
Lumenis · Model Vision One
Voice Confirmation - The Vision One is equipped with a unique voice confirmation feature, which allows the user to change any of the key parameters, while receiving a vocal confirmation of the dialed choice. This feature allows the operator to adjust parameters also during treatment, without having to shift view from the treatment site to the unit's control panel. Dependability you can count on - Dependability is of crucial importance in both the OR and Office Setting. Convenience & Flexibility - Changing delivery devises is fast and easy. The Vision One remembers the settings that were last used with the selected delivery device allowing for a smoother transition. Memory Settings - The Vision One has five memory setting that can be programmed to remember the most used treatment parameters. Smart™ Fiber Technology - The Vision One features Smart fiber technology that allows the laser system to distinguish an LIO from an endoprobe or LaserLink and will automatically adjust power settings to increase safety parameters. The Lumenis Smart fiber technology also alerts the surgeon and staff if the physician eye safety filter, footswitch and delivery devices are not properly attached to the laser console. User-Friendly - A color touch screen and illuminated remote keypad put all operations literally at your fingertips. Easily adjust parameters or instantly switch between treatment wavelengths. Conveniently position the remote control on either side of the slit lamp, or in a sterile cover for the operating room.
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: Weak or no output at the delivery device, treatment ineffective, power not reaching the set value.
Root cause: Laser module / lamp / diode-bar ageing, a damaged delivery fibre / handpiece / applicator, or a driver / power-supply fault.
Symptoms: Unit shuts down after a period, over-temperature or low-flow alarm.
Root cause: Chiller / TEC fault, low or contaminated coolant, a failed pump, or blocked airflow.
Symptoms: Burn marks at the tip, high loss, intermittent output, applicator not recognised.
Root cause: Damaged or contaminated fibre / applicator / connector.
Symptoms: Skin cooling not delivered, cooling / cryogen alarm.
Root cause: Contact-cooling / cryogen supply, a valve, or the tip.
Symptoms: Laser will not fire, key / interlock / footswitch error.
Root cause: Footswitch, door interlock, or key-switch fault.
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.
Power re-calibration required after replacement.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Laser module / lamp / diode bar Power re-calibration required after replacement. | Periodic replacement | $$$$ | Expert-level |
| Delivery fibre / handpiece / applicator | Frequent wear item | $$$ | Fairly easy |
| Chiller / TEC components & coolant filter | Periodic replacement | $$$ | Difficult |
| Contact-cooling tip / cryogen valve (aesthetic) | Periodic replacement | $$ | Moderate |
| Footswitch | 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 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.
Lumenis has initiated a recall on certain models of Vision One System due to a potential for unintended laser exposure to the user.
Software anomaly recorded incorrect filter in patient database and this may lead to patient skin burns.
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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