Current through Register Vol. 39, No. 6, September 16, 2024
(a) Persons
possessing generally licensed items, manufactured or initially transferred
pursuant to Subpart B of 10 CFR 32, shall comply with the provisions of 10 CFR
31, which are hereby incorporated by reference including subsequent amendments
and editions, as follows:
(1) Reports,
notifications, and responses to agency requests for information required by
this Rule shall be made to the agency at the address shown in Rule .0111 of
this Chapter unless directed otherwise by the agency;
(2)
10 CFR
31.1, "Purpose and scope;"
(3)
10 CFR
31.2, "Terms and conditions;"
(4)
10 CFR
31.5, "Certain detecting, measuring, gauging,
or controlling devices and certain devices for producing light or an ionized
atmosphere," except that the fee required by
10 CFR
170.31 shall not apply. Persons using devices
described in 31.5(a) shall be registered with the agency. Device registration
shall be made in accordance with Paragraph (b) of this Rule and shall contain
the information required by 31.5(c)(13)(iii);
(5)
10 CFR
31.6, "General license to install devices
generally licensed in 10 CFR
31.5;"
(6)
10 CFR
31.7, "Luminous safety devices in
aircraft;"
(7)
10 CFR
31.8, "Americium-241 and radium-226 in the
form of calibration or reference sources;"
(8)
10 CFR
31.9, "General license to own byproduct
material;"
(9)
10 CFR
31.10, "General license for strontium 90 in
ice detection devices;"
(10)
10 CFR
31.11, "General license for use of byproduct
material for certain in vitro clinical or laboratory testing," except that
persons required by 31.11(b) to register devices with the agency shall comply
with the provisions of Paragraph (b) of this Rule;
(11)
10 CFR
31.12, "General license for certain items and
self-luminous products containing radium-226;" and
(12)
10 CFR
31.21, "Maintenance of
records;"
(b) Persons
registering devices shall use General License Application for Registration
forms provided by the agency. These forms are available free of charge at:
https://radiation.ncdhhs.gov/rms/rmsgenlicforms.htm. Applications and
supporting material shall be submitted to the agency by e-mail at
Licensing.ram@dhhs.nc.gov, or at the address shown in Rule .0111 of this
Chapter in lieu of the United States Nuclear Regulatory Commission. The
following information shall appear on the application:
(1) facility name, mailing address, physical
address if different from the mailing address, and the name of the county where
the facility is located;
(2) type
of device;
(3) device
manufacturer;
(4) device model
numbers and serial numbers;
(5)
number of devices being registered, isotopes, and activity;
(6) indicate if the devices have been leak
tested by checking the corresponding check box;
(7) if the devices have been leak tested,
write down the frequency that leak tests are required;
(8) the name of the person or company
performing the leak test;
(9)
describe the method of device disposal; and
(10) the signature, printed name, title, date
the form is signed and telephone number of the contact person.
(c) Copies of the regulations
incorporated by this Rule are available free of charge at
https://www.nrc.gov/reading-rm/doc-collections/cfr/part031/.
Authority
G.S.
104E-7;
104E-10(b);
Eff. February 1, 1980;
Amended Eff. June 1, 1989; October 1, 1984;
October 1, 1980;
Transferred and Recodified from
15A NCAC
11.0302 Eff. February 1, 2015;
Amended Eff. March 1, 2017.
