Diode Laser Therapy Machine
Beijing ADSS Development Co., Ltd. · Model FG2000-D+
Diode Laser Therapy Machine.
Intended use: A mains electricity (AC-powered) device assembly in which input energy is used to excite a diode to emit a high-power therapeutic laser beam designed to perform dermatological procedures such as body hair removal (e.g., armpit, leg/arm, back, chest, bikini line, and face) and/or skin resurfacing (e.g., treatment of benign lesions, wrinkle reduction). It is intended to be used by a trained professional to emit pulsed light of a specific wavelength (e.g., around 808 nm or 1060 nm), delivered by a dedicated handpiece. It typically includes a control unit with dedicated software and user interface, delivery handpiece, and footswitch.
Key tips
- ·When no category-specific guidance fits, default to the manufacturer's own service manual and the general troubleshooting method in the Engineer's Guide.
- ·Run an incoming and annual electrical safety test regardless of how niche the device is.
Typical Failure Modes
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.
No or low laser output
HighSymptoms: 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.
Cooling / thermal shutdown
HighSymptoms: 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.
Delivery fibre / handpiece / applicator fault
MediumSymptoms: Burn marks at the tip, high loss, intermittent output, applicator not recognised.
Root cause: Damaged or contaminated fibre / applicator / connector.
Skin-cooling / contact-cooling fault (aesthetic)
MediumSymptoms: Skin cooling not delivered, cooling / cryogen alarm.
Root cause: Contact-cooling / cryogen supply, a valve, or the tip.
Footswitch / interlock / key fault
MediumSymptoms: Laser will not fire, key / interlock / footswitch error.
Root cause: Footswitch, door interlock, or key-switch fault.
Serviceable Parts & Consumables
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.
Laser module / lamp / diode bar
Power re-calibration required after replacement.
Class Periodic replacementRel. cost $$$$R&R Expert-level
Delivery fibre / handpiece / applicator
Class Frequent wear itemRel. cost $$$R&R Fairly easy
Chiller / TEC components & coolant filter
Class Periodic replacementRel. cost $$$R&R Difficult
Contact-cooling tip / cryogen valve (aesthetic)
Class Periodic replacementRel. cost $$R&R Moderate
Footswitch
Class Periodic replacementRel. cost $$R&R Fairly easy
| Part | Service class | Relative cost | R&R difficulty |
|---|---|---|---|
| Laser module / lamp / diode bar Power re-calibration required after replacement. | Periodic replacement | $$$$ | Expert-level |
| Delivery fibre / handpiece / applicator | Frequent wear item | $$$ | 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.
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.
- ·Follow the manufacturer's PM schedule
- ·Perform incoming and annual electrical safety testing per facility biomedical program
Troubleshooting Approach
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.
Symptom: No or low output
- Measure output at the delivery device with a laser power meter against the setting.
- Fit a known-good delivery fibre / handpiece / applicator.
- Confirm the cooling system runs and coolant is at level and clean.
- Check the key, interlock and footswitch are satisfied.
- Escalate a confirmed laser-module or driver fault to the OEM; recalibrate power after any module work.
Symptom: Thermal shutdown
- Confirm the cooling fans / pump run and airflow is clear.
- Check the coolant level and replace the coolant filter.
- Let the unit cool and restart.
- Clean the air filters / vents.
- Monitor for recurrence during a treatment.
Technical Specs
- MRI safety
- Labeling does not contain MRI Safety Information
- Sterile
- No
- Single use
- No
- FDA distribution status
- In Commercial Distribution
- Device type (GMDN)
- Dermatological diode laser system
- FDA product classification
- Powered Laser Surgical Instrument
Typical Location
Where this class of equipment is typically deployed - general reference, not this unit's own placement record.
- Varies by device - check the unit's own manual for facility placement guidance
Documents & Manuals
No documents available for this device yet.
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