[Code of Federal Regulations]
[Title 10, Volume 1]
[Revised as of January 1, 2001]
From the U.S. Government Printing Office via GPO Access
[CITE: 10CFR35.60]

[Page 566]
 
                            TITLE 10--ENERGY
 
                CHAPTER I--NUCLEAR REGULATORY COMMISSION
 
PART 35--MEDICAL USE OF BYPRODUCT MATERIAL--Table of Contents
 
                Subpart C--General Technical Requirements
 
Sec. 35.60  Syringe shields and labels.

    (a) A licensee shall keep syringes that contain byproduct material 
to be administered in a radiation shield.
    (b) To identify its contents, a licensee shall conspicuously label 
each syringe or syringe radiation shield that contains a syringe with a 
radiopharmaceutical. The label must show the radiopharmaceutical name or 
its abbreviation, the clinical procedure to be performed, or the 
patient's or the human research subject's name.
    (c) A licensee shall require each individual who prepares a 
radiopharmaceutical kit to use a syringe radiation shield when preparing 
the kit and shall require each individual to use a syringe radiation 
shield when administering a radiopharmaceutical by injection unless the 
use of the shield is contraindicated for that patient or human research 
subject.

[51 FR 36951, Oct. 16, 1986, as amended at 59 FR 61784, Dec. 2, 1994]