Sign up to save your podcasts
Or
Share COFEPRIS Uncovered: Comparing Mexico's Device Classification to FDA and EU Rules
Share to email
Share to Facebook
Share to X
Share to email
Share to Facebook
Share to X
Or
COFEPRIS Uncovered: Comparing Mexico's Device Classification to FDA and EU Rules
This episode provides a detailed overview of Mexico's three-tiered medical device classification system managed by COFEPRIS. We explore how Class I, Class II, and Class III devices are defined by risk and highlight the key differences between Mexico's framework and the systems used by the US FDA and the European Union. Understanding these nuances is the critical first step for successful market entry.
- How does Mexico's COFEPRIS classify medical devices?
- What are the three risk-based classes for medical devices in Mexico?
- Is there a special category for low-risk Class I devices in Mexico?
- Can a device's US FDA classification be used for registration in Mexico?
- How does Mexico's 3-class system differ from the EU's 4-class model?
- Why is it a mistake to assume classifications are the same across regions?
- Which regulation governs device classification in Mexico?
- What determines the regulatory pathway and cost for market access in Mexico?
Pure Global offers end-to-end regulatory consulting for MedTech and IVD companies, streamlining global market access with local expertise and advanced AI tools. We act as your local representative in over 30 markets, developing efficient regulatory strategies and using AI to compile and submit technical dossiers. Our integrated approach allows a single registration process to access multiple markets, saving you time and resources. To accelerate your global expansion and ensure ongoing compliance, visit us at https://pureglobal.com, contact [email protected], or explore our FREE AI tools and database at https://pureglobal.ai.
View all episodes
By Pure GlobalThis episode provides a detailed overview of Mexico's three-tiered medical device classification system managed by COFEPRIS. We explore how Class I, Class II, and Class III devices are defined by risk and highlight the key differences between Mexico's framework and the systems used by the US FDA and the European Union. Understanding these nuances is the critical first step for successful market entry.
- How does Mexico's COFEPRIS classify medical devices?
- What are the three risk-based classes for medical devices in Mexico?
- Is there a special category for low-risk Class I devices in Mexico?
- Can a device's US FDA classification be used for registration in Mexico?
- How does Mexico's 3-class system differ from the EU's 4-class model?
- Why is it a mistake to assume classifications are the same across regions?
- Which regulation governs device classification in Mexico?
- What determines the regulatory pathway and cost for market access in Mexico?
Pure Global offers end-to-end regulatory consulting for MedTech and IVD companies, streamlining global market access with local expertise and advanced AI tools. We act as your local representative in over 30 markets, developing efficient regulatory strategies and using AI to compile and submit technical dossiers. Our integrated approach allows a single registration process to access multiple markets, saving you time and resources. To accelerate your global expansion and ensure ongoing compliance, visit us at https://pureglobal.com, contact [email protected], or explore our FREE AI tools and database at https://pureglobal.ai.