AirLife™ Reduced Heparin Arterial Blood Sampler - SFDA Registration ME0000002202SFDAA00060

Access comprehensive regulatory information for AirLife™ Reduced Heparin Arterial Blood Sampler 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 ME0000002202SFDAA00060 and manufactured by CareFusion.

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.