MAMays & Asscoiates · Model OmniPro EEG System
OmniPro EEG System used in EEG physiological data collection
Intended use: An electrically-powered device designed for noninvasive recording of the electrical activity of the brain for display in the form of a graph [electroencephalogram (EEG)], typically to study a variety of neurological conditions, evaluate psychiatric disorders, and/or assist in localizing tumours or lesions on or near the surface of the brain. It is designed to acquire electrical signals from electrodes typically attached to the scalp and ear lobes. The results may be displayed via print-out or electronically; data interpretation and/or telemetry features may also be included.
Failure patterns typical of this equipment class - general BMET reference, not verified against this exact unit's own service history unless flagged. Severity is a category-level estimate.
Symptoms: Noisy / flat channels, impedance alarm.
Root cause: Dry gel, poor contact.
Symptoms: Dead channel, artifact.
Root cause: Front-end amplifier failure.
Symptoms: No stimulus delivered.
Root cause: Stimulator circuit wear.
Symptoms: 50/60 Hz interference.
Root cause: Shield/ground break.
The parts a BMET typically services on this class of equipment. Service class and relative cost are general engineering estimates for the category, not figures from this unit's documentation. Part numbers appear only when pulled from this unit's own service manual. Always confirm intervals and pricing against the manufacturer.
Consumable.
Frequent R&R.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Patient electrode gel Consumable. | Consumable | $ | Easy |
| Amplifier channel module | Periodic replacement | $$$ | Difficult |
| Stimulator cable | Periodic replacement | $$ | Fairly easy |
| EEG electrode cap / cup Frequent R&R. | Periodic replacement | $$ | Easy |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
Preventive-maintenance tasks typical of this equipment class. Perform to the manufacturer's procedure and your facility's policy - this is general reference, not a schedule for this specific unit.
A structured starting point derived from the failure modes above. Follow the manufacturer's service documentation for the actual procedure.
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
No documents available for this device yet.
Describe a symptom or error code. Bio answers from this device's own documented error codes, failure modes, parts, and guides.
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