Infrastructure and Medical Device Administration
IMDA- EN
- Infrastructure and Medical Device Administration
- VI
- Cục Hạ tầng và Thiết bị y tế
- JA
- Cục Hạ tầng và Thiết bị y tế（IMDA）
The MOH directorate responsible for medical-device regulation — separate from DAV. Issues Class C/D marketing authorisation certificates, runs the Reference-Country fast-track, maintains the foreign-manufacturer registry, and issues the Vietnamese CFS for device exports.
Contact
- Portal
- https://imda.moh.gov.vn
- Address
- 138A Giảng Võ, phường Kim Mã, quận Ba Đình, Hà Nội
- Hotline
- +84 24 6273 2272
Additional links
- Legacy DMEC portal — https://dmec.moh.gov.vn
- Legal documents hub — https://imda.moh.gov.vn/van-ban-phap-quy
Regulatory scope
IMDA was renamed in 2025 from the prior Cục Cơ sở Hạ tầng và Thiết bị y tế. The current portal imda.moh.gov.vn went live on 1 January 2025; the legacy dmec.moh.gov.vn portal ran in parallel through end-2024. Legal basis: Decree 98/2021/NĐ-CP as amended by Decrees 07/2023 and 04/2025.
- Last reviewed:
- 2026-06-28
- Page updated:
- 2026-06-28