Esaote · Model C-Scan
Maintenance-free open permanent magnet 0.2 Tesla field No RF Shielding required Very compact, installation space of 9 m2 required Low Power Consumption: only 1 Kw in normal 220/110V power outlet Ergonomic design for maximum patient comfort (no claustrophobia) Complete set of dedicated optimized coils All imaging sequences used in MSK settings Full set of pre-defined sequences and protocols User defined sequences and customized examination protocols Multi planar score Windows based user interface Extensive image viewing, analysis and elaboration tools Sophisticated storage functionality particularly useful for systems connected to PACS network Full DICOM connectivity
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.
Synced live from the FDA openFDA API.
The device is being recalled because dynamic loading forces from larger patients can fracture the extremity portion of the patient table. Additionally, a weight limit is added to the patient seat for weight-bearing examinations.
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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