Current through Register Vol. 39, No. 6, September 16, 2024
(a)
Unless specifically provided otherwise by the rules in this Chapter, the
requirements in this Rule shall apply to all x-ray systems, except for
fluoroscopic and dental intraoral x-ray systems. The useful beam of x-ray
systems subject to provisions of this Rule shall be limited to the area of
clinical interest or the image receptor, whichever is smaller.
(1) General purpose stationary and mobile
x-ray systems shall meet the following special requirements:
(A) There shall be provided a means for
stepless adjustment of the size of the x-ray field. The minimum field size at a
SID of 100 centimeters shall be equal to or less than five centimeters by five
centimeters.
(B) Means shall be
provided for visually defining the perimeter of the x-ray field. The total
misalignment of the edges of the visually defined field with the respective
edges of the x-ray field along either the length or width of the visually
defined field shall not exceed two percent of the distance from the source to
the center of the visually defined field when the surface upon which it appears
is perpendicular to the axis of the x-ray beam.
(C) Notwithstanding Parts (a)(1)(A) and (B)
of this Rule, equipment manufactured before August 1, 1974 may employ fixed
cones and diaphragms or variable collimators without beam defining
lights.
(2) In addition
to the requirements of Subparagraph (a)(1) of this Rule, all stationary x-ray
systems, except equipment originally manufactured before the effective date of
this Rule, shall meet the following requirements:
(A) Means shall be provided to indicate when
the axis of the x-ray beam is perpendicular to the plane of the image receptor,
to align the center of the x-ray field with respect to the center of the image
receptor to within two percent of the SID, and to indicate the SID to within
two percent;
(B) The beam limiting
device shall numerically indicate the field size in the plane of the image
receptor to which it is adjusted;
(C) Indication of field size dimensions and
SID's shall be specified in inches or centimeters and shall be such that
aperture adjustments result in x-ray field dimensions in the plane of the image
receptor which correspond to those of the image receptor to within two percent
of the SID when the beam axis is perpendicular to the plane of the image
receptor.
(3)
Radiographic equipment designed for only one image receptor size at a fixed SID
shall be provided with means to limit the field at the plane of the image
receptor to dimensions no greater than those of the image receptor and to align
the center of the x-ray field with the center of the image receptor to within
two percent of the SID.
(4) Special
purpose x-ray systems shall meet the following requirements:
(A) These systems shall be provided with
means to limit the x-ray field in the plane of the image receptor so that such
field does not exceed each dimension of the image receptor by more than two
percent of the SID when the axis of the x-ray beam is perpendicular to the
plane of the image receptor.
(B)
Such systems shall also be provided with means to align the center of the x-ray
field with the center of the image receptor to within two percent of the
SID.
(C) The requirements in Parts
(a)(4)(A) and (B) of this Rule may be met with a system that meets the
requirements for a general purpose x-ray system as specified in Subparagraph
(a)(1) of this Rule or, when alignment means are also provided, as follows:
(i) an assortment of removable,
fixed-aperture, beam-limiting devices sufficient to meet the requirement for
each combination of image receptor size and SID for which the unit is designed,
where each device has clear and permanent markings to indicate the image
receptor size and SID for which it is designed; or
(ii) a beam-limiting device having multiple
fixed apertures sufficient to meet the requirement for each combination of
image receptor size and SID for which the unit is designed, where the device
has permanent, clearly legible, markings indicating image receptor size and SID
for which the unit is designed, where the device has permanent, clearly
legible, markings indicating image receptor size and SID for which each
aperture is designated and indicating which aperture is in position for
use.
(b) Radiation exposure control devices shall
meet the following requirements:
(1) Means
shall be provided to terminate the exposure after a preset time interval,
preset product of current and time, a preset number of pulses or a preset
radiation exposure to the image receptor. In addition:
(A) Termination of exposure shall cause
automatic resetting of the timer to its initial setting or to zero except
during serial radiography, and
(B)
It shall not be possible to make an exposure when the timer is set to a zero or
"off" position if either position is provided.
(2) Control over x-ray exposures shall be in
accordance with the following requirements:
(A) A control shall be incorporated into each
x-ray system such that the operator can terminate an exposure at any time
except for serial radiography where means may be provided to permit completion
of any single exposure of the series in process.
(B) Each x-ray control shall be located in
such a way as to meet the following criteria.
(i) For stationary x-ray systems, the control
shall be permanently mounted in a protected area so that the operator is
required to remain in that protected area during the entire exposure;
and
(ii) The x-ray control shall
provide visual indication observable at or from the operator's protected
position whenever x-rays are produced. In addition, except for equipment
originally manufactured before the effective date of this Rule, a signal
audible to the operator shall indicate that the exposure has
terminated.
(3) When an automatic exposure control (e.g.,
phototimer) is provided the following requirements shall be met, except
equipment originally manufactured before the effective date of this Rule:
(A) Indication shall be made on the control
panel when this mode of operation is selected;
(B) When the x-ray tube potential is equal to
or greater than 50 kVp, the minimum exposure time for field emission equipment
rated for pulsed operation shall be equal to or less than a time interval
equivalent to two pulses;
(C) The
minimum exposure time for all equipment other than that specified in Part
(b)(3)(B) of this Rule shall be equal to or less than 1/60 second or a time
interval required to deliver five mAs, whichever is greater;
(D) Either the product of peak x-ray tube
potential, current and exposure time shall be limited to not more than 60 kWs
per exposure or the product of x-ray tube current and exposure time shall be
limited to not more than 600 mAs per exposure except when the x-ray tube
potential is less than 50 kVp, in which case the product of x-ray tube current
and exposure time shall be limited to not more than 2000 mAs per exposure;
and
(E) A visible signal shall
indicate when an exposure has been terminated at the limits described in Part
(b)(3)(D) of this Rule and manual resetting shall be required before further
automatically timed exposures can be made.
(4) When four timer tests are performed at
identical timer setting equal to 5.0 seconds or less, the average time period
(T) shall be greater than five times the difference between the maximum period
(Tmax) and the minimum period (Tmin) in accordance with the formula:
T > 5(Tmax-Tmin)
(c) Source-skin or source-image receptor
distance shall meet the following requirement:
All radiographic systems shall be provided with a durable,
securely fastened means to limit the source-skin distance to at least 30
centimeters. This is considered to be met when the collimator or cone provides
the required limits.
(d)
The exposure produced shall be reproducible to within the following criteria:
When all technique factors are held constant, the coefficient
of variation shall not exceed 0.10. This shall be deemed to be met if, when
four exposures at identical technique factors are made, the value of the
average exposure (E)is greater than five times the difference between the
maximum exposure (Emax) and the minimum exposure (Emin) in accordance with the
formula:
E > 5(Emax-Emin)
(e) Standby radiation from capacitor energy
storage equipment, when the exposure switch or timer is not activated, shall
not exceed a rate of two milliroentgens per hour at five centimeters from any
accessible surface of the diagnostic source assembly with the beam-limiting
device fully open.
(f) Linearity
(1) When the equipment allows a choice of
x-ray tube current settings, the average ratios of exposure to the indicated
milliampere-seconds product, i.e., mR/mAs, obtained at any two consecutive tube
current settings shall not differ by more than 0.10 times their sum, i.e.,
/mean of x1- x2/(LESS THAN EQUAL TO)minus 0.10 mean of (x1+ x2), where the mean
of x1 and x2 are the average mR/mAs values obtained at each of two consecutive
tube current settings.
(2)
Compliance shall be determined at the most commonly used mA stations by
measuring mR/mAs at those stations and at one adjacent station to
each.
(g) Timer accuracy
(1) For indicated values of 0.10 seconds and
above, the measured value shall be within plus or minus 15 percent of the
indicated values for equipment manufactured before August 1, 1974.
(2) For equipment manufactured after August
1, 1974, the deviation of measured values from indicated values shall not
exceed the limits specified for that system by its manufacturer.
Authority
G.S.
104E-7;
Eff. February 1,
1980;
Amended Eff. May 1, 1993; November 1, 1989; October 1,
1980;
Transferred and Recodified from
15A NCAC
11.0606 Eff. February 1,
2015.