OrthoScan · Model Mobile DI
OrthoScans new mini c-arm with flat detector offers surgeons increased image quality, a smaller thin design, improved reliability, and more efficient imaging. Once again OrthoScan is setting the new standard in mini c-arm imaging.
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.
Synced live from the FDA openFDA API.
Ziehm Imaging, Inc., distributor, have been informed by manufacturer, Ziehm Imaging GmbH that installed devices may not fully meet the requirements of IEC 60601-2-54 and or 21 CFR 1020.32(c) with respect to wired hand switch may fail when being exposed to mechanical stress such as shocks (e.g. dropping) or impacts can irreversibly damage the switching element in the hand switch. A defective switching element may then potentially initiate unintended radiation of the connected mobile X-ray unit.
OrthoScan Inc. discovered during investigation of a non-standard work flow a non-conformity of the devices. Specifically, the system software allows a user to activate the Digital Zoom feature in the course of taking a live image exposing a larger x-ray field than can be viewed by the user
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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