Ellex 2RT for professional procurement
Ellex 2RT is an ophthalmic laser cleared in the United States under 510(k) K122202. Published device literature describes a short-pulse 532 nm ophthalmic laser platform; exact treatment parameters and indications should be confirmed against the supplied unit, software revision and local labeling.
Evaluate the exact Ellex 2RT configuration
Ellex 2RT is an ophthalmic laser cleared in the United States under 510(k) K122202. Published device literature describes a short-pulse 532 nm ophthalmic laser platform; exact treatment parameters and indications should be confirmed against the supplied unit, software revision and local labeling.
This listing is prepared for professional B2B procurement. Confirm the exact serialised unit, installed software, probes/handpieces/accessories, power requirements, regulatory labeling and included documentation before purchase.
Three steps before purchase
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.
Review the product and supplied configuration
Reference images support model identification. The final quotation should match the exact unit, accessories and condition being supplied.
Product capabilities and procurement-relevant details
Product-specific facts below are preserved from the researched listing; configuration-sensitive items should be verified against the exact supplied unit.
Ophthalmic laser platform
Ophthalmic laser platform
FDA 510(k) K122202
FDA 510(k) K122202
Published 532 nm treatment wavelength
Published 532 nm treatment wavelength
Short-pulse laser architecture
Short-pulse laser architecture
Designed for professional ophthalmic use
Designed for professional ophthalmic use
Where this product can fit
Suitability depends on the exact configuration, professional use case, manufacturer instructions and destination-market requirements.
Professional ophthalmic laser workflow
Confirm suitability for the intended workflow before deployment.
Retinal/ophthalmic applications within cleared/local labeling
Confirm suitability for the intended workflow before deployment.
Replacement or system procurement
Confirm suitability for the intended workflow before deployment.
Product data for purchasing review
Exact specifications can vary by revision, region and installed options. The serial-number-specific configuration and manufacturer documentation take precedence.
- Brand / model
- Ellex 2RT
- Device class
- Ophthalmic laser
- FDA clearance
- K122202
- Published wavelength
- 532 nm
- Published pulse duration
- Approximately 3 ns in device literature
- Published spot size
- 400 µm in device literature
- Product entity
- Ellex 2RT
- Manufacturer / brand
- Ellex
- Manufacturer model
- 2RT
- Device type
- Laser – Yag
- A — Regulatory/clinical registry
- U.S. FDA device/regulatory record
- A — Manufacturer/official
- Quantel Medical / Ellex official product resource
- Brand
- 2RT, Ellex
- SKU
- MED-2RT
Confirm the complete supplied configuration
The final commercial offer defines what is included. For high-value or configuration-sensitive equipment, request an itemized packing list before payment.
Quotation should confirm
- Exact model and serial-number label.
- Installed options, software revision and licensed features.
- Included probes, handpieces, cables, footswitches, accessories and consumables.
- Power input, plug type and compatibility with the destination facility.
- Functional test results, preventive-maintenance/service history and available manuals.
- Local regulatory, import, installation and professional-use requirements.
Condition and compatibility
- Current photographs should match the supplied unit.
- Model, serial and part-number labels should be readable.
- Required accessories and host-system compatibility should be confirmed.
- Service, maintenance or functional-test information should be reviewed where applicable.
- Power, plug, facility and installation requirements should match the destination.
Exact package contents and condition are controlled by the written quotation and order documentation.
Review authoritative documentation before purchase
Use manufacturer, regulatory and technical references to validate product-family information. The exact supplied unit still requires serial-specific verification.
www.accessdata.fda.gov
External technical reference for product verification and procurement review.
Quantel Medical / Ellex official product resource
External technical reference for product verification and procurement review.
Support from quotation to delivery
Site readiness
Review power, space, environment, network, consumable or facility requirements where applicable.
Inspection coordination
Confirm exact-unit photographs, identification labels, condition and functional evidence before dispatch.
Global logistics
Coordinate export packing, insured freight and shipment documentation for approved destinations.
Handover support
Plan installation, commissioning, training or local technical support where required and available.
Frequently asked questions
Answers distinguish product-family information from the serial-specific configuration that must be confirmed in the quotation.
Is Ellex 2RT in stock?
Yes. AI Robot Supplier currently lists this product as in stock. Confirm the exact configuration and shipping destination when requesting the commercial invoice.
Does every unit have the same configuration?
No. Medical and scientific equipment can vary by production year, software, installed modules and accessories. The final quotation should identify the supplied configuration.
Can this equipment be shipped internationally?
International B2B shipment can be arranged subject to destination-country import, carrier and regulatory requirements.
What this product is
Ellex 2RT is an ophthalmic laser cleared in the United States under 510(k) K122202. Published device literature describes a short-pulse 532 nm ophthalmic laser platform; exact treatment parameters and indications should be confirmed against the supplied unit, software revision and local labeling.
What should be confirmed before ordering Ellex 2RT?
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.
Does every Ellex 2RT have the same configuration?
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.
2RT product documentation
Review available manufacturer documentation, model labels, compatibility information and regional requirements before ordering. Manufacturer names and trademarks are used for product identification.
One procurement partner from quotation to delivery
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.
Request a destination-specific Ellex 2RT quote
Include delivery country, quantity, required configuration and target purchase date.
Ellex 2RT technical references and related resources
Review relevant technical references and AI Robot Supplier procurement resources before ordering.
