Cal. Code Regs. tit. 17, § 30192.5
(a) A general license is hereby issued to any physician, veterinarian, clinical laboratory or hospital to possess and use radioactive material in prepackaged units for in vitro clinical testing, not exceeding the following:
Radionuclide
Maximum uCi* per unit
Maximum uCi total
Tritium
50
2,000
Carbon-14
10
2,000
Iron-59
20
200
Selenium-75
10
200
Cobalt-57
10
200
Iodine-125 or Iodine-131
10
200
Mock Iodine-125
Reference Source
Iodine-129
0.05
-
Americium-241
0.005
-
* microcurie (uCi)
(b) The general licensee shall not possess or use radioactive material under the general license issued pursuant to subsection (a):
(2) Unless the prepackaged unit bears a label or is accompanied by a package insert containing the following or a substantially similar statement:
“This radioactive material may be received and used only by physicians, veterinarians, clinical laboratories or hospitals, and only for in vitro clinical or laboratory tests not involving internal or external administration of the material or the radiation therefrom to human beings or animals. The receipt, possession, use and transfer of this material is subject to the regulations and general license of the United States Nuclear Regulatory Commission or a state with which the Commission has entered into an agreement for the exercise of regulatory authority.”
Note: Authority cited: Sections 114975, 115000 and 131200, Health and Safety Code. Reference: Sections 114965, 114970, 114985(g), 115000, 115060, 115165, 115230, 115235, 131050, 131051 and 131052, Health and Safety Code.
1. New section filed 7-7-86; effective thirtieth day thereafter (Register 86, No. 28).
2. Amendment of subsection (c) and Note filed 9-9-97; operative 10-9-97 (Register 97, No. 37).
3. Amendment of section and Note filed 6-8-2011; operative 7-8-2011 (Register 2011, No. 23).
4. Editorial correction amending column heading in subsection (a) (Register 2011, No. 24).