Medical Device Regulatory Requirements in Kyrgyzstan
| Regulatory Authority |
Department of Medicinal Products and Medical Devices |
| Regulatory Authority Website Link |
Click Here
|
| Device Classification |
I, IIa, IIb and III |
| Medical Device Regulations |
Medical Device Regulation
| Click Here
|
| Registration Process |
Medical Device Registration
| Click Here
|
| Registration Timeline |
4 to 8 months depending on classification |
| Requirement of Authorized Representative |
Yes |
| Language Requirement |
Labels must be in Kyrgyz, and/or Russian Language |
Disclaimer: This website sources information from regulatory authorities and aims for accuracy, but regulations may change without notice. Users are advised to verify details with relevant authorities before making compliance decisions. We are not responsible for errors, omissions, or outdated content.
The above information is last updated on 09/Apr/2025