The recognition pathway explained
2026-02-10 · 4 min read
How Uzbekistan's recognition procedure differs from general registration, and which existing approvals matter.
What Changed
Uzbekistan operates a recognition procedure alongside general registration. It allows a shorter assessment where a device already holds approval from certain recognised international regulatory systems.
Who Is Affected
Manufacturers holding CE, FDA, MHRA, PMDA, MFDS approval or WHO prequalification for the device being registered in Uzbekistan.
What It Means
Where recognition applies, laboratory testing and local clinical investigation are not normally expected, and the official review period is shorter than the general route.
What Manufacturers Should Do
Confirm that the approval certificate covers the exact models and configurations you intend to register, and that the scope statement matches your intended local labelling.
Source: REGVIA regulatory practice note