In this episode of LATAM MedTech Insights, we explore the intricate details of Mexico's medical device labeling standard, NOM-137-SSA1-2008. As one of Latin America's largest MedTech markets, Mexico presents a huge opportunity, but access is strictly controlled by its regulatory body, COFEPRIS. We break down the most common mistakes foreign manufacturers make, from language requirements to the specific data that must be present on your packaging. Learn how to navigate the nuances of primary versus secondary labels, the correct way to use supplementary stickers, and why your local distributor's information is a critical component for avoiding customs delays. Case Study: Imagine your multi-million dollar shipment of medical devices, fully approved in the US and EU, gets stuck indefinitely in Mexican customs. The reason? A single line of missing text on a small sticker. We explore a real-world scenario where a simple labeling mistake involving the distributor's address cost a company months of delays and significant financial loss—a completely avoidable problem. Key questions answered in this episode: 1. Why is simply translating my existing label into Spanish not enough for COFEPRIS?. 2. What specific information about my Mexican distributor must be on the packaging?. 3. How do labeling rules differ for primary sterile packaging versus the outer box?. 4. Can I use stickers to add Mexican requirements, and what are the rules to avoid rejection?. 5. What is a Sanitary Registration number and where must it appear on my label?. 6. Are there upcoming changes to NOM-137 that I need to be aware of right now?. 7. How must the 'Hecho en' (Made in) information be formatted to ensure compliance?. Pure Global offers end-to-end regulatory consulting for MedTech and IVD companies, combining local expertise with advanced AI to streamline global market access. Let us help you navigate the complexities of markets like Mexico. Contact us at [email protected] or visit https://pureglobal.com/ to learn more.