For purposes of this chapter, the terms in this part have the meanings given them.
"Absorbed dose" means the energy imparted by ionizing radiation per unit mass of irradiated material. The special unit of absorbed dose is the rad under the conventional system of measurement and is the gray under the SI system of measurement.
"Absorbed dose rate" means absorbed dose per unit time for machine with timers, or dose-monitor unit per unit time for linear accelerators.
"Accelerator" means any machine capable of accelerating electrons, protons, deuterons, or other charged particles in a vacuum and of discharging the resultant particulate or other radiation into a medium at energies usually in excess of 1 MeV. For purposes of this definition, linear accelerator, particle accelerator, and cyclotron are equivalent terms.
"Added filtration" means filtration that is in addition to the inherent filtration.
"Adult" means an individual 18 or more years of age or older.
"Air kerma (K)" means the kinetic energy released in air by ionizing radiation. Kerma is determined as the quotient of dE by dM, where dE is the sum of the initial kinetic energies of all the charged ionizing particles liberated by uncharged ionizing particles in air of mass dM. The special name for the unit of kerma is the gray (Gy). The SI unit is joule per kilogram.
"Aluminum equivalent" means the thickness of type 1100 aluminum alloy affording the same attenuation, under specified conditions, as the material in question.
"Annual" means an activity is done or is performed at intervals not to exceed 12 months.
"Appropriate limit" or "appropriate limits" means the maximum permissible dose or doses of radiation that may be administered to the whole body or a given part of a human being.
"As low as reasonably achievable" or "ALARA" means making every reasonable effort to maintain exposure to radiation as far below the dose limits as is practical, consistent with the purpose for which the registered activity is undertaken, taking into account the state of technology, the economics of improvement in relation to benefits to the public health and safety, and other societal and socioeconomic considerations.
"Attenuation" means the reduction of exposure rate upon passage of radiation through matter.
"Attenuation block" means a block or stack, having dimensions 20 centimeters or larger by 20 centimeters or larger by 3.8 centimeters, of type 1100 aluminum alloy or other materials having equivalent attenuation that is large enough to intercept the entire x-ray beam.
"Audit" means a planned and documented activity performed according to procedures to determine, by examination and evaluation of objective evidence, the adequacy of and extent to which applicable elements of the quality assurance program have been developed, documented, and effectively implemented.
"Automatic exposure control" or "AEC" means a device that automatically controls one or more technique factors in order to obtain a required quantity of radiation at a preselected location or locations.
"Base plus fog density" means the optical density of a film due to its base density plus any action of the developer on the unexposed silver halide crystals.
"Beam axis" means a line from the source through the centers of the x-ray fields, or for therapy the axis of rotation of the beam-limiting device.
"Beam-limiting device" or "BLD" means a device used to restrict the dimensions of the x-ray field or useful beam.
"Beam-monitoring system" means a system designed and installed to detect and measure the radiation present in the useful beam.
"Beam-scattering filter" or "foil" means a thin piece of material, usually metallic, placed in the beam to scatter a beam of electrons in order to provide a more uniform electron distribution in the useful beam.
"Bent beam linear accelerator" means a linear accelerator geometry in which the accelerated electron beam must change direction by passing through a bending magnet.
"Bone densitometry system" means a medical device that uses electronically produced ionizing radiation to determine the density of bone structures of human patients.
"C-arm system" means an x-ray system in which the image receptor and the x-ray tube housing assembly are connected by a common mechanical support system to maintain a desired spatial relation.
"Cabinet x-ray system" means an x-ray system with the x-ray tube installed in an enclosure independent of existing architectural structure except the floor on which it may be placed. The cabinet x-ray system is intended to:
contain at least that portion of a material being irradiated;
provide radiation attenuation; and
exclude personnel from its interior during generation of radiation.
Included are all x-ray systems designed primarily for the inspection of carry-on baggage at airline, railroad, and bus terminals and in similar facilities. An x-ray tube used within a shielded part of a building or x-ray equipment that may temporarily or occasionally incorporate portable shielding is not considered a cabinet x-ray system.
the determination of the response or reading of an instrument relative to a series of known radiation values over the range of the instrument;
the determination of the radiation dose or exposure rate at a designated distance from a radiation source under specified conditions of measurement;
to check, adjust, or systematically standardize to graduations of a quantitative measuring instrument; and
to check, adjust, or systematically bring radiation-producing equipment into manufacturer's specifications.
"Cephalometric device" means a device intended for the radiographic visualization and measurement of the dimensions of the human head.
"Certified cabinet x-ray system" means an x-ray system that has been certified according to Code of Federal Regulations, title 21, section 1010.2, as being manufactured and assembled pursuant to Code of Federal Regulations, title 21, section 1020.40.
"Certified components" means components of x-ray systems that are subject to the x-ray equipment performance standards adopted under Public Law 90-602, the Radiation Control for Health and Safety Act of 1968.
"Certified system" means an x-ray system that has one or more certified components.
"Changeable filters" means any filter, exclusive of inherent filtration, that can be removed from the useful beam through any electronic, mechanical, or physical process.
"Clinical range" means the range of control console technique settings that a facility would use in its routine x-ray projections. Equipment performance tests are performed over clinical ranges.
"Coefficient of variation" or "C" means the standard deviation divided by the average of the parameters measured.
"Collimation" means the restriction of the useful beam to an appropriate area.
"Collimator" means a device used to limit the size, shape, and direction of the primary beam.
"Commissioner" means the commissioner of the Department of Health.
"Computed radiography" means a system of creating digital radiographic images that utilizes a storage-phosphor plate instead of film in a cassette. Once the plate is exposed, a laser beam scans it to produce the digital data that is translated into an image.
"Computed tomography" or "CT" means the production of a tomogram by the acquisition and computer processing of x-ray transmission data.
"Control panel" means the part of the x-ray control upon which the switches, knobs, push buttons, and other hardware necessary for manually setting the technique factors are mounted.
"CT conditions of operation" means all selectable parameters governing the operation of a CT system including, but not limited to, nominal tomographic section thickness, filtration, and the technique factors defined in subpart 195.
"CT dose index" or "CTDI" means the integral from minus 7T to plus 7T of the dose profile along a line perpendicular to the tomographic plane divided by the product of the nominal tomographic section thickness (T) and the number of tomograms produced in a single scan (n), that is:
z = position along a line perpendicular to the tomographic plane;
D(z) = dose at position z;
T = nominal tomographic section thickness; and
n = number of tomograms produced in a single scan.
This definition assumes that the dose profile is centered around z=0 and that, for a multiple tomogram system, the increment of adjacent scans is nT.
"CT gantry" means the tube housing assemblies, beam-limiting devices, and detectors, as well as the supporting structures and frames that hold those components.
"CT number" means the number used to represent the x-ray attenuation associated with each elemental area of the CT image.
"CT scan" means the complete process of collecting x-ray transmission data for the production of a tomogram. This includes data collected simultaneously during a single scan for the production of one or more tomogram.
"CT scan increment" means the amount of relative displacement of the patient with respect to the CT system between successive scans measured along the direction of the displacement.
"CT scan time" means the time between the beginning and end of x-ray transmission data accumulation for a CT scan.
"Dead-man switch" means a switch so constructed that a circuit-closing contact can be maintained only by continuous pressure on the switch by the operator.
"Declared pregnant woman" means a woman who has voluntarily informed the registrant, in writing, of her pregnancy and the estimated date of conception. The declaration remains in effect until the declared pregnant woman withdraws the declaration in writing or is no longer pregnant.
"Densitometer" means an instrument that measures the degree of blackening or radiographic density of a film due to radiation or light by measuring the ratio of the light intensity incident on the film to the light intensity transmitted by the film.
"Diagnostic radiological physicist" means an individual who is qualified to practice independently in the appropriate subfields for medical diagnostic physics and is:
certified in radiological physics or diagnostic radiological physics by the American Board of Radiology;
certified in diagnostic physics by the American Board of Medical Physics;
certified in diagnostic physics by the Canadian College of Medical Physics; or
a holder of a masters degree in medical physics, radiological sciences, or an equivalent field involving graduate study in physics applied to the application of radiation to humans from an accredited college or university and has at least two years of full-time practical training or supervised experience under an individual who meets the qualifications in item A, B, or C.
"Diagnostic x-ray imaging system" means an assemblage of components for the generation, emissions, and reception of x-rays and the transformation, storage, and visual display of the resultant x-ray image which are designed and used for irradiation of any part of a body for the purpose of diagnosis or visualization.
"Digital radiography" means a radiographic image displayed on a video monitor after computer processing.
"Direct supervision" means guidance and instruction by a qualified individual who is physically present and watching the performance of the radiological operation or procedure and in such proximity that contact can be maintained and immediate assistance can be given as required.
"Dose" means absorbed radiation dose, radiation dose equivalent, effective radiation dose equivalent, committed radiation dose equivalent, committed effective radiation dose equivalent, or total effective radiation dose equivalent. For purposes of this chapter, "radiation dose" is an equivalent term.
"Dose equivalent" or "DE" means a quantity used for radiation protection purposes that expresses on a common scale for all radiations the irradiation incurred by exposed persons. It is defined as the product of the absorbed radiation dose and the quality factor. For x-rays and gamma rays, the dose equivalent in rem is usually assumed to be numerically equal to either the exposure in roentgens or the absorbed dose in rad. The special unit radiation dose equivalent is the rem under the conventional measurement system and is the sievert under the SI measurement system.
"Dose limits" or "limits" means the permissible upper bounds of radiation doses.
"Dose-monitoring system" means a system of devices for the detection, measurement, and display of quantities of radiation that can be related to the absorbed dose at a given location within a defined geometry.
"Dose-monitor unit" means a unit response from the dose-monitoring system from which the absorbed radiation dose has been calculated.
"Effective dose equivalent" or "HE" means the sum of the products of the dose equivalent to each organ or tissue (HT) and the weighting factor (wT) applicable to each of the body organs or tissues that are irradiated.
"Electron-beam generator" means a type of electron accelerator in which the electron beam is brought out into the atmosphere for irradiation purposes.
"Electronic signature" means an electronic sound, symbol, or process attached to or logically associated with a record, and executed or adopted by a person with the intent to sign the record according to Minnesota Statutes, chapter 325L.
"Exposure" means being exposed to ionizing radiation. The unit of exposure is the Roentgen in air (R). The SI unit is 2.58 x 10-4 coulombs per kilogram.
"Exposure rate" means the exposure per unit of time, such as roentgen per minute, milliroentgen per hour. The SI unit is 10-4 coulombs per kilogram per hour.
"External beam radiation therapy" means therapeutic irradiation in which the source of radiation is at a distance from the body.
"Facility" means the location at which one or more sources of radiation are installed or located within one building, one vehicle, at one address, and are under the same administrative control.
"Field emission equipment" means equipment that uses an x-ray tube in which electron emission from the cathode is due solely to the action of an electric field.
"Field-flattening filter" means a filter used to homogenize the absorbed dose rate over the radiation field.
"Filmless radiography" or "photostimulable storage phosphor (PSP) imaging" means a system that could employ reusable imaging plates, associated hardware and software to acquire and display digital projection radiographs. These imaging devices are known by a number of names including computed radiography (CR), photostimulable storage phosphor (PSP) imaging, or digital radiography (DR). In the digital form, PSP images are readily put into picture archiving and communications systems and viewed on a monitor rather than viewing an image on x-ray film.
"Filter" or "filtration" means material placed in the useful beam to preferentially absorb selected radiations.
"Fluoroscopic imaging assembly" means a subsystem in which x-ray photons produce a set of fluoroscopic or radiographic recorded images from the fluoroscopic image receptor. Fluoroscopic imaging assembly includes image receptors such as the image intensifier and spot-film device, electrical interlocks, if any, and structural material providing linkage between the image receptor and diagnostic source assembly.
"Focal spot" means the area of the anode of the x-ray tube bombarded by the electrons accelerated from the cathode and from which the useful beam originates.
"Gantry" means the part of the system supporting and allowing possible movements of the radiation head.
"General purpose radiographic x-ray system" means a radiographic x-ray system that, by design, is not limited to radiographic examination of specific anatomical regions.
"Gonad shield" means a protective barrier for the testes or ovaries.
"Gray" or "Gy" means the unit of absorbed radiation dose equal to one joule per kilogram. The conventional system equivalent is 100 rad.
"Half-value layer" or "HVL" means the thickness of a specified material that attenuates the beam of radiation to such an extent that the exposure rate is reduced to one-half of its original value. The contribution of all scattered radiation, other than any that might be present initially in the beam concerned, is considered excluded.
"Healing arts" means health professions for diagnostic or healing treatment of human and animal maladies that are regulated under Minnesota Statutes, chapter 147, 153, or 156; or section 148.01, 148.106, or 150A.05, subdivision 1, clause (4), for the lawful practice of medicine, dentistry, veterinary medicine, osteopathic medicine, chiropractic, and podiatry.
"Healing arts screening" or "screening" means the testing of individuals with x-ray equipment to detect or evaluate health conditions when the tests are not specifically and individually ordered by a licensed practitioner of the healing arts who is legally authorized to prescribe the tests for the purpose of diagnosis or treatment.
"High radiation area" means any area, accessible to individuals, in which radiation levels from radiation sources external to the body could result in an individual receiving a radiation dose equivalent in excess of 0.1 rem (1.0 mSv) in one hour at 30 centimeters from any source of radiation or 30 centimeters from any surface that the radiation penetrates.
"Image intensifier" means a device, installed in its housing, that instantaneously converts an x-ray pattern into a corresponding light image of higher energy intensity.
"Image quality" means the overall clarity and detail of a radiographic image. Limiting spatial resolution (or resolving power), image sharpness, and image contrast are three common measures of image quality.
"Image receptor" means a device such as a fluorescent screen or radiographic film, solid-state detector, or gaseous detector that transforms incident x-ray photons either into a visible image or into another form that can be made into a visible image by further transformations.
"Individual" means a human being.
"Individual monitoring" means the assessment of dose equivalent by the use of individual monitoring devices or by the use of radiation survey data.
"Individual monitoring devices" means devices designed to be worn by a single individual for the assessment of dose equivalent. For purposes of this chapter, "personal dosimeter" and "dosimeter" are equivalent terms. Examples of individual monitoring devices are film badges, thermoluminescent devices, pocket ionization chambers, and optically stimulated luminescence devices.
"Industrial cabinet baggage system" has the meaning given for cabinet x-ray systems in subpart 24.
"Industrial vault radiography" means industrial radiography conducted in an enclosure, shielded so that radiation levels at every location on the exterior meet the unrestricted limitations in this chapter.
"Industrial radiographer" means any individual who performs or who, in attendance at the site where ionizing radiation sources are being used, personally supervises industrial radiographic operations and who is responsible to the registrant for ensuring compliance with this chapter.
"Industrial radiographer's assistant" means an individual who uses radiographic exposure devices or radiation survey instruments in industrial radiography under the supervision of an industrial radiographer.
"Industrial radiography" means an examination of the structure of materials by the nondestructive methods of utilizing ionizing radiation to make images. Industrial radiography does not include cabinet x-ray or the use of ionizing radiation-producing equipment to measure thickness, to identify levels and material in containers, or to analyze the chemical compositions. Industrial x-ray does not include the use of ionizing radiation-producing equipment in forensic, medical, or veterinary research.
"Inherent filtration" means the filtration of the useful beam provided by the permanently installed components of the tube housing assembly.
"Inspection" means an official examination or observation, including but not limited to tests, radiation surveys, and monitoring to determine compliance with rules, regulations, and requirements of the commissioner.
"Instrument traceability" for ionizing radiation measurements means the ability to show that an instrument has been calibrated at specified time intervals using a national standard or a transfer standard. If a transfer standard is used, the calibration must be at a laboratory accredited by a program that requires continuing participation in measurement quality assurance with the National Institute of Standards and Technology (NIST), or other equivalent national or international programs.
"Interlock" means a device that automatically causes a reduction of the exposure rate upon entry by personnel into a high radiation area. An interlocking device must prevent the start or continued operation of equipment unless certain predetermined conditions prevail.
"Ionizing radiation" means any radiation capable of producing displacing electrons from atoms or molecules, thereby producing ions. Examples: alpha, beta, gamma, x-ray, and neutron radiation.
"Irradiation" means the exposure of a living being or matter to ionizing radiation.
"Isocenter" means a fixed point in space through which pass the central axes of radiation beams for all possible beam orientations and field sizes.
"Kilovolt peak" or "kVp" has the meaning given for peak tube potential in subpart 120.
"Lead equivalence" or "lead equivalent" means the thickness of lead affording the same attenuation, under specified conditions, as the material in question.
"Leakage radiation" means radiation emanating from the radiation source assembly except for the useful beam and radiation produced when the exposure switch or timer is not activated.
"Leakage technique factors" means the technique factors associated with the diagnostic or therapeutic source assembly that are used in measuring leakage radiation.
"Licensed practitioner of the healing arts" means health professionals for diagnostic or healing treatment of human and animal maladies, which are licensed under Minnesota Statutes, chapter 147, 153, or 156; or section 148.01, 148.106, or 150A.05, subdivision 1, clause (4), for the lawful practice of medicine, dentistry, veterinary medicine, osteopathic medicine, chiropractic, and podiatry.
"Light field" means the area of the intersection of the light beam from the beam-limiting device and one of the set of planes parallel to and including the plane of the image receptor whose perimeter is the locus of points at which the illumination is one-fourth of the maximum in the intersection.
"Line-voltage regulation" means the difference between the no-load and the load line potentials expressed as a percent of the load line potential. It is calculated using the following equation:
Percent line-voltage regulation = 100 (Vn - V1)/V1
|Vn = no-load line potential; and|
|V1 = load line potential.|
"mA" means milliampere.
"mAs" means milliampere-second.
"Maximum line current" means the root-mean-square current in the supply line of an x-ray system operating at its maximum rating.
"Medical event" means the administration of radiation received from radiation-producing equipment and includes:
therapeutic administration involving:
the wrong patient;
the wrong treatment modality;
a dose to tissue other than the treatment site that is 50 percent or more of the dose expected from the administration defined in the written directive;
a total radiation dose delivered that differs from the prescribed dose by 20 percent or more;
a total radiation dosage delivered that differs from the prescribed dosage by 20 percent or more or falls outside the prescribed dosage range; or
a fractionated radiation dose delivered that differs from the prescribed dose, for a single fraction, by 50 percent or more; and
when the patient radiation dose during a fluoroscopic procedure exceeds 600 rads for an adult.
"Medical particle accelerator" has the meaning given for accelerator in subpart 4.
"Medical physicist" has the meaning given for diagnostic radiological physicist in subpart 49, or therapeutic radiological physicist in subpart 200.
"Medical uses" means the intentional internal or external administration of radiation to human and animal patients or human research subjects.
"Megavolt," "MV," or "mega electron volt," "MeV," means the energy equal to that acquired by a particle with one electron charge in passing through a potential difference of 1,000,000 volts in a vacuum. Current convention is to use MV for photons and MeV for electrons.
"Moving beam radiation therapy" means radiation therapy with continuous displacement of one or more mechanical axes relative to the patient during irradiation. It includes arc therapy, skip therapy, conformal therapy, and rotational therapy.
"Nominal tomographic section thickness" means the full width at half-maximum at the center of the cross-sectional volume over which x-ray transmission data are collected.
"Nominal treatment distance" means:
for electron irradiation, the distance from the scattering foil, virtual source, or exit window of the electron beam to the entrance surface of the irradiated object along the central axis of the useful beam;
for x-ray irradiation, the virtual source or target to isocenter distance along the central axis of the useful beam; and
for nonisocentric equipment, the distance specified by the manufacturer.
"Nonstochastic effects" means health effects the severity of which varies with the radiation dose, and for which a threshold is believed to exist. Radiation-induced cataract formation is an example of a nonstochastic effect.
"Occupational dose" means the dose received by an individual in the course of employment in which the individual's assigned duties for the registrant involve exposure to radiation-producing equipment, whether or not the radiation-producing equipment is in the possession of the registrant. Occupational dose does not include doses received from background radiation, from any medical administration the individual has received, from exposure to individuals administered radioactive material and released in accordance with chapter 4731, from voluntary participation in medical research programs, or as a member of the public.
"Open-beam configuration" means an analytical x-ray system in which an individual could accidentally place some part of the body in the primary beam or secondary scattered beam path during normal operation.
"Optical density" or "O.D." means the logarithm of the incident light intensity minus the logarithm of the transmitted light intensity.
"Patient" means an individual or animal subjected to healing arts examination, diagnosis, or treatment.
"Peak tube potential" means the maximum value of the potential difference across the x-ray tube during an exposure.
"Permanent radiographic installation" means a shielded enclosed room, cell, vault, or structure that is not moved and is not located at a temporary job site. The installation is designed or intended for radiography, and in which radiography is regularly performed.
"Person" means any individual, corporation, partnership, firm, association, trust, estate, public or private institution, group, agency, political subdivision of this state, and any legal successor, representative, agent or agency of the foregoing, excluding federal government agencies.
"Personal protective garments" mean garments, including aprons, gloves, and thyroid collars made of radiation absorbing materials used to reduce radiation exposure.
"Personal monitoring dosimeter" has the meaning given for individual monitoring devices in subpart 84.
"Phantom" means a volume of material behaving in a manner similar to tissue with respect to the attenuation and scattering of radiation.
"Phototimer" means a method for controlling radiation exposures to image receptors by measuring the amount of radiation that reaches a radiation monitoring device. A radiation monitoring device is part of an electronic circuit that controls the duration of time the x-ray tube is activated. "Phototimer" includes the meaning given for automatic exposure control in subpart 15.
"Physician assistant" means a person registered according to Minnesota Statutes, chapter 147A, who is qualified by academic, practical training, or both to provide patient services as specified in the physician-physician assistant agreement recognized by the Minnesota Board of Medical Practice.
"Pixel" or "picture element" means an elemental area of a digital image.
"Port film" or "portal imaging" means a radiographic film or electronic image taken with a therapeutic x-ray system to verify proper setup of the treatment field.
"Positive beam limiting or limitation" or "PBL" means the automatic or semiautomatic adjustment of an x-ray beam to the size of the selected image receptor, whereby exposures cannot be made without this adjustment.
"Position-indicating device" or "PID" means a device on dental x-ray equipment used to indicate the beam position and to establish the source-to-skin distance.
"Prescribed dose" means the total radiation dose and radiation dose per fraction as documented in the written directive or therapeutic order.
"Primary beam" means radiation that passes through an aperture of the source housing by a direct path from the x-ray tube located in the radiation-producing equipment housing.
"Primary dose-monitoring system" means a system that will monitor the useful beam during irradiation and will terminate irradiation when a preselected number of dose monitor units have been acquired.
"Primary protective barrier" means the material, excluding filters, placed in the useful beam for protection purposes to reduce the radiation exposure.
"Protective apron" see personal protective garments in subpart 123.
"Protective barrier" or "barrier" means a barrier of radiation absorbing materials used to reduce radiation exposure.
"Protective glove," see personal protective garments in subpart 123.
"Pulsed mode" means operation of an x-ray system so that the x-ray tube current is pulsed by the x-ray control to produce one or more exposure intervals of less than one-half second duration.
"Quality assurance program" means an all-encompassing program including quality control that extends to administrative, education, and preventive maintenance methods. It includes a continuing evaluation of the adequacy and effectiveness of the overall imaging program, with a view to initiating corrective measures when necessary. The nature and extent of this program will vary with the size and type of the facility, and the type of activities conducted.
"Quality control" means a series of distinct technical procedures that ensure the production of a satisfactory product. Its aim is to provide quality that is not only satisfactory but also dependable and economic. The quality control procedures are concerned directly with the equipment.
"Quarter" means at intervals not to exceed 12 consecutive weeks.
"Rad" means the special unit of absorbed dose. The SI equivalent is 0.01 gray.
"Radiation" means ionizing radiation.
"Radiation area" means an area accessible to individuals in which the radiation levels could result in an individual receiving a dose equivalent in excess of 0.005 rem (0.05 mSv) in one hour at 30 centimeters from the source of radiation or from any surface that the radiation penetrates.
"Radiation detector" or "detector" means a device that in the presence of radiation provides a signal or other indication suitable for use in measuring one or more quantities of incident radiation.
"Radiation head" means the structure from which the useful beam emerges.
"Radiation-producing equipment" means any device capable of producing radiation.
"Radiation protection" means the use of time, distance, shielding, and other personnel protective garments.
"Radiation safety officer" means an individual who has the knowledge and training to apply appropriate radiation protection standards, and has been assigned such responsibility by the registrant.
"Radiation therapy simulation system" means a radiographic, fluoroscopic, or CT x-ray system including all software applicable to the process intended for localizing the volume to be exposed during radiation therapy and confirming the position and size of the therapeutic irradiation field.
"Radiograph" means an image produced on a radiosensitive surface, such as a photographic film or digital plate, by radiation other than visible light, such as by x-rays passed through an object or by photographing a fluoroscopic image that results in a permanent record.
"Radiographic imaging system" means any system where a permanent or semipermanent image is recorded on an image receptor by the action of ionizing radiation.
"Radiology practitioner assistant" or "RPA" means an individual who is an advanced level radiographer registered with the American Registry of Radiologic Technologists and certified by the Certification Board for Radiology Practitioner Assistants. The individual is qualified by completion of an educational program recognized by the Board of Directors of the Certification Board for Radiology Practitioner Assistants. The RPA may provide patient services as specified in an agreement with a supervising radiologist.
"Rated line voltage" means the range of potentials, in volts, of the supply line specified by the manufacturer at which the radiation-producing equipment is designed to operate.
"Rating" means the operating limits as specified by the component manufacturer.
"Recording" means producing a retrievable form of an image resulting from x-ray photons.
"Reference man" means a hypothetical aggregation of human physical and physiological characteristics. These characteristics may be used by researchers and public health workers to standardize results of experiments and to relate biological insult to a common base.
"Reference plane" means a plane that is displaced from and parallel to the tomographic plane.
"Registered radiologist assistant" or "RRA" means a person who is an advanced level radiographer certified and registered in radiography by the American Registry of Radiologic Technologists and has successfully completed all elements of a radiologist assistant educational program recognized by the ARRT. The RRA would be able to provide patient services as specified in an agreement with a supervising radiologist.
a person having administrative control of any radiation-producing equipment except those specifically exempted under this chapter and who is legally obligated to register with the commissioner according to this chapter; or
a person who is legally obligated to register with the commissioner as a service provider.
"Registration" means registration with the commissioner according to this chapter.
"Rem" means a special unit of dose equivalence. The SI equivalent is 0.01 sievert.
"Restricted area" means any area to which access or egress may be limited by the registrant for purposes of protection of individuals from exposure to radiation.
"Retake" or "reject" means any diagnostic radiographic imaging that had to be retaken, reexposing the patient to radiation because of some error, failure, or degradation in the radiographic imaging process.
"Retake or reject analysis program" means an ongoing analysis of retakes or rejects that provides information about existing imaging problems in a radiology department.
"Roentgen" or "R" means a special unit of exposure. The roentgen is equal to 2.58 x 10-4 coulombs per kilogram of air.
"Scattered radiation" or "secondary radiation" means radiation that, during passage through matter, has been deviated in direction and may have also been modified by a decrease in energy.
"Secondary dose-monitoring system" means a system that will terminate irradiation if the primary dose-monitoring system fails.
"Secondary protective barrier" means a barrier sufficient to attenuate stray radiation.
"Sensitometer" means an instrument designed to reproducibly expose a piece of film to a number of different levels of light intensity.
"Sensitometric strip" means a film exposed by a sensitometer, resulting in a gray scale range. The strips are used to measure the range of densities from minimum to maximum.
"Sensitometry" means a quantitative measurement of the response of film to exposure and development. Sensitometry is used to test the processor setup and stability.
"Service provider" means a person engaged in the business of assembling, installing, repairing, or replacing one or more components into diagnostic or industrial radiation-producing equipment system or subsystem or conducting equipment performance evaluations on diagnostic or industrial equipment. Service providers must be registered with the commissioner under part 4732.0275.
"Shadow tray" means a device attached to the radiation head to support auxiliary beam-limiting material.
"Shutter" means a device attached to the tube housing assembly that can totally intercept the useful beam and has a lead equivalency not less than that of the tube housing assembly.
"SI equivalent" means units that conform to the international system of units.
"Sievert" or "Sv" means the SI unit of any quantities expressed as dose equivalent. The conventional system equivalent is the rem.
"Source" means the target or focal spot of the x-ray tube or accelerator.
"Source of radiation" means a device or equipment that emits or is capable of producing radiation. For purposes of this chapter, this is equivalent to radiation-producing equipment.
"Source-to-image distance" or "SID" means the distance from the source to the center of the input surface of the image receptor.
"Source-to-skin distance" or "SSD" means the distance between the source and the skin of the patient.
"Spot check" means a procedure that is performed to ensure that a previous calibration continues to be valid.
"Spot film" means a radiograph that is made during a fluoroscopic procedure to permanently record conditions that exist during that fluoroscopic procedure.
"Spot-film device" means a device intended to transport and position a radiographic image receptor between the x-ray source and fluoroscopic image receptor. Spot-film device includes a device intended to hold a cassette over the input end of the fluoroscopic image receptor to produce a radiograph.
"Stationary beam therapy" means radiation therapy without relative displacement of the useful beam and the patient during irradiation.
"Step wedge" means a quality control test tool made of type 1100 aluminum with 11 steps.
"Stepless adjustment" means a method of adjusting collimator blades continuously rather than in fixed increments.
"Stochastic effects" means health effects that occur randomly and for which the probability of the effect occurring, rather than its severity, is assumed to be a linear function of dose without threshold. Hereditary effects and cancer incidence are examples of stochastic effects.
"Storage" means a condition in which a device or radiation-producing equipment is not being used for an extended period of time and has been made inoperable.
"Storage area" means a location, facility, or vehicle that is locked or has a physical barrier to prevent accidental exposure to, tampering with, or unauthorized removal of the device, container, or source.
"Stray radiation" means the sum of leakage radiation and scattered radiation.
"Supervising physician" means a Minnesota licensed physician who accepts full medical responsibility for the performance, practice, and activities of a registered radiologist assistant or a radiology practitioner assistant.
"Survey" or "radiation survey" means an evaluation of the radiological conditions and potential hazards incident to the use of radiation-producing equipment. When appropriate, such evaluation includes, but is not limited to, tests, physical examinations, and measurements of levels of radiation.
"Target" means the part of an x-ray tube or accelerator onto which a beam of accelerated particles is directed to produce ionizing radiation or other particles.
"Technique factors" means the conditions of operation, specified as follows:
for capacitor energy storage equipment, peak tube potential in kV and quantity of charge in mAs;
for field emission equipment rated for pulsed operation, peak tube potential in kV, and number of x-ray pulses;
for CT x-ray systems designed for pulsed operation, peak tube potential in kV, scan time in seconds, and either tube current in mA, x-ray pulse width in seconds, and the number of x-ray pulses per scan, or the product of milliamperage, x-ray pulse width, and the number of x-ray pulses in mAs;
for CT x-ray systems not designed for pulsed operation, peak tube potential in kV, and either the tube current in mA and scan time in seconds, or the product of milliamperage and exposure time in mAs and the scan time when the scan time and exposure time are equivalent;
for phototimed or automatic exposure controlled equipment, all necessary indicators including anatomical, if applicable, that must be activated before exposure; and
for all other equipment, peak tube potential in kV and either tube current in mA and exposure time in seconds, or the product of milliamperage and exposure time in mAs.
"Television receiver" means an electronic product designed to receive and display a television picture through broadcast, cable, or closed-circuit television.
"Temporary job site" means a location where radiography is performed, other than a location listed in a registration.
"Termination of irradiation" means the stopping of irradiation in a fashion that will not permit continuance of irradiation without the resetting of operating conditions at the control panel.
"Therapeutic radiation machine" means x-ray or electron-producing equipment designed and used for external beam radiation therapy.
"Therapeutic radiological physicist" means an individual qualified to practice independently in the subfields for medical therapeutic physics who:
is certified in radiological physics or therapeutic radiological physics by the American Board of Radiology;
is certified in therapeutic radiological physics by the American Board of Medical Physics;
is certified in therapeutic radiological physics by the Canadian College of Medical Physics; or
holds a masters degree or doctor's degree in medical physics, radiological sciences, or an equivalent field involving graduate study in physics applied to the application of radiation to humans from an accredited college or university and have at least one year of full-time practical training and experience involving work in a radiation therapy facility under an individual who meets the qualifications in this item or item A, B, or C.
"Therapeutic-type protective tube housing" means the definitions in items A to C.
For x-ray therapy equipment not capable of operating at 500 kilovolt peak (kVp) or above, the following definition applies: an x-ray tube housing so constructed that the leakage radiation at a distance of one meter from the source does not exceed one rad (0.01 Gy) in an hour when the tube is operated at its maximum rated continuous current for the maximum rated tube potential.
For x-ray therapy equipment capable of operation at 500 kilovolt peak (kVp) or above, the following definition applies: an x-ray tube housing so constructed that leakage radiation at a distance of one meter from the source does not exceed either one rad (0.01 Gy) in an hour or 0.1 percent of the useful beam dose rate at one meter from the source, whichever is greater, when the machine is operated at its maximum rated continuous current for the maximum rated accelerating potential.
In either case, small areas of reduced protection are acceptable provided the average reading over any 100 square centimeters area at one meter distance from the source does not exceed the values given in items A and B.
"Tomogram" means an x-ray image of a thin section of the body.
"Tomographic plane" means the geometric plane that is identified as corresponding to the output tomogram.
"Tomographic section" means the volume of an object whose x-ray attenuation properties are imaged in a tomogram.
"Traceable to a standard" means a comparison, either directly or indirectly, to a standard maintained by the National Institute of Standards and Technology (NIST) and that all comparisons have been documented.
"Tube housing assembly" means the tube housing with tube installed. It includes high voltage and filament transformers and other appropriate elements when contained within the tube housing.
"Tube rating chart" means the set of curves that specify the rated limits of operation of the tube in terms of the technique factors.
"Type 1100 aluminum alloy" means an alloy of aluminum that has a nominal chemical composition of 99 percent minimum aluminum and 0.12 percent copper.
"Useful beam" means the radiation emanating from the tube housing port or the radiation head and passing through the aperture of the beam-limiting device when the exposure controls are in a mode to cause the system to produce radiation.
"Utilization log" means a record of procedures conducted in a certain time frame and following a set of requirements:
"Variable-aperture beam-limiting device" means a beam-limiting device that has a capacity for stepless adjustment of the x-ray field size at a given SID.
"Very high radiation area" means an area accessible to individuals, where radiation levels from radiation-producing equipment external to the body could result in an individual receiving an absorbed dose in excess of 500 rad (5 Gy) in one hour at one meter from any surface that the radiation penetrates.
"Virtual source" means a point from which radiation appears to originate.
"Visible area" means the portion of the input surface of the image receptor over which incident x-ray photons are producing a visible image.
"Wedge filter" means an added filter effecting continuous change in transmission on all or part of the useful beam.
"Worker" means an individual who engages in activities with sources of ionizing radiation that require registration by the commissioner and that are controlled by a registrant.
"Written directive" or "written order" means a dated order either in writing or electronically for a specific patient, specific procedure, and has an indication of the licensed practitioner of the healing arts ordering the procedure.
"X-ray control" means a device, switch, or other similar means by which an operator initiates and terminates the radiation exposure. The x-ray exposure control may include associated equipment such as timers and back-up timers.
"X-ray equipment" means an x-ray system, subsystem, or component. Types of x-ray equipment are listed in items A to D.
"Mobile x-ray equipment" means x-ray equipment mounted in a self-contained transport vehicle.
"Portable industrial x-ray equipment" means industrial x-ray equipment designed to be brought to a temporary job site to perform temporary industrial radiography.
"Portable x-ray equipment" means x-ray equipment on wheels or casters and designed to be brought to a patient when the patient's condition does not permit transfer to a fixed location.
"Stationary x-ray equipment" means x-ray equipment installed in a fixed location within a facility.
"X-ray field" means the area of the intersection of the useful beam and any one of the set of planes parallel to and including the plane of the image receptor, whose perimeter is the locus of points at which the exposure rate is one-fourth of the maximum in the intersection.
"X-ray generator" means a type of electron accelerator in which the electron beam is used mainly for the production of x-rays.
"X-ray high-voltage generator" means a device that transforms electrical energy from the potential supplied by the x-ray control to the tube operating potential. The device may also include means for transforming alternating current to direct current filament transformers for the x-ray tube, high-voltage switches, electrical protective devices, and other appropriate elements.
"X-ray system" means an assemblage of components for the controlled production of x-rays. It includes minimally an x-ray high-voltage generator, an x-ray control, a tube housing assembly, a beam-limiting device, and the necessary supporting structures. Additional components that function with the system are considered integral parts of the system.
"X-ray tube" or "tube" means an electron tube designed to be used primarily for the production of x-rays.
"Year" means a period of time consisting of 12 consecutive months.
MS s 144.12
32 SR 777; L 2016 c 119 s 7
October 13, 2021
Official Publication of the State of Minnesota
Revisor of Statutes