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Medical devices are regulated by the State Department of Medicine Provision and Medical Equipment, under the Kyrgyz Republic Ministry of Health.
Kyrgyzstan follows the EU model of risk-based classification into Classes I, IIa, IIb and III.
The approval process takes between one and six months, depending on the documentation and class of the device.
Licenses are valid for five years.
An authorized representative is required.
Last updated on January 10 2018.
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