1450 nm diode-laser architecture
1450 nm diode-laser architecture
$3,952
Candela SmoothBeam is a legacy Candela dermatology laser using a 1450 nm diode wavelength with epidermal cooling. The model appears in FDA 510(k) records as the Candela SmoothBeam Laser System; exact accessories and cleared indications depend on the system revision and market. Available for international procurement subject to exact configuration, condition and destination requirements.
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Candela SmoothBeam is a legacy Candela dermatology laser using a 1450 nm diode wavelength with epidermal cooling. The model appears in FDA 510(k) records as the Candela SmoothBeam Laser System; exact accessories and cleared indications depend on the system revision and market.
Candela SmoothBeam is a legacy Candela dermatology laser using a 1450 nm diode wavelength with epidermal cooling. The model appears in FDA 510(k) records as the Candela SmoothBeam Laser System; exact accessories and cleared indications depend on the system revision and market.
This is a legacy or configuration-sensitive product. The final quotation should identify the exact model revision, manufacture year where available, serial-number configuration, condition, included accessories, software/licenses and service history.
For purchasing, compare the exact offered configuration rather than the model name alone. AI Robot Supplier can prepare a destination-specific quotation covering the equipment, documented accessories, shipping scope and available technical documentation.
Match model/serial labels, condition and included configuration to the written quotation.
Check accessories, software, power, facility and host-system requirements where applicable.
Confirm packing, freight, insurance, documentation, warranty and commissioning responsibilities.
Reference images support model identification. The final quotation should match the exact unit, accessories and condition being supplied.

Product-specific facts below are preserved from the researched listing; configuration-sensitive items should be verified against the exact supplied unit.
1450 nm diode-laser architecture
Non-ablative dermatology platform
Dynamic epidermal cooling/cooling workflow associated with the SmoothBeam platform
FDA 510(k) record available for the device family
Legacy unit condition and laser/handpiece service history should be verified
Suitability depends on the exact configuration, professional use case, manufacturer instructions and destination-market requirements.
Confirm suitability for the intended workflow before deployment.
Confirm suitability for the intended workflow before deployment.
Confirm suitability for the intended workflow before deployment.
Exact specifications can vary by revision, region and installed options. The serial-number-specific configuration and manufacturer documentation take precedence.
The final commercial offer defines what is included. For high-value or configuration-sensitive equipment, request an itemized packing list before payment.
Exact package contents and condition are controlled by the written quotation and order documentation.
Use manufacturer, regulatory and technical references to validate product-family information. The exact supplied unit still requires serial-specific verification.
External technical reference for product verification and procurement review.
External technical reference for product verification and procurement review.
External technical reference for product verification and procurement review.
Review power, space, environment, network, consumable or facility requirements where applicable.
Confirm exact-unit photographs, identification labels, condition and functional evidence before dispatch.
Coordinate export packing, insured freight and shipment documentation for approved destinations.
Plan installation, commissioning, training or local technical support where required and available.
Answers distinguish product-family information from the serial-specific configuration that must be confirmed in the quotation.
Only the items written in the final quotation should be considered included. Many aesthetic systems were sold in multiple handpiece, wavelength and software configurations.
No. Cleared or authorized indications, labeling and accessory availability can vary by market. Buyers should confirm local requirements before clinical use.
Review the exact revision, shot/pulse count where available, handpiece condition, cooling system, optics, software, service history, safety accessories and availability of ongoing technical support.
Confirm the exact model and serial label, condition, included accessories, installed options or software where applicable, power requirements, documentation and the destination-country requirements shown in the written quotation.
No. Configuration can vary by production revision, installed options, accessories and prior service history. The serial-number-specific quotation and packing list should take precedence over generic product-family information.
International B2B shipment can be arranged subject to destination-country import rules, carrier restrictions and any product-specific transport requirements. Freight and insurance terms should be confirmed before payment.
Review available manufacturer documentation, model labels, compatibility information and regional requirements before ordering. Manufacturer names and trademarks are used for product identification.
Exact-model details, configuration and documentation are reviewed before commercial confirmation.
Freight options, export packing and shipment documentation for approved destinations.
Support for configuration checks, installation planning and procurement documentation.
Written quotation, packing scope, delivery terms and warranty conditions before order approval.
Include delivery country, quantity, required configuration and target purchase date.
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