Varian Medical Systems · Model TrueBeam STx
Radical minds deserve radical technology. The TrueBeam STx system is a radically new solution that is faster and more powerful, giving clinicians the ability to navigate the complexities of cancer care with confidence, including challenging cases in the brain, spine, lung, liver and prostate. The system uses sophisticated imaging and respiration synchronization tools to visualize soft tissue during treatment and make changes accordingly. With new beam-shaping capabilities using the High-Intensity Mode, it enables the delivery of larger doses in smaller places. Now clinicians can perform radiosurgery procedures with exceptional ease and speed, with most treatments taking only a few minutes a day. TrueBeam STx - innovative, intelligent and intuitive.
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 |
|---|---|---|---|
| Workstation / GPU | Periodic replacement | $$$ | Difficult |
| Power supply unit | Major service part | $$ | Moderate |
| Network interface card | Major service part | $ | Fairly easy |
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.
Synced live from the FDA openFDA API.
Reports have been received of an anomaly that can result in a treatment without intended gating (respiratory tracking/monitoring). This issue occurs when a patient planned with gating is treated on more than one system.
Medical device for patient treatment does not meet electrical safety standards.
Describe a symptom or error code. Bio answers from this device's own documented error codes, failure modes, parts, and guides.
Ask Bio →