Kyrgyzstan
REGULATORY AUTHORITY: 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 and III.

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 January 10 2018.



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