
GE HealthCare · Model Definium 8000
From image acquisition to interpretation to archiving, the Definium 8000 helps you maximize productivity and quality every step of the way. Definium 8000 offers multiple configurations for ultimate flexibility, from a wall stand to a full, comprehensive radiographic room. It combines excellent image quality with proven dose efficiency. Exceptionally fast processing speed. An easy, intuitive user-friendliness. New automated features and innovative clinical applications. All this comes with GE’s market leadership and experience in digital radiography, with thousands of digital X-ray flat panel detectors shipped worldwide. Complete control over system design and manufacturing for the utmost reliability. And one of the best customer care networks in the industry.
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: Panel not detected, images not received, wireless / tethered link drops mid-exam.
Root cause: Detector battery (wireless), Wi-Fi / tether cable, a docking / connector fault, or detector electronics.
Symptoms: Fixed-pattern artefacts, non-uniformity, dead pixels / lines, calibration overdue or failing.
Root cause: Detector gain / offset calibration, a bad pixel map, or physical detector (drop) damage.
Symptoms: Exposure inhibited, kV / mAs error, no exposure captured, AEC over/under.
Root cause: HV generator, tube, filament supply, or an AEC / interface fault.
Symptoms: Tube column, wall stand or table bucky will not track, detent, or auto-position.
Root cause: Drive motor, brake, encoder, or the auto-positioning interface.
Symptoms: Images will not display, process or send; worklist missing; slow processing.
Root cause: Workstation PC, software, or the DICOM / network configuration.
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 |
|---|---|---|---|
| Flat-panel detector (exchange) | Major service part | $$$$ | Moderate |
| Detector battery (wireless) | Periodic replacement | $$ | Easy |
| Tether cable / access point | Periodic replacement | $$ | Fairly easy |
| Positioner drive / brake / encoder | Major service part | $$$ | Difficult |
| Acquisition workstation PC | Major service part | $$$ | Moderate |
| AEC ion chamber | Major service part | $$$ | Difficult |
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.
Synced live from the FDA openFDA API.
Loss of image data: Software anomaly in the Processing Software on the Definium 8000 system may impact patient safety when using the VolumeRAD advanced application (option). The slice visualization of VolumeRAD exams acquired on the Wallstand receptor will be offset by 17mm. This prevents the visualization of anatomy WITHIN a distance of 17mm from the wallstand patient barrier (receptor cover).
Radiation dose reading greater than actual dose: Error in the generator software on the GE Healthcare Revolution XR/d configured with HP 8200 PC consoles and all Definium 8000 systems may impact patient safety. Occasional generator software errors may cause light X-ray Images with reported mAs readings higher than was actually exposed to the patient using the overhead X-ray tube. The mAs rea
Not properly labeling the manual switch for disabling positive beam limitation (PBL) located on the overhead tube support user interface as required
Necessary certification labels are missing from the x-ray contol.
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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