Nasal Postpac - SFDA Registration ME0000000294SFDAA00081

Access comprehensive regulatory information for Nasal Postpac in the Saudi Arabia medical device market through Pure Global AI's free database. This Class I device is registered with Saudi Arabia SFDA under registration number ME0000000294SFDAA00081 and manufactured by Medtronic XOMED, Inc.

This page provides complete registration details including product category (MD), manufacturer information, model details, and regulatory compliance data from the official Saudi Arabia SFDA medical device database. Pure Global AI offers free access to Saudi Arabia's complete medical device registry, helping global MedTech companies navigate SFDA regulations efficiently.