Togo medical device regulations
Official sources linkedMinistère de la Santé / DPML 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 |
|---|---|---|---|---|
| Loi n° 2009-007 du 15 mai 2009 | Code de la santé publique de la République togolaise Complete 57-page Gazette publication supplied by Togo’s official trade-information portal. Book IV includes the medical-device title, notably Articles 378–379, within the broader statutory framework for medicines, medical devices and pharmacy. OCR preserves the original French two-column publication. This source is the original 2009 expression, not an asserted current consolidation. | General | — | Official |
| Avis n° 005/2026/OTR/CG/CDDI/DEL | Conditions d’importation et d’enlèvement des médicaments et autres produits de santé Complete original one-page customs notice signed 4 June 2026 and published by OTR on 8 June. Expressly includes medical devices and recalls two cumulative import conditions: a marketing/commercialisation authorisation and importer approval, or a special import authorisation from the pharmacy director; removal also requires a pharmacy-director release authorisation. Cites national Customs Code Law 2018-007 and Ministerial Order 304/2025 of 31 December 2025. This notice is an implementation original, not the missing complete text of that ministerial order; publication, signature and retrieval dates are distinguished. | Registration | — | 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.
Continue from regulations into practical research
Keep Togo as the target market while you move into registration records, classification, cross-country product research, or pathway planning.
Compare products across markets
Search the same product in multiple country registries.
Build a registration plan
Estimate pathway, government fees, preparation, and review time.
Build a reusable product master
Structure company, product, model, approval, and evidence facts once.
Map dossier reuse and deltas
Compare existing evidence against Togo needs.
Build a market-launch workpaper
Connect route, evidence, labels, representatives, and launch dependencies.
Assess a regulatory change
Test a current Ministère de la Santé / DPML update against one product and its evidence.