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.
ARE YOU INTERESTED IN REGISTRATION IN KYRGYZSTAN? REQUEST A FREE QUOTE>