
GE HealthCare · Model Proteus XR/i
Flexible and User-Friendly. The broad clinical flexibility of Proteus XR/i system enables you to undertake a wide variety of radiographic studies, including tomography as an option. The floor-mounted tube stand, the floating Bucky table and the electromagnetic brakes make for quick and easy patient positioning. The elevating table is equipped with central foot switches. The wall stand with oscillating Bucky allows fast and accurate positioning. Image Quality. The Proteus XR/i benefits from GE Healthcares uncompromising quality standards that ensure very high uptime ratings. The high-power, high-frequency generator with its very short minimum exposure time provides excellent reproducibility that results in consistent image quality. Automatic Exposure Control (AEC) reduces the number of retakes, and the Anatomical Programmer (APR) accommodates a full range of studies. The system can be equipped with the Dose Area Product (DAP) measurement device with printer as an option. Reliability and Ease of Use. To enhance your productivity and ensure maximum uptime, the system is equipped with a single-phase or three-phase high-frequency generator (50/64 kW) that is suitable for almost all applications. Ergonomic and easy-to-use Touch screen console. A very wide range of accessories such as lateral cassette holder, compression band, hand grips, etc.
Compiled for this model from its own documentation and established engineering knowledge for this equipment class - not from a verified service record. Confirm against the manufacturer's service manual.
Symptoms: Exposure inhibited, generator error / fault code, images consistently under- or over-exposed.
Root cause: HV generator / inverter fault, an exposure-switch / contactor fault, an HT-cable fault, or a tube-load / thermal interlock.
Symptoms: Output does not match the console, techniques drift, generator calibration fails.
Root cause: Inverter / HV-tank fault, a filament-supply fault, or a calibration issue.
Symptoms: Auto-exposure images consistently over- or under-exposed, chambers not tracking.
Root cause: AEC ion chamber(s) or the AEC calibration.
Symptoms: Column, wall stand, table or bucky will not track / detent; collimator light out; grid errors.
Root cause: Drive / brake / detent hardware, the collimator lamp / drive, or a bucky-motor fault.
Symptoms: Exposures inhibited after a series, tube-heat alarm.
Root cause: Tube housing heat limit reached or a cooling-fan fault.
Serviceable items for this model, compiled from its documentation and engineering knowledge for this equipment class. Service class and relative cost are estimates, not manufacturer figures; no part numbers are given. Confirm intervals and pricing against the manufacturer.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| HV generator / inverter components | Major service part | $$$$ | Expert-level |
| HT cables | Major service part | $$$ | Difficult |
| X-ray tube assembly | Major service part | $$$$ | Expert-level |
| AEC ion chamber | Major service part | $$$ | Difficult |
| Collimator lamp / drive assembly | Periodic replacement | $$ | Moderate |
| Bucky / grid motor | Major service part | $$ | Moderate |
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 starting sequence for this model, compiled from its documentation and engineering knowledge for this equipment class. 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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