Verathon · Model BladderScan i10
Large 10.1” (25.6 cm) optically bonded touchscreen reduces glare Interface uses intuitive graphics, automatic bladder location detection and BladderTraqTM contour tracking to guide the user through every step Simple charting tool easily transfers exam results to any electronic healthcare record system
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: Inaccurate volume readings, or no image.
Root cause: Transducer element or cable wear.
Symptoms: Won't hold charge, shuts down mid-scan.
Root cause: Aged rechargeable battery pack.
Symptoms: Scan targets wrong anatomy, inaccurate volume.
Root cause: Internal aiming-icon calibration drift.
Symptoms: Unresponsive controls, frozen screen.
Root cause: Touchscreen digitizer or display aging.
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.
Core consumable; most-replaced assembly.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Touchscreen / display module | Major service part | $$$ | Moderate |
| Ultrasound transducer / probe head Core consumable; most-replaced assembly. | Periodic replacement | $$$$ | Moderate |
| Rechargeable battery pack | Periodic replacement | $$ | Fairly easy |
| Probe cable | Periodic replacement | $$ | Fairly easy |
Relative cost: $ lowest · $$$$ 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.
Due to a change in handle material and process, probe handle may crack.
Describe a symptom or error code. Bio answers from this device's own documented error codes, failure modes, parts, and guides.
Ask Bio →