Keep Standard and Optional Wavelengths Separate
The DEPELITE legacy page publishes 1064 and 532 nm and separately describes 755, 1320, 585, and 650 nm as customized wavelength language. A comparison should identify which wavelengths are included in the offered configuration, which require a separate option, and which handpiece or accessory is associated with each confirmed choice. Do not present every listed value as one standard package.
Use the current signed specification to confirm the 350 ps pulse width, 1–10 Hz frequency, 20–3,000 mJ energy range, 2–10 mm spot size, input voltage, and power. Keep those values attached to the exact DEPELITE quotation rather than mixing them with another picosecond or Q-switch system.
Turn Interface Features Into Demonstration Questions
The page describes SP, PTP, and MP interface modes, suggestions for 11 items, a seven-joint articulated arm, and more than 30 self-check points. Ask the supplier to demonstrate the functions included in the offered unit and explain the operating materials used for training. A feature label is useful for structuring the demonstration, but it does not by itself establish a clinical outcome or local intended use.
Record the interface version, included handpieces, articulated-arm configuration, accessories, operating language, and self-check information shown during the demonstration. Distributors should also agree on the route for escalating software, accessory, or technical questions from clinic customers.
Prepare a Traceable DEPELITE Purchase Record
A focused inquiry includes the destination market, buyer type, intended professional service category, operator setting, expected quantity, preferred configuration, and required documents. Ask for current size and weight, packing information, delivery terms, training, warranty coverage, maintenance communication, and spare-parts availability.
Before using DEPELITE information in sales material, compare every public value and option with the current model document. Keep optional wavelengths clearly labeled and remove any statement that implies an unverified medical result or market authorization. The quotation, signed specification, accessory list, and applicable document set should control the final purchasing and publication record.
When comparing quotations, list the included wavelengths, handpieces, articulated arm, interface functions, accessories, and training materials in separate rows. This prevents optional wavelength language or a demonstration accessory from being carried into the final comparison as part of the standard package.
