IDS Ltd.

IDS PICO PREMIUM Picosecond Laser

Officially documented 300 ps picosecond Nd:YAG platform

Overview

IDS describes PICO PREMIUM as a picosecond Nd:YAG platform with a 300 ps pulse duration, six handpieces and six wavelengths. The official page also documents a fractional hexagonal-lens handpiece. Confirm the exact supplied configuration and regional documentation.

Manufacturer-Documented Platform Features

  • 300 ps pulse duration reported by IDS
  • Six handpieces
  • Six wavelengths described in manufacturer material
  • Fractional hexagonal-lens handpiece

Technical Specifications

ManufacturerIDS Ltd.
ModelPICO PREMIUM
TechnologyPicosecond Nd:YAG laser
Pulse duration300 ps, manufacturer-reported
HandpiecesSix
Wavelength optionsSix described by IDS; confirm supplied set
Primary sourceIDS official PICO PREMIUM page

Procurement and Cost Review

  • Confirm every wavelength and handpiece included
  • Request documented pulse and output testing
  • Include optics, service and downtime in ownership cost
  • Require training and model-matched local evidence

Regulatory and Certification Evidence

NEES Medical does not publish a model-specific Pakistan authorization or certification document for this device on this page. Request the current declaration or certificate, issuer, standard, scope, model match and validity details before purchase.

Manufacturer Source

Specifications above were checked against the manufacturer page on 2026-09-02. Source pages can change; the signed quotation and model documentation should control the purchase.

IDS official PICO PREMIUM page

Questions to Ask Before Purchase

Is the listed configuration final?

No. Confirm the exact model, handpieces, accessories, software and consumables in the signed quotation.

What evidence should a clinic request?

Request manufacturer documentation, model-matched Pakistan authorization evidence, warranty terms, training scope and service coverage.

Does this page guarantee treatment outcomes?

No. Manufacturer-described features do not replace professional training, patient assessment, local requirements or the supplied device instructions.