Multilayer self-healing membrane for septal closure of medical devices

JP7899214B2Active Publication Date: 2026-08-03BECTON DICKINSON & CO
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Patent Information

Authority / Receiving Office
JP · JP
Patent Type
Patents
Current Assignee / Owner
BECTON DICKINSON & CO
Filing Date
2022-04-18
Publication Date
2026-08-03

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Abstract

The membrane for the medical device includes a first portion having a first material and a second portion having a second material, the first material being an ionomer and the second material being at least one of a thermoplastic elastomer, a thermoplastic polyurethane, and a thermoplastic olefin. At least one of the first material and the second material can include a lubricant additive.
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Claims

1. A first part containing the first material, A second part containing a second material, A membrane for medical devices, including The first material comprises an ionomer configured to have self-healing properties to minimize fragmentation when the needle passes through the membrane, The second material comprises at least one of thermoplastic elastomers, thermoplastic polyurethanes, and thermoplastic olefins. The aforementioned medical device is a patient connector, The patient connector is for connecting one component of a closed-system transport device or closed-system transport system to a patient's venous line. The membrane is a membrane for a medical device, characterized in that it is used in any component of the closed-system transport device or the closed-system transport system.

2. The film according to claim 1, characterized in that at least one of the first material and the second material contains a lubricating additive.

3. The film according to claim 2, characterized in that the lubricating additive comprises at least one of boron nitride, polytetrafluoroethylene, wax, and mineral oil.

4. The film according to claim 3, characterized in that the lubricating additive is 10% by weight or less of the first portion and the second portion.

5. The film according to claim 1, characterized in that the first material has a Shore D hardness of 39 to 68.

6. The film according to claim 1, characterized in that the first material has a tensile strength of 2.1 to 5.4 kpsi.

7. The film according to claim 1, characterized in that the first material comprises an ethylene acrylic acid copolymer.

8. The film according to claim 1, characterized in that the second material comprises at least one of a styrene-based thermoplastic elastomer and an olefin-based thermoplastic elastomer.

9. The membrane according to claim 1, characterized in that the first portion includes 25% or less of the volume of the membrane.

10. The film according to claim 1, characterized in that the first portion is an outer layer surrounding the second portion.

11. The film according to claim 1, characterized in that the first portion and the second portion are formed separately.

12. The film according to claim 1, characterized in that the first portion and the second portion are formed integrally.

13. A body having a first end and a second end, comprising a body defining a passage, A line connection is provided at the second end of the main body, A film according to any one of claims 1 to 12 is disposed at the first end of the main body, A patient connector characterized by including [a specific feature].

14. The patient connector according to claim 13, characterized in that the membrane is received by an opening defined by the main body.