MyoTrac Infiniti
™
User Guide
6
by conditioning hot, dry air. It is recommended that all staff involved with the unit receive an
explanation of the ESD symbol and the precautions described above as a minimum.
Do not apply any electrode gel or equivalent directly on the sensor snaps. Always use
electrodes as a medium between the sensor and the client.
Not for diagnostic purposes, not defibrillator proof, not for critical patient monitoring.
To prevent voiding warranty by breaking connector pins, carefully align white guiding dot on
sensor plug with slot on sensor input.
Make sure to remove electrodes from sensor snaps immediately after use.
Do not plug third party sensors directly into instrument inputs. Plug only Thought
Technology Active Sensor cable connectors into instrument inputs. All electrodes and third
party sensors must be connected to active sensors, either directly or through an adapter.
Remove batteries when the device is not being used for an extended period of time. Please
dispose of battery following local regulations.
ADVERSE REACTIONS
Skin irritation and burns beneath the electrodes have been reported with the use of powered muscle
stimulators.
CONTRAINDICATIONS
Powered muscle stimulators should not be used on patients with cardiac demand
pacemakers.
INTENDED PURPOSE
Biofeedback, Relaxation & Muscle Re-Education purposes
Relaxation of muscle spasms
Prevention or retardation of disuse atrophy
Increasing local blood circulation
Stroke Rehab by Muscle re-education
Immediate post-surgical stimulation of calf muscles to prevent venous thrombosis
Maintaining or increasing range of motion
Acute and ongoing treatment of stress, urge or mixed urinary incontinence and where the
following results may improve urinary control: Inhibition of the detruser muscle through
reflexive mechanisms.
Incontinence treatment for assessing EMG activity of the pelvic floor and accessory muscles such
as the abdominal or gluteal muscles
Powered muscle stimulators should only be used under medical supervision for adjunctive
therapy for the treatment of medical diseases and conditions
NOTE
No preventative inspections required; maintenance must be performed by qualified personnel.
Factory re-calibration can be requested.
The supplier will make available, upon request, circuit diagrams, component parts lists and
description or other information required for the repair of product by qualified personnel.
The operator must be familiar with typical characteristics of signals acquired by this
equipment, and be able to detect anomalies in the acquired signal that could interfere with
treatment effectiveness. Depending on the importance of signal integrity, it may be advisable
to continuously monitor the raw signals, in time and/or frequency domain, while the device is
being used for biofeedback or other purposes. If anomalies are observed on acquired signals,
and if you suspect a problem with electromagnetic interference, contact Thought Technology
for a technical note on identification and remediation.
This product conforms to standards EN60601-1, EN60601-2-10 and EN60601-2-40; some
encoder labeling may indicate superceded standards.
MAINTENANCE AND CALIBRATION
Wipe encoder with a clean cloth
Factory testing and calibration ensure equipment accuracy and frequency response. Contact
Thought Technology for factory re-calibration if necessary.
STORAGE
Store in its original case at up to 90% humidity / 30C°
TRANSPORTATION
Transport in its original case
Manual # SA9810US Rev 5
