Current through Register No. 40, October 3, 2024
(a) An application
for a specific license to manufacture or initially transfer devices containing
byproduct material, excluding special nuclear material, to persons generally
licensed under He-P 4031.04, or equivalent
regulations of the NRC, or an agreement state as established by the Atomic
Energy Act of 1954, or a licensing state shall be approved if:
(1) The applicant satisfies the general
requirements of He-P 4030.09;
(2) The applicant submits complete
information relating to the design, manufacture, prototype testing, quality
control, labels, proposed uses, installation, servicing, leak testing,
operating and safety instructions, and potential hazards of the device which
shall ensure that:
a. The device can be
safely operated by persons not having training in radiological
protection;
b. Under ordinary
conditions of handling, storage, and the use of the device, the byproduct
material contained in the device cannot be released or inadvertently removed
from the device;
c. Under ordinary
conditions of handling, storage, and the use of the device, it is unlikely that
any person will receive in one year a dose in excess of 10% of the annual
limits specified in He-P 4020.05; and
d. Under accident conditions (such as fire
and explosion) associated with handling, storage, and use of the device, it is
unlikely that any person would receive an external radiation dose or dose
commitment in excess of the organ doses in Table 4032.1 below:
Table 4032.1 Organ Doses Under Accident Conditions
Body Part
|
Organ Dose
|
Whole body; head and trunk; active blood-forming
organs; gonads, or lens of eye
|
15 rems (150 mSv)
|
Hands and forearms; feet and localized areas of
skin averaged over areas no longer than 1 square centimeter
|
200 rems (2 Sv)
|
Other organs
|
50 rems (500 mSv);
|
(3) Each device bears a durable, legible,
clearly visible label or labels, which contain in a clearly identified and
separate statement:
a. Instructions and
precautions necessary to ensure safe installation, operation, and servicing of
the device or identification of operating and service manuals used to provide
this information;
b. The
requirement, or exemption of a requirement, for leak testing, or for testing
any on-off mechanism and indicator, to include the maximum time interval for
such testing, the identification of radioactive material by isotope, the
quantity of radioactivity, and the date of determination of the quantity;
and
c. The information called for
in the following statement in the same form:
1. "The receipt, possession, use and transfer
of this device Model_____ Serial No._____ are subject to a general license or
the equivalent and the regulations of the NRC, the Agreement State or the
Licensing State which has regulatory authority.";
2. "This label shall be maintained on the
device in a legible condition.";
3.
"Removal of this label is prohibited.";
4. The words, "CAUTION - RADIOACTIVE
MATERIAL"; and
5. The name of the
manufacturer or distributor;
(4) Each device having a separable source
housing that provides the primary shielding for the source also bears on the
source housing, a durable label containing:
a. The device model number and serial
number;
b. The isotope and
quantity;
c. The words, "CAUTION -
RADIOACTIVE MATERIAL";
d. The
radiation symbol described in
He-P
4022.11; and
e. The name of the manufacturer or initial
distributor;
(5) Each
device meeting the criteria of
He-P
4031.04(e) (15) , bears a permanent,
such as embossed, etched, stamped, or engraved, label affixed to the source
housing if separable, or the device if the source housing is not separable,
that includes the words, "CAUTION-RADIOACTIVE MATERIAL", and, if practicable,
the radiation symbol described in
He-P
4022.11; and
(6) The device has been registered in the NRC
Sealed Source and Device Registry.
(b) Should an applicant under
He-P
4032.03(a) (3) b. desire that a
device be required to be leak tested or tested for proper operation of the
on-off mechanism and indicator, at intervals greater than 6 months, DHHS/RHS
shall consider at least the following information in determining the acceptable
interval:
(1) Primary containment (source
capsule);
(2) Protection of primary
containment;
(3) Method of sealing
containment;
(4) Containment
construction materials;
(5) Form of
contained radioactive material;
(6)
Maximum temperature withstood during prototype test;
(7) Maximum pressure withstood during
prototype tests;
(8) Maximum
quantity of contained radioactive material;
(9) Radiotoxicity of contained radioactive
material; and
(10) Operating
experience with identical devices or similarly designed and constructed
devices.
(c) In the
event the applicant under
He-P
4032.03(a) desires that the general
licensee under He-P 4031, or under equivalent regulations of the NRC, an
agreement state, or a licensing state, be authorized to install the device,
collect the sample to be analyzed by a specific licensee for leakage of
byproduct material, service the device, test the on-off mechanism and
indicator, or remove the device from installation, the applicant shall:
(1) Include written instructions to be
followed by the general licensee;
(2) Include the estimated calendar-quarter
doses associated with such activity or activities, and bases for such
estimates; and
(3) Demonstrate that
performance of such activity or activities by an individual untrained in
radiological protection is unlikely to cause that individual to receive a
calendar-quarter dose in excess of 10% of the limits specified in
He-P
4020.06(a) .
(d) If a device containing byproduct material
is to be transferred for use under the general license contained in
He-P
4031.04(b) , each person that is
licensed under He-P 4032.03 shall provide to
each person to whom a device is to be transferred, prior to transferring the
device, the following:
(1) A copy of the
general license contained in
He-P
4031.04(b) , except if paragraphs
He-P
4031.04(e) (2) through (e) (4) or
He-P
4031.04(e) (15) do not apply to the
particular device, those paragraphs may be omitted;
(2) A copy of
He-P
4031.02,
He-P
4030.10(n) ,
He-P
4021.12,
He-P
4021.13, and
He-P
4021.19;
(3) A list of the services that can only be
performed by a specific licensee;
(4) Information on acceptable disposal
options including estimated costs of disposal; and
(5) An indication that DHHS/RHS shall take
enforcement action for improper disposal.
(e) If the transfer specified in
He-P
4032.03(d) is through an
intermediate person, the information to be provided as described in
He-P
4032.03(d) shall also be provided to
the intended user prior to initial transfer to the intermediate
person.
(f) If byproduct material
is to be transferred in a device for use under the equivalent general license
of an agreement state or equivalent regulations of the NRC, or a licensing
state each person that is licensed under
He-P
4032.03 shall provide to each person to whom a device
is to be transferred, prior to transferring the device, the following:
(1) A copy of the agreement state's
regulations equivalent to
He-P
4031.04,
He-P
4031.02,
He-P
4030.10(n) ,
He-P
4021.12, and
He-P
4021.13, a copy of 10 CFR §§31.5, 31.2,
30.51, 20.2201, and 20.2202, or
(2)
A copy of He-P 4031.04,
He-P
4030.02,
He-P
4030.10(n) ,
He-P
4021.12, and
He-P
4021.13, except if certain paragraphs of these rules
do not apply to the particular device, those paragraphs may be disregarded;
a. If a copy of the agreement state's
regulations equivalent to New Hampshire rules as listed in this paragraph, is
provided to a prospective general licensee in lieu of the applicable agreement
state's, licensing state's or NRC regulations, the copy of the agreement
state's, licensing state's or equivalent regulations of the NRC shall be
accompanied by a note explaining that use of the device is regulated by the
agreement state, licensing state or NRC, as applicable; and
b. If certain paragraphs of the regulations
do not apply to the particular device, those paragraphs may be
omitted;
(3) A list of
the services that can only be performed by a specific licensee;
(4) Information on acceptable disposal
options including estimated costs of disposal; and
(5) The name or title, address, and phone
number of the contact at the agreement state or licensing state regulatory
agency or NRC from which additional information may be obtained.
(g) If the transfer specified in
He-P
4032.03(f) is through an
intermediate person, the information to be provided as described in
He-P
4032.03(f) shall also be provided to
the intended user prior to initial transfer to the intermediate
person.
(h) In lieu of the
requirements of He-P 4032.03(d) through (g)
above, the applicant may propose an
alternative approach to informing customers, subject to approval by DHHS/RHS.
In its review of such a request, DHHS/RHS shall ensure that the proposed
alternative approach to informing customers:
(1) Meets the essential objectives of
He-P
4032.03(d) through (g) ;
(2) Provides the same information as required
by He-P
4032.03(d) through (g) ;
and
(3) Is not harmful to public
health and safety.
(i)
Each device that is transferred after November 17, 2005, shall meet the
labeling requirements in
He-P
4032.03(a) (3) through (a) (5) .
(j) If a notification of
bankruptcy has been made under
He-P
4030.10(h) or the license is to be
terminated, each person licensed under
He-P
4032.03 shall provide, upon request, to DHHS/RHS, the
NRC, any appropriate agreement state, or licensing state records of final
disposition required under
He-P
4032.03(m) and (n) .
(k) Each person licensed under
He-P
4032.03 to initially transfer devices to generally
licensed persons shall:
(1) Report, in a
clear and legible report, to DHHS/RHS all transfers of such devices to persons
for use under the general license in
He-P
4031.03 and all receipts of devices from persons
licensed under He-P 4031.03 including:
a. The identity of each general licensee by
name and mailing address, and address location of use. If there is no mailing
address for the location of use, an alternative address for the general
licensee shall be submitted along with information on the actual location of
use;
b. The name, title, and
telephone number of the individual identified by the general licensee as having
knowledge of and authority to take required actions to ensure compliance with
the applicable rules, and who may constitute a point of contact between
DHHS/RHS and the general licensee;
c. The date of transfer;
d. The type, model number, and serial number
of device transferred;
e. The
quantity and type of byproduct material contained in the device;
f. If one or more intermediate persons will
temporarily possess the device at the intended place of use prior to its
possession by the user, the general licensee shall provide the same information
for both the intended user and each intermediate person, which shall clearly
designate and identify the intermediate person(s); and
g. The identity of the specific licensee
submitting the report, including the license number of the specific
licensee;
(2) Report, in
a clear and legible report, to DHHS/RHS all receipts of devices from persons
licensed under He-P 4031.03, including, for
devices received from persons generally licensed under
He-P
4031.03:
a. The
identity of the general licensee by name and address;
b. The type, model number, and serial number
of the device received;
c. The date
of receipt, and, in the case of devices not initially transferred by the
reporting licensee, the name of the manufacturer or initial transferor;
and
(3) Report to
DHHS/RHS the identity of the general licensee, the device, and the changes to
information on the device label, if the licensee authorized under
He-P
4032.03 makes changes to a device possessed by a
general licensee authorized under
He-P
4031.04(b) , such that the label must
be changed to update required information;
(4) Report to DHHS/RHS if no transfers have
been made to or from persons generally licensed under
He-P
4031.04(b) during the reporting
period;
(5) Report to the NRC, on
NRC Form 653 "Transfers of Industrial Devices Report" or in a clear and legible
report containing all data required by the form, all transfers of such devices
to persons for use under the NRC general license in section 31.5 of 10 CFR
31;
(6) Report to the responsible
agreement state, licensing state agency or the NRC all transfers of such
devices to persons for use under a general license in the agreement state's
licensing state's or NRC regulations equivalent to He-P 4031;
(7) Identify in the report required by
He-P
4032.03(k) (5) or (6) , the
following:
a. The identity of each general
licensee by name and mailing address, and address location of use; if there is
no mailing address for the location of use, an alternative address for the
general licensee shall be submitted along with information on the actual
location of use;
b. The name,
title, and telephone number of the individual identified by the general
licensee as having knowledge of and authority to take required actions to
ensure compliance with the applicable rules, and who may constitute a point of
contact between the agency and the general licensee;
c. The date of transfer;
d. The type, model, and serial number of the
device transferred;
e. The quantity
and type of byproduct material contained in the device; and
f. The identity of the specific licensee
submitting the report, including the license number of the specific
licensee;
(8) Report to
the NRC, on NRC Form 653 "Transfers of Industrial Devices Report" or in a clear
and legible report containing all data required by the form, all receipts of
such devices from persons authorized under the NRC general license in section
31.5 of 10 CFR 31;
(9) Report to
the responsible agreement state, or licensing state agency or the NRC all
receipts of such devices from persons authorized under a general license in the
agreement state's, licensing state's or NRC regulations equivalent to
He-P
4031.04;
(10) Include in the report for devices
received from persons generally licensed under agreement state, licensing
state, or NRC regulations equivalent to
He-P
4031.04:
a. The
identity of the general licensee by name and address;
b. The type, model number, and serial number
of the device received;
c. The date
of receipt, and, in the case of devices not initially transferred by the
reporting licensee, the name of the manufacturer or initial transferor;
and
d. The identity of the specific
licensee submitting the report, including the license number of the specific
licensee;
(11) Report to
the responsible agreement state or licensing state agency or the NRC, the
identity of the general licensee, the device, and the changes to information on
the device label, if the licensee authorized under
He-P
4032.03 makes changes to a device possessed by a
general licensee authorized under regulations equivalent to
He-P
4031.04(b) , such that the label must
be changed to update required information;
(12) Report to the NRC, if no transfers have
been made to or from NRC general licensees during the reporting
period;
(13) Report to the
agreement state or licensing state agency or the NRC regulated state if no
transfers have been made to or from that agreement state or licensing state or
the NRC regulated state during the reporting period;
(14) Keep records showing:
a. The name of each general licensee or
intermediate person to whom transfers of byproduct material in devices for use
pursuant to the general license provided in
He-P
4031.04, or equivalent regulations of the NRC, an
agreement state or licensing state have been made;
b. Address of each general licensee or
intermediate person to whom transfers of byproduct material in devices for use
pursuant to the general license provided in
He-P
4031.04, or equivalent regulations of the NRC, an
agreement state or licensing state have been made;
c. The point of contact for each general
licensee or intermediate person to whom transfers of byproduct material in
devices for use pursuant to the general license provided in
He-P
4031.04, or equivalent regulations of the NRC, an
agreement state or licensing state have been made;
d. The date of each transfer of byproduct
material;
e. Identification of the
radioisotope contained in each device transferred;
f. The quantity of radioactivity in each
device transferred;
g. The identity
of any intermediate person; and
h.
The requirements of He-P 4031 specifics for this transfer;
(15) Cover each calendar quarter in its
reports submitted under He-P 4032;
(16) Submit reports required in
He-P
4032.03 within 30 days of the end of the calendar
quarter; and
(17) Indicate in
reports required in He-P 4032.03, the period covered
by the report.
(l) In
the event that one or more intermediate persons will temporarily possess the
device at the intended place of use prior to its possession by the user, the
licensee shall provide the same information for both the intended user and each
intermediate person, and shall clearly designate the identity of the
intermediate person(s); and
(m)
Each person licensed under
He-P
4032.03 shall maintain all information concerning
transfers and receipts of devices that supports the reports required by this
section.
(n) Records required by
(l) shall be maintained for a period of 3 years following the date of the
recorded event.
(See Revision Note at part heading for He-P 4032) #6942,
eff 2-1-99; ss by #8488, eff 11-18-05; ss by #8959, eff
8-7-07