
Alcon · Model ACCURUS
Digital Infusion Pressure and Irrigation Pressure Provides fast response to increase or decrease IOP Surgeon controlled pressurized infusion provides chamber stability Fluid/Air Exchange Digital control of air pressure for precise Fluid/Air exchange Diathermy Available from the foot pedal anytime, even during U/S tuning Illumination The ACCURUS Xenon Illuminator provides unbiased color contrast for improved visibility during surgery Dual high-intensity illuminators provide the color and power needed for the most demanding surgeries Vitrectomy Technology Touching the Vit icon provides you a quick menu from which to select either the Proportional Vacuum, Momentary, or 3D Technology modes Fragmentation The Frag icon allows you to select four different fragmentation modes 3D Frag provides simultaneous control of power and vacuum Linear Frag Fixed Frag Momentary Frag Pulsed Frag is available in all modes except 3D Scissors Press the Scissors icon and you can select Proportional, Multi-cut, or MPC modes Vacuum assist for tissue manipulation is available in MPC and Multi-cut scissors modes Extrusion The Extrude icon gives you the option of three different extrusion vacuum settings: High, Medium, and Low Viscous Fluid Control Touch the Viscous Fluid Controller (VFC) icon and choose whether you want to inject or extract viscous fluids Wireless Remote Control Provides convenient access to important surgical modes for selection and parameter adjustment.
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 ultrasonic power, poor followability, vacuum will not build or holds poorly, surge.
Root cause: Worn phaco handpiece / tip, a cracked or worn tubing / cassette, or a pump / vacuum-sensor fault.
Symptoms: Handpiece will not tune, overheats, no irrigation / aspiration, cutter not cutting (vit).
Root cause: Worn or damaged handpiece, or its connector / cable.
Symptoms: Cassette not recognised, priming / tuning fails, fluid leaks at the cassette.
Root cause: Cassette-detection switch, the peristaltic / Venturi pump, or fluidics seals.
Symptoms: Pedal positions not registering, wireless pedal not pairing.
Root cause: Worn footpedal or its cable / wireless module.
Symptoms: Cut rate low or erratic, cutter will not drive.
Root cause: Internal pneumatic valve or a supply-pressure 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.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Phaco / I-A / vitrectomy handpiece | Periodic replacement | $$$ | Fairly easy |
| Peristaltic / Venturi pump components | Periodic replacement | $$$ | Difficult |
| Cassette-detection switch / fluidics seals | Periodic replacement | $$ | Moderate |
| Footpedal / wireless module | Periodic replacement | $$ | Fairly easy |
| Pneumatic valve (vitrectomy) | Major service part | $$ | Moderate |
Relative cost: $ lowest · $$$$ 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.
Insufficient seal on the outside packaging, potentially affecting the sterility of the product.
This medical device correction is related to Alcon products that present a 23G non-valved trocar cannula and infusion cannula together because of an issue regarding the loose fit between the 23G non-valved trocar cannula and infusion cannula that could potentially cause a detachment between the non-valved trocar cannula and infusion cannula during surgery.
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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