NEUROPROBE
®
500 PRO USER MANUAL 35
COPYRIGHT © 2006 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED
SPECIFICATIONS (Cont.)
SLD INFRARED PADS:
Wavelengths:
630nm with 875 nm
Diodes and Dimensions:
15 x 630nm & 24 x 875nm on each 4.5" x 7.5" pad in dual pad configuration
110 x 630 nm and 48x875 nm on a 29" x 14" L.E. Pad
TIMER FUNCTIONS:
Treatment Timer:
Adjustable for 1-99 minutes in one-minute increments in IFC modes. In probe mode the time is
adjustable from 1-999 seconds. Tums output to zero and system off and sounds 10-second
buzzer to indicate completion of treatment in IFC modes. In probe mode the system returns to
the detection mode following time out.
PROBE DETECTION:
Sensitivity:
Adjustable from 200K to 5 Meg ohms
Display:
Bar graph and numeric indicator 0-200uA
Audio:
Variable frequency increases with skin conductivity
PATIENT SAFETY SYSTEMS:
Activation:
By patient safety hand control which shuts down output. Output modality may not be changed
during operation. Output levels are reset to zero at the start and completion of treatment.
MISC:
Auto Intensity:
Output intensity is gradually increased during treatment from 0 to 20% automatically in a linear manner
over the duration of treatment when the anti-adaptation mode is selected. The amount of increase is user
programmable.
Treatment Programs:
Infrared Therapy: 1 Preset
Sensory-Motor: 7 Presets
Noxious: 1 Preset
Nerve Block: 2 Presets
For program details see Page 24
Certificates and Approvals:
Device is designed to meet or exceed all safety requirements of a medical device in it’s class, per
IEC 60601 and CSA C22.2 No. 601.1
Caution:
Federal law restricts this device to sale by or on the order of a physician (or other health
practitioner licensed by their state).
NOTE:
ACP reserves the right to change technical specifications and product availability without notice.
