
Ellex · Model Ultra Q
IOL-Friendly Photodisruption - Ultra Q™ achieves the industry’s lowest energy optical breakdown at 1.8mJ (in air) to cut tissue more efficiently with fewer shots and less cumulative energy. Featuring an Ultra Gaussian beam profile, Ultra Q™ focuses more energy into the center of the beam profile to deliver greater energy density. Not only does this reduce the amount of energy needed to effectively perform capsulotomy and iridotomy treatments, it also greatly reduces the risk of lens pitting. Capsulotomy for Presbyopic IOLs - A precise capsulotomy is essential for IOLs that correct presbyopia through implantation in the posterior chamber’s capsular bag. Good IOL centration, in terms of the pupil, optimizes lens performance. In contrast, decentration can cause halos and poor vision. The goal is a perfectly centered, precise capsulotomy that will not affect the tension of the bag and the position of the IOL in the visual axis. The precision and ultra-low energy optical breakdown provided by Ultra Q™ creates a capsulotomy opening that is precisely controlled, without causing damage to the lens – even if the lack of a ridge makes the capsule adhere to the optic. Iridotomy for Phakic IOLs - Refractive IOLs that are designed to correct myopia, or hyperopia (also known as Phakic IOLs) can be placed in front of the iris or between the iris and the natural lens. To prevent any possibility of IOL-induced pupillary block, these lenses require peripheral iridotomies prior to surgery. The iridotomy aperture must be large enough to ensure a balanced aqueous flow, yet small enough so that no light is transmitted back to the pupil, which can cause double vision. Ultra Q™ enables you to create a precise size of the iridotomy, often in a single shot that uses lower energy than other YAG lasers.
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.
No documents available for this device yet.
Synced live from the FDA openFDA API.
Unintended laser emission while the user was moving the joystick for targeting.
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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