Registrations

MedyMar registers products market by market, and we publish our status honestly — we do not make blanket, pan-regional approval claims. Regulatory requirements differ by country, and a device approved in one market is not automatically approved in another.

How we handle registration

• Per-market status. Registration is pursued and listed for each country individually — Oman, Rwanda and each East African market as it is completed.
• Clear disclosure. Where a product is pending registration in your country, we tell you before you buy rather than implying approval.
• Documentation on request. Registration certificates and supporting documents are available for procurement and tender files.

Current status by market

Registration status is maintained per country and updated as approvals complete. For the current status of a specific product in your market, contact us through the Contact page or the Tender Desk and we will provide the relevant documentation.

Medical-device advertising and registration are reviewed for compliance in each market before any clinical claim is made.