UNIMED Procedure Pack General Pack Core Kit - SFDA Registration ME0000002294SFDAA00340

Access comprehensive regulatory information for UNIMED Procedure Pack General Pack Core Kit in the Saudi Arabia medical device market through Pure Global AI's free database. This 2 device is registered with Saudi Arabia SFDA under registration number ME0000002294SFDAA00340 and manufactured by United Medical Industries Limited Co. L.L.C.

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.