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Uzbekistan Medical Device Registration2026 Field Guide

Resolution 738, the 155-working-day clock, and the 5-year certificate — with dossier language and practical notes.

Registration clock
155 WDs
Feb 2026 reset
Res. 738
Certificate validity
5 yrs

Sourced from Uzbek regulatory guidance and verified 2026 publications.

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What's inside

Five pages, zero fluff

Every figure in this guide traces to a named source — Uzbek regulatory guidance and verified 2026 publications.

The Resolution 738 reset

Resolution 738 (effective 26 Feb 2026) rewrites state registration — with 4 safety levels and clinical-trial-backed decisions under Decree PF-137.

The 155-working-day clock

155 working days from filing to decision (remarks excluded) — practice: 6–9 months, Class III up to a year, 5-year validity.

Dossier language and notes

English dossier with Russian translation, Uzbek/Russian IFU, and no retail-sales license — retail runs on notification.

Sources & scope

  • omcmedical.com, Uzbekistan Medical Device Registration | MoH.
  • zenodo.org, MPHAPP analysis of Presidential Decree PF-137 (Aug 19, 2025).
  • Arazy Group, Uzbekistan Regulatory Update — March 2026 (YouTube).

This guide is market-access intelligence, not regulatory or legal advice. Uzbek timelines, fees, and review practice change — professional review is required before business use.

Market Access Strategy Session

Uzbekistan on your roadmap? Start with the full picture.

A Market Access Strategy Session maps your Uzbek route — Resolution 738 sequencing, clinical-trial and GMP readiness, and renewal planning.

Professional review is required before business use.