We are entering the final phase to incorporate UDI-DI coding for Class IIa medical devices in Colombia.

According to legislation, the requirement to include the corresponding UDI-DI coding for products registered before February 2024 will expire on February 8, 2026.

Failure to incorporate the UDI-DI coding within the established term will result in the inability to commercialize the product in Colombia, as INVIMA will consider the registration noncompliant with current regulatory requirements.

We encourage you to review your portfolio to confirm that all Class IIa product registrations comply with this requirement and remain aligned with INVIMA’s regulatory standards. 

If you require support in verifying or submitting your UDI-DI coding, our team is available to guide you through each step of the process.