Installation calibration tests must be conducted prior to any patient use. Any adjustments must be made to bring the equipment up to a nationally recognized standard, such as Code of Federal Regulations, title 21, section 892, or manufacturer's specifications and to ensure compliance with this chapter prior to first use.
Equipment performance tests must be conducted over all clinical ranges, when applicable. For equipment performance tests, any adjustments must be made to bring equipment to compliance with a nationally recognized standard, such as Code of Federal Regulations, title 21, section 892, or manufacturer's specifications and to ensure compliance with this chapter prior to using the equipment again.
TEST TYPE | MINIMUM TEST INTERVAL | TOLERANCE |
A. AAPM - accredited dosimetry calibration laboratory calibration | Intercomparison every 12 months At intervals not to exceed 24 months traceable to NIST Standard |
Documented and correction applied or noted in report of measurement when appropriate |
B. Linearity | At intervals not to exceed 48 months | 0.5 percent |
C. Venting | At intervals not to exceed 48 months | Documented and correction applied |
D. Extracameral signal | Initial use | 0.5 percent |
E. Leakage | Each use | 0.1 percent |
F. Recombination | Initial use | Documented and correction applied |
G. Collecting potential | Each use | Documented and correction applied |
TEST TYPE | MINIMUM TEST INTERVAL | TOLERANCE |
A. Local standard comparison | At intervals not to exceed 24 months | 1 percent |
B. Linearity | At intervals not to exceed 24 months | Documented and correction applied |
C. Venting | At intervals not to exceed 24 months | Documented and correction applied |
D. Extracameral signal | At intervals not to exceed 24 months | Documented and correction applied |
E. Leakage | Each use | 1 percent |
F. Recombination | Initial use | Documented and correction applied |
G. Collecting potential | Each use | Documented and correction applied |
TEST TYPE | MINIMUM TEST INTERVAL | TOLERANCE |
A. Thermoluminescent Dosimeter | ||
(1) Calibration | Each batch or box | Documented and correction applied |
(2) Linearity | Initial use | Documented and correction applied |
B. Film | ||
(1) Dose and response | Each batch or box | Documented and correction applied |
(2) Densitometer linearity | At intervals not to exceed 12 months | Documented and correction applied |
C. Air ionization chamber system | ||
(1) Linearity | At intervals not to exceed 12 months | Documented and correction applied |
(2) Extracameral signal | Initial use | 1 percent |
D. Diode system | ||
(1) Energy dependence | Initial use | Documented and correction applied |
(2) Extracameral signal | Initial use | Documented and correction applied |
(3) Linearity | Initial use | Documented and correction applied |
TEST TYPE | MINIMUM TEST INTERVAL | TOLERANCE |
A. Calibration | At intervals not to exceed 12 months | Documented and correction applied |
B. Linearity | At intervals not to exceed 12 months | Documented and correction applied |
C. Constancy | Each use | 5 percent |
TEST TYPE | MINIMUM TEST INTERVAL | TOLERANCE |
A. Accuracy | Daily before patient use | 2 mm |
B. Hysteresis | Each use | 2 mm |
TEST TYPE | MINIMUM TEST INTERVAL | TOLERANCE |
A. Thickness | Initial use | Documented and correction applied |
B. Density | Initial use | Documented and correction applied |
C. Phantom stacked density | Initial use | Documented and correction applied |
D. Detector fit | Initial use | Documented and correction applied |
TEST TYPE | MINIMUM TEST INTERVAL | TOLERANCE |
A. Thermometer calibration | Initial use | 0.1 degree/C |
B. Barometer (aneroid) | ||
(1) Calibration Hg | Initial use | 1 mm Hg |
(2) Intercomparison | At intervals not to exceed 12 months | 1 mm Hg |
MS s 144.12
32 SR 777
December 10, 2007
Official Publication of the State of Minnesota
Revisor of Statutes