10 CFR § 35.49 - Suppliers for sealed sources or devices for medical use.

---
identifier: "/us/cfr/t10/s35.49"
source: "ecfr"
legal_status: "authoritative_unofficial"
title: "10 CFR § 35.49 - Suppliers for sealed sources or devices for medical use."
title_number: 10
title_name: "Energy"
section_number: "35.49"
section_name: "Suppliers for sealed sources or devices for medical use."
chapter_name: "NUCLEAR REGULATORY COMMISSION"
part_number: "35"
part_name: "MEDICAL USE OF BYPRODUCT MATERIAL"
positive_law: false
currency: "2026-03-24"
last_updated: "2026-03-24"
format_version: "1.1.0"
generator: "[email protected]"
authority: "Atomic Energy Act of 1954, secs. 81, 161, 181, 182, 183, 223, 234, 274 (42 U.S.C. 2111, 2201, 2231, 2232, 2233, 2273, 2282, 2021); Energy Reorganization Act of 1974, secs. 201, 206 (42 U.S.C. 5841, 5846); 44 U.S.C. 3504 note."
regulatory_source: "67 FR 20370, Apr. 24, 2002, unless otherwise noted."
cfr_part: "35"
---


# 35.49 Suppliers for sealed sources or devices for medical use.

For medical use, a licensee may only use—

(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;

(b) Sealed sources or devices non-commercially transferred from a Part 35 licensee or an Agreement State medical use licensee.

(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.

[67 FR 20370, Apr. 24, 2002, as amended at 71 FR 15008, Mar. 27, 2006]