Uzbekistan · Horizon published 12 Oct 2026 · Source published 24 November 2025 · Reviewed 12 Oct 2026
Uzbekistan clarifies medical-device registration requirements
Uzbekistan’s official resources set out state registration, a State Register and category-specific application routes for medical devices and equipment. The framework provides manufacturers, regulatory teams and prospective local representatives with a clear starting point for preparing a product-specific Uzbekistan health-market file.
Verified facts
- Uzbekistan’s legal database publishes Cabinet of Ministers Resolution No. 738 of 24 November 2025 on procedures for state registration of medicines and medical equipment, with subsequent amendments shown in the current text.
- The official REGMED portal describes state registration for medical devices and medical equipment, identifies the State Center for Pharmaceutical Products Safety as the relevant executive body and distinguishes some category-specific pathways and exceptions.
- The Unified Portal of Interactive Public Services describes a medical-device registration service, cites the registration legal basis and displays service information. Its general timing and fee information do not decide a particular device file or outcome.
- The Center for Pharmaceutical Products Safety publishes State Register material and 2026 supplements. A register must be checked against the exact product, manufacturer, model, status and current amendment rather than inferred from similar products.
- The World Bank’s 2025 health-system strategy proposal provides independent context for reform and service needs, but it does not establish an adopted procurement, buyer, funding package, product demand or supplier route.
Horizon view
The decision-relevant unit is an exact product and intended use with a defined manufacturer, applicant or representative, regulatory dossier, current register position, import and quality path, facility or user context and contracting route. The official resources make it possible to structure preparation early, while registration, import handling, clinical use, procurement, servicing and payment remain distinct workstreams.
Commercial implication and next step
Before approaching a hospital, importer or public buyer, create a product file containing intended use, device classification, model and accessories, manufacturer evidence, quality-system documentation, labelling/instructions, authorised applicant or local role, current registration/register check, import/customs questions, storage and service model, clinical/technical acceptance, facility diligence, procurement authority, price/payment, warranty, adverse-event and recall processes. Seek current specialist confirmation for the actual product and parties. Do not ship samples, make clinical or registration claims, appoint a distributor, use patient data or describe a buyer route on the basis of a portal or policy source alone.
What to verify before acting
The sources do not establish product registration, exemption, import permission, customs clearance, certificate, clinical acceptance, manufacturer inspection result, hospital demand, procurement, buyer authority, supplier eligibility, price, payment, contract or transaction. This is not Uzbekistan medical-device, pharmaceutical, clinical, regulatory, customs, procurement, tax, data-protection, insurance or legal advice.
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