AGFA · Model DX D 100+
Fully motorized, heavy duty solution Wireless mobility for improved flexibility and infection control Batteries and configuration provide maximum power and autonomy Powerful generator reduces exposure times and delivers sharper images Ergonomic and maneuverable in restricted spaces MUSICA empowered FreeView Technology
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.
Steel cable installed inside the mobile column which supports the weight of the telescopic arm with the tube head has potential risk -an interference could cause the safety system which blocks the arm if the cable is cut off does not work properly, may result in patient injury
When using the DX-D 100 unit, sporadic unintended movements caused by an electrostatic discharge of the unit to the ground may occur.
When liquid comes in contact with the DX-D 100 touch screen, the device may incorrectly recognize this as user input altering device settings.
Unit was mislabeled with a factory label showing 32 KW output power.
Customers could potentially experience intermittent, unintended and illogical movement when using the product.
A localized fog pattern appears on the film.
Users of affected systems may experience a loss of images, the need to repeat the imaging procedure and possibly a short delay in diagnosis.
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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