GE HealthCare · Model Precision 600FP
Sharp Image A cesium iodide based flat-panel detector and super noise reduction coupled with a comprehensive post-processing and visualization suite make for ultra-vivid imaging. Comprehensive Dose Management Precision 600FP includes features such as grid controlled pulse, adjustable frame rate and dose settings, and virtual collimation that allow reduced dose for you and your patient. Streamlined Workflow We designed Precision 600FP to be bariatric friendly and easy to use with flexible tableside controls. Optimized Cost of Ownership The small footprint is designed to fit your current fluoro room and GE’s reliable service support is always there to assist you when needed.
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: Unexpected shutdown, unit won't power on.
Root cause: PSU or backup battery aging.
Symptoms: Frozen console, acquisition timeout.
Root cause: Workstation or storage degradation.
Symptoms: Images fail to transfer, PACS timeout.
Root cause: Network configuration or interface card fault.
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.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Network interface card | Major service part | $ | Fairly easy |
| Workstation / GPU | Periodic replacement | $$$ | Difficult |
| Power supply unit | Major service part | $$ | 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 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.
A reported incident of a monitor that fell from the suspension. A fall of a monitor could result in an injury to a patient or operator. Recall affects the single and dual LCD monitor suspensions used on Precision 500D Classical R & F system, Precision RXi 23A/32A Analog System, Precision RXi Digital system and Precision MPi fluoroscopic imaging systems.
It was reported that when the GE Precision 500D foot pedal is repeatedly activated, a defect in the fluoro-timer will cause the dose measurement to report a higher value than was actually received by the patient. Patient will receive a lower dosage irradiation time which will result in indication of cumulative air kerma higher than that to which the patient was actually exposed.
Inaccurate cassette size display reading/ Inaccurate mAs reading: 1. When the device is in PBL mode and a larger film cassette is inserted into the table Bucky (replacing a smaller cassette) after a protocol is selected on the console, the collimator will not adjust to the larger cassette size. The collimator stays at the original smaller cassette size and allows the operator to take an exposure.
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