Omnifilm - SFDA Registration ME0000001558SFDAA00239

Access comprehensive regulatory information for Omnifilm 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 ME0000001558SFDAA00239 and manufactured by PAUL HARTMANN AG.

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.