechanism of the injection device 8.

[0029] In FIG. 3, the device 1 described above and the drawer unit 13 with the syringe 5 are shown separately. It will be seen that the syringe needle 6 is largely shielded by the drawer unit 13, thus making it possible to prevent a user from injuring himself on the needle. The drawer unit 13 is pushed into a drawer region 14 of the device 1, as a result of which the syringe needle 6 is guided into the needle receiver 8 and the septum 7 is pierced.

[0030] FIGS. 4 to 7 show the insertion of the syringe 5 into the drawer unit 13 and the pulling-off of a protective cap 16 from the syringe 5. In FIG. 4, the drawer unit 13 with a pull-off element 15, on the one hand, and the syringe 5 with the protective cap 16, on the other hand, are shown individually. In FIG. 5, the syringe 5 is inserted into the drawer unit 13. It will be seen that engagement elements 23 of the pull-off element 15 engage in a groove 24 of the protective cap 16. In FIG. 6, the protective cap 16 has already been pulled off with the pull-off element 15 from the syringe 5. FIG. 7 shows the drawer unit 13 with the inserted syringe 5 ready to be pushed into the device 1. It will be seen that the syringe needle 6 of the syringe 5 is substantially shielded by the drawer unit 13, thus making it possible to prevent a user from injuring himself on the syringe needle 6.