Code of Federal Regulations > Title 10 > Chapter I > Part 35 - PART 35—MEDICAL USE OF BYPRODUCT MATERIAL

U.S. Code of Federal Regulations

Regulations most recently checked for updates: Aug 27, 2025

Subpart A [§ 35.1 - § 35.19] - Subpart A—General Information

Subpart B [§ 35.24 - § 35.59] - Subpart B—General Administrative Requirements

Subpart C [§ 35.60 - § 35.92] - Subpart C—General Technical Requirements

Subpart D [§ 35.100 - § 35.290] - Subpart D—Unsealed Byproduct Material—Written Directive Not Required

Subpart E [§ 35.300 - § 35.396] - Subpart E—Unsealed Byproduct Material—Written Directive Required

Subpart F [§ 35.400 - § 35.491] - Subpart F—Manual Brachytherapy

Subpart G [§ 35.500 - § 35.590] - Subpart G—Sealed Sources for Diagnosis

Subpart H [§ 35.600 - § 35.690] - Subpart H—Photon Emitting Remote Afterloader Units, Teletherapy Units, and Gamma Stereotactic Radiosurgery Units

Subpart I - Subparts I-J [Reserved]

Subpart K [§ 35.1000 - § 35.1000] - Subpart K—Other Medical Uses of Byproduct Material or Radiation From Byproduct Material

Subpart L [§ 35.2024 - § 35.2655] - Subpart L—Records

Subpart M [§ 35.3045 - § 35.3204] - Subpart M—Reports

Subpart N [§ 35.4001 - § 35.4002] - Subpart N—Enforcement