Medical Device Registration and Approval in Mexico

General country-specific regulatory information is provided on this page for medical device registration and approval in Mexico.

We review our Regulatory Information frequently; please check back often for updates

Medical Device Regulations and Classification in Mexico


Federal Commission for the Protection against Sanitary Risk (Comisión Federal para la Protección contra Riesgos Sanitarios) (COFEPRIS)



Medical Devices/IVDs: I/II/III



Standard Route

3-6 months (excluding time to respond feedback/request from COPEFRIS). The anticipated timeline during the COVID-19 pandemic, however, has increased to 10-12 months.

Expedited Route (Third Party Route-TPR)

2-5 months (excluding time to respond feedback/request from COPEFRIS).

Equivalency Route (Applicable for all medical devices approved in the US, Canada, and Japan):

3-8 months (excluding time to respond feedback/request from COPEFRIS).

Specific Route for certain Class I (Low-Risk Medical Devices) products

1-3 months.



Testing performed outside of Mexico according to International standards is accepted, however, for some devices such as condoms, x-ray /radiation equipment, HIV/HCV/HPV test kits, and the surface antigen of Hepatitis B, in-country testing is required before submitting the registration to COFEPRIS.

Local clinical trial is not required because Clinical data from countries outside of Mexico is generally acceptable. For the US and Canada equivalency route, summaries of clinical data are acceptable. While for the Japan equivalency route, clinical data is not required.



Standard/Equivalency Route:

Class I – USD 630

Class II – USD 920

Class III – USD 1170

Expedited Route:

Fees vary from USD 2935 – USD 5870 as it set by the third party and depending on the device classification.


LOCAL FEES (Manufacturer): 

No manufacturer review fees are required.



As of mid-December 2021, an initial product registration license will be issued with 5 years validity and it will become indefinite (no expiry date) after the first renewal, however, license must still be renewed every 5 years.

For the second renewal and forward, only notification is required unless there are product safety issues which requires product change and/or COPEFRIS requests more technical documents to be submitted.

Renewals must be submitted under the same route as the original registration, no later than 270 calendar days before the expiration date.



License transfers are possible in Mexico. The procedure for the transfer of rights will follow what is established for the modifications to the registration conditions.



Foreign manufacturers without a location in Mexico must appoint a License Holder (LH) authorized by the COFEPRIS through an “Operation Notice” (Aviso de Funcionamiento).

Other North American Countries: CanadaUnited States of America

Last Update January 2023

Blue and grey circles used in Licensale logo

For detailed device-specific compliance information for each market, including Mexico, to expedite the preparation of your medical device or IVD registration application.


Did you know you can onboard your medical device or IVD compliance information to our system in less than 15 minutes?

And, in less than a minute, you can start your device-specific registration application and a complete county-specific registration process in this country or any of the other 140+ countries available for you through the Arazy Group Medtech registration platform.

Ready to Get Started?