
GE HealthCare · Model Lunar Prodigy Advance
ScanCheck - ScanCheck automatically identifies potential acquisition and analysis errors and provides multimedia help. It also alerts of incorrect positioning, unusual anatomy, high-density areas and artifacts, and makes recommendations for correction. PRODIGY: DualFemur - The DualFemur option automatically scans both femurs in one seamless acquisition without repositioning, and identifies the weakest side to enhance confidence in treatment decisions. The trending function enables seamless follow-up of changes. PRODIGY: Total body/body composition - Body composition scans with DXA provide precise and accurate data on bone and tissue composition, including bone mineral density (BMD), lean and fat tissue mass, and %fat. They provide both total body data and regional results. PRODIGY: Dual-energy Vertebral Assessment (DVA) - DVA aids in the identification and assessment of vertebral deformations. DVA provides rapid single- and dual-energy images of the AP and lateral spine, allowing clinicians to visually assess the presence of vertebral deformations. PRODIGY: Composer - Automated physician reporting comes complete with the National Osteoporosis Foundation (NOF) treatment guidelines and World Health Organization (WHO) diagnostic criteria for a complete osteoporosis assessment. Composer™ is designed to follow diagnostic guidelines proposed by the International Society of Clinical Densitometry (ISCD), determining the lowest T-score based on defined regions. Recommendation text is inserted to aid productivity.
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: Daily spine / block phantom BMD trends out of control limits, or calibration fails.
Root cause: X-ray source output drift, detector degradation, or a calibration-drum / reference fault.
Symptoms: The scanning arm or table will not move smoothly, position error, scan aborts, image geometry wrong.
Root cause: Drive motor, belt, or an encoder / limit-sensor fault.
Symptoms: Exposure inhibited, kV error, no counts / very noisy scan.
Root cause: X-ray tube / HV supply, or the filter-wheel / calibration-drum.
Symptoms: Missing scan lines, non-uniform image, detector-error message.
Root cause: Detector element / electronics degradation.
Symptoms: Analysis software hangs, scans will not archive or transfer.
Root cause: Workstation PC or software 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 |
|---|---|---|---|
| X-ray tube / HV supply | Major service part | $$$$ | Expert-level |
| Detector assembly | Major service part | $$$$ | Difficult |
| Scanning-drive motor / belt / encoder | Major service part | $$$ | Difficult |
| Calibration drum / filter wheel | Major service part | $$$ | Difficult |
| Workstation PC | Major service part | $$$ | 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.
Aortic Length over-estimated: incorrect measurements when using the Aorta analysis protocol or customized protocols. Until a new software version is installed the aorta analysis protocol or the customized protocols for an aneurysm should NOT BE USED.
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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