MEDICAL USE OF BYPRODUCT MATERIAL

10 C.F.R. Part 35

in effectEffective: 2024-07-01

Contents

subpartA. General Information subpartB. General Administrative Requirements subpartC. General Technical Requirements subpartD. Unsealed Byproduct Material—Written Directive Not Required subpartE. Unsealed Byproduct Material—Written Directive Required subpartF. Manual Brachytherapy subpartG. Sealed Sources for Diagnosis subpartH. Photon Emitting Remote Afterloader Units, Teletherapy Units, and Gamma Stereotactic Radiosurgery Units subpartI-J. Subparts I-J [Reserved]subpartK. Other Medical Uses of Byproduct Material or Radiation From Byproduct Material subpartL. Records subpartM. Reports subpartN. Enforcement

Source: eCFRURL: https://www.ecfr.gov/api/versioner/v1/full/2024-07-01/title-10.xmlFetched: 7/26/2026