MEDICAL DEVICE REPORTING REQUIREMENTS
DYNATRON® 25 SERIES™ | OPERATOR’S MANUAL 101
Reporting any Incident of Patient Discomfort
Dynatronics recommends that if discomfort of any level is reported by the patient, the treatment be stopped immediately.
e device and all accessories in use during that treatment should be isolated and held for inspection. Make a note of
treatment parameters that were in use during the treatment including intensity settings. Also note environmental factors
that were observed during the treatment (oce lights ickering, static electricity discharge, other devices in use on the same
power source or in the same room, etc.)
e incident should be reported immediately to Dynatronics Customer Service at 1-800-874-6251. e customer service
representative will inform you if it is necessary to send the device and/or accessories to Dynatronics for inspection.
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