
High level control maximum output at tabletop or equivalent minimum SSDĮrror between fluorographic beam size and observed image size must be no more than ± 3% of SID for all modes and at any tower heightĮrror between actual fluorographic beam size at image receptor and indicated image size must be no more than ± 3% of SID for all modes and at any tower heightįluoroscopic high contrast resolution and distortion
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< 5 R (1.3 mC/kg) per minute for manual < 10 R (2.6 mC/kg) per minute for automatic exposure rate control systems Maximum output at tabletop or equivalent minimum SSDĪt intervals not to exceed 12 months and every tube change For facilities with fluoroscopes and C-arm fluoroscopes, except radiation therapy simulators, manufactured before May 19, 1995.

Spot film reproducibility (fluoroscopy units with manual mode) and over the range as specified by the manufacturer of the averaged exposures when measured at > 1.2 O.D. of the averaged exposures over the range specified by the manufacturer At times shorter than 100 milliseconds, use manufacturers' specifications ± 2% of SID any one direction, ± 3% of SID, both directions (total)Ĭoefficient of variation 100 milliseconds. All diagnostic radiographic tubes required when applicable. THERAPEUTIC EQUIPMENT PERFORMANCE TESTS AND LIMITS FOR MEASUREMENT EQUIPMENT.ĮQUIPMENT PERFORMANCE TESTS FOR EXTERNAL BEAM TELETHERAPY AND SIMULATION SYSTEMS. INSTALLATION CALIBRATION TESTS AND EQUIPMENT PERFORMANCE TESTS FOR A QUALITY ASSURANCE PROGRAM. POSTING REQUIREMENTS FOR INDUSTRIAL RADIOGRAPHY. WARNING DEVICES FOR INDUSTRIAL RADIOGRAPHY FACILITIES. INSTRUCTION AND TRAINING FOR INDUSTRIAL RADIOGRAPHY. INDUSTRIAL RADIOGRAPHY IN A TEMPORARY JOB SITE. INDUSTRIAL RADIOGRAPHIC OPERATING AND EMERGENCY PROCEDURES. REQUIREMENTS FOR PERMANENT INDUSTRIAL RADIOGRAPHIC INSTALLATIONS. INDUSTRIAL FACILITY REQUIREMENTS FOR USING RADIATION-PRODUCING EQUIPMENT IN MANUFACTURING PROCESSES, GAUGES, AND CABINETS. REQUIREMENTS FOR X-RAY FLUORESCENT ANALYZERS AND BOMB DETECTION UNITS. THERAPEUTIC RADIATION MACHINES - PHOTON THERAPY SYSTEMS (500 KV AND ABOVE) AND ELECTRON THERAPY SYSTEMS (500 KEV AND ABOVE). THERAPEUTIC RADIATION MACHINES OF LESS THAN 500 KV. GENERAL REQUIREMENTS FOR THERAPEUTIC EQUIPMENT. GENERAL REQUIREMENTS FOR FACILITIES USING ACCELERATORS. REQUIREMENTS FOR STEREOTACTIC MAMMOGRAPHIC EQUIPMENT. REQUIREMENTS FOR COMPUTED RADIOGRAPHY, DIGITAL RADIOGRAPHY, OR PHOTOSTIMULABLE STORAGE PHOSPHOR RADIATION-PRODUCING EQUIPMENT.ĬOMPUTERIZED TOMOGRAPHY DESIGNED FOR VISUALIZATION OF THE HEAD AND SOFT TISSUE OF THE NECK. GENERAL PURPOSE DIAGNOSTIC RADIATION-PRODUCING EQUIPMENT MANUFACTURED BEFORE 1973.įLUOROSCOPIC X-RAY SYSTEMS EXCEPT RADIATION THERAPY SIMULATORS. GENERAL EQUIPMENT REQUIREMENTS FOR ALL DIAGNOSTIC RADIATION-PRODUCING SYSTEMS. RADIATION SURVEY OR MEASUREMENT INSTRUMENTS. WARNING AND CONTROL DEVICES FOR HIGH AND VERY HIGH RADIATION AREAS. REPORTS OF MEDICAL EVENTS OR INCIDENTS INVOLVING RADIATION-PRODUCING EQUIPMENT. REPORTS OF THEFT OR LOSS OF RADIATION-PRODUCING EQUIPMENT. INDIVIDUALS OPERATING X-RAY EQUIPMENT DURING TRAINING. REGISTRANT REQUIREMENTS FOR OPERATORS IN FACILITIES USING X-RAY EQUIPMENT. ORDERING OF DIAGNOSTIC RADIOGRAPHIC OR THERAPEUTIC PROCEDURES. PROCEDURES AND SAFETY INSTRUCTION FOR FACILITIES. RADIATION SAFETY OFFICER RESPONSIBILITIES. GENERAL REQUIREMENTS FOR SHIELDING AGAINST IONIZING RADIATION.ĪDDITIONAL SHIELDING REQUIREMENTS FOR DENTAL FACILITIES.ĪDDITIONAL SHIELDING REQUIREMENTS FOR INDUSTRIAL FACILITIES USING RADIATION-PRODUCING EQUIPMENT.ĭETERMINATION OF ACCUMULATED OCCUPATIONAL DOSE.ĭOSE LIMITS FOR INDIVIDUAL MEMBERS OF THE PUBLIC.


RECIPROCITY FOR OUT-OF-STATE RADIATION-PRODUCING EQUIPMENT.
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REGISTRATION REQUIREMENTS FOR RADIATION-PRODUCING EQUIPMENT AND OTHER ELECTRONIC DEVICES THAT PRODUCE RADIATION.
