Medical Device Regulatory Requirements in Nepal
| Regulatory Authority |
Department of Drug Administration (DDA) |
| Regulatory Authority Website Link |
Click Here
|
| Device Classification |
Not yet classified |
| Medical Device Regulations |
Health Technology Product an Medical Device Directive 2074
| Click Here
|
| Requirement of Authorized Representative |
Yes |
| Language Requirement |
Labels must be in 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 We are not responsible for errors, omissions, or outdated content.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