Lumenis · Model LightSheer DESIRE
• Satisfied Patients - Treatments are cost effective and large areas can be treated in less than 10 minutes, so you can see more satisfied patients. • Faster Learning Curve - The system is simple to operate and has a friendly Graphic User Interface (GUI) and preset programs- For a faster learning curve and easy treatment delegation. • Treatment Versatility - The handpieces have been ergonomically designed and can be switched using a simple 'Plug and Play' method-To allow versatility in treatment options and improved system handling. • Multi-Location-Usage - The system is light and portable and can easily be transported from one place to another- To enable multi-location use. • Upgrade - The system is up-gradable so it can grow with your business-To fit your needs in any given time and match your practice requirements so you can maximize revenues. • Desirable Clinical Results - The LightSheer technology by Lumenis has been validated in numerous clinical studies and peer reviewed articles. Thousands of satisfied customers have been and are still benefiting from the gold standard performance and patient satisfaction. • Faster Treatment - High-Speed Integrated Technology (HIT™) reduces treatment time by more than 75%. Using the 22x35mm spot size, large areas as the back and legs can be treated in less than 10 minutes. THE HIT ™ eliminates the lengthy preparation time need need for cooling or anesthetics. • Ultimate Patient Comfort - High-Speed Integrated Technology (HIT™) uses a unique vacuum mechanism that activates the skin's tactile and pressure receptors to inhibit the transmission of pain. ChillTip™ Technology improves patient comfort by cooling the skin prior to treatment and continuously cooling it throughout the treatment. • Clinically Validated Efficacy - Numerous clinical studies and peer review articles have validated the safety and efficacy of the technologies powering the LightSheer DESIRE. Thousands of satisfied customers have been and are still benefiting from the gold standard performance and patient satisfaction.
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: Reduced output power, inconsistent treatment fluence.
Root cause: Normal diode/gain-medium wear over lamp/diode hours.
Symptoms: Overheat shutdown mid-treatment, error code on startup.
Root cause: Coolant pump, TEC element, or filter degradation.
Symptoms: Uneven beam delivery, connector arcing, or no output at the handpiece.
Root cause: Fiber or articulated-arm optics degraded by flex/heat cycling.
Symptoms: Won't fire, safety interlock fault on the display.
Root cause: Door/footswitch interlock or shutter mechanism failure.
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.
High-turnover; keep spares.
Core consumable; major cost driver.
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Cooling system (pump / TEC / filter) | Periodic replacement | $$$ | Moderate |
| Handpiece / delivery fiber assembly High-turnover; keep spares. | Periodic replacement | $$$ | Fairly easy |
| Footswitch / interlock assembly | Major service part | $$ | Fairly easy |
| Laser diode / flashlamp module Core consumable; major cost driver. | Periodic replacement | $$$$ | Difficult |
Relative cost: $ lowest · $$$$ 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.
Device software treatment preset parameters for the XC treatment handpiece do not match the Operator Manual, and exceed recommended settings. Operator Manual parameters are lower than indicated for specific hair color and Fitzpatrick skin type resulting in insufficient treatment effect. May result in patient burns and hypopigmentation.
During hair removal treatment, patients' skin can experience burns due to debris accumulating on the sapphire crystal tip.
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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