Medical devices are regulated by the State Department of Medicine Provision and Medical Equipment, under the Kyrgyz Republic Ministry of Health. CLASSIFICATION SYSTEM:
Kyrgyzstan follows the EU model of risk-based classification into Classes I, IIa, IIb, III, and IV. TIMEFRAME:
The approval process takes between one and six months, depending on the documentation and class of the device. LICENSE VALIDITY:
Licenses are valid for five years. AUTHORIZED REPRESENTATIVE:
An authorized representative is required.
Last updated on February 9 2015.
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