Medical Device Registration in Uzbekistan

UZ NOW coordinates registration work for foreign medical device manufacturers and suppliers that need an organized local process and one accountable point of contact in Uzbekistan.

What we coordinate

• Product scope and documentation readiness review
• Registration pathway and dossier planning with qualified local specialists
• Translations, formalities and local evidence where required
• Liaison with specialists, laboratories and authorities as applicable
• Submission workflow, follow-up and issue tracking
• Importer, distributor and launch preparation after registration

How the work starts

We review the product family, intended use, manufacturer documents and existing approvals. CE marking, EU certification or FDA clearance can support the assessment but do not automatically replace local requirements.

The exact route, documents, timing and local roles depend on the device. UZ NOW is not a government authority and does not guarantee approval.

Frequently asked questions

Does a foreign manufacturer need a local company in Uzbekistan?

The suitable structure depends on the product, registration route, importer and commercial model. We clarify the roles before a filing plan is agreed.

How long does medical device registration take?

Timing depends on the device, classification, dossier readiness and any local review or testing requirements. A working schedule is prepared after the initial assessment.