Radifocus Guide Wire M - SFDA Registration ME0000000975SFDAA00162

Access comprehensive regulatory information for Radifocus Guide Wire M in the Saudi Arabia medical device market through Pure Global AI's free database. This Class III device is registered with Saudi Arabia SFDA under registration number ME0000000975SFDAA00162 and manufactured by Terumo Europe N.V..

This page provides complete registration details including product category (MD), manufacturer information, 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.