Villa Sistemi Apollo EZ
Villa Sistemi · Model Apollo EZ
In the spirit of renewal Based on an upgraded, high performance hardware architecture, the new remote control console introduces features and solutions that further increase ease of use and efficiency of the system, thus helping to speed up the workflow and increase productivity in the R/F room. Versatility and efficiency Rapid and concurrent movements reduce dramatically the patient preparation time and increase workflow. On the film-based versions, the powerful spot film device, available with either line or cross divisions, can fit virtually any application need, while the one-hand cassette loading and unloading mechanism grants a maximized speed for this frequent operation. Safety and patient care Special attention is always by us given to patient's dose reduction, by employing a number of provisions, such as reduced skin-to-film-distance, automatic collimation, fully automatic parameter settings in both fluoro and exposure. Additionally, in order to grant the highest level of safety, a dedicated anti-collision device on the vertical tilting movement stops the motion in case of contact with foreign objects The spot film device, compatible with numerous formats of radiographic cassettes, makes the preparation of the examination simple and fast through the automatic cassette loading and alignment mechanism, thus allowing multiple images to be acquired in succession on the same film through the line and cross divisions
Key tips
- ·Never bypass a radiation interlock to "just get the image" - this is one of the few true zero-tolerance rules in BMET work.
- ·Trend image-quality phantom results over time - drift shows up before an outright failure does.
- ·Portable/mobile units take real physical abuse from transport - check wheel locks and cable strain reliefs more often than fixed units.
Typical Failure Modes
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.
X-ray tube overheating / filament failure
HighSymptoms: Tube won't fire, heat-capacity alarm.
Root cause: Filament wear, cooling failure.
Cooling system fault
HighSymptoms: Tube temp alarm, duty-cycle limited.
Root cause: Pump/radiator or coolant loss.
Generator / high-voltage fault
HighSymptoms: Exposure fails, kV/mA out of range error.
Root cause: HV tank or generator board fault.
Recon / system software hang
LowSymptoms: Frozen console, acquisition timeout.
Root cause: Workstation or RAID degradation.
Serviceable Parts & Consumables
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.
X-ray tube insert
Major R&R; track mAs history.
Class Major service partRel. cost $$$$R&R Expert-level
Flat-panel detector
Class Major service partRel. cost $$$$R&R Expert-level
Cooling pump & radiator
Class Periodic replacementRel. cost $$$R&R Difficult
High-voltage generator
Class Major service partRel. cost $$$$R&R Expert-level
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| X-ray tube insert Major R&R; track mAs history. | Major service part | $$$$ | Expert-level |
| Flat-panel detector | Major service part | $$$$ | Expert-level |
| Cooling pump & radiator | Periodic replacement | $$$ | Difficult |
| High-voltage generator | Major service part | $$$$ | Expert-level |
Relative cost: $ lowest · $$$$ highest service-part cost for this equipment class. Not a price.
PM Checklist
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.
- ·Daily QC per modality: image-quality phantom test
- ·Tube and detector inspection
- ·Annual state-required radiation safety survey
- ·Vendor-scheduled preventive maintenance
Troubleshooting Approach
A structured starting point derived from the failure modes above. Follow the manufacturer's service documentation for the actual procedure.
Symptom: X-ray tube overheating / filament failure
- Confirm the presentation - typically tube won't fire, heat-capacity alarm - and note the exact alarm or message and the conditions when it occurs.
- Check the most likely cause first: filament wear, cooling failure.
- Isolate the affected subsystem using the manufacturer's functional check or self-test, where one is provided.
- If the fault is confirmed and not a field adjustment, service or replace the x-ray tube insert per the manufacturer's service documentation.
- Return the device to service only after the manufacturer's functional and applicable electrical-safety checks pass.
- Record the findings, any parts used, and the verification results in the maintenance history.
Symptom: Detector calibration drift
- Confirm the presentation - typically image noise, artifacts, low SNR - and note the exact alarm or message and the conditions when it occurs.
- Check the most likely cause first: flat-panel / sensor aging.
- Isolate the affected subsystem using the manufacturer's functional check or self-test, where one is provided.
- If the fault is confirmed and not a field adjustment, service or replace the flat-panel detector per the manufacturer's service documentation.
- Return the device to service only after the manufacturer's functional and applicable electrical-safety checks pass.
- Record the findings, any parts used, and the verification results in the maintenance history.
Typical Location
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
- Radiology / Imaging department
- Emergency Department (portable units)
- Operating Room (C-arms)
- Cath lab
- Bedside ICU (portable X-ray)
Documents & Manuals
No documents available for this device yet.
Safety & Recalls
Synced live from the FDA openFDA API.
- RECALL
It has been discovered that due to lack of information accompanying documents the product fails to comply with 21CfR 1020.33(c),1020.33(d),1020.33(g),and 1020.330).
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