Home / Agencies / Treasury / 2026-11761
Final Rule

Publication of the List of Medical Devices Requiring Specific Authorization for the North Korea Sanctions Regulations

Agency
Document Number
2026-11761
Published
June 11, 2026
Effective Date
June 11, 2026

Abstract

The Department of the Treasury's Office of Foreign Assets Control (OFAC) is publishing a list of medical devices that may not be exported or reexported to North Korea pursuant to the general license authorizing the exportation or reexportation to North Korea of certain agricultural commodities, medicine, medical devices, and replacement parts and components. The exportation or re-exportation of these excluded medical devices to North Korea requires specific authorization from OFAC.

Federal Register Source

This document is published by the Office of the Federal Register, National Archives and Records Administration. Access the full regulatory text, preamble, and docket comments below.

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Frequently Asked Questions

What is the 2026-11761 Federal Register document?
Document 2026-11761 is a Final Rule published by the Department of the Treasury in the Federal Register on June 11, 2026, with an effective date of June 11, 2026. The Department of the Treasury's Office of Foreign Assets Control (OFAC) is publishing a list of medical devices that may not be exported or reexported to North Korea pursuant to the general license authorizing the exportation or reexportation to North Korea of certain agricultural commodities, medicine, medical devices, and replacement parts and components. The exportation or re-exportation of these excluded medical devices to North Korea requires specific authorization from OFAC. View the original at https://www.federalregister.gov/documents/2026/06/11/2026-11761/publication-of-the-list-of-medical-devices-requiring-specific-authorization-for-the-north-korea.
Is document 2026-11761 an economically significant rule?
No. Document 2026-11761 is not classified as economically significant under Executive Order 12866. Economically significant rules require OIRA review and are estimated to have impacts of $100 million or more per year.
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