Bausch & Lomb MILLENNIUM
Bausch & Lomb · Model MILLENNIUM
MODULAR SYSTEM FOR CATARACT AND VITREOUS REMOVAL The Millennium microsurgical system delivers on the promise of a platform with innovative technology. For the latest advancement in fluidics control for the cataract surgeon, Bausch & Lomb Surgical offers Millennium™ Advanced Flow System (AFS) and Custom Control Software (CCS) which take you beyond cold phaco with a new hyper-cool level of control with your choice of either a venturi or peristaltic system. The Dual Linear™ control feature allows for simultaneous control of either flow or vacuum, and ultrasound power. Additionally, surgeons can use both flow and vacuum response in the same procedure. The powerful Quad-crystal ultrasound handpiece delivers excellent cutting with smooth efficiency. Programming options allow for virtually unlimited parameters of storage and surgeon-controlled mode switching. With its modular design, the Millennium system integrates innovation for today and the future.
Key tips
- ·Verify laser output with a real power meter, not the unit's own display - the display can drift independently of true output.
- ·Take "the image looks a little off" reports seriously - optical alignment drift is usually gradual, not sudden.
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.
Light source / lamp failure
MediumSymptoms: Dim illumination, lamp error.
Root cause: Xenon/LED aging.
Probe / handpiece fault
HighSymptoms: No phaco power, error.
Root cause: Tip or handpiece wear.
Pump / fluidics fault
MediumSymptoms: Unstable anterior chamber.
Root cause: Peristaltic pump wear.
Imaging sensor drift
LowSymptoms: Blurry/offset image.
Root cause: Camera calibration drift.
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.
Illumination lamp / LED
Class Periodic replacementRel. cost $$$R&R Moderate
Peristaltic pump tubing
Consumable.
Class Frequent wear itemRel. cost $R&R Easy
Imaging camera module
Class Periodic replacementRel. cost $$$R&R Difficult
Phaco handpiece / tip
High-value, track usage.
Class Periodic replacementRel. cost $$$$R&R Difficult
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Illumination lamp / LED | Periodic replacement | $$$ | Moderate |
| Peristaltic pump tubing Consumable. | Frequent wear item | $ | Easy |
| Imaging camera module | Periodic replacement | $$$ | Difficult |
| Phaco handpiece / tip High-value, track usage. | Periodic replacement | $$$$ | Difficult |
Relative cost: $ lowest · $$$$ 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.
- ·Optical alignment / calibration check
- ·Lamp or laser output verification
- ·Annual full PM
Troubleshooting Approach
A structured starting point derived from the failure modes above. Follow the manufacturer's service documentation for the actual procedure.
Symptom: Light source / lamp failure
- Confirm the presentation - typically dim illumination, lamp error - and note the exact alarm or message and the conditions when it occurs.
- Check the most likely cause first: xenon/LED 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 phaco handpiece / tip 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: Probe / handpiece fault
- Confirm the presentation - typically no phaco power, error - and note the exact alarm or message and the conditions when it occurs.
- Check the most likely cause first: tip or handpiece wear.
- 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 illumination lamp / LED 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.
- Eye clinic / ophthalmology suite
- Operating Room (ophthalmic surgery)
Documents & Manuals
No documents available for this device yet.
Safety & Recalls
Synced live from the FDA openFDA API.
- RECALL
The AC power cords used on these products are subject to an FDA Alert -- Safety Investigation of Certain Medical Device Power Cords: Initial Communication, Date Issued: October 19, 2009.
- RECALL
Users may incorrectly assemble the plastic needle wrench to the phacoemulsification needle resulting in the generation of plastic particulate
- RECALL
The directions for use are printed with the incorrect symbols to indicate the product is packaged as sterile and nonreusable
- RECALL
The cutter probe tip breaks during use.
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