{"data":{"id":"us/10-cfr-35.49","jurisdiction":"us","citation":"10 CFR 35.49","heading":"Suppliers for sealed sources or devices for medical use.","body":"For medical use, a licensee may only use—\n(a) Sealed sources or devices manufactured, labeled, packaged, and distributed in accordance with a license issued under 10 CFR Part 30 and 10 CFR 32.74 of this chapter or equivalent requirements of an Agreement State;\n(b) Sealed sources or devices non-commercially transferred from a Part 35 licensee or an Agreement State medical use licensee.\n(c) Teletherapy sources manufactured and distributed in accordance with a license issued under 10 CFR Part 30 or the equivalent requirements of an Agreement State.","path":["Title 10—Energy","CHAPTER I—NUCLEAR REGULATORY COMMISSION","PART 35—MEDICAL USE OF BYPRODUCT MATERIAL","Subpart B—General Administrative Requirements"],"source_url":"https://www.ecfr.gov/api/versioner/v1/full/2026-08-25/title-10.xml","current_through":"2026-08-25","vintage":"","retrieved_at":"2026-08-27T02:24:09Z","sha256":"d75ba0163dcb0d63b304e6f5b2de214d2788405418d22a00ae44ea4f22408fce","source_id":"us-cfr","stale":true,"prev":"us/10-cfr-35.41","next":"us/10-cfr-35.50"},"notice":"GroundRules: Original legal text. Not legal advice."}