Drug delivery device with sterile fluid flowpath and related method of assembly
US-2019374707-A1 · Dec 12, 2019 · US
US12377220B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12377220-B2 |
| Application number | US-202017017182-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 10, 2020 |
| Priority date | Mar 15, 2018 |
| Publication date | Aug 5, 2025 |
| Grant date | Aug 5, 2025 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
An assembly for an injection or infusion device includes i) a cartridge being closed by a septum and the surface of the septum being sterile and covered by a first continuous flexible strip, and ii) a fluid path unit comprising a cartridge holder and a fluid path compartment comprising a needle in an interior, the needle is configured to penetrate the septum of the cartridge through a passage in the fluid path compartment. The passage is closed by a second continuous flexible strip keeping the interior of the fluid path compartment in a sterile condition. The cartridge is inserted into the cartridge holder aligning the septum with the passage and sandwiching both strips between the septum and the fluid path compartment. Both strips may be simultaneously removable from the cartridge and fluid path compartment thereby, establishing a sterile connection between the septum and the interior of the fluid path compartment.
Opening claim text (preview).
What is claimed is: 1. An assembly for an injection or infusion device, the assembly comprising a cartridge for a sterile liquid medicament, formed as a barrel, the cartridge being closed by a septum fastened to the barrel by a crimp, wherein a first surface of the septum opposite a second surface contacting the liquid medicament is recessed from a surface of the crimp, is sterile and is covered by a first area of a first continuous flexible strip, the first area of a first continuous flexible strip being attached to the surface of the crimp without contacting the first surface of the septum, thereby keeping the first surface of the septum in a sterile condition; and a fluid path unit comprising a cartridge holder and a fluid path compartment comprising a needle or spike in an interior of the fluid path compartment, wherein the needle or spike is configured to penetrate the septum of the cartridge through a passage defined in a surface of the fluid path compartment, wherein the passage of the fluid path compartment is closed by a second continuous flexible strip attached to the surface of the fluid path compartment, the second continuous flexible strip comprising a second area covering the passage thereby keeping the interior of the fluid path compartment in a sterile condition, wherein the cartridge is arranged in the cartridge holder of the fluid path unit such that the septum is aligned with the passage of the fluid path compartment and the first continuous flexible strip and the second continuous flexible strip contact each other and are sandwiched between the septum and the fluid path compartment, wherein the first continuous flexible strip has a first free end and the second continuous flexible strip has a second free end, the first and second free ends are arranged substantially parallel to one another adjacent the passage of the fluid path compartment, and wherein, by simultaneously pulling the first free end and the second free end, the first continuous flexible strip and the second continuous flexible strip are detachable from the assembly upon removal from the surface of the crimp and the surface of the fluid path compartment for establishing a sterile connection between the opposite first surface of the septum and the interior of the fluid path compartment. 2. The assembly for an injection or infusion device according to claim 1 , wherein the barrel of the cartridge defines a first axis which is aligned with an axis of the spike or needle, and wherein the first free end and the second free end of the first continuous flexible strip and the second continuous flexible strip adjacent to the passage are oriented substantially perpendicular to the first axis. 3. The assembly for an injection or infusion device according to claim 1 , wherein the first continuous flexible strip and the second continuous flexible strip sandwiched between the septum and the fluid path compartment are compressed against each other by a biasing element. 4. The assembly for an injection or infusion device according to claim 3 , wherein the biasing element is a spring or ratchet acting on the barrel of the cartridge biasing the cartridge towards the fluid path compartment and/or is at least one resilient element positioned between the crimp of the cartridge and the fluid path compartment. 5. The assembly for an injection or infusion device according to claim 4 , wherein the resilient element comprises an O-ring, elastic double sided adhesive tape or a flexible arm. 6. The assembly for an injection or infusion device according to claim 1 , wherein the first continuous flexible strip and the second continuous flexible strip are made of a porous membrane, the porous membrane being permeable to sterilization gases. 7. The assembly for an injection or infusion device according to claim 6 , wherein the porous membrane comprises polyethylene or polypropylene fibers. 8. The assembly for an injection or infusion device according to claim 6 , wherein the sterilization gasses to which the porous membrane is permeable comprise one or more of ethylene oxide gas or hydrogen peroxide gas. 9. The assembly for an injection or infusion device according to claim 1 , wherein the first area of the first continuous flexible strip is attached or attachable to an end surface of the crimp. 10. The assembly for an injection or infusion device according to claim 9 , wherein the first area of the first continuous flexible strip is attached or attachable to the end surface of the crimp by one or more of heat sealing, an adhesive glue, a hot melt or using double sided adhesive tape. 11. The assembly for an injection or infusion device according to claim 1 , wherein the second area of the second continuous flexible strip covering the passage is attached to the surface of the fluid path compartment by one or more of heat sealing, an adhesive glue, a hot melt or using double sided adhesive tape. 12. The assembly for an injection or infusion device according to claim 1 , wherein the second area of the second continuous flexible strip is connected to the free end of the second continuous flexible strip by at least one U-shaped fold and/or the first area of the first continuous flexible strip is connected to the free end of the first continuous flexible strip by at least one U-shaped fold. 13. The assembly for an injection or infusion device according to claim 1 , wherein the first free end and the second free end of the first continuous flexible strip and the second continuous flexible strip are connected to each other, or connected to a protective cap, or connected to a removable release liner protecting an adhesive layer configured for attaching the injection or infusion device to the skin of a patient. 14. A method for assembling an assembly for an injection or infusion device, comprising the steps of: providing a cartridge comprising a sterile liquid medicament, formed as a barrel, the cartridge being closed by a septum fastened to the barrel by a crimp, a surface of the septum opposite to a surface contacting the liquid medicament being sterile and covered by a first area of a first continuous flexible strip attached to a surface of the crimp, thereby keeping the opposite surface of the septum in a sterile condition; providing a fluid path unit comprising a cartridge holder and a fluid path compartment comprising a needle or spike in an interior of the fluid path compartment, wherein the needle or spike is configured to penetrate the septum of the cartridge through a passage defined in a surface of the fluid path compartment, wherein the passage is closed by a second continuous flexible strip that is attached to the surface of the fluid path compartment, the second continuous flexible strip having a second area covering the passage thereby keeping the interior of the fluid path compartment in a sterile condition; and inserting the cartridge in the cartridge holder of the fluid path unit such that the septum is aligned with the passage of the fluid path compartment and that the first continuous flexible strip and the second continuous flexible strip contact each other and are sandwiched between the septum and the fluid path compartment, wherein the first continuous flexible strip comprises a first free end and the second continuous flexible strip comprises a second free end, the first free end and the second free end arranged substantially parallel to another adjacent from the passage during insertion, and wherein, by pulling the first and second free ends, the first and second continuous flexible strips are detachable from the assembly upon removal from the surface of the crimp and the surface o
Methods of manufacture, assembly or production · CPC title
with fixed or steady piercing means, e.g. piercing under movement of ampoule · CPC title
of the skin patch type · CPC title
via the proximal end of a syringe, i.e. syringe end opposite to needle cannula mounting end · CPC title
comprising sealing means, e.g. severable caps, to be removed prior to injection by, e.g. tearing or twisting · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.