Sao Tome and Principe medical device regulations
Official sources linkedMinistério da Saúde rules and guidance for medical device market access, registration, and lifecycle compliance. Each code opens a metadata page with the official source and readable HTML when available.
| Code | Regulation | Category | Effective | Provenance |
|---|---|---|---|---|
| Lei n° 09/2018 | Lei Base de Saúde Complete sixteen-page official health law preserved by WHO. Article 24 expressly includes the production, sale, import and export of medical devices within pharmaceutical activity and subjects it to ministerial discipline and supervision. This is a framework health law, not a device-specific registration procedure. The two-column Gazette is extracted in column reading order. | General | — | Official |
Exports carry source + retrieval dateWhat these codes are
Each row above represents one regulatory instrument. Its code is the authority’s identifier. A regulation page collects the metadata and official source; when readable HTML is available, article links can open and highlight the exact cited passage.
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