Toshiba · Model Infinix
Instant image display at fluoroscopy initiation to ensure critical information is immediately available Head-to-toe coverage Designed to fit in conventionally sized cardiovascular suites Advanced image processing technology to increase resolution and virtually eliminate lag 3D imaging Parallel processing Freedom to configure room set up based on procedure needs Low contrast imaging option High speed acquisition Flexible and accurate C-arm positioning reduces overall exposure by shortening exam times
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: Tube won't fire, heat-capacity alarm.
Root cause: Filament wear, cooling failure.
Symptoms: Image noise, artifacts, low SNR.
Root cause: Flat-panel / sensor aging.
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.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Flat-panel detector | Major service part | $$$$ | Expert-level |
| Cooling pump & radiator | Periodic replacement | $$$ | Difficult |
| High-voltage generator | Major service part | $$$$ | Expert-level |
| Workstation RAID / GPU | Periodic replacement | $$$ | 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.
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.
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