URETERO-RENO FIBERSCOPE - SFDA Registration ME0000002522SFDAA00173

Access comprehensive regulatory information for URETERO-RENO FIBERSCOPE in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIa device is registered with Saudi Arabia SFDA under registration number ME0000002522SFDAA00173 and manufactured by Olympus Medical Systems Corp..

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.