This episode of MENA MedTech Insights provides a detailed guide to registering a Class II medical device in Jordan. We explore the critical role of the Jordan Food and Drug Administration (JFDA) and break down the essential steps for foreign manufacturers, from appointing a local representative to compiling a compliant technical dossier. We delve into the specific documentation required, including the importance of prior approval from reference markets like the EU or USA. Learn about common pitfalls, such as translation requirements and the complex process of document legalization, which can cause significant delays if not handled correctly. **Key Takeaways From This Episode:** * Why is appointing a registered Authorized Representative your non-negotiable first step in Jordan? * Does the JFDA accept FDA 510(k) clearance, or is a CE mark mandatory for Class II devices? * What is the single most common documentation error that stalls applications with the JFDA? * Are English-only labels and Instructions for Use (IFU) sufficient for the Jordanian market? * How can improper document legalization at the embassy level halt your entire market entry strategy? * What is the realistic timeline for approval, from submission to receiving your registration certificate? * How can you leverage your existing regulatory approvals to fast-track your entry into Jordan? At Pure Global, we offer end-to-end regulatory consulting to help MedTech and IVD companies seamlessly access over 30 global markets, including Jordan. Our combination of local expertise and advanced AI tools ensures your submission is efficient and compliant. Let us be your strategic partner in global expansion. Contact us at [email protected] or visit https://pureglobal.com/ to learn more.