
AGFA · Model ADC Compact
Completely automated computed radiography (CR)plate reading. “Drop-and-go” buffer. Compact footprint and ergonomic design. Building block for digital X-ray department.
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: Banding, streaks, ghost images, non-uniform density, dust artefacts.
Root cause: Dirty light guide / scanning optics, a worn erase-lamp array, imaging-plate wear, or contaminated transport rollers.
Symptoms: Plate jams in the reader, transport error, plate not returned.
Root cause: Worn or contaminated transport rollers / belts, or a sensor fault.
Symptoms: A faint previous image appears on the next exposure.
Root cause: Erase-lamp array degradation or a driver fault.
Symptoms: No or very noisy image, scan-error message.
Root cause: Scanning laser or the photomultiplier / detection chain.
Symptoms: Images will not display, annotate or send to PACS.
Root cause: Workstation PC or the DICOM configuration.
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.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Transport rollers / belts | Periodic replacement | $$ | Moderate |
| Erase-lamp array | Periodic replacement | $$$ | Moderate |
| Imaging plates / cassettes | Periodic replacement | $$$ | Easy |
| Light guide / scanning optics | Major service part | $$$ | Difficult |
| Workstation PC | 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 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.
Users of affected systems may experience one or more of four (4) problems the clinical impact could be a loss of image(s), 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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