Legion PS XLPE High flexion Articular Insert - SFDA Registration ME0000009019SFDAA00171

Access comprehensive regulatory information for Legion PS XLPE High flexion Articular Insert in the Saudi Arabia medical device market through Pure Global AI's free database. This Class II device is registered with Saudi Arabia SFDA under registration number ME0000009019SFDAA00171 and manufactured by Smith & Nephew Inc..

This page provides complete registration details including product category (Medical Device), 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.