Arizona Administrative Code
Title 9 - HEALTH SERVICES
Chapter 7 - DEPARTMENT OF HEALTH SERVICES - RADIATION CONTROL
Article 6 - USE OF X-RAYS IN THE HEALING ARTS
Section R9-7-603 - Operational Standards, Shielding, and Darkroom Requirements
Universal Citation: AZ Admin Code R 9-7-603
Current through Register Vol. 30, No. 38, September 20, 2024
A. A person shall not make, sell, lease, transfer, lend, or install x-ray equipment or the supplies used in connection with the equipment unless the supplies and equipment, when properly placed in operation and properly used, meets the requirements of 9 A.A.C. 7.
B. A registrant shall direct the operation of x-ray machines under the registrant's control and assure that all of the following provisions are met in the operation of x-ray machines:
1. The
registrant shall not permit any individual to engage in the practice of
"Healing Arts Radiography" using equipment under the registrant's control,
unless the individual possesses, and displays in the primary employer's
facility, an official certificate issued by, or is exempt from, the Medical
Radiologic Technology Board of Examiners that contains an original signature of
its Director or designee. A copy of the certificate shall be posted at any
secondary employment location with documentation that verifies that the
employer has physically seen the official certificate and has annotated on the
copy the location where the official certificate may be viewed by Department
staff.
2. The registrant shall
maintain records documenting compliance with subsection (B)(1) for each
individual practicing "Healing Arts Radiography" using equipment under the
registrant's control,
3. The
registrant shall provide safety rules to each individual operating x-ray
equipment under the registrant's control, including any restrictions in
operating procedures necessary for the safe use of the equipment and require
that the operator demonstrate familiarity with 9 A.A.C. 7.
C. Shielding
1. Each registrant shall provide each
installation with primary and secondary protective barriers that are necessary
to assure compliance with 9 A.A.C. 7, Article 4.
2. A registrant shall ensure that attenuation
provided by a protective barrier meets or exceeds the level of protection
established in Report No. 147 Structural Shielding Design for Medical X-ray
Imaging Facilities, November 19, 2004, by the National Council on Radiation
Protection and Measurements, (NCRP), NCRP Publications, 7910 Woodmount Ave.,
Suite 400, Bethesda, MD 20814-3095. This report is incorporated by reference
and available under
R9-7-101. The incorporated material
contains no future editions or amendments. Copies of the report are available
from NCRP Publications: online at http://www.ncrppublications.org ;
toll free at (800) 229-2652 (Ext. 25); or e-mail at NCRPpubs@NCRPonline.org.
Each registrant shall use this incorporated material to provide sufficient
shielding to prevent a public exposure that exceeds the limits in
R9-7-416.
3. A registrant shall:
a. Mount each lead barrier so that the
barrier will not sag or cold flow because of its own weight and protect the
barrier from damage;
b. Use
barriers designed so that joints between different ends of protective material
do not impair the overall protection of the barriers;
c. Use barriers designed so that joints at
the floor and ceiling do not impair the overall protection of the
barriers;
d. Use windows, window
frames, doors, and door frames that have the same lead equivalence required in
the adjacent walls; and
e. Cover
holes in protective barriers so that overall attenuation is not
impaired.
4. A
registrant shall also meet the structural shielding requirements in
R9-7-607(C), if the x-ray system in question is not a mobile fluoroscopic unit,
dental panoramic, cephalometric, dental CT, or intraoral radiographic
system.
D. Film Processing and Darkroom Requirements. A registrant shall:
1. Ensure that the darkroom is light-tight
and use proper safe-lighting such that any film type in use exposed in a
cassette to x-ray radiation sufficient to produce an optical density from 1 to
2 when processed shall not suffer an increase in density greater than 0.1 (0.05
for mammography) when exposed in the darkroom for two minutes with all
safe-lights illuminated. (A processor with a daylight loader satisfies this
requirement.);
2. Ensure that film
is stored in a cool, dry place and is protected from radiation exposure; and
that film located in open packages is stored in a light-tight
container;
3. Ensure that film
cassettes and intensifying screens are inspected annually, cleaned, and
replaced as necessary;
4. Ensure
that film cassettes contain film and intensifying screens that have the same
sensitivity;
5. Ensure that
automatic film processors develop film in accordance with time-temperature
relationships recommended by the film manufacturer;
6. Ensure that manually developed film is
developed in accordance with the time-temperature relationships recommended by
the manufacturer, and that a timer, thermometer, and a time-temperature chart
are available and used in the darkroom;
7. Ensure that film processing solutions are
prepared and maintained in accordance with the directions of the
manufacturer;
8. Ensure that
outdated film is not used for diagnostic radiographs;
9. Follow manufacturer's recommendations for
cleaning or inspection of computed radiography (CR) cassettes, but not less
than annually;
10. Follow
manufacturer's recommendations for preventive maintenance on digital
radiography panels or cassettes, but not less than annually; and
11. Maintain documentation that demonstrates
that requirements of this subsection are being met for three years for
Department review from the date of inspection.
Disclaimer: These regulations may not be the most recent version. Arizona may have more current or accurate information. We make no warranties or guarantees about the accuracy, completeness, or adequacy of the information contained on this site or the information linked to on the state site. Please check official sources.
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