Landolt Raspatory - SFDA Registration ME0000006290SFDAA00129

Access comprehensive regulatory information for Landolt Raspatory 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 ME0000006290SFDAA00129 and manufactured by RZ-Medizintechnik GmbH.

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.