Regulatory & Market Access

Regulatory status differs by country, and a device approved in one market is not automatically approved in another. MedyMar supports market access with honest, per-market registration references and the paperwork procurement teams and ministries ask for.

What we provide

• Registration references for products registered in Oman, Rwanda and each East African market as approvals complete.
• Conformity documentation — CE certificates, ISO 13485 certificates, declarations of conformity and instructions for use.
• Manufacturer authorisation letters for tenders that require them.
• Registration-file support for manufacturers entering our markets, where offered.

Our disclosure policy

Where a product is pending registration in your country, we say so before you buy rather than implying approval. Read more under Registrations and Authenticity & traceability.

For the current status of a specific product in your market, contact us with the product name and destination.