# US 11,433,228 B2 · Single use caps and covers for vascular access devices, and kits and methods for using the same

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- Number: US 11,433,228 B2
- Document ID: US11433228B2
- Status: Granted
- Kind: B2
- Application number: 17/180,661
- Filed: 2021-02-19
- Published: 2021-06-10
- Granted: 2022-09-06
- Earliest claimed: 2019-11-11
- Assignees: CleanSite Medical, Inc.
- Applicants: CleanSite Medical, Inc.
- Inventors: John Grant; Daniel M. Chambers
- Web page: https://patentgrep.com/patent/US11433228B2

## CPC

- A61M 39/20: Closure caps or plugs for connectors or open ends of tubes
- A61M 5/50: having means for preventing re-use, or for indicating if defective, used, tampered with or unsterile {(retractable needles or needle protectors with means for preventing re-use A61M5/321)}
- A61M 39/0208: {Subcutaneous access sites (implantable infusion devices A61M5/14276; transcutaneous access sites A61M39/0247)}
- A61M 39/165: {Shrouds or protectors for aseptically enclosing the connector}
- A61M 5/14: Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
- A61M 5/1413: {Modular systems comprising interconnecting elements}
- A61M 5/162: Needle sets, i.e. connections by puncture between reservoir and tube
- A61M 39/105: {Multi-channel connectors or couplings, e.g. for connecting multi-lumen tubes (multi-channel connectors in general F16L37/56)}
- A61M 39/162: {with antiseptic agent incorporated within the connector}
- A61M 2039/0229: {having means for facilitating assembling, e.g. snap-fit housing or modular design}
- A61M 2039/0288: {protectors, caps or covers therefor}
- A61M 2039/205: {comprising air venting means}
- A61M 2205/273: preventing reuse, e.g. of disposables
- A61M: DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY (introducing media into or onto the bodies of animals A61D7/00; means for inserting tampons A61F13/26; devices for administering food or medicines orally A61J; containers for collecting, storing or administering blood or medical fluids A61J1/05); DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY (surgery A61B; chemical aspects of surgical articles A61L); DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR {(Electrotherapy, e.g. producing anaesthesia by the use of alternating or intermittent currents A61N1/36021)}

## Abstract

This invention concerns improved single use caps or covers for vascular access devices such as needlefree connectors that are used, for example, in intravenous administration sets and extension sets. Removal of a single use cap or cover according to the invention from a vascular access device destroys the cap such that the cap cannot be reused. Said single use caps or covers will help ensure compliance with infection prevention protocols in healthcare settings, which will assist in reducing incidences of healthcare-associated infections (HAIs), particularly catheter-related blood stream infections. Assemblies and kits including said caps or covers, for example, IV administration and extension sets that include one or more needlefree connectors, as well as methods for using said caps or covers, are also described.

## Claims

### Claim 1

A vascular access assembly, comprising:
a. a needlefree connector that comprises a vascular access port that comprises a valve region that comprises a valve surface, exterior threads, and a collar disposed below the exterior threads; and
b. a single use cap removably attached to the valve region of the vascular access port, the cap being configured to (i) be snap fit to the collar of the valve region without threading onto the exterior threads and (ii) be destroyed upon removal so as to prevent reuse of the cap, the cap comprising:
i. a cap body comprised of a plastic, wherein the cap body comprises a sidewall integrated with a closed end wall, wherein the sidewall and the closed end wall form a cavity, wherein the sidewall and the closed end wall are configured to cover the valve surface, the exterior threads, and the collar of the valve region of the vascular access port upon snap fitting the cap to the collar;
ii. an opening defined by a first edge of the sidewall and opposite the closed end wall, wherein the opening is sized to allow the cap to be placed over the valve region such that at least the valve surface, the exterior threads, and the collar of the valve region are disposed inside the cavity when the cap is removably attached via the snap fit to the valve region;
iii. a circumferential channel formed into an interior surface of the sidewall of the cap, wherein the channel is configured to matingly snap fit to the collar on the valve region so as to allow the cap to be retained on the vascular access port;
iv. at least one separating region in the cap body configured to allow the sidewall to be separated so as to allow the cap to be removed from the valve region of the vascular access port to which the cap has been attached and to prevent functional reattachment of the cap to the same valve region or a valve region of a vascular access port of a different needlefree connector; and
v. a pull tab connected to a portion of the sidewall proximate to the first edge of the sidewall and the at least one separating region, wherein the pull tab is configured for grasping by a user, and when pulled, to cause the sidewall to separate in at least a portion of the at least one separating region so as to allow the user to then remove the cap from the valve region of the vascular access port to which the cap is removably attached.

### Claim 2 (depends on 1)

The assembly according to claim 1, wherein the cavity is substantially cylindrical.

### Claim 3 (depends on 1)

The assembly according to claim 1, wherein the at least one separating region of the cap comprises a tear strip bounded by two spaced tearable regions.

### Claim 4 (depends on 1)

The assembly according to claim 1 wherein the at least one separating region of the cap comprises a tear strip bounded by a pair of spaced, substantially parallel, separating lines, the tear strip extending at least from the first edge of the sidewall toward the closed end wall of the cap and wherein the pull tab is connected to the tear strip.

### Claim 5 (depends on 1)

The assembly according to claim 1 wherein the plastic comprising the cap body is comprised of a thermoplastic resin.

### Claim 6 (depends on 1)

The assembly according to claim 1 wherein the cap further comprises a vent and a gas-permeable barrier to allow gas but not microorganisms to pass through the vent.

### Claim 7 (depends on 1)

The assembly according to claim 1 wherein the needlefree connector is selected from the group consisting of a Y-site that comprises a needlefree connector portion that includes the vascular access port and a T-site that comprises a needlefree connector portion that includes the vascular access port.

### Claim 8 (depends on 1)

The assembly according to claim 1 wherein the needlefree connector is (i) a packaged needlefree connector or (ii) a packaged vascular access connector that comprises the vascular access port wherein the vascular access connector is included in an IV set, a primary IV administration set, a secondary IV administration set, or an IV extension set.

### Claim 9 (depends on 8)

A kit that comprises the assembly according to claim 8 packaged in a sealed, sterilized container.

### Claim 10 (depends on 1)

A method of capping, covering, or protecting the vascular access port of the needlefree connector, comprising using the assembly according to claim 1 to protect the vascular access port to be capped, covered, or protected, thereby capping, covering, or protecting the vascular access port of the needlefree connector.

### Claim 11 (depends on 1)

A method of uncapping, uncovering, or de-protecting the vascular access port of the needlefree connector included in the assembly according to claim 1, comprising using the pull tab to tear a seam in the sidewall of the cap and removing the cap to thereby uncap, uncover, or de-protect the vascular access port of the needlefree connector.

### Claim 12 (depends on 1)

The assembly according to claim 1 wherein the cap further comprises a port-engaging element that is configured to engage an exterior valve surface of the vascular access port, wherein the port-engaging element is configured to provide continuing antimicrobial action when the cap is attached to a vascular access port.

### Claim 13 (depends on 12)

The assembly according to claim 12 wherein the port-engaging element comprises a compressible medical grade foam.

### Claim 14 (depends on 12)

The assembly according to claim 12 wherein the continuing antimicrobial action is provided by a liquid disinfectant.

### Claim 15 (depends on 14)

The assembly according to claim 14 wherein the liquid disinfectant comprises 70% isopropyl alcohol.

### Claim 16 (depends on 12)

A method of cleaning the vascular access port of the needlefree connector that is included in the assembly according to claim 12, the method comprising rotating the cap in relation to the vascular access port, thereby cleaning the vascular access port.
