
Toshiba · Model Infinix-i 4D CT
Improve visualization and device manipulation. Offer anatomical and functional information. Eliminate patient transfer. Confirm procedural goal. 12" × 16" Flat Panel Detector. 3D Angiography. Volume Navigation 3D roadmapping. 3D Multi-Modality Fusion. Tableside Controls.
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: Ring or band artefacts, excessive noise, HU non-uniformity, failed daily air/water calibration.
Root cause: Detector-channel drift or a bad detector module, a DAS fault, or air-cal / tube-output drift.
Symptoms: Tube-arc errors, exposure aborts, kV/mA faults, spits, or noisy bearing; tube pulls high heat units.
Root cause: Anode / bearing wear or vacuum degradation - the CT tube is a wear item.
Symptoms: Rotation faults, comms errors during rotation, brush dust, drive alarms.
Root cause: Worn slip-ring brushes, a drive-belt / bearing fault, or the data-transmission link.
Symptoms: Table drifts, will not index to the correct position, height or cradle errors.
Root cause: Table drive, encoder, or brake fault.
Symptoms: Recon hangs or is slow, images will not send to PACS, console errors.
Root cause: Recon-hardware or console-PC fault, or the network / storage.
Symptoms: Over-temperature warnings, exposures inhibited after a series, coolant alarm.
Root cause: Chiller pump / fan, low coolant, or a blocked heat exchanger.
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.
Major planned replacement; track heat-unit history.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| CT X-ray tube assembly Major planned replacement; track heat-unit history. | Periodic replacement | $$$$ | Expert-level |
| Detector module / DAS board | Major service part | $$$$ | Expert-level |
| Slip-ring brush set | Periodic replacement | $$ | Moderate |
| Gantry drive belt / bearings | Major service part | $$$ | Difficult |
| Table drive / encoder | Major service part | $$$ | Difficult |
| Chiller pump / coolant | Periodic replacement | $$ | Moderate |
Relative cost: $ lowest · $$$$ 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.
Synced live from the FDA openFDA API.
It was found that during a procedure the Peak Skin Dose (PSD) value displayed by the Dose Tracking System (DTS) was larger than the DTS expected value. This issue occurs when the power for the Angio Workstation is turned on after the power for the Infinix system is turned on.
Although the Flat Panel Detector (FPD) touch sensor is activated during use, the error message is displayed and the audible signal continues sounding during the table movement of longitudinal tilt, the movement of longitudinal tilt does not stop.
Lost and incorrect images. When using the "F-Rec" fluoroscopy image acquisition recording option in the "manual mode" an infrequent software error may cause images from another study to be displayed on the monitor. The acquired images may be lost requiring additional image acquisitions to be performed.
Under some conditions during high doses procedures the cumulative air kerma display may reach its maximum capability and fail to display the accrued value.
Audible signal is not available at all times when using the HLC fluoroscopy mode. Special means of activation are not designed in for selection of High Level Controls, as required by regulation.
System Lock-up: When performing DAS One Shot, the system may lockup due to a software timing error.
It was found during a study, arcing might occur in the transformer of the high voltage generator, XTP-8100G and XTBP-8100G displaying an error message and interrupting fluoroscopy.
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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