Medical Device Regulatory Requirements in Sudan

Regulatory Authority National Medicine and Poison Board (NMPB)
Regulatory Authority Website Link Click Here
Device Classification A,B,C,D
Registration Process Medical equipment and supplies Registration | Click Here
Registration Timeline 4 months
Requirement of Authorized Representative YES
Language Requirement Labels must be in Arabic and/or English Language
Additional Information

All documents must be in English and/or Arabic
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 We are not responsible for errors, omissions, or outdated content.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/May/2025

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