GE HealthCare · Model OEC Fluorostar 7900
Imaging processing 1K x 1K Pulsed Fluoroscopy, pre-defined modes for dose optimization PreView Iris/ Dual leaf collimator enables placement of shutter, reducing overall dose to patients and staff Dual side Laser Aimer helps align anatomy with precision from Image Intensifier and tube side SIMPLE Touch Screen User Interface 60,000 image storage in system hard drive CD Burner for image transfer in bmp or jpeg format USB port for plug-and-play image transfer to user's PC Integrated DICOM
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: 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: Exposure fails, kV/mA out of range error.
Root cause: HV tank or generator board fault.
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 |
|---|---|---|---|
| Workstation RAID / GPU | Periodic replacement | $$$ | Difficult |
| X-ray tube insert Major R&R; track mAs history. | Major service part | $$$$ | Expert-level |
| Flat-panel detector | Major service part | $$$$ | Expert-level |
| Cooling pump & radiator | Periodic replacement | $$$ | 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 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.
The alarm timer is reset after each exposure and therefore never reaches the five minute alarm state unless one exposure exceeds 5 minutes in duration.
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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