
AGFA · Model DR 800
Full Leg/Full Spine capabilities come standard, including tube and detector positioning, acquisition of up to four images. With EasyStitch™, you can add extensive orthopedic tools. Seamless automatic stitching directly on the table allowing horizontal and vertical Full Leg/Full Spine (FLFS) procedures. EasyStitch uses single focus, distortion free imaging technology providing simple, precise Full Leg/Full Spine (FLFS) imaging. Implementing the DR 800 with digital tomosynthesis will add a key new tool to your imaging portfolio: one that gives your hospital’s radiologists more choices than found in legacy equipment. By using multislice image reconstruction, the DR 800 provides the depth to see beyond dense structures, revealing more details than classical X-rays. Yet it uses the low radiation dose and fast workflow of general radiography. The DR 800 offers improved diagnostic visualization for interventional procedures, with real-time subtraction and masking (roadmapping) for guidance in the positioning and placement of catheters, stents and balloons.
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: Panel not detected, images not received, wireless / tethered link drops mid-exam.
Root cause: Detector battery (wireless), Wi-Fi / tether cable, a docking / connector fault, or detector electronics.
Symptoms: Fixed-pattern artefacts, non-uniformity, dead pixels / lines, calibration overdue or failing.
Root cause: Detector gain / offset calibration, a bad pixel map, or physical detector (drop) damage.
Symptoms: Exposure inhibited, kV / mAs error, no exposure captured, AEC over/under.
Root cause: HV generator, tube, filament supply, or an AEC / interface fault.
Symptoms: Tube column, wall stand or table bucky will not track, detent, or auto-position.
Root cause: Drive motor, brake, encoder, or the auto-positioning interface.
Symptoms: Images will not display, process or send; worklist missing; slow processing.
Root cause: Workstation PC, software, or the DICOM / network 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 |
|---|---|---|---|
| Flat-panel detector (exchange) | Major service part | $$$$ | Moderate |
| Detector battery (wireless) | Periodic replacement | $$ | Easy |
| Tether cable / access point | Periodic replacement | $$ | Fairly easy |
| Positioner drive / brake / encoder | Major service part | $$$ | Difficult |
| Acquisition workstation PC | Major service part | $$$ | Moderate |
| AEC ion chamber | Major service part | $$$ | 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 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.
No documents available for this device yet.
Synced live from the FDA openFDA API.
It is possible to exceed the maximum allowed Air Kerma rate (AKR) of 88mGy/min for pulsed fluoro exams. This can happen in case the framerate is increased on the NX workstation when ABS is not enabled.
Potential for the front lever chain of the DR 800 table to fail.
Under specific conditions (Fluoroscopic exam, ABS=OFF, manual change of parameters) wrong calculation of the dose/minute for fluoroscopy exams can be possible
Tomosynthesis image acquisition sequence did not stop automatically after expected number of exposures.
The exposed area of fluo exams possibly does not match the active area of the detector within specified limits.
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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