GE HealthCare · Model Proteus
• Jedi high-frequency generator with programmable APR's, touch screen LCD console, and self-calibrating reliability. • Elevating table with 4-way floating tabletop. Includes variable SID, auto-collimation, photo-timing, oscillating grid, and foot pedal controls. • Overhead tube crane with automatic SID detenting, auto-collimator, technique selection, image receptor selection, and variable vertical SID. • Bucky wall stand includes photo-timing and cassette sizing for auto-collimation.
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: Tube won't fire, heat-capacity alarm.
Root cause: Filament wear, cooling failure.
Symptoms: Image noise, artifacts, low SNR.
Root cause: Flat-panel / sensor aging.
Symptoms: Tube temp alarm, duty-cycle limited.
Root cause: Pump/radiator or coolant loss.
Symptoms: Frozen console, acquisition timeout.
Root cause: Workstation or RAID degradation.
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.
Major R&R; track mAs history.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Cooling pump & radiator | Periodic replacement | $$$ | Difficult |
| High-voltage generator | Major service part | $$$$ | Expert-level |
| Workstation RAID / GPU | Periodic replacement | $$$ | Difficult |
| X-ray tube insert Major R&R; track mAs history. | Major service part | $$$$ | Expert-level |
Relative cost: $ lowest · $$$$ 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.
Synced live from the FDA openFDA API.
Potential breakage of the steel cable which supports the bucky device in certain wall stands of Proteus XR/a X-ray imaging systems. A fall of a bucky while the system is in use could result in an injury to a patient or operator.
The warning label that is required by 21 CFR 1020.30(j) was not on the control console of the Proteus XR/a Radiographic X-ray System, Model 2259976.
The actual average illuminance for the collimators are approximately 140-lux. This does not meet the 160-lux requirement. GE will be correcting the units by replacing all collimators.
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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